Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807029698/ng2284sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807029698/ng2284Isup2.hkl |
CCDC reference: 654798
N-salicldimine-4-phenylthiosemicarbazone ligand was synthesized by condensing salicylaldehyde with 4-phenylthiosemicarbazide in ethonal for 2.5 h, and the hydrazone ligand was isolated as yellow crystals from the resulting solution. The title compound was prepared by the addition of nickel(II) acetate tetrahydrate (1 mmol) and pyridine (1 ml) to a methanol solution (15 ml) of the ligand (1 mmol). The mixture was refluxed for 1 h, cooled slowly to room temperature and filtered. Red-brown crystals were isolated from the solution after three days. Analysis calculated for C19H16N4OSNi: C 56.06, H 3.96, N 13.76%; found: C 56.01, H 3.94, N 13.79%.
C-bound H atoms were placed in calculated positions, with C—H = 0.93 and Uiso(H) = 1.2Ueq(C), and were included in the refinement in the riding-model approximation. H atoms on the N atoms were located in Fourier difference maps and refined with the restraints N—H = 0.86 (1) Å, and with Uiso(H) = 1.2Ueq(N). The Flack parameter was refined from 3366 Friedel paris.
Up to now, a number of metal complexes of N-salicyldimine-4-phenylthiosemicarbazide have been synthesized, and most of them are mononuclear (Milanesio et al., 2000; Prabhakaran et al., 2005; Soriano-García et al., 1985; Naik et al., 2003; Thomas et al., 2004). Recently, a dinuclear complex has been reported (Deng et al., 2007). In these complexs, the hydrazone ligand chelates in a terdentate manner. In the title mononuclear complex, [Ni(C14H11N3OS)(C5H5N)], the ligand binds in a similar mode. As shown in Fig. 1, the NiII atom is N,O,S-chelated by deprotonated salicylaldimine-4-phenylthiosemicarbazide dianion. It is also coordinated by pyridine molecule, and a square planar geometry results. The mononuclear units are linked into a chain structure along b axis by N—H···S intermolecular hydrogen bonds and weak π-π stacking interactions between the pyridine rings [centroid···centroid = 3.758 (3) Å] (Fig. 2).
For other metal derivatives of N-salicylaldimine-4-phenylthiosemicarbazide, see: Milanesio et al. (2000) for vanadium, Prabhakaran et al. (2005) and Soriano-García et al. (1985) for nickel, Naik et al. (2003) and Thomas et al. (2004) for copper, Deng et al. (2007) for zinc.
Data collection: RAPID-AUTO (Rigaku, 1998); cell refinement: RAPID-AUTO; data reduction: CrystalStructure (Rigaku/MSC, 2002); program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: ORTEPII (Johnson, 1976); software used to prepare material for publication: SHELXL97.
[Ni(C14H11N3OS)(C5H5N)] | F(000) = 840 |
Mr = 407.13 | Dx = 1.550 Mg m−3 |
Monoclinic, Pc | Mo Kα radiation, λ = 0.71073 Å |
Hall symbol: P -2yc | Cell parameters from 11939 reflections |
a = 5.7294 (11) Å | θ = 3.0–27.5° |
b = 12.924 (3) Å | µ = 1.25 mm−1 |
c = 23.683 (5) Å | T = 295 K |
β = 95.64 (3)° | Prism, colorless |
V = 1745.2 (6) Å3 | 0.35 × 0.24 × 0.17 mm |
Z = 4 |
Rigaku R-AXIS RAPID diffractometer | 7370 independent reflections |
