Buy article online - an online subscription or single-article purchase is required to access this article.
Download citation
Download citation
link to html
The first metal complex of di-2-pyridyl­methanone p-nitro­phenyl­hydrazone (dpknph), i.e. the title compound, fac-[ReCl(C17H13N5O2)(CO)3]·C2H6OS, crystallizes as well separated pseudo-tetrahedral DMSO (DMSO is di­methyl sul­foxide) and pseudo-octahedral fac-[ReCl(dpknph)(CO)3] moieties. Two N atoms from dpknph, three C atoms from the carbonyl groups and one chloride ion occupy the coordination sphere around rhenium. The coordinated dpknph ligand forms a six-membered ring in a boat conformation, with the pyridine rings in a butterfly formation. The p-nitro­phenyl­hydrazone moiety is planar, with all C and N atoms in sp2-hybridized forms. The mol­ecules pack as stacks of interlocked fac-[ReCl(dpknph)(CO)3]·DMSO units via a network of non-covalent bonds that include solute–solute, solvent–solute and π–π interactions.

Supporting information

cif

Crystallographic Information File (CIF) https://doi.org/10.1107/S0108270101013890/da1194sup1.cif
Contains datablocks global, I

hkl

Structure factor file (CIF format) https://doi.org/10.1107/S0108270101013890/da1194Isup2.hkl
Contains datablock I

CCDC reference: 179248

Comment top

The development of molecular systems sensitive to their surroundings is of interest for their rich physicochemical properties, reactivity patterns and applications in devices employed in photonic, electronic and sensing techniques (Drain et al., 2001; Luo et al., 2001; Prasad et al., 1991; Bosshard et al., 1995; Czerney & Grummt, 1997). The synthesis of di-2-pyridylmethanone p-nitrophenylhydrazone (dpknph) and its rhenium tricarbonyl compound, fac-[ReCl(dpknph)(CO)3], have been reported (Bakir & Abdur-Rashid, 1999). Optical and thermodynamic measurements on fac-[ReCl(dpknph)(CO)3] in polar solvents have revealed strong solvent–solute and solute–solute interactions, and facile interconversion between two charge–transfer bands (Bakir et al., 2000). Manipulation of the charge-transfer bands in fac-[ReCl(dpknph)(CO)3]·DMSO, (I), led to the use of these systems {fac-[ReCl(dpknph)(CO)3] and surrounding solvent molecules} as spectrophotometric sensors for a variety of substrates that include metal ions. The structure of (I) is reported here and compared to the structures of tricabonylrhenium compounds containing α-diimine ligands, e.g. di-2-pyridylketoneoxime (dpk.oxime) and hydroxyd(2-pyridyl)methoxide (dpkO,OH).

An ORTEP view of (I) is shown in Fig. 1, and Table 1 contains selected bond distances and angles. Two N atoms of the bidentate chelating dpknph ligand and two C atoms from two carbonyl groups occupy the equatorial positions in fac-[ReCl(dpknph)(CO)3] and the two axial positions are occupied by a carbonyl C atom and a Cl atom. The N,N-chelating dpknph molecule forms a six-membered (Re1—N1—C15—C—C25—N2) metallocyclic ring in a boat conformation. The N,N-bite angle of 83.32 (12)° is of the same order as those reported for tricabonylrhenium compounds of N,N-bidentate polypyridyl-like ligands containing six-membered rings (Bakir, 2001; Gerber et al., 1993, 1995). For example, an N,N-bite angle of 84.6 (4)° was reported for dpkO,OH in [ReOCl2(dpkO,OH)] (Gerber et al., 1995, 1993) and a bite angle of 80.27 (19)° was observed for dpk.oxime in fac-[ReCl(dpk.oxime)(CO)3]·DMSO (Bakir, 2001). The carbonyl groups are in facial positions, with an average C—Re—C bond angle of 89.4 (3)°. The Re—C, Re—N and Re—Cl bonds distances are normal and similar to those reported for fac-[ReCl(dpk.oxime)(CO)3]·DMSO (Bakir, 2001) and a variety of tricarbonylrhenium compounds of the type fac-[ReCl(L—L)(CO)3], where L—L is an α-diimine ligand (Horn & Snow, 1980; Xue et al., 1998; Yam et al., 1995, 1998; Gibson et al., 1998). For example, in fac-[ReCl(tBu2bpy)(CO)3], the Re—C, Re—N and Re—Cl bond distances are 1.935 (9)/1.935 (9)/1.896 (3), 2.169 (6)/2.170 (5) and 2.476 (2) Å, respectively (Yam et al., 1995). The p-nitrophenylhydrazone moiety in (I) is planar with all C and N atoms in sp2-hybridized forms.

