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Crystal structures of 2,3,7,8,12,13,17,18-octa­bromo-5,10,15,20-tetra­kis­(penta­fluoro­phen­yl)porphyrin as the chloro­form monosolvate and tetra­hydro­furan monosolvate

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aSchool of Chemistry, Trinity Biomedical Science Institute, 152–160 Pearse Street, Trinity College Dublin, The University of Dublin, Dublin 2, Ireland
*Correspondence e-mail: sengem@tcd.ie

Edited by B. Therrien, University of Neuchâtel, Switzerland (Received 16 December 2019; accepted 14 January 2020; online 17 January 2020)

The crystal structures of the title compounds, two solvates (CHCl3 and THF) of a symmetric and highly substituted porphyrin, C44H2Br8F20N4 or OBrTPFPP, are described. These structures each feature a non-planar porphyrin ring, exhibiting a similar conformation of the strained ring independent of solvent identity. These distorted porphyrins are able to form hydrogen bonds and sub-van der Waals halogen inter­actions with enclathrated solvent; supra­molecular inter­actions of proximal macrocycles are additionally affected by solvent choice. The crystal studied for compound 1·CHCl3 was refined as an inversion twin. One penta­fluoro­phenyl group was modelled as disordered over two sites [occupancy ratio = 0.462 (7):0.538 (7)]. The chloro­form solvate was also modelled as disordered over two orientations [occupancy ratio = 0.882 (7): 0.118 (7).

1. Chemical context

Highly substituted porphyrins are a subclass of porphyrin compounds where the meso and β positions are substituted with non-H atoms. When large substituents are introduced to the periphery of the porphyrin ring, this tends to overcrowd the macrocycle and induce conformational distortion, increasing with the steric demand (Senge & Kalisch, 1997[Senge, M. O. & Kalisch, W. W. (1997). Inorg. Chem. 36, 6103-6116.]; Medforth et al., 1992[Medforth, C. J., Senge, M. O., Smith, K. M., Sparks, L. D. & Shelnutt, J. A. (1992). J. Am. Chem. Soc. 114, 9859-9869.]). Among the most studied substitution patterns are those with variously functionalized aryl rings at the 5,10,15,20-positions and with halogen, alkane and aryl substituents at the 2,3,7,8,12,13,17,18-positions (Senge, 2000[Senge, M. O. (2000). The Porphyrin Handbook, edited by K. M. Kadish, K. M. Smith and S. R. Guillard; Vol. 1, pp. 239-347; Academic Press, San Diego.], 2006[Senge, M. O. (2006). Chem. Commun. pp. 243-256.])

There are numerous approaches used to introduce conformational distortion to porphyrins, including coordination of specific metal centers, incorporation of a strapping motif, or decorating the ring with sterically demanding substituents (Schindler et al., 2018[Schindler, J., Kupfer, S., Ryan, A. A., Flanagan, K. J., Senge, M. O. & Dietzek, B. (2018). Coord. Chem. Rev. 360, 1-16.]; Senge, 2006[Senge, M. O. (2006). Chem. Commun. pp. 243-256.]). Recent publications show uses for distorted porphyrins as free-base catalysts and sensors, and these compounds demonstrate unique and tuneable porphyrin inner core inter­actions (Aoki et al., 2019[Aoki, E., Suzuki, W., Kotani, H., Ishizuka, T., Sakai, H., Hasobe, T. & Kojima, T. (2019). Chem. Commun. 55, 4925-4928.]; Norvaiša et al., 2019[Norvaiša, K., Flanagan, K. J., Gibbons, D. & Senge, M. O. (2019). Angew. Chem. Int. Ed.]; Kielmann et al., 2019[Kielmann, M., Grover, N., Kalisch, W. W. & Senge, M. O. (2019). Eur. J. Org. Chem. pp. 2448-2452.]; Kielmann & Senge, 2019[Kielmann, M. & Senge, M. O. (2019). Angew. Chem. Int. Ed. 58, 418-441.]). For example, non-planar metal-free porphyrins show promise as organocatalysts, acting as hydrogen-bond donors (Kielmann et al., 2019[Kielmann, M., Grover, N., Kalisch, W. W. & Senge, M. O. (2019). Eur. J. Org. Chem. pp. 2448-2452.]). Moreover, the porphyrin scaffold is customizable, and the potential for tuneable basicity and catalytic activity based on variable substitution patterns has been explored (Roucan et al., 2017[Roucan, M., Kielmann, M., Connon, S. J., Bernhard, S. S. R. & Senge, M. O. (2017). Chem. Commun. 54, 26-29.]). The distortion of the porphyrin ring, when compared to the planar parent compound, affects the photophysical and electronic properties of both free-base macrocycles and of derived metal complexes (Parusel et al., 2000[Parusel, A. B. J., Wondimagegn, T. & Ghosh, A. (2000). J. Am. Chem. Soc. 122, 6371-6374.]; Gentemann et al., 1994[Gentemann, S., Medforth, C. J., Forsyth, T. P., Nurco, D. J., Smith, K. M., Fajer, J. & Holten, D. (1994). J. Am. Chem. Soc. 116, 7363-7368.]; Röder et al., 2010[Röder, B., Büchner, M., Rückmann, I. & Senge, M. O. (2010). Photochem. Photobiol. Sci. 9, 1152-1158.]). With this in mind, halogenated porphyrins specifically are of inter­est as ligands in catalytic metal complexes, owing to non-planar conformation, as well as the electron-deficient character of the porphyrin ring (Dolphin et al., 1997[Dolphin, D., Traylor, T. G. & Xie, L. Y. (1997). Acc. Chem. Res. 30, 251-259.]; Henling et al., 1993[Henling, L. M., Schaefer, W. P., Hodge, J. A., Hughes, M. E., Gray, H. B., Lyons, J. E. & Ellis, P. E. (1993). Acta Cryst. C49, 1743-1747.]).

[Scheme 1]

The title compound has been previously characterized as a di­chloro­benzene solvate (Takeuchi et al., 1994[Takeuchi, T., Gray, H. B. & Goddard, W. A. (1994). J. Am. Chem. Soc. 116, 9730-9732.]). Structural differences between this literature compound and the structures presented herein arise from inter­molecular inter­actions with chloro­form and THF. Additionally, in the published structure, the solvent could not be adequately modelled. These three structures are compared below.

2. Structural commentary

The crystal structure of the title compound (2,3,7,8,12,13,17,18-octa­bromo-5,10,15,20-tetra­kis­(penta­fluoro­phen­yl)por­phyrin mono­chloro­form solvate, (1·CHCl­3) shows a single H2OBrTPFPP mol­ecule and one chloro­form solvate in the asymmetric unit. This highly substituted porphyrin ring exhibits peri inter­actions from the appended bromine atoms crowding with penta­fluoro­phenyl rings, forcing the bromine atoms substanti­ally out of the mean plane of the porphyrin ring at a mean deviation of 2.14 (14) Å. One of these penta­fluoro­phenyl rings is disordered over two positions, related by a co-planar shift; the co-crystallized CHCl3 is also disordered over two orientations. A view of the mol­ecular structure of H2OBrTPFPP is shown in Fig. 1[link].

[Figure 1]
Figure 1
View of the mol­ecular structure of the main residue of 1·CHCl3; displacement ellipsoids are drawn at the 50% probability level. A second disordered orientation of the C151–156 ring and the solvent chloro­form mol­ecule are omitted for clarity.

A second crystal structure of (2,3,7,8,12,13,17,18-octa­bromo-5,10,15,20-tetra­kis­(penta­fluoro­phen­yl)porphyrin mono­tetra­hydro­furan solvate (1·THF) displays essentially the same conformation of the macrocycle; differences in the packing of these compounds are discussed below. The Δ24 values, a summation of atomic deviations from mean plane of the macrocycle are similar in 1·CHCl­3 and 1·THF; a view of the skeletal deviations from the mean-plane in the crystal structure of these two compounds is shown in Fig. 4[link]b.

[Figure 4]
Figure 4
(a) Diagram of porphyrin mol­ecules which are used for comparison within this text. (b) Comparative mean-plane deviations of compounds 1·CHCl3 and 1·THF. (c) Comparative mean-plane deviations for atoms within the β-octa-substituted 5,10,15,20-tetra­kis­(penta­fluoro­phen­yl)porphyrin structures H2X8TPFPP [2: X = H (HALZUP), 3: X = F (GODYON), 4: X = Cl (ZALHUP), 1·C6H4Cl2: X = Br (ZALJEB)]. (d) Comparative mean-plane deviations for atoms within structures with the formula H2[EtxH8 - x(TPP)]: 6: x = 2 (TATPOT01), 7: x = 4 (TATPUZ01), 8: x = 6 (TATQEK01), 9: x = 8 (SATQOU).

Normal Structure Decomposition (NSD, Jentzen et al., 1995[Jentzen, W., Simpson, M. C., Hobbs, J. D., Song, X., Ema, T., Nelson, N. Y., Medforth, C. J., Smith, K. M., Veyrat, M., Mazzanti, M., Ramasseul, R., Marchon, J., Takeuchi, T., Goddard, W. A. III & Shelnutt, J. A. (1995). J. Am. Chem. Soc. 117, 11085-11097.]; Schindler et al., 2018[Schindler, J., Kupfer, S., Ryan, A. A., Flanagan, K. J., Senge, M. O. & Dietzek, B. (2018). Coord. Chem. Rev. 360, 1-16.]) analysis is the standard method of comparing the mode and extent of distortion between porphyrin structures. NSD is the decomposition of the atomic coordinates of a porphyrin into defined in-plane and out-of-plane distortion modes, based on a least-squares fit of the atomic coordinates to the calculated lowest frequency vibrational modes. The porphyrin rings of the title compounds are shown to exhibit significant out-of-plane saddle-type [B2u (min)] distortion in both crystal structures reported here. This saddling distortion is a direct result of large substituents appended to the porphyrin ring – the saddle distortion allevi­ates steric demand by removing the restraint of co-planarity from the Br and aryl groups. Slight isotropic contraction, or bre mode distortion, of this porphyrin ring when projected into the xy-plane [A1g (min)] is an effect of the large skewing, or pyrrole tilt – the reported Cl8TPFPP and F8TPFPP porphyrins do not show this A1g contraction with similar bond distances reported, as shown in Table 3[link] and Fig. 5[link].

Table 3
Calculated mean distances, angles and structural parameters (Å, °) for compounds 1–6

Measured mean bond distances, angles, mean-plane angles, calculated NSD values, intra­molecular contacts and mean-plane deviations for atom groups.

  Br8TPFPP·CHCl3 Br8TPFPP1·THF H8TPFPP·dioxane F8TPFPP Cl8TPFPP Br8TPFPP·C6H4Cl2 Br8TPP·DMF
  1·CHCl3 1·THF 2 3 4 1·C6H4Cl2 6
  This work This work (HALZUP; Dog- (GODYON; Leroy (ZALHUP; Birn- (ZALJEB; Birn- (RONROB; Spyr-
      utan et al., 2010[Dogutan, D. K., Bediako, D. K., Teets, T. S., Schwalbe, M. & Nocera, D. G. (2010). Org. Lett. 12, 1036-1039.]) et al., 1999[Leroy, J., Bondon, A. & Toupet, L. (1999). Acta Cryst. C55, 464-466.]) baum et al., 1995[Birnbaum, E. R., Hodge, J. A., Grinstaff, M. W., Schaefer, W. P., Henling, L., Labinger, J. A., Bercaw, J. E. & Gray, H. B. (1995). Inorg. Chem. 34, 3625-3632.]) baum et al., 1995[Birnbaum, E. R., Hodge, J. A., Grinstaff, M. W., Schaefer, W. P., Henling, L., Labinger, J. A., Bercaw, J. E. & Gray, H. B. (1995). Inorg. Chem. 34, 3625-3632.]) oulias et al., 1997[Spyroulias, G. A., Despotopoulos, A., Raptopoulou, C. P., Terzis, A. & Coutsolelos, A. G. (1997). Chem. Commun. pp. 783-784.])
Bond lengths
N—Ca 1.368 (7) 1.366 (6) 1.358 1.370 1.372 1.367 1.362
Ca—Cb 1.440 (20) 1.450 (2) 1.450 1.438 1.448 1.457 1.435
Ca—Cm 1.406 (10) 1.408 (4) 1.395 1.399 1.402 1.406 1.415
Cb—Cb 1.361 (10) 1.357 (12) 1.345 1.332 1.347 1.349 1.348
               
Bond angles
N—Ca—Cm 123.1 (7) 123.7 (12) 126.1 126.6 125.4 124.5 123.1
N—Ca—Cb 110.0 (6) 110.0 (6) 108.8 107.5 107.2 108.1 107.5
Ca—N—Ca 109.0 (4) 109.0 (3) 108.1 108.7 109.5 108.7 109.4
Ca—Cm—Ca 123.0 (9) 123.8 (7) 125.8 125.4 125.7 123.4 120.9
Ca—Cb—Cb 107.4 (12) 107.5 (9) 107.1 108.1 108.0 107.4 107.7
Cm—Ca—Cb 129.0 (2) 128.3 (14) 125.0 125.9 127.2 127.1 129.3
               
Pyrrole mean-plane incline angles
<pyrN21 27.8 25.6 0.7 3.1 14.6 25.6 39.1
<pyrN22 26.9 29.5 0.4 3.4 15.7 20.4 39.1
<pyrN23 36.9 36.5 0.7 3.1 14.9 25.6 39.1
<pyrN24 32.1 22.3 0.4 3.4 14.0 20.4 39.1
Mean(<pyr) 30.0 28.5 0.6 3.2 14.8 23.0 39.1
               
Structural parameters
Δipa 0.59 (11) 0.42 (10) 0.182 (12) 0.23 (2) 0.07 (4) 0.31 (7) 0.8 (2)
Δoopb 3.46 (7) 3.17 (7) 0.01 (9) 0.246 (8) 1.91 (2) 2.73 (5) 3.790 (120)
N21⋯N22 2.866 (3) 2.43 (5) 2.927 2.921 2.943 2.923 2.958
N22⋯N23 2.931 (3) 2.32 (5) 2.895 2.942 2.939 2.86 2.958
N23⋯N24 2.895 (3) 2.61 (6) 2.927 2.921 2.942 2.923 2.958
N24⋯N21 2.928 (3) 2.60 (6) 2.895 2.942 2.925 2.86 2.958
Δ24c 0.543 0.497 0.008 0.046 0.308 0.442 0.616
ΔNd 0.075 0.090 0.018 0.046 0.088 0.077 0.034
ΔCme 0.036 0.017 0.009 0.061 0.009 0.091 0.317
ΔCaf 0.418 0.379 0.007 0.029 0.250 0.339 0.409
ΔCbg 1.156 1.060 0.005 0.055 0.626 0.903 1.264
(a) Simulated total in-plane distortion; (b) simulated total out-of-plane distortion; (c) average deviation from the least-squares plane of the 24-macrocycle atoms; (d) simulated displacement of the four inter­nal nitro­gen atoms from the 24-atom mean plane; (e) average deviation of the meso-carbon atoms from the 24-atom mean plane; (f) Average deviation of the α-carbon atoms from the 24-atom mean plane; (g) Average deviation of the β-carbon atoms from the 24-atom mean plane.
[Figure 5]
Figure 5
NSD analysis of the β-octa-substituted 5,10,15,20-tetra­kis­(penta­fluoro­phen­yl)porphyrin structures H2X8TPFPP (X = H, F, Cl, Br, Br, Br).

