Supporting information
Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536807057613/om2174sup1.cif | |
Structure factor file (CIF format) https://doi.org/10.1107/S1600536807057613/om2174Isup2.hkl |
CCDC reference: 672683
Key indicators
- Single-crystal X-ray study
- T = 293 K
- Mean (C-C) = 0.003 Å
- R factor = 0.026
- wR factor = 0.062
- Data-to-parameter ratio = 20.0
checkCIF/PLATON results
No syntax errors found
Alert level C PLAT066_ALERT_1_C Predicted and Reported Transmissions Identical . ? PLAT180_ALERT_3_C Check Cell Rounding: # of Values Ending with 0 = 4 PLAT220_ALERT_2_C Large Non-Solvent C Ueq(max)/Ueq(min) ... 2.78 Ratio PLAT241_ALERT_2_C Check High Ueq as Compared to Neighbors for O1
Alert level G PLAT199_ALERT_1_G Check the Reported _cell_measurement_temperature 293 K PLAT200_ALERT_1_G Check the Reported _diffrn_ambient_temperature . 293 K
0 ALERT level A = In general: serious problem 0 ALERT level B = Potentially serious problem 4 ALERT level C = Check and explain 2 ALERT level G = General alerts; check 3 ALERT type 1 CIF construction/syntax error, inconsistent or missing data 2 ALERT type 2 Indicator that the structure model may be wrong or deficient 1 ALERT type 3 Indicator that the structure quality may be low 0 ALERT type 4 Improvement, methodology, query or suggestion 0 ALERT type 5 Informative message, check
Metal-organic coordination polymers with aromatic N-donor ligands have attracted special attention owing to their interesting structural and chemical properties (Carlucci et al., 2004; Cui et al., 2005; Dobrzańska et al., 2005). Aromatic N-donor ligands with different character are selected for constructing new organotin compounds (Li et al., 2006; Ma et al., 2004). The Sn—N and Sn—Cl distances are in reported ranges (Pettinari et al., 1998).
A mixture of hydroquinone (1.0 g, 10 mmol) and NaOH (0.8 g, 20 mmol) in DMSO (20 ml) was stirred at 60°C for 1 h, then 3-(chloromethyl)pyridine (2.6 g, 20 mmol) was added. The mixture was cooled to room temperature after stirring at 60°C for 24 h, and then poured into 100 ml of water. A colorless solid of 1,4-bis(pyridin-3-ylmethoxy)benzene formed immediately, which was isolated by filtration in 68% yield after drying in air.
A mixture of dibenzyldichlorostannane (37 mg, 0.1 mmol) (obtained from commercial sources) with 1,4-bis(pyridin-3-ylmethoxy)benzene (29 mg, 0.1 mmol) in EtOH and CH2Cl2 (25 ml, v:v = 1:1) was stirred for a few minutes and then filtered. Single crystals suitable for X-ray analysis were obtained by slow evaporation of the filtrate at room temperature for several days (yield: 35%). Analysis calculated for C32H30Cl2N2O2Sn: C 57.86, H 4.55, N 4.22%; found: C 57.82, H 4.59, N 4.19%.
All H atoms on C atoms were positioned geometrically and refined as riding atoms, with C—H = 0.93 Å for aromatic hydrogen atoms and C—H = 0.97 Å for methylene hydrogen atoms, and Uiso=1.2Ueq(C).
Data collection: SMART (Bruker, 1997); cell refinement: SMART (Bruker, 1997); data reduction: SAINT (Bruker, 1999); program(s) used to solve structure: SHELXS97 (Sheldrick, 1997); program(s) used to refine structure: SHELXL97 (Sheldrick, 1997); molecular graphics: SHELXTL-Plus (Sheldrick, 1990); software used to prepare material for publication: SHELXL97 (Sheldrick, 1997).
