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The anti­biotic ciprofloxacin [systematic name: 1-cyclo­propyl-6-fluoro-4-oxo-7-(piperazin-4-ium-1-yl)-1,4-dihydro­quinoline-3-carboxyl­ate], has been crystallized as a 2:3 solvate with 2,2-difluoro­ethanol, 2C17H18FN3O3·3C2H4O2, (I), and as a 3:14.5 hydrate, 3C17H18FN3O3·14.5H2O, (II). The structure of (I) was determined using synchrotron X-ray diffraction data and refined as a two-component nonmerohedral twin. Both structures contain several independent mol­ecules in the asymmetric unit: (I) contains two zwitterionic ciprofloxacin mol­ecules and three difluoro­ethanol solvent mol­ecules, while (II) contains three zwitterionic ciprofloxacin mol­ecules and a mixture of ordered and disordered water mol­ecules. The inter­molecular inter­actions were analysed using fingerprint plots derived from Hirshfeld surfaces, providing a detailed description of the unique environment of each independent ciprofloxacin mol­ecule.

Supporting information

cif

Crystallographic Information File (CIF) https://doi.org/10.1107/S0108270111005488/bi3008sup1.cif
Contains datablocks I, II, global

hkl

Structure factor file (CIF format) https://doi.org/10.1107/S0108270111005488/bi3008Isup2.hkl
Contains datablock I

hkl

Structure factor file (CIF format) https://doi.org/10.1107/S0108270111005488/bi3008IIsup3.hkl
Contains datablock II

CCDC references: 819309; 819310

Comment top

Ciprofloxacin (Cf) belongs to the quinolone class of semisynthetic antibiotics (Turel, 2002; Mitscher, 2005). A search of the Cambridge Structural Database (Version 5.31 with updates to May 2010; Allen, 2002) reveals 68 crystal structures containing the Cf molecule. These include the structures of the anhydrous form (Fabbiani et al., 2009; Mahapatra et al., 2010), a hexahydrate (Turel et al., 1997; Fabbiani & Dittrich, 2008), hydrated sodium salts crystallized under high-pressure conditions and recoverable to ambient pressure (Fabbiani et al., 2009), a lactate sesquihydrate (Prasanna & Guru Row, 2001), a hemi-methanolate (Li et al., 2006), a hydrochloride 1.34-hydrate (Turel & Golobič, 2003), and several coordination complexes with group II or lanthanide elements.

While the crystal structures of coordination complexes of Cf often contain more than one Cf molecule in the asymmetric unit, (I) and (II) are the only examples known to date of non-coordination complexes where this is the case: two and three independent Cf molecules are found in (I) and (II), respectively (Figs. 1 and 2). Some differences in torsion angles are observed for the Cf molecules in the two structures (Table 1), indicating conformational variations in the relative orientation of the piperazinium ring and, in particular, of the cyclopropyl and carboxylate groups relative to the planar dihydroquinoline ring structure. In both (I) and (II), Cf exists as a zwitterion. Previous literature (Główka et al. 2003) has suggested that an in-plane conformation for quinolones, as observed for (I), is predominantly associated with a protonated carboxyl group, with exceptions being characterized by significant differences in C—O bond lengths compared with those normally observed in zwitterions. For (I) and (II), we are confident of our zwitterionic assignment on the basis of (i) the observed bond lengths of the carboxylate group, which, although significantly different for most of the molecules, are well below the expected value of 1.31 Å for a C—OH single bond [Reference for standard value?], and (ii) the fact that the H atoms of the NH2+ groups are visible in difference Fourier maps.

The supramolecular architecture of both structures is dominated by three-dimensional hydrogen-bonding patterns, with different hydrogen-bonding capabilities satisfied by the symmetry-independent Cf molecules. Hydrogen-bond parameters are given in Tables 2 and 3. In (I), both Cf molecules form similarly bifurcated N—H···O(carboxylate) hydrogen bonds that define cross-linked chains of molecules A and B running in nearly perpendicular directions along the c and b axes, respectively. Symmetry-equivalent chains stack pairwise via face-to-face ππ interactions. Each of the three symmetry-independent 2,2-difluoroethanol molecules donates a hydrogen bond to the carboxylate O atom antiperiplanar to the carbonyl group: 2,2-difluoroethanol molecules B and C to Cf molecule B, and 2,2-difluoroethanol molecule A to Cf molecule A. These hydrogen bonds, together with weaker C—H···F and C—H···O interactions, contribute to the formation of the three-dimensional network (Fig. 3). The conformation of the hydroxyl group differs in the three independent 2,2-difluoroethanol molecules, with values for the C19—C18—O4—H4 torsion angle of 151, 98 and 160° for molecules A, B and C, respectively.

Although significant disorder is observed for the water molecules in (II), hydrogen bonds involving the Cf molecules are well defined, since the majority of water molecules interacting directly with Cf are ordered and their H-atom positions could be assigned from the experimental data. As in (I), each of the symmetry-independent Cf molecules forms infinite hydrogen-bonded N—H···O(carboxylate) chains. In (II), however, the hydrogen bonds in these chains are not bifurcated and involve N—H34 rather than N—H33. In addition, rather than being nearly orthogonal to each other, the chains all run along the a axis. Cross-linking of the chains occurs via a second set of N—H···O(carbonyl) hydrogen bonds, leading to the formation of trimers about a pseudo-31screw axis. This is in marked contrast with the structure of Cf hexahydrate, which forms a layered structure with no direct Cf···Cf contacts (Turel et al., 1997; Fabbiani & Dittrich, 2008 ?). The trimers in (II) are arranged in a hexameric fashion centred about the inversion centre at the unit-cell origin (Fig. 4). This arrangement creates channels approximately 4.5 Å in diameter that contain predominantly disordered water molecules (OW1–OW7 and OW15), as well as those that were modelled as ordered but exhibit the largest displacement parameters (OW12–OW14). The better defined water molecules, OW8–OW11, act as hydrogen-bond donor bridges, linking molecules within a trimer (OW8) and pairs of symmetry-related molecules (OW9–OW11), thereby connecting the trimers (Fig. 4 and Table 3). Within the hexameric arrangement, face-to-face ππ interactions link symmetry-equivalent Cf hydrogen-bonded chains in a manner similar to that found for the pairwise stacks of hydrogen-bonded chains in (I), albeit at slightly larger interplanar separations [3.4854 (8), 3.4980 (9) and 3.6165 (7) Å for pairwise stacks of molecules A, B and C, respectively, in (II); 3.2642 (14) and 3.4023 (14) Å for molecules A and B, respectively, in (I)]. As in the structure of (I), there are a number of C—H···O, C—H···F and C—H···π interactions that contribute to the stability of the structure.

Hirshfeld surfaces (Spackman & Byrom, 1997; McKinnon et al., 1998) and fingerprint plots (Spackman & McKinnon, 2002) have been shown to be useful tools for comparing and elucidating intermolecular interactions of molecules in different crystalline environments, including symmetry-independent molecules in the asymmetric unit (McKinnon et al., 2004, 2007). The analysis of fingerprint plots is restricted here to the structure of (I), since several water H atoms are missing from the structure of (II). Fingerprint plots for the two symmetry-independent Cf molecules and three symmetry-independent 2,2-difluoroethanol molecules in (I) are shown in Figs. 5 and 6, respectively. At first glance, the plots for Cf look quite similar in shape, which reflects the not-too-dissimilar packing environment around the two molecules. On closer inspection, the `thickness' and point density of some features, e.g. the long spikes denoting hydrogen bonding or the regions at high values of de and di, are distinct for each molecule. The asymmetry about the plot diagonal is typical of a structure that contains more than one molecule in the crystallographic asymmetric unit. Some interactions, e.g. H···H, O···H, H···O and C···H, labelled in Fig. 5 as 1, 2, 3 and 4, respectively, manifest themselves with characteristic features in the plots. For instance, it is immediately obvious that two distinct C···H interactions, namely π···H, are present, and on comparison with the plots shown in Fig. 6, the complementary H···π interactions are visible: Cf molecule A with solvent molecule C, and Cf molecule B with solvent molecule A, while solvent molecule B does not participate in such contacts. The diffuse set of points labelled 5 in Fig. 6 corresponds to H···H contacts involved in a cyclic interaction; the hydroxyl atoms O4 and H4 of solvent molecule A are approximately coplanar with atoms O1 and H5 of Cf molecule A, so that, in addition to the stronger O4—H4···O1 hydrogen bond, a much weaker C5—H5···O4 interaction [C5···O4 = 3.669 (5) Å] is also present.

Related literature top

For related literature, see: Allen (2002); Fabbiani & Dittrich (2008); Fabbiani et al. (2009); Główka et al. (2003); Li et al. (2006); Mahapatra et al. (2010); McKinnon et al. (1998, 2004, 2007); Mitscher (2005); Prasanna & Guru Row (2001); Sheldrick (2008a, 2008b); Spackman & Byrom (1997); Spackman & McKinnon (2002); Turel (2002); Turel & Golobič (2003); Turel et al. (1997).

Experimental top

Ciprofloxacin (Sigma Aldrich) was used as received. Single crystals were obtained by recrystallization from 2,2-difluoroethanol for (I) or from water–NaOH at ca pH 12 for (II), by slow evaporation of saturated solutions under ambient conditions. Crystals of (II) were identified from a mixture also containing crystals of the known Cf hexahydrate. They can be easily distinguished by their characteristic thick block habit, compared with the thin plates typically displayed by the hexahydrate. While we have not studied in detail the conditions under which preferential or controlled crystallization of (II) occurs, we have also observed concomitant crystallisation of the two hydrates from water–NaOH (ca pH 12) at the lower temparature of 278 K. These crystals appear to be stable when kept suspended in solution for weeks under ambient conditions. Crystals of (II) have also been obtained by crystallization from an aqueous Ba(OH)2 solution.

For (I), several crystals of various size were screened and all were found to be two-component twins. Smaller crystals were found to be better suited for data collection in terms of low mosaicity and good reflection profiles, e.g. absence of peak splitting, though data resolution was limited even using a synchrotron source. The non-merohedral twin law corresponds to a twofold rotation about the [011] direct-lattice direction. The fractional contribution of the major component was refined to 0.519 (2).

Refinement top

The program TWINABS (Sheldrick, 2008a) was used to generate a merged reflection file for (I) in the SHELXL HKLF5 format (Sheldrick, 2008b). Data statistics were as follows: 20118 data (4526 unique) for domain 1 only with mean I/σ(I) = 14.3; 20116 data (4515 unique) for domain 2 only with mean I/σ(I) = 14.5, and 7592 data (1975 unique) for both domains with mean I/σ(I) = 20.0. The quoted Rint value (0.07) comes from scaling all single and composite reflections involving domain 1. For the generation of an HKLF5 file, all observations containing domain 1 were chosen. Single reflections that also occur in composites were omitted for merging.

Given the low data-to-parameter ratio, non-H atoms of Cf in (I) were subjected to rigid-bond and similarity restraints, and bonds in the two Cf molecules were restrained to be the same with an s.u. of 0.02 Å. In the structure of (II), seven water O atoms (OW1–OW7) were modelled with split sites, with their occupancies set to either 50:50 or 60:40, one O atom (OW14) was modelled as half-occupied and the remaining six as fully occupied. The strategy for assigning site occupancies for OW1–OW7 and OW14 consisted of refining different models in which a variable number of occupancies were fixed and/or allowed to refine, so as to obtain an optimal R factor. Occupancies were fixed in the final refinement.

For both structures, H atoms belonging to Cf were positioned geometrically and constrained to ride on their parent atoms, with Uiso(H) = 1.2Ueq(parent). In both structures, N-bound H atoms in the Cf molecules were clearly visible in a difference Fourier map but were positioned geometrically and constrained to ride during refinement. For (I), hydroxyl H atoms were first located in a difference Fourier map and subsequently constrained to ride on their parent atom using a variable C—C—O—H torsion angle (AFIX 147 instruction in SHELXL97). For (II), H atoms for the eight ordered water molecules were clearly visible in a difference Fourier map. Their positions were refined subject to bond-distance and bond-angle restraints, with Uiso(H) = 1.5Ueq(O). The H atoms of the disordered water molecules could not be located, and they cannot easily be placed to form a consistent hydrogen-bonding pattern. These H atoms were therefore omitted from the structure.

Computing details top

For both compounds, data collection: APEX2 (Bruker, 2007); cell refinement: SAINT (Bruker, 2007); data reduction: SAINT (Bruker, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008b); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008b); molecular graphics: ORTEP-3 for Windows (Burnett & Johnson, 1996) and Mercury (Macrae et al., 2008); software used to prepare material for publication: publCIF (Westrip, 2010).