3. Supra­molecular features

In 1·CHCl3, solvent chloro­form mol­ecules are nestled between two adjacent porphyrin rings and disordered over two similar orientations. In the dominant orientation, CHCl3 mol­ecules show weak C—H⋯N inter­actions (≃2.7 Å H⋯N) to imine pyrrole rings of one porphyrin, and Cl⋯π inter­actions (≃3.3 Å) as well as Cl⋯F contact (≃3.0 Å) to an adjacent porphyrin (Table 1[link]). These inter­actions are shown in Fig. 2[link].

Table 1
Hydrogen-bond geometry (Å, °) for 1·CHCl3[link]

D—H⋯A D—H H⋯A DA D—H⋯A
N21—H21⋯N22 0.88 2.34 2.866 (3) 119
N21—H21⋯N24 0.88 2.42 2.928 (3) 117
N23—H23⋯N22 0.88 2.48 2.931 (3) 113
N23—H23⋯N24 0.88 2.46 2.895 (3) 111
[Figure 2]
Figure 2
Inter­actions between 1·CHCl3 and enclathrated chloro­form solvate, showing proximal Cl⋯F and C—H⋯N inter­actions, indicated by dashed lines. Only the major occupancy component of the chloroform solvent is shown.

This solvent-mediated supra­molecular motif serves to arrange the porphyrin rings directly above and below one another, in an approximately face-to-face arrangement. As a result of this arrangement, the porphyrin mol­ecules form stacks which extend along the b-axis direction. The adjacent stacks of porphyrin units in the ac direction inter­digitate with one another, as shown in Fig. 3[link].

[Figure 3]
Figure 3
Packing diagram showing the inter­digital arrangement of adjacent stacks of 1·CHCl3. The chloroform solvent is not shown.

In 1·THF, the central core of the porphyrin displays traditional hydrogen bonding (Table 2[link]) from one pyrrole group to the THF oxygen atom [N⋯O 2.849 (6) Å], with a longer distance to the other available pyrrole N—H group (N⋯O = 3.8 Å). The THF solvate is not observed to form similar bimodal intra­molecular inter­actions as the chloro­form solvate, and porphyrin mol­ecules do not form the infinite stacking arrangements seen in 1·CHCl3. The porphyrin mol­ecules display multiple halogen–halogen inter­actions from the bromine and fluorine atoms in both structures.

Table 2
Hydrogen-bond geometry (Å, °) for 1·THF[link]

D—H⋯A D—H H⋯A DA D—H⋯A
N22—H22⋯O25 0.97 (1) 1.92 (2) 2.849 (6) 158 (5)

4. Database survey

Previous structures of H2X8-F20TPP·solvent have been described for X = H (Birnbaum et al., 1995[Birnbaum, E. R., Hodge, J. A., Grinstaff, M. W., Schaefer, W. P., Henling, L., Labinger, J. A., Bercaw, J. E. & Gray, H. B. (1995). Inorg. Chem. 34, 3625-3632.]; Dogutan et al., 2010[Dogutan, D. K., Bediako, D. K., Teets, T. S., Schwalbe, M. & Nocera, D. G. (2010). Org. Lett. 12, 1036-1039.]), F (Leroy et al., 1999[Leroy, J., Bondon, A. & Toupet, L. (1999). Acta Cryst. C55, 464-466.]), Cl (Birnbaum et al., 1995[Birnbaum, E. R., Hodge, J. A., Grinstaff, M. W., Schaefer, W. P., Henling, L., Labinger, J. A., Bercaw, J. E. & Gray, H. B. (1995). Inorg. Chem. 34, 3625-3632.]), and Br (Birnbaum et al., 1995[Birnbaum, E. R., Hodge, J. A., Grinstaff, M. W., Schaefer, W. P., Henling, L., Labinger, J. A., Bercaw, J. E. & Gray, H. B. (1995). Inorg. Chem. 34, 3625-3632.]) (Fig. 4[link]a). The increasing distortion of macrocycles with increasingly larger halogens can be observed in the plot of skeletal deviations shown in Fig. 4[link]c.

The macrocycle structures of 1·CHCl3 and 1·THF can be directly compared to the previous structure 1·C6H4Cl2; these three structures all exhibit approximately the same macrocycle bond distances and angles, shown in Table 3[link]. The supra­molecular inter­actions of 1·C6H4Cl2 could not be reliably determined given that the solvent was only partially modelled in the reported structure. The face-to-face stacking centroid-to-centroid distance of porphyrin macrocycles in 1·C6H4Cl2 was 6.93 Å, whereas for 1·CHCl3, the separation was 6.83 Å. It is additionally possible that the solvent in the former case was in fact di­chloro­methane, which was present in the crystallization solution and displays a similar Cl⋯Cl separation.

The NSD analysis parameters of similar literature structures are summarized in Fig. 5[link], as a comparator to the structures in this work. The NSD parameter, in Å, is equal to one quarter of the sum of the displacements of all 24 atoms of the simplified distortion model, which can be attributed to this distortion mode; the error value shown is the sum error (δoop) of the least-squares fit of all six lowest frequency modes. As expected, an increasing saddle-type distortion is found for increasing size of the halogen atom, with little deviation from planarity apparent where X = H or F [sad = −0.001 (9) Å (H) and 0.000 (0) Å (F)]. Significant saddling distortion was apparent for X = Cl [sad = 1.91 (2) Å], and greater for X = Br [1·C6H4Cl2 sad = 2.72 (5) Å, 1·CHCl3 sad = 3.45 (7) Å and 1·THF sad = 3.16 (7)], showing the dependence of distortion on steric bulk, which outweighs solvent contributions.

Analogous studies of porphyrins with increasing steric demand have observed increasing distortion for the porphyrin structures (eth­yl)x-5,10,15,20-tetra­phenyl­porphyrin (X = 2, 4, 6, or 8; Fig. 4[link]a) (Senge & Kalisch, 1997[Senge, M. O. & Kalisch, W. W. (1997). Inorg. Chem. 36, 6103-6116.]; Kielmann et al., 2019[Kielmann, M., Grover, N., Kalisch, W. W. & Senge, M. O. (2019). Eur. J. Org. Chem. pp. 2448-2452.]); comparatively, this result shows that this manner of distortion is not dependent on inductive contributions from the halogen atoms (Fig. 4[link]a and 4d). The non-fluorinated analogue structure 2,3,7,8,12,13,17,18-octa­bromo-5,10,15,20-tetra­phenyl­porphyrin (5, Spyroulias et al., 1997[Spyroulias, G. A., Despotopoulos, A., Raptopoulou, C. P., Terzis, A. & Coutsolelos, A. G. (1997). Chem. Commun. pp. 783-784.]; Fig. 4[link]a and Table 3[link]) shows slightly greater distortion [sad = 3.68 (12) Å] and similar bond lengths to the title compounds. These observations would imply that the inductive or steric contribution of the fluoro substituents is negligible in causing increased distortion of the macrocycle.

5. Synthesis and crystallization

This compound was synthesized by a previously reported procedure (Mandon et al., 1992[Mandon, D., Ochsenbein, P., Fischer, J., Weiss, R., Jayaraj, K., Austin, R. N., Gold, A., White, P. S., Brigaud, O., Battioni, P. & Mansuy, D. (1992). Inorg. Chem. 31, 2044-2049.]). Crystallization was performed by slow evaporation of a partially covered homogeneous solution at room temperature; of chloro­form for 1·CHCl3 and THF for 1·THF.

6. Refinement

Crystal data, data collection and structure refinement details are summarized in Table 4[link].

Table 4
Experimental details

  1·CHCl3 1·THF
Crystal data
Chemical formula C44H2Br8F20N4·CHCl3 C44H2Br8F20N4·C4H8O
Mr 1725.14 1677.88
Crystal system, space group Monoclinic, P21 Monoclinic, P21/n
Temperature (K) 100 100
a, b, c (Å) 15.5162 (7), 6.8288 (3), 24.5631 (12) 21.524 (9), 9.545 (4), 26.020 (11)
β (°) 104.683 (1) 107.426 (7)
V3) 2517.6 (2) 5101 (4)
Z 2 4
Radiation type Mo Kα Mo Kα
μ (mm−1) 6.65 6.41
Crystal size (mm) 0.31 × 0.30 × 0.11 0.42 × 0.11 × 0.09
 
Data collection
Diffractometer Bruker APEXII CCD Bruker APEXII CCD
Absorption correction Multi-scan (SADABS; Bruker, 2016[Bruker (2016). SADABS, Bruker AXS Inc., Madison, WI, USA.]) Multi-scan (SADABS; Bruker, 2016[Bruker (2016). SADABS, Bruker AXS Inc., Madison, WI, USA.])
Tmin, Tmax 0.458, 0.746 0.455, 0.746
No. of measured, independent and observed [I > 2σ(I)] reflections 107677, 18291, 17164 148293, 12689, 10079
Rint 0.028 0.082
(sin θ/λ)max−1) 0.758 0.668
 
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.020, 0.043, 1.03 0.054, 0.095, 1.21
No. of reflections 18291 12689
No. of parameters 763 908
No. of restraints 244 718
H-atom treatment H-atom parameters constrained H atoms treated by a mixture of independent and constrained refinement
     
Δρmax, Δρmin (e Å−3) 0.52, −0.46 1.63, −0.98
Absolute structure Refined as an inversion twin.
Absolute structure parameter 0.010 (4)
Computer programs: APEX3 (Bruker, 2017[Bruker (2017). APEX3. Bruker AXS Inc., Madison, WI, USA.]), SAINT (Bruker, 2015[Bruker (2015). SAINT. Bruker AXS Inc., Madison, WI, USA.]), SHELXT (Sheldrick, 2015a[Sheldrick, G. M. (2015a). Acta Cryst. A71, 3-8.]), SHELXL (Sheldrick, 2015b[Sheldrick, G. M. (2015b). Acta Cryst. C71, 3-8.]), Shelxle (Hübschle et al., 2011[Hübschle, C. B., Sheldrick, G. M. & Dittrich, B. (2011). J. Appl. Cryst. 44, 1281-1284.]) and OLEX2 (Dolomanov et al., 2009[Dolomanov, O. V., Bourhis, L. J., Gildea, R. J., Howard, J. A. K. & Puschmann, H. (2009). J. Appl. Cryst. 42, 339-341.]).

Compound 1·CHCl3 was refined as an inversion twin, with a Flack parameter of 0.010 (4), indicating a small inversion impurity in the single crystal. The penta­fluoro­phenyl group bound to C5 was modelled as disordered over two equivalent [0.462 (7):0.538 (7)] coplanar positions, displaced by ≃0.3 Å at the centroid, which were constrained to have equal Uij parameters for atoms sharing sites, similar Uij parameters for bonded atoms, and idealized ring geometry. The most distant fluorine atoms had to be held to additional isotropic Uij restraints. The chloro­form solvate was also modelled as disordered over two orientations, sharing approximate carbon and hydrogen positions. This second orientation was related by a partial rotation around the threefold axis and modelled such that these two orientations had a sum occupancy of one mol­ecule. The dominant orientation was refined to 0.882 (7) occupancy, and C—Cl distances in the minor component had to be restrained to idealized bond distances. C atoms were held to equal Uij restraints and Cl atoms were restrained to similar Uij parameters.

In compound 1·THF penta­fluoro­phenyl rings were modelled as disordered over two orientations with dominant orientations of 0.748 (18) and 0.694 (17) occupancy. Porphyrin-to-phenyl distances and carbon atom displacement parameters (Uij) were restrained. Idealized geometric constraints were imposed on the least occupied phenyl ring C10A–C10F. The ipso phenyl carbon atoms were constrained to have equal Uij parameters and positions. Pyrrole hydrogen atoms were located in the difference-Fourier map and restrained using idealized bond distances.

Supporting information


Computing details top

For both structures, data collection: APEX3 (Bruker, 2017); cell refinement: SAINT (Bruker, 2015); data reduction: SAINT (Bruker, 2015); program(s) used to solve structure: SHELXT (Sheldrick, 2015a); program(s) used to refine structure: SHELXL (Sheldrick, 2015b); molecular graphics: Shelxle (Hübschle et al., 2011); software used to prepare material for publication: OLEX2 (Dolomanov et al., 2009).

2,3,7,8,12,13,17,18-Octabromo-5,10,15,20-tetrakis(pentafluorophenyl)porphyrin chloroform monosolvate (1_CHCl3) top
Crystal data top
C44H2Br8F20N4·CHCl3F(000) = 1624
Mr = 1725.14Dx = 2.276 Mg m3
Monoclinic, P21Mo Kα radiation, λ = 0.71073 Å
a = 15.5162 (7) ÅCell parameters from 9974 reflections
b = 6.8288 (3) Åθ = 2.6–32.5°
c = 24.5631 (12) ŵ = 6.65 mm1
β = 104.683 (1)°T = 100 K
V = 2517.6 (2) Å3Block, blue
Z = 20.31 × 0.30 × 0.11 mm
Data collection top
Bruker APEXII CCD
diffractometer
18291 independent reflections
Radiation source: microfocus sealed X-ray tube, graphite-monochromated17164 reflections with I > 2σ(I)
Mirror optics monochromatorRint = 0.028
Detector resolution: 7.9 pixels mm-1θmax = 32.6°, θmin = 1.4°
φ and ω scansh = 2323
Absorption correction: multi-scan
(SADABS; Bruker, 2016)
k = 1010
Tmin = 0.458, Tmax = 0.746l = 3736
107677 measured reflections
Refinement top
Refinement on F2Hydrogen site location: inferred from neighbouring sites
Least-squares matrix: fullH-atom parameters constrained
R[F2 > 2σ(F2)] = 0.020 w = 1/[σ2(Fo2) + (0.0025P)2 + 1.005P]
where P = (Fo2 + 2Fc2)/3
wR(F2) = 0.043(Δ/σ)max = 0.002
S = 1.03Δρmax = 0.52 e Å3
18291 reflectionsΔρmin = 0.46 e Å3
763 parametersAbsolute structure: Refined as an inversion twin.
244 restraintsAbsolute structure parameter: 0.010 (4)
Primary atom site location: dual
Special details top