Fig. 1. A view of the molecule of the title compound. Displacement ellipsoids are drawn at the 30% probability level. Symmetry code: (i) = 1 - x, 1 - y, 1 - z; (ii) = 2 - x, 1 - y, -z. |
[SnCl2(C7H7)2(C18H16N2O2)] | Z = 2 |
Mr = 664.17 | F(000) = 672 |
Monoclinic, P21/c | Dx = 1.451 Mg m−3 |
Hall symbol: -P 2ybc | Mo Kα radiation, λ = 0.71069 Å |
a = 7.2380 (5) Å | θ = 2.0–28.5° |
b = 14.3560 (9) Å | µ = 1.05 mm−1 |
c = 14.6290 (9) Å | T = 293 K |
β = 90.098 (1)° | Block, colorless |
V = 1520.08 (17) Å3 | 0.38 × 0.33 × 0.28 mm |
Bruker APEX CCD area-detector diffractometer | 3558 independent reflections |
Radiation source: fine-focus sealed tube | 3144 reflections with I > 2σ(I) |
Graphite monochromator | Rint = 0.032 |
ω scans | θmax = 28.5°, θmin = 2.0° |
Absorption correction: multi-scan (SADABS; Sheldrick, 1996) | h = −5→9 |
Tmin = 0.678, Tmax = 0.746 | k = −18→18 |
9019 measured reflections | l = −18→16 |
Refinement on F2 | Primary atom site location: structure-invariant direct methods |
Least-squares matrix: full | Secondary atom site location: difference Fourier map |
R[F2 > 2σ(F2)] = 0.026 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.062 | H-atom parameters constrained |
S = 1.06 | w = 1/[σ2(Fo2) + (0.025P)2 + 0.426P] where P = (Fo2 + 2Fc2)/3 |
3558 reflections | (Δ/σ)max < 0.001 |
178 parameters | Δρmax = 0.31 e Å−3 |
0 restraints | Δρmin = −0.80 e Å−3 |
[SnCl2(C7H7)2(C18H16N2O2)] | V = 1520.08 (17) Å3 |
Mr = 664.17 | Z = 2 |
Monoclinic, P21/c | Mo Kα radiation |
a = 7.2380 (5) Å | µ = 1.05 mm−1 |
b = 14.3560 (9) Å | T = 293 K |
c = 14.6290 (9) Å | 0.38 × 0.33 × 0.28 mm |
β = 90.098 (1)° |
Bruker APEX CCD area-detector diffractometer | 3558 independent reflections |
Absorption correction: multi-scan (SADABS; Sheldrick, 1996) | 3144 reflections with I > 2σ(I) |
Tmin = 0.678, Tmax = 0.746 | Rint = 0.032 |
9019 measured reflections |
R[F2 > 2σ(F2)] = 0.026 | 0 restraints |
wR(F2) = 0.062 | H-atom parameters constrained |
S = 1.06 | Δρmax = 0.31 e Å−3 |
3558 reflections | Δρmin = −0.80 e Å−3 |
178 parameters |
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. |
x | y | z | Uiso*/Ueq | ||
Sn1 | 0.5000 | 0.5000 | 0.5000 | 0.03137 (6) | |
Cl1 | 0.20749 (7) | 0.43159 (4) | 0.57024 (3) | 0.05319 (13) | |
C1 | 0.8020 (3) | 0.29921 (14) | 0.38280 (14) | 0.0532 (5) | |
