metal-organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

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ISSN: 2056-9890

[N′-(3-Meth­­oxy-2-oxido­benzyl­­idene)nicotinohydrazidato]di­phenyl­tin(IV)

aDepartment of Chemistry and Chemical Engineering, Jining University, Shandong 273155, People's Republic of China
*Correspondence e-mail: zhongjungao@sina.com

(Received 1 August 2009; accepted 20 August 2009; online 26 August 2009)

The asymmetric unit of the title compound, [Sn(C6H5)2(C14H11N3O3)], contains two crystallographically independent mol­ecules that differ predominantly in the torsion of the phenyl rings. In both mol­ecules, the SnIV ion is in a distored trigonal-bipyramidal geometry. The Sn—O distances are in the range 2.055 (2)–2.143 (2) Å.

Related literature

For covalent radii see: Sanderson (1967[Sanderson, R. T. (1967). Inorganic Chemistry, p. 74. New York: Reinhold.]). For a related structure see: Yearwood et al. (2002[Yearwood, B., Parkin, C. H. & Atwood, D. A. (2002). Inorg. Chim. Acta, 333, 124-131.]).

[Scheme 1]

Experimental

Crystal data
  • [Sn(C6H5)2(C14H11N3O3)]

  • Mr = 542.15

  • Monoclinic, P 21

  • a = 8.9653 (14) Å

  • b = 20.771 (3) Å

  • c = 12.903 (2) Å

  • β = 106.015 (2)°

  • V = 2309.5 (6) Å3

  • Z = 4

  • Mo Kα radiation

  • μ = 1.14 mm−1

  • T = 298 K

  • 0.49 × 0.45 × 0.34 mm

Data collection
  • Bruker SMART CCD area-detector diffractometer

  • Absorption correction: multi-scan (SADABS; Sheldrick, 1996[Sheldrick, G. M. (1996). SADABS. University of Göttingen, Germany.]) Tmin = 0.605, Tmax = 0.698

  • 9743 measured reflections

  • 7970 independent reflections

  • 7720 reflections with I > 2σ(I)

  • Rint = 0.019

Refinement
  • R[F2 > 2σ(F2)] = 0.024

  • wR(F2) = 0.057

  • S = 1.02

  • 7970 reflections

  • 597 parameters

  • 1 restraint

  • H-atom parameters constrained

  • Δρmax = 0.26 e Å−3

  • Δρmin = −0.49 e Å−3

  • Absolute structure: Flack (1983[Flack, H. D. (1983). Acta Cryst. A39, 876-881.]), 3753 Friedel pairs

  • Flack parameter: 0.0342

Table 1
Selected geometric parameters (Å, °)

C15—Sn1 2.115 (3)
C21—Sn1 2.115 (3)
C41—Sn2 2.111 (3)
C47—Sn2 2.110 (3)
N1—Sn1 2.159 (3)
N4—Sn2 2.143 (3)
O1—Sn1 2.055 (2)
O3—Sn1 2.129 (2)
O4—Sn2 2.143 (2)
O5—Sn2 2.059 (2)
O1—Sn1—C21 97.12 (12)
O1—Sn1—C15 94.22 (12)
C21—Sn1—C15 117.09 (12)
O1—Sn1—O3 156.71 (9)
C21—Sn1—O3 96.90 (11)
C15—Sn1—O3 95.83 (12)
O1—Sn1—N1 83.12 (11)
C21—Sn1—N1 121.10 (11)
C15—Sn1—N1 121.65 (12)
O3—Sn1—N1 73.72 (11)
O5—Sn2—C47 100.04 (12)
O5—Sn2—C41 95.16 (12)
C47—Sn2—C41 117.07 (13)
O5—Sn2—O4 155.61 (9)
C47—Sn2—O4 95.87 (11)
C41—Sn2—O4 93.89 (12)
O5—Sn2—N4 83.65 (11)
C47—Sn2—N4 112.89 (12)
C41—Sn2—N4 129.37 (12)
O4—Sn2—N4 73.13 (11)

Data collection: SMART (Siemens, 1996[Siemens (1996). SMART and SAINT. Siemens Analytical X-ray Instruments Inc., Madison, Wisconsin, USA.]); cell refinement: SAINT (Siemens, 1996[Siemens (1996). SMART and SAINT. Siemens Analytical X-ray Instruments Inc., Madison, Wisconsin, USA.]); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); molecular graphics: SHELXTL (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]); software used to prepare material for publication: SHELXTL.

Supporting information


Comment top

The structure determination was undertaken as a part of a project on the synthesis and structural characterization of Schiff base complexes. In the crystal structure of the title compound two crystallographically independent molecules are found. Differences are found predominantly in the torsion of the phenyl rings. The Sn1 atoms are five-coordinated by two O atoms, two C atoms and one N atom in a disorted trigonal-bipyramidal coodination (Table 1). The Schiff base is coordinated to the Sn1 atom as a tridentate ligand via the azomethine N atom, the hydroxyl O atom and the carbonyl O atom. The Sn1—N1 distances are close to the sum of the covalent radii of 2.15 Å (Sanderson, 1967), indicating a strong Sn—N interaction. Very similar structural parameters were observed in the compound studied by Yearwood et al. (2002).

Related literature top

For covalent radii see: Sanderson (1967). For a related structure see: Yearwood et al. (2002).

Experimental top

A mixture of diphenyltin oxide (0.5778 g, 2.0 mmol) and 3-Methoxy-2-oxideobenzaldehyde(3-pyridyl)methyl-hydrazone (0.5420 g, 2.0 mmol) in methanol (60 ml) was heated under reflux for 6 h. The obtained clear solution was evaporated under vacuum. The product was crystallized from a mixture of dichloromethane/ethanol (1:1) to yield blocks of (I). Yield 0.8347 g, 77%, m.p. 476 K, analysis, calculated for C26H21N3O3Sn: C 57.60, H, 3.90; N 7.75%; found: C 57.66, H 3.93, N, 7.71%.

