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Acta Crystallogr Sect E Struct Rep Online. 2008 May 1; 64(Pt 5): o898.
Published online 2008 April 23. doi:  10.1107/S1600536808010817
PMCID: PMC2961173

Tris[2-(deuteriomethyl­sulfan­yl)­phen­yl]­phosphine deuteriochloro­form 0.125-solvate

Abstract

The title deuterated tripodal phosphine, C21H12D9PS3·0.125CDCl3, crystallizes as two independent mol­ecules, one of which lies on a general position and the other about a threefold rotation axis, and as a deuteriochloro­form solvate. The solvent mol­ecule is disordered about a site of symmetry 3, so that the ratio of phosphine to solvent is 8:1. The P atom adopts a pyramidal coordination geometry.

Related literature

For the synthesis and crystal structure of tris­[(2-methyl­sulfan­yl)phen­yl]phosphine, see: Meek et al. (1976 [triangle]); Uttecht et al. (2005 [triangle]).

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Object name is e-64-0o898-scheme1.jpg

Experimental

Crystal data

  • C21H12D9PS3·0.125CDCl3
  • M r = 424.63
  • Hexagonal, An external file that holds a picture, illustration, etc.
Object name is e-64-0o898-efi1.jpg
  • a = 23.090 (1) Å
  • c = 25.144 (1) Å
  • V = 11610 (1) Å3
  • Z = 24
  • Mo Kα radiation
  • μ = 0.52 mm−1
  • T = 100 (2) K
  • 0.20 × 0.15 × 0.10 mm

Data collection

  • Bruker SMART APEX diffractometer
  • Absorption correction: multi-scan (SADABS; Sheldrick, 1996 [triangle]) T min = 0.925, T max = 1.000 (expected range = 0.878–0.949)
  • 36814 measured reflections
  • 5929 independent reflections
  • 4200 reflections with I > 2σ(I)
  • R int = 0.089

Refinement

  • R[F 2 > 2σ(F 2)] = 0.062
  • wR(F 2) = 0.194
  • S = 1.18
  • 5929 reflections
  • 329 parameters
  • 12 restraints
  • H-atom parameters constrained
  • Δρmax = 1.14 e Å−3
  • Δρmin = −0.49 e Å−3

Data collection: APEX2 (Bruker, 2007 [triangle]); cell refinement: SAINT (Bruker, 2007 [triangle]); data reduction: SAINT; program(s) used to solve structure: SHELXS97 (Sheldrick, 2008 [triangle]); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 [triangle]); molecular graphics: X-SEED (Barbour, 2001 [triangle]); software used to prepare material for publication: publCIF (Westrip, 2008 [triangle]).

Supplementary Material

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536808010817/tk2251sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536808010817/tk2251Isup2.hkl

Additional supplementary materials: crystallographic information; 3D view; checkCIF report

Acknowledgments

We thank the ScienceFund MOSTI (03-01-03-SF0209) for funding the study, and the University of Malaya for the purchase of the diffractometer.

supplementary crystallographic information

Comment

Tris[(2-methylsulfanyl)phenyl]phosphine is a tripodal ligand that yields a number of adducts with transition metals. The compound crystallizes without any solvent (Uttecht et al., 2005). We intended to synthesize the deuterated title compound to examine their coordination patterns. The present deuteriochloroform solvate (Scheme I, Fig. 1) is isostructural with the reported solvent-free compound, whose crystal structure has been described in detail. The deuterated chloroform molecule is disordered, and appears to occupy a only small portion of the unit cell. Its presence is not sufficient to cause much change in the unit cell volume.

Experimental

The procedure was adapted from a reported procedure (Meek et al., 1976). d3-2-Bromothioanisole (2.50 g, 0.012 mol) was dissolved in dry ether (13 ml) at 273 K. To the solution was added over 2 h 1.6 M n-butyllithium in n-hexane (8 ml). A white precipitate separated after half the n-butyllithium was added. After the full quantity of the reagent was added, stirring was continued for another hour. Phosphorus trichloride (0.56 g, 0.004 mol) in ether (8 ml) was added over 3 h. The mixture was then allowed to warm up to room temperature before being hydrolyzed with 0.2 N hydrochloric acid (8 ml). The white solid was collected and washed with distilled water, ethanol and ether. The compound (1.216 g, 0.003 mol, 70% yield) was recrystallized from deuterated chloroform.