The packing of molecules (Fig. 2) shows antiparallel stacks of (I) having the p-nitrophenylhydrazone (P—NO2—C6H4—NH—N) moieties from adjacent stacks face-to-face. The interplanar distance between the phenyl rings of approximately 3.45 Å is of the same order as the π-stacking in aromatic and charge-transfer compounds and is shorter than the interplanar distance of 4.97 Å reported for the pure benzene dimer (Glusker et al., 1994; Batchelor et al., 2000; Williams, 1993). The antiparallel arrangement of the p-nitrophenylhydrazone moieties facilitates the formation of intermolecular non-classical C—H···O hydrogen bonds between the nitro O4 and O5 atoms and the pyridine H14 and H24 atoms. A classical intramolecular N—H···O hydrogen bond, a non-classical intramolecular C—H···O hydrogen bond and a non-classical intermolecular C—H···Cl hydrogen bonds were observed between DMSO and fac-[ReCl(dpknph)(CO)3] (Fig. 3). In addition, side-to-side intermolecular hydrogen bonds were observed between adjacent carbonyl groups, nitro groups and pyridine rings, i.e. C22—H22A···O2 and C23—H23A···O5. The bond distances and angles (Table 2) of the classical hydrogen bonds between the DMSO O6 atom and the amino N4—H4 group of the hydrazone moiety are similar to those reported for a variety of N—H···O hydrogen bonds (Bakir, 2001; Sherrington & Taskinen, 2001; Uppadine et al., 2001; Glusker et al., 1994; Pan et al., 1997). For example, in 5-nitro-2-thiophenecarboxaldehyde-4-methylphenylhydrazone form I (NTMPH-I), two different N—H···O hydrogen bonds, with O—H = 2.0–2.3 Å, N—O = 3.01–3.18 Å and N—H···O = 161–160° were observed (Pan et al., 1997). The non-classical hydrogen bonds are of the same order as the sum of their van der Waals radii; for example, the van der Waals O—H distance is about 2.8 Å (Glusker et al., 1994; Pan et al., 1997). The non-covalent interactions observed in this interlocking system (solute–solute and solvent–solute) may account for the optical and molecular sensing behavior of (I), as any slight interaction between this system and its surroundings may disrupt the weak non-covalent interactions present. This is consistent with the low values of the activation parameters reported for the interconversion between the charge-transfer bands in fac-[ReCl(dpknph)(CO)3] (Bakir et al., 2000) and the low values for the bond energies of non-covalent interactions (Vishweshwar et al., 2001). The layer arrangement of (I) and the planar hydrazone moiety may also account for the observed fast electronic transfer in fac-[ReCl(dpknph)(CO)3] compared with dpknph (Bakir & Abdur-Rashid, 1999). Studies are in progress to grow single crystals of the uncoordinated dpknph molecule and compare its structure with the structure of (I).

In conclusion, structural studies on (I) revealed the presence of weak non-covalent interactions that include solvent–solute, solute–solute and π-stacking interactions, which may account for the interlocked charge-transfer bands and molecular sensitivity of fac-[ReCl(dpknph)(CO)3] in polar solvents.

Related literature top

For related literature, see: Bakir & Abdur-Rashid (1999); Bakir et al. (2000); Batchelor et al. (2000); Bosshard et al. (1995); Czerney & Grummt (1997); Drain et al. (2001); Gerber et al. (1993, 1995); Gibson et al. (1998); Glusker et al. (1994); Horn & Snow (1980); Luo et al. (2001); Pan et al. (1997); Prasad & Williams (1991); Sherrington & Taskinen (2001); Uppadine et al. (2001); Vishweshwar et al. (2001); Williams (1993); Xue et al. (1998); Yam et al. (1995, 1998).