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/UeqOcc. (<1)
C10.79032 (16)0.5406 (4)0.87273 (10)0.0134 (4)
Br10.87104 (2)0.43518 (5)0.99180 (2)0.02349 (6)
C20.86821 (16)0.5046 (4)0.91809 (10)0.0152 (4)
Br21.05536 (2)0.43897 (5)0.93835 (2)0.02288 (6)
C30.94138 (16)0.5053 (4)0.89661 (10)0.0153 (4)
Br31.06413 (2)0.81653 (4)0.70329 (2)0.02160 (6)
C40.91257 (15)0.5427 (4)0.83707 (10)0.0132 (4)
Br40.92250 (2)0.68017 (4)0.57534 (2)0.01783 (5)
C50.96138 (16)0.5753 (4)0.79756 (10)0.0145 (4)
Br50.67971 (2)0.08433 (4)0.56768 (2)0.02307 (5)
C60.92364 (15)0.5776 (4)0.73877 (10)0.0134 (4)
F60.94084 (10)0.1746 (3)0.61796 (6)0.0201 (3)
Br60.49352 (2)0.08753 (4)0.62177 (2)0.02119 (5)
C70.96548 (16)0.6523 (4)0.69563 (10)0.0154 (4)
F70.98329 (10)0.0661 (3)0.52270 (7)0.0227 (3)
Br70.37497 (2)0.69017 (4)0.73639 (2)0.01604 (5)
C80.91110 (16)0.5994 (4)0.64558 (10)0.0139 (4)
F80.86376 (11)0.1210 (3)0.42128 (7)0.0246 (4)
Br80.51364 (2)0.86107 (4)0.86350 (2)0.01969 (5)
C90.83861 (15)0.4866 (3)0.65798 (10)0.0133 (4)
F90.70704 (11)0.3005 (3)0.41561 (6)0.0247 (3)
C100.77912 (15)0.3636 (4)0.62036 (10)0.0139 (4)
F100.66599 (10)0.4240 (3)0.51083 (6)0.0229 (3)
C110.70159 (15)0.2861 (4)0.63184 (10)0.0137 (4)
F110.41703 (10)0.4175 (3)0.58292 (6)0.0224 (3)
C120.64841 (16)0.1194 (4)0.60940 (10)0.0150 (4)
F120.24742 (11)0.2960 (3)0.54385 (7)0.0268 (4)
C130.57470 (16)0.1181 (4)0.63059 (10)0.0149 (4)
F130.16081 (11)0.1268 (3)0.61447 (9)0.0321 (4)
C140.57932 (15)0.2834 (4)0.66693 (10)0.0130 (4)
F140.24506 (11)0.0721 (3)0.72457 (8)0.0270 (4)
C150.51835 (15)0.3577 (3)0.69576 (10)0.0127 (4)
F150.41634 (10)0.1838 (2)0.76383 (6)0.0196 (3)
C160.54601 (15)0.4764 (3)0.74374 (10)0.0126 (4)
F160.59460 (13)0.3120 (3)0.91627 (7)0.0328 (4)
C170.49068 (15)0.6028 (3)0.76885 (10)0.0138 (4)
F170.54619 (14)0.3700 (4)1.01268 (8)0.0471 (6)
C180.54346 (15)0.6649 (4)0.81857 (10)0.0141 (4)
F180.60364 (13)0.6916 (4)1.07618 (7)0.0433 (5)
C190.63021 (15)0.5740 (4)0.82428 (10)0.0133 (4)
F190.71156 (14)0.9551 (4)1.04248 (8)0.0435 (5)
C200.70187 (16)0.5724 (4)0.87352 (10)0.0140 (4)
F200.76215 (12)0.8962 (3)0.94747 (8)0.0315 (4)
N210.82117 (13)0.5520 (3)0.82522 (8)0.0122 (3)
H210.7864010.5639720.7909970.015*
N220.84463 (13)0.4908 (3)0.71443 (8)0.0129 (4)
N230.65875 (13)0.3736 (3)0.66794 (8)0.0136 (4)
H230.6797010.4752960.6891860.016*
Cl1S0.8289 (3)1.0578 (6)0.84825 (15)0.0405 (6)0.882 (7)
F51.0834 (12)0.304 (4)0.7761 (9)0.0289 (15)0.462 (7)
F41.2643 (6)0.3383 (11)0.8118 (4)0.0363 (11)0.462 (7)
F31.3335 (5)0.6633 (11)0.8705 (3)0.0379 (10)0.462 (7)
F21.2238 (5)0.9445 (11)0.8947 (3)0.0382 (11)0.462 (7)
F11.0460 (9)0.900 (3)0.8631 (7)0.0303 (14)0.462 (7)
C1S0.7822 (3)1.0817 (7)0.7756 (2)0.0287 (9)0.882 (7)
H0.7628291.2208370.7678730.034*0.882 (7)
Cl2S0.68818 (11)0.9313 (2)0.75235 (8)0.0489 (5)0.882 (7)
Cl3S0.86152 (16)1.0294 (2)0.73764 (8)0.0461 (4)0.882 (7)
N240.63172 (13)0.4721 (3)0.77706 (8)0.0132 (4)
C511.0608 (6)0.603 (3)0.8183 (10)0.0210 (7)0.462 (7)
C521.0984 (7)0.767 (2)0.8488 (8)0.0255 (12)0.462 (7)
C531.1905 (7)0.7875 (14)0.8658 (6)0.0287 (14)0.462 (7)
C541.2450 (6)0.6439 (12)0.8522 (5)0.0292 (14)0.462 (7)
C551.2074 (9)0.4800 (15)0.8217 (6)0.0280 (13)0.462 (7)
C561.1154 (9)0.460 (2)0.8047 (8)0.0241 (9)0.462 (7)
C2S0.770 (2)1.107 (6)0.7747 (14)0.0287 (9)0.118 (7)
HA0.7634291.2507250.7666300.034*0.118 (7)
C51B1.0594 (5)0.616 (2)0.8184 (8)0.0210 (7)0.538 (7)
C52B1.0853 (6)0.793 (2)0.8456 (7)0.0255 (12)0.538 (7)
C53B1.1752 (6)0.8393 (12)0.8646 (5)0.0287 (14)0.538 (7)
C54B1.2393 (5)0.7081 (11)0.8564 (4)0.0292 (14)0.538 (7)
C55B1.2134 (7)0.5311 (12)0.8292 (5)0.0280 (13)0.538 (7)
C56B1.1235 (8)0.4852 (18)0.8102 (7)0.0241 (9)0.538 (7)
F1B1.0276 (8)0.927 (2)0.8547 (6)0.0303 (14)0.538 (7)
F2B1.2028 (4)1.0127 (9)0.8910 (3)0.0382 (11)0.538 (7)
F3B1.3255 (4)0.7480 (10)0.8757 (3)0.0379 (10)0.538 (7)
F4B1.2721 (5)0.4032 (10)0.8213 (3)0.0363 (11)0.538 (7)
F5B1.0987 (10)0.315 (4)0.7843 (8)0.0289 (15)0.538 (7)
C1010.80163 (15)0.3017 (4)0.56770 (10)0.0137 (4)
C1020.88211 (16)0.2099 (4)0.56870 (10)0.0148 (4)
C1030.90484 (16)0.1527 (4)0.52009 (11)0.0158 (4)
C1040.84515 (17)0.1824 (4)0.46866 (10)0.0180 (4)
C1050.76466 (16)0.2730 (4)0.46601 (10)0.0171 (5)
C1060.74383 (15)0.3321 (4)0.51480 (10)0.0159 (4)
C1510.42329 (15)0.3018 (4)0.67476 (10)0.0127 (4)
C1520.37698 (16)0.3310 (4)0.61870 (10)0.0156 (4)
C1530.28927 (17)0.2728 (4)0.59851 (11)0.0188 (5)
C1540.24496 (15)0.1857 (4)0.63424 (12)0.0206 (5)
C1550.28786 (16)0.1582 (4)0.69014 (12)0.0189 (5)
C1560.37625 (16)0.2150 (4)0.70987 (10)0.0149 (4)
C2010.67914 (16)0.6031 (4)0.92807 (10)0.0167 (5)
C2020.62418 (17)0.4721 (4)0.94653 (11)0.0214 (5)
C2030.59867 (19)0.5003 (5)0.99606 (12)0.0291 (7)
C2040.62785 (19)0.6622 (6)1.02837 (11)0.0306 (7)
C2050.68316 (19)0.7956 (5)1.01145 (12)0.0276 (6)
C2060.70860 (18)0.7645 (4)0.96233 (11)0.0212 (5)
Cl4S0.8187 (18)0.975 (3)0.7296 (6)0.069 (4)0.118 (7)
Cl5S0.6705 (9)0.989 (2)0.7786 (10)0.068 (5)0.118 (7)
Cl6S0.839 (2)1.047 (5)0.8409 (12)0.049 (6)0.118 (7)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
C10.0128 (10)0.0167 (10)0.0107 (10)0.0011 (8)0.0027 (8)0.0002 (8)
Br10.02061 (12)0.03766 (15)0.01195 (10)0.00155 (11)0.00370 (9)0.00789 (11)
C20.0145 (11)0.0201 (11)0.0109 (10)0.0009 (8)0.0028 (8)0.0020 (8)
Br20.01293 (10)0.03700 (15)0.01655 (11)0.00356 (11)0.00026 (8)0.00561 (11)
C30.0113 (10)0.0210 (11)0.0123 (10)0.0005 (8)0.0005 (8)0.0023 (8)
Br30.01564 (11)0.03080 (14)0.01819 (12)0.01240 (10)0.00399 (9)0.00174 (10)
C40.0095 (9)0.0170 (10)0.0118 (10)0.0019 (8)0.0001 (8)0.0004 (8)
Br40.01723 (11)0.02391 (11)0.01397 (10)0.00445 (10)0.00694 (8)0.00244 (9)
C50.0118 (10)0.0193 (11)0.0127 (10)0.0041 (8)0.0037 (8)0.0012 (8)
Br50.02230 (12)0.02245 (12)0.02858 (13)0.00561 (10)0.01408 (10)0.01180 (10)
C60.0099 (9)0.0176 (10)0.0126 (10)0.0019 (8)0.0023 (8)0.0002 (8)
F60.0148 (6)0.0309 (8)0.0135 (7)0.0038 (7)0.0017 (5)0.0026 (6)
Br60.01599 (11)0.01999 (12)0.02962 (13)0.00840 (10)0.00952 (9)0.00895 (10)
C70.0120 (10)0.0205 (12)0.0142 (10)0.0053 (8)0.0041 (8)0.0001 (8)
F70.0154 (7)0.0339 (9)0.0219 (8)0.0074 (7)0.0103 (6)0.0043 (7)
Br70.01161 (10)0.01818 (10)0.01770 (11)0.00211 (9)0.00253 (8)0.00019 (9)
C80.0120 (10)0.0191 (11)0.0116 (10)0.0025 (8)0.0047 (8)0.0023 (8)
F80.0231 (8)0.0395 (10)0.0144 (7)0.0028 (7)0.0105 (6)0.0013 (6)
Br80.01666 (11)0.02534 (12)0.01741 (11)0.00252 (9)0.00493 (9)0.00738 (9)
C90.0100 (10)0.0175 (10)0.0128 (10)0.0026 (8)0.0037 (8)0.0001 (8)
F90.0191 (7)0.0417 (10)0.0109 (7)0.0042 (7)0.0004 (6)0.0005 (7)
C100.0106 (9)0.0192 (10)0.0121 (10)0.0008 (8)0.0035 (8)0.0003 (8)
F100.0136 (6)0.0366 (9)0.0176 (7)0.0075 (7)0.0026 (5)0.0001 (7)
C110.0114 (10)0.0179 (11)0.0119 (10)0.0016 (8)0.0033 (8)0.0017 (8)
F110.0190 (7)0.0339 (9)0.0147 (7)0.0046 (7)0.0046 (5)0.0036 (7)
C120.0127 (10)0.0191 (10)0.0141 (10)0.0018 (8)0.0049 (8)0.0044 (8)
F120.0194 (8)0.0364 (9)0.0186 (8)0.0014 (7)0.0059 (6)0.0008 (7)
C130.0113 (10)0.0174 (10)0.0163 (11)0.0050 (8)0.0037 (8)0.0035 (8)
F130.0092 (7)0.0391 (10)0.0436 (11)0.0090 (7)0.0015 (7)0.0024 (8)
C140.0106 (9)0.0178 (11)0.0108 (10)0.0036 (8)0.0029 (8)0.0016 (8)
F140.0167 (7)0.0310 (9)0.0364 (10)0.0066 (7)0.0128 (7)0.0085 (7)
C150.0100 (9)0.0160 (10)0.0117 (10)0.0029 (8)0.0024 (7)0.0003 (8)
F150.0187 (7)0.0241 (7)0.0160 (7)0.0034 (7)0.0044 (5)0.0046 (6)
C160.0094 (9)0.0155 (10)0.0132 (10)0.0019 (8)0.0035 (8)0.0008 (8)
F160.0387 (10)0.0377 (10)0.0246 (9)0.0199 (8)0.0130 (8)0.0029 (8)
C170.0121 (10)0.0155 (10)0.0142 (10)0.0010 (8)0.0043 (8)0.0008 (8)
F170.0390 (11)0.0824 (18)0.0253 (9)0.0214 (12)0.0179 (8)0.0062 (10)
C180.0129 (10)0.0165 (11)0.0142 (10)0.0020 (8)0.0061 (8)0.0021 (8)
F180.0316 (10)0.0870 (17)0.0141 (8)0.0069 (11)0.0110 (7)0.0063 (10)
C190.0115 (10)0.0166 (10)0.0119 (10)0.0015 (8)0.0031 (8)0.0009 (8)
F190.0423 (11)0.0587 (14)0.0298 (10)0.0051 (10)0.0096 (8)0.0288 (10)
C200.0130 (10)0.0177 (10)0.0114 (10)0.0029 (8)0.0030 (8)0.0009 (8)
F200.0314 (9)0.0332 (10)0.0319 (9)0.0137 (8)0.0119 (7)0.0134 (8)
N210.0085 (8)0.0167 (9)0.0105 (9)0.0010 (7)0.0008 (7)0.0010 (7)