Radiation source: fine-focus sealed tube | 4892 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.044 |
Detector resolution: 10.000 pixels mm-1 | θmax = 27.5°, θmin = 3.0° |
ω scans | h = −6→7 |
Absorption correction: multi-scan (ABSCOR; Higashi, 1995) | k = −16→16 |
Tmin = 0.669, Tmax = 0.816 | l = −30→30 |
16815 measured reflections |
Refinement on F2 | Secondary atom site location: difference Fourier map |
Least-squares matrix: full | Hydrogen site location: inferred from neighbouring sites |
R[F2 > 2σ(F2)] = 0.037 | H atoms treated by a mixture of independent and constrained refinement |
wR(F2) = 0.089 | w = 1/[σ2(Fo2) + (0.022P)2 + 0.9787P] where P = (Fo2 + 2Fc2)/3 |
S = 1.06 | (Δ/σ)max = 0.001 |
7370 reflections | Δρmax = 0.60 e Å−3 |
475 parameters | Δρmin = −0.57 e Å−3 |
4 restraints | Absolute structure: Flack (1983), with 3366 Friedel pairs |
Primary atom site location: structure-invariant direct methods | Absolute structure parameter: 0.029 (17) |
[Ni(C14H11N3OS)(C5H5N)] | V = 1745.2 (6) Å3 |
Mr = 407.13 | Z = 4 |
Monoclinic, Pc | Mo Kα radiation |
a = 5.7294 (11) Å | µ = 1.25 mm−1 |
b = 12.924 (3) Å | T = 295 K |
c = 23.683 (5) Å | 0.35 × 0.24 × 0.17 mm |
β = 95.64 (3)° |
Rigaku R-AXIS RAPID diffractometer | 7370 independent reflections |
Absorption correction: multi-scan (ABSCOR; Higashi, 1995) | 4892 reflections with I > 2σ(I) |
Tmin = 0.669, Tmax = 0.816 | Rint = 0.044 |
16815 measured reflections |
R[F2 > 2σ(F2)] = 0.037 | H atoms treated by a mixture of independent and constrained refinement |
wR(F2) = 0.089 | Δρmax = 0.60 e Å−3 |
S = 1.06 | Δρmin = −0.57 e Å−3 |
7370 reflections | Absolute structure: Flack (1983), with 3366 Friedel pairs |
475 parameters | Absolute structure parameter: 0.029 (17) |
4 restraints |
x | y | z | Uiso*/Ueq | ||
Ni1 | 0.42415 (9) | 0.92246 (4) | 0.75792 (3) | 0.03968 (16) | |
Ni2 | 0.30864 (10) | 0.32924 (4) | 0.63710 (3) | 0.03927 (16) | |
S1 | 0.1296 (2) | 1.01932 (11) | 0.72961 (6) | 0.0479 (4) | |
S2 | 0.6011 (3) | 0.23095 (11) | 0.66440 (6) | 0.0486 (4) | |
O1 | 0.6638 (8) | 0.8306 (2) | 0.78157 (17) | 0.0491 (11) | |
O2 | 0.0683 (7) | 0.4217 (2) | 0.61431 (17) | 0.0479 (11) | |
N1 | 0.5015 (8) | 1.0198 (3) | 0.81387 (19) | 0.0399 (10) | |
N2 | 0.3641 (8) | 1.1071 (3) | 0.8204 (2) | 0.0444 (11) | |
N3 | 0.0183 (8) | 1.1876 (4) | 0.78621 (19) | 0.0464 (11) | |
H3N | −0.096 (6) | 1.185 (4) | 0.7596 (16) | 0.056* | |
N4 | 0.3432 (8) | 0.8267 (3) | 0.69777 (19) | 0.0372 (11) | |
N5 | 0.2299 (7) | 0.2349 (3) | 0.57989 (19) | 0.0381 (10) | |
N6 | 0.3675 (8) | 0.1466 (3) | 0.57220 (19) | 0.0451 (11) | |
N7 | 0.7084 (8) | 0.0632 (4) | 0.60734 (18) | 0.0464 (11) | |
H7N | 0.825 (6) | 0.066 (4) | 0.6330 (17) | 0.056* | |
N8 | 0.3873 (8) | 0.4238 (3) | 0.69807 (19) | 0.0380 (11) | |
C1 | 0.8281 (16) | 0.8445 (6) | 0.8244 (4) | 0.0414 (19) | |
C2 | 0.995 (2) | 0.7658 (7) | 0.8368 (4) | 0.057 (3) | |
H2 | 0.9801 | 0.7038 | 0.8169 | 0.069* | |
C3 | 1.176 (2) | 0.7786 (8) | 0.8771 (4) | 0.062 (3) | |
H3 | 1.2856 | 0.7256 | 0.8826 | 0.075* | |
C4 | 1.2076 (16) | 0.8661 (7) | 0.9108 (4) | 0.054 (2) | |
H4 | 1.3329 | 0.8726 | 0.9387 | 0.065* | |
C5 | 1.0409 (13) | 0.9432 (6) | 0.9004 (3) | 0.053 (2) | |