Experimental top

fac-[ReCl(dpknph)(CO)3] was synthesized as described previously (Bakir & Abdur-Rashid, 1999). Reagent grade DMSO used for the crystallization was thoroughly deoxygenated prior to use. When fac-[ReCl(dpknph)(CO)3] was allowed to stand in DMSO for several days at room temperature, yellow–green crystals of (I) were obtained. A single-crystal was selected and mounted on a glass fiber with epoxy cement and used for data collection.

Refinement top

The H atom involved in the amine-H to solvent O hydrogen bond was refined without contraints. All other H-atom positions were assigned by assuming idealized geometry with C—H distances of 0.96 and 0.93 Å for aliphatic and aromatic H atoms, respectively. The DMSO molecule is slightly disordered such that the S atom exists in two different positions; the major orientation has an occupancy of 0.847 (4).

Computing details top

Data collection: XSCANS (Siemens, 1996); cell refinement: XSCANS; data reduction: SHELXTL (Bruker, 1997); program(s) used to solve structure: SHELXS97 (Sheldrick, 1990); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL.

Figures top
[Figure 1] Fig. 1. A view of the structure of (I), with displacement ellipsoids drawn at the 30% probability level.
[Figure 2] Fig. 2. A view showing the packing of (I).
[Figure 3] Fig. 3. A view showing classical and non-classical hydrogen bonds between DMSO and fac-[ReCl(dpknph)(CO)3] moieties. [Symmetry codes: (A) x, y, z, (B) x, 2 - y, 1/2 + z, (C) X, 1 - y, 1/2 + z and (D) 1 - x, 2 - y, 2 - z.]
fac-Tricarbonylchloro(di-2-pyridylmethanone p-nitrophenylhydrazone)rhenium(I) dimethyl sulfoxide solvate top
Crystal data top
[ReCl(C17H13N5O2)(CO)3]·C2H6OSDx = 1.799 Mg m3
Mr = 703.13Melting point: not measured K
Monoclinic, C2/cMo Kα radiation, λ = 0.71073 Å
a = 21.104 (2) ÅCell parameters from 30 reflections
b = 14.486 (2) Åθ = 10.7–22.4°
c = 18.962 (2) ŵ = 4.91 mm1
β = 116.408 (7)°T = 298 K
V = 5192.0 (10) Å3Irregular, yellow-green
Z = 80.42 × 0.38 × 0.34 mm
F(000) = 2736
Data collection top
Bruker P4
diffractometer
3969 reflections with I > 2σ(I)
Radiation source: fine-focus sealed tubeRint = 0.027
Graphite monochromatorθmax = 25.0°, θmin = 1.8°
2θ/ω scansh = 125
Absorption correction: ψ scan
(XSCANS; Bruker, 1996)
k = 117
Tmin = 0.157, Tmax = 0.188l = 2220
5397 measured reflections3 standard reflections every 97 reflections
4562 independent reflections intensity decay: none
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)] = 0.027Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.064H atoms treated by a mixture of independent and constrained refinement
S = 1.08 w = 1/[σ2(Fo2) + (0.026P)2 + 8.P]
where P = (Fo2 + 2Fc2)/3
4562 reflections(Δ/σ)max = 0.002