Figures top
[Figure 1] Fig. 1. The asymmetric unit of (I), with displacement ellipsoids drawn at the 50% probability level. H atoms have been omitted for clarity. Suffixes A, B and C denote symmetry-independent molecules.
[Figure 2] Fig. 2. The asymmetric unit of (II), with displacement ellipsoids drawn at the 50% probability level. H atoms have been omitted for clarity. For Cf, suffixes A, B and C denote symmetry-independent molecules. For the water molecules (OW), suffixes A and B denote disordered parts.
[Figure 3] Fig. 3. The crystal packing of (I), viewed along the b axis, illustrating the hydrogen-bonded arrangements of Cf molecules A (green in the electronic version of the paper) and B (blue). Symmetry-independent solvent molecules are coloured differently [red (molecule A), yellow (molecule B) and magenta (molecule C) in the electronic version of the paper]. O—H···O and N+—H···O hydrogen bonds are shown as dashed lines.
[Figure 4] Fig. 4. The crystal packing of (II), viewed along the a axis, illustrating the hexameric arrangement of trimeric hydrogen-bonded columns of Cf molecules A (green in the electronic version of the paper), B (blue) and C (magenta). Hydrogen bonds are shown as dashed lines, and the pseudo-31 screw axis is highlighted in the upper part of the diagram. Fully occupied water molecules OW8–OW11, which are hydrogen-bonded to Cf molecules, are shown as balls and sticks. Disordered water molecules occupying the channel along the a axis are depicted as orange spheres. [Symmetry codes: (i) 1 - x, 1 - y, 1 - z; (ii) -x, 1 - y, 1 - z; (iii) x, -1 + y, z; (iv) 1 - x, -y, -z; (v) x, -1 + y, z.]
[Figure 5] Fig. 5. Fingerprint plots of Cf molecules A and B in (I). Close contacts are labelled as follows: 1 = H···H, 2 = H···O, 3 = O···H and 4 = C···H.
[Figure 6] Fig. 6. Fingerprint plots of solvent molecules A, B and C in (I). Close contacts are labelled as follows: 5 = H···H.
(I) 1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-4-ium-1-yl)-1,4-dihydroquinoline-3- carboxylate–2,2-difluoroethanol (2/3) top
Crystal data top
2C17H18FN3O3·3C2H4F2OZ = 2
Mr = 908.84F(000) = 948
Triclinic, P1Dx = 1.463 Mg m3
Hall symbol: -P 1Synchrotron radiation, λ = 0.7000 Å
a = 10.9848 (4) ÅCell parameters from 9991 reflections
b = 13.9800 (4) Åθ = 2.3–24.6°
c = 13.9802 (4) ŵ = 0.13 mm1
α = 105.6488 (18)°T = 120 K
β = 90.352 (2)°Block, yellow
γ = 93.364 (2)°0.1 × 0.08 × 0.08 mm
V = 2063.22 (11) Å3
Data collection top
Bruker SMART APEXII CCD area-detector
diffractometer
7072 independent reflections
Radiation source: fine-focus sealed tube5962 reflections with I > 2σ(I)
Silicon monochromatorRint = 0.08
ω scansθmax = 24.6°, θmin = 1.5°
Absorption correction: multi-scan
(TWINABS; Sheldrick, 2008a)
h = 1313
Tmin = 0.58, Tmax = 0.74k = 1616
51821 measured reflectionsl = 016
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.068Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.202H-atom parameters constrained
S = 1.16 w = 1/[σ2(Fo2) + (0.0922P)2 + 1.8862P]
where P = (Fo2 + 2Fc2)/3
7072 reflections(Δ/σ)max < 0.001
571 parametersΔρmax = 0.58 e Å3
522 restraintsΔρmin = 0.46 e Å3
Crystal data top
2C17H18FN3O3·3C2H4F2Oγ = 93.364 (2)°
Mr = 908.84V = 2063.22 (11) Å3
Triclinic, P1Z = 2
a = 10.9848 (4) ÅSynchrotron radiation, λ = 0.7000 Å
b = 13.9800 (4) ŵ = 0.13 mm1
c = 13.9802 (4) ÅT = 120 K
α = 105.6488 (18)°0.1 × 0.08 × 0.08 mm
β = 90.352 (2)°
Data collection top
Bruker SMART APEXII CCD area-detector
diffractometer
7072 independent reflections
Absorption correction: multi-scan
(TWINABS; Sheldrick, 2008a)
5962 reflections with I > 2σ(I)
Tmin = 0.58, Tmax = 0.74Rint = 0.08
51821 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.068522 restraints
wR(F2) = 0.202H-atom parameters constrained
S = 1.16Δρmax = 0.58 e Å3
7072 reflectionsΔρmin = 0.46 e Å3
571 parameters
Special details top