Refinement

Carbon-bound H-atoms were placed in calculated positions (C—H 0.95 to 1.00 Å) and were included in the refinement in the riding model approximation, with U(H) set to 1.2 to 1.5U(C). Scattering factors used for deuterium were those of hydrogen.

The CDCl3 molecule was refined as a complete molecule of 1/8 occupancy about a site of symmetry, 3. The displacement factors of the three chloride atoms were restrained to be identical. The three C–Cl distances were restrained to within 0.01 Å of each other as were the Cl···Cl distances; the anisotropic temperature factors of the carbon atom were restrained to be nearly isotropic.

The final difference Fourier map had a peak 1 Å from P1 but was otherwise featureless.

Figures

Fig. 1.
Thermal ellipsoid plot (Barbour, 2001) of the two independent (CD3S-2-C6H4)3P molecules showing atom labelling; the P2-molecule is located on a threefold axis of symmetry. Displacement ellipsoids are drawn at the 70% probability level. The disordered ...

Crystal data

C21H12D9PS3·0.125CDCl3Z = 24
Mr = 424.63F000 = 5214
Hexagonal, R3Dx = 1.458 Mg m3
Hall symbol: -R 3Mo Kα radiation λ = 0.71073 Å
a = 23.090 (1) ÅCell parameters from 2990 reflections
b = 23.090 Åθ = 2.6–21.9º
c = 25.144 (1) ŵ = 0.52 mm1
α = 90ºT = 100 (2) K
β = 90ºDiamondoid, colorless
γ = 120º0.20 × 0.15 × 0.10 mm
V = 11610 (1) Å3

Data collection

Bruker SMART APEX diffractometer5929 independent reflections
Radiation source: fine-focus sealed tube4200 reflections with I > 2σ(I)
Monochromator: graphiteRint = 0.089
T = 100(2) Kθmax = 27.5º
[var phi] and ω scansθmin = 1.3º
Absorption correction: Multi-scan(SADABS; Sheldrick, 1996)h = −29→29
Tmin = 0.925, Tmax = 1.000k = −29→30
36814 measured reflectionsl = −30→32

Refinement

Refinement on F2Secondary atom site location: difference Fourier map
Least-squares matrix: fullHydrogen site location: inferred from neighbouring sites
R[F2 > 2σ(F2)] = 0.062H-atom parameters constrained
wR(F2) = 0.194  w = 1/[σ2(Fo2) + (0.1P)2] where P = (Fo2 + 2Fc2)/3
S = 1.18(Δ/σ)max = 0.001
5929 reflectionsΔρmax = 1.14 e Å3
329 parametersΔρmin = −0.49 e Å3
12 restraintsExtinction correction: none
Primary atom site location: structure-invariant direct methods

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2)