Refinement top

H atoms were positioned with idelaized geometry with C-H = 0.93 Å for aromatic H atoms and 0.96 Å for methyl H atoms and were constrained to ride on their parent atoms with Uiso(H) = 1.2Ueq(C) or 1.5Ueq(for methyl groups). The absolute structure was determined on the basis of 3753 Friedel pairs.

Computing details top

Data collection: SMART (Siemens, 1996); cell refinement: SAINT (Siemens, 1996); data reduction: SAINT (Siemens, 1996); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXTL (Sheldrick, 2008).

Figures top
[Figure 1] Fig. 1. The molecular structure of the title complex with labeling and 30% displacement ellipsoids (H atoms omitted for clarity).
[N'-(3-Methoxy-2-oxidobenzylidene)nicotinohydrazidato]diphenyltin(IV) top
Crystal data top
[Sn(C6H5)2(C14H11N3O3)]F(000) = 1088
Mr = 542.15Dx = 1.559 Mg m3
Monoclinic, P21Mo Kα radiation, λ = 0.71073 Å
Hall symbol: P 2ybCell parameters from 9021 reflections
a = 8.9653 (14) Åθ = 2.4–28.1°
b = 20.771 (3) ŵ = 1.14 mm1
c = 12.903 (2) ÅT = 298 K
β = 106.015 (2)°Block, yellow
V = 2309.5 (6) Å30.49 × 0.45 × 0.34 mm
Z = 4
Data collection top
Bruker SMART CCD area-detector
diffractometer
7970 independent reflections
Radiation source: fine-focus sealed tube7720 reflections with I > 2σ(I)
Graphite monochromatorRint = 0.019
ϕ and ω scansθmax = 25.0°, θmin = 1.9°
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)
h = 1010
Tmin = 0.605, Tmax = 0.698k = 2423
9743 measured reflectionsl = 159
Refinement top
Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.024H-atom parameters constrained
wR(F2) = 0.057 w = 1/[σ2(Fo2) + (0.0304P)2]
where P = (Fo2 + 2Fc2)/3
S = 1.02(Δ/σ)max = 0.001
7970 reflectionsΔρmax = 0.26 e Å3
597 parametersΔρmin = 0.49 e Å3
1 restraintAbsolute structure: Flack (1983), 3753 Friedel pairs
Primary atom site location: structure-invariant direct methodsAbsolute structure parameter: 0.0342
Crystal data top
[Sn(C6H5)2(C14H11N3O3)]V = 2309.5 (6) Å3
Mr = 542.15Z = 4
Monoclinic, P21Mo Kα radiation
a = 8.9653 (14) ŵ = 1.14 mm1
b = 20.771 (3) ÅT = 298 K
c = 12.903 (2) Å0.49 × 0.45 × 0.34 mm
β = 106.015 (2)°
Data collection top
Bruker SMART CCD area-detector
diffractometer
7970 independent reflections
Absorption correction: multi-scan
(SADABS; Sheldrick, 1996)
7720 reflections with I > 2σ(I)
Tmin = 0.605, Tmax = 0.698Rint = 0.019
9743 measured reflections
Refinement top
R[F2 > 2σ(F2)] = 0.024H-atom parameters constrained
wR(F2) = 0.057Δρmax = 0.26 e Å3
S = 1.02Δρmin = 0.49 e Å3
7970 reflectionsAbsolute structure: Flack (1983), 3753 Friedel pairs
597 parametersAbsolute structure parameter: 0.0342
1 restraint
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*/Ueq
C10.8744 (5)0.6897 (3)0.3633 (3)0.0776 (13)
H10.91240.67240.41740.093*
C20.8341 (5)0.6481 (2)0.2940 (3)0.0701 (11)
H20.84510.60380.30000.084*
C30.7773 (5)0.67369 (19)0.2162 (3)0.0616 (10)
H30.74830.64640.16800.074*
C40.7615 (4)0.73871 (18)0.2066 (3)0.0464 (8)
C50.8047 (5)0.7776 (2)0.2807 (3)0.0636 (9)
H50.79280.82190.27650.076*
C60.7003 (3)0.76720 (19)0.1211 (2)0.0439 (7)
C70.6190 (4)0.9109 (2)0.0230 (3)0.0493 (8)
H70.64550.93690.07390.059*
C80.5591 (4)0.94252 (17)0.0557 (3)0.0450 (7)
C90.5271 (5)1.00873 (19)0.0427 (3)0.0617 (10)
H90.55051.03060.01370.074*
C100.4628 (5)1.04139 (19)0.1105 (3)0.0663 (11)
H100.44331.08530.10080.080*
C110.4258 (4)1.00908 (19)0.1950 (3)0.0562 (9)
H110.37981.03150.24050.067*