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

Refinement. Refinement of F2 against ALL reflections. From TWINABS: 23224 data (5427 unique) involve domain 1 only, mean I/σ 12.7 23236 data (5429 unique) involve domain 2 only, mean I/σ 12.9 9155 data (2475 unique) involve 2 domains, mean I/σ 17.1 The quoted Rint value (0.08) comes from scaling all single and composite reflections involving domain 1. For the generation of an HKLF5 file, all observations containing domain 1 were chosen. Data were merged in TWINABS according to point group -1; single reflections that also occur in composites were omitted.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
C1A0.9157 (4)0.6677 (3)0.9873 (3)0.0288 (8)
H1A0.99130.65680.95010.035*
C2A0.8581 (5)0.5807 (3)1.0157 (3)0.0420 (11)
H2A10.81700.59321.07870.050*
H2A20.89860.51880.99700.050*
C3A0.8011 (4)0.6155 (3)0.9344 (3)0.0386 (10)
H3A10.72600.64930.94830.046*
H3A20.80770.57480.86660.046*
C4A0.8842 (3)0.8470 (3)1.0175 (3)0.0235 (8)
C5A0.9123 (3)0.7794 (3)1.1540 (3)0.0266 (8)
H5A0.93170.72501.17620.032*
C6A0.8930 (3)0.8662 (3)1.2250 (3)0.0249 (8)
C7A0.9057 (3)0.8645 (3)1.3323 (3)0.0255 (8)
C8A0.8585 (3)0.9511 (3)1.1929 (2)0.0219 (7)
C9A0.8628 (3)0.9378 (3)1.0849 (3)0.0241 (8)
C10A0.8422 (3)1.0192 (3)1.0475 (3)0.0237 (8)
H10A0.82661.08051.09050.028*
C11A0.8452 (3)1.0080 (3)0.9483 (3)0.0248 (8)
C12A0.8640 (3)0.9176 (3)0.8782 (2)0.0222 (7)
C13A0.9126 (3)0.8245 (3)0.7086 (2)0.0243 (8)
H13A0.85020.77040.69710.029*
H13B0.98410.80440.73730.029*
C14A0.9448 (3)0.8467 (3)0.6104 (3)0.0240 (8)
H14A1.01370.89530.62120.029*
H14B0.96870.78630.56350.029*
C15A0.7919 (3)0.9719 (3)0.6399 (2)0.0245 (8)
H15A0.72010.99200.61150.029*
H15B0.85251.02750.65460.029*
C16A0.7589 (3)0.9448 (3)0.7348 (3)0.0246 (8)
H16A0.72781.00180.78220.030*
H16B0.69580.89120.72070.030*
C17A0.8836 (3)0.8363 (3)0.9151 (3)0.0243 (8)
H17A0.89620.77470.87150.029*
F1A0.8334 (2)1.09146 (15)0.91582 (15)0.0284 (5)
N1A0.9055 (3)0.7661 (2)1.0551 (2)0.0251 (7)
N2A0.8682 (3)0.9135 (2)0.7771 (2)0.0239 (7)
N3A0.8410 (3)0.8854 (2)0.5674 (2)0.0228 (6)
H3A40.78140.83680.54810.027*
H3A30.86560.90370.51330.027*
O1A0.9278 (3)0.7830 (2)1.3494 (2)0.0404 (8)
O2A0.8963 (2)0.94404 (19)1.39869 (17)0.0276 (6)
O3A0.8274 (2)1.03187 (18)1.24727 (17)0.0253 (6)
C1B0.4484 (4)0.5514 (3)0.8104 (3)0.0319 (9)
H1B0.52070.59620.81130.038*
C2B0.4191 (4)0.5314 (3)0.9062 (3)0.0395 (10)
H2B10.47330.56180.96270.047*
H2B20.38380.46570.90490.047*
C3B0.3424 (4)0.5984 (3)0.8669 (3)0.0384 (10)
H3B10.26100.57310.84150.046*
H3B20.35060.66920.89930.046*
C4B0.3889 (3)0.5089 (3)0.6346 (3)0.0254 (8)
C5B0.4229 (3)0.3788 (3)0.7091 (3)0.0260 (8)
H5B0.44540.36020.76550.031*
C6B0.3937 (3)0.3040 (3)0.6251 (3)0.0256 (8)
C7B0.4001 (3)0.1985 (3)0.6308 (3)0.0245 (8)
C8B0.3571 (3)0.3298 (3)0.5358 (3)0.0242 (8)
C9B0.3582 (3)0.4370 (3)0.5460 (3)0.0254 (8)
C10B0.3259 (3)0.4710 (3)0.4636 (3)0.0250 (8)
H10B0.30400.42540.40330.030*
C11B0.3266 (3)0.5694 (3)0.4719 (3)0.0267 (8)
C12B0.3567 (3)0.6433 (3)0.5603 (3)0.0240 (7)
C13B0.4146 (4)0.8152 (3)0.6520 (3)0.0282 (8)
H13C0.49080.79160.66930.034*
H13D0.36010.82070.70730.034*
C14B0.4377 (3)0.9162 (3)0.6323 (3)0.0268 (8)
H14C0.47010.96380.69230.032*
H14D0.49810.91150.58110.032*
C15B0.2663 (4)0.8780 (3)0.5124 (3)0.0273 (8)
H15C0.31930.87000.45590.033*
H15D0.18970.90110.49520.033*
C16B0.2436 (3)0.7792 (3)0.5365 (3)0.0260 (8)
H16C0.18850.78680.59170.031*
H16D0.20570.73050.47950.031*
C17B0.3875 (3)0.6100 (3)0.6421 (3)0.0260 (8)
H17B0.40750.65610.70260.031*
F1B0.3010 (2)0.59818 (16)0.38806 (15)0.0318 (5)
N1B0.4220 (3)0.4767 (2)0.7173 (2)0.0278 (7)
N2B0.3597 (3)0.7443 (2)0.5626 (2)0.0261 (7)
N3B0.3242 (3)0.9521 (2)0.5999 (2)0.0247 (7)
H3B30.34181.00980.58440.030*
H3B40.27160.96400.65030.030*
O1B0.4321 (3)0.18655 (19)0.71462 (19)0.0313 (6)
O2B0.3747 (2)0.12815 (18)0.55542 (18)0.0277 (6)
O3B0.3268 (2)0.27002 (19)0.45403 (18)0.0280 (6)
O4A0.1169 (3)0.4141 (2)0.7139 (2)0.0451 (8)
H4A0.11990.35360.69350.068*
C18A0.0222 (5)0.4457 (4)0.6626 (4)0.0489 (12)
H18A0.05430.44240.69610.059*
H18B0.01290.40270.59540.059*
C19A0.0542 (4)0.5481 (3)0.6604 (4)0.0414 (11)
H19A0.13430.55220.63060.050*
F2A0.0329 (3)0.5799 (2)0.6068 (2)0.0654 (9)
F3A0.0543 (4)0.6118 (2)0.7516 (3)0.0825 (12)
O4B0.3352 (3)0.8446 (2)0.2558 (2)0.0403 (7)
H4B0.40260.83370.27470.061*
C18B0.2516 (4)0.7633 (3)0.2550 (3)0.0383 (10)
H18C0.17350.78810.27850.046*
H18D0.28120.72730.30000.046*
C19B0.2353 (4)0.6951 (3)0.1550 (3)0.0430 (11)
H19B0.21780.73320.10760.052*
F2B0.3369 (3)0.6442 (2)0.1268 (2)0.0624 (8)
F3B0.1414 (3)0.6267 (2)0.1530 (2)0.0614 (8)
O4C0.6097 (3)0.7792 (3)1.0868 (2)0.0481 (8)
H4C0.60470.78331.14620.072*
C18C0.5157 (4)0.8319 (4)1.0576 (3)0.0440 (11)
H18E0.50370.89231.10940.053*
H18F0.43970.79111.04650.053*
C19C0.5525 (4)0.8567 (3)0.9642 (3)0.0363 (10)
H19C0.62690.90090.97560.044*
F2C0.5685 (3)0.7732 (2)0.89043 (19)0.0515 (7)
F3C0.4582 (3)0.9011 (2)0.9317 (2)0.0612 (8)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
C1A0.048 (2)0.0223 (19)0.0177 (18)0.0075 (16)0.0020 (16)0.0068 (15)
C2A0.077 (3)0.024 (2)0.027 (2)0.001 (2)0.002 (2)0.0107 (18)
C3A0.063 (3)0.026 (2)0.026 (2)0.0006 (19)0.0047 (19)0.0069 (17)
C4A0.0321 (19)0.0214 (18)0.0194 (18)0.0018 (14)0.0003 (14)0.0100 (15)
C5A0.038 (2)0.028 (2)0.0186 (18)0.0029 (16)0.0004 (15)0.0143 (16)
C6A0.0349 (19)0.0246 (19)0.0164 (17)0.0029 (15)0.0012 (14)0.0072 (15)
C7A0.038 (2)0.025 (2)0.0145 (17)0.0028 (16)0.0018 (15)0.0072 (15)
C8A0.0328 (18)0.0212 (19)0.0120 (16)0.0001 (14)0.0015 (14)0.0055 (14)
C9A0.0332 (19)0.0243 (19)0.0169 (17)0.0020 (15)0.0015 (14)0.0093 (14)
C10A0.0352 (19)0.0184 (18)0.0174 (17)0.0026 (15)0.0010 (14)0.0046 (14)
C11A0.0348 (19)0.0227 (19)0.0210 (18)0.0049 (15)0.0008 (15)0.0121 (15)
C12A0.0295 (18)0.0232 (18)0.0162 (17)0.0008 (14)0.0009 (14)0.0092 (14)
C13A0.0358 (19)0.0249 (19)0.0146 (17)0.0045 (15)0.0012 (14)0.0092 (15)
C14A0.0335 (19)0.0245 (19)0.0170 (17)0.0057 (15)0.0002 (14)0.0099 (15)
C15A0.040 (2)0.0199 (18)0.0154 (17)0.0032 (15)0.0028 (15)0.0080 (15)
C16A0.0342 (19)0.027 (2)0.0150 (17)0.0044 (15)0.0008 (14)0.0093 (15)
C17A0.0346 (19)0.0216 (19)0.0177 (17)0.0017 (15)0.0011 (14)0.0073 (15)
F1A0.0510 (13)0.0198 (11)0.0181 (10)0.0041 (9)0.0005 (9)0.0109 (9)
N1A0.0407 (17)0.0211 (16)0.0151 (15)0.0041 (13)0.0005 (12)0.0072 (12)
N2A0.0356 (16)0.0231 (16)0.0153 (14)0.0063 (13)0.0001 (12)0.0082 (13)
N3A0.0382 (17)0.0204 (16)0.0119 (14)0.0013 (13)0.0009 (12)0.0080 (12)
O1A0.081 (2)0.0256 (15)0.0194 (14)0.0147 (14)0.0003 (14)0.0119 (12)
O2A0.0469 (15)0.0248 (14)0.0140 (12)0.0034 (11)0.0014 (11)0.0098 (11)
O3A0.0427 (14)0.0208 (14)0.0140 (12)0.0049 (11)0.0016 (10)0.0065 (11)
C1B0.050 (2)0.0227 (19)0.0229 (19)0.0040 (17)0.0087 (17)0.0060 (16)
C2B0.067 (3)0.029 (2)0.022 (2)0.007 (2)0.0081 (19)0.0064 (18)
C3B0.058 (3)0.033 (2)0.025 (2)0.0082 (19)0.0037 (18)0.0078 (18)
C4B0.0324 (19)0.0245 (19)0.0224 (18)0.0033 (15)0.0000 (15)0.0114 (15)
C5B0.037 (2)0.0247 (19)0.0198 (18)0.0040 (15)0.0019 (15)0.0110 (15)
C6B0.0346 (19)0.0217 (18)0.0223 (18)0.0040 (15)0.0011 (15)0.0084 (15)
C7B0.0319 (19)0.0218 (19)0.0224 (19)0.0028 (14)0.0023 (15)0.0099 (16)
C8B0.0309 (18)0.0231 (19)0.0212 (18)0.0036 (15)0.0024 (14)0.0099 (15)
C9B0.0324 (19)0.0256 (19)0.0211 (18)0.0023 (15)0.0004 (15)0.0110 (15)
C10B0.0367 (19)0.0238 (19)0.0147 (17)0.0011 (15)0.0015 (14)0.0059 (15)
C11B0.038 (2)0.0271 (19)0.0203 (18)0.0049 (16)0.0020 (15)0.0143 (16)
C12B0.0319 (18)0.0220 (18)0.0198 (18)0.0061 (14)0.0047 (14)0.0080 (15)
C13B0.039 (2)0.0210 (19)0.026 (2)0.0050 (15)0.0018 (16)0.0084 (16)
C14B0.037 (2)0.0183 (18)0.0246 (19)0.0035 (15)0.0046 (15)0.0041 (15)
C15B0.045 (2)0.0183 (18)0.0199 (18)0.0042 (16)0.0024 (16)0.0069 (15)
C16B0.036 (2)0.0210 (18)0.0235 (19)0.0038 (15)0.0010 (15)0.0097 (15)
C17B0.036 (2)0.0194 (18)0.0207 (18)0.0013 (15)0.0011 (15)0.0027 (15)
F1B0.0569 (14)0.0227 (11)0.0194 (11)0.0031 (10)0.0017 (10)0.0119 (9)
N1B0.0401 (18)0.0218 (16)0.0236 (16)0.0029 (13)0.0057 (13)0.0097 (13)
N2B0.0340 (17)0.0207 (16)0.0244 (16)0.0041 (13)0.0005 (13)0.0070 (13)
N3B0.0419 (17)0.0183 (15)0.0180 (15)0.0052 (13)0.0064 (13)0.0110 (13)
O1B0.0516 (17)0.0241 (14)0.0210 (13)0.0048 (12)0.0052 (12)0.0104 (11)
O2B0.0454 (15)0.0202 (14)0.0202 (13)0.0018 (11)0.0003 (11)0.0104 (11)
O3B0.0444 (15)0.0205 (13)0.0200 (13)0.0004 (11)0.0037 (11)0.0076 (11)
O4A0.062 (2)0.0324 (17)0.0471 (19)0.0062 (15)0.0055 (15)0.0204 (15)
C18A0.055 (3)0.038 (3)0.058 (3)0.007 (2)0.012 (2)0.020 (2)
C19A0.046 (2)0.038 (3)0.047 (3)0.012 (2)0.001 (2)0.020 (2)
F2A0.082 (2)0.0524 (18)0.070 (2)0.0205 (16)0.0186 (17)0.0274 (16)
F3A0.136 (3)0.0416 (18)0.064 (2)0.0282 (19)0.030 (2)0.0004 (16)
O4B0.0512 (18)0.0315 (16)0.0423 (18)0.0083 (13)0.0043 (14)0.0157 (14)
C18B0.052 (2)0.031 (2)0.030 (2)0.0073 (19)0.0047 (19)0.0051 (19)
C19B0.054 (3)0.040 (3)0.036 (2)0.004 (2)0.000 (2)0.011 (2)
F2B0.0654 (19)0.0564 (19)0.0539 (18)0.0114 (15)0.0123 (14)0.0068 (15)
F3B0.0675 (19)0.0444 (17)0.065 (2)0.0007 (14)0.0004 (15)0.0039 (15)
O4C0.058 (2)0.060 (2)0.0307 (17)0.0122 (16)0.0048 (15)0.0194 (16)
C18C0.045 (3)0.054 (3)0.034 (2)0.003 (2)0.0048 (19)0.013 (2)
C19C0.044 (2)0.036 (2)0.027 (2)0.0015 (18)0.0041 (17)0.0047 (19)
F2C0.0802 (19)0.0406 (16)0.0323 (14)0.0010 (14)0.0011 (13)0.0084 (12)
F3C0.0677 (19)0.071 (2)0.0512 (17)0.0159 (16)0.0091 (14)0.0253 (16)
Geometric parameters (Å, º) top
C1A—N1A1.456 (5)C5B—N1B1.343 (5)
C1A—C2A1.487 (5)C5B—C6B1.366 (5)
C1A—C3A1.502 (6)C5B—H5B0.930
C1A—H1A0.980C6B—C8B1.450 (5)
C2A—C3A1.498 (6)C6B—C7B1.505 (5)
C2A—H2A10.970C7B—O2B1.249 (4)
C2A—H2A20.970C7B—O1B1.278 (4)
C3A—H3A10.970C8B—O3B1.250 (4)
C3A—H3A20.970C8B—C9B1.466 (5)
C4A—C9A1.395 (5)C9B—C10B1.411 (5)
C4A—C17A1.397 (5)C10B—C11B1.348 (5)
C4A—N1A1.400 (4)C10B—H10B0.930
C5A—N1A1.346 (4)C11B—F1B1.370 (4)
C5A—C6A1.373 (5)C11B—C12B1.404 (5)
C5A—H5A0.930C12B—C17B1.392 (5)
C6A—C8A1.446 (5)C12B—N2B1.402 (4)
C6A—C7A1.512 (5)C13B—N2B1.470 (5)
C7A—O2A1.251 (4)C13B—C14B1.518 (5)
C7A—O1A1.263 (4)C13B—H13C0.970
C8A—O3A1.246 (4)C13B—H13D0.970
C8A—C9A1.473 (5)C14B—N3B1.483 (5)
C9A—C10A1.404 (5)C14B—H14C0.970
C10A—C11A1.353 (5)C14B—H14D0.970
C10A—H10A0.930C15B—N3B1.485 (5)
C11A—F1A1.374 (4)C15B—C16B1.515 (5)
C11A—C12A1.402 (5)C15B—H15C0.970
C12A—C17A1.396 (5)C15B—H15D0.970
C12A—N2A1.400 (4)C16B—N2B1.470 (4)
C13A—N2A1.462 (4)C16B—H16C0.970
C13A—C14A1.526 (5)C16B—H16D0.970
C13A—H13A0.970C17B—H17B0.930
C13A—H13B0.970N3B—H3B30.900
C14A—N3A1.481 (4)N3B—H3B40.900
C14A—H14A0.970O4A—C18A1.417 (5)
C14A—H14B0.970O4A—H4A0.820
C15A—N3A1.484 (4)C18A—C19A1.463 (6)
C15A—C16A1.515 (5)C18A—H18A0.970
