3,4′,5-Trichloro­biphenyl-4-yl 2,2,2-trichloro­ethyl sulfate

Lehmler, H.-J.; He, X.; Duffel, M.W.; Parkin, S.

doi:10.1107/S1600536813007976

3,4',5-Trichlorobiphenyl-4-yl 2,2,2-trichloroethyl sulfate

H.-J. Lehmler, X. He, M. W. Duffel and S. Parkin

Crystals of the title compound, C₁₄H₈Cl₆O₄S, are twinned by inversion, with unequal components [0.85 (3):0.15 (3)]. The asymmetric unit contains two independent molecules that are related by a pseudo-inversion center. The C_ar-O [1.393 (9) and 1.397 (9) Å] and ester S-O bond lengths [1.600 (5) and 1.590 (5) Å] of both molecules are comparable to the structurally related 2,3,5,5-trichlorobiphenyl-4-yl 2,2,2-trichloroethyl sulfate. The dihedral angles between the benzene rings in the two molecules are 37.8 (2) and 35.0 (2)°.

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Supporting information

	Crystallographic Information File (CIF) https://doi.org/10.1107/S1600536813007976/yk2088sup1.cif Contains datablocks I, global
	Structure factor file (CIF format) https://doi.org/10.1107/S1600536813007976/yk2088Isup2.hkl Contains datablock I
	Chemical Markup Language (CML) file https://doi.org/10.1107/S1600536813007976/yk2088Isup3.cml Supplementary material

CCDC reference: 935710

checkCIF report

Key indicators

Single-crystal X-ray study
T = 90 K
Mean (C-C) = 0.011 Å
R factor = 0.064
wR factor = 0.161
Data-to-parameter ratio = 22.0

checkCIF/PLATON results

No syntax errors found



Alert level B
PLAT340_ALERT_3_B Low Bond Precision on  C-C Bonds ...............     0.0111 Ang
PLAT934_ALERT_3_B Number of (Iobs-Icalc)/SigmaW .gt. 10 Outliers .          1

Alert level C
PLAT911_ALERT_3_C Missing # FCF Refl Between THmin & STh/L=  0.600         14

Alert level G
PLAT005_ALERT_5_G No _iucr_refine_instructions_details  in the CIF          ?
PLAT083_ALERT_2_G SHELXL Second Parameter in WGHT Unusually Large.      21.37
PLAT434_ALERT_2_G Short Inter HL..HL Contact  Cl2B   ..  Cl3A    .       3.38 Ang.
PLAT720_ALERT_4_G Number of Unusual/Non-Standard Labels ..........         24
PLAT912_ALERT_4_G Missing # of FCF Reflections Above STh/L=  0.600         44

   0 ALERT level A = Most likely a serious problem - resolve or explain
   2 ALERT level B = A potentially serious problem, consider carefully
   1 ALERT level C = Check. Ensure it is not caused by an omission or oversight
   5 ALERT level G = General information/check it is not something unexpected

   0 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
   3 ALERT type 3 Indicator that the structure quality may be low
   2 ALERT type 4 Improvement, methodology, query or suggestion
   1 ALERT type 5 Informative message, check

Comment top

Sulfuric acid monoesters of hydroxylated polychlorinated biphenyls (OHPCBs) are emerging as an important class of metabolites of polychlorinated biphenyls (PCBs). Two recent in vivo studies report the formation of PCB sulfates by rats (Dhakal et al., 2012) and poplar plants (Zhai et al., 2013). In vitro studies demonstrate that PCB sulfates are both substrates and inhibitors of mammalian cytosolic sulfotransferases (Liu et al., 2006; Wang et al., 2006; Liu et al., 2009). Only limited structural information about sulfate mono- and diesters of hydroxylated PCBs is available to support structure-activity or structure-property relationship studies. Here we report the structure of the title compound, a biphenyl-4-yl 2,2,2-trichloroethyl sulfate with two chlorine substituents ortho to the sulfate group, to contribute to the number of available crystal structures.

The two independent molecules of the title compound in the asymmetric unit are related by a pseudo-inversion center. The length of the C_aromatic—O bonds of the two molecules are 1.393 (9) and 1.397 (9) Å, respectively. These bond lengths are comparable to the C_aromatic—O bond length (1.405 Å) reported for the structurally related 2',3,5,5'-trichloro-biphenyl-4-yl 2,2,2-trichloroethyl sulfate (Li et al., 2010b). In contrast, biphenyl-4-yl 2,2,2-trichloroethyl sulfates without electronegative chlorine substituents ortho to the sulfate group have slightly longer C_aromatic—O bond length ranging from 1.426 to 1.449 Å (Li et al., 2008; Li et al., 2010b; Li et al., 2010a; Li et al., 2010c).