339 parametersΔρmax = 0.37 e Å3
0 restraintsΔρmin = 0.85 e Å3
Crystal data top
[ReCl(C17H13N5O2)(CO)3]·C2H6OSV = 5192.0 (10) Å3
Mr = 703.13Z = 8
Monoclinic, C2/cMo Kα radiation
a = 21.104 (2) ŵ = 4.91 mm1
b = 14.486 (2) ÅT = 298 K
c = 18.962 (2) Å0.42 × 0.38 × 0.34 mm
β = 116.408 (7)°
Data collection top
Bruker P4
diffractometer
3969 reflections with I > 2σ(I)
Absorption correction: ψ scan
(XSCANS; Bruker, 1996)
Rint = 0.027
Tmin = 0.157, Tmax = 0.1883 standard reflections every 97 reflections
5397 measured reflections intensity decay: none
4562 independent reflections
Refinement top
R[F2 > 2σ(F2)] = 0.0270 restraints
wR(F2) = 0.064H atoms treated by a mixture of independent and constrained refinement
S = 1.08Δρmax = 0.37 e Å3
4562 reflectionsΔρmin = 0.85 e Å3
339 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)
Re10.264771 (8)0.534013 (12)0.880100 (9)0.04002 (7)
Cl10.29956 (7)0.39331 (9)0.96173 (8)0.0638 (3)
N10.37510 (17)0.5386 (2)0.89800 (19)0.0369 (7)
N20.30833 (19)0.6044 (3)0.9944 (2)0.0465 (8)
C10.1708 (3)0.5319 (4)0.8690 (3)0.0616 (13)
C20.2359 (2)0.4629 (4)0.7857 (3)0.0542 (11)
C30.2420 (2)0.6436 (4)0.8184 (3)0.0534 (11)
O10.1137 (2)0.5325 (3)0.8630 (3)0.0916 (14)
O20.2222 (2)0.4193 (4)0.7311 (2)0.0897 (14)
O30.2270 (2)0.7070 (3)0.7778 (2)0.0802 (12)
C110.4016 (2)0.4659 (3)0.8744 (3)0.0446 (9)
H11A0.37370.41350.85480.053*
C120.4682 (2)0.4672 (3)0.8785 (3)0.0488 (10)
H12A0.48450.41680.86090.059*
C130.5105 (2)0.5431 (3)0.9086 (3)0.0494 (11)
H13A0.55590.54480.91230.059*
C140.4842 (2)0.6167 (3)0.9332 (2)0.0441 (10)
H14A0.51230.66870.95430.053*
C150.4159 (2)0.6138 (3)0.9268 (2)0.0379 (8)
C0.3890 (2)0.6892 (3)0.9588 (2)0.0400 (9)
C210.2816 (3)0.5859 (4)1.0454 (3)0.0676 (15)
H21A0.24580.54221.03140.081*
C220.3048 (3)0.6287 (5)1.1175 (3)0.0772 (17)
H22A0.28560.61351.15160.093*
C230.3570 (3)0.6940 (5)1.1379 (3)0.0737 (16)
H23A0.37330.72491.18580.088*
C240.3848 (3)0.7131 (4)1.0864 (3)0.0576 (12)
H24A0.42070.75661.09960.069*
C250.3595 (2)0.6677 (3)1.0149 (2)0.0433 (9)
N30.39610 (19)0.7769 (2)0.9520 (2)0.0444 (8)
N40.4223 (2)0.8112 (3)0.9045 (2)0.0474 (9)
H40.422 (2)0.777 (3)0.863 (3)0.055 (14)*
C310.4247 (2)0.9072 (3)0.9001 (2)0.0433 (9)
C320.4070 (2)0.9644 (3)0.9472 (3)0.0498 (10)
H32A0.39420.93930.98410.060*
C330.4086 (3)1.0587 (3)0.9388 (3)0.0574 (12)
H33A0.39631.09770.96980.069*
C340.4284 (2)1.0951 (3)0.8845 (3)0.0548 (12)
C350.4475 (2)1.0403 (3)0.8391 (3)0.0568 (12)
H35A0.46161.06650.80360.068*
C360.4459 (2)0.9442 (3)0.8461 (3)0.0525 (11)
H36A0.45870.90580.81530.063*
N50.4294 (2)1.1951 (3)0.8765 (3)0.0723 (14)
O40.4130 (3)1.2433 (3)0.9193 (3)0.118 (2)
O50.4466 (2)1.2259 (3)0.8276 (3)0.0939 (14)
O60.4230 (3)0.7309 (4)0.7719 (2)0.1154 (19)