C120.4566 (4)0.94435 (17)0.2120 (3)0.0451 (8)
C130.5281 (3)0.9105 (2)0.1433 (2)0.0423 (7)
C140.3611 (6)0.9384 (2)0.3658 (3)0.0778 (14)
H14A0.42950.97130.40400.117*
H14B0.34450.90700.41610.117*
H14C0.26360.95720.32780.117*
C150.7839 (4)0.73385 (18)0.1970 (3)0.0467 (8)
C160.8784 (4)0.7704 (3)0.2785 (3)0.0642 (10)
H160.86720.81500.27830.077*
C170.9909 (5)0.7405 (3)0.3613 (3)0.0903 (17)
H171.05560.76500.41580.108*
C181.0053 (6)0.6746 (4)0.3617 (4)0.0964 (19)
H181.07990.65470.41700.116*
C190.9121 (5)0.6382 (3)0.2823 (4)0.0799 (13)
H190.92180.59360.28380.096*
C200.8033 (4)0.6679 (2)0.1997 (3)0.0619 (10)
H200.74150.64290.14460.074*
C210.3786 (4)0.73152 (16)0.0491 (2)0.0431 (7)
C220.2814 (4)0.75321 (18)0.1083 (3)0.0557 (9)
H220.31080.78790.15500.067*
C230.1402 (5)0.7230 (2)0.0975 (4)0.0725 (12)
H230.07530.73720.13800.087*
C240.0961 (5)0.6727 (2)0.0281 (4)0.0723 (12)
H240.00050.65300.02050.087*
C250.1911 (5)0.6512 (2)0.0301 (3)0.0703 (11)
H250.16050.61690.07750.084*
C260.3332 (4)0.68023 (18)0.0189 (3)0.0525 (8)
H260.39880.66480.05790.063*
C270.0013 (5)0.9828 (3)1.1151 (4)0.0785 (14)
H270.03410.99801.17190.094*
C280.0037 (5)0.9185 (3)1.1010 (3)0.0764 (11)
H280.02800.89071.14740.092*
C290.0535 (5)0.8947 (2)1.0178 (3)0.0643 (11)
H290.05530.85061.00610.077*
C300.1012 (4)0.93724 (18)0.9516 (3)0.0499 (8)
C310.0949 (5)1.0015 (2)0.9724 (3)0.0693 (11)
H310.12681.03020.92740.083*
C320.1608 (4)0.9145 (2)0.8613 (2)0.0474 (7)
C330.2466 (4)0.7762 (2)0.7514 (2)0.0496 (8)
H330.21180.74880.79680.060*
C340.3089 (4)0.74560 (17)0.6728 (3)0.0457 (8)
C350.3156 (5)0.67813 (19)0.6717 (3)0.0589 (9)
H350.27720.65470.72020.071*
C360.3774 (5)0.64637 (19)0.6007 (3)0.0630 (10)
H360.38090.60160.60080.076*
C370.4350 (5)0.68106 (19)0.5283 (3)0.0565 (9)
H370.47770.65940.48020.068*
C380.4295 (4)0.74709 (17)0.5272 (3)0.0478 (8)
C390.3666 (4)0.78110 (17)0.6002 (2)0.0443 (7)
C400.5481 (6)0.7553 (2)0.3835 (3)0.0762 (13)
H40A0.63480.72930.42070.114*
H40B0.58230.78750.34180.114*
H40C0.47110.72860.33640.114*
C410.4735 (4)0.97590 (17)0.6996 (3)0.0476 (8)
C420.4710 (5)1.03547 (19)0.7470 (3)0.0603 (10)
H420.38371.04770.76780.072*
C430.5954 (6)1.0772 (2)0.7640 (4)0.0797 (13)
H430.59161.11720.79550.096*
C440.7229 (6)1.0592 (3)0.7345 (5)0.0973 (17)
H440.80711.08700.74620.117*
C450.7294 (6)1.0005 (3)0.6876 (5)0.0980 (17)
H450.81820.98860.66840.118*
C460.6038 (5)0.9588 (2)0.6685 (3)0.0699 (11)
H460.60730.91940.63500.084*
C470.0803 (4)0.94225 (17)0.5471 (3)0.0460 (7)
C480.0773 (5)1.0006 (2)0.4981 (3)0.0672 (11)
H480.16311.02760.51970.081*
C490.0503 (6)1.0207 (3)0.4169 (4)0.0865 (15)
H490.05151.06120.38590.104*
C500.1721 (5)0.9809 (3)0.3834 (4)0.0833 (14)
H500.25680.99370.32750.100*
C510.1740 (5)0.9226 (3)0.4294 (4)0.0919 (15)
H510.25970.89580.40580.110*
C520.0482 (5)0.9032 (2)0.5116 (4)0.0753 (13)
H520.04990.86320.54360.090*
N10.6398 (3)0.84948 (14)0.0300 (2)0.0438 (6)
N20.6926 (4)0.82985 (15)0.1167 (2)0.0502 (7)
N30.1728 (4)0.85239 (16)0.8523 (2)0.0571 (8)
N40.2328 (3)0.83689 (15)0.7669 (2)0.0473 (7)
N50.8630 (5)0.7541 (2)0.3585 (3)0.0853 (13)
N60.0461 (5)1.0262 (2)1.0533 (3)0.0824 (11)
O10.5663 (3)0.84980 (12)0.16702 (17)0.0551 (6)
O20.4289 (3)0.90798 (15)0.29086 (18)0.0591 (7)
O30.6595 (3)0.72733 (11)0.05616 (18)0.0519 (6)
O40.1992 (3)0.95651 (12)0.8002 (2)0.0596 (7)
O50.3664 (3)0.84455 (12)0.5949 (2)0.0608 (7)
O60.4834 (3)0.78554 (13)0.4596 (2)0.0646 (7)
Sn10.60021 (2)0.773826 (10)0.074059 (15)0.03996 (6)