The lengths of the PCB sulfate ester bond of the title compound (i.e., S1—O1) are 1.600 (5) and 1.590 (5) Å. In contrast, biphenyl-4-yl 2,2,2-trichloroethyl sulfates without chlorine substituents ortho to the sulfate group typically have shorter sulfate ester bond lengths ranging from 1.563 to 1.586 Å (Li et al., 2008; Li et al., 2010b; Li et al., 2010a; Li et al., 2010c). Similar to aromatic sulfate monoesters (Brandao et al., 2005; Denehy et al., 2006), this difference suggests that chlorine substituents ortho to the sulfate group decrease the stability of the S—O ester bond.

The dihedral angle of the biphenyl moiety of PCB derivatives is a structural parameter associated with the affinity of PCB derivatives for cellular target molecules. The two molecules of the title compound have solid state dihedral angles of 37.8 (2)° and 35.0 (2)°. Similarly, structurally related biphenyl-4-yl 2,2,2-trichloroethyl sulfates have dihedral angles ranging from 4.9° to 41.8° in the solid state (Li et al., 2008; Li et al., 2010a; Li et al., 2010c). The fact that biphenyl-4-yl 2,2,2-trichloroethyl sulfates without ortho chlorine substituents adopt a range of dihedral angles can be explained by crystal packing effects, which force the biphenyl moiety to adopt an energetically less favorable conformation in the solid state.

Related literature top

For related structures of biphenyl-4-yl ester 2,2,2-trichloro-ethyl esters of sulfuric acid, see: Li et al. (2008, 2010a,b,c). For a review of structures of sulfuric acid aryl mono esters, see: Brandao et al. (2005); Denehy et al. (2006). For additional background to sulfate metabolites of polychlorinated biphenyls, see: Liu et al. (2006, 2009); Wang et al. (2006); Dhakal et al. (2012); Zhai et al. (2013).

Experimental top

The title compound was synthesized from 3,4',5-trichlorobiphenyl-4-ol and 2,2,2-trichloroethyl sulfonyl chloride using 4-dimethylaminopyridine as catalyst as reported previously (Li et al., 2008). Crystals suitable for X-ray diffraction analysis were obtained by slow evaporation of a methanolic solution.

Computing details top

Data collection: APEX2 (Bruker, 2006); cell refinement: SAINT (Bruker, 2006); data reduction: SAINT (Bruker, 2006); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: XP in SHELXTL (Sheldrick, 2008); software used to prepare material for publication: SHELXL97 (Sheldrick, 2008) and local procedures.

Figures top

Fig. 1. View of the title compound showing the atom-labeling scheme. Displacement ellipsoids are drawn at the 50% probability level.

3,4',5-Trichlorobiphenyl-4-yl 2,2,2-trichloroethyl sulfate top

Crystal data top

C₁₄H₈Cl₆O₄S	F(000) = 1936
M_r = 484.96	D_x = 1.741 Mg m⁻³
Orthorhombic, Pca2₁	Cu Kα radiation, λ = 1.54178 Å
Hall symbol: P 2c -2ac	Cell parameters from 9992 reflections
a = 13.993 (3) Å	θ = 3.1–68.3°
b = 9.1890 (18) Å	µ = 9.71 mm⁻¹
c = 28.778 (6) Å	T = 90 K
V = 3700.3 (13) Å³	Flake, colourless
Z = 8	0.17 × 0.09 × 0.02 mm

Data collection top

Bruker X8 Proteum diffractometer	6651 independent reflections
Radiation source: fine-focus rotating anode	6238 reflections with I > 2σ(I)
Graded multilayer optics monochromator	R_int = 0.062
Detector resolution: 5.6 pixels mm^-1	θ_max = 68.4°, θ_min = 3.1°
ϕ and ω scans	h = −14→16
Absorption correction: multi-scan (SADABS; Bruker, 2006)	k = −10→11
T_min = 0.504, T_max = 0.830	l = −34→34
45894 measured reflections

Refinement top

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)] = 0.064	H-atom parameters constrained
wR(F²) = 0.161	w = 1/[σ²(F_o²) + (0.0514P)² + 21.3733P] where P = (F_o² + 2F_c²)/3
S = 1.15	(Δ/σ)_max < 0.001
6651 reflections	Δρ_max = 0.96 e Å⁻³
302 parameters	Δρ_min = −0.85 e Å⁻³
1 restraint	Absolute structure: Flack (1983), 3176 Friedel pairs
Primary atom site location: structure-invariant direct methods	Absolute structure parameter: 0.15 (3)

Crystal data top

C₁₄H₈Cl₆O₄S	V = 3700.3 (13) Å³
M_r = 484.96	Z = 8
Orthorhombic, Pca2₁	Cu Kα radiation
a = 13.993 (3) Å	µ = 9.71 mm⁻¹
b = 9.1890 (18) Å	T = 90 K
c = 28.778 (6) Å	0.17 × 0.09 × 0.02 mm