S10.39660 (12)0.68617 (13)0.69270 (10)0.0793 (7)0.847 (4)
C40.3052 (5)0.6638 (7)0.6605 (5)0.140 (4)0.847 (4)
H4A0.29960.61560.69210.210*0.847 (4)
H4B0.28420.64490.60640.210*0.847 (4)
H4C0.28220.71880.66570.210*0.847 (4)
C50.3868 (4)0.7737 (5)0.6256 (4)0.095 (2)0.847 (4)
H5A0.43260.79560.63410.143*0.847 (4)
H5B0.36030.82370.63270.143*0.847 (4)
H5C0.36200.75020.57290.143*0.847 (4)
S1'0.3543 (7)0.7550 (8)0.6972 (6)0.083 (4)0.153 (4)
C4'0.3052 (5)0.6638 (7)0.6605 (5)0.140 (4)0.153 (4)
H4'A0.28380.64590.69380.210*0.153 (4)
H4'B0.33390.61410.65740.210*0.153 (4)
H4'C0.26880.67770.60880.210*0.153 (4)
C5'0.3868 (4)0.7737 (5)0.6256 (4)0.095 (2)0.153 (4)
H5'A0.41820.82580.64100.143*0.153 (4)
H5'B0.34770.78560.57520.143*0.153 (4)
H5'C0.41170.71980.62220.143*0.153 (4)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
Re10.03414 (10)0.04760 (11)0.04102 (10)0.00310 (8)0.01916 (7)0.00309 (8)
Cl10.0682 (8)0.0559 (7)0.0678 (7)0.0105 (6)0.0306 (6)0.0110 (6)
N10.0338 (16)0.0377 (18)0.0405 (17)0.0018 (14)0.0176 (14)0.0007 (15)
N20.048 (2)0.053 (2)0.0458 (19)0.0042 (18)0.0276 (17)0.0036 (18)
C10.047 (3)0.083 (4)0.062 (3)0.005 (3)0.031 (2)0.008 (3)
C20.039 (2)0.070 (3)0.055 (3)0.002 (2)0.022 (2)0.008 (3)
C30.048 (3)0.064 (3)0.055 (3)0.009 (2)0.029 (2)0.001 (2)
O10.050 (2)0.132 (4)0.108 (3)0.012 (2)0.049 (2)0.012 (3)
O20.055 (2)0.135 (4)0.072 (2)0.001 (2)0.021 (2)0.049 (3)
O30.085 (3)0.081 (3)0.086 (3)0.029 (2)0.048 (2)0.028 (2)
C110.046 (2)0.039 (2)0.050 (2)0.0053 (19)0.021 (2)0.008 (2)
C120.048 (2)0.046 (2)0.058 (3)0.009 (2)0.029 (2)0.002 (2)
C130.041 (2)0.053 (3)0.062 (3)0.005 (2)0.030 (2)0.008 (2)
C140.036 (2)0.043 (2)0.053 (2)0.0044 (18)0.0207 (19)0.001 (2)
C150.039 (2)0.042 (2)0.0353 (19)0.0004 (17)0.0184 (17)0.0025 (17)
C0.037 (2)0.039 (2)0.044 (2)0.0058 (17)0.0186 (18)0.0060 (18)
C210.069 (3)0.087 (4)0.065 (3)0.024 (3)0.047 (3)0.015 (3)
C220.089 (4)0.102 (5)0.064 (3)0.021 (4)0.055 (3)0.020 (3)
C230.075 (4)0.100 (5)0.056 (3)0.008 (3)0.039 (3)0.029 (3)
C240.057 (3)0.065 (3)0.058 (3)0.010 (2)0.033 (2)0.016 (2)
C250.045 (2)0.046 (2)0.044 (2)0.0003 (19)0.0249 (19)0.0031 (19)
N30.0446 (19)0.042 (2)0.048 (2)0.0036 (16)0.0227 (17)0.0004 (16)
N40.054 (2)0.043 (2)0.053 (2)0.0005 (17)0.0305 (19)0.0019 (18)
C310.037 (2)0.040 (2)0.047 (2)0.0016 (18)0.0123 (18)0.0015 (19)
C320.051 (2)0.046 (3)0.050 (2)0.000 (2)0.020 (2)0.002 (2)
C330.059 (3)0.043 (3)0.060 (3)0.001 (2)0.018 (2)0.009 (2)
C340.049 (3)0.041 (3)0.057 (3)0.005 (2)0.008 (2)0.001 (2)
C350.044 (2)0.058 (3)0.061 (3)0.002 (2)0.017 (2)0.019 (3)
C360.049 (3)0.058 (3)0.055 (3)0.002 (2)0.026 (2)0.001 (2)
N50.062 (3)0.045 (3)0.076 (3)0.005 (2)0.001 (2)0.012 (2)
O40.184 (6)0.043 (2)0.118 (4)0.004 (3)0.058 (4)0.009 (3)