xyzUiso*/UeqOcc. (<1)
Cl10.3613 (6)0.7404 (8)0.1620 (5)0.0398 (13)0.17
Cl20.2520 (7)0.6046 (7)0.1699 (7)0.0398 (13)0.17
Cl30.3839 (7)0.6288 (7)0.1538 (7)0.0398 (13)0.17
S10.23386 (5)0.27581 (5)0.07002 (4)0.0297 (3)
S20.07625 (5)0.35610 (5)0.07921 (4)0.0307 (3)
S30.22138 (5)0.41664 (5)−0.09462 (4)0.0308 (3)
S40.03527 (5)−0.10870 (5)0.16513 (4)0.0260 (2)
P10.21057 (5)0.38934 (5)0.02920 (4)0.0231 (2)
P20.00000.00000.13345 (6)0.0185 (3)
C10.29317 (18)0.39837 (19)0.02368 (14)0.0241 (8)
C20.34626 (18)0.45189 (19)−0.00033 (15)0.0268 (8)
H20.34150.4884−0.01210.032*
C30.4062 (2)0.4540 (2)−0.00774 (15)0.0302 (9)
H30.44170.4910−0.02550.036*
C40.41479 (19)0.4038 (2)0.01014 (16)0.0304 (9)
H40.45670.40620.00550.036*
C50.36333 (19)0.3492 (2)0.03509 (15)0.0286 (9)
H50.37010.31430.04800.034*
C60.30210 (18)0.34504 (18)0.04128 (14)0.0243 (8)
C70.2637 (2)0.2188 (2)0.07750 (18)0.0359 (10)
H7A0.22670.17490.08800.054*
H7B0.29850.23530.10490.054*
H7C0.28240.21470.04370.054*
C80.20467 (18)0.39982 (18)0.10092 (15)0.0233 (8)
C90.2594 (2)0.4248 (2)0.13414 (16)0.0347 (10)
H90.30290.44250.11940.042*
C100.2520 (2)0.4246 (3)0.18775 (17)0.0403 (11)
H100.29040.43990.20980.048*
C110.1919 (3)0.4032 (2)0.21056 (17)0.0413 (11)
H110.18810.40500.24810.050*
C120.1353 (2)0.3784 (2)0.17813 (16)0.0316 (9)
H120.09220.36190.19340.038*
C130.14268 (19)0.37816 (18)0.12409 (16)0.0257 (8)
C140.0046 (2)0.3277 (2)0.1209 (2)0.0464 (13)
H14A−0.03570.30980.09890.070*
H14B0.00870.36520.14210.070*
H14C0.00150.29260.14470.070*
C150.22337 (17)0.46852 (18)0.00343 (15)0.0243 (8)
C160.22705 (18)0.51897 (19)0.03555 (16)0.0279 (9)
H160.22790.51410.07300.034*
C170.2295 (2)0.5742 (2)0.01652 (17)0.0376 (10)
H170.23040.60670.04020.045*
C180.2308 (2)0.5838 (2)−0.03719 (17)0.0327 (9)
H180.23370.6235−0.05090.039*
C190.22791 (19)0.53560 (19)−0.07160 (17)0.0290 (9)
H190.22900.5422−0.10900.035*
C200.22342 (17)0.47825 (18)−0.05158 (15)0.0241 (8)
C210.1884 (2)0.4301 (2)−0.15450 (15)0.0305 (9)
H21A0.17740.3932−0.17920.046*
H21B0.22190.4723−0.17080.046*
H21C0.14800.4322−0.14640.046*
C220.06906 (16)−0.00245 (17)0.10086 (14)0.0181 (7)
C230.10721 (17)0.04262 (17)0.06167 (14)0.0209 (7)
H230.09510.07390.04910.025*
C240.16278 (17)0.04311 (17)0.04031 (14)0.0202 (7)
H240.18870.07480.01370.024*
C250.17988 (18)−0.00197 (18)0.05765 (14)0.0225 (8)
H250.2178−0.00200.04300.027*
C260.14256 (17)−0.04786 (18)0.09647 (14)0.0223 (8)
H260.1550−0.07920.10810.027*
C270.08693 (17)−0.04882 (17)0.11873 (14)0.0204 (7)
C280.08728 (19)−0.13719 (19)0.19390 (15)0.0273 (8)
H28A0.0631−0.16860.22280.041*
H28B0.1280−0.09890.20800.041*
H28C0.0993−0.15970.16670.041*
C290.3291 (7)0.6581 (8)0.1414 (7)0.032 (5)0.17
H290.32250.65700.10200.038*0.17

Atomic displacement parameters (Å2)