Sn20.27721 (3)0.915473 (10)0.672005 (17)0.04469 (7)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
C10.085 (3)0.100 (4)0.061 (2)0.023 (3)0.042 (2)0.005 (2)
C20.094 (3)0.064 (3)0.064 (2)0.010 (2)0.043 (2)0.008 (2)
C30.082 (3)0.056 (2)0.057 (2)0.008 (2)0.039 (2)0.0040 (17)
C40.0432 (17)0.060 (2)0.0395 (17)0.0020 (16)0.0167 (14)0.0014 (15)
C50.082 (2)0.061 (2)0.059 (2)0.009 (2)0.0384 (18)0.009 (2)
C60.0449 (16)0.055 (2)0.0354 (15)0.0008 (17)0.0168 (12)0.0034 (16)
C70.061 (2)0.047 (2)0.0442 (17)0.0035 (19)0.0220 (14)0.0087 (17)
C80.0499 (18)0.0440 (19)0.0437 (17)0.0006 (15)0.0172 (14)0.0031 (14)
C90.079 (3)0.051 (2)0.066 (2)0.008 (2)0.038 (2)0.0156 (17)
C100.088 (3)0.042 (2)0.080 (3)0.010 (2)0.041 (2)0.0101 (18)
C110.062 (2)0.053 (2)0.059 (2)0.0109 (18)0.0256 (18)0.0009 (17)
C120.0495 (19)0.0454 (19)0.0402 (17)0.0005 (15)0.0120 (14)0.0025 (14)
C130.0419 (16)0.0421 (19)0.0403 (16)0.0008 (16)0.0071 (12)0.0020 (17)
C140.115 (4)0.075 (3)0.059 (2)0.025 (3)0.050 (2)0.006 (2)
C150.0395 (17)0.062 (2)0.0421 (17)0.0066 (15)0.0179 (13)0.0091 (16)
C160.056 (2)0.084 (3)0.053 (2)0.003 (2)0.0153 (16)0.009 (2)
C170.058 (3)0.159 (6)0.049 (2)0.005 (3)0.007 (2)0.018 (3)
C180.068 (3)0.152 (6)0.072 (3)0.044 (4)0.022 (3)0.035 (4)
C190.067 (3)0.091 (3)0.086 (3)0.027 (3)0.027 (2)0.032 (3)
C200.050 (2)0.069 (3)0.072 (2)0.0092 (18)0.0244 (18)0.019 (2)
C210.0407 (16)0.0498 (19)0.0387 (16)0.0030 (14)0.0107 (13)0.0099 (14)
C220.0511 (19)0.060 (2)0.062 (2)0.0048 (16)0.0253 (17)0.0002 (16)
C230.056 (2)0.084 (3)0.087 (3)0.008 (2)0.036 (2)0.008 (3)
C240.050 (2)0.087 (3)0.082 (3)0.013 (2)0.022 (2)0.012 (3)
C250.073 (3)0.074 (3)0.062 (2)0.025 (2)0.015 (2)0.004 (2)
C260.060 (2)0.057 (2)0.0459 (18)0.0020 (17)0.0219 (16)0.0008 (16)
C270.070 (3)0.110 (4)0.062 (3)0.025 (3)0.030 (2)0.009 (3)
C280.079 (3)0.099 (4)0.062 (2)0.003 (3)0.037 (2)0.003 (3)
C290.073 (3)0.067 (3)0.062 (2)0.004 (2)0.034 (2)0.0059 (19)
C300.0490 (19)0.060 (2)0.0419 (18)0.0080 (16)0.0142 (15)0.0009 (15)
C310.085 (3)0.065 (3)0.067 (3)0.012 (2)0.038 (2)0.005 (2)
C320.0539 (18)0.0483 (19)0.0430 (16)0.0005 (19)0.0186 (14)0.0032 (18)
C330.064 (2)0.0441 (19)0.0452 (17)0.005 (2)0.0219 (14)0.0073 (18)
C340.0499 (18)0.0388 (18)0.0484 (19)0.0013 (15)0.0135 (15)0.0012 (13)
C350.076 (3)0.047 (2)0.060 (2)0.0009 (18)0.0286 (19)0.0061 (17)
C360.080 (3)0.039 (2)0.075 (3)0.0052 (19)0.029 (2)0.0006 (18)
C370.067 (2)0.050 (2)0.054 (2)0.0110 (18)0.0191 (18)0.0052 (17)
C380.051 (2)0.0458 (19)0.0454 (19)0.0032 (15)0.0121 (15)0.0017 (14)
C390.0524 (18)0.0377 (18)0.0407 (16)0.0022 (16)0.0093 (13)0.0019 (15)
C400.108 (4)0.076 (3)0.057 (2)0.017 (3)0.043 (2)0.001 (2)
C410.055 (2)0.0483 (19)0.0407 (17)0.0021 (15)0.0143 (14)0.0044 (14)
C420.067 (2)0.053 (2)0.068 (2)0.0056 (19)0.030 (2)0.0070 (18)
C430.097 (3)0.071 (3)0.075 (3)0.028 (3)0.031 (3)0.013 (2)
C440.088 (4)0.104 (4)0.110 (4)0.045 (3)0.045 (3)0.031 (3)
C450.068 (3)0.121 (5)0.119 (4)0.021 (3)0.049 (3)0.032 (4)
C460.067 (3)0.072 (3)0.076 (3)0.001 (2)0.029 (2)0.012 (2)
C470.0522 (19)0.0438 (18)0.0445 (17)0.0013 (15)0.0177 (14)0.0047 (14)
C480.062 (2)0.061 (2)0.070 (3)0.007 (2)0.0053 (19)0.017 (2)
C490.079 (3)0.078 (3)0.088 (3)0.004 (3)0.002 (3)0.027 (3)
C500.067 (3)0.083 (4)0.085 (3)0.012 (3)0.005 (2)0.018 (3)
C510.068 (3)0.077 (3)0.115 (4)0.017 (3)0.001 (3)0.039 (3)
C520.066 (3)0.055 (3)0.100 (3)0.014 (2)0.016 (2)0.014 (2)
N10.0552 (17)0.0433 (17)0.0377 (14)0.0021 (13)0.0209 (12)0.0029 (12)