O50.079 (3)0.068 (3)0.106 (3)0.019 (2)0.015 (3)0.029 (3)
O60.154 (5)0.133 (4)0.051 (2)0.042 (4)0.038 (3)0.012 (3)
S10.1192 (16)0.0656 (11)0.0626 (10)0.0243 (10)0.0489 (11)0.0037 (8)
C40.180 (10)0.163 (9)0.124 (7)0.066 (8)0.109 (7)0.043 (7)
C50.106 (5)0.099 (5)0.073 (4)0.008 (4)0.034 (4)0.009 (4)
S1'0.105 (8)0.087 (8)0.066 (6)0.003 (6)0.046 (6)0.015 (5)
C4'0.180 (10)0.163 (9)0.124 (7)0.066 (8)0.109 (7)0.043 (7)
C5'0.106 (5)0.099 (5)0.073 (4)0.008 (4)0.034 (4)0.009 (4)
Geometric parameters (Å, º) top
Re1—C11.900 (5)C21—C221.377 (7)
Re1—C31.902 (5)C22—C231.371 (8)
Re1—C21.914 (5)C23—C241.372 (7)
Re1—N22.193 (4)C24—C251.383 (6)
Re1—N12.200 (3)N3—N41.345 (5)
Re1—Cl12.4654 (13)N4—C311.394 (6)
N1—C151.344 (5)N4—H40.93 (5)
N1—C111.359 (5)C31—C321.385 (6)
N2—C251.335 (6)C31—C361.395 (6)
N2—C211.346 (6)C32—C331.377 (7)
C1—O11.158 (6)C33—C341.378 (7)
C2—O21.135 (6)C34—C351.358 (7)
C3—O31.150 (6)C34—N51.458 (7)
C11—C121.373 (6)C35—C361.400 (7)
C12—C131.370 (6)N5—O51.220 (6)
C13—C141.376 (6)N5—O41.232 (7)
C14—C151.394 (5)O6—S11.498 (4)
C15—C1.478 (6)O6—S1'1.550 (13)
C—N31.293 (5)S1—C51.743 (7)
C—C251.487 (6)S1—C41.776 (9)
C1—Re1—C388.8 (2)N3—C—C15127.1 (4)
C1—Re1—C290.3 (2)N3—C—C25112.4 (4)
C3—Re1—C289.2 (2)C15—C—C25119.9 (4)
C1—Re1—N294.29 (18)N2—C21—C22123.2 (5)
C3—Re1—N295.75 (17)C23—C22—C21118.5 (5)
C2—Re1—N2173.34 (17)C22—C23—C24118.8 (5)
C1—Re1—N1177.59 (17)C23—C24—C25120.0 (5)
C3—Re1—N191.75 (16)N2—C25—C24121.5 (4)
C2—Re1—N192.06 (16)N2—C25—C118.5 (4)
N2—Re1—N183.32 (12)C24—C25—C120.0 (4)
C1—Re1—Cl193.50 (17)C—N3—N4122.0 (4)
C3—Re1—Cl1177.63 (15)H4—N4—N3121 (3)
C2—Re1—Cl191.40 (16)H4—N4—C31118 (3)
N2—Re1—Cl183.52 (10)N3—N4—C31116.4 (4)
N1—Re1—Cl185.93 (9)C32—C31—N4122.1 (4)
C15—N1—C11118.6 (3)C32—C31—C36120.6 (4)
C15—N1—Re1122.0 (3)N4—C31—C36117.3 (4)
C11—N1—Re1119.2 (3)C33—C32—C31119.5 (5)
C25—N2—C21118.0 (4)C32—C33—C34119.8 (5)
C25—N2—Re1122.4 (3)C35—C34—C33121.7 (4)
C21—N2—Re1119.5 (3)C35—C34—N5119.5 (5)
O1—C1—Re1178.5 (5)C33—C34—N5118.9 (5)
O2—C2—Re1176.5 (4)C34—C35—C36119.6 (5)
O3—C3—Re1176.6 (4)C31—C36—C35118.8 (5)
N1—C11—C12122.1 (4)O5—N5—O4124.0 (5)
C13—C12—C11119.7 (4)O5—N5—C34117.8 (6)
C12—C13—C14118.5 (4)O4—N5—C34118.1 (5)
C13—C14—C15120.3 (4)S1—O6—S1'53.2 (4)
N1—C15—C14120.7 (4)O6—S1—C5106.8 (3)
N1—C15—C118.2 (3)O6—S1—C4106.6 (4)
C14—C15—C120.8 (4)C5—S1—C497.1 (4)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N4—H4···O60.93 (5)1.85 (5)2.775 (5)169 (4)
C5—H5C···Cl1i0.962.833.716 (7)153
C4—H4C···O30.962.853.364 (8)115
C14—H14A···O4ii0.932.553.353 (7)145
C24—H24A···O5ii0.932.533.308 (7)142
C22—H22A···O2iii0.932.473.393 (6)174
C23—H23A···O5iv0.932.543.436 (7)163
Symmetry codes: (i) x, y+1, z1/2; (ii) x+1, y+2, z+2; (iii) x, y+1, z+1/2; (iv) x, y+2, z+1/2.