Data collection top

Bruker X8 Proteum diffractometer	6651 independent reflections
Absorption correction: multi-scan (SADABS; Bruker, 2006)	6238 reflections with I > 2σ(I)
T_min = 0.504, T_max = 0.830	R_int = 0.062
45894 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.064	H-atom parameters constrained
wR(F²) = 0.161	w = 1/[σ²(F_o²) + (0.0514P)² + 21.3733P] where P = (F_o² + 2F_c²)/3
S = 1.15	Δρ_max = 0.96 e Å⁻³
6651 reflections	Δρ_min = −0.85 e Å⁻³
302 parameters	Absolute structure: Flack (1983), 3176 Friedel pairs
1 restraint	Absolute structure parameter: 0.15 (3)

Special details top

Experimental. The crystal was twinned by inversion, but with unequal sized pieces of each component. The refined Flack parameter indicates major:minor fractions of 0.85 (3):0.15 (3).

Geometry. All s.u.'s (except the s.u. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell s.u.'s are taken into account individually in the estimation of s.u.'s in distances, angles and torsion angles; correlations between s.u.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell s.u.'s is used for estimating s.u.'s involving l.s. planes.

Refinement. Refinement of F² against all reflections. The weighted R-value wR and goodness of fit S are based on F². Conventional R-values R are based on F, with F set to zero for negative F². The threshold expression of F² > 2σ(F²) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-values based on F² are statistically about twice as large as those based on F, and R-values based on ALL data will be even larger.