N20.0674 (19)0.0473 (19)0.0445 (16)0.0007 (15)0.0301 (14)0.0017 (13)
N30.074 (2)0.054 (2)0.0528 (18)0.0053 (16)0.0345 (16)0.0043 (15)
N40.0607 (18)0.0429 (18)0.0456 (17)0.0028 (14)0.0268 (13)0.0037 (13)
N50.104 (3)0.100 (3)0.075 (2)0.021 (2)0.063 (2)0.013 (2)
N60.104 (3)0.077 (3)0.078 (2)0.022 (2)0.045 (2)0.008 (2)
O10.0940 (19)0.0379 (13)0.0410 (12)0.0060 (13)0.0315 (12)0.0007 (11)
O20.0863 (17)0.0531 (16)0.0475 (12)0.0106 (15)0.0347 (12)0.0042 (12)
O30.0746 (16)0.0436 (13)0.0481 (14)0.0028 (12)0.0350 (12)0.0007 (11)
O40.0888 (19)0.0440 (14)0.0577 (15)0.0000 (13)0.0397 (14)0.0001 (12)
O50.099 (2)0.0379 (14)0.0622 (16)0.0050 (13)0.0495 (14)0.0031 (12)
O60.0962 (19)0.0523 (17)0.0597 (15)0.0075 (14)0.0455 (14)0.0014 (12)
Sn10.04690 (12)0.04038 (12)0.03702 (11)0.00066 (11)0.01897 (8)0.00278 (10)
Sn20.05794 (14)0.03805 (12)0.04156 (12)0.00031 (11)0.01956 (10)0.00249 (10)
Geometric parameters (Å, º) top
C1—N51.345 (6)C28—H280.9300
C1—C21.361 (6)C29—C301.377 (5)
C1—H10.9300C29—H290.9300
C2—C31.354 (5)C30—C311.367 (5)
C2—H20.9300C30—C321.487 (5)
C3—C41.367 (5)C31—N61.340 (5)
C3—H30.9300C31—H310.9300
C4—C51.386 (5)C32—O41.285 (4)
C4—C61.485 (4)C32—N31.302 (5)
C5—N51.345 (5)C33—N41.288 (6)
C5—H50.9300C33—C341.434 (5)
C6—O31.300 (4)C33—H330.9300
C6—N21.305 (5)C34—C391.399 (5)
C7—N11.296 (5)C34—C351.403 (5)
C7—C81.432 (5)C35—C361.365 (5)
C7—H70.9300C35—H350.9300
C8—C131.404 (5)C36—C371.387 (5)
C8—C91.405 (5)C36—H360.9300
C9—C101.355 (5)C37—C381.372 (5)
C9—H90.9300C37—H370.9300
C10—C111.396 (5)C38—O61.366 (4)
C10—H100.9300C38—C391.413 (5)
C11—C121.378 (5)C39—O51.320 (4)
C11—H110.9300C40—O61.417 (4)
C12—O21.344 (4)C40—H40A0.9600
C12—C131.416 (5)C40—H40B0.9600
C13—O11.321 (5)C40—H40C0.9600
C14—O21.424 (4)C41—C461.382 (5)
C14—H14A0.9600C41—C421.383 (5)
C14—H14B0.9600C41—Sn22.111 (3)
C14—H14C0.9600C42—C431.381 (6)
C15—C201.381 (6)C42—H420.9300
C15—C161.383 (5)C43—C441.354 (7)
C15—Sn12.115 (3)C43—H430.9300
C16—C171.396 (7)C44—C451.370 (8)
C16—H160.9300C44—H440.9300
C17—C181.374 (8)C45—C461.388 (7)
C17—H170.9300C45—H450.9300
C18—C191.359 (8)C46—H460.9300
C18—H180.9300C47—C481.364 (5)
C19—C201.375 (6)C47—C521.380 (5)
C19—H190.9300C47—Sn22.110 (3)
C20—H200.9300C48—C491.386 (6)
C21—C261.369 (5)C48—H480.9300
C21—C221.382 (5)C49—C501.342 (7)
C21—Sn12.115 (3)C49—H490.9300
C22—C231.385 (6)C50—C511.351 (8)
C22—H220.9300C50—H500.9300
C23—C241.363 (7)C51—C521.379 (7)
C23—H230.9300C51—H510.9300
C24—C251.357 (6)C52—H520.9300
C24—H240.9300N1—N21.390 (4)
C25—C261.381 (5)N1—Sn12.159 (3)
C25—H250.9300N3—N41.390 (4)
C26—H260.9300N4—Sn22.143 (3)
C27—N61.337 (6)O1—Sn12.055 (2)
C27—C281.350 (8)O3—Sn12.129 (2)
C27—H270.9300O4—Sn22.143 (2)
C28—C291.364 (6)O5—Sn22.059 (2)
N5—C1—C2124.3 (4)N4—C33—C34128.1 (3)
N5—C1—H1117.8N4—C33—H33116.0
C2—C1—H1117.8C34—C33—H33116.0
C3—C2—C1117.4 (4)C39—C34—C35119.7 (3)
C3—C2—H2121.3C39—C34—C33121.9 (3)
C1—C2—H2121.3C35—C34—C33118.4 (3)
C2—C3—C4121.6 (4)C36—C35—C34121.0 (4)
C2—C3—H3119.2C36—C35—H35119.5
C4—C3—H3119.2C34—C35—H35119.5
C3—C4—C5117.3 (3)C35—C36—C37119.8 (4)
C3—C4—C6122.0 (3)C35—C36—H36120.1
C5—C4—C6120.7 (4)C37—C36—H36120.1
N5—C5—C4122.9 (5)C38—C37—C36120.5 (4)
N5—C5—H5118.6C38—C37—H37119.8
C4—C5—H5118.6C36—C37—H37119.8
O3—C6—N2125.4 (3)O6—C38—C37125.0 (3)
O3—C6—C4116.9 (3)O6—C38—C39114.2 (3)
N2—C6—C4117.7 (3)C37—C38—C39120.8 (3)
N1—C7—C8126.1 (3)O5—C39—C34124.4 (3)
N1—C7—H7116.9O5—C39—C38117.4 (3)