H5 | 1.0548 | 1.0034 | 0.9220 | 0.064* | |
C6 | 0.8511 (12) | 0.9335 (5) | 0.8582 (3) | 0.0424 (16) | |
C7 | 0.6850 (9) | 1.0158 (4) | 0.8509 (2) | 0.0404 (12) | |
H7 | 0.7103 | 1.0723 | 0.8750 | 0.049* | |
C8 | 0.1818 (9) | 1.1111 (4) | 0.7833 (2) | 0.0390 (12) | |
C9 | 0.0002 (17) | 1.2640 (6) | 0.8284 (4) | 0.041 (2) | |
C10 | −0.2062 (17) | 1.3186 (6) | 0.8283 (5) | 0.051 (2) | |
H10 | −0.3307 | 1.3035 | 0.8014 | 0.062* | |
C11 | −0.2306 (14) | 1.3955 (5) | 0.8679 (3) | 0.0557 (19) | |
H11 | −0.3713 | 1.4315 | 0.8670 | 0.067* | |
C12 | −0.0527 (15) | 1.4192 (6) | 0.9080 (4) | 0.057 (2) | |
H12 | −0.0701 | 1.4715 | 0.9342 | 0.068* | |
C13 | 0.1552 (17) | 1.3640 (7) | 0.9090 (5) | 0.061 (3) | |
H13 | 0.2778 | 1.3783 | 0.9366 | 0.074* | |
C14 | 0.1808 (17) | 1.2872 (6) | 0.8688 (4) | 0.047 (2) | |
H14 | 0.3217 | 1.2513 | 0.8694 | 0.056* | |
C15 | 0.4957 (11) | 0.8095 (4) | 0.6593 (3) | 0.0456 (14) | |
H15 | 0.6289 | 0.8508 | 0.6602 | 0.055* | |
C16 | 0.4640 (11) | 0.7341 (4) | 0.6189 (2) | 0.0508 (15) | |
H16 | 0.5721 | 0.7253 | 0.5925 | 0.061* | |
C17 | 0.2700 (11) | 0.6712 (5) | 0.6180 (2) | 0.0537 (14) | |
H17 | 0.2463 | 0.6180 | 0.5916 | 0.064* | |
C18 | 0.1127 (10) | 0.6887 (4) | 0.6568 (2) | 0.0484 (14) | |
H18 | −0.0200 | 0.6473 | 0.6571 | 0.058* | |
C19 | 0.1518 (10) | 0.7674 (4) | 0.6951 (2) | 0.0459 (13) | |
H19 | 0.0405 | 0.7802 | 0.7202 | 0.055* | |
C20 | −0.0943 (17) | 0.4123 (6) | 0.5718 (4) | 0.0416 (19) | |
C21 | −0.2597 (18) | 0.4920 (7) | 0.5611 (4) | 0.050 (2) | |
H21 | −0.2470 | 0.5516 | 0.5832 | 0.059* | |
C22 | −0.4421 (19) | 0.4834 (7) | 0.5179 (4) | 0.059 (3) | |
H22 | −0.5520 | 0.5361 | 0.5115 | 0.071* | |
C23 | −0.4570 (17) | 0.3963 (8) | 0.4851 (5) | 0.061 (3) | |
H23 | −0.5804 | 0.3898 | 0.4567 | 0.074* | |
C24 | −0.2986 (14) | 0.3196 (6) | 0.4926 (3) | 0.052 (2) | |
H24 | −0.3117 | 0.2624 | 0.4687 | 0.062* | |
C25 | −0.1122 (12) | 0.3246 (5) | 0.5364 (3) | 0.0417 (17) | |
C26 | 0.0501 (9) | 0.2410 (4) | 0.5421 (2) | 0.0439 (13) | |
H26 | 0.0254 | 0.1862 | 0.5168 | 0.053* | |
C27 | 0.5462 (10) | 0.1413 (4) | 0.6101 (2) | 0.0403 (13) | |
C28 | 0.7199 (17) | −0.0134 (6) | 0.5662 (4) | 0.0381 (19) | |
C29 | 0.9279 (18) | −0.0694 (6) | 0.5667 (4) | 0.047 (2) | |
H29 | 1.0531 | −0.0532 | 0.5933 | 0.057* | |
C30 | 0.9513 (14) | −0.1482 (6) | 0.5287 (3) | 0.057 (2) | |
H30 | 1.0917 | −0.1845 | 0.5298 | 0.069* | |
C31 | 0.7675 (15) | −0.1739 (6) | 0.4886 (4) | 0.052 (2) | |
H31 | 0.7825 | −0.2272 | 0.4628 | 0.062* | |
C32 | 0.5649 (16) | −0.1191 (6) | 0.4881 (4) | 0.051 (2) | |
H32 | 0.4408 | −0.1366 | 0.4616 | 0.061* | |
C33 | 0.5341 (17) | −0.0390 (6) | 0.5250 (4) | 0.045 (2) | |
H33 | 0.3936 | −0.0026 | 0.5229 | 0.054* | |
C34 | 0.5814 (9) | 0.4822 (4) | 0.7015 (2) | 0.0435 (13) | |
H34 | 0.6953 | 0.4691 | 0.6770 | 0.052* | |
C35 | 0.6158 (11) | 0.5614 (5) | 0.7404 (2) | 0.0534 (15) | |
H35 | 0.7476 | 0.6035 | 0.7407 | 0.064* | |
C36 | 0.4544 (11) | 0.5779 (5) | 0.7788 (2) | 0.0548 (14) | |
H36 | 0.4754 | 0.6311 | 0.8053 | 0.066* | |
C37 | 0.2619 (11) | 0.5145 (4) | 0.7774 (2) | 0.0509 (15) | |
H37 | 0.1531 | 0.5223 | 0.8038 | 0.061* | |