H1 | 0.9066 | 0.3322 | 0.4006 | 0.064* | |
C2 | 0.8068 (5) | 0.24379 (18) | 0.30446 (18) | 0.0773 (9) | |
H2 | 0.9140 | 0.2404 | 0.2697 | 0.093* | |
C3 | 0.6534 (6) | 0.19451 (18) | 0.27899 (18) | 0.0898 (11) | |
H3 | 0.6568 | 0.1576 | 0.2268 | 0.108* | |
C4 | 0.4961 (5) | 0.19903 (18) | 0.3293 (2) | 0.0842 (9) | |
H4 | 0.3929 | 0.1650 | 0.3113 | 0.101* | |
C5 | 0.4881 (4) | 0.25374 (15) | 0.40689 (17) | 0.0596 (6) | |
H5 | 0.3798 | 0.2562 | 0.4409 | 0.072* | |
C6 | 0.6417 (3) | 0.30517 (12) | 0.43423 (12) | 0.0415 (4) | |
C7 | 0.6336 (3) | 0.36578 (13) | 0.51685 (13) | 0.0450 (4) | |
H7A | 0.7589 | 0.3765 | 0.5380 | 0.054* | |
H7B | 0.5694 | 0.3320 | 0.5646 | 0.054* | |
C8 | 0.5061 (2) | 0.45295 (11) | 0.28016 (10) | 0.0322 (3) | |
H8 | 0.6321 | 0.4607 | 0.2901 | 0.039* | |
C9 | 0.4468 (2) | 0.42783 (12) | 0.19347 (11) | 0.0346 (3) | |
C10 | 0.2592 (3) | 0.41791 (16) | 0.17951 (13) | 0.0507 (5) | |
H10 | 0.2141 | 0.4004 | 0.1225 | 0.061* | |
C11 | 0.1393 (3) | 0.43422 (18) | 0.25106 (13) | 0.0556 (6) | |
H11 | 0.0124 | 0.4293 | 0.2423 | 0.067* | |
C12 | 0.2089 (2) | 0.45780 (15) | 0.33514 (12) | 0.0429 (4) | |
H12 | 0.1274 | 0.4680 | 0.3832 | 0.051* | |
C13 | 0.5846 (3) | 0.41269 (13) | 0.11814 (12) | 0.0410 (4) | |
H13A | 0.6507 | 0.3547 | 0.1276 | 0.049* | |
H13B | 0.5223 | 0.4098 | 0.0595 | 0.049* | |
C14 | 0.8871 (3) | 0.42179 (13) | −0.00519 (12) | 0.0436 (4) | |
H14 | 0.8118 | 0.3695 | −0.0092 | 0.052* | |
C15 | 0.8503 (3) | 0.49061 (12) | 0.05819 (13) | 0.0396 (4) | |
C16 | 0.9622 (3) | 0.56830 (14) | 0.06280 (13) | 0.0460 (4) | |
H16 | 0.9362 | 0.6147 | 0.1052 | 0.055* | |
O1 | 0.7078 (2) | 0.48820 (10) | 0.12015 (12) | 0.0590 (5) | |
N1 | 0.39040 (19) | 0.46651 (11) | 0.35020 (9) | 0.0328 (3) |
U11 | U22 | U33 | U12 | U13 | U23 | |
Sn1 | 0.02965 (9) | 0.03914 (10) | 0.02533 (9) | 0.00382 (6) | 0.00442 (6) | −0.00170 (5) |
Cl1 | 0.0395 (2) | 0.0754 (3) | 0.0447 (3) | −0.0091 (2) | 0.00994 (19) | −0.0005 (2) |
C1 | 0.0660 (13) | 0.0428 (10) | 0.0509 (12) | 0.0122 (9) | 0.0140 (10) | 0.0053 (9) |
C2 | 0.125 (2) | 0.0526 (13) | 0.0544 (14) | 0.0342 (15) | 0.0313 (15) | 0.0074 (11) |
C3 | 0.180 (4) | 0.0434 (13) | 0.0463 (14) | 0.0161 (17) | −0.0108 (18) | −0.0093 (10) |
C4 | 0.129 (3) | 0.0485 (14) | 0.0748 (18) | −0.0162 (15) | −0.0235 (18) | −0.0062 (12) |