C8—C7—H7116.9C34—C39—C38118.2 (3)
C13—C8—C9118.7 (3)O6—C40—H40A109.5
C13—C8—C7123.4 (4)O6—C40—H40B109.5
C9—C8—C7117.9 (3)H40A—C40—H40B109.5
C10—C9—C8121.5 (3)O6—C40—H40C109.5
C10—C9—H9119.3H40A—C40—H40C109.5
C8—C9—H9119.3H40B—C40—H40C109.5
C9—C10—C11119.9 (4)C46—C41—C42118.5 (4)
C9—C10—H10120.0C46—C41—Sn2122.0 (3)
C11—C10—H10120.0C42—C41—Sn2119.5 (3)
C12—C11—C10120.9 (3)C43—C42—C41121.4 (4)
C12—C11—H11119.6C43—C42—H42119.3
C10—C11—H11119.6C41—C42—H42119.3
O2—C12—C11126.7 (3)C44—C43—C42119.3 (5)
O2—C12—C13113.9 (3)C44—C43—H43120.3
C11—C12—C13119.3 (3)C42—C43—H43120.3
O1—C13—C8122.8 (3)C43—C44—C45120.8 (5)
O1—C13—C12117.5 (3)C43—C44—H44119.6
C8—C13—C12119.6 (4)C45—C44—H44119.6
O2—C14—H14A109.5C44—C45—C46120.2 (5)
O2—C14—H14B109.5C44—C45—H45119.9
H14A—C14—H14B109.5C46—C45—H45119.9
O2—C14—H14C109.5C41—C46—C45119.8 (4)
H14A—C14—H14C109.5C41—C46—H46120.1
H14B—C14—H14C109.5C45—C46—H46120.1
C20—C15—C16118.7 (4)C48—C47—C52117.5 (4)
C20—C15—Sn1118.4 (3)C48—C47—Sn2119.6 (3)
C16—C15—Sn1122.8 (3)C52—C47—Sn2123.0 (3)
C15—C16—C17119.9 (5)C47—C48—C49121.7 (4)
C15—C16—H16120.0C47—C48—H48119.2
C17—C16—H16120.0C49—C48—H48119.2
C18—C17—C16119.6 (5)C50—C49—C48119.1 (5)
C18—C17—H17120.2C50—C49—H49120.4
C16—C17—H17120.2C48—C49—H49120.4
C19—C18—C17120.9 (5)C49—C50—C51121.2 (4)
C19—C18—H18119.6C49—C50—H50119.4
C17—C18—H18119.6C51—C50—H50119.4
C18—C19—C20119.5 (5)C50—C51—C52119.6 (4)
C18—C19—H19120.3C50—C51—H51120.2
C20—C19—H19120.3C52—C51—H51120.2
C19—C20—C15121.5 (5)C51—C52—C47120.9 (5)
C19—C20—H20119.3C51—C52—H52119.5
C15—C20—H20119.3C47—C52—H52119.5
C26—C21—C22119.1 (3)C7—N1—N2115.6 (3)
C26—C21—Sn1121.4 (2)C7—N1—Sn1128.4 (2)
C22—C21—Sn1119.3 (3)N2—N1—Sn1115.9 (2)
C21—C22—C23119.7 (4)C6—N2—N1111.2 (3)
C21—C22—H22120.2C32—N3—N4111.1 (3)
C23—C22—H22120.2C33—N4—N3115.1 (3)
C24—C23—C22120.3 (4)C33—N4—Sn2128.0 (2)
C24—C23—H23119.8N3—N4—Sn2116.7 (2)
C22—C23—H23119.8C1—N5—C5116.5 (4)
C25—C24—C23120.2 (4)C27—N6—C31115.0 (4)
C25—C24—H24119.9C13—O1—Sn1131.97 (19)
C23—C24—H24119.9C12—O2—C14117.9 (3)
C24—C25—C26120.0 (4)C6—O3—Sn1113.3 (2)
C24—C25—H25120.0C32—O4—Sn2113.7 (2)
C26—C25—H25120.0C39—O5—Sn2133.2 (2)
C21—C26—C25120.6 (4)C38—O6—C40117.9 (3)
C21—C26—H26119.7O1—Sn1—C2197.12 (12)
C25—C26—H26119.7O1—Sn1—C1594.22 (12)
N6—C27—C28124.7 (4)C21—Sn1—C15117.09 (12)
N6—C27—H27117.7O1—Sn1—O3156.71 (9)
C28—C27—H27117.7C21—Sn1—O396.90 (11)
C27—C28—C29119.0 (5)C15—Sn1—O395.83 (12)
C27—C28—H28120.5O1—Sn1—N183.12 (11)
C29—C28—H28120.5C21—Sn1—N1121.10 (11)
C28—C29—C30118.8 (4)C15—Sn1—N1121.65 (12)
C28—C29—H29120.6O3—Sn1—N173.72 (11)
C30—C29—H29120.6O5—Sn2—C47100.04 (12)
C31—C30—C29117.9 (4)O5—Sn2—C4195.16 (12)
C31—C30—C32120.6 (4)C47—Sn2—C41117.07 (13)
C29—C30—C32121.5 (4)O5—Sn2—O4155.61 (9)
N6—C31—C30124.5 (4)C47—Sn2—O495.87 (11)
N6—C31—H31117.7C41—Sn2—O493.89 (12)
C30—C31—H31117.7O5—Sn2—N483.65 (11)
O4—C32—N3125.2 (3)C47—Sn2—N4112.89 (12)
O4—C32—C30118.6 (4)C41—Sn2—N4129.37 (12)
N3—C32—C30116.2 (3)O4—Sn2—N473.13 (11)
N5—C1—C2—C30.7 (8)C7—N1—N2—C6175.9 (3)
C1—C2—C3—C40.3 (7)Sn1—N1—N2—C63.4 (4)
C2—C3—C4—C50.6 (6)O4—C32—N3—N40.2 (5)
C2—C3—C4—C6179.6 (4)C30—C32—N3—N4178.6 (3)
C3—C4—C5—N51.3 (6)C34—C33—N4—N3177.8 (3)
C6—C4—C5—N5178.9 (4)C34—C33—N4—Sn26.4 (5)
C3—C4—C6—O31.1 (5)C32—N3—N4—C33179.1 (3)
C5—C4—C6—O3178.6 (3)C32—N3—N4—Sn22.8 (4)
C3—C4—C6—N2178.5 (4)C2—C1—N5—C51.4 (8)
C5—C4—C6—N21.8 (5)C4—C5—N5—C11.7 (7)
N1—C7—C8—C136.3 (6)C28—C27—N6—C310.4 (7)
N1—C7—C8—C9172.4 (4)C30—C31—N6—C270.2 (7)