C38 | 0.2330 (11) | 0.4391 (4) | 0.7362 (2) | 0.0443 (14) | |
H38 | 0.1008 | 0.3971 | 0.7349 | 0.053* |
U11 | U22 | U33 | U12 | U13 | U23 | |
Ni1 | 0.0444 (4) | 0.0343 (3) | 0.0392 (4) | 0.0006 (3) | −0.0018 (3) | −0.0047 (3) |
Ni2 | 0.0437 (4) | 0.0347 (3) | 0.0380 (4) | 0.0012 (3) | −0.0026 (3) | −0.0043 (3) |
S1 | 0.0541 (9) | 0.0433 (7) | 0.0433 (8) | 0.0063 (7) | −0.0103 (7) | −0.0090 (6) |
S2 | 0.0550 (9) | 0.0426 (7) | 0.0452 (9) | 0.0087 (7) | −0.0105 (7) | −0.0087 (7) |
O1 | 0.057 (3) | 0.043 (2) | 0.044 (3) | 0.0073 (17) | −0.007 (2) | −0.0095 (16) |
O2 | 0.053 (3) | 0.040 (2) | 0.048 (3) | 0.0083 (17) | −0.010 (2) | −0.0123 (16) |
N1 | 0.043 (3) | 0.036 (2) | 0.041 (3) | 0.002 (2) | 0.000 (2) | 0.000 (2) |
N2 | 0.044 (3) | 0.033 (2) | 0.054 (3) | 0.011 (2) | −0.009 (2) | −0.007 (2) |
N3 | 0.048 (3) | 0.043 (3) | 0.045 (3) | 0.009 (2) | −0.012 (2) | −0.005 (2) |
N4 | 0.038 (3) | 0.034 (2) | 0.039 (3) | 0.0015 (19) | 0.001 (2) | −0.0015 (19) |
N5 | 0.038 (3) | 0.031 (2) | 0.044 (3) | 0.0033 (19) | −0.001 (2) | −0.0020 (19) |
N6 | 0.049 (3) | 0.037 (2) | 0.048 (3) | 0.008 (2) | −0.001 (2) | −0.008 (2) |
N7 | 0.046 (3) | 0.046 (3) | 0.043 (3) | 0.009 (2) | −0.014 (2) | −0.009 (2) |
N8 | 0.043 (3) | 0.035 (2) | 0.036 (3) | 0.002 (2) | 0.002 (2) | −0.0005 (19) |
C1 | 0.039 (4) | 0.044 (4) | 0.041 (4) | 0.009 (3) | −0.001 (3) | 0.009 (3) |
C2 | 0.075 (7) | 0.051 (5) | 0.044 (5) | 0.019 (4) | −0.004 (4) | −0.013 (4) |
C3 | 0.072 (6) | 0.068 (5) | 0.045 (5) | 0.034 (4) | −0.004 (4) | 0.005 (4) |
C4 | 0.047 (4) | 0.071 (5) | 0.042 (5) | 0.014 (4) | −0.008 (4) | −0.006 (4) |
C5 | 0.048 (4) | 0.060 (4) | 0.049 (4) | 0.004 (3) | −0.009 (4) | −0.005 (3) |
C6 | 0.044 (4) | 0.042 (3) | 0.040 (4) | 0.002 (3) | 0.001 (3) | −0.003 (3) |
C7 | 0.038 (3) | 0.041 (3) | 0.041 (3) | 0.000 (2) | −0.005 (2) | −0.007 (2) |
C8 | 0.045 (3) | 0.032 (3) | 0.039 (3) | 0.006 (2) | −0.002 (2) | 0.003 (2) |
C9 | 0.049 (5) | 0.036 (4) | 0.036 (4) | −0.001 (3) | 0.001 (3) | 0.000 (3) |
C10 | 0.037 (4) | 0.053 (4) | 0.061 (5) | 0.012 (3) | −0.007 (4) | 0.003 (4) |
C11 | 0.053 (5) | 0.056 (4) | 0.060 (5) | 0.015 (4) | 0.011 (4) | 0.003 (4) |
C12 | 0.062 (6) | 0.052 (4) | 0.059 (5) | 0.007 (4) | 0.017 (4) | −0.008 (3) |
C13 | 0.063 (6) | 0.062 (5) | 0.058 (6) | −0.005 (4) | 0.002 (5) | −0.022 (4) |
C14 | 0.046 (4) | 0.046 (4) | 0.047 (5) | 0.013 (3) | −0.002 (3) | −0.005 (3) |
C15 | 0.043 (4) | 0.045 (3) | 0.049 (4) | 0.002 (3) | 0.005 (3) | 0.003 (3) |
C16 | 0.062 (4) | 0.048 (3) | 0.042 (3) | 0.015 (3) | 0.007 (3) | −0.004 (3) |
C17 | 0.068 (4) | 0.042 (3) | 0.049 (3) | 0.006 (3) | −0.007 (3) | −0.008 (3) |
C18 | 0.054 (3) | 0.044 (3) | 0.047 (3) | −0.010 (3) | 0.003 (3) | −0.009 (3) |
C19 | 0.049 (3) | 0.046 (3) | 0.042 (3) | −0.001 (3) | 0.004 (3) | −0.005 (3) |
C20 | 0.054 (5) | 0.043 (3) | 0.027 (3) | 0.000 (3) | 0.000 (3) | −0.003 (3) |
C21 | 0.059 (6) | 0.045 (4) | 0.043 (4) | 0.020 (4) | −0.005 (4) | 0.000 (3) |
C22 | 0.066 (6) | 0.064 (5) | 0.045 (5) | 0.025 (4) | −0.009 (4) | −0.002 (4) |
C23 | 0.052 (4) | 0.076 (6) | 0.052 (5) | 0.018 (4) | −0.018 (4) | −0.009 (4) |
C24 | 0.052 (5) | 0.057 (4) | 0.044 (4) | 0.009 (3) | −0.013 (3) | −0.015 (3) |