C5 | 0.0737 (15) | 0.0441 (11) | 0.0610 (13) | −0.0067 (10) | −0.0047 (11) | 0.0067 (9) |
C6 | 0.0542 (11) | 0.0330 (8) | 0.0373 (9) | 0.0084 (8) | 0.0019 (8) | 0.0047 (7) |
C7 | 0.0515 (11) | 0.0466 (10) | 0.0368 (9) | 0.0134 (8) | −0.0011 (8) | 0.0007 (8) |
C8 | 0.0274 (7) | 0.0404 (9) | 0.0290 (8) | −0.0003 (6) | 0.0033 (6) | 0.0018 (6) |
C9 | 0.0352 (8) | 0.0431 (9) | 0.0255 (7) | −0.0043 (7) | 0.0064 (6) | 0.0024 (6) |
C10 | 0.0404 (10) | 0.0822 (15) | 0.0296 (9) | −0.0124 (10) | −0.0009 (7) | −0.0004 (9) |
C11 | 0.0296 (9) | 0.1006 (18) | 0.0367 (10) | −0.0086 (10) | 0.0001 (7) | 0.0035 (10) |
C12 | 0.0300 (8) | 0.0652 (12) | 0.0334 (9) | 0.0003 (8) | 0.0067 (7) | 0.0024 (8) |
C13 | 0.0430 (9) | 0.0498 (10) | 0.0303 (8) | −0.0100 (8) | 0.0094 (7) | −0.0059 (7) |
C14 | 0.0444 (10) | 0.0481 (10) | 0.0383 (9) | −0.0156 (8) | 0.0119 (7) | −0.0131 (8) |
C15 | 0.0380 (9) | 0.0495 (10) | 0.0313 (9) | −0.0067 (7) | 0.0113 (7) | −0.0080 (7) |
C16 | 0.0466 (10) | 0.0505 (10) | 0.0410 (10) | −0.0130 (8) | 0.0171 (8) | −0.0188 (8) |
O1 | 0.0566 (9) | 0.0633 (9) | 0.0572 (10) | −0.0258 (7) | 0.0344 (8) | −0.0252 (7) |
N1 | 0.0302 (7) | 0.0419 (7) | 0.0263 (7) | 0.0009 (6) | 0.0031 (5) | 0.0013 (6) |
Sn1—C7 | 2.1696 (18) | C8—H8 | 0.9300 |
Sn1—N1 | 2.3784 (14) | C9—C10 | 1.380 (2) |
Sn1—Cl1 | 2.5515 (5) | C9—C13 | 1.504 (2) |
C1—C6 | 1.387 (3) | C10—C11 | 1.381 (3) |
C1—C2 | 1.396 (3) | C10—H10 | 0.9300 |
C1—H1 | 0.9300 | C11—C12 | 1.371 (3) |
C2—C3 | 1.368 (5) | C11—H11 | 0.9300 |
C2—H2 | 0.9300 | C12—N1 | 1.338 (2) |
C3—C4 | 1.358 (5) | C12—H12 | 0.9300 |
C3—H3 | 0.9300 | C13—O1 | 1.404 (2) |
C4—C5 | 1.382 (4) | C13—H13A | 0.9700 |
C4—H4 | 0.9300 | C13—H13B | 0.9700 |
C5—C6 | 1.393 (3) | C14—C15 | 1.381 (2) |
C5—H5 | 0.9300 | C14—C16i | 1.387 (2) |
C6—C7 | 1.491 (3) | C14—H14 | 0.9300 |
C7—H7A | 0.9700 | C15—O1 | 1.375 (2) |
C7—H7B | 0.9700 | C15—C16 | 1.380 (3) |
C8—N1 | 1.339 (2) | C16—C14i | 1.387 (2) |
C8—C9 | 1.386 (2) | C16—H16 | 0.9300 |
C7—Sn1—N1 | 94.19 (6) | C10—C9—C13 | 122.04 (15) |
C7—Sn1—Cl1 | 88.98 (6) | C8—C9—C13 | 120.23 (15) |
N1—Sn1—Cl1 | 91.01 (4) | C9—C10—C11 | 119.34 (17) |
C6—C1—C2 | 120.2 (2) | C9—C10—H10 | 120.3 |
C6—C1—H1 | 119.9 | C11—C10—H10 | 120.3 |
C2—C1—H1 | 119.9 | C12—C11—C10 | 119.43 (17) |
C3—C2—C1 | 119.8 (3) | C12—C11—H11 | 120.3 |