C13—C8—C9—C102.1 (6)C8—C13—O1—Sn125.6 (5)
C7—C8—C9—C10176.6 (4)C12—C13—O1—Sn1156.2 (2)
C8—C9—C10—C110.5 (7)C11—C12—O2—C140.1 (6)
C9—C10—C11—C121.3 (6)C13—C12—O2—C14178.3 (3)
C10—C11—C12—O2179.0 (4)N2—C6—O3—Sn16.7 (4)
C10—C11—C12—C130.6 (6)C4—C6—O3—Sn1172.9 (2)
C9—C8—C13—O1174.2 (3)N3—C32—O4—Sn23.0 (4)
C7—C8—C13—O17.2 (5)C30—C32—O4—Sn2178.6 (2)
C9—C8—C13—C124.0 (5)C34—C39—O5—Sn25.2 (5)
C7—C8—C13—C12174.6 (3)C38—C39—O5—Sn2174.8 (2)
O2—C12—C13—O13.6 (4)C37—C38—O6—C401.0 (6)
C11—C12—C13—O1175.0 (3)C39—C38—O6—C40179.9 (3)
O2—C12—C13—C8178.1 (3)C13—O1—Sn1—C2198.2 (3)
C11—C12—C13—C83.3 (5)C13—O1—Sn1—C15143.8 (3)
C20—C15—C16—C170.1 (5)C13—O1—Sn1—O328.4 (5)
Sn1—C15—C16—C17175.7 (3)C13—O1—Sn1—N122.4 (3)
C15—C16—C17—C180.8 (7)C26—C21—Sn1—O1173.8 (3)
C16—C17—C18—C190.3 (8)C22—C21—Sn1—O110.7 (3)
C17—C18—C19—C200.9 (8)C26—C21—Sn1—C1587.7 (3)
C18—C19—C20—C151.6 (7)C22—C21—Sn1—C1587.8 (3)
C16—C15—C20—C191.1 (6)C26—C21—Sn1—O312.5 (3)
Sn1—C15—C20—C19174.7 (3)C22—C21—Sn1—O3172.0 (3)
C26—C21—C22—C230.2 (5)C26—C21—Sn1—N187.6 (3)
Sn1—C21—C22—C23175.8 (3)C22—C21—Sn1—N196.9 (3)
C21—C22—C23—C240.9 (6)C20—C15—Sn1—O1148.8 (3)
C22—C23—C24—C250.9 (7)C16—C15—Sn1—O126.8 (3)
C23—C24—C25—C260.1 (7)C20—C15—Sn1—C2148.6 (3)
C22—C21—C26—C251.3 (5)C16—C15—Sn1—C21127.0 (3)
Sn1—C21—C26—C25176.8 (3)C20—C15—Sn1—O352.3 (3)
C24—C25—C26—C211.2 (6)C16—C15—Sn1—O3132.1 (3)
N6—C27—C28—C290.7 (8)C20—C15—Sn1—N1126.7 (3)
C27—C28—C29—C300.7 (7)C16—C15—Sn1—N157.7 (3)
C28—C29—C30—C310.5 (6)C6—O3—Sn1—O10.4 (4)
C28—C29—C30—C32178.3 (4)C6—O3—Sn1—C21126.2 (2)
C29—C30—C31—N60.2 (7)C6—O3—Sn1—C15115.5 (2)
C32—C30—C31—N6178.5 (4)C6—O3—Sn1—N15.8 (2)
C31—C30—C32—O43.3 (5)C7—N1—Sn1—O18.3 (3)
C29—C30—C32—O4178.0 (3)N2—N1—Sn1—O1172.5 (2)
C31—C30—C32—N3175.3 (4)C7—N1—Sn1—C2185.9 (3)
C29—C30—C32—N33.5 (5)N2—N1—Sn1—C2193.3 (3)
N4—C33—C34—C390.6 (6)C7—N1—Sn1—C1599.0 (3)
N4—C33—C34—C35178.7 (4)N2—N1—Sn1—C1581.8 (3)
C39—C34—C35—C360.1 (6)C7—N1—Sn1—O3174.1 (3)
C33—C34—C35—C36178.3 (4)N2—N1—Sn1—O35.0 (2)
C34—C35—C36—C370.1 (6)C39—O5—Sn2—C47103.9 (3)
C35—C36—C37—C380.4 (6)C39—O5—Sn2—C41137.4 (3)
C36—C37—C38—O6179.8 (3)C39—O5—Sn2—O426.1 (5)
C36—C37—C38—C390.6 (6)C39—O5—Sn2—N48.3 (3)
C35—C34—C39—O5179.7 (3)C48—C47—Sn2—O5109.5 (3)
C33—C34—C39—O51.6 (5)C52—C47—Sn2—O570.5 (3)
C35—C34—C39—C380.3 (5)C48—C47—Sn2—C418.4 (4)
C33—C34—C39—C38178.4 (3)C52—C47—Sn2—C41171.6 (3)
O6—C38—C39—O50.2 (4)C48—C47—Sn2—O489.0 (3)
C37—C38—C39—O5179.4 (3)C52—C47—Sn2—O491.0 (3)
O6—C38—C39—C34179.8 (3)C48—C47—Sn2—N4163.2 (3)
C37—C38—C39—C340.6 (5)C52—C47—Sn2—N416.8 (3)
C46—C41—C42—C430.5 (6)C46—C41—Sn2—O51.4 (3)
Sn2—C41—C42—C43178.4 (3)C42—C41—Sn2—O5176.4 (3)
C41—C42—C43—C440.5 (7)C46—C41—Sn2—C47105.4 (3)
C42—C43—C44—C450.3 (9)C42—C41—Sn2—C4772.4 (3)
C43—C44—C45—C460.7 (10)C46—C41—Sn2—O4155.9 (3)
C42—C41—C46—C451.5 (6)C42—C41—Sn2—O426.2 (3)
Sn2—C41—C46—C45179.4 (4)C46—C41—Sn2—N484.6 (3)
C44—C45—C46—C411.7 (9)C42—C41—Sn2—N497.5 (3)
C52—C47—C48—C491.0 (7)C32—O4—Sn2—O521.6 (4)
Sn2—C47—C48—C49179.0 (4)C32—O4—Sn2—C47109.0 (3)
C47—C48—C49—C502.0 (8)C32—O4—Sn2—C41133.2 (2)
C48—C49—C50—C511.8 (9)C32—O4—Sn2—N43.2 (2)
C49—C50—C51—C520.6 (8)C33—N4—Sn2—O58.6 (3)
C50—C51—C52—C470.5 (8)N3—N4—Sn2—O5175.7 (3)
C48—C47—C52—C510.3 (7)C33—N4—Sn2—C4789.7 (3)
Sn2—C47—C52—C51179.7 (3)N3—N4—Sn2—C4786.1 (3)
C8—C7—N1—N2177.0 (3)C33—N4—Sn2—C41100.1 (3)
C8—C7—N1—Sn12.1 (5)N3—N4—Sn2—C4184.2 (3)
O3—C6—N2—N12.2 (5)C33—N4—Sn2—O4179.0 (3)
C4—C6—N2—N1177.4 (3)N3—N4—Sn2—O43.2 (2)