C25 | 0.043 (4) | 0.043 (3) | 0.038 (4) | 0.007 (3) | 0.001 (3) | 0.000 (3) |
C26 | 0.046 (3) | 0.040 (3) | 0.043 (3) | −0.002 (2) | −0.006 (3) | −0.007 (2) |
C27 | 0.046 (3) | 0.036 (3) | 0.037 (3) | 0.003 (2) | −0.004 (2) | 0.000 (2) |
C28 | 0.045 (4) | 0.030 (3) | 0.040 (4) | 0.005 (3) | 0.007 (3) | 0.006 (3) |
C29 | 0.049 (4) | 0.049 (4) | 0.044 (4) | 0.003 (3) | 0.003 (3) | −0.007 (4) |
C30 | 0.056 (5) | 0.059 (5) | 0.057 (5) | 0.020 (4) | 0.005 (4) | 0.001 (4) |
C31 | 0.070 (6) | 0.044 (4) | 0.043 (4) | 0.010 (3) | 0.010 (4) | −0.006 (3) |
C32 | 0.052 (5) | 0.054 (5) | 0.043 (5) | 0.012 (4) | −0.009 (4) | −0.010 (4) |
C33 | 0.037 (4) | 0.045 (4) | 0.052 (5) | 0.002 (3) | −0.004 (3) | −0.008 (4) |
C34 | 0.044 (3) | 0.048 (3) | 0.038 (3) | −0.003 (3) | 0.002 (2) | −0.004 (3) |
C35 | 0.055 (4) | 0.053 (4) | 0.051 (3) | −0.005 (3) | −0.002 (3) | −0.003 (3) |
C36 | 0.067 (4) | 0.044 (3) | 0.051 (4) | 0.009 (3) | −0.004 (3) | −0.014 (3) |
C37 | 0.057 (4) | 0.053 (3) | 0.044 (3) | 0.008 (3) | 0.012 (3) | 0.002 (3) |
C38 | 0.045 (4) | 0.045 (3) | 0.042 (3) | −0.003 (3) | 0.000 (3) | 0.002 (3) |
Ni1—N1 | 1.849 (4) | C12—C13 | 1.387 (12) |
Ni1—O1 | 1.859 (4) | C12—H12 | 0.9300 |
Ni1—N4 | 1.909 (4) | C13—C14 | 1.394 (12) |
Ni1—S1 | 2.1547 (15) | C13—H13 | 0.9300 |
Ni2—N5 | 1.845 (4) | C14—H14 | 0.9300 |
Ni2—O2 | 1.863 (4) | C15—C16 | 1.366 (8) |
Ni2—N8 | 1.911 (4) | C15—H15 | 0.9300 |
Ni2—S2 | 2.1507 (15) | C16—C17 | 1.375 (8) |
S1—C8 | 1.744 (5) | C16—H16 | 0.9300 |
S2—C27 | 1.736 (5) | C17—C18 | 1.367 (8) |
O1—C1 | 1.327 (10) | C17—H17 | 0.9300 |
O2—C20 | 1.308 (10) | C18—C19 | 1.367 (7) |
N1—C7 | 1.302 (6) | C18—H18 | 0.9300 |
N1—N2 | 1.393 (6) | C19—H19 | 0.9300 |
N2—C8 | 1.297 (6) | C20—C21 | 1.406 (12) |
N3—C8 | 1.368 (7) | C20—C25 | 1.407 (11) |
N3—C9 | 1.415 (10) | C21—C22 | 1.392 (11) |
N3—H3N | 0.86 (4) | C21—H21 | 0.9300 |
N4—C19 | 1.334 (6) | C22—C23 | 1.366 (13) |
N4—C15 | 1.341 (7) | C22—H22 | 0.9300 |
N5—C26 | 1.298 (6) | C23—C24 | 1.343 (12) |
N5—N6 | 1.410 (5) | C23—H23 | 0.9300 |
N6—C27 | 1.295 (6) | C24—C25 | 1.415 (10) |
N7—C27 | 1.378 (7) | C24—H24 | 0.9300 |
N7—C28 | 1.397 (10) | C25—C26 | 1.424 (8) |
N7—H7N | 0.86 (4) | C26—H26 | 0.9300 |
N8—C38 | 1.340 (7) | C28—C29 | 1.393 (13) |
N8—C34 | 1.340 (6) | C28—C33 | 1.410 (11) |
C1—C6 | 1.400 (11) | C29—C30 | 1.375 (12) |
C1—C2 | 1.406 (12) | C29—H29 | 0.9300 |
C2—C3 | 1.348 (12) | C30—C31 | 1.386 (11) |
C2—H2 | 0.9300 | C30—H30 | 0.9300 |
C3—C4 | 1.386 (13) | C31—C32 | 1.359 (12) |
C3—H3 | 0.9300 | C31—H31 | 0.9300 |
C4—C5 | 1.386 (12) | C32—C33 | 1.377 (12) |
C4—H4 | 0.9300 | C32—H32 | 0.9300 |
C5—C6 | 1.409 (10) | C33—H33 | 0.9300 |
C5—H5 | 0.9300 | C34—C35 | 1.379 (7) |
C6—C7 | 1.426 (8) | C34—H34 | 0.9300 |
C7—H7 | 0.9300 | C35—C36 | 1.376 (8) |
C9—C14 | 1.372 (11) | C35—H35 | 0.9300 |
C9—C10 | 1.377 (13) | C36—C37 | 1.371 (8) |
C10—C11 | 1.382 (12) | C36—H36 | 0.9300 |
C10—H10 | 0.9300 | C37—C38 | 1.378 (8) |
C11—C12 | 1.358 (11) | C37—H37 | 0.9300 |
C11—H11 | 0.9300 | C38—H38 | 0.9300 |
N1—Ni1—O1 | 95.77 (17) | C9—C14—C13 | 120.6 (10) |
N1—Ni1—N4 | 177.51 (19) | C9—C14—H14 | 119.7 |
O1—Ni1—N4 | 85.93 (17) | C13—C14—H14 | 119.7 |