U11U22U33U12U13U23
Cl10.055 (4)0.037 (5)0.028 (5)0.024 (3)0.006 (3)0.003 (2)
Cl20.055 (4)0.037 (5)0.028 (5)0.024 (3)0.006 (3)0.003 (2)
Cl30.055 (4)0.037 (5)0.028 (5)0.024 (3)0.006 (3)0.003 (2)
S10.0303 (5)0.0261 (5)0.0302 (6)0.0122 (4)0.0060 (4)0.0036 (4)
S20.0232 (5)0.0291 (5)0.0390 (6)0.0125 (4)−0.0012 (4)−0.0026 (4)
S30.0447 (6)0.0364 (6)0.0198 (5)0.0268 (5)−0.0003 (4)0.0004 (4)
S40.0226 (5)0.0253 (5)0.0301 (6)0.0121 (4)0.0043 (4)0.0102 (4)
P10.0226 (5)0.0268 (5)0.0186 (5)0.0114 (4)0.0006 (4)0.0006 (4)
P20.0195 (5)0.0195 (5)0.0166 (8)0.0097 (2)0.0000.000
C10.0242 (19)0.031 (2)0.0183 (19)0.0145 (16)0.0002 (14)−0.0035 (15)
C20.026 (2)0.026 (2)0.023 (2)0.0084 (16)−0.0042 (15)−0.0034 (15)
C30.031 (2)0.032 (2)0.025 (2)0.0142 (18)0.0017 (17)−0.0015 (17)
C40.0223 (19)0.034 (2)0.031 (2)0.0114 (17)−0.0014 (16)−0.0081 (17)
C50.030 (2)0.035 (2)0.024 (2)0.0191 (18)0.0000 (16)−0.0044 (16)
C60.028 (2)0.0250 (19)0.0163 (19)0.0112 (16)−0.0056 (15)−0.0038 (15)
C70.036 (2)0.029 (2)0.041 (3)0.0158 (19)−0.0034 (19)0.0022 (18)
C80.0282 (19)0.0280 (19)0.0192 (19)0.0181 (17)0.0027 (15)0.0035 (15)
C90.029 (2)0.055 (3)0.026 (2)0.025 (2)−0.0013 (17)−0.0074 (19)
C100.043 (3)0.078 (3)0.026 (2)0.050 (3)−0.0058 (19)−0.003 (2)
C110.074 (3)0.055 (3)0.018 (2)0.050 (3)0.001 (2)0.0003 (19)
C120.048 (2)0.036 (2)0.022 (2)0.029 (2)0.0137 (18)0.0120 (17)
C130.031 (2)0.0224 (19)0.029 (2)0.0171 (16)0.0040 (16)0.0039 (15)
C140.031 (2)0.035 (2)0.074 (4)0.016 (2)0.019 (2)0.002 (2)
C150.0212 (18)0.0258 (19)0.027 (2)0.0123 (16)−0.0007 (15)−0.0003 (15)
C160.030 (2)0.029 (2)0.020 (2)0.0112 (17)−0.0014 (16)−0.0098 (16)
C170.043 (3)0.033 (2)0.033 (3)0.017 (2)0.000 (2)−0.0094 (19)
C180.034 (2)0.029 (2)0.036 (2)0.0163 (18)−0.0002 (18)0.0026 (18)
C190.030 (2)0.033 (2)0.025 (2)0.0169 (18)0.0003 (16)0.0043 (17)
C200.0192 (18)0.0257 (19)0.027 (2)0.0110 (15)−0.0006 (15)−0.0027 (16)
C210.035 (2)0.038 (2)0.022 (2)0.0209 (19)−0.0017 (17)−0.0005 (17)
C220.0165 (16)0.0204 (17)0.0174 (18)0.0092 (14)−0.0027 (13)−0.0026 (14)
C230.0232 (18)0.0244 (18)0.0173 (19)0.0135 (15)−0.0037 (14)−0.0009 (14)
C240.0208 (17)0.0188 (17)0.0174 (18)0.0072 (14)0.0005 (14)−0.0008 (14)
C250.0216 (18)0.0274 (19)0.0178 (19)0.0117 (15)0.0020 (14)−0.0002 (15)
C260.0232 (18)0.0216 (18)0.023 (2)0.0118 (15)−0.0017 (15)0.0010 (15)
C270.0187 (17)0.0180 (17)0.0198 (19)0.0058 (14)−0.0022 (14)−0.0009 (14)
C280.032 (2)0.031 (2)0.024 (2)0.0200 (18)−0.0015 (16)0.0055 (16)
C290.035 (8)0.027 (9)0.035 (7)0.018 (7)0.004 (10)−0.018 (8)

Geometric parameters (Å, °)