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

	x	y	z	U_iso*/U_eq
S1A	0.77740 (12)	0.4047 (2)	0.35290 (7)	0.0283 (2)
O1A	0.8439 (4)	0.2785 (5)	0.33235 (19)	0.0273 (7)
O2A	0.8158 (4)	0.4167 (6)	0.40377 (19)	0.0313 (7)
O3A	0.7985 (4)	0.5393 (6)	0.3314 (2)	0.0302 (7)
O4A	0.6838 (4)	0.3483 (6)	0.3531 (2)	0.0349 (7)
Cl1A	1.03327 (13)	0.3420 (2)	0.37524 (7)	0.0380 (3)
Cl2A	0.78298 (12)	0.2737 (2)	0.23480 (7)	0.0318 (2)
Cl3A	1.37897 (13)	0.5084 (2)	0.10448 (8)	0.0378 (3)
Cl4A	0.8960 (2)	0.4431 (3)	0.50012 (9)	0.0563 (4)
Cl5A	0.69326 (19)	0.4810 (2)	0.48583 (9)	0.0487 (4)
Cl6A	0.76595 (19)	0.2066 (2)	0.52014 (8)	0.0489 (4)
C1A	1.0641 (5)	0.3630 (7)	0.2372 (3)	0.0240 (9)
C2A	1.0822 (5)	0.3612 (8)	0.2847 (3)	0.0273 (9)
H2A	1.1456	0.3760	0.2956	0.033*
C3A	1.0090 (5)	0.3381 (8)	0.3166 (3)	0.0276 (9)
C4A	0.9162 (5)	0.3143 (8)	0.3011 (3)	0.0252 (9)
C5A	0.8987 (5)	0.3119 (7)	0.2542 (3)	0.0259 (9)
C6A	0.9704 (5)	0.3381 (8)	0.2223 (3)	0.0273 (9)
H6A	0.9560	0.3393	0.1900	0.033*
C7A	0.7997 (6)	0.2919 (9)	0.4344 (3)	0.0326 (10)
H7A1	0.8546	0.2241	0.4332	0.039*
H7A2	0.7412	0.2386	0.4251	0.039*
C8A	0.7887 (7)	0.3548 (10)	0.4822 (3)	0.0431 (12)
C1'A	1.1400 (5)	0.3932 (8)	0.2034 (3)	0.0284 (9)
C2'A	1.1233 (5)	0.4783 (9)	0.1639 (3)	0.0314 (11)
H2'A	1.0607	0.5138	0.1581	0.038*
C3'A	1.1959 (5)	0.5118 (9)	0.1333 (3)	0.0307 (10)
H3'A	1.1833	0.5691	0.1065	0.037*
C4'A	1.2877 (5)	0.4609 (9)	0.1420 (3)	0.0284 (10)
C5'A	1.3053 (5)	0.3752 (8)	0.1800 (3)	0.0293 (10)
H5'A	1.3677	0.3379	0.1850	0.035*
C6'A	1.2329 (5)	0.3424 (8)	0.2113 (3)	0.0285 (9)
H6'A	1.2464	0.2854	0.2380	0.034*
S1B	0.48992 (12)	0.0952 (2)	0.44025 (7)	0.0283 (2)
O1B	0.4243 (3)	0.2207 (5)	0.46086 (19)	0.0273 (7)
O2B	0.4512 (4)	0.0835 (6)	0.38944 (19)	0.0313 (7)
O3B	0.4667 (4)	−0.0367 (6)	0.4615 (2)	0.0302 (7)
O4B	0.5834 (4)	0.1524 (6)	0.4402 (2)	0.0349 (7)
Cl1B	0.23508 (13)	0.1574 (2)	0.41731 (7)	0.0380 (3)
Cl2B	0.48229 (12)	0.2267 (2)	0.55864 (7)	0.0318 (2)
Cl3B	−0.11866 (13)	0.0187 (2)	0.68821 (8)	0.0378 (3)
Cl4B	0.3715 (2)	0.0537 (3)	0.29351 (9)	0.0563 (4)
Cl5B	0.50048 (19)	0.2929 (2)	0.27257 (8)	0.0487 (4)
Cl6B	0.57633 (19)	0.0222 (3)	0.30941 (8)	0.0489 (4)
C1B	0.2034 (5)	0.1376 (8)	0.5547 (3)	0.0240 (9)
C2B	0.1855 (5)	0.1373 (8)	0.5077 (3)	0.0273 (9)
H2B	0.1222	0.1221	0.4967	0.033*
C3B	0.2590 (5)	0.1590 (8)	0.4759 (3)	0.0276 (9)
C4B	0.3515 (5)	0.1866 (8)	0.4923 (3)	0.0252 (9)
C5B	0.3684 (5)	0.1883 (8)	0.5392 (3)	0.0259 (9)
C6B	0.2963 (5)	0.1672 (8)	0.5714 (3)	0.0273 (9)
H6B	0.3089	0.1725	0.6038	0.033*
C7B	0.4686 (6)	0.2041 (9)	0.3589 (3)	0.0326 (10)
H7B1	0.5276	0.2556	0.3684	0.039*
H7B2	0.4146	0.2736	0.3604	0.039*
C8B	0.4791 (7)	0.1461 (10)	0.3102 (3)	0.0431 (12)
C1'B	0.1230 (5)	0.1095 (8)	0.5886 (3)	0.0284 (9)
C2'B	0.1395 (5)	0.0364 (9)	0.6294 (3)	0.0314 (11)
H2'B	0.2024	0.0042	0.6364	0.038*
C3'B	0.0659 (5)	0.0087 (8)	0.6607 (3)	0.0307 (10)
H3'B	0.0784	−0.0421	0.6888	0.037*
C4'B	−0.0243 (5)	0.0551 (9)	0.6506 (3)	0.0284 (10)
C5'B	−0.0442 (5)	0.1307 (8)	0.6098 (3)	0.0293 (10)
H5'B	−0.1072	0.1629	0.6031	0.035*
C6'B	0.0308 (5)	0.1580 (8)	0.5789 (3)	0.0285 (9)
H6'B	0.0188	0.2102	0.5510	0.034*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
S1A	0.0183 (5)	0.0276 (5)	0.0392 (6)	0.0017 (4)	0.0002 (4)	0.0039 (4)
O1A	0.0202 (14)	0.0205 (15)	0.0411 (17)	−0.0046 (12)	0.0037 (13)	0.0031 (12)
O2A	0.0285 (16)	0.0267 (16)	0.0386 (17)	−0.0036 (13)	0.0023 (13)	0.0059 (13)