N1—Ni1—S1 | 87.31 (14) | N4—C15—C16 | 122.9 (5) |
O1—Ni1—S1 | 175.83 (13) | N4—C15—H15 | 118.5 |
N4—Ni1—S1 | 91.08 (13) | C16—C15—H15 | 118.5 |
N5—Ni2—O2 | 95.19 (17) | C15—C16—C17 | 119.0 (6) |
N5—Ni2—N8 | 178.16 (19) | C15—C16—H16 | 120.5 |
O2—Ni2—N8 | 85.50 (17) | C17—C16—H16 | 120.5 |
N5—Ni2—S2 | 87.57 (13) | C18—C17—C16 | 118.5 (5) |
O2—Ni2—S2 | 176.29 (13) | C18—C17—H17 | 120.8 |
N8—Ni2—S2 | 91.81 (14) | C16—C17—H17 | 120.8 |
C8—S1—Ni1 | 95.46 (18) | C19—C18—C17 | 119.5 (6) |
C27—S2—Ni2 | 95.30 (18) | C19—C18—H18 | 120.2 |
C1—O1—Ni1 | 126.3 (4) | C17—C18—H18 | 120.2 |
C20—O2—Ni2 | 127.8 (4) | N4—C19—C18 | 122.7 (5) |
C7—N1—N2 | 112.7 (4) | N4—C19—H19 | 118.7 |
C7—N1—Ni1 | 125.2 (4) | C18—C19—H19 | 118.7 |
N2—N1—Ni1 | 122.1 (3) | O2—C20—C21 | 119.2 (7) |
C8—N2—N1 | 112.6 (4) | O2—C20—C25 | 122.6 (8) |
C8—N3—C9 | 129.6 (5) | C21—C20—C25 | 118.3 (8) |
C8—N3—H3N | 114 (4) | C22—C21—C20 | 121.2 (9) |
C9—N3—H3N | 116 (4) | C22—C21—H21 | 119.4 |
C19—N4—C15 | 117.4 (5) | C20—C21—H21 | 119.4 |
C19—N4—Ni1 | 123.1 (4) | C23—C22—C21 | 118.9 (9) |
C15—N4—Ni1 | 119.1 (4) | C23—C22—H22 | 120.5 |
C26—N5—N6 | 112.1 (4) | C21—C22—H22 | 120.5 |
C26—N5—Ni2 | 125.9 (4) | C24—C23—C22 | 121.9 (10) |
N6—N5—Ni2 | 122.0 (3) | C24—C23—H23 | 119.0 |
C27—N6—N5 | 111.5 (4) | C22—C23—H23 | 119.0 |
C27—N7—C28 | 129.1 (5) | C23—C24—C25 | 121.0 (8) |
C27—N7—H7N | 115 (4) | C23—C24—H24 | 119.5 |
C28—N7—H7N | 116 (4) | C25—C24—H24 | 119.5 |
C38—N8—C34 | 118.3 (5) | C20—C25—C24 | 118.6 (7) |
C38—N8—Ni2 | 118.8 (4) | C20—C25—C26 | 123.1 (7) |
C34—N8—Ni2 | 122.6 (4) | C24—C25—C26 | 118.3 (6) |
O1—C1—C6 | 124.6 (7) | N5—C26—C25 | 125.3 (5) |
O1—C1—C2 | 118.6 (8) | N5—C26—H26 | 117.4 |
C6—C1—C2 | 116.8 (8) | C25—C26—H26 | 117.4 |
C3—C2—C1 | 121.2 (9) | N6—C27—N7 | 119.8 (5) |
C3—C2—H2 | 119.4 | N6—C27—S2 | 123.5 (4) |
C1—C2—H2 | 119.4 | N7—C27—S2 | 116.7 (4) |
C2—C3—C4 | 123.8 (10) | C29—C28—N7 | 117.4 (8) |
C2—C3—H3 | 118.1 | C29—C28—C33 | 118.2 (9) |
C4—C3—H3 | 118.1 | N7—C28—C33 | 124.4 (8) |
C5—C4—C3 | 115.8 (9) | C30—C29—C28 | 121.1 (9) |
C5—C4—H4 | 122.1 | C30—C29—H29 | 119.5 |
C3—C4—H4 | 122.1 | C28—C29—H29 | 119.5 |
C4—C5—C6 | 122.2 (8) | C29—C30—C31 | 120.7 (8) |
C4—C5—H5 | 118.9 | C29—C30—H30 | 119.7 |
C6—C5—H5 | 118.9 | C31—C30—H30 | 119.7 |
C1—C6—C5 | 120.1 (7) | C32—C31—C30 | 118.1 (8) |
C1—C6—C7 | 121.3 (7) | C32—C31—H31 | 121.0 |
C5—C6—C7 | 118.6 (6) | C30—C31—H31 | 121.0 |
N1—C7—C6 | 126.6 (5) | C31—C32—C33 | 123.3 (9) |
N1—C7—H7 | 116.7 | C31—C32—H32 | 118.3 |
C6—C7—H7 | 116.7 | C33—C32—H32 | 118.3 |
N2—C8—N3 | 120.3 (5) | C32—C33—C28 | 118.7 (9) |
N2—C8—S1 | 122.4 (4) | C32—C33—H33 | 120.7 |
N3—C8—S1 | 117.3 (4) | C28—C33—H33 | 120.7 |
C14—C9—C10 | 118.5 (9) | N8—C34—C35 | 121.4 (5) |
C14—C9—N3 | 122.8 (9) | N8—C34—H34 | 119.3 |
C10—C9—N3 | 118.7 (8) | C35—C34—H34 | 119.3 |
C9—C10—C11 | 120.8 (9) | C36—C35—C34 | 119.7 (6) |
C9—C10—H10 | 119.6 | C36—C35—H35 | 120.1 |
C11—C10—H10 | 119.6 | C34—C35—H35 | 120.1 |
C12—C11—C10 | 121.2 (8) | C37—C36—C35 | 118.9 (5) |
C12—C11—H11 | 119.4 | C37—C36—H36 | 120.6 |
C10—C11—H11 | 119.4 | C35—C36—H36 | 120.6 |
C11—C12—C13 | 118.7 (8) | C36—C37—C38 | 118.7 (6) |