C15A—H15A0.970C18A—H18B0.970
C15A—H15B0.970C19A—F3A1.344 (6)
C16A—N2A1.475 (4)C19A—F2A1.376 (5)
C16A—H16A0.970C19A—H19A0.980
C16A—H16B0.970O4B—C18B1.416 (5)
C17A—H17A0.930O4B—H4B0.820
N3A—H3A40.900C18B—C19B1.467 (6)
N3A—H3A30.900C18B—H18C0.970
C1B—N1B1.449 (5)C18B—H18D0.970
C1B—C2B1.474 (5)C19B—F3B1.360 (6)
C1B—C3B1.494 (6)C19B—F2B1.362 (5)
C1B—H1B0.980C19B—H19B0.980
C2B—C3B1.502 (6)O4C—C18C1.422 (6)
C2B—H2B10.970O4C—H4C0.820
C2B—H2B20.970C18C—C19C1.491 (6)
C3B—H3B10.970C18C—H18E0.970
C3B—H3B20.970C18C—H18F0.970
C4B—C17B1.390 (5)C19C—F2C1.354 (5)
C4B—C9B1.393 (5)C19C—F3C1.374 (5)
C4B—N1B1.402 (4)C19C—H19C0.980
N1A—C1A—C2A118.0 (3)C9B—C4B—N1B118.1 (3)
N1A—C1A—C3A117.2 (3)N1B—C5B—C6B125.7 (3)
C2A—C1A—C3A60.2 (3)N1B—C5B—H5B117.2
N1A—C1A—H1A116.5C6B—C5B—H5B117.2
C2A—C1A—H1A116.5C5B—C6B—C8B118.9 (3)
C3A—C1A—H1A116.5C5B—C6B—C7B117.8 (3)
C1A—C2A—C3A60.4 (3)C8B—C6B—C7B123.3 (3)
C1A—C2A—H2A1117.7O2B—C7B—O1B123.6 (3)
C3A—C2A—H2A1117.7O2B—C7B—C6B119.7 (3)
C1A—C2A—H2A2117.7O1B—C7B—C6B116.7 (3)
C3A—C2A—H2A2117.7O3B—C8B—C6B126.3 (3)
H2A1—C2A—H2A2114.9O3B—C8B—C9B119.2 (3)
C2A—C3A—C1A59.4 (3)C6B—C8B—C9B114.5 (3)
C2A—C3A—H3A1117.8C4B—C9B—C10B117.2 (3)
C1A—C3A—H3A1117.8C4B—C9B—C8B123.2 (3)
C2A—C3A—H3A2117.8C10B—C9B—C8B119.6 (3)
C1A—C3A—H3A2117.8C11B—C10B—C9B120.3 (3)
H3A1—C3A—H3A2115.0C11B—C10B—H10B119.9
C9A—C4A—C17A121.3 (3)C9B—C10B—H10B119.9
C9A—C4A—N1A118.1 (3)C10B—C11B—F1B117.7 (3)
C17A—C4A—N1A120.6 (3)C10B—C11B—C12B123.6 (3)
N1A—C5A—C6A125.7 (3)F1B—C11B—C12B118.6 (3)
N1A—C5A—H5A117.2C17B—C12B—N2B123.1 (3)
C6A—C5A—H5A117.2C17B—C12B—C11B116.3 (3)
C5A—C6A—C8A118.5 (3)N2B—C12B—C11B120.5 (3)
C5A—C6A—C7A116.8 (3)N2B—C13B—C14B109.4 (3)
C8A—C6A—C7A124.6 (3)N2B—C13B—H13C109.8
O2A—C7A—O1A123.9 (3)C14B—C13B—H13C109.8
O2A—C7A—C6A118.4 (3)N2B—C13B—H13D109.8
O1A—C7A—C6A117.7 (3)C14B—C13B—H13D109.8
O3A—C8A—C6A126.5 (3)H13C—C13B—H13D108.3
O3A—C8A—C9A118.9 (3)N3B—C14B—C13B111.4 (3)
C6A—C8A—C9A114.6 (3)N3B—C14B—H14C109.3
C4A—C9A—C10A118.3 (3)C13B—C14B—H14C109.3
C4A—C9A—C8A122.9 (3)N3B—C14B—H14D109.3
C10A—C9A—C8A118.8 (3)C13B—C14B—H14D109.3
C11A—C10A—C9A119.5 (3)H14C—C14B—H14D108.0
C11A—C10A—H10A120.2N3B—C15B—C16B109.5 (3)
C9A—C10A—H10A120.2N3B—C15B—H15C109.8
C10A—C11A—F1A117.4 (3)C16B—C15B—H15C109.8
C10A—C11A—C12A123.8 (3)N3B—C15B—H15D109.8
F1A—C11A—C12A118.8 (3)C16B—C15B—H15D109.8
C17A—C12A—N2A123.4 (3)H15C—C15B—H15D108.2
C17A—C12A—C11A116.7 (3)N2B—C16B—C15B109.8 (3)
N2A—C12A—C11A119.8 (3)N2B—C16B—H16C109.7
N2A—C13A—C14A109.5 (3)C15B—C16B—H16C109.7
N2A—C13A—H13A109.8N2B—C16B—H16D109.7
C14A—C13A—H13A109.8C15B—C16B—H16D109.7
N2A—C13A—H13B109.8H16C—C16B—H16D108.2
C14A—C13A—H13B109.8C4B—C17B—C12B120.9 (3)
H13A—C13A—H13B108.2C4B—C17B—H17B119.6
N3A—C14A—C13A111.9 (3)C12B—C17B—H17B119.6
N3A—C14A—H14A109.2C5B—N1B—C4B119.6 (3)
C13A—C14A—H14A109.2C5B—N1B—C1B122.3 (3)
N3A—C14A—H14B109.2C4B—N1B—C1B118.0 (3)
C13A—C14A—H14B109.2C12B—N2B—C13B116.6 (3)
H14A—C14A—H14B107.9C12B—N2B—C16B115.1 (3)
N3A—C15A—C16A110.1 (3)C13B—N2B—C16B110.1 (3)
N3A—C15A—H15A109.6C14B—N3B—C15B111.2 (3)
C16A—C15A—H15A109.6C14B—N3B—H3B3109.4
N3A—C15A—H15B109.6C15B—N3B—H3B3109.4
C16A—C15A—H15B109.6C14B—N3B—H3B4109.4
H15A—C15A—H15B108.2C15B—N3B—H3B4109.4
N2A—C16A—C15A109.4 (3)H3B3—N3B—H3B4108.0
N2A—C16A—H16A109.8C18A—O4A—H4A109.5
C15A—C16A—H16A109.8O4A—C18A—C19A108.3 (4)
N2A—C16A—H16B109.8O4A—C18A—H18A110.0
C15A—C16A—H16B109.8C19A—C18A—H18A110.0
H16A—C16A—H16B108.2O4A—C18A—H18B110.0
C12A—C17A—C4A120.3 (3)C19A—C18A—H18B110.0
C12A—C17A—H17A119.9H18A—C18A—H18B108.4
C4A—C17A—H17A119.9F3A—C19A—F2A104.9 (4)
C5A—N1A—C4A119.6 (3)F3A—C19A—C18A111.7 (4)
C5A—N1A—C1A120.4 (3)F2A—C19A—C18A110.0 (4)
C4A—N1A—C1A120.0 (3)F3A—C19A—H19A110.0
C12A—N2A—C13A118.2 (3)F2A—C19A—H19A110.0
C12A—N2A—C16A115.8 (3)C18A—C19A—H19A110.0
C13A—N2A—C16A110.5 (3)C18B—O4B—H4B109.5
C14A—N3A—C15A111.6 (3)O4B—C18B—C19B111.5 (4)
C14A—N3A—H3A4109.3O4B—C18B—H18C109.3
C15A—N3A—H3A4109.3C19B—C18B—H18C109.3
C14A—N3A—H3A3109.3O4B—C18B—H18D109.3
C15A—N3A—H3A3109.3C19B—C18B—H18D109.3
H3A4—N3A—H3A3108.0H18C—C18B—H18D108.0
N1B—C1B—C2B121.1 (3)F3B—C19B—F2B107.3 (4)
N1B—C1B—C3B117.2 (4)F3B—C19B—C18B110.3 (4)
C2B—C1B—C3B60.8 (3)F2B—C19B—C18B111.2 (4)
N1B—C1B—H1B115.5F3B—C19B—H19B109.4
C2B—C1B—H1B115.5F2B—C19B—H19B109.4
C3B—C1B—H1B115.5C18B—C19B—H19B109.4
C1B—C2B—C3B60.3 (3)C18C—O4C—H4C109.5
C1B—C2B—H2B1117.7O4C—C18C—C19C108.2 (4)
C3B—C2B—H2B1117.7O4C—C18C—H18E110.1
C1B—C2B—H2B2117.7C19C—C18C—H18E110.1
C3B—C2B—H2B2117.7O4C—C18C—H18F110.1
H2B1—C2B—H2B2114.9C19C—C18C—H18F110.1
C1B—C3B—C2B58.9 (3)H18E—C18C—H18F108.4
C1B—C3B—H3B1117.9F2C—C19C—F3C105.3 (3)
C2B—C3B—H3B1117.9F2C—C19C—C18C111.1 (4)
C1B—C3B—H3B2117.9F3C—C19C—C18C108.5 (4)
C2B—C3B—H3B2117.9F2C—C19C—H19C110.6
H3B1—C3B—H3B2115.0F3C—C19C—H19C110.6
C17B—C4B—C9B121.7 (3)C18C—C19C—H19C110.6
C17B—C4B—N1B120.2 (3)
N1A—C1A—C2A—C3A107.0 (4)N1B—C5B—C6B—C7B179.9 (4)
N1A—C1A—C3A—C2A108.3 (4)C5B—C6B—C7B—O2B179.6 (3)
N1A—C5A—C6A—C8A2.1 (6)C8B—C6B—C7B—O2B1.0 (6)
N1A—C5A—C6A—C7A179.9 (4)C5B—C6B—C7B—O1B0.3 (5)
C5A—C6A—C7A—O2A175.6 (4)C8B—C6B—C7B—O1B179.0 (3)
C8A—C6A—C7A—O2A6.5 (6)C5B—C6B—C8B—O3B179.3 (4)
C5A—C6A—C7A—O1A3.0 (5)C7B—C6B—C8B—O3B0.0 (6)
C8A—C6A—C7A—O1A174.9 (4)C5B—C6B—C8B—C9B1.2 (5)
C5A—C6A—C8A—O3A173.2 (4)C7B—C6B—C8B—C9B179.4 (3)
C7A—C6A—C8A—O3A4.7 (6)C17B—C4B—C9B—C10B0.3 (5)
C5A—C6A—C8A—C9A7.3 (5)N1B—C4B—C9B—C10B179.7 (3)
C7A—C6A—C8A—C9A174.8 (3)C17B—C4B—C9B—C8B179.1 (3)
C17A—C4A—C9A—C10A1.0 (5)N1B—C4B—C9B—C8B0.9 (5)
N1A—C4A—C9A—C10A179.6 (3)O3B—C8B—C9B—C4B179.1 (3)
C17A—C4A—C9A—C8A177.8 (3)C6B—C8B—C9B—C4B1.4 (5)
N1A—C4A—C9A—C8A1.6 (5)O3B—C8B—C9B—C10B0.4 (5)
O3A—C8A—C9A—C4A173.2 (3)C6B—C8B—C9B—C10B179.1 (3)
C6A—C8A—C9A—C4A7.2 (5)C4B—C9B—C10B—C11B0.6 (5)
O3A—C8A—C9A—C10A5.5 (5)C8B—C9B—C10B—C11B179.9 (3)
C6A—C8A—C9A—C10A174.0 (3)C9B—C10B—C11B—F1B176.5 (3)
C4A—C9A—C10A—C11A0.8 (5)C9B—C10B—C11B—C12B1.0 (6)
C8A—C9A—C10A—C11A179.6 (3)C10B—C11B—C12B—C17B0.4 (6)
C9A—C10A—C11A—F1A175.4 (3)F1B—C11B—C12B—C17B177.1 (3)
C9A—C10A—C11A—C12A2.2 (6)C10B—C11B—C12B—N2B177.7 (4)
C10A—C11A—C12A—C17A1.6 (6)F1B—C11B—C12B—N2B0.3 (5)
F1A—C11A—C12A—C17A175.9 (3)N2B—C13B—C14B—N3B56.2 (4)
C10A—C11A—C12A—N2A178.7 (4)N3B—C15B—C16B—N2B59.4 (4)
F1A—C11A—C12A—N2A1.2 (5)C9B—C4B—C17B—C12B0.9 (6)
N2A—C13A—C14A—N3A55.0 (4)N1B—C4B—C17B—C12B179.1 (3)
N3A—C15A—C16A—N2A58.8 (4)N2B—C12B—C17B—C4B176.7 (3)
N2A—C12A—C17A—C4A176.7 (3)C11B—C12B—C17B—C4B0.5 (5)
C11A—C12A—C17A—C4A0.2 (5)C6B—C5B—N1B—C4B0.1 (6)
C9A—C4A—C17A—C12A1.5 (6)C6B—C5B—N1B—C1B176.9 (4)
N1A—C4A—C17A—C12A179.1 (3)C17B—C4B—N1B—C5B180.0 (3)
C6A—C5A—N1A—C4A4.1 (6)C9B—C4B—N1B—C5B0.1 (5)
C6A—C5A—N1A—C1A173.7 (4)C17B—C4B—N1B—C1B2.8 (5)
C9A—C4A—N1A—C5A4.2 (5)C9B—C4B—N1B—C1B177.2 (3)
C17A—C4A—N1A—C5A176.4 (3)C2B—C1B—N1B—C5B30.5 (6)
C9A—C4A—N1A—C1A173.7 (3)C3B—C1B—N1B—C5B101.2 (4)
C17A—C4A—N1A—C1A5.8 (5)C2B—C1B—N1B—C4B146.5 (4)
C2A—C1A—N1A—C5A37.9 (5)C3B—C1B—N1B—C4B75.8 (5)
C3A—C1A—N1A—C5A106.8 (4)C17B—C12B—N2B—C13B8.7 (5)
C2A—C1A—N1A—C4A139.9 (4)C11B—C12B—N2B—C13B168.5 (3)
C3A—C1A—N1A—C4A71.0 (5)C17B—C12B—N2B—C16B122.4 (4)
C17A—C12A—N2A—C13A9.3 (5)C11B—C12B—N2B—C16B60.4 (4)
C11A—C12A—N2A—C13A167.6 (3)C14B—C13B—N2B—C12B166.6 (3)
C17A—C12A—N2A—C16A125.2 (4)C14B—C13B—N2B—C16B59.9 (4)
C11A—C12A—N2A—C16A58.0 (4)C15B—C16B—N2B—C12B163.5 (3)
C14A—C13A—N2A—C12A163.6 (3)C15B—C16B—N2B—C13B62.2 (4)
C14A—C13A—N2A—C16A59.7 (4)C13B—C14B—N3B—C15B54.8 (4)
C15A—C16A—N2A—C12A159.8 (3)C16B—C15B—N3B—C14B55.7 (4)
C15A—C16A—N2A—C13A62.4 (4)O4A—C18A—C19A—F3A66.8 (5)
C13A—C14A—N3A—C15A53.0 (4)O4A—C18A—C19A—F2A177.1 (4)
C16A—C15A—N3A—C14A54.6 (4)O4B—C18B—C19B—F3B170.6 (4)
N1B—C1B—C2B—C3B105.9 (4)O4B—C18B—C19B—F2B70.6 (5)
N1B—C1B—C3B—C2B112.2 (4)O4C—C18C—C19C—F2C60.4 (5)
N1B—C5B—C6B—C8B0.5 (6)O4C—C18C—C19C—F3C175.6 (4)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N3A—H3A3···O1Ai0.902.583.176 (4)125
N3A—H3A3···O2Ai0.901.862.758 (4)173
N3A—H3A4···O2Bii0.902.392.885 (4)114
N3A—H3A4···O3Bii0.901.852.717 (4)162
N3B—H3B3···O1Biii0.902.773.376 (4)126
N3B—H3B3···O2Biii0.901.822.724 (4)179
N3B—H3B4···O2Aiv0.902.502.894 (4)107
N3B—H3B4···O3Aiv0.901.792.687 (4)171
O4A—H4A···O1Av0.821.882.672 (4)162
O4B—H4B···O1Bii0.821.872.666 (4)165
O4C—H4C···O1Bv0.821.932.733 (4)168
C2A—H2A2···F3Bii0.972.513.207 (5)128
C14A—H14A···O2Avi0.972.493.350 (5)148
C14A—H14A···O3Avi0.972.493.274 (4)138
C16A—H16A···O4Bvii0.972.483.148 (5)126
C1B—H1B···F2C0.982.453.200 (5)133
C14B—H14D···O2Bii0.972.343.295 (4)170
C15B—H15D···O2Aiv0.972.513.131 (5)122
C18B—H18D···F1B0.972.463.396 (5)161
Symmetry codes: (i) x, y, z1; (ii) x+1, y+1, z+1; (iii) x, y+1, z; (iv) x+1, y+2, z+2; (v) x+1, y+1, z+2; (vi) x+2, y+2, z+2; (vii) x+1, y+2, z+1.
(II) 1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-4-ium-1-yl)-1,4-dihydroquinoline-3- carboxylate–water (3/14.5) top
Crystal data top
3C17H18FN3O3·14.5H2OZ = 2
Mr = 1255.26F(000) = 1334
Triclinic, P1Dx = 1.402 Mg m3
Hall symbol: -P 1Mo Kα radiation, λ = 0.71073 Å
a = 13.8760 (12) ÅCell parameters from 6396 reflections
b = 15.8760 (13) Åθ = 2.4–31.4°
c = 16.528 (2) ŵ = 0.12 mm1
α = 115.755 (7)°T = 100 K
β = 103.610 (7)°Block, colourless
γ = 102.325 (5)°0.30 × 0.25 × 0.20 mm
V = 2972.8 (5) Å3
Data collection top
Bruker APEXII CCD area-detector
diffractometer
12150 independent reflections
Radiation source: fine-focus sealed tube9655 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.038
ω scansθmax = 26.4°, θmin = 2.2°
Absorption correction: multi-scan
(SADABS; Sheldrick, 2008a)
h = 1717
Tmin = 0.40, Tmax = 0.43k = 1919
55842 measured reflectionsl = 2020
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.043Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.122H atoms treated by a mixture of independent and constrained refinement
S = 1.03 w = 1/[σ2(Fo2) + (0.0595P)2 + 1.7881P]
where P = (Fo2 + 2Fc2)/3
12150 reflections(Δ/σ)max < 0.001
907 parametersΔρmax = 0.57 e Å3
34 restraintsΔρmin = 0.42 e Å3
Crystal data top
3C17H18FN3O3·14.5H2Oγ = 102.325 (5)°
Mr = 1255.26V = 2972.8 (5) Å3
Triclinic, P1Z = 2
a = 13.8760 (12) ÅMo Kα radiation
b = 15.8760 (13) ŵ = 0.12 mm1
c = 16.528 (2) ÅT = 100 K
α = 115.755 (7)°0.30 × 0.25 × 0.20 mm
β = 103.610 (7)°
Data collection top
Bruker APEXII CCD area-detector
diffractometer
12150 independent reflections
Absorption correction: multi-scan
(SADABS; Sheldrick, 2008a)
9655 reflections with I > 2σ(I)
Tmin = 0.40, Tmax = 0.43Rint = 0.038
55842 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.04334 restraints
wR(F2) = 0.122H atoms treated by a mixture of independent and constrained refinement
S = 1.03Δρmax = 0.57 e Å3
12150 reflectionsΔρmin = 0.42 e Å3
907 parameters
Special details top