O3A	0.0248 (17)	0.0217 (16)	0.0442 (18)	0.0022 (12)	0.0006 (13)	0.0063 (13)
O4A	0.0187 (15)	0.0370 (18)	0.0491 (19)	−0.0033 (13)	−0.0001 (14)	0.0041 (15)
Cl1A	0.0219 (5)	0.0543 (7)	0.0379 (6)	−0.0016 (5)	−0.0044 (5)	0.0037 (5)
Cl2A	0.0167 (5)	0.0340 (6)	0.0447 (6)	−0.0060 (4)	−0.0047 (4)	0.0021 (5)
Cl3A	0.0279 (6)	0.0455 (7)	0.0399 (6)	−0.0032 (5)	0.0037 (5)	0.0000 (6)
Cl4A	0.0802 (11)	0.0341 (6)	0.0545 (8)	−0.0139 (7)	−0.0252 (7)	0.0035 (5)
Cl5A	0.0709 (11)	0.0286 (7)	0.0465 (9)	0.0093 (7)	0.0109 (8)	0.0067 (7)
Cl6A	0.0715 (11)	0.0299 (8)	0.0454 (9)	0.0031 (7)	0.0054 (8)	0.0030 (7)
C1A	0.018 (2)	0.0134 (18)	0.040 (2)	0.0007 (16)	0.0015 (18)	0.0006 (17)
C2A	0.0137 (19)	0.023 (2)	0.045 (3)	−0.0001 (16)	−0.0014 (17)	0.0013 (19)
C3A	0.019 (2)	0.020 (2)	0.044 (2)	0.0014 (17)	−0.0017 (18)	0.0002 (18)
C4A	0.0122 (18)	0.0156 (19)	0.048 (3)	−0.0009 (15)	−0.0002 (18)	0.0014 (17)
C5A	0.017 (2)	0.0120 (18)	0.048 (3)	0.0000 (16)	0.0010 (18)	0.0004 (17)
C6A	0.020 (2)	0.022 (2)	0.040 (2)	−0.0008 (17)	−0.0039 (18)	−0.0016 (18)
C7A	0.033 (2)	0.027 (2)	0.038 (2)	0.001 (2)	−0.002 (2)	0.0039 (19)
C8A	0.060 (3)	0.028 (2)	0.041 (3)	−0.002 (2)	−0.007 (3)	0.000 (2)
C1'A	0.017 (2)	0.024 (2)	0.044 (2)	0.0023 (17)	−0.0018 (18)	−0.0069 (19)
C2'A	0.017 (2)	0.034 (3)	0.043 (2)	0.0000 (19)	−0.0038 (19)	0.000 (2)
C3'A	0.025 (2)	0.030 (2)	0.037 (2)	0.002 (2)	−0.005 (2)	0.000 (2)
C4'A	0.019 (2)	0.026 (2)	0.040 (2)	−0.0023 (18)	0.0028 (18)	−0.0037 (19)
C5'A	0.019 (2)	0.026 (2)	0.043 (3)	0.0008 (18)	−0.0034 (18)	−0.003 (2)
C6'A	0.019 (2)	0.023 (2)	0.042 (3)	−0.0013 (17)	−0.0001 (19)	0.001 (2)
S1B	0.0183 (5)	0.0276 (5)	0.0392 (6)	0.0017 (4)	0.0002 (4)	0.0039 (4)
O1B	0.0202 (14)	0.0205 (15)	0.0411 (17)	−0.0046 (12)	0.0037 (13)	0.0031 (12)
O2B	0.0285 (16)	0.0267 (16)	0.0386 (17)	−0.0036 (13)	0.0023 (13)	0.0059 (13)
O3B	0.0248 (17)	0.0217 (16)	0.0442 (18)	0.0022 (12)	0.0006 (13)	0.0063 (13)
O4B	0.0187 (15)	0.0370 (18)	0.0491 (19)	−0.0033 (13)	−0.0001 (14)	0.0041 (15)
Cl1B	0.0219 (5)	0.0543 (7)	0.0379 (6)	−0.0016 (5)	−0.0044 (5)	0.0037 (5)
Cl2B	0.0167 (5)	0.0340 (6)	0.0447 (6)	−0.0060 (4)	−0.0047 (4)	0.0021 (5)
Cl3B	0.0279 (6)	0.0455 (7)	0.0399 (6)	−0.0032 (5)	0.0037 (5)	0.0000 (6)
Cl4B	0.0802 (11)	0.0341 (6)	0.0545 (8)	−0.0139 (7)	−0.0252 (7)	0.0035 (5)
Cl5B	0.0709 (11)	0.0286 (7)	0.0465 (9)	0.0093 (7)	0.0109 (8)	0.0067 (7)
Cl6B	0.0715 (11)	0.0299 (8)	0.0454 (9)	0.0031 (7)	0.0054 (8)	0.0030 (7)
C1B	0.018 (2)	0.0134 (18)	0.040 (2)	0.0007 (16)	0.0015 (18)	0.0006 (17)
C2B	0.0137 (19)	0.023 (2)	0.045 (3)	−0.0001 (16)	−0.0014 (17)	0.0013 (19)
C3B	0.019 (2)	0.020 (2)	0.044 (2)	0.0014 (17)	−0.0017 (18)	0.0002 (18)
C4B	0.0122 (18)	0.0156 (19)	0.048 (3)	−0.0009 (15)	−0.0002 (18)	0.0014 (17)
C5B	0.017 (2)	0.0120 (18)	0.048 (3)	0.0000 (16)	0.0010 (18)	0.0004 (17)
C6B	0.020 (2)	0.022 (2)	0.040 (2)	−0.0008 (17)	−0.0039 (18)	−0.0016 (18)
C7B	0.033 (2)	0.027 (2)	0.038 (2)	0.001 (2)	−0.002 (2)	0.0039 (19)
C8B	0.060 (3)	0.028 (2)	0.041 (3)	−0.002 (2)	−0.007 (3)	0.000 (2)
C1'B	0.017 (2)	0.024 (2)	0.044 (2)	0.0023 (17)	−0.0018 (18)	−0.0069 (19)
C2'B	0.017 (2)	0.034 (3)	0.043 (2)	0.0000 (19)	−0.0038 (19)	0.000 (2)
C3'B	0.025 (2)	0.030 (2)	0.037 (2)	0.002 (2)	−0.005 (2)	0.000 (2)
C4'B	0.019 (2)	0.026 (2)	0.040 (2)	−0.0023 (18)	0.0028 (18)	−0.0037 (19)
C5'B	0.019 (2)	0.026 (2)	0.043 (3)	0.0008 (18)	−0.0034 (18)	−0.003 (2)
C6'B	0.019 (2)	0.023 (2)	0.042 (3)	−0.0013 (17)	−0.0001 (19)	0.001 (2)