C3—C2—H2 | 120.1 | C10—C11—H11 | 120.3 |
C1—C2—H2 | 120.1 | N1—C12—C11 | 122.02 (16) |
C4—C3—C2 | 120.6 (2) | N1—C12—H12 | 119.0 |
C4—C3—H3 | 119.7 | C11—C12—H12 | 119.0 |
C2—C3—H3 | 119.7 | O1—C13—C9 | 107.17 (14) |
C3—C4—C5 | 120.6 (3) | O1—C13—H13A | 110.3 |
C3—C4—H4 | 119.7 | C9—C13—H13A | 110.3 |
C5—C4—H4 | 119.7 | O1—C13—H13B | 110.3 |
C4—C5—C6 | 120.2 (3) | C9—C13—H13B | 110.3 |
C4—C5—H5 | 119.9 | H13A—C13—H13B | 108.5 |
C6—C5—H5 | 119.9 | C15—C14—C16i | 119.17 (17) |
C1—C6—C5 | 118.7 (2) | C15—C14—H14 | 120.4 |
C1—C6—C7 | 120.68 (19) | C16i—C14—H14 | 120.4 |
C5—C6—C7 | 120.66 (19) | O1—C15—C16 | 115.42 (15) |
C6—C7—Sn1 | 116.39 (12) | O1—C15—C14 | 124.78 (16) |
C6—C7—H7A | 108.2 | C16—C15—C14 | 119.80 (17) |
Sn1—C7—H7A | 108.2 | C15—C16—C14i | 121.03 (16) |
C6—C7—H7B | 108.2 | C15—C16—H16 | 119.5 |
Sn1—C7—H7B | 108.2 | C14i—C16—H16 | 119.5 |
H7A—C7—H7B | 107.3 | C15—O1—C13 | 118.87 (14) |
N1—C8—C9 | 123.04 (15) | C12—N1—C8 | 118.41 (14) |
N1—C8—H8 | 118.5 | C12—N1—Sn1 | 119.77 (11) |
C9—C8—H8 | 118.5 | C8—N1—Sn1 | 121.78 (11) |
C10—C9—C8 | 117.73 (15) | ||
C6—C1—C2—C3 | −0.7 (3) | C8—C9—C13—O1 | −46.9 (2) |
C1—C2—C3—C4 | 0.0 (4) | C16i—C14—C15—O1 | −178.7 (2) |
C2—C3—C4—C5 | 0.2 (4) | C16i—C14—C15—C16 | 0.6 (3) |
C3—C4—C5—C6 | 0.2 (4) | O1—C15—C16—C14i | 178.7 (2) |
C2—C1—C6—C5 | 1.1 (3) | C14—C15—C16—C14i | −0.6 (4) |
C2—C1—C6—C7 | −178.63 (18) | C16—C15—O1—C13 | 178.23 (19) |
C4—C5—C6—C1 | −0.8 (3) | C14—C15—O1—C13 | −2.5 (3) |
C4—C5—C6—C7 | 178.9 (2) | C9—C13—O1—C15 | 179.19 (18) |
C1—C6—C7—Sn1 | 100.43 (18) | C11—C12—N1—C8 | 1.0 (3) |
C5—C6—C7—Sn1 | −79.3 (2) | C11—C12—N1—Sn1 | −176.86 (17) |
N1ii—Sn1—C7—C6 | −171.71 (16) | C9—C8—N1—C12 | −1.8 (3) |
N1—Sn1—C7—C6 | 8.29 (16) | C9—C8—N1—Sn1 | 175.98 (13) |
Cl1ii—Sn1—C7—C6 | −80.77 (15) | C7—Sn1—N1—C12 | 112.89 (15) |
Cl1—Sn1—C7—C6 | 99.23 (15) | C7ii—Sn1—N1—C12 | −67.11 (15) |
N1—C8—C9—C10 | 0.9 (3) | Cl1ii—Sn1—N1—C12 | −156.17 (14) |
N1—C8—C9—C13 | −179.33 (16) | Cl1—Sn1—N1—C12 | 23.83 (14) |
C8—C9—C10—C11 | 0.8 (3) | C7—Sn1—N1—C8 | −64.88 (14) |
C13—C9—C10—C11 | −179.0 (2) | C7ii—Sn1—N1—C8 | 115.12 (14) |
C9—C10—C11—C12 | −1.5 (4) | Cl1ii—Sn1—N1—C8 | 26.06 (13) |
C10—C11—C12—N1 | 0.7 (4) | Cl1—Sn1—N1—C8 | −153.94 (13) |
C10—C9—C13—O1 | 132.9 (2) |
Symmetry codes: (i) −x+2, −y+1, −z; (ii) −x+1, −y+1, −z+1. |