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

Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R-factors based on ALL data will be even larger.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/UeqOcc. (<1)
C1A0.01030 (13)0.05863 (13)0.75199 (12)0.0162 (3)
H1A0.01860.00630.72030.019*
C2A0.00057 (14)0.08955 (14)0.84785 (13)0.0210 (4)
H2A10.00040.04360.87180.025*
H2A20.04600.12780.86420.025*
C3A0.10167 (13)0.13991 (13)0.84351 (13)0.0187 (4)
H3A10.11750.20830.85710.022*
H3A20.16310.12410.86470.022*
C4A0.00372 (13)0.11147 (12)0.63089 (12)0.0149 (3)
C5A0.15004 (13)0.07864 (13)0.67699 (13)0.0165 (3)
H5A0.18030.05610.71180.020*
C6A0.21164 (13)0.10248 (13)0.61823 (12)0.0166 (3)
C7A0.32080 (13)0.09554 (13)0.62078 (13)0.0185 (4)
C8A0.17049 (13)0.13364 (12)0.55932 (12)0.0154 (3)
C9A0.06323 (13)0.13288 (12)0.56604 (12)0.0155 (3)
C10A0.01854 (13)0.14943 (13)0.50339 (12)0.0161 (3)
H10A0.05650.16210.45830.019*
C11A0.08030 (13)0.14676 (12)0.50921 (12)0.0155 (3)
C12A0.14544 (13)0.13332 (12)0.57909 (12)0.0146 (3)
C13A0.30262 (13)0.11202 (13)0.65625 (12)0.0164 (3)
H13A0.25640.05120.64790.020*
H13B0.31780.16650.72060.020*
C14A0.40542 (13)0.09951 (13)0.64716 (13)0.0174 (3)
H14A0.44170.08970.69840.021*
H14B0.38960.04040.58560.021*
C15A0.42007 (13)0.20740 (14)0.57800 (13)0.0187 (4)
H15A0.40350.15100.51430.022*
H15B0.46590.26690.58380.022*
C16A0.31815 (13)0.22165 (13)0.58904 (13)0.0170 (3)
H16A0.33530.28100.65080.020*
H16B0.28130.23170.53820.020*
C17A0.10022 (13)0.11484 (13)0.63909 (12)0.0157 (3)
H17A0.13960.10450.68560.019*
F1A0.11574 (8)0.15200 (8)0.44057 (7)0.0193 (2)
N1A0.04887 (11)0.08558 (11)0.68779 (10)0.0152 (3)
N2A0.24798 (11)0.13337 (11)0.58360 (10)0.0152 (3)
N3A0.47622 (11)0.18885 (11)0.65348 (11)0.0168 (3)
H3A30.49570.24290.71250.020*
H3A40.53540.17860.64520.020*
O1A0.36156 (10)0.03730 (10)0.64688 (10)0.0256 (3)
O2A0.36312 (10)0.14924 (11)0.59960 (10)0.0244 (3)
O3A0.22068 (9)0.15653 (9)0.50312 (9)0.0194 (3)
C1B0.29467 (14)0.23071 (13)0.30397 (12)0.0182 (4)
H1C0.32800.25880.27070.022*
C2B0.20504 (15)0.13171 (13)0.24003 (13)0.0223 (4)
H2C10.18450.10230.17060.027*
H2D20.14690.11880.26130.027*
C3B0.31166 (15)0.13773 (14)0.29628 (14)0.0247 (4)
H3C10.31750.12860.35130.030*
H3D20.35510.11200.26060.030*
C4B0.38410 (13)0.36527 (12)0.47548 (12)0.0149 (3)
C5B0.19722 (13)0.31214 (13)0.39923 (13)0.0167 (3)
H5C0.13690.27280.34270.020*
C6B0.18425 (13)0.37441 (13)0.48112 (13)0.0166 (3)
C7B0.07127 (14)0.36530 (13)0.47227 (13)0.0193 (4)
C8B0.27616 (13)0.44012 (13)0.57029 (12)0.0159 (3)
C9B0.37795 (13)0.43309 (13)0.56186 (12)0.0155 (3)
C10B0.47369 (14)0.49694 (13)0.64258 (12)0.0166 (3)
H10C0.47280.54320.70100.020*
C11B0.56765 (13)0.49026 (13)0.63440 (12)0.0164 (3)
C12B0.57591 (13)0.41920 (13)0.55003 (12)0.0152 (3)
C13B0.67626 (13)0.35036 (13)0.45292 (12)0.0168 (3)
H13C0.63880.36520.40640.020*
H13D0.63940.28090.43200.020*
C14B0.78931 (14)0.36560 (14)0.45669 (13)0.0187 (4)
H14C0.78800.31970.39370.022*
H14D0.82390.43340.47190.022*
C15B0.84785 (14)0.41153 (15)0.62718 (13)0.0217 (4)
H15C0.88440.48170.65030.026*
H15D0.88420.39540.67320.026*
C16B0.73346 (14)0.39399 (14)0.62038 (13)0.0188 (4)
H16C0.69810.32480.60120.023*
H16D0.73230.43680.68330.023*
C17B0.48173 (13)0.35762 (12)0.46986 (12)0.0151 (3)
H17C0.48330.31090.41200.018*
F1B0.65970 (8)0.55830 (8)0.71088 (7)0.0204 (2)
N1B0.29006 (11)0.30310 (11)0.39370 (10)0.0162 (3)
N2B0.67632 (11)0.41602 (11)0.54880 (10)0.0158 (3)
N3B0.85125 (11)0.34822 (11)0.53093 (11)0.0188 (3)
H3B30.82420.28320.51280.023*
H3B40.91920.36260.53510.023*
O1B0.00013 (10)0.31583 (10)0.38875 (10)0.0269 (3)
O2B0.05349 (10)0.40641 (10)0.54905 (10)0.0247 (3)
O3B0.27442 (10)0.50037 (9)0.64887 (9)0.0203 (3)
C1C0.10738 (14)0.31041 (13)0.07593 (13)0.0183 (4)
H1E0.04370.27270.01640.022*
C2C0.16026 (14)0.24825 (14)0.10174 (13)0.0214 (4)
H2E10.23710.27600.13350.026*
H2F20.13020.17620.05790.026*
C3C0.09685 (15)0.29607 (14)0.15790 (14)0.0221 (4)
H3E10.02870.25280.14760.027*
H3F20.13550.35260.22330.027*
C4C0.12151 (13)0.48096 (13)0.11331 (12)0.0166 (3)
C5C0.27096 (13)0.43313 (13)0.10391 (12)0.0170 (3)
H5E0.29960.38300.09040.020*
C6C0.33560 (13)0.52667 (13)0.12925 (12)0.0174 (4)
C7C0.45042 (14)0.54273 (14)0.14200 (12)0.0187 (4)
C8C0.29293 (14)0.60469 (13)0.14454 (12)0.0178 (4)
C9C0.18149 (14)0.57680 (13)0.13538 (12)0.0179 (4)
C10C0.13191 (14)0.64792 (14)0.14996 (13)0.0208 (4)
H10E0.16890.71160.16350.025*
C11C0.02942 (15)0.62282 (14)0.14418 (13)0.0218 (4)
C12C0.03129 (14)0.52869 (14)0.12660 (12)0.0193 (4)
C13C0.20246 (14)0.40775 (15)0.08716 (14)0.0250 (4)
H13E0.17880.38680.13300.030*
H13F0.19680.36390.02690.030*
C14C0.31720 (15)0.40022 (16)0.07001 (14)0.0299 (5)
H14E0.34220.41610.02040.036*
H14F0.36120.33200.04700.036*
C15C0.25400 (16)0.57458 (15)0.20396 (15)0.0254 (4)
H15E0.25810.61690.26560.031*
H15F0.27500.60020.16160.031*
C16C0.14139 (15)0.57851 (14)0.21914 (13)0.0224 (4)
H16E0.09450.64680.24590.027*
H16F0.11850.55710.26470.027*
C17C0.01608 (14)0.45761 (13)0.10949 (12)0.0180 (4)
H17E0.02190.39390.09530.022*
F1C0.01800 (9)0.69140 (8)0.15369 (9)0.0294 (3)
N1C0.16929 (11)0.40926 (11)0.09739 (10)0.0163 (3)
N2C0.13518 (12)0.51201 (12)0.12542 (11)0.0210 (3)
N3C0.32810 (12)0.47000 (12)0.16036 (11)0.0234 (3)
H3C40.39540.46850.14680.028*
H3C30.31440.44950.20330.028*
O1C0.47208 (10)0.46445 (10)0.10160 (10)0.0244 (3)
O2C0.51768 (10)0.62985 (9)0.19216 (9)0.0225 (3)
O3C0.34399 (10)0.69030 (9)0.16331 (10)0.0236 (3)
OW1A0.6940 (3)0.1254 (3)1.0564 (2)0.0384 (7)0.50
OW1B0.6126 (4)0.0704 (3)1.0436 (3)0.0669 (12)0.50
OW2A0.3200 (2)0.0970 (2)0.04907 (19)0.0393 (6)0.60
OW2B0.2159 (2)0.0042 (2)0.0927 (2)0.0223 (7)0.40
OW3A0.5083 (2)0.2178 (2)0.2245 (2)0.0319 (7)0.50
OW3B0.4730 (4)0.2825 (4)0.1750 (3)0.0823 (16)0.50
OW4A0.2248 (2)0.97205 (19)0.74736 (18)0.0330 (6)0.60
OW4B0.1614 (3)0.8795 (3)0.7071 (2)0.0295 (8)0.40
OW5A0.6790 (2)0.2961 (2)0.1828 (2)0.0257 (6)0.50
OW5B0.6683 (3)0.2485 (3)0.2086 (2)0.0454 (8)0.50
OW6A0.8952 (3)0.0356 (3)0.0276 (2)0.0237 (7)0.50
OW6B0.9370 (3)0.0326 (3)0.0136 (3)0.0265 (7)0.50
OW7A0.3738 (3)0.1689 (3)0.9555 (3)0.0413 (9)0.60
OW7B0.3657 (5)0.1445 (4)0.9120 (3)0.0257 (12)0.40
OW80.33039 (15)0.85648 (12)0.16362 (12)0.0434 (4)
H810.347 (2)0.8994 (17)0.2238 (9)0.065*
H820.335 (2)0.8006 (13)0.157 (2)0.065*
OW90.45285 (10)0.88062 (10)0.58803 (10)0.0245 (3)
H910.4050 (14)0.8686 (18)0.5370 (12)0.037*
H920.5089 (12)0.9297 (13)0.6042 (16)0.037*
OW100.88366 (12)0.39539 (11)0.29624 (10)0.0312 (3)
H1010.9215 (18)0.3725 (18)0.3245 (17)0.047*
H1020.887 (2)0.4539 (11)0.3383 (15)0.047*
OW110.37127 (11)0.31620 (10)0.08836 (10)0.0278 (3)
H1110.4046 (18)0.3286 (18)0.1224 (15)0.042*
H1120.4023 (18)0.3647 (14)0.0296 (9)0.042*
OW120.62077 (15)0.10562 (12)0.27024 (12)0.0409 (4)
H1210.601 (2)0.111 (2)0.3170 (16)0.061*
H1220.623 (2)0.1469 (18)0.251 (2)0.061*
OW130.85309 (12)0.17866 (13)0.01946 (13)0.0421 (4)
H1310.8028 (17)0.165 (2)0.0700 (14)0.063*
H1320.825 (2)0.156 (2)0.0111 (19)0.063*
OW140.51312 (19)0.07464 (14)0.89016 (13)0.0582 (5)
H1410.548 (2)0.116 (2)0.9534 (8)0.087*
H1420.548 (2)0.093 (3)0.860 (2)0.087*
OW150.93634 (19)0.12971 (18)0.22207 (17)0.0181 (5)0.50
H1510.882 (2)0.095 (2)0.224 (3)0.027*0.50
H1520.961 (3)0.1890 (11)0.265 (2)0.027*0.50
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
C1A0.0143 (8)0.0174 (8)0.0199 (9)0.0075 (7)0.0071 (7)0.0109 (7)
C2A0.0192 (9)0.0233 (9)0.0202 (9)0.0064 (7)0.0080 (7)0.0112 (8)
C3A0.0149 (8)0.0190 (9)0.0209 (9)0.0057 (7)0.0043 (7)0.0105 (7)
C4A0.0135 (8)0.0134 (8)0.0176 (8)0.0048 (6)0.0068 (6)0.0074 (7)
C5A0.0121 (8)0.0151 (8)0.0212 (9)0.0041 (6)0.0073 (7)0.0083 (7)
C6A0.0128 (8)0.0147 (8)0.0202 (8)0.0054 (6)0.0060 (7)0.0071 (7)
C7A0.0129 (8)0.0189 (9)0.0206 (9)0.0053 (7)0.0057 (7)0.0081 (7)
C8A0.0129 (8)0.0119 (8)0.0174 (8)0.0055 (6)0.0036 (6)0.0049 (7)
C9A0.0119 (8)0.0134 (8)0.0189 (8)0.0045 (6)0.0045 (6)0.0070 (7)
C10A0.0139 (8)0.0155 (8)0.0175 (8)0.0061 (7)0.0035 (6)0.0080 (7)
C11A0.0168 (8)0.0134 (8)0.0152 (8)0.0049 (6)0.0070 (6)0.0062 (7)
C12A0.0129 (8)0.0121 (8)0.0170 (8)0.0056 (6)0.0056 (6)0.0055 (7)
C13A0.0129 (8)0.0192 (8)0.0195 (8)0.0071 (7)0.0066 (7)0.0110 (7)
C14A0.0150 (8)0.0181 (8)0.0216 (9)0.0080 (7)0.0073 (7)0.0111 (7)
C15A0.0145 (8)0.0231 (9)0.0226 (9)0.0079 (7)0.0084 (7)0.0138 (8)
C16A0.0142 (8)0.0171 (8)0.0223 (9)0.0072 (7)0.0072 (7)0.0112 (7)
C17A0.0138 (8)0.0165 (8)0.0185 (8)0.0073 (7)0.0057 (7)0.0096 (7)
F1A0.0166 (5)0.0259 (5)0.0185 (5)0.0085 (4)0.0083 (4)0.0128 (4)
N1A0.0134 (7)0.0156 (7)0.0182 (7)0.0061 (6)0.0061 (6)0.0095 (6)
N2A0.0117 (7)0.0172 (7)0.0191 (7)0.0066 (6)0.0066 (6)0.0101 (6)
N3A0.0127 (7)0.0185 (7)0.0196 (7)0.0068 (6)0.0071 (6)0.0089 (6)
O1A0.0163 (6)0.0268 (7)0.0387 (8)0.0071 (5)0.0127 (6)0.0200 (6)
O2A0.0184 (6)0.0354 (8)0.0327 (7)0.0177 (6)0.0144 (6)0.0222 (6)
O3A0.0141 (6)0.0219 (6)0.0241 (6)0.0081 (5)0.0061 (5)0.0131 (5)
C1B0.0177 (8)0.0193 (9)0.0145 (8)0.0067 (7)0.0048 (7)0.0067 (7)
C2B0.0215 (9)0.0178 (9)0.0198 (9)0.0054 (7)0.0046 (7)0.0057 (7)
C3B0.0272 (10)0.0202 (9)0.0216 (9)0.0111 (8)0.0052 (8)0.0074 (8)
C4B0.0151 (8)0.0140 (8)0.0170 (8)0.0049 (6)0.0048 (7)0.0097 (7)