Geometric parameters (Å, º) top

S1A—O4A	1.408 (5)	S1B—O3B	1.396 (6)
S1A—O3A	1.414 (6)	S1B—O4B	1.409 (5)
S1A—O2A	1.563 (6)	S1B—O2B	1.563 (6)
S1A—O1A	1.600 (5)	S1B—O1B	1.590 (5)
O1A—C4A	1.393 (9)	O1B—C4B	1.397 (9)
O2A—C7A	1.464 (9)	O2B—C7B	1.434 (9)
Cl1A—C3A	1.722 (9)	Cl1B—C3B	1.720 (8)
Cl2A—C5A	1.749 (7)	Cl2B—C5B	1.726 (7)
Cl3A—C4'A	1.730 (8)	Cl3B—C4'B	1.739 (8)
Cl4A—C8A	1.783 (10)	Cl4B—C8B	1.793 (10)
Cl5A—C8A	1.772 (10)	Cl5B—C8B	1.755 (9)
Cl6A—C8A	1.774 (9)	Cl6B—C8B	1.774 (10)
C1A—C2A	1.391 (11)	C1B—C2B	1.378 (11)
C1A—C6A	1.400 (10)	C1B—C6B	1.412 (10)
C1A—C1'A	1.467 (10)	C1B—C1'B	1.510 (10)
C2A—C3A	1.390 (11)	C2B—C3B	1.389 (11)
C2A—H2A	0.9500	C2B—H2B	0.9500
C3A—C4A	1.390 (10)	C3B—C4B	1.401 (10)
C4A—C5A	1.373 (11)	C4B—C5B	1.370 (11)
C5A—C6A	1.381 (11)	C5B—C6B	1.384 (11)
C6A—H6A	0.9500	C6B—H6B	0.9500
C7A—C8A	1.500 (12)	C7B—C8B	1.509 (12)
C7A—H7A1	0.9900	C7B—H7B1	0.9900
C7A—H7A2	0.9900	C7B—H7B2	0.9900
C1'A—C6'A	1.399 (10)	C1'B—C2'B	1.373 (12)
C1'A—C2'A	1.400 (12)	C1'B—C6'B	1.393 (10)
C2'A—C3'A	1.380 (12)	C2'B—C3'B	1.391 (12)
C2'A—H2'A	0.9500	C2'B—H2'B	0.9500
C3'A—C4'A	1.389 (11)	C3'B—C4'B	1.364 (10)
C3'A—H3'A	0.9500	C3'B—H3'B	0.9500
C4'A—C5'A	1.369 (12)	C4'B—C5'B	1.392 (12)
C5'A—C6'A	1.388 (11)	C5'B—C6'B	1.399 (11)
C5'A—H5'A	0.9500	C5'B—H5'B	0.9500
C6'A—H6'A	0.9500	C6'B—H6'B	0.9500