Cl1—C291.737 (9)C10—H100.9500
Cl2—C291.736 (9)C11—C121.398 (6)
Cl3—C291.736 (9)C11—H110.9500
S1—C71.776 (4)C12—C131.370 (5)
S1—C61.744 (4)C12—H120.9500
S2—C141.783 (4)C14—H14A0.9800
S2—C131.762 (4)C14—H14B0.9800
S3—C211.783 (4)C14—H14C0.9800
S3—C201.769 (4)C15—C161.385 (5)
S4—C271.745 (4)C15—C201.401 (5)
S4—C281.786 (4)C16—C171.337 (6)
P1—C11.817 (4)C16—H160.9500
P1—C151.819 (4)C17—C181.367 (6)
P1—C81.834 (4)C17—H170.9500
P2—C22i1.819 (3)C18—C191.385 (6)
P2—C221.819 (3)C18—H180.9500
P2—C22ii1.819 (3)C19—C201.371 (5)
C1—C21.371 (5)C19—H190.9500
C1—C61.417 (5)C21—H21A0.9800
C2—C31.373 (5)C21—H21B0.9800
C2—H20.9500C21—H21C0.9800
C3—C41.346 (6)C22—C231.383 (5)
C3—H30.9500C22—C271.400 (5)
C4—C51.378 (5)C23—C241.386 (5)
C4—H40.9500C23—H230.9500
C5—C61.377 (5)C24—C251.357 (5)
C5—H50.9500C24—H240.9500
C7—H7A0.9800C25—C261.380 (5)
C7—H7B0.9800C25—H250.9500
C7—H7C0.9800C26—C271.391 (5)
C8—C131.387 (5)C26—H260.9500
C8—C91.378 (5)C28—H28A0.9800
C9—C101.358 (6)C28—H28B0.9800
C9—H90.9500C28—H28C0.9800
C10—C111.347 (6)C29—H291.0000
C7—S1—C6102.45 (19)H14A—C14—H14C109.5
C14—S2—C13104.0 (2)H14B—C14—H14C109.5
C21—S3—C20102.65 (18)C16—C15—C20116.5 (3)
C27—S4—C28104.09 (17)C16—C15—P1123.3 (3)
C1—P1—C15102.93 (17)C20—C15—P1120.0 (3)
C1—P1—C8101.70 (16)C17—C16—C15123.3 (4)
C15—P1—C8101.72 (17)C17—C16—H16118.3
C22i—P2—C22101.27 (14)C15—C16—H16118.3
C22i—P2—C22ii101.27 (14)C16—C17—C18119.7 (4)
C22—P2—C22ii101.27 (14)C16—C17—H17120.1
C2—C1—C6117.9 (3)C18—C17—H17120.1
C2—C1—P1123.4 (3)C17—C18—C19119.9 (4)
C6—C1—P1118.5 (3)C17—C18—H18120.1
C3—C2—C1121.5 (4)C19—C18—H18120.1
C3—C2—H2119.2C20—C19—C18119.8 (4)
C1—C2—H2119.2C20—C19—H19120.1
C4—C3—C2120.3 (4)C18—C19—H19120.1
C4—C3—H3119.9C19—C20—C15120.7 (4)
C2—C3—H3119.9C19—C20—S3120.7 (3)
C3—C4—C5120.6 (4)C15—C20—S3118.5 (3)
C3—C4—H4119.7S3—C21—H21A109.5
C5—C4—H4119.7S3—C21—H21B109.5
C4—C5—C6120.0 (4)H21A—C21—H21B109.5
C4—C5—H5120.0S3—C21—H21C109.5
C6—C5—H5120.0H21A—C21—H21C109.5
C5—C6—C1119.7 (4)H21B—C21—H21C109.5
C5—C6—S1122.4 (3)C23—C22—C27118.9 (3)
C1—C6—S1117.9 (3)C23—C22—P2122.4 (3)
S1—C7—H7A109.5C27—C22—P2118.5 (3)
S1—C7—H7B109.5C24—C23—C22121.4 (3)
H7A—C7—H7B109.5C24—C23—H23119.3
S1—C7—H7C109.5C22—C23—H23119.3
H7A—C7—H7C109.5C25—C24—C23119.5 (3)
H7B—C7—H7C109.5C25—C24—H24120.2
C13—C8—C9117.5 (4)C23—C24—H24120.2
C13—C8—P1119.8 (3)C24—C25—C26120.4 (3)
C9—C8—P1122.6 (3)C24—C25—H25119.8
C10—C9—C8120.8 (4)C26—C25—H25119.8
C10—C9—H9119.6C25—C26—C27120.9 (3)