C5B0.0146 (8)0.0163 (8)0.0189 (8)0.0052 (7)0.0039 (7)0.0101 (7)
C6B0.0149 (8)0.0168 (8)0.0213 (9)0.0070 (7)0.0063 (7)0.0119 (7)
C7B0.0172 (8)0.0174 (9)0.0255 (9)0.0083 (7)0.0076 (7)0.0119 (8)
C8B0.0172 (8)0.0155 (8)0.0194 (9)0.0078 (7)0.0076 (7)0.0111 (7)
C9B0.0157 (8)0.0153 (8)0.0181 (8)0.0063 (7)0.0063 (7)0.0102 (7)
C10B0.0189 (8)0.0157 (8)0.0165 (8)0.0074 (7)0.0078 (7)0.0083 (7)
C11B0.0149 (8)0.0152 (8)0.0157 (8)0.0034 (7)0.0019 (6)0.0079 (7)
C12B0.0149 (8)0.0161 (8)0.0179 (8)0.0062 (7)0.0072 (7)0.0106 (7)
C13B0.0157 (8)0.0175 (8)0.0179 (8)0.0060 (7)0.0073 (7)0.0091 (7)
C14B0.0173 (8)0.0201 (9)0.0229 (9)0.0083 (7)0.0099 (7)0.0124 (7)
C15B0.0174 (9)0.0263 (10)0.0205 (9)0.0105 (7)0.0060 (7)0.0106 (8)
C16B0.0174 (8)0.0228 (9)0.0194 (9)0.0096 (7)0.0077 (7)0.0119 (7)
C17B0.0161 (8)0.0147 (8)0.0163 (8)0.0061 (7)0.0070 (7)0.0086 (7)
F1B0.0141 (5)0.0195 (5)0.0175 (5)0.0036 (4)0.0022 (4)0.0044 (4)
N1B0.0146 (7)0.0161 (7)0.0161 (7)0.0056 (6)0.0049 (6)0.0071 (6)
N2B0.0140 (7)0.0178 (7)0.0173 (7)0.0074 (6)0.0063 (6)0.0093 (6)
N3B0.0148 (7)0.0192 (7)0.0240 (8)0.0082 (6)0.0086 (6)0.0108 (6)
O1B0.0168 (6)0.0294 (7)0.0252 (7)0.0116 (6)0.0025 (5)0.0076 (6)
O2B0.0159 (6)0.0274 (7)0.0263 (7)0.0085 (5)0.0098 (5)0.0089 (6)
O3B0.0182 (6)0.0227 (7)0.0185 (6)0.0093 (5)0.0076 (5)0.0080 (5)
C1C0.0165 (8)0.0145 (8)0.0184 (8)0.0049 (7)0.0038 (7)0.0058 (7)
C2C0.0199 (9)0.0164 (9)0.0243 (9)0.0068 (7)0.0040 (7)0.0094 (7)
C3C0.0211 (9)0.0193 (9)0.0231 (9)0.0054 (7)0.0067 (7)0.0102 (8)
C4C0.0180 (8)0.0177 (8)0.0139 (8)0.0095 (7)0.0044 (7)0.0073 (7)
C5C0.0162 (8)0.0196 (9)0.0150 (8)0.0092 (7)0.0047 (7)0.0080 (7)
C6C0.0159 (8)0.0193 (9)0.0156 (8)0.0068 (7)0.0045 (7)0.0082 (7)
C7C0.0185 (8)0.0224 (9)0.0150 (8)0.0072 (7)0.0066 (7)0.0092 (7)
C8C0.0176 (8)0.0184 (9)0.0141 (8)0.0050 (7)0.0021 (7)0.0081 (7)
C9C0.0184 (8)0.0195 (9)0.0153 (8)0.0086 (7)0.0043 (7)0.0086 (7)
C10C0.0221 (9)0.0177 (9)0.0208 (9)0.0090 (7)0.0049 (7)0.0091 (7)
C11C0.0259 (9)0.0212 (9)0.0215 (9)0.0158 (8)0.0079 (7)0.0106 (8)
C12C0.0187 (8)0.0229 (9)0.0144 (8)0.0103 (7)0.0039 (7)0.0079 (7)
C13C0.0166 (9)0.0254 (10)0.0228 (9)0.0103 (8)0.0034 (7)0.0049 (8)
C14C0.0188 (9)0.0340 (11)0.0238 (10)0.0117 (8)0.0042 (8)0.0050 (9)
C15C0.0303 (10)0.0260 (10)0.0291 (10)0.0178 (8)0.0169 (8)0.0150 (8)
C16C0.0246 (9)0.0220 (9)0.0202 (9)0.0120 (8)0.0089 (7)0.0085 (8)
C17C0.0172 (8)0.0177 (8)0.0170 (8)0.0071 (7)0.0047 (7)0.0076 (7)
F1C0.0303 (6)0.0266 (6)0.0427 (7)0.0212 (5)0.0169 (5)0.0204 (5)
N1C0.0149 (7)0.0154 (7)0.0171 (7)0.0069 (6)0.0046 (6)0.0071 (6)
N2C0.0185 (7)0.0237 (8)0.0193 (7)0.0118 (6)0.0069 (6)0.0079 (6)
N3C0.0197 (8)0.0316 (9)0.0229 (8)0.0149 (7)0.0077 (6)0.0147 (7)
O1C0.0187 (6)0.0216 (7)0.0273 (7)0.0087 (5)0.0097 (5)0.0067 (6)
O2C0.0169 (6)0.0200 (7)0.0240 (7)0.0042 (5)0.0065 (5)0.0076 (6)
O3C0.0218 (6)0.0180 (6)0.0282 (7)0.0056 (5)0.0053 (5)0.0122 (6)
OW1A0.050 (2)0.0358 (18)0.0405 (18)0.0213 (16)0.0268 (16)0.0207 (15)
OW1B0.082 (3)0.067 (3)0.042 (2)0.039 (3)0.014 (2)0.018 (2)
OW2A0.0341 (14)0.0446 (16)0.0382 (15)0.0130 (12)0.0123 (11)0.0216 (13)
OW2B0.0217 (16)0.0223 (16)0.0280 (17)0.0101 (13)0.0123 (14)0.0146 (14)
OW3A0.0267 (14)0.0359 (16)0.0224 (14)0.0036 (12)0.0099 (12)0.0094 (12)
OW3B0.085 (3)0.068 (3)0.054 (3)0.050 (3)0.007 (2)0.001 (2)
OW4A0.0333 (13)0.0323 (13)0.0374 (14)0.0109 (11)0.0165 (11)0.0197 (11)
OW4B0.0233 (17)0.037 (2)0.0246 (18)0.0037 (15)0.0057 (14)0.0178 (16)
OW5A0.0289 (15)0.0242 (14)0.0308 (15)0.0075 (12)0.0152 (12)0.0185 (13)
OW5B0.0363 (18)0.044 (2)0.0357 (18)0.0080 (16)0.0062 (14)0.0112 (17)
OW6A0.0188 (17)0.0277 (16)0.0255 (16)0.0103 (14)0.0095 (13)0.0128 (13)
OW6B0.0272 (19)0.0295 (16)0.0300 (17)0.0131 (16)0.0167 (15)0.0165 (14)
OW7A0.0261 (16)0.032 (2)0.074 (3)0.0125 (15)0.020 (2)0.032 (2)
OW7B0.040 (2)0.018 (2)0.015 (2)0.0085 (18)0.017 (2)0.0027 (19)
OW80.0617 (11)0.0246 (8)0.0324 (8)0.0128 (8)0.0011 (8)0.0159 (7)
OW90.0197 (7)0.0246 (7)0.0289 (7)0.0057 (6)0.0064 (6)0.0158 (6)
OW100.0415 (9)0.0324 (8)0.0265 (8)0.0219 (7)0.0149 (7)0.0157 (6)
OW110.0333 (8)0.0222 (7)0.0231 (7)0.0059 (6)0.0104 (6)0.0097 (6)
OW120.0581 (11)0.0306 (8)0.0416 (9)0.0172 (8)0.0319 (8)0.0174 (7)
OW130.0231 (8)0.0475 (10)0.0426 (10)0.0131 (7)0.0076 (7)0.0144 (8)
OW140.0996 (17)0.0378 (10)0.0370 (10)0.0229 (10)0.0308 (11)0.0171 (8)
OW150.0155 (12)0.0135 (12)0.0188 (12)0.0029 (10)0.0080 (10)0.0032 (10)
Geometric parameters (Å, º) top
C1A—N1A1.455 (2)C13B—H13D0.970
C1A—C2A1.497 (2)C14B—N3B1.490 (2)
C1A—C3A1.505 (2)C14B—H14C0.970
C1A—H1A0.980C14B—H14D0.970
C2A—C3A1.507 (2)C15B—N3B1.486 (2)
C2A—H2A10.970C15B—C16B1.520 (2)
C2A—H2A20.970C15B—H15C0.970
C3A—H3A10.970C15B—H15D0.970
C3A—H3A20.970C16B—N2B1.479 (2)
C4A—N1A1.396 (2)C16B—H16C0.970
C4A—C9A1.402 (2)C16B—H16D0.970
C4A—C17A1.404 (2)C17B—H17C0.930
C5A—N1A1.347 (2)N3B—H3B30.900
C5A—C6A1.372 (2)N3B—H3B40.900
C5A—H5A0.930C1C—N1C1.457 (2)
C6A—C8A1.442 (2)C1C—C2C1.491 (3)
C6A—C7A1.507 (2)C1C—C3C1.502 (3)
C7A—O2A1.253 (2)C1C—H1E0.980
C7A—O1A1.265 (2)C2C—C3C1.506 (3)
C8A—O3A1.256 (2)C2C—H2E10.970
C8A—C9A1.469 (2)C2C—H2F20.970
C9A—C10A1.412 (2)C3C—H3E10.970
C10A—C11A1.363 (2)C3C—H3F20.970
C10A—H10A0.930C4C—N1C1.396 (2)
C11A—F1A1.3649 (19)C4C—C9C1.405 (3)
C11A—C12A1.415 (2)C4C—C17C1.409 (2)
C12A—C17A1.389 (2)C5C—N1C1.345 (2)
C12A—N2A1.407 (2)C5C—C6C1.378 (2)
C13A—N2A1.472 (2)C5C—H5E0.930
C13A—C14A1.514 (2)C6C—C8C1.435 (3)
C13A—H13A0.970C6C—C7C1.507 (2)
C13A—H13B0.970C7C—O2C1.249 (2)
C14A—N3A1.489 (2)C7C—O1C1.270 (2)
C14A—H14A0.970C8C—O3C1.251 (2)
C14A—H14B0.970C8C—C9C1.466 (2)
C15A—N3A1.487 (2)C9C—C10C1.407 (3)
C15A—C16A1.519 (2)C10C—C11C1.361 (3)
C15A—H15A0.970C10C—H10E0.930
C15A—H15B0.970C11C—F1C1.360 (2)
C16A—N2A1.479 (2)C11C—C12C1.413 (3)
C16A—H16A0.970C12C—C17C1.383 (3)
C16A—H16B0.970C12C—N2C1.403 (2)
C17A—H17A0.930C13C—N2C1.471 (2)
N3A—H3A30.900C13C—C14C1.519 (3)
N3A—H3A40.900C13C—H13E0.970
C1B—N1B1.456 (2)C13C—H13F0.970
C1B—C2B1.496 (2)C14C—N3C1.490 (2)
C1B—C3B1.500 (3)C14C—H14E0.970
C1B—H1C0.980C14C—H14F0.970
C2B—C3B1.509 (3)C15C—N3C1.489 (3)
C2B—H2C10.970C15C—C16C1.506 (3)
C2B—H2D20.970C15C—H15E0.970
C3B—H3C10.970C15C—H15F0.970
C3B—H3D20.970C16C—N2C1.484 (2)
C4B—N1B1.402 (2)C16C—H16E0.970
C4B—C9B1.402 (2)C16C—H16F0.970
C4B—C17B1.407 (2)C17C—H17E0.930
C5B—N1B1.346 (2)N3C—H3C40.900
C5B—C6B1.367 (3)N3C—H3C30.900
C5B—H5C0.930OW8—H810.862 (10)
C6B—C8B1.449 (2)OW8—H820.864 (10)
C6B—C7B1.509 (2)OW9—H910.856 (10)
C7B—O1B1.258 (2)OW9—H920.863 (10)
C7B—O2B1.262 (2)OW10—H1010.861 (10)
C8B—O3B1.244 (2)OW10—H1020.869 (10)
C8B—C9B1.474 (2)OW11—H1110.865 (10)
C9B—C10B1.410 (2)OW11—H1120.856 (10)
C10B—C11B1.363 (2)OW12—H1210.858 (10)
C10B—H10C0.930OW12—H1220.841 (10)
C11B—F1B1.3641 (19)OW13—H1310.856 (10)
C11B—C12B1.412 (2)OW13—H1320.850 (10)
C12B—C17B1.390 (2)OW14—H1410.889 (10)
C12B—N2B1.409 (2)OW14—H1420.868 (10)
C13B—N2B1.470 (2)OW15—H1510.854 (10)
C13B—C14B1.517 (2)OW15—H1520.821 (10)
C13B—H13C0.970
N1A—C1A—C2A118.73 (15)N2B—C13B—H13C109.6
N1A—C1A—C3A118.99 (15)C14B—C13B—H13C109.6
C2A—C1A—C3A60.26 (11)N2B—C13B—H13D109.6
N1A—C1A—H1A115.8C14B—C13B—H13D109.6
C2A—C1A—H1A115.8H13C—C13B—H13D108.1
C3A—C1A—H1A115.8N3B—C14B—C13B111.25 (14)
C1A—C2A—C3A60.11 (11)N3B—C14B—H14C109.4
C1A—C2A—H2A1117.8C13B—C14B—H14C109.4
C3A—C2A—H2A1117.8N3B—C14B—H14D109.4
C1A—C2A—H2A2117.8C13B—C14B—H14D109.4
C3A—C2A—H2A2117.8H14C—C14B—H14D108.0
H2A1—C2A—H2A2114.9N3B—C15B—C16B110.43 (14)
C1A—C3A—C2A59.63 (11)N3B—C15B—H15C109.6
C1A—C3A—H3A1117.8C16B—C15B—H15C109.6
C2A—C3A—H3A1117.8N3B—C15B—H15D109.6
C1A—C3A—H3A2117.8C16B—C15B—H15D109.6
C2A—C3A—H3A2117.8H15C—C15B—H15D108.1
H3A1—C3A—H3A2114.9N2B—C16B—C15B110.21 (14)
N1A—C4A—C9A119.47 (15)N2B—C16B—H16C109.6
N1A—C4A—C17A119.37 (15)C15B—C16B—H16C109.6
C9A—C4A—C17A121.15 (15)N2B—C16B—H16D109.6
N1A—C5A—C6A124.66 (16)C15B—C16B—H16D109.6
N1A—C5A—H5A117.7H16C—C16B—H16D108.1
C6A—C5A—H5A117.7C12B—C17B—C4B120.60 (16)
C5A—C6A—C8A120.10 (15)C12B—C17B—H17C119.7
C5A—C6A—C7A116.51 (15)C4B—C17B—H17C119.7
C8A—C6A—C7A123.38 (15)C5B—N1B—C4B119.40 (14)
O2A—C7A—O1A124.93 (16)C5B—N1B—C1B121.16 (14)
O2A—C7A—C6A118.16 (15)C4B—N1B—C1B119.44 (14)
O1A—C7A—C6A116.87 (16)C12B—N2B—C13B114.80 (13)
O3A—C8A—C6A124.85 (15)C12B—N2B—C16B114.05 (13)
O3A—C8A—C9A120.64 (15)C13B—N2B—C16B110.00 (14)
C6A—C8A—C9A114.46 (15)C15B—N3B—C14B110.99 (14)
C4A—C9A—C10A117.65 (15)C15B—N3B—H3B3109.4
C4A—C9A—C8A121.85 (15)C14B—N3B—H3B3109.4
C10A—C9A—C8A120.43 (15)C15B—N3B—H3B4109.4
C11A—C10A—C9A119.85 (16)C14B—N3B—H3B4109.4
C11A—C10A—H10A120.1H3B3—N3B—H3B4108.0
C9A—C10A—H10A120.1N1C—C1C—C2C120.98 (15)
C10A—C11A—F1A117.96 (15)N1C—C1C—C3C119.02 (15)
C10A—C11A—C12A123.61 (15)C2C—C1C—C3C60.45 (12)
F1A—C11A—C12A118.34 (14)N1C—C1C—H1E115.2
C17A—C12A—N2A122.20 (15)C2C—C1C—H1E115.2
C17A—C12A—C11A116.19 (15)C3C—C1C—H1E115.2
N2A—C12A—C11A121.52 (15)C1C—C2C—C3C60.15 (12)
N2A—C13A—C14A111.29 (14)C1C—C2C—H2E1117.8
N2A—C13A—H13A109.4C3C—C2C—H2E1117.8
C14A—C13A—H13A109.4C1C—C2C—H2F2117.8
N2A—C13A—H13B109.4C3C—C2C—H2F2117.8
C14A—C13A—H13B109.4H2E1—C2C—H2F2114.9
H13A—C13A—H13B108.0C1C—C3C—C2C59.40 (12)
N3A—C14A—C13A111.20 (14)C1C—C3C—H3E1117.8
N3A—C14A—H14A109.4C2C—C3C—H3E1117.8