O4A—S1A—O3A	121.2 (3)	O3B—S1B—O4B	122.7 (3)
O4A—S1A—O2A	109.9 (3)	O3B—S1B—O2B	105.6 (3)
O3A—S1A—O2A	106.0 (3)	O4B—S1B—O2B	110.3 (3)
O4A—S1A—O1A	106.0 (3)	O3B—S1B—O1B	109.4 (3)
O3A—S1A—O1A	110.5 (3)	O4B—S1B—O1B	105.4 (3)
O2A—S1A—O1A	101.4 (3)	O2B—S1B—O1B	101.4 (3)
C4A—O1A—S1A	119.3 (4)	C4B—O1B—S1B	120.0 (4)
C7A—O2A—S1A	117.1 (5)	C7B—O2B—S1B	117.5 (5)
C2A—C1A—C6A	118.1 (7)	C2B—C1B—C6B	120.1 (7)
C2A—C1A—C1'A	121.5 (7)	C2B—C1B—C1'B	119.9 (6)
C6A—C1A—C1'A	120.3 (7)	C6B—C1B—C1'B	120.0 (7)
C3A—C2A—C1A	121.1 (7)	C1B—C2B—C3B	120.8 (7)
C3A—C2A—H2A	119.5	C1B—C2B—H2B	119.6
C1A—C2A—H2A	119.5	C3B—C2B—H2B	119.6
C4A—C3A—C2A	120.0 (8)	C2B—C3B—C4B	119.3 (8)
C4A—C3A—Cl1A	120.1 (6)	C2B—C3B—Cl1B	119.9 (6)
C2A—C3A—Cl1A	119.8 (6)	C4B—C3B—Cl1B	120.7 (6)
C5A—C4A—C3A	119.0 (7)	C5B—C4B—O1B	120.6 (6)
C5A—C4A—O1A	120.1 (6)	C5B—C4B—C3B	119.5 (7)
C3A—C4A—O1A	120.5 (7)	O1B—C4B—C3B	119.8 (7)
C4A—C5A—C6A	121.5 (7)	C4B—C5B—C6B	122.2 (7)
C4A—C5A—Cl2A	118.8 (6)	C4B—C5B—Cl2B	118.7 (6)
C6A—C5A—Cl2A	119.7 (6)	C6B—C5B—Cl2B	119.0 (6)
C5A—C6A—C1A	120.3 (8)	C5B—C6B—C1B	118.1 (7)
C5A—C6A—H6A	119.9	C5B—C6B—H6B	121.0
C1A—C6A—H6A	119.9	C1B—C6B—H6B	121.0
O2A—C7A—C8A	105.4 (6)	O2B—C7B—C8B	108.2 (7)
O2A—C7A—H7A1	110.7	O2B—C7B—H7B1	110.0
C8A—C7A—H7A1	110.7	C8B—C7B—H7B1	110.0
O2A—C7A—H7A2	110.7	O2B—C7B—H7B2	110.0
C8A—C7A—H7A2	110.7	C8B—C7B—H7B2	110.0
H7A1—C7A—H7A2	108.8	H7B1—C7B—H7B2	108.4
C7A—C8A—Cl5A	112.5 (6)	C7B—C8B—Cl5B	108.6 (6)
C7A—C8A—Cl6A	106.7 (6)	C7B—C8B—Cl6B	108.2 (6)
Cl5A—C8A—Cl6A	109.3 (5)	Cl5B—C8B—Cl6B	110.8 (6)
C7A—C8A—Cl4A	110.8 (7)	C7B—C8B—Cl4B	109.5 (7)
Cl5A—C8A—Cl4A	108.6 (5)	Cl5B—C8B—Cl4B	110.0 (5)
Cl6A—C8A—Cl4A	108.8 (5)	Cl6B—C8B—Cl4B	109.7 (5)
C6'A—C1'A—C2'A	118.2 (7)	C2'B—C1'B—C6'B	118.9 (7)
C6'A—C1'A—C1A	120.1 (7)	C2'B—C1'B—C1B	120.7 (6)
C2'A—C1'A—C1A	121.6 (6)	C6'B—C1'B—C1B	120.4 (7)
C3'A—C2'A—C1'A	121.3 (7)	C1'B—C2'B—C3'B	121.2 (7)
C3'A—C2'A—H2'A	119.3	C1'B—C2'B—H2'B	119.4
C1'A—C2'A—H2'A	119.3	C3'B—C2'B—H2'B	119.4
C2'A—C3'A—C4'A	119.3 (8)	C4'B—C3'B—C2'B	119.4 (8)
C2'A—C3'A—H3'A	120.3	C4'B—C3'B—H3'B	120.3
C4'A—C3'A—H3'A	120.3	C2'B—C3'B—H3'B	120.3
C5'A—C4'A—C3'A	120.3 (7)	C3'B—C4'B—C5'B	121.3 (8)
C5'A—C4'A—Cl3A	120.7 (6)	C3'B—C4'B—Cl3B	120.7 (7)
C3'A—C4'A—Cl3A	118.9 (7)	C5'B—C4'B—Cl3B	118.0 (6)
C4'A—C5'A—C6'A	120.7 (7)	C4'B—C5'B—C6'B	118.5 (7)
C4'A—C5'A—H5'A	119.6	C4'B—C5'B—H5'B	120.8
C6'A—C5'A—H5'A	119.6	C6'B—C5'B—H5'B	120.8
C5'A—C6'A—C1'A	120.0 (8)	C1'B—C6'B—C5'B	120.6 (8)
C5'A—C6'A—H6'A	120.0	C1'B—C6'B—H6'B	119.7
C1'A—C6'A—H6'A	120.0	C5'B—C6'B—H6'B	119.7