N220.0103 (8)0.0171 (9)0.0109 (9)0.0028 (7)0.0022 (7)0.0005 (7)
N230.0102 (8)0.0179 (9)0.0137 (9)0.0050 (7)0.0048 (7)0.0047 (7)
Cl1S0.0756 (12)0.0204 (8)0.0225 (8)0.0033 (7)0.0072 (7)0.0020 (7)
F50.011 (4)0.043 (2)0.030 (5)0.008 (4)0.001 (3)0.002 (3)
F40.0166 (13)0.053 (3)0.041 (2)0.007 (2)0.0093 (14)0.006 (2)
F30.0136 (12)0.066 (3)0.0308 (14)0.014 (2)0.0003 (9)0.008 (2)
F20.030 (2)0.051 (3)0.0291 (13)0.0231 (19)0.0003 (16)0.007 (2)
F10.026 (4)0.038 (4)0.024 (4)0.012 (3)0.001 (3)0.009 (2)
C1S0.044 (2)0.0133 (18)0.0273 (15)0.0029 (14)0.0058 (15)0.0024 (12)
Cl2S0.0507 (7)0.0301 (6)0.0534 (9)0.0098 (5)0.0100 (6)0.0206 (6)
Cl3S0.0720 (11)0.0283 (6)0.0474 (8)0.0150 (6)0.0326 (8)0.0138 (5)
N240.0100 (8)0.0178 (9)0.0117 (9)0.0008 (7)0.0027 (7)0.0017 (7)
C510.0106 (10)0.038 (2)0.0130 (11)0.0062 (11)0.0011 (9)0.0038 (14)
C520.014 (2)0.047 (3)0.0141 (19)0.012 (2)0.000 (2)0.001 (2)
C530.019 (3)0.051 (4)0.0150 (13)0.016 (3)0.0008 (19)0.001 (3)
C540.0128 (14)0.055 (4)0.0175 (18)0.012 (3)0.0001 (13)0.007 (3)
C550.0096 (16)0.055 (4)0.019 (3)0.004 (3)0.0040 (17)0.008 (3)
C560.0091 (19)0.047 (3)0.015 (3)0.0042 (16)0.0001 (16)0.0050 (19)
C2S0.044 (2)0.0133 (18)0.0273 (15)0.0029 (14)0.0058 (15)0.0024 (12)
C51B0.0106 (10)0.038 (2)0.0130 (11)0.0062 (11)0.0011 (9)0.0038 (14)
C52B0.014 (2)0.047 (3)0.0141 (19)0.012 (2)0.000 (2)0.001 (2)
C53B0.019 (3)0.051 (4)0.0150 (13)0.016 (3)0.0008 (19)0.001 (3)
C54B0.0128 (14)0.055 (4)0.0175 (18)0.012 (3)0.0001 (13)0.007 (3)
C55B0.0096 (16)0.055 (4)0.019 (3)0.004 (3)0.0040 (17)0.008 (3)
C56B0.0091 (19)0.047 (3)0.015 (3)0.0042 (16)0.0001 (16)0.0050 (19)
F1B0.026 (4)0.038 (4)0.024 (4)0.012 (3)0.001 (3)0.009 (2)
F2B0.030 (2)0.051 (3)0.0291 (13)0.0231 (19)0.0003 (16)0.007 (2)
F3B0.0136 (12)0.066 (3)0.0308 (14)0.014 (2)0.0003 (9)0.008 (2)
F4B0.0166 (13)0.053 (3)0.041 (2)0.007 (2)0.0093 (14)0.006 (2)
F5B0.011 (4)0.043 (2)0.030 (5)0.008 (4)0.001 (3)0.002 (3)
C1010.0109 (9)0.0190 (10)0.0118 (10)0.0015 (8)0.0039 (8)0.0007 (8)
C1020.0121 (10)0.0187 (11)0.0137 (10)0.0012 (8)0.0036 (8)0.0011 (8)
C1030.0127 (10)0.0203 (12)0.0165 (11)0.0011 (8)0.0076 (8)0.0024 (8)
C1040.0187 (11)0.0232 (11)0.0139 (10)0.0010 (10)0.0078 (8)0.0004 (10)
C1050.0143 (11)0.0254 (12)0.0108 (10)0.0016 (9)0.0017 (8)0.0001 (9)
C1060.0113 (10)0.0204 (11)0.0166 (11)0.0007 (8)0.0047 (8)0.0004 (9)
C1510.0095 (9)0.0155 (10)0.0134 (10)0.0018 (8)0.0034 (8)0.0021 (8)
C1520.0137 (10)0.0190 (11)0.0141 (10)0.0026 (9)0.0036 (8)0.0008 (8)
C1530.0146 (11)0.0212 (12)0.0178 (12)0.0003 (9)0.0011 (9)0.0020 (9)
C1540.0071 (9)0.0209 (11)0.0314 (13)0.0036 (9)0.0003 (9)0.0004 (11)
C1550.0119 (10)0.0183 (12)0.0284 (13)0.0023 (9)0.0087 (9)0.0030 (10)
C1560.0129 (10)0.0165 (11)0.0161 (11)0.0003 (8)0.0053 (8)0.0005 (8)
C2010.0119 (10)0.0268 (12)0.0109 (10)0.0014 (9)0.0022 (8)0.0014 (9)
C2020.0163 (11)0.0328 (14)0.0151 (11)0.0054 (10)0.0040 (9)0.0002 (10)
C2030.0191 (13)0.054 (2)0.0155 (12)0.0046 (12)0.0070 (10)0.0053 (12)
C2040.0180 (12)0.063 (2)0.0108 (11)0.0059 (14)0.0043 (9)0.0027 (13)
C2050.0209 (13)0.0445 (17)0.0154 (12)0.0019 (12)0.0010 (10)0.0117 (12)
C2060.0163 (11)0.0303 (13)0.0172 (12)0.0024 (10)0.0045 (9)0.0051 (10)
Cl4S0.123 (11)0.048 (7)0.037 (5)0.045 (7)0.024 (7)0.015 (5)
Cl5S0.052 (6)0.044 (6)0.097 (10)0.017 (5)0.003 (6)0.036 (6)
Cl6S0.075 (10)0.025 (5)0.032 (8)0.003 (7)0.015 (8)0.010 (6)
Geometric parameters (Å, º) top
C1—C21.442 (3)F19—C2051.339 (4)
C1—C201.394 (3)C20—C2011.484 (3)
C1—N211.371 (3)F20—C2061.336 (3)
Br1—C21.861 (2)N21—H210.8800
C2—C31.368 (3)N23—H230.8800
Br2—C31.862 (2)Cl1S—C1S1.755 (5)
C3—C41.439 (3)F5—C561.30 (3)
Br3—C71.868 (2)F4—C551.372 (13)
C4—C51.392 (3)F3—C541.338 (11)
C4—N211.375 (3)F2—C531.317 (11)
Br4—C81.862 (2)F1—C521.32 (2)
C5—C61.414 (3)C1S—H1.0000
C5—C511.510 (9)C1S—Cl2S1.757 (5)
C5—C51B1.504 (8)C1S—Cl3S1.760 (5)
Br5—C121.864 (2)C51—C521.3900
C6—C71.467 (3)C51—C561.3900
C6—N221.357 (3)C52—C531.3900
F6—C1021.339 (3)C53—C541.3900
Br6—C131.862 (2)C54—C551.3900
C7—C81.352 (3)C55—C561.3900
F7—C1031.340 (3)C2S—HA1.0000
Br7—C171.868 (2)C2S—Cl4S1.75 (3)
C8—C91.458 (3)C2S—Cl5S1.76 (3)
F8—C1041.336 (3)C2S—Cl6S1.76 (3)
Br8—C181.867 (2)C51B—C52B1.3900
C9—C101.407 (3)C51B—C56B1.3900
C9—N221.366 (3)C52B—C53B1.3900
F9—C1051.344 (3)C52B—F1B1.335 (16)
C10—C111.407 (3)C53B—C54B1.3900
C10—C1011.484 (3)C53B—F2B1.366 (10)
F10—C1061.343 (3)C54B—C55B1.3900
C11—C121.432 (3)C54B—F3B1.330 (9)
C11—N231.372 (3)C55B—C56B1.3900
F11—C1521.336 (3)C55B—F4B1.312 (11)
C12—C131.371 (3)C56B—F5B1.34 (2)
F12—C1531.344 (3)C101—C1021.392 (3)
C13—C141.430 (3)C101—C1061.395 (3)
F13—C1541.335 (3)C102—C1031.384 (3)
C14—C151.412 (3)C103—C1041.379 (3)
C14—N231.372 (3)C104—C1051.380 (4)
F14—C1551.337 (3)C105—C1061.378 (3)
C15—C161.405 (3)C151—C1521.397 (3)
C15—C1511.484 (3)C151—C1561.395 (3)
F15—C1561.331 (3)C152—C1531.383 (3)
C16—C171.460 (3)C153—C1541.380 (4)
C16—N241.374 (3)C154—C1551.378 (4)
F16—C2021.336 (3)C155—C1561.389 (3)
C17—C181.354 (3)C201—C2021.389 (4)
F17—C2031.338 (4)C201—C2061.391 (4)
C18—C191.456 (3)C202—C2031.385 (4)
F18—C2041.336 (3)C203—C2041.369 (5)
C19—C201.420 (3)C204—C2051.385 (5)
C19—N241.358 (3)C205—C2061.378 (4)
C20—C1—C2130.6 (2)F3—C54—C55121.0 (6)
N21—C1—C2105.2 (2)C55—C54—C53120.0
N21—C1—C20124.1 (2)F4—C55—C54117.6 (8)
C1—C2—Br1127.12 (18)F4—C55—C56122.4 (8)
C3—C2—C1108.4 (2)C54—C55—C56120.0
C3—C2—Br1123.99 (19)F5—C56—C51122.3 (14)
C2—C3—Br2123.52 (19)F5—C56—C55117.7 (14)
C2—C3—C4108.6 (2)C55—C56—C51120.0
C4—C3—Br2127.57 (19)Cl4S—C2S—HA114.7
C5—C4—C3130.8 (2)Cl4S—C2S—Cl5S109 (2)
N21—C4—C3105.2 (2)Cl4S—C2S—Cl6S102 (2)
N21—C4—C5124.0 (2)Cl5S—C2S—HA114.7
C4—C5—C6123.8 (2)Cl6S—C2S—HA114.7
C4—C5—C51118.4 (10)Cl6S—C2S—Cl5S100 (2)
C4—C5—C51B118.3 (8)C52B—C51B—C5118.1 (9)
C6—C5—C51117.8 (10)C52B—C51B—C56B120.0
C6—C5—C51B117.9 (8)C56B—C51B—C5121.9 (9)
C5—C6—C7126.6 (2)C53B—C52B—C51B120.0
N22—C6—C5122.6 (2)F1B—C52B—C51B123.4 (10)
N22—C6—C7110.5 (2)F1B—C52B—C53B116.6 (10)
C6—C7—Br3129.58 (18)C52B—C53B—C54B120.0
C8—C7—Br3123.96 (18)F2B—C53B—C52B121.4 (6)
C8—C7—C6106.0 (2)F2B—C53B—C54B118.6 (6)
C7—C8—Br4125.40 (18)C53B—C54B—C55B120.0
C7—C8—C9106.7 (2)F3B—C54B—C53B120.5 (5)
C9—C8—Br4127.57 (18)F3B—C54B—C55B119.5 (5)
C10—C9—C8126.2 (2)C54B—C55B—C56B120.0
N22—C9—C8110.1 (2)F4B—C55B—C54B121.6 (6)
N22—C9—C10122.9 (2)F4B—C55B—C56B118.4 (7)
C9—C10—C101118.8 (2)C55B—C56B—C51B120.0
C11—C10—C9123.0 (2)F5B—C56B—C51B120.0 (11)
C11—C10—C101118.0 (2)F5B—C56B—C55B120.0 (11)
C10—C11—C12131.3 (2)C102—C101—C10121.4 (2)
N23—C11—C10123.0 (2)C102—C101—C106116.5 (2)
N23—C11—C12105.6 (2)C106—C101—C10122.1 (2)
C11—C12—Br5126.88 (18)F6—C102—C101119.9 (2)
C13—C12—Br5124.21 (19)F6—C102—C103117.7 (2)
C13—C12—C11108.3 (2)C103—C102—C101122.4 (2)
C12—C13—Br6124.44 (19)F7—C103—C102120.7 (2)
C12—C13—C14108.5 (2)F7—C103—C104120.0 (2)
C14—C13—Br6126.40 (18)C104—C103—C102119.3 (2)
C15—C14—C13131.5 (2)F8—C104—C103120.6 (2)
N23—C14—C13105.6 (2)F8—C104—C105119.5 (2)
N23—C14—C15122.9 (2)C103—C104—C105119.9 (2)
C14—C15—C151117.8 (2)F9—C105—C104119.2 (2)
C16—C15—C14121.8 (2)F9—C105—C106120.8 (2)
C16—C15—C151120.4 (2)C106—C105—C104119.9 (2)
C15—C16—C17127.5 (2)F10—C106—C101119.4 (2)
N24—C16—C15122.1 (2)F10—C106—C105118.6 (2)
N24—C16—C17110.2 (2)C105—C106—C101122.0 (2)
C16—C17—Br7127.80 (18)C152—C151—C15121.6 (2)
C18—C17—Br7125.52 (19)C156—C151—C15121.6 (2)
C18—C17—C16106.3 (2)C156—C151—C152116.8 (2)
C17—C18—Br8125.01 (18)F11—C152—C151120.2 (2)
C17—C18—C19106.6 (2)F11—C152—C153118.1 (2)
C19—C18—Br8127.61 (17)C153—C152—C151121.7 (2)
C20—C19—C18126.2 (2)F12—C153—C152120.4 (2)
N24—C19—C18110.6 (2)F12—C153—C154119.6 (2)
N24—C19—C20123.0 (2)C154—C153—C152120.0 (2)
C1—C20—C19123.4 (2)F13—C154—C153119.9 (2)
C1—C20—C201119.6 (2)F13—C154—C155120.2 (2)
C19—C20—C201117.0 (2)C155—C154—C153120.0 (2)
C1—N21—C4112.39 (19)F14—C155—C154119.9 (2)
C1—N21—H21123.8F14—C155—C156120.5 (2)
C4—N21—H21123.8C154—C155—C156119.6 (2)
C6—N22—C9106.16 (19)F15—C156—C151119.9 (2)
C11—N23—H23124.1F15—C156—C155118.3 (2)
C14—N23—C11111.9 (2)C155—C156—C151121.9 (2)
C14—N23—H23124.1C202—C201—C20120.6 (2)
Cl1S—C1S—H108.0C202—C201—C206116.6 (2)