C13A—C14A—H14A109.4C1C—C3C—H3F2117.8
N3A—C14A—H14B109.4C2C—C3C—H3F2117.8
C13A—C14A—H14B109.4H3E1—C3C—H3F2115.0
H14A—C14A—H14B108.0N1C—C4C—C9C118.64 (15)
N3A—C15A—C16A110.34 (14)N1C—C4C—C17C120.17 (16)
N3A—C15A—H15A109.6C9C—C4C—C17C121.17 (16)
C16A—C15A—H15A109.6N1C—C5C—C6C124.62 (16)
N3A—C15A—H15B109.6N1C—C5C—H5E117.7
C16A—C15A—H15B109.6C6C—C5C—H5E117.7
H15A—C15A—H15B108.1C5C—C6C—C8C119.74 (16)
N2A—C16A—C15A110.85 (14)C5C—C6C—C7C117.49 (16)
N2A—C16A—H16A109.5C8C—C6C—C7C122.76 (15)
C15A—C16A—H16A109.5O2C—C7C—O1C124.40 (16)
N2A—C16A—H16B109.5O2C—C7C—C6C119.19 (16)
C15A—C16A—H16B109.5O1C—C7C—C6C116.39 (15)
H16A—C16A—H16B108.1O3C—C8C—C6C124.30 (16)
C12A—C17A—C4A121.23 (16)O3C—C8C—C9C120.89 (16)
C12A—C17A—H17A119.4C6C—C8C—C9C114.81 (15)
C4A—C17A—H17A119.4C4C—C9C—C10C118.05 (16)
C5A—N1A—C4A119.16 (14)C4C—C9C—C8C122.34 (16)
C5A—N1A—C1A120.73 (14)C10C—C9C—C8C119.61 (16)
C4A—N1A—C1A119.92 (14)C11C—C10C—C9C119.53 (17)
C12A—N2A—C13A114.72 (13)C11C—C10C—H10E120.2
C12A—N2A—C16A114.86 (13)C9C—C10C—H10E120.2
C13A—N2A—C16A111.41 (13)F1C—C11C—C10C118.11 (17)
C15A—N3A—C14A110.07 (13)F1C—C11C—C12C118.16 (16)
C15A—N3A—H3A3109.6C10C—C11C—C12C123.71 (17)
C14A—N3A—H3A3109.6C17C—C12C—N2C124.13 (17)
C15A—N3A—H3A4109.6C17C—C12C—C11C116.91 (16)
C14A—N3A—H3A4109.6N2C—C12C—C11C118.95 (16)
H3A3—N3A—H3A4108.2N2C—C13C—C14C109.37 (16)
N1B—C1B—C2B118.88 (15)N2C—C13C—H13E109.8
N1B—C1B—C3B118.66 (15)C14C—C13C—H13E109.8
C2B—C1B—C3B60.49 (12)N2C—C13C—H13F109.8
N1B—C1B—H1C115.8C14C—C13C—H13F109.8
C2B—C1B—H1C115.8H13E—C13C—H13F108.2
C3B—C1B—H1C115.8N3C—C14C—C13C111.28 (15)
C1B—C2B—C3B59.90 (12)N3C—C14C—H14E109.4
C1B—C2B—H2C1117.8C13C—C14C—H14E109.4
C3B—C2B—H2C1117.8N3C—C14C—H14F109.4
C1B—C2B—H2D2117.8C13C—C14C—H14F109.4
C3B—C2B—H2D2117.8H14E—C14C—H14F108.0
H2C1—C2B—H2D2114.9N3C—C15C—C16C110.83 (15)
C1B—C3B—C2B59.61 (12)N3C—C15C—H15E109.5
C1B—C3B—H3C1117.8C16C—C15C—H15E109.5
C2B—C3B—H3C1117.8N3C—C15C—H15F109.5
C1B—C3B—H3D2117.8C16C—C15C—H15F109.5
C2B—C3B—H3D2117.8H15E—C15C—H15F108.1
H3C1—C3B—H3D2114.9N2C—C16C—C15C109.68 (15)
N1B—C4B—C9B118.69 (15)N2C—C16C—H16E109.7
N1B—C4B—C17B119.79 (15)C15C—C16C—H16E109.7
C9B—C4B—C17B121.51 (15)N2C—C16C—H16F109.7
N1B—C5B—C6B125.37 (16)C15C—C16C—H16F109.7
N1B—C5B—H5C117.3H16E—C16C—H16F108.2
C6B—C5B—H5C117.3C12C—C17C—C4C120.53 (16)
C5B—C6B—C8B119.56 (16)C12C—C17C—H17E119.7
C5B—C6B—C7B116.10 (15)C4C—C17C—H17E119.7
C8B—C6B—C7B124.27 (16)C5C—N1C—C4C119.74 (15)
O1B—C7B—O2B123.89 (16)C5C—N1C—C1C121.74 (15)
O1B—C7B—C6B117.96 (16)C4C—N1C—C1C118.50 (14)
O2B—C7B—C6B118.14 (15)C12C—N2C—C13C116.74 (15)
O3B—C8B—C6B125.38 (16)C12C—N2C—C16C114.00 (14)
O3B—C8B—C9B120.20 (15)C13C—N2C—C16C109.68 (15)
C6B—C8B—C9B114.40 (15)C15C—N3C—C14C111.43 (15)
C4B—C9B—C10B117.85 (15)C15C—N3C—H3C4109.3
C4B—C9B—C8B122.46 (15)C14C—N3C—H3C4109.3
C10B—C9B—C8B119.69 (15)C15C—N3C—H3C3109.3
C11B—C10B—C9B119.48 (16)C14C—N3C—H3C3109.3
C11B—C10B—H10C120.3H3C3—N3C—H3C3108.0
C9B—C10B—H10C120.3H81—OW8—H82110 (2)
C10B—C11B—F1B118.33 (15)H91—OW9—H92109 (2)
C10B—C11B—C12B123.95 (15)H101—OW10—H102110 (2)
F1B—C11B—C12B117.68 (15)H111—OW11—H112108 (2)
C17B—C12B—N2B123.35 (15)H121—OW12—H122124 (3)
C17B—C12B—C11B116.47 (15)H131—OW13—H132107 (2)
N2B—C12B—C11B120.13 (15)H141—OW14—H142109 (3)
N2B—C13B—C14B110.37 (14)H151—OW15—H152114 (3)
N1A—C1A—C2A—C3A108.87 (17)F1B—C11B—C12B—N2B4.0 (2)
N1A—C1A—C3A—C2A108.44 (17)N2B—C13B—C14B—N3B56.51 (18)
N1A—C5A—C6A—C8A2.7 (3)N3B—C15B—C16B—N2B57.95 (19)
N1A—C5A—C6A—C7A176.41 (16)N2B—C12B—C17B—C4B179.26 (15)
C5A—C6A—C7A—O2A153.83 (17)C11B—C12B—C17B—C4B1.9 (2)
C8A—C6A—C7A—O2A25.3 (2)N1B—C4B—C17B—C12B179.50 (15)
C5A—C6A—C7A—O1A24.3 (2)C9B—C4B—C17B—C12B1.4 (2)
C8A—C6A—C7A—O1A156.57 (17)C6B—C5B—N1B—C4B3.9 (3)
C5A—C6A—C8A—O3A179.70 (16)C6B—C5B—N1B—C1B176.80 (16)
C7A—C6A—C8A—O3A1.2 (3)C9B—C4B—N1B—C5B2.0 (2)
C5A—C6A—C8A—C9A2.3 (2)C17B—C4B—N1B—C5B178.83 (15)
C7A—C6A—C8A—C9A178.65 (15)C9B—C4B—N1B—C1B178.68 (15)
N1A—C4A—C9A—C10A174.15 (15)C17B—C4B—N1B—C1B0.5 (2)
C17A—C4A—C9A—C10A5.4 (2)C2B—C1B—N1B—C5B35.8 (2)
N1A—C4A—C9A—C8A3.0 (2)C3B—C1B—N1B—C5B105.94 (19)
C17A—C4A—C9A—C8A177.51 (15)C2B—C1B—N1B—C4B144.94 (16)
O3A—C8A—C9A—C4A177.45 (16)C3B—C1B—N1B—C4B74.8 (2)
C6A—C8A—C9A—C4A5.0 (2)C17B—C12B—N2B—C13B6.7 (2)
O3A—C8A—C9A—C10A5.5 (2)C11B—C12B—N2B—C13B170.61 (15)
C6A—C8A—C9A—C10A172.03 (15)C17B—C12B—N2B—C16B121.56 (18)
C4A—C9A—C10A—C11A1.6 (2)C11B—C12B—N2B—C16B61.2 (2)
C8A—C9A—C10A—C11A178.83 (15)C14B—C13B—N2B—C12B170.59 (14)
C9A—C10A—C11A—F1A172.86 (15)C14B—C13B—N2B—C16B59.17 (18)
C9A—C10A—C11A—C12A3.5 (3)C15B—C16B—N2B—C12B169.26 (14)
C10A—C11A—C12A—C17A4.8 (2)C15B—C16B—N2B—C13B60.10 (18)
F1A—C11A—C12A—C17A171.57 (14)C16B—C15B—N3B—C14B55.05 (19)
C10A—C11A—C12A—N2A178.52 (16)C13B—C14B—N3B—C15B54.50 (19)
F1A—C11A—C12A—N2A5.1 (2)N1C—C1C—C2C—C3C108.07 (18)
N2A—C13A—C14A—N3A55.52 (18)N1C—C1C—C3C—C2C111.22 (18)
N3A—C15A—C16A—N2A57.45 (19)N1C—C5C—C6C—C8C4.1 (3)
N2A—C12A—C17A—C4A177.60 (15)N1C—C5C—C6C—C7C174.44 (15)
C11A—C12A—C17A—C4A0.9 (2)C5C—C6C—C7C—O2C158.08 (16)
N1A—C4A—C17A—C12A175.42 (15)C8C—C6C—C7C—O2C20.5 (3)
C9A—C4A—C17A—C12A4.1 (3)C5C—C6C—C7C—O1C20.4 (2)
C6A—C5A—N1A—C4A5.1 (3)C8C—C6C—C7C—O1C161.07 (16)
C6A—C5A—N1A—C1A179.94 (16)C5C—C6C—C8C—O3C176.59 (16)
C9A—C4A—N1A—C5A2.1 (2)C7C—C6C—C8C—O3C4.9 (3)
C17A—C4A—N1A—C5A177.44 (15)C5C—C6C—C8C—C9C2.7 (2)
C9A—C4A—N1A—C1A177.12 (15)C7C—C6C—C8C—C9C175.83 (15)
C17A—C4A—N1A—C1A2.4 (2)N1C—C4C—C9C—C10C179.16 (15)
C2A—C1A—N1A—C5A41.2 (2)C17C—C4C—C9C—C10C2.4 (2)
C3A—C1A—N1A—C5A111.10 (18)N1C—C4C—C9C—C8C1.5 (2)
C2A—C1A—N1A—C4A143.87 (16)C17C—C4C—C9C—C8C176.92 (16)
C3A—C1A—N1A—C4A73.9 (2)O3C—C8C—C9C—C4C179.29 (16)
C17A—C12A—N2A—C13A0.2 (2)C6C—C8C—C9C—C4C0.0 (2)
C11A—C12A—N2A—C13A176.26 (15)O3C—C8C—C9C—C10C1.4 (3)
C17A—C12A—N2A—C16A130.78 (17)C6C—C8C—C9C—C10C179.31 (16)
C11A—C12A—N2A—C16A52.7 (2)C4C—C9C—C10C—C11C1.2 (3)
C14A—C13A—N2A—C12A172.25 (14)C8C—C9C—C10C—C11C178.12 (16)
C14A—C13A—N2A—C16A55.09 (18)C9C—C10C—C11C—F1C176.68 (16)
C15A—C16A—N2A—C12A171.26 (14)C9C—C10C—C11C—C12C1.8 (3)
C15A—C16A—N2A—C13A56.16 (18)F1C—C11C—C12C—C17C174.93 (15)
C16A—C15A—N3A—C14A57.54 (18)C10C—C11C—C12C—C17C3.5 (3)
C13A—C14A—N3A—C15A56.72 (18)F1C—C11C—C12C—N2C3.7 (2)
N1B—C1B—C2B—C3B108.50 (18)C10C—C11C—C12C—N2C177.80 (17)
N1B—C1B—C3B—C2B108.85 (18)N2C—C13C—C14C—N3C57.0 (2)
N1B—C5B—C6B—C8B2.4 (3)N3C—C15C—C16C—N2C57.8 (2)
N1B—C5B—C6B—C7B174.69 (16)N2C—C12C—C17C—C4C179.16 (16)
C5B—C6B—C7B—O1B12.3 (2)C11C—C12C—C17C—C4C2.3 (3)
C8B—C6B—C7B—O1B170.77 (16)N1C—C4C—C17C—C12C179.02 (16)
C5B—C6B—C7B—O2B166.61 (16)C9C—C4C—C17C—C12C0.6 (3)
C8B—C6B—C7B—O2B10.3 (3)C6C—C5C—N1C—C4C2.5 (3)
C5B—C6B—C8B—O3B179.39 (17)C6C—C5C—N1C—C1C176.19 (16)
C7B—C6B—C8B—O3B3.8 (3)C9C—C4C—N1C—C5C0.3 (2)
C5B—C6B—C8B—C9B0.9 (2)C17C—C4C—N1C—C5C178.11 (15)
C7B—C6B—C8B—C9B177.68 (15)C9C—C4C—N1C—C1C179.11 (15)
N1B—C4B—C9B—C10B178.26 (15)C17C—C4C—N1C—C1C0.7 (2)
C17B—C4B—C9B—C10B2.6 (2)C2C—C1C—N1C—C5C26.9 (2)
N1B—C4B—C9B—C8B1.1 (2)C3C—C1C—N1C—C5C98.0 (2)
C17B—C4B—C9B—C8B177.97 (15)C2C—C1C—N1C—C4C151.79 (16)
O3B—C8B—C9B—C4B178.87 (16)C3C—C1C—N1C—C4C80.7 (2)
C6B—C8B—C9B—C4B2.5 (2)C17C—C12C—N2C—C13C11.0 (3)
O3B—C8B—C9B—C10B1.7 (2)C11C—C12C—N2C—C13C167.59 (16)
C6B—C8B—C9B—C10B176.85 (15)C17C—C12C—N2C—C16C118.60 (19)
C4B—C9B—C10B—C11B0.5 (2)C11C—C12C—N2C—C16C62.8 (2)
C8B—C9B—C10B—C11B179.91 (15)C14C—C13C—N2C—C12C167.24 (16)
C9B—C10B—C11B—F1B174.64 (15)C14C—C13C—N2C—C16C61.17 (19)
C9B—C10B—C11B—C12B3.0 (3)C15C—C16C—N2C—C12C164.97 (16)
C10B—C11B—C12B—C17B4.2 (3)C15C—C16C—N2C—C13C62.01 (19)
F1B—C11B—C12B—C17B173.48 (14)C16C—C15C—N3C—C14C53.8 (2)
C10B—C11B—C12B—N2B178.37 (16)C13C—C14C—N3C—C15C53.4 (2)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N3A—H3A3···O2Ci0.902.032.866 (2)153
N3A—H3A3···O3Ci0.902.292.903 (2)125
N3A—H3A4···O2Aii0.901.802.684 (2)166
N3B—H3B3···O3Aii0.901.902.782 (3)168
N3B—H3B4···O2Bii0.901.762.660 (2)173
N3C—H3C4···O1Ciii0.901.792.682 (2)170
N3C—H3C3···OW5Aiii0.902.292.959 (4)131
N3C—H3C3···O3Biv0.902.102.859 (2)142
OW8—H81···O1Aiv0.86 (1)1.86 (1)2.702 (2)165 (3)
OW8—H82···O3C0.86 (3)1.83 (3)2.683 (3)170 (3)
OW9—H91···O2Aiv0.86 (2)2.07 (2)2.836 (2)149 (2)
OW9—H91···O3Aiv0.86 (2)2.38 (2)3.021 (2)133 (2)
OW9—H92···O1Av0.86 (2)1.92 (2)2.784 (2)176 (2)
OW10—H101···O1Bii0.86 (3)1.96 (3)2.816 (2)179 (3)
OW10—H102···O2Bi0.87 (2)1.99 (2)2.826 (2)158 (3)
OW10—H102···O3Bi0.87 (2)2.52 (3)3.091 (2)126 (2)
OW11—H111···O2Cvi0.87 (3)1.97 (3)2.830 (2)175 (2)
OW11—H112···O1C0.86 (1)1.88 (1)2.731 (2)176 (2)
OW15—H152···O1Bii0.82 (3)1.99 (3)2.787 (3)163 (4)
OW12—H121···OW9i0.86 (3)1.86 (3)2.712 (2)176 (3)
OW12—H122···OW3A0.84 (3)2.20 (3)2.825 (4)131 (3)
OW12—H122···OW5B0.84 (3)2.06 (3)2.882 (5)165 (3)
OW13—H131···OW8vi0.86 (2)1.96 (2)2.803 (3)166 (2)
OW13—H132···OW1Avii0.85 (3)2.16 (3)2.930 (4)150 (3)
OW13—H132···OW6A0.85 (3)2.41 (3)2.827 (5)111 (2)
OW14—H141···OW1A0.89 (1)2.25 (2)2.910 (4)131 (2)
OW14—H141···OW1B0.89 (1)2.03 (3)2.623 (5)123 (3)
OW14—H142···OW8i0.86 (4)1.91 (4)2.728 (3)157 (3)
OW15—H151···OW4Ai0.85 (3)1.91 (3)2.75 (3)170 (4)
Symmetry codes: (i) x+1, y+1, z+1; (ii) x+1, y, z; (iii) x1, y, z; (iv) x, y+1, z+1; (v) x+1, y+1, z; (vi) x+1, y+1, z; (vii) x, y, z1.