C11—C12—H12 | 120.7 | C36—C37—H37 | 120.7 |
C13—C12—H12 | 120.7 | C38—C37—H37 | 120.7 |
C12—C13—C14 | 120.2 (10) | N8—C38—C37 | 122.8 (5) |
C12—C13—H13 | 119.9 | N8—C38—H38 | 118.6 |
C14—C13—H13 | 119.9 | C37—C38—H38 | 118.6 |
N1—Ni1—S1—C8 | −3.0 (2) | C9—C10—C11—C12 | −0.3 (13) |
N4—Ni1—S1—C8 | 178.9 (2) | C10—C11—C12—C13 | −0.6 (13) |
N5—Ni2—S2—C27 | 2.4 (2) | C11—C12—C13—C14 | 1.2 (14) |
N8—Ni2—S2—C27 | −179.4 (2) | C10—C9—C14—C13 | 0.2 (15) |
N1—Ni1—O1—C1 | −2.1 (6) | N3—C9—C14—C13 | 179.3 (8) |
N4—Ni1—O1—C1 | 176.1 (6) | C12—C13—C14—C9 | −1.1 (15) |
N5—Ni2—O2—C20 | 1.4 (6) | C19—N4—C15—C16 | −1.0 (8) |
N8—Ni2—O2—C20 | −176.9 (6) | Ni1—N4—C15—C16 | 172.3 (4) |
O1—Ni1—N1—C7 | 5.3 (5) | N4—C15—C16—C17 | −1.3 (8) |
S1—Ni1—N1—C7 | −177.5 (5) | C15—C16—C17—C18 | 1.7 (8) |
O1—Ni1—N1—N2 | −174.8 (4) | C16—C17—C18—C19 | 0.0 (9) |
S1—Ni1—N1—N2 | 2.3 (4) | C15—N4—C19—C18 | 2.9 (8) |
C7—N1—N2—C8 | 179.8 (5) | Ni1—N4—C19—C18 | −170.1 (4) |
Ni1—N1—N2—C8 | −0.1 (6) | C17—C18—C19—N4 | −2.4 (8) |
O1—Ni1—N4—C19 | 108.6 (4) | Ni2—O2—C20—C21 | −179.2 (7) |
S1—Ni1—N4—C19 | −68.5 (4) | Ni2—O2—C20—C25 | 1.4 (12) |
O1—Ni1—N4—C15 | −64.3 (4) | O2—C20—C21—C22 | −177.1 (9) |
S1—Ni1—N4—C15 | 118.6 (4) | C25—C20—C21—C22 | 2.4 (15) |
O2—Ni2—N5—C26 | −3.7 (5) | C20—C21—C22—C23 | −1.0 (17) |
S2—Ni2—N5—C26 | 178.8 (5) | C21—C22—C23—C24 | −1.2 (17) |
O2—Ni2—N5—N6 | 175.2 (4) | C22—C23—C24—C25 | 2.0 (16) |
S2—Ni2—N5—N6 | −2.4 (4) | O2—C20—C25—C24 | 177.9 (8) |
C26—N5—N6—C27 | 180.0 (5) | C21—C20—C25—C24 | −1.6 (12) |
Ni2—N5—N6—C27 | 1.0 (6) | O2—C20—C25—C26 | −2.8 (12) |
O2—Ni2—N8—C38 | 64.2 (4) | C21—C20—C25—C26 | 177.8 (8) |
S2—Ni2—N8—C38 | −118.3 (4) | C23—C24—C25—C20 | −0.6 (13) |
O2—Ni2—N8—C34 | −109.7 (4) | C23—C24—C25—C26 | −179.9 (8) |
S2—Ni2—N8—C34 | 67.8 (4) | N6—N5—C26—C25 | −175.6 (5) |
Ni1—O1—C1—C6 | −2.1 (12) | Ni2—N5—C26—C25 | 3.4 (9) |
Ni1—O1—C1—C2 | 179.2 (7) | C20—C25—C26—N5 | 0.3 (11) |
O1—C1—C2—C3 | 175.1 (10) | C24—C25—C26—N5 | 179.6 (6) |
C6—C1—C2—C3 | −3.8 (16) | N5—N6—C27—N7 | −176.3 (4) |
C1—C2—C3—C4 | 2.9 (19) | N5—N6—C27—S2 | 1.7 (7) |
C2—C3—C4—C5 | −0.9 (17) | C28—N7—C27—N6 | 3.9 (10) |
C3—C4—C5—C6 | −0.1 (14) | C28—N7—C27—S2 | −174.2 (6) |
O1—C1—C6—C5 | −175.9 (8) | Ni2—S2—C27—N6 | −3.0 (5) |
C2—C1—C6—C5 | 2.8 (12) | Ni2—S2—C27—N7 | 175.1 (4) |
O1—C1—C6—C7 | 4.2 (12) | C27—N7—C28—C29 | 166.5 (7) |
C2—C1—C6—C7 | −177.0 (8) | C27—N7—C28—C33 | −14.8 (13) |
C4—C5—C6—C1 | −1.0 (13) | N7—C28—C29—C30 | 178.1 (7) |
C4—C5—C6—C7 | 178.9 (7) | C33—C28—C29—C30 | −0.6 (13) |
N2—N1—C7—C6 | 175.4 (5) | C28—C29—C30—C31 | 0.0 (13) |
Ni1—N1—C7—C6 | −4.7 (9) | C29—C30—C31—C32 | 0.1 (12) |
C1—C6—C7—N1 | −0.6 (11) | C30—C31—C32—C33 | 0.5 (14) |
C5—C6—C7—N1 | 179.5 (6) | C31—C32—C33—C28 | −1.2 (15) |
N1—N2—C8—N3 | 175.1 (4) | C29—C28—C33—C32 | 1.2 (14) |
N1—N2—C8—S1 | −3.3 (7) | N7—C28—C33—C32 | −177.5 (8) |
C9—N3—C8—N2 | −6.5 (10) | C38—N8—C34—C35 | −4.6 (7) |
C9—N3—C8—S1 | 171.9 (6) | Ni2—N8—C34—C35 | 169.4 (4) |
Ni1—S1—C8—N2 | 4.3 (5) | N8—C34—C35—C36 | 3.5 (8) |
Ni1—S1—C8—N3 | −174.1 (4) | C34—C35—C36—C37 | 0.1 (9) |
C8—N3—C9—C14 | 14.8 (13) | C35—C36—C37—C38 | −2.4 (9) |
C8—N3—C9—C10 | −166.2 (7) | C34—N8—C38—C37 | 2.2 (8) |