Cl1S—C1S—Cl2S111.8 (3)C206—C201—C20122.8 (2)
Cl1S—C1S—Cl3S110.9 (3)F16—C202—C201119.9 (2)
Cl2S—C1S—H108.0F16—C202—C203117.9 (3)
Cl2S—C1S—Cl3S110.1 (3)C203—C202—C201122.2 (3)
Cl3S—C1S—H108.0F17—C203—C202120.5 (3)
C19—N24—C16105.90 (19)F17—C203—C204119.8 (3)
C52—C51—C5122.6 (11)C204—C203—C202119.7 (3)
C52—C51—C56120.0F18—C204—C203120.4 (3)
C56—C51—C5117.4 (11)F18—C204—C205119.9 (3)
F1—C52—C51119.4 (12)C203—C204—C205119.7 (3)
F1—C52—C53120.5 (11)F19—C205—C204120.2 (3)
C53—C52—C51120.0F19—C205—C206119.9 (3)
F2—C53—C52118.4 (7)C206—C205—C204119.9 (3)
F2—C53—C54121.6 (7)F20—C206—C201120.0 (2)
C52—C53—C54120.0F20—C206—C205118.1 (3)
F3—C54—C53118.9 (6)C205—C206—C201121.9 (3)
C1—C2—C3—Br2173.32 (18)C18—C19—C20—C1158.9 (3)
C1—C2—C3—C40.3 (3)C18—C19—C20—C20122.2 (4)
C1—C20—C201—C202117.1 (3)C18—C19—N24—C166.5 (3)
C1—C20—C201—C20664.9 (4)F18—C204—C205—F190.9 (5)
Br1—C2—C3—Br20.6 (3)F18—C204—C205—C206179.6 (3)
Br1—C2—C3—C4172.97 (18)C19—C20—C201—C20261.9 (3)
C2—C1—C20—C19169.3 (3)C19—C20—C201—C206116.1 (3)
C2—C1—C20—C2019.6 (4)F19—C205—C206—F200.5 (4)
C2—C1—N21—C45.1 (3)F19—C205—C206—C201178.5 (3)
C2—C3—C4—C5173.4 (3)C20—C1—C2—Br114.5 (4)
C2—C3—C4—N213.2 (3)C20—C1—C2—C3173.1 (3)
Br2—C3—C4—C513.4 (4)C20—C1—N21—C4171.1 (2)
Br2—C3—C4—N21170.02 (19)C20—C19—N24—C16167.9 (2)
C3—C4—C5—C6169.0 (3)C20—C201—C202—F163.1 (4)
C3—C4—C5—C519.0 (9)C20—C201—C202—C203177.3 (3)
C3—C4—C5—C51B12.9 (8)C20—C201—C206—F202.4 (4)
C3—C4—N21—C15.2 (3)C20—C201—C206—C205176.7 (3)
Br3—C7—C8—Br40.7 (3)N21—C1—C2—Br1169.59 (18)
Br3—C7—C8—C9174.94 (18)N21—C1—C2—C32.8 (3)
C4—C5—C6—C7165.5 (2)N21—C1—C20—C1915.5 (4)
C4—C5—C6—N2221.1 (4)N21—C1—C20—C201165.6 (2)
C4—C5—C51—C5268.3 (13)N21—C4—C5—C615.0 (4)
C4—C5—C51—C56113.2 (9)N21—C4—C5—C51167.0 (8)
C4—C5—C51B—C52B69.1 (10)N21—C4—C5—C51B163.1 (7)
C4—C5—C51B—C56B112.2 (8)N22—C6—C7—Br3169.45 (19)
Br4—C8—C9—C1022.4 (4)N22—C6—C7—C82.7 (3)
Br4—C8—C9—N22167.51 (18)N22—C9—C10—C1122.5 (4)
C5—C4—N21—C1171.6 (2)N22—C9—C10—C101153.4 (2)
C5—C6—C7—Br316.5 (4)N23—C11—C12—Br5168.58 (18)
C5—C6—C7—C8171.4 (2)N23—C11—C12—C132.6 (3)
C5—C6—N22—C9167.7 (2)N23—C14—C15—C1625.9 (4)
C5—C51—C52—F13.7 (15)N23—C14—C15—C151155.8 (2)
C5—C51—C52—C53178.5 (18)F4—C55—C56—F54 (2)
C5—C51—C56—F51.1 (18)F4—C55—C56—C51176.7 (13)
C5—C51—C56—C55178.6 (17)F3—C54—C55—F40.9 (14)
C5—C51B—C52B—C53B178.7 (15)F3—C54—C55—C56177.8 (12)
C5—C51B—C52B—F1B1.0 (13)F2—C53—C54—F32.1 (13)
C5—C51B—C56B—C55B178.6 (15)F2—C53—C54—C55179.9 (13)
C5—C51B—C56B—F5B1.6 (15)F1—C52—C53—F22.1 (17)
Br5—C12—C13—Br60.4 (3)F1—C52—C53—C54177.8 (17)
Br5—C12—C13—C14171.48 (18)N24—C16—C17—Br7169.92 (17)
C6—C5—C51—C52113.6 (10)N24—C16—C17—C183.0 (3)
C6—C5—C51—C5664.9 (12)N24—C19—C20—C127.6 (4)
C6—C5—C51B—C52B109.1 (8)N24—C19—C20—C201151.4 (2)
C6—C5—C51B—C56B69.6 (11)C51—C5—C6—C716.5 (9)
C6—C7—C8—Br4171.98 (18)C51—C5—C6—N22156.9 (8)
C6—C7—C8—C92.2 (3)C51—C52—C53—F2179.9 (12)
F6—C102—C103—F70.4 (4)C51—C52—C53—C540.0
F6—C102—C103—C104178.5 (2)C52—C51—C56—F5180 (2)
Br6—C13—C14—C1514.4 (4)C52—C51—C56—C550.0
Br6—C13—C14—N23168.31 (18)C52—C53—C54—F3177.8 (12)
C7—C6—N22—C96.7 (3)C52—C53—C54—C550.0
C7—C8—C9—C10163.6 (2)C53—C54—C55—F4176.9 (12)
C7—C8—C9—N226.5 (3)C53—C54—C55—C560.0
F7—C103—C104—F81.7 (4)C54—C55—C56—F5180 (2)
F7—C103—C104—C105179.5 (2)C54—C55—C56—C510.0
Br7—C17—C18—Br83.3 (3)C56—C51—C52—F1177.8 (17)
Br7—C17—C18—C19174.12 (17)C56—C51—C52—C530.0
C8—C9—C10—C11168.6 (2)C51B—C5—C6—C712.6 (8)
C8—C9—C10—C10115.5 (4)C51B—C5—C6—N22160.8 (7)
C8—C9—N22—C68.1 (3)C51B—C52B—C53B—C54B0.0
F8—C104—C105—F91.0 (4)C51B—C52B—C53B—F2B179.5 (10)
F8—C104—C105—C106178.2 (2)C52B—C51B—C56B—C55B0.0
Br8—C18—C19—C2020.1 (4)C52B—C51B—C56B—F5B179.8 (17)
Br8—C18—C19—N24165.68 (18)C52B—C53B—C54B—C55B0.0
C9—C10—C11—C12158.5 (3)C52B—C53B—C54B—F3B178.1 (10)
C9—C10—C11—N2325.2 (4)C53B—C54B—C55B—C56B0.0
C9—C10—C101—C10254.8 (3)C53B—C54B—C55B—F4B179.3 (11)
C9—C10—C101—C106125.1 (3)C54B—C55B—C56B—C51B0.0
F9—C105—C106—F102.3 (4)C54B—C55B—C56B—F5B179.8 (17)
F9—C105—C106—C101178.6 (2)C56B—C51B—C52B—C53B0.0
C10—C9—N22—C6162.4 (2)C56B—C51B—C52B—F1B179.6 (15)
C10—C11—C12—Br514.6 (4)F1B—C52B—C53B—C54B179.7 (14)
C10—C11—C12—C13174.2 (3)F1B—C52B—C53B—F2B0.2 (14)
C10—C11—N23—C14172.7 (2)F2B—C53B—C54B—C55B179.5 (10)
C10—C101—C102—F60.5 (4)F2B—C53B—C54B—F3B2.4 (11)
C10—C101—C102—C103179.3 (2)F3B—C54B—C55B—C56B178.1 (10)
C10—C101—C106—F101.5 (4)F3B—C54B—C55B—F4B1.2 (12)
C10—C101—C106—C105179.5 (2)F4B—C55B—C56B—C51B179.3 (11)
C11—C10—C101—C102121.3 (3)F4B—C55B—C56B—F5B0.5 (16)
C11—C10—C101—C10658.8 (3)C101—C10—C11—C1217.4 (4)
C11—C12—C13—Br6171.15 (18)C101—C10—C11—N23158.9 (2)
C11—C12—C13—C140.0 (3)C101—C102—C103—F7179.5 (2)
F11—C152—C153—F122.7 (4)C101—C102—C103—C1041.7 (4)
F11—C152—C153—C154179.0 (2)C102—C101—C106—F10178.4 (2)
C12—C11—N23—C144.4 (3)C102—C101—C106—C1050.6 (4)
C12—C13—C14—C15174.7 (3)C102—C103—C104—F8177.1 (2)
C12—C13—C14—N232.6 (3)C102—C103—C104—C1051.7 (4)
F12—C153—C154—F130.6 (4)C103—C104—C105—F9179.8 (2)
F12—C153—C154—C155178.9 (3)C103—C104—C105—C1060.5 (4)
C13—C14—C15—C16157.2 (3)C104—C105—C106—F10178.4 (2)
C13—C14—C15—C15121.1 (4)C104—C105—C106—C1010.6 (4)
C13—C14—N23—C114.4 (3)C106—C101—C102—F6179.6 (2)
F13—C154—C155—F140.1 (4)C106—C101—C102—C1030.6 (4)
F13—C154—C155—C156178.1 (2)C151—C15—C16—C1718.9 (4)
C14—C15—C16—C17162.8 (2)C151—C15—C16—N24154.5 (2)
C14—C15—C16—N2423.7 (4)C151—C152—C153—F12177.4 (2)
C14—C15—C151—C15253.8 (3)C151—C152—C153—C1540.8 (4)
C14—C15—C151—C156125.3 (3)C152—C151—C156—F15179.7 (2)
F14—C155—C156—F150.9 (4)C152—C151—C156—C1550.6 (4)
F14—C155—C156—C151178.8 (2)C152—C153—C154—F13178.9 (3)
C15—C14—N23—C11173.2 (2)C152—C153—C154—C1550.6 (4)
C15—C16—C17—Br716.0 (4)C153—C154—C155—F14179.4 (2)
C15—C16—C17—C18171.1 (2)C153—C154—C155—C1561.3 (4)
C15—C16—N24—C19168.6 (2)C154—C155—C156—F15178.9 (2)
C15—C151—C152—F112.5 (4)C154—C155—C156—C1510.7 (4)
C15—C151—C152—C153177.7 (2)C156—C151—C152—F11178.4 (2)
C15—C151—C156—F151.2 (4)C156—C151—C152—C1531.4 (4)
C15—C151—C156—C155178.5 (2)C201—C202—C203—F17179.5 (3)
C16—C15—C151—C152127.9 (3)C201—C202—C203—C2040.1 (5)
C16—C15—C151—C15653.1 (3)C202—C201—C206—F20179.6 (2)
C16—C17—C18—Br8169.77 (17)C202—C201—C206—C2051.4 (4)
C16—C17—C18—C191.0 (3)C202—C203—C204—F18179.9 (3)
F16—C202—C203—F170.2 (4)C202—C203—C204—C2050.5 (5)
F16—C202—C203—C204179.8 (3)C203—C204—C205—F19179.5 (3)
C17—C16—N24—C195.9 (3)C203—C204—C205—C2060.1 (5)
C17—C18—C19—C20169.4 (2)C204—C205—C206—F20179.9 (3)
C17—C18—C19—N244.8 (3)C204—C205—C206—C2011.1 (5)
F17—C203—C204—F180.5 (5)C206—C201—C202—F16178.8 (2)
F17—C203—C204—C205179.1 (3)C206—C201—C202—C2030.8 (4)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N21—H21···N220.882.342.866 (3)119
N21—H21···N240.882.422.928 (3)117
N23—H23···N220.882.482.931 (3)113
N23—H23···N240.882.462.895 (3)111
2,3,7,8,12,13,17,18-Octabromo-5,10,15,20-tetrakis(pentafluorophenyl)porphyrin tetrahydrofuran monosolvate (1_THF) top
Crystal data top
C44H2Br8F20N4·C4H8OF(000) = 3176
Mr = 1677.88Dx = 2.185 Mg m3
Monoclinic, P21/nMo Kα radiation, λ = 0.71073 Å
a = 21.524 (9) ÅCell parameters from 9873 reflections
b = 9.545 (4) Åθ = 2.3–28.3°
c = 26.020 (11) ŵ = 6.41 mm1
β = 107.426 (7)°T = 100 K
V = 5101 (4) Å3Block fragment, blue
Z = 40.42 × 0.11 × 0.09 mm
Data collection top
Bruker APEXII CCD
diffractometer
12689 independent reflections
Radiation source: microfocus sealed X-ray tube, graphite-monochromated10079 reflections with I > 2σ(I)
Mirror optics monochromatorRint = 0.082
Detector resolution: 7.9 pixels mm-1θmax = 28.3°, θmin = 1.5°
φ and ω scansh = 2828
Absorption correction: multi-scan
(SADABS; Bruker, 2016)
k = 1212
Tmin = 0.455, Tmax = 0.746l = 3434
148293 measured reflections
Refinement top
Refinement on F2Primary atom site location: dual
Least-squares matrix: fullHydrogen site location: mixed
R[F2 > 2σ(F2)] = 0.054H atoms treated by a mixture of independent and constrained refinement
wR(F2) = 0.095 w = 1/[σ2(Fo2) + 36.9739P]
where P = (Fo2 + 2Fc2)/3
S = 1.21(Δ/σ)max = 0.001
12689 reflectionsΔρmax = 1.63 e Å3
908 parametersΔρmin = 0.98 e Å3
718 restraints
Special details top