Experimental details

(I)(II)
Crystal data
Chemical formula2C17H18FN3O3·3C2H4F2O3C17H18FN3O3·14.5H2O
Mr908.841255.26
Crystal system, space groupTriclinic, P1Triclinic, P1
Temperature (K)120100
a, b, c (Å)10.9848 (4), 13.9800 (4), 13.9802 (4)13.8760 (12), 15.8760 (13), 16.528 (2)
α, β, γ (°)105.6488 (18), 90.352 (2), 93.364 (2)115.755 (7), 103.610 (7), 102.325 (5)
V3)2063.22 (11)2972.8 (5)
Z22
Radiation typeSynchrotron, λ = 0.7000 ÅMo Kα
µ (mm1)0.130.12
Crystal size (mm)0.1 × 0.08 × 0.080.30 × 0.25 × 0.20
Data collection
DiffractometerBruker SMART APEXII CCD area-detector
diffractometer
Bruker APEXII CCD area-detector
diffractometer
Absorption correctionMulti-scan
(TWINABS; Sheldrick, 2008a)
Multi-scan
(SADABS; Sheldrick, 2008a)
Tmin, Tmax0.58, 0.740.40, 0.43
No. of measured, independent and
observed [I > 2σ(I)] reflections
51821, 7072, 5962 55842, 12150, 9655
Rint0.080.038
(sin θ/λ)max1)0.5960.625
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.068, 0.202, 1.16 0.043, 0.122, 1.03
No. of reflections707212150
No. of parameters571907
No. of restraints52234
H-atom treatmentH-atom parameters constrainedH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å3)0.58, 0.460.57, 0.42

Computer programs: APEX2 (Bruker, 2007), SAINT (Bruker, 2007), SHELXS97 (Sheldrick, 2008b), SHELXL97 (Sheldrick, 2008b), ORTEP-3 for Windows (Burnett & Johnson, 1996) and Mercury (Macrae et al., 2008), publCIF (Westrip, 2010).

Hydrogen-bond geometry (Å, º) for (I) top
D—H···AD—HH···AD···AD—H···A
N3A—H3A3···O1Ai0.902.583.176 (4)125
N3A—H3A3···O2Ai0.901.862.758 (4)173
N3A—H3A4···O2Bii0.902.392.885 (4)114
N3A—H3A4···O3Bii0.901.852.717 (4)162
N3B—H3B3···O1Biii0.902.773.376 (4)126
N3B—H3B3···O2Biii0.901.822.724 (4)179
N3B—H3B4···O2Aiv0.902.502.894 (4)107
N3B—H3B4···O3Aiv0.901.792.687 (4)171
O4A—H4A···O1Av0.821.882.672 (4)162
O4B—H4B···O1Bii0.821.872.666 (4)165
O4C—H4C···O1Bv0.821.932.733 (4)168
C2A—H2A2···F3Bii0.972.513.207 (5)128
C14A—H14A···O2Avi0.972.493.350 (5)148
C14A—H14A···O3Avi0.972.493.274 (4)138
C16A—H16A···O4Bvii0.972.483.148 (5)126
C1B—H1B···F2C0.982.453.200 (5)133
C14B—H14D···O2Bii0.972.343.295 (4)170
C15B—H15D···O2Aiv0.972.513.131 (5)122
C18B—H18D···F1B0.972.463.396 (5)161
Symmetry codes: (i) x, y, z1; (ii) x+1, y+1, z+1; (iii) x, y+1, z; (iv) x+1, y+2, z+2; (v) x+1, y+1, z+2; (vi) x+2, y+2, z+2; (vii) x+1, y+2, z+1.
Hydrogen-bond geometry (Å, º) for (II) top
D—H···AD—HH···AD···AD—H···A
N3A—H3A3···O2Ci0.902.032.866 (2)153
N3A—H3A3···O3Ci0.902.292.903 (2)125
N3A—H3A4···O2Aii0.901.802.684 (2)166
N3B—H3B3···O3Aii0.901.902.782 (3)168
N3B—H3B4···O2Bii0.901.762.660 (2)173
N3C—H3C4···O1Ciii0.901.792.682 (2)170
N3C—H3C3···OW5Aiii0.902.292.959 (4)131
N3C—H3C3···O3Biv0.902.102.859 (2)142
OW8—H81···O1Aiv0.862 (14)1.861 (14)2.702 (2)165 (3)
OW8—H82···O3C0.86 (3)1.83 (3)2.683 (3)170 (3)
OW9—H91···O2Aiv0.855 (19)2.067 (19)2.836 (2)149 (2)
OW9—H91···O3Aiv0.855 (19)2.38 (2)3.021 (2)132.9 (18)
OW9—H92···O1Av0.86 (2)1.92 (2)2.784 (2)176.1 (19)
OW10—H101···O1Bii0.86 (3)1.96 (3)2.816 (2)179 (3)
OW10—H102···O2Bi0.87 (2)1.99 (2)2.826 (2)158 (3)
OW10—H102···O3Bi0.87 (2)2.52 (3)3.091 (2)126 (2)
OW11—H111···O2Cvi0.87 (3)1.97 (3)2.830 (2)175 (2)
OW11—H112···O1C0.858 (14)1.876 (13)2.731 (2)176 (2)
OW15—H152···O1Bii0.82 (3)1.99 (3)2.787 (3)163 (4)
OW12—H121···OW9i0.86 (3)1.86 (3)2.712 (2)176 (3)
OW12—H122···OW3A0.84 (3)2.20 (3)2.825 (4)131 (3)
OW12—H122···OW5B0.84 (3)2.06 (3)2.882 (5)165 (3)
OW13—H131···OW8vi0.86 (2)1.96 (2)2.803 (3)166 (2)
OW13—H132···OW1Avii0.85 (3)2.16 (3)2.930 (4)150 (3)
OW13—H132···OW6A0.85 (3)2.41 (3)2.827 (5)111 (2)
OW14—H141···OW1A0.888 (13)2.25 (2)2.910 (4)131 (2)
OW14—H141···OW1B0.888 (13)2.03 (3)2.623 (5)123 (3)
OW14—H142···OW8i0.86 (4)1.91 (4)2.728 (3)157 (3)
OW15—H151···OW4Ai0.85 (3)1.91 (3)2.75 (3)170 (4)
Symmetry codes: (i) x+1, y+1, z+1; (ii) x+1, y, z; (iii) x1, y, z; (iv) x, y+1, z+1; (v) x+1, y+1, z; (vi) x+1, y+1, z; (vii) x, y, z1.
Selected torsion angles (°) for the Cf molecules in (I) and (II) top
θ1 = C2—C1—N1—C5, θ2 = C5—C6—C7—O1 and θ3 = C11—C12—N2—C16.
Moleculeθ1θ2θ3
(I) A37.9 (5)-3.0 (5)-58.0 (4)
(I) B-30.5 (6)0.3 (5)60.4 (4)
(II) A-41.2 (2)-24.3 (2)52.7 (2)
(II) B-35.8 (2)-12.3 (2)61.2 (2)
(II) C26.9 (2)20.4 (2)-62.8 (2)
 

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