Experimental details
Crystal data | |
Chemical formula | [SnCl2(C7H7)2(C18H16N2O2)] |
Mr | 664.17 |
Crystal system, space group | Monoclinic, P21/c |
Temperature (K) | 293 |
a, b, c (Å) | 7.2380 (5), 14.3560 (9), 14.6290 (9) |
β (°) | 90.098 (1) |
V (Å3) | 1520.08 (17) |
Z | 2 |
Radiation type | Mo Kα |
µ (mm−1) | 1.05 |
Crystal size (mm) | 0.38 × 0.33 × 0.28 |
Data collection | |
Diffractometer | Bruker APEX CCD area-detector diffractometer |
Absorption correction | Multi-scan (SADABS; Sheldrick, 1996) |
Tmin, Tmax | 0.678, 0.746 |
No. of measured, independent and observed [I > 2σ(I)] reflections | 9019, 3558, 3144 |
Rint | 0.032 |
(sin θ/λ)max (Å−1) | 0.670 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.026, 0.062, 1.06 |
No. of reflections | 3558 |
No. of parameters | 178 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.31, −0.80 |
Computer programs: SMART (Bruker, 1997), SAINT (Bruker, 1999), SHELXS97 (Sheldrick, 1997), SHELXL97 (Sheldrick, 1997), SHELXTL-Plus (Sheldrick, 1990).
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In recent years, metal-organic coordination polymers with aromatic N-donor ligands have attracted special attention owing to their interesting structural and chemical properties (Carlucci et al., 2004; Cui et al., 2005; Dobrzańska et al., 2005). Aromatic N-donor ligands with different character are selected for constructing new compounds with organotin (Li et al., 2006; Ma et al., 2004). In this case, 1,4-bis(pyridin-3-ylmethoxy)benzene and dibenzyldichlorostannane were selected to construct complexes with a polymeric structure.
In the title compound, {(C7H7)2SnCl2(C18H16O2N2)}n , the asymmetric unit contains one Sn(IV) atom located on a center of inversion. As shown in Figure 1, the Sn has a distorted octahedral coordination geometry that consists of two benzyl groups,two Cl- ions and two nitrogen atoms from different 1,4-bis(pyridin-3-ylmethoxy)benzene ligands. All the distances of Sn—N and Sn—Cl are in the reported ranges (Pettinari et al., 1998). In addition, the dihedral angle of the phenyl ring and pyridine ring is 49.5 (4)°. Each dibenzyldichlorostannane is linked by the neutral 1,4-bis(pyridin-3-ylmethoxy)benzene ligands to generate an infinite coordination polymeric chain, and all chains are parallel in the structure.