Geometry. All esds (except the esd in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell esds are taken into account individually in the estimation of esds in distances, angles and torsion angles; correlations between esds in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell esds is used for estimating esds involving l.s. planes.

Refinement. Two perfluoro rings were modelled as disordered over two locations with restraints (SADI, SIMU) and constraints (EXYZ, EADP for ipso carbons C12/C12a and C21/C21a) with occupancies of 75:25 and 70:30%. Pyrrole hydrogens located on the difference map and refined using restraints (DFIX). There is a short intermolecular HL..HL contact Br5···Br5 of 3.23 Angstroms (symmetry code = 1-x,-y,1-z = 3_656). See ALERT B

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/UeqOcc. (<1)
Br10.52232 (2)0.99320 (5)0.17627 (2)0.01967 (11)
Br20.65964 (2)0.99488 (5)0.28686 (2)0.01897 (11)
Br30.82447 (2)0.44087 (5)0.35875 (2)0.01795 (11)
Br40.77566 (3)0.15494 (6)0.41730 (2)0.02278 (12)
Br50.49322 (3)0.11413 (6)0.45284 (2)0.02566 (13)
Br60.35528 (3)0.08167 (6)0.34382 (2)0.02386 (12)
Br70.35141 (3)0.15311 (6)0.10022 (2)0.02311 (12)
Br80.39813 (3)0.44804 (6)0.04830 (2)0.02922 (14)
F1B0.3598 (14)0.762 (2)0.1217 (9)0.024 (3)0.306 (17)
F2B0.3219 (10)0.893 (2)0.0271 (8)0.034 (3)0.306 (17)
F3B0.4084 (10)0.924 (2)0.0300 (7)0.037 (3)0.306 (17)
F4B0.5320 (10)0.819 (2)0.0078 (7)0.033 (3)0.306 (17)
F5B0.5669 (13)0.674 (3)0.1029 (10)0.022 (3)0.306 (17)
F60.73871 (14)0.7001 (3)0.23590 (11)0.0205 (7)
F70.85729 (15)0.8205 (3)0.25703 (12)0.0241 (7)
F80.92243 (15)0.9035 (4)0.35882 (14)0.0313 (8)
F90.86678 (15)0.8738 (3)0.43919 (12)0.0255 (7)
F100.75021 (15)0.7465 (3)0.41955 (11)0.0222 (7)
F11B0.6146 (14)0.081 (4)0.3942 (12)0.025 (3)0.252 (18)
F12B0.6698 (11)0.231 (3)0.4832 (9)0.030 (3)0.252 (18)
F13B0.7274 (11)0.093 (3)0.5776 (9)0.032 (3)0.252 (18)
F14B0.7159 (12)0.188 (3)0.5826 (10)0.033 (3)0.252 (18)
F15B0.6587 (12)0.339 (3)0.4930 (12)0.028 (3)0.252 (18)
F160.40450 (15)0.0892 (3)0.23781 (13)0.0266 (7)
F170.28883 (18)0.2265 (4)0.20717 (15)0.0360 (9)
F180.17533 (17)0.0789 (4)0.17611 (17)0.0441 (10)
F190.17774 (15)0.2053 (4)0.17564 (16)0.0395 (9)
F200.29175 (15)0.3428 (3)0.20559 (13)0.0261 (7)
N210.57239 (19)0.6076 (4)0.25003 (16)0.0150 (9)
N220.63177 (19)0.4305 (4)0.34616 (16)0.0153 (9)
H220.5882 (12)0.470 (5)0.339 (2)0.015 (14)*
N230.5165 (2)0.2459 (4)0.30937 (16)0.0159 (9)
N240.4668 (2)0.4152 (5)0.21131 (16)0.0163 (9)
H240.492 (2)0.442 (6)0.2476 (10)0.032 (17)*
C10.4597 (2)0.4950 (6)0.16626 (19)0.0154 (10)
C20.4854 (2)0.6308 (5)0.1660 (2)0.0170 (10)
C30.5348 (2)0.6877 (5)0.2093 (2)0.0164 (10)
C40.5587 (2)0.8328 (5)0.21547 (19)0.0147 (10)
C50.6130 (2)0.8340 (5)0.2584 (2)0.0150 (10)
C60.6230 (2)0.6905 (5)0.27870 (19)0.0148 (10)
C70.6794 (2)0.6364 (5)0.31605 (19)0.0149 (10)
C80.6838 (2)0.5035 (5)0.33991 (19)0.0154 (10)
C90.7404 (2)0.4180 (5)0.36414 (19)0.0143 (10)
C100.7210 (2)0.3030 (5)0.3861 (2)0.0154 (10)
C110.6514 (2)0.3098 (5)0.37521 (19)0.0158 (10)
C120.6088 (3)0.2197 (5)0.3909 (2)0.0181 (11)
C12A0.6362 (3)0.1253 (6)0.4380 (2)0.0225 (9)0.252 (18)
C12F0.6624 (10)0.1997 (13)0.4855 (4)0.0246 (15)0.252 (18)
C12E0.6914 (12)0.129 (3)0.5333 (3)0.0259 (16)0.252 (18)
C12D0.6943 (11)0.017 (3)0.5336 (6)0.0258 (16)0.252 (18)
C12C0.6680 (13)0.0913 (13)0.4861 (9)0.0250 (16)0.252 (18)
C12B0.6390 (10)0.0202 (6)0.4383 (6)0.0234 (15)0.252 (18)
C130.5419 (3)0.2086 (5)0.3621 (2)0.0176 (10)
C140.4905 (2)0.1467 (6)0.38137 (18)0.0166 (10)
C150.4364 (2)0.1415 (6)0.3390 (2)0.0190 (11)
C160.4536 (2)0.2014 (5)0.29310 (19)0.0145 (10)
C170.4142 (2)0.2103 (5)0.2392 (2)0.0151 (10)
C180.4276 (2)0.2986 (5)0.2003 (2)0.0159 (10)
C190.3984 (2)0.2980 (5)0.14292 (19)0.0160 (10)
C200.4176 (2)0.4162 (6)0.12187 (19)0.0175 (10)
C21B0.4602 (3)0.7128 (6)0.1155 (2)0.0194 (9)0.306 (17)
C22B0.4009 (18)0.775 (4)0.0944 (13)0.0222 (16)0.306 (17)
C23B0.3830 (13)0.846 (3)0.0440 (11)0.0258 (16)0.306 (17)
C24B0.4304 (15)0.854 (3)0.0173 (9)0.0268 (16)0.306 (17)
C25B0.4895 (12)0.802 (3)0.0375 (11)0.0259 (16)0.306 (17)
C26B0.5064 (16)0.729 (4)0.0845 (15)0.0226 (15)0.306 (17)
C710.7412 (2)0.7171 (5)0.3271 (2)0.0149 (10)
C720.7695 (2)0.7413 (5)0.28649 (19)0.0159 (10)
C730.8303 (2)0.8037 (5)0.2964 (2)0.0175 (10)
C740.8631 (2)0.8463 (5)0.3483 (2)0.0195 (11)
C750.8353 (2)0.8286 (5)0.3890 (2)0.0176 (10)
C760.7754 (2)0.7640 (5)0.3785 (2)0.0177 (10)
C1710.3519 (2)0.1309 (6)0.22187 (19)0.0165 (10)
C1720.3489 (3)0.0143 (6)0.2218 (2)0.0210 (11)
C1730.2904 (3)0.0867 (6)0.2065 (2)0.0271 (13)
C1740.2327 (3)0.0110 (7)0.1905 (3)0.0315 (14)
C1750.2339 (3)0.1325 (6)0.1905 (2)0.0252 (12)
C1760.2929 (3)0.2012 (6)0.2059 (2)0.0207 (11)
F1A0.3574 (5)0.7361 (10)0.1329 (4)0.0236 (17)0.694 (17)
F2A0.3068 (4)0.8801 (10)0.0399 (4)0.0346 (19)0.694 (17)
F3A0.3808 (5)0.9315 (9)0.0262 (3)0.0399 (19)0.694 (17)
F4A0.5055 (5)0.8370 (9)0.0000 (3)0.0370 (17)0.694 (17)
F5A0.5569 (6)0.6956 (12)0.0924 (4)0.0267 (18)0.694 (17)
F11A0.6002 (5)0.0773 (12)0.3832 (4)0.0261 (16)0.748 (18)
F12A0.6504 (4)0.2514 (7)0.4669 (4)0.0321 (15)0.748 (18)
F13A0.7155 (4)0.1454 (10)0.5655 (3)0.0349 (16)0.748 (18)
F14A0.7237 (4)0.1351 (10)0.5815 (3)0.0362 (16)0.748 (18)
F15A0.6742 (4)0.3116 (9)0.4979 (4)0.0303 (16)0.748 (18)
O250.5156 (2)0.5565 (5)0.3555 (2)0.0452 (12)
C260.4822 (3)0.6868 (7)0.3386 (3)0.0428 (17)
H26A0.4400360.6703820.3106280.051*
H26B0.5088740.7502680.3236980.051*
C270.4714 (3)0.7495 (8)0.3890 (3)0.0485 (19)
H27A0.4319870.8092810.3798030.058*
H27B0.5093940.8058390.4093270.058*
C280.4628 (4)0.6212 (8)0.4209 (3)0.0492 (19)
H28A0.4767000.6406980.4601020.059*
H28B0.4170270.5888210.4097340.059*
C290.5061 (5)0.5173 (9)0.4068 (4)0.073 (3)
H29A0.5486200.5147970.4352830.088*
H29B0.4863560.4229130.4039660.088*
C21A0.4602 (3)0.7128 (6)0.1155 (2)0.0194 (9)0.694 (17)
C22A0.3956 (8)0.7599 (15)0.1009 (5)0.0214 (15)0.694 (17)
C23A0.3688 (5)0.8339 (11)0.0536 (4)0.0242 (15)0.694 (17)
C24A0.4061 (6)0.8611 (11)0.0197 (4)0.0271 (15)0.694 (17)
C25A0.4697 (6)0.8157 (12)0.0333 (4)0.0258 (14)0.694 (17)
C26A0.4955 (6)0.7428 (16)0.0809 (6)0.0227 (14)0.694 (17)
C1210.6362 (3)0.1253 (6)0.4380 (2)0.0225 (9)0.748 (18)
C1220.6306 (4)0.0197 (8)0.4319 (3)0.0222 (11)0.748 (18)
C1230.6566 (5)0.1134 (9)0.4740 (4)0.0253 (12)0.748 (18)
C1240.6892 (4)0.0585 (11)0.5241 (4)0.0253 (13)0.748 (18)
C1250.6943 (5)0.0823 (12)0.5328 (3)0.0255 (13)0.748 (18)
C1260.6682 (4)0.1736 (10)0.4902 (3)0.0240 (12)0.748 (18)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Br10.0205 (2)0.0128 (2)0.0221 (3)0.0018 (2)0.00074 (19)0.0039 (2)
Br20.0225 (2)0.0116 (2)0.0198 (2)0.0023 (2)0.00176 (19)0.0003 (2)
Br30.0163 (2)0.0166 (2)0.0195 (2)0.0006 (2)0.00298 (19)0.0003 (2)
Br40.0204 (3)0.0165 (3)0.0274 (3)0.0033 (2)0.0011 (2)0.0070 (2)
Br50.0309 (3)0.0302 (3)0.0177 (3)0.0009 (2)0.0100 (2)0.0056 (2)
Br60.0197 (3)0.0276 (3)0.0268 (3)0.0009 (2)0.0107 (2)0.0072 (2)
Br70.0259 (3)0.0183 (3)0.0216 (3)0.0048 (2)0.0017 (2)0.0021 (2)
Br80.0433 (3)0.0249 (3)0.0145 (2)0.0085 (3)0.0011 (2)0.0009 (2)
F1B0.024 (4)0.021 (5)0.022 (5)0.004 (4)0.001 (5)0.008 (4)
F2B0.037 (5)0.022 (4)0.029 (5)0.001 (4)0.012 (4)0.006 (4)
F3B0.048 (6)0.028 (5)0.022 (4)0.002 (6)0.008 (5)0.009 (4)
F4B0.044 (6)0.032 (5)0.021 (5)0.007 (5)0.007 (5)0.010 (4)
F5B0.027 (6)0.022 (6)0.018 (6)0.001 (5)0.008 (5)0.011 (5)
F60.0234 (16)0.0227 (17)0.0141 (14)0.0004 (13)0.0034 (12)0.0023 (12)
F70.0283 (17)0.0228 (17)0.0242 (16)0.0036 (14)0.0126 (13)0.0019 (14)
F80.0222 (16)0.033 (2)0.0364 (19)0.0134 (15)0.0055 (14)0.0040 (16)
F90.0270 (17)0.0245 (18)0.0193 (15)0.0054 (14)0.0019 (13)0.0059 (13)
F100.0260 (16)0.0264 (17)0.0151 (15)0.0026 (14)0.0073 (12)0.0020 (13)
F11B0.022 (6)0.025 (5)0.026 (6)0.000 (5)0.002 (5)0.010 (5)
F12B0.030 (5)0.030 (5)0.031 (5)0.008 (5)0.008 (4)0.015 (5)
F13B0.028 (5)0.039 (6)0.028 (5)0.013 (5)0.008 (4)0.019 (5)
F14B0.034 (5)0.041 (6)0.019 (5)0.003 (6)0.001 (4)0.008 (6)
F15B0.025 (6)0.031 (6)0.024 (5)0.002 (5)0.001 (5)0.003 (5)
F160.0236 (16)0.0167 (17)0.0383 (19)0.0016 (13)0.0075 (14)0.0057 (14)
F170.040 (2)0.0193 (18)0.049 (2)0.0109 (16)0.0139 (18)0.0005 (16)
F180.0234 (18)0.040 (2)0.064 (3)0.0194 (17)0.0056 (17)0.002 (2)
F190.0142 (16)0.042 (2)0.058 (2)0.0033 (15)0.0050 (16)0.0043 (19)
F200.0218 (16)0.0203 (17)0.0354 (19)0.0020 (13)0.0074 (14)0.0020 (14)
N210.015 (2)0.014 (2)0.014 (2)0.0024 (17)0.0015 (16)0.0022 (17)
N220.013 (2)0.013 (2)0.018 (2)0.0050 (17)0.0025 (16)0.0034 (17)
N230.016 (2)0.016 (2)0.014 (2)0.0011 (17)0.0011 (16)0.0026 (17)
N240.018 (2)0.018 (2)0.0109 (19)0.0022 (18)0.0011 (16)0.0020 (17)
C10.015 (2)0.016 (2)0.014 (2)0.004 (2)0.0034 (18)0.003 (2)
C20.017 (2)0.018 (3)0.014 (2)0.003 (2)0.0029 (19)0.003 (2)
C30.015 (2)0.016 (3)0.017 (2)0.001 (2)0.0032 (19)0.004 (2)
C40.015 (2)0.013 (2)0.017 (2)0.0019 (19)0.0045 (19)0.003 (2)
C50.018 (2)0.009 (2)0.017 (2)0.0016 (19)0.0039 (19)0.0008 (19)
C60.015 (2)0.016 (3)0.014 (2)0.0005 (19)0.0052 (19)0.0027 (19)
C70.019 (2)0.011 (2)0.013 (2)0.0016 (19)0.0036 (19)0.0010 (19)
C80.017 (2)0.015 (2)0.012 (2)0.002 (2)0.0022 (18)0.000 (2)
C90.015 (2)0.012 (2)0.014 (2)0.0000 (19)0.0006 (18)0.0020 (19)
C100.017 (2)0.011 (2)0.016 (2)0.0024 (19)0.0005 (19)0.0025 (19)
C110.020 (2)0.013 (2)0.012 (2)0.000 (2)0.0015 (19)0.0008 (19)
C120.024 (3)0.015 (3)0.014 (2)0.001 (2)0.004 (2)0.002 (2)
C12A0.0202 (17)0.0260 (18)0.0209 (17)0.0001 (16)0.0055 (15)0.0079 (16)
C12F0.023 (3)0.028 (3)0.021 (2)0.000 (3)0.004 (2)0.009 (2)
C12E0.025 (2)0.030 (3)0.021 (2)0.001 (3)0.005 (2)0.010 (3)
C12D0.024 (2)0.030 (3)0.023 (3)0.004 (3)0.007 (2)0.011 (3)
C12C0.023 (3)0.027 (3)0.025 (3)0.004 (2)0.008 (2)0.010 (3)