Experimental details

Crystal data
Chemical formula[Sn(C6H5)2(C14H11N3O3)]
Mr542.15
Crystal system, space groupMonoclinic, P21
Temperature (K)298
a, b, c (Å)8.9653 (14), 20.771 (3), 12.903 (2)
β (°) 106.015 (2)
V3)2309.5 (6)
Z4
Radiation typeMo Kα
µ (mm1)1.14
Crystal size (mm)0.49 × 0.45 × 0.34
Data collection
DiffractometerBruker SMART CCD area-detector
diffractometer
Absorption correctionMulti-scan
(SADABS; Sheldrick, 1996)
Tmin, Tmax0.605, 0.698
No. of measured, independent and
observed [I > 2σ(I)] reflections
9743, 7970, 7720
Rint0.019
(sin θ/λ)max1)0.596
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.024, 0.057, 1.02
No. of reflections7970
No. of parameters597
No. of restraints1
H-atom treatmentH-atom parameters constrained
Δρmax, Δρmin (e Å3)0.26, 0.49
Absolute structureFlack (1983), 3753 Friedel pairs
Absolute structure parameter0.0342

Computer programs: SMART (Siemens, 1996), SAINT (Siemens, 1996), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), SHELXTL (Sheldrick, 2008).

Selected geometric parameters (Å, º) top
C15—Sn12.115 (3)N4—Sn22.143 (3)
C21—Sn12.115 (3)O1—Sn12.055 (2)
C41—Sn22.111 (3)O3—Sn12.129 (2)
C47—Sn22.110 (3)O4—Sn22.143 (2)
N1—Sn12.159 (3)O5—Sn22.059 (2)
O1—Sn1—C2197.12 (12)O5—Sn2—C47100.04 (12)
O1—Sn1—C1594.22 (12)O5—Sn2—C4195.16 (12)
C21—Sn1—C15117.09 (12)C47—Sn2—C41117.07 (13)
O1—Sn1—O3156.71 (9)O5—Sn2—O4155.61 (9)
C21—Sn1—O396.90 (11)C47—Sn2—O495.87 (11)
C15—Sn1—O395.83 (12)C41—Sn2—O493.89 (12)
O1—Sn1—N183.12 (11)O5—Sn2—N483.65 (11)
C21—Sn1—N1121.10 (11)C47—Sn2—N4112.89 (12)
C15—Sn1—N1121.65 (12)C41—Sn2—N4129.37 (12)
O3—Sn1—N173.72 (11)O4—Sn2—N473.13 (11)
 

Acknowledgements

We acknowledge financial support by the Jining University Science Foundation and the State Key Laboratory of Crystal Materials, Shandong University.

References

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