Experimental details

Crystal data
Chemical formula[ReCl(C17H13N5O2)(CO)3]·C2H6OS
Mr703.13
Crystal system, space groupMonoclinic, C2/c
Temperature (K)298
a, b, c (Å)21.104 (2), 14.486 (2), 18.962 (2)
β (°) 116.408 (7)
V3)5192.0 (10)
Z8
Radiation typeMo Kα
µ (mm1)4.91
Crystal size (mm)0.42 × 0.38 × 0.34
Data collection
DiffractometerBruker P4
diffractometer
Absorption correctionψ scan
(XSCANS; Bruker, 1996)
Tmin, Tmax0.157, 0.188
No. of measured, independent and
observed [I > 2σ(I)] reflections
5397, 4562, 3969
Rint0.027
(sin θ/λ)max1)0.595
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.027, 0.064, 1.08
No. of reflections4562
No. of parameters339
H-atom treatmentH atoms treated by a mixture of independent and constrained refinement
Δρmax, Δρmin (e Å3)0.37, 0.85

Computer programs: XSCANS (Siemens, 1996), XSCANS, SHELXTL (Bruker, 1997), SHELXS97 (Sheldrick, 1990), SHELXL97 (Sheldrick, 1997), SHELXTL.

Selected geometric parameters (Å, º) top
Re1—C11.900 (5)N3—N41.345 (5)
Re1—C31.902 (5)N4—C311.394 (6)
Re1—C21.914 (5)N4—H40.93 (5)
Re1—N22.193 (4)C34—N51.458 (7)
Re1—N12.200 (3)N5—O51.220 (6)
Re1—Cl12.4654 (13)N5—O41.232 (7)
C—N31.293 (5)
C1—Re1—C388.8 (2)N2—Re1—N183.32 (12)
C1—Re1—C290.3 (2)C3—Re1—Cl1177.63 (15)
C3—Re1—C289.2 (2)C—N3—N4122.0 (4)
C3—Re1—N295.75 (17)N3—N4—C31116.4 (4)
C2—Re1—N2173.34 (17)O5—N5—O4124.0 (5)
C2—Re1—N192.06 (16)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
N4—H4···O60.93 (5)1.85 (5)2.775 (5)169 (4)
C5—H5C···Cl1i0.962.833.716 (7)153
C4—H4C···O30.962.853.364 (8)115
C14—H14A···O4ii0.932.553.353 (7)145
C24—H24A···O5ii0.932.533.308 (7)142
C22—H22A···O2iii0.932.473.393 (6)174
C23—H23A···O5iv0.932.543.436 (7)163
Symmetry codes: (i) x, y+1, z1/2; (ii) x+1, y+2, z+2; (iii) x, y+1, z+1/2; (iv) x, y+2, z+1/2.
 

Subscribe to Acta Crystallographica Section C: Structural Chemistry

The full text of this article is available to subscribers to the journal.

If you have already registered and are using a computer listed in your registration details, please email support@iucr.org for assistance.

Buy online

You may purchase this article in PDF and/or HTML formats. For purchasers in the European Community who do not have a VAT number, VAT will be added at the local rate. Payments to the IUCr are handled by WorldPay, who will accept payment by credit card in several currencies. To purchase the article, please complete the form below (fields marked * are required), and then click on `Continue'.
E-mail address* 
Repeat e-mail address* 
(for error checking) 

Format*   PDF (US $40)
   HTML (US $40)
   PDF+HTML (US $50)
In order for VAT to be shown for your country javascript needs to be enabled.

VAT number 
(non-UK EC countries only) 
Country* 
 

Terms and conditions of use
Contact us

Follow Acta Cryst. C
Sign up for e-alerts
Follow Acta Cryst. on Twitter
Follow us on facebook
Sign up for RSS feeds