C12B0.021 (3)0.026 (3)0.023 (3)0.002 (2)0.007 (2)0.008 (2)
C130.024 (3)0.012 (2)0.016 (2)0.002 (2)0.006 (2)0.002 (2)
C140.024 (3)0.019 (3)0.007 (2)0.000 (2)0.0043 (19)0.0037 (19)
C150.018 (2)0.015 (3)0.025 (3)0.003 (2)0.008 (2)0.002 (2)
C160.017 (2)0.010 (2)0.016 (2)0.0008 (19)0.0046 (19)0.0028 (19)
C170.013 (2)0.015 (2)0.017 (2)0.0013 (19)0.0045 (19)0.002 (2)
C180.013 (2)0.014 (2)0.019 (2)0.0030 (19)0.0004 (19)0.002 (2)
C190.016 (2)0.018 (3)0.014 (2)0.000 (2)0.0031 (19)0.001 (2)
C200.019 (2)0.019 (3)0.011 (2)0.002 (2)0.0000 (19)0.002 (2)
C21B0.0267 (19)0.0146 (17)0.0141 (17)0.0026 (16)0.0018 (15)0.0026 (15)
C22B0.029 (3)0.016 (3)0.017 (3)0.001 (2)0.000 (2)0.003 (2)
C23B0.032 (3)0.019 (2)0.019 (2)0.002 (2)0.003 (2)0.005 (2)
C24B0.035 (3)0.020 (2)0.019 (2)0.003 (3)0.001 (3)0.005 (2)
C25B0.034 (3)0.021 (3)0.019 (2)0.003 (3)0.001 (3)0.005 (2)
C26B0.030 (3)0.018 (3)0.017 (2)0.003 (3)0.002 (3)0.005 (2)
C710.018 (2)0.006 (2)0.017 (2)0.0018 (19)0.0010 (19)0.0012 (19)
C720.020 (2)0.011 (2)0.014 (2)0.002 (2)0.0007 (19)0.0003 (19)
C730.020 (3)0.012 (2)0.022 (3)0.001 (2)0.009 (2)0.003 (2)
C740.016 (2)0.010 (2)0.029 (3)0.003 (2)0.003 (2)0.001 (2)
C750.019 (2)0.013 (2)0.017 (2)0.002 (2)0.001 (2)0.003 (2)
C760.021 (3)0.013 (3)0.019 (3)0.003 (2)0.005 (2)0.000 (2)
C1710.019 (2)0.018 (3)0.013 (2)0.002 (2)0.0061 (19)0.001 (2)
C1720.020 (3)0.019 (3)0.024 (3)0.001 (2)0.006 (2)0.003 (2)
C1730.030 (3)0.020 (3)0.032 (3)0.011 (2)0.011 (3)0.004 (2)
C1740.019 (3)0.035 (4)0.038 (3)0.014 (3)0.005 (2)0.000 (3)
C1750.017 (3)0.028 (3)0.030 (3)0.001 (2)0.006 (2)0.002 (3)
C1760.022 (3)0.020 (3)0.020 (3)0.003 (2)0.006 (2)0.000 (2)
F1A0.022 (2)0.021 (4)0.027 (4)0.004 (3)0.006 (3)0.009 (3)
F2A0.030 (4)0.027 (3)0.033 (4)0.002 (3)0.010 (3)0.008 (3)
F3A0.051 (4)0.032 (3)0.023 (3)0.001 (3)0.010 (3)0.013 (2)
F4A0.048 (4)0.038 (3)0.024 (3)0.008 (3)0.010 (3)0.008 (2)
F5A0.031 (4)0.029 (4)0.022 (4)0.001 (3)0.011 (3)0.009 (3)
F11A0.028 (4)0.022 (2)0.025 (4)0.002 (3)0.003 (3)0.002 (3)
F12A0.036 (4)0.022 (3)0.041 (4)0.006 (2)0.015 (3)0.015 (3)
F13A0.033 (3)0.041 (4)0.030 (3)0.010 (3)0.009 (2)0.020 (3)
F14A0.036 (3)0.044 (4)0.021 (2)0.003 (3)0.003 (2)0.008 (3)
F15A0.034 (4)0.028 (3)0.021 (3)0.002 (3)0.004 (3)0.003 (2)
O250.044 (3)0.029 (3)0.072 (4)0.013 (2)0.031 (3)0.010 (2)
C260.031 (4)0.029 (4)0.068 (5)0.009 (3)0.015 (3)0.007 (3)
C270.032 (4)0.040 (4)0.075 (5)0.001 (3)0.018 (4)0.012 (4)
C280.051 (5)0.042 (4)0.055 (5)0.012 (4)0.017 (4)0.001 (4)
C290.112 (8)0.040 (5)0.090 (7)0.039 (5)0.064 (6)0.023 (5)
C21A0.0267 (19)0.0146 (17)0.0141 (17)0.0026 (16)0.0018 (15)0.0026 (15)
C22A0.028 (3)0.016 (2)0.016 (3)0.002 (2)0.000 (2)0.003 (2)
C23A0.031 (3)0.017 (2)0.018 (2)0.001 (2)0.003 (2)0.003 (2)
C24A0.035 (3)0.019 (2)0.020 (2)0.003 (2)0.003 (2)0.005 (2)
C25A0.034 (3)0.021 (2)0.019 (2)0.004 (2)0.001 (2)0.005 (2)
C26A0.029 (3)0.018 (2)0.018 (2)0.003 (2)0.002 (2)0.003 (2)
C1210.0202 (17)0.0260 (18)0.0209 (17)0.0001 (16)0.0055 (15)0.0079 (16)
C1220.020 (2)0.025 (2)0.022 (2)0.0027 (19)0.0075 (19)0.009 (2)
C1230.023 (2)0.027 (2)0.027 (2)0.004 (2)0.009 (2)0.009 (2)
C1240.023 (2)0.030 (3)0.023 (2)0.005 (2)0.0083 (19)0.012 (2)
C1250.024 (2)0.030 (3)0.021 (2)0.000 (2)0.0046 (18)0.009 (2)
C1260.023 (2)0.027 (2)0.021 (2)0.000 (2)0.0042 (18)0.008 (2)
Geometric parameters (Å, º) top
Br1—C41.876 (5)C13—C141.468 (7)
Br2—C51.862 (5)C14—C151.343 (7)
Br3—C91.869 (5)C15—C161.468 (7)
Br4—C101.863 (5)C16—C171.408 (7)
Br5—C141.869 (5)C17—C181.411 (7)
Br6—C151.877 (5)C17—C1711.488 (7)
Br7—C191.870 (5)C18—C191.437 (7)
Br8—C201.858 (5)C19—C201.370 (7)
F1B—C22B1.30 (4)C21B—C22B1.37 (4)
F2B—C23B1.33 (3)C21B—C26B1.46 (4)
F3B—C24B1.35 (3)C22B—C23B1.42 (3)
F4B—C25B1.37 (3)C23B—C24B1.40 (3)
F5B—C26B1.35 (3)C24B—C25B1.32 (3)
F6—C721.343 (5)C25B—C26B1.36 (4)
F7—C731.329 (6)C71—C721.389 (7)
F8—C741.339 (6)C71—C761.392 (7)
F9—C751.350 (5)C72—C731.389 (7)
F10—C761.346 (6)C73—C741.386 (7)
F11B—C12B1.25 (3)C74—C751.373 (8)
F12B—C12C1.34 (2)C75—C761.380 (7)
F13B—C12D1.36 (2)C171—C1721.388 (7)
F14B—C12E1.36 (3)C171—C1761.385 (7)
F15B—C12F1.35 (3)C172—C1731.385 (7)
F16—C1721.349 (6)C173—C1741.390 (9)
F17—C1731.335 (7)C174—C1751.370 (9)
F18—C1741.344 (6)C175—C1761.378 (7)
F19—C1751.346 (6)F1A—C22A1.354 (15)
F20—C1761.352 (6)F2A—C23A1.348 (12)
N21—C31.358 (6)F3A—C24A1.334 (12)
N21—C61.371 (6)F4A—C25A1.337 (13)
N22—H220.974 (10)F5A—C26A1.344 (15)
N22—C81.369 (6)F11A—C1221.356 (12)
N22—C111.373 (6)F12A—C1231.331 (11)
N23—C131.363 (6)F13A—C1241.343 (9)
N23—C161.361 (6)F14A—C1251.334 (11)
N24—H240.975 (10)F15A—C1261.333 (11)
N24—C11.368 (6)O25—C261.439 (8)
N24—C181.374 (6)O25—C291.459 (9)
C1—C21.410 (7)C26—H26A0.9900
C1—C201.448 (7)C26—H26B0.9900
C2—C31.407 (7)C26—C271.521 (10)
C2—C21B1.487 (7)C27—H27A0.9900
C2—C21A1.487 (7)C27—H27B0.9900
C3—C41.469 (7)C27—C281.522 (11)
C4—C51.354 (7)C28—H28A0.9900
C5—C61.461 (7)C28—H28B0.9900
C6—C71.407 (7)C28—C291.481 (10)
C7—C81.403 (7)C29—H29A0.9900
C7—C711.490 (7)C29—H29B0.9900
C8—C91.446 (7)C21A—C22A1.400 (18)
C9—C101.361 (7)C21A—C26A1.370 (19)
C10—C111.440 (7)C22A—C23A1.385 (15)
C11—C121.404 (7)C23A—C24A1.385 (14)
C12—C12A1.493 (7)C24A—C25A1.377 (13)
C12—C131.414 (7)C25A—C26A1.384 (16)
C12—C1211.493 (7)C121—C1221.395 (11)
C12A—C12F1.3900C121—C1261.405 (10)
C12A—C12B1.3900C122—C1231.396 (10)
C12F—C12E1.3900C123—C1241.385 (11)
C12E—C12D1.3900C124—C1251.362 (12)
C12D—C12C1.3900C125—C1261.389 (11)
C12C—C12B1.3900
C3—N21—C6106.8 (4)C24B—C25B—C26B121 (3)
C8—N22—H22124 (3)C26B—C25B—F4B122 (2)
C8—N22—C11111.4 (4)F5B—C26B—C21B120 (3)
C11—N22—H22123 (3)F5B—C26B—C25B119 (3)
C16—N23—C13107.0 (4)C25B—C26B—C21B120 (2)
C1—N24—H24125 (4)C72—C71—C7120.6 (4)
C1—N24—C18111.7 (4)C72—C71—C76116.8 (5)
C18—N24—H24123 (4)C76—C71—C7122.5 (5)
N24—C1—C2124.9 (5)F6—C72—C71119.8 (4)
N24—C1—C20106.1 (4)F6—C72—C73117.9 (4)
C2—C1—C20128.9 (5)C73—C72—C71122.3 (5)
C1—C2—C21B116.6 (4)F7—C73—C72120.9 (5)
C1—C2—C21A116.6 (4)F7—C73—C74120.2 (5)
C3—C2—C1123.7 (5)C74—C73—C72118.9 (5)
C3—C2—C21B119.6 (5)F8—C74—C73119.7 (5)
C3—C2—C21A119.6 (5)F8—C74—C75120.2 (5)
N21—C3—C2122.5 (5)C75—C74—C73120.2 (5)
N21—C3—C4109.8 (4)F9—C75—C74119.8 (4)
C2—C3—C4127.3 (5)F9—C75—C76120.2 (5)
C3—C4—Br1129.5 (4)C74—C75—C76119.9 (5)
C5—C4—Br1123.9 (4)F10—C76—C71120.0 (5)
C5—C4—C3106.6 (4)F10—C76—C75118.2 (4)
C4—C5—Br2124.4 (4)C75—C76—C71121.9 (5)
C4—C5—C6106.7 (4)C172—C171—C17123.1 (5)
C6—C5—Br2128.8 (4)C176—C171—C17120.4 (5)
N21—C6—C5109.7 (4)C176—C171—C172116.5 (5)
N21—C6—C7123.0 (5)F16—C172—C171119.5 (5)
C7—C6—C5126.7 (5)F16—C172—C173118.0 (5)
C6—C7—C71118.7 (4)C173—C172—C171122.4 (5)
C8—C7—C6124.6 (5)F17—C173—C172121.3 (5)
C8—C7—C71116.3 (4)F17—C173—C174120.0 (5)
N22—C8—C7124.3 (5)C172—C173—C174118.7 (5)
N22—C8—C9105.9 (4)F18—C174—C173119.8 (6)
C7—C8—C9129.8 (5)F18—C174—C175119.9 (6)
C8—C9—Br3127.6 (4)C175—C174—C173120.3 (5)
C10—C9—Br3123.6 (4)F19—C175—C174120.0 (5)
C10—C9—C8108.2 (4)F19—C175—C176120.5 (5)
C9—C10—Br4124.1 (4)C174—C175—C176119.5 (5)
C9—C10—C11108.3 (4)F20—C176—C171120.0 (5)
C11—C10—Br4127.2 (4)F20—C176—C175117.4 (5)
N22—C11—C10106.0 (4)C175—C176—C171122.6 (5)
N22—C11—C12123.7 (5)C26—O25—C29107.9 (5)
C12—C11—C10130.3 (5)O25—C26—H26A110.6
C11—C12—C12A118.4 (5)O25—C26—H26B110.6
C11—C12—C13122.8 (5)O25—C26—C27105.5 (6)
C11—C12—C121118.4 (5)H26A—C26—H26B108.8
C13—C12—C12A118.6 (5)C27—C26—H26A110.6
C13—C12—C121118.6 (5)C27—C26—H26B110.6
C12F—C12A—C12112.2 (7)C26—C27—H27A111.1
C12F—C12A—C12B120.0C26—C27—H27B111.1
C12B—C12A—C12127.8 (7)C26—C27—C28103.3 (6)
F15B—C12F—C12A127.2 (14)H27A—C27—H27B109.1
F15B—C12F—C12E112.5 (14)C28—C27—H27A111.1
C12E—C12F—C12A120.0C28—C27—H27B111.1
F14B—C12E—C12F125.8 (14)C27—C28—H28A111.3
F14B—C12E—C12D114.2 (14)C27—C28—H28B111.3
C12F—C12E—C12D120.0H28A—C28—H28B109.2
F13B—C12D—C12E123.0 (15)C29—C28—C27102.4 (6)
F13B—C12D—C12C116.7 (15)C29—C28—H28A111.3
C12E—C12D—C12C120.0C29—C28—H28B111.3
F12B—C12C—C12D123.2 (14)O25—C29—C28109.1 (6)
F12B—C12C—C12B116.8 (14)O25—C29—H29A109.9
C12B—C12C—C12D120.0O25—C29—H29B109.9
F11B—C12B—C12A116.8 (18)C28—C29—H29A109.9
F11B—C12B—C12C123.2 (18)C28—C29—H29B109.9
C12C—C12B—C12A120.0H29A—C29—H29B108.3
N23—C13—C12123.4 (5)C22A—C21A—C2118.6 (6)
N23—C13—C14109.5 (4)C26A—C21A—C2124.3 (6)
C12—C13—C14126.9 (5)C26A—C21A—C22A117.1 (7)
C13—C14—Br5127.2 (4)F1A—C22A—C21A121.1 (9)
C15—C14—Br5124.8 (4)F1A—C22A—C23A117.6 (13)
C15—C14—C13106.9 (4)C23A—C22A—C21A121.3 (10)
C14—C15—Br6123.5 (4)F2A—C23A—C22A121.3 (10)
C14—C15—C16106.6 (4)F2A—C23A—C24A119.1 (8)
C16—C15—Br6129.7 (4)C24A—C23A—C22A119.7 (10)
N23—C16—C15109.8 (4)F3A—C24A—C23A120.4 (9)
N23—C16—C17122.5 (4)F3A—C24A—C25A119.7 (10)
C17—C16—C15127.7 (4)C25A—C24A—C23A119.9 (9)
C16—C17—C18123.9 (5)F4A—C25A—C24A120.5 (10)
C16—C17—C171119.4 (4)F4A—C25A—C26A120.1 (10)
C18—C17—C171116.6 (4)C24A—C25A—C26A119.4 (10)
N24—C18—C17125.5 (5)F5A—C26A—C21A119.1 (10)
N24—C18—C19105.6 (4)F5A—C26A—C25A118.1 (13)
C17—C18—C19128.5 (5)C21A—C26A—C25A122.7 (10)
C18—C19—Br7127.7 (4)C122—C121—C12120.3 (6)
C20—C19—Br7123.0 (4)C122—C121—C126115.9 (6)
C20—C19—C18108.8 (4)C126—C121—C12123.7 (6)
C1—C20—Br8129.1 (4)F11A—C122—C121120.7 (8)
C19—C20—Br8123.0 (4)F11A—C122—C123116.2 (8)
C19—C20—C1107.5 (4)C121—C122—C123123.1 (8)
C22B—C21B—C2129.4 (13)F12A—C123—C122121.7 (8)
C22B—C21B—C26B116.1 (17)F12A—C123—C124120.4 (7)
C26B—C21B—C2114.5 (12)C124—C123—C122117.9 (8)
F1B—C22B—C21B116 (2)F13A—C124—C123119.6 (8)
F1B—C22B—C23B121 (3)F13A—C124—C125118.9 (8)
C21B—C22B—C23B123 (3)C125—C124—C123121.5 (7)
F2B—C23B—C22B116 (2)F14A—C125—C124121.5 (7)
F2B—C23B—C24B128 (2)F14A—C125—C126118.9 (8)
C24B—C23B—C22B116 (2)C124—C125—C126119.6 (7)
F3B—C24B—C23B112 (2)F15A—C126—C121117.8 (7)
C25B—C24B—F3B125 (2)F15A—C126—C125120.1 (8)