C14—C9—C10—C11 | 0.4 (14) | Ni2—N8—C38—C37 | −172.0 (4) |
N3—C9—C10—C11 | −178.6 (7) | C36—C37—C38—N8 | 1.3 (8) |
D—H···A | D—H | H···A | D···A | D—H···A |
N3—H3N···S2i | 0.86 (4) | 2.77 (4) | 3.605 (4) | 163 (5) |
N7—H7N···S1ii | 0.86 (4) | 2.80 (2) | 3.627 (4) | 161 (5) |
Symmetry codes: (i) x−1, y+1, z; (ii) x+1, y−1, z. |
Experimental details
Crystal data | |
Chemical formula | [Ni(C14H11N3OS)(C5H5N)] |
Mr | 407.13 |
Crystal system, space group | Monoclinic, Pc |
Temperature (K) | 295 |
a, b, c (Å) | 5.7294 (11), 12.924 (3), 23.683 (5) |
β (°) | 95.64 (3) |
V (Å3) | 1745.2 (6) |
Z | 4 |
Radiation type | Mo Kα |
µ (mm−1) | 1.25 |
Crystal size (mm) | 0.35 × 0.24 × 0.17 |
Data collection | |
Diffractometer | Rigaku R-AXIS RAPID |
Absorption correction | Multi-scan (ABSCOR; Higashi, 1995) |
Tmin, Tmax | 0.669, 0.816 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 16815, 7370, 4892 |
Rint | 0.044 |
(sin θ/λ)max (Å−1) | 0.649 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.037, 0.089, 1.06 |
No. of reflections | 7370 |
No. of parameters | 475 |
No. of restraints | 4 |
H-atom treatment | H atoms treated by a mixture of independent and constrained refinement |
Δρmax, Δρmin (e Å−3) | 0.60, −0.57 |
Absolute structure | Flack (1983), with 3366 Friedel pairs |
Absolute structure parameter | 0.029 (17) |
Computer programs: RAPID-AUTO (Rigaku, 1998), RAPID-AUTO, CrystalStructure (Rigaku/MSC, 2002), SHELXS97 (Sheldrick, 1997), SHELXL97 (Sheldrick, 1997), ORTEPII (Johnson, 1976), SHELXL97.
Ni1—N1 | 1.849 (4) | Ni2—N5 | 1.845 (4) |
Ni1—O1 | 1.859 (4) | Ni2—O2 | 1.863 (4) |
Ni1—N4 | 1.909 (4) | Ni2—N8 | 1.911 (4) |
Ni1—S1 | 2.1547 (15) | Ni2—S2 | 2.1507 (15) |
N1—Ni1—O1 | 95.77 (17) | N5—Ni2—O2 | 95.19 (17) |
N1—Ni1—N4 | 177.51 (19) | N5—Ni2—N8 | 178.16 (19) |
O1—Ni1—N4 | 85.93 (17) | O2—Ni2—N8 | 85.50 (17) |
N1—Ni1—S1 | 87.31 (14) | N5—Ni2—S2 | 87.57 (13) |
O1—Ni1—S1 | 175.83 (13) | O2—Ni2—S2 | 176.29 (13) |
N4—Ni1—S1 | 91.08 (13) | N8—Ni2—S2 | 91.81 (14) |
D—H···A | D—H | H···A | D···A | D—H···A |
N3—H3N···S2i | 0.86 (4) | 2.77 (4) | 3.605 (4) | 163 (5) |
N7—H7N···S1ii | 0.86 (4) | 2.80 (2) | 3.627 (4) | 161 (5) |
Symmetry codes: (i) x−1, y+1, z; (ii) x+1, y−1, z. |
Up to now, a number of metal complexes of N-salicyldimine-4-phenylthiosemicarbazide have been synthesized, and most of them are mononuclear (Milanesio et al., 2000; Prabhakaran et al., 2005; Soriano-García et al., 1985; Naik et al., 2003; Thomas et al., 2004). Recently, a dinuclear complex has been reported (Deng et al., 2007). In these complexs, the hydrazone ligand chelates in a terdentate manner. In the title mononuclear complex, [Ni(C14H11N3OS)(C5H5N)], the ligand binds in a similar mode. As shown in Fig. 1, the NiII atom is N,O,S-chelated by deprotonated salicylaldimine-4-phenylthiosemicarbazide dianion. It is also coordinated by pyridine molecule, and a square planar geometry results. The mononuclear units are linked into a chain structure along b axis by N—H···S intermolecular hydrogen bonds and weak π-π stacking interactions between the pyridine rings [centroid···centroid = 3.758 (3) Å] (Fig. 2).