C8—C9—H9119.6C25—C26—H26119.5
C11—C10—C9121.9 (4)C27—C26—H26119.5
C11—C10—H10119.0C26—C27—C22118.8 (3)
C9—C10—H10119.0C26—C27—S4122.8 (3)
C10—C11—C12118.9 (4)C22—C27—S4118.3 (3)
C10—C11—H11120.5S4—C28—H28A109.5
C12—C11—H11120.5S4—C28—H28B109.5
C11—C12—C13119.2 (4)H28A—C28—H28B109.5
C11—C12—H12120.4S4—C28—H28C109.5
C13—C12—H12120.4H28A—C28—H28C109.5
C8—C13—C12121.6 (4)H28B—C28—H28C109.5
C8—C13—S2115.3 (3)Cl1—C29—Cl3112.2 (7)
C12—C13—S2123.0 (3)Cl1—C29—Cl2112.4 (7)
S2—C14—H14A109.5Cl3—C29—Cl2109.7 (7)
S2—C14—H14B109.5Cl1—C29—H29107.5
H14A—C14—H14B109.5Cl3—C29—H29107.5
S2—C14—H14C109.5Cl2—C29—H29107.5
C15—P1—C1—C2−6.0 (4)C1—P1—C15—C16−104.6 (3)
C8—P1—C1—C2−111.1 (3)C8—P1—C15—C160.5 (4)
C15—P1—C1—C6179.1 (3)C1—P1—C15—C2081.7 (3)
C8—P1—C1—C674.0 (3)C8—P1—C15—C20−173.2 (3)
C6—C1—C2—C30.6 (6)C20—C15—C16—C171.0 (6)
P1—C1—C2—C3−174.3 (3)P1—C15—C16—C17−172.9 (3)
C1—C2—C3—C4−2.1 (6)C15—C16—C17—C18−2.3 (6)
C2—C3—C4—C51.3 (6)C16—C17—C18—C191.5 (6)
C3—C4—C5—C60.9 (6)C17—C18—C19—C200.3 (6)
C4—C5—C6—C1−2.4 (6)C18—C19—C20—C15−1.6 (6)
C4—C5—C6—S1177.3 (3)C18—C19—C20—S3−178.7 (3)
C2—C1—C6—C51.6 (5)C16—C15—C20—C190.9 (5)
P1—C1—C6—C5176.7 (3)P1—C15—C20—C19175.0 (3)
C2—C1—C6—S1−178.1 (3)C16—C15—C20—S3178.1 (3)
P1—C1—C6—S1−3.0 (4)P1—C15—C20—S3−7.8 (4)
C7—S1—C6—C5−7.1 (4)C21—S3—C20—C19−25.5 (4)
C7—S1—C6—C1172.6 (3)C21—S3—C20—C15157.3 (3)
C1—P1—C8—C13−161.9 (3)C22i—P2—C22—C23103.4 (2)
C15—P1—C8—C1392.1 (3)C22ii—P2—C22—C23−0.7 (3)
C1—P1—C8—C913.9 (4)C22i—P2—C22—C27−81.1 (4)
C15—P1—C8—C9−92.2 (4)C22ii—P2—C22—C27174.9 (3)
C13—C8—C9—C103.6 (6)C27—C22—C23—C24−0.6 (5)
P1—C8—C9—C10−172.2 (3)P2—C22—C23—C24174.9 (3)
C8—C9—C10—C11−3.3 (7)C22—C23—C24—C250.8 (5)
C9—C10—C11—C122.3 (7)C23—C24—C25—C26−0.3 (5)
C10—C11—C12—C13−1.7 (6)C24—C25—C26—C27−0.2 (5)
C9—C8—C13—C12−3.1 (6)C25—C26—C27—C220.3 (5)
P1—C8—C13—C12172.8 (3)C25—C26—C27—S4176.2 (3)
C9—C8—C13—S2172.8 (3)C23—C22—C27—C260.1 (5)
P1—C8—C13—S2−11.3 (4)P2—C22—C27—C26−175.6 (3)
C11—C12—C13—C82.2 (6)C23—C22—C27—S4−176.0 (3)
C11—C12—C13—S2−173.4 (3)P2—C22—C27—S48.3 (4)
C14—S2—C13—C8177.7 (3)C28—S4—C27—C2623.3 (4)
C14—S2—C13—C12−6.5 (4)C28—S4—C27—C22−160.7 (3)

Symmetry codes: (i) −x+y, −x, z; (ii) −y, xy, z.

Footnotes

Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: TK2251).

References

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  • Westrip, S. P. (2008). publCIF In preparation.

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