C25B—C24B—C23B123 (2)C125—C126—C121122.0 (8)
C24B—C25B—F4B117 (2)
Br1—C4—C5—Br21.5 (7)C12A—C12—C13—N23154.4 (5)
Br1—C4—C5—C6177.4 (3)C12A—C12—C13—C1420.2 (8)
Br2—C5—C6—N21171.6 (4)C12A—C12F—C12E—F14B177 (3)
Br2—C5—C6—C717.4 (8)C12A—C12F—C12E—C12D0.0
Br3—C9—C10—Br43.2 (6)C12F—C12A—C12B—F11B180 (2)
Br3—C9—C10—C11170.2 (3)C12F—C12A—C12B—C12C0.0
Br4—C10—C11—N22172.6 (4)C12F—C12E—C12D—F13B173 (2)
Br4—C10—C11—C129.5 (8)C12F—C12E—C12D—C12C0.0
Br5—C14—C15—Br66.7 (7)C12E—C12D—C12C—F12B179 (3)
Br5—C14—C15—C16168.6 (4)C12E—C12D—C12C—C12B0.0
Br6—C15—C16—N23172.5 (4)C12D—C12C—C12B—F11B180 (3)
Br6—C15—C16—C179.6 (8)C12D—C12C—C12B—C12A0.0
Br7—C19—C20—Br81.0 (6)C12B—C12A—C12F—F15B174 (3)
Br7—C19—C20—C1172.6 (4)C12B—C12A—C12F—C12E0.0
F1B—C22B—C23B—F2B2 (4)C13—N23—C16—C154.3 (6)
F1B—C22B—C23B—C24B179 (3)C13—N23—C16—C17173.7 (5)
F2B—C23B—C24B—F3B3 (4)C13—C12—C12A—C12F120.0 (10)
F2B—C23B—C24B—C25B179 (3)C13—C12—C12A—C12B61.6 (13)
F3B—C24B—C25B—F4B0 (4)C13—C12—C121—C12256.6 (9)
F3B—C24B—C25B—C26B178 (3)C13—C12—C121—C126122.9 (7)
F4B—C25B—C26B—F5B1 (4)C13—C14—C15—Br6175.7 (4)
F4B—C25B—C26B—C21B180 (2)C13—C14—C15—C160.5 (6)
F6—C72—C73—F70.8 (7)C14—C15—C16—N232.4 (6)
F6—C72—C73—C74179.6 (4)C14—C15—C16—C17175.6 (5)
F7—C73—C74—F80.5 (7)C15—C16—C17—C18163.5 (5)
F7—C73—C74—C75179.8 (5)C15—C16—C17—C17111.8 (8)
F8—C74—C75—F92.5 (8)C16—N23—C13—C12170.8 (5)
F8—C74—C75—C76177.2 (5)C16—N23—C13—C144.6 (6)
F9—C75—C76—F100.8 (7)C16—C17—C18—N2420.9 (8)
F9—C75—C76—C71179.4 (5)C16—C17—C18—C19167.4 (5)
F12B—C12C—C12B—F11B1 (2)C16—C17—C171—C17264.6 (7)
F12B—C12C—C12B—C12A179 (2)C16—C17—C171—C176113.9 (6)
F13B—C12D—C12C—F12B5 (3)C17—C18—C19—Br718.5 (8)
F13B—C12D—C12C—C12B173.8 (19)C17—C18—C19—C20169.5 (5)
F14B—C12E—C12D—F13B10 (3)C17—C171—C172—F160.3 (8)
F14B—C12E—C12D—C12C177 (2)C17—C171—C172—C173178.8 (5)
F15B—C12F—C12E—F14B2 (2)C17—C171—C176—F200.5 (8)
F15B—C12F—C12E—C12D175 (2)C17—C171—C176—C175178.8 (5)
F16—C172—C173—F170.4 (8)C18—N24—C1—C2169.7 (5)
F16—C172—C173—C174179.2 (5)C18—N24—C1—C206.1 (6)
F17—C173—C174—F180.4 (9)C18—C17—C171—C172119.7 (6)
F17—C173—C174—C175179.1 (6)C18—C17—C171—C17661.8 (7)
F18—C174—C175—F190.4 (9)C18—C19—C20—Br8173.3 (4)
F18—C174—C175—C176179.2 (5)C18—C19—C20—C10.2 (6)
F19—C175—C176—F200.1 (8)C20—C1—C2—C3168.4 (5)
F19—C175—C176—C171179.5 (5)C20—C1—C2—C21B8.4 (8)
N21—C3—C4—Br1173.3 (4)C20—C1—C2—C21A8.4 (8)
N21—C3—C4—C53.7 (6)C21B—C2—C3—N21161.3 (5)
N21—C6—C7—C819.1 (8)C21B—C2—C3—C411.7 (8)
N21—C6—C7—C71153.7 (5)C21B—C22B—C23B—F2B175 (3)
N22—C8—C9—Br3168.2 (4)C21B—C22B—C23B—C24B2 (4)
N22—C8—C9—C103.2 (5)C22B—C21B—C26B—F5B178 (3)
N22—C11—C12—C12A157.2 (5)C22B—C21B—C26B—C25B1 (4)
N22—C11—C12—C1326.5 (8)C22B—C23B—C24B—F3B180 (2)
N22—C11—C12—C121157.2 (5)C22B—C23B—C24B—C25B2 (4)
N23—C13—C14—Br5165.5 (4)C23B—C24B—C25B—F4B178 (2)
N23—C13—C14—C153.2 (6)C23B—C24B—C25B—C26B4 (4)
N23—C16—C17—C1818.8 (8)C24B—C25B—C26B—F5B178 (3)
N23—C16—C17—C171165.9 (5)C24B—C25B—C26B—C21B3 (4)
N24—C1—C2—C316.8 (8)C26B—C21B—C22B—F1B180 (3)
N24—C1—C2—C21B166.5 (5)C26B—C21B—C22B—C23B3 (4)
N24—C1—C2—C21A166.5 (5)C71—C7—C8—N22162.3 (5)
N24—C1—C20—Br8169.3 (4)C71—C7—C8—C915.1 (8)
N24—C1—C20—C193.8 (6)C71—C72—C73—F7177.3 (5)
N24—C18—C19—Br7168.5 (4)C71—C72—C73—C741.6 (8)
N24—C18—C19—C203.4 (6)C72—C71—C76—F10178.7 (4)
C1—N24—C18—C17167.2 (5)C72—C71—C76—C751.5 (7)
C1—N24—C18—C196.0 (6)C72—C73—C74—F8178.4 (5)
C1—C2—C3—N2115.3 (8)C72—C73—C74—C750.9 (8)
C1—C2—C3—C4171.6 (5)C73—C74—C75—F9178.2 (5)
C1—C2—C21B—C22B73 (2)C73—C74—C75—C762.1 (8)
C1—C2—C21B—C26B107.6 (17)C74—C75—C76—F10178.9 (5)
C1—C2—C21A—C22A69.4 (9)C74—C75—C76—C710.9 (8)
C1—C2—C21A—C26A108.8 (10)C76—C71—C72—F6179.2 (4)
C2—C1—C20—Br815.1 (8)C76—C71—C72—C732.8 (7)
C2—C1—C20—C19171.9 (5)C171—C17—C18—N24154.5 (5)
C2—C3—C4—Br112.9 (8)C171—C17—C18—C1917.1 (8)
C2—C3—C4—C5170.1 (5)C171—C172—C173—F17179.5 (5)
C2—C21B—C22B—F1B0 (4)C171—C172—C173—C1740.1 (9)
C2—C21B—C22B—C23B177.5 (18)C172—C171—C176—F20179.1 (5)
C2—C21B—C26B—F5B1 (4)C172—C171—C176—C1750.2 (8)
C2—C21B—C26B—C25B180 (2)C172—C173—C174—F18179.2 (5)
C2—C21A—C22A—F1A2.4 (16)C172—C173—C174—C1750.5 (9)
C2—C21A—C22A—C23A178.5 (9)C173—C174—C175—F19179.1 (5)
C2—C21A—C26A—F5A0.4 (17)C173—C174—C175—C1760.6 (10)
C2—C21A—C26A—C25A177.9 (10)C174—C175—C176—F20179.5 (5)
C3—N21—C6—C56.2 (5)C174—C175—C176—C1710.2 (9)
C3—N21—C6—C7165.2 (5)C176—C171—C172—F16178.8 (4)
C3—C2—C21B—C22B110 (2)C176—C171—C172—C1730.2 (8)
C3—C2—C21B—C26B69.2 (17)F1A—C22A—C23A—F2A0.3 (17)
C3—C2—C21A—C22A113.8 (9)F1A—C22A—C23A—C24A179.8 (10)
C3—C2—C21A—C26A68.0 (11)F2A—C23A—C24A—F3A0.3 (14)
C3—C4—C5—Br2175.6 (4)F2A—C23A—C24A—C25A179.5 (10)
C3—C4—C5—C60.2 (6)F3A—C24A—C25A—F4A2.5 (15)
C4—C5—C6—N214.0 (6)F3A—C24A—C25A—C26A180.0 (11)
C4—C5—C6—C7167.1 (5)F4A—C25A—C26A—F5A0.3 (19)
C5—C6—C7—C8170.9 (5)F4A—C25A—C26A—C21A177.2 (11)
C5—C6—C7—C7116.2 (8)F11A—C122—C123—F12A1.5 (12)
C6—N21—C3—C2168.1 (5)F11A—C122—C123—C124178.6 (9)
C6—N21—C3—C46.1 (6)F12A—C123—C124—F13A0.9 (12)
C6—C7—C8—N2224.6 (8)F12A—C123—C124—C125177.8 (9)
C6—C7—C8—C9157.9 (5)F13A—C124—C125—F14A1.1 (13)
C6—C7—C71—C7262.6 (7)F13A—C124—C125—C126179.0 (8)
C6—C7—C71—C76121.4 (5)F14A—C125—C126—F15A1.8 (12)
C7—C8—C9—Br314.0 (8)F14A—C125—C126—C121179.6 (9)
C7—C8—C9—C10174.6 (5)O25—C26—C27—C2832.3 (7)
C7—C71—C72—F64.6 (7)C26—O25—C29—C283.1 (10)
C7—C71—C72—C73173.4 (5)C26—C27—C28—C2933.1 (8)
C7—C71—C76—F105.2 (7)C27—C28—C29—O2523.0 (10)
C7—C71—C76—C75174.6 (5)C29—O25—C26—C2718.4 (8)
C8—N22—C11—C102.7 (6)C21A—C2—C3—N21161.3 (5)
C8—N22—C11—C12175.5 (5)C21A—C2—C3—C411.7 (8)
C8—C7—C71—C72110.8 (5)C21A—C22A—C23A—F2A179.5 (10)
C8—C7—C71—C7665.1 (6)C21A—C22A—C23A—C24A0.6 (17)
C8—C9—C10—Br4175.0 (4)C22A—C21A—C26A—F5A177.8 (12)
C8—C9—C10—C111.7 (6)C22A—C21A—C26A—C25A0.3 (18)
C9—C10—C11—N220.5 (6)C22A—C23A—C24A—F3A179.6 (10)
C9—C10—C11—C12177.5 (5)C22A—C23A—C24A—C25A0.6 (15)
C10—C11—C12—C12A20.4 (8)C23A—C24A—C25A—F4A177.7 (10)
C10—C11—C12—C13155.8 (5)C23A—C24A—C25A—C26A0.2 (16)
C10—C11—C12—C12120.4 (8)C24A—C25A—C26A—F5A177.8 (11)
C11—N22—C8—C7174.3 (5)C24A—C25A—C26A—C21A0.3 (19)
C11—N22—C8—C93.6 (5)C26A—C21A—C22A—F1A179.3 (12)
C11—C12—C12A—C12F63.7 (11)C26A—C21A—C22A—C23A0.2 (17)
C11—C12—C12A—C12B114.7 (12)C121—C12—C13—N23154.4 (5)
C11—C12—C13—N2321.8 (8)C121—C12—C13—C1420.2 (8)
C11—C12—C13—C14163.6 (5)C121—C122—C123—F12A180.0 (9)
C11—C12—C121—C122119.7 (7)C121—C122—C123—C1240.2 (11)
C11—C12—C121—C12660.7 (9)C122—C121—C126—F15A179.5 (9)
C12—C12A—C12F—F15B8 (3)C122—C121—C126—C1251.8 (11)
C12—C12A—C12F—C12E178.5 (7)C122—C123—C124—F13A179.3 (8)
C12—C12A—C12B—F11B2 (3)C122—C123—C124—C1252.0 (12)
C12—C12A—C12B—C12C178.3 (8)C123—C124—C125—F14A177.6 (9)
C12—C13—C14—Br519.3 (8)C123—C124—C125—C1262.3 (12)
C12—C13—C14—C15172.1 (5)C124—C125—C126—F15A178.3 (9)
C12—C121—C122—F11A0.0 (12)C124—C125—C126—C1210.3 (12)
C12—C121—C122—C123178.3 (6)C126—C121—C122—F11A179.6 (9)
C12—C121—C126—F15A0.0 (12)C126—C121—C122—C1232.1 (11)
C12—C121—C126—C125178.6 (6)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N22—H22···O250.97 (1)1.92 (2)2.849 (6)158 (5)
Calculated mean distances, angles and structural parameters (Å, °) for compounds 1–6 top
Measured mean bond distances, angles, mean-plane angles, calculated NSD values, intramolecular contacts and mean-plane deviations for atom groups.
Br8TPFPP·CHCl3Br8TPFPP1·THFH8TPFPP·dioxaneF8TPFPPCl8TPFPPBr8TPFPP·C6H4Cl2Br8TPP·DMF
1·CHCl31·THF2341·C6H4Cl26
This workThis work(HALZUP; Dogutan et al., 2010)(GODYON; Leroy et al., 1999)(ZALHUP; Birnbaum et al., 1995)(ZALJEB; Birnbaum et al., 1995)(RONROB; Spyroulias et al., 1997)
Bond lengths
N-Ca1.368 (7)1.366 (6)1.3581.3701.3721.3671.362
Ca-Cb1.440 (20)1.450 (2)1.4501.4381.4481.4571.435
Ca-Cm1.406 (10)1.408 (4)1.3951.3991.4021.4061.415
Cb-Cb1.361 (10)1.357 (12)1.3451.3321.3471.3491.348
Bond angles
N-Ca-Cm123.1 (7)123.7 (12)126.1126.6125.4124.5123.1
N-Ca-Cb110.0 (6)110.0 (6)108.8107.5107.2108.1107.5
Ca-N-Ca109.0 (4)109.0 (3)108.1108.7109.5108.7109.4
Ca-Cm-Ca123.0 (9)123.8 (7)125.8125.4125.7123.4120.9
Ca-Cb-Cb107.4 (12)107.5 (9)107.1108.1108.0107.4107.7
Cm-Ca-Cb129.0 (2)128.3 (14)125.0125.9127.2127.1129.3
Pyrrole mean-plane incline angles
<pyrN2127.825.60.73.114.625.639.1
<pyrN2226.929.50.43.415.720.439.1
<pyrN2336.936.50.73.114.925.639.1
<pyrN2432.122.30.43.414.020.439.1
Mean(<pyr)30.028.50.63.214.823.039.1
Structural parameters
Δipa0.59 (11)0.42 (10)0.182 (12)0.23 (2)0.07 (4)0.31 (7)0.8 (2)
Δoopb3.46 (7)3.17 (7)0.01 (9)0.246 (8)1.91 (2)2.73 (5)3.790 (120)
N21···N222.866 (3)2.43 (5)2.9272.9212.9432.9232.958
N22···N232.931 (3)2.32 (5)2.8952.9422.9392.862.958
N23···N242.895 (3)2.61 (6)2.9272.9212.9422.9232.958
N24···N212.928 (3)2.60 (6)2.8952.9422.9252.862.958
Δ24c0.5430.4970.0080.0460.3080.4420.616
ΔNd0.0750.0900.0180.0460.0880.0770.034
ΔCme0.0360.0170.0090.0610.0090.0910.317
ΔCaf0.4180.3790.0070.0290.2500.3390.409
ΔCbg1.1561.0600.0050.0550.6260.9031.264
(a) Simulated total in-plane distortion; (b) simulated total out-of-plane distortion; (c) average deviation from the least-squares plane of the 24-macrocycle atoms; (d) simulated displacement of the four internal nitrogen atoms from the 24-atom mean plane; (e) average deviation of the meso-carbon atoms from the 24-atom mean plane; (f) Average deviation of the α-carbon atoms from the 24-atom mean plane; (g) Average deviation of the β-carbon atoms from the 24-atom mean plane.
 

Funding information

Funding for this research was provided by: Science Foundation Ireland (SFI, IvP 13/IA/1894) and has received funding from the European Union's Horizon 2020 research and innovation programme under the FET–OPEN grant agreement No. 828779.

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