O4A—S1A—O1A—C4A	138.7 (5)	O3B—S1B—O1B—C4B	−4.9 (6)
O3A—S1A—O1A—C4A	5.6 (6)	O4B—S1B—O1B—C4B	−138.6 (6)
O2A—S1A—O1A—C4A	−106.4 (5)	O2B—S1B—O1B—C4B	106.3 (6)
O4A—S1A—O2A—C7A	45.2 (6)	O3B—S1B—O2B—C7B	−177.9 (5)
O3A—S1A—O2A—C7A	177.8 (5)	O4B—S1B—O2B—C7B	−43.3 (6)
O1A—S1A—O2A—C7A	−66.7 (5)	O1B—S1B—O2B—C7B	68.0 (6)
C6A—C1A—C2A—C3A	−1.2 (11)	C6B—C1B—C2B—C3B	3.1 (11)
C1'A—C1A—C2A—C3A	177.5 (7)	C1'B—C1B—C2B—C3B	−178.2 (7)
C1A—C2A—C3A—C4A	0.9 (11)	C1B—C2B—C3B—C4B	−2.3 (11)
C1A—C2A—C3A—Cl1A	−178.0 (6)	C1B—C2B—C3B—Cl1B	179.7 (6)
C2A—C3A—C4A—C5A	1.0 (11)	S1B—O1B—C4B—C5B	91.6 (8)
Cl1A—C3A—C4A—C5A	179.9 (5)	S1B—O1B—C4B—C3B	−92.2 (7)
C2A—C3A—C4A—O1A	174.4 (6)	C2B—C3B—C4B—C5B	1.6 (11)
Cl1A—C3A—C4A—O1A	−6.7 (10)	Cl1B—C3B—C4B—C5B	179.5 (6)
S1A—O1A—C4A—C5A	−92.0 (7)	C2B—C3B—C4B—O1B	−174.6 (6)
S1A—O1A—C4A—C3A	94.7 (7)	Cl1B—C3B—C4B—O1B	3.3 (10)
C3A—C4A—C5A—C6A	−2.6 (11)	O1B—C4B—C5B—C6B	174.4 (6)
O1A—C4A—C5A—C6A	−176.0 (6)	C3B—C4B—C5B—C6B	−1.8 (11)
C3A—C4A—C5A—Cl2A	177.1 (5)	O1B—C4B—C5B—Cl2B	−2.3 (10)
O1A—C4A—C5A—Cl2A	3.7 (9)	C3B—C4B—C5B—Cl2B	−178.5 (5)
C4A—C5A—C6A—C1A	2.3 (11)	C4B—C5B—C6B—C1B	2.5 (11)
Cl2A—C5A—C6A—C1A	−177.4 (5)	Cl2B—C5B—C6B—C1B	179.2 (5)
C2A—C1A—C6A—C5A	−0.4 (11)	C2B—C1B—C6B—C5B	−3.2 (11)
C1'A—C1A—C6A—C5A	−179.1 (6)	C1'B—C1B—C6B—C5B	178.2 (6)
S1A—O2A—C7A—C8A	−148.3 (6)	S1B—O2B—C7B—C8B	148.2 (6)
O2A—C7A—C8A—Cl5A	58.7 (8)	O2B—C7B—C8B—Cl5B	−180.0 (5)
O2A—C7A—C8A—Cl6A	178.5 (5)	O2B—C7B—C8B—Cl6B	−59.6 (8)
O2A—C7A—C8A—Cl4A	−63.2 (7)	O2B—C7B—C8B—Cl4B	59.9 (8)
C2A—C1A—C1'A—C6'A	36.2 (11)	C2B—C1B—C1'B—C2'B	145.8 (8)
C6A—C1A—C1'A—C6'A	−145.1 (7)	C6B—C1B—C1'B—C2'B	−35.5 (11)
C2A—C1A—C1'A—C2'A	−140.7 (8)	C2B—C1B—C1'B—C6'B	−34.4 (11)
C6A—C1A—C1'A—C2'A	38.0 (11)	C6B—C1B—C1'B—C6'B	144.2 (7)
C6'A—C1'A—C2'A—C3'A	0.1 (12)	C6'B—C1'B—C2'B—C3'B	0.8 (12)
C1A—C1'A—C2'A—C3'A	177.0 (7)	C1B—C1'B—C2'B—C3'B	−179.4 (7)
C1'A—C2'A—C3'A—C4'A	−0.5 (12)	C1'B—C2'B—C3'B—C4'B	0.0 (13)
C2'A—C3'A—C4'A—C5'A	1.7 (12)	C2'B—C3'B—C4'B—C5'B	−0.5 (12)
C2'A—C3'A—C4'A—Cl3A	−177.9 (6)	C2'B—C3'B—C4'B—Cl3B	178.5 (6)
C3'A—C4'A—C5'A—C6'A	−2.4 (12)	C3'B—C4'B—C5'B—C6'B	0.3 (12)
Cl3A—C4'A—C5'A—C6'A	177.1 (6)	Cl3B—C4'B—C5'B—C6'B	−178.8 (6)
C4'A—C5'A—C6'A—C1'A	2.0 (12)	C2'B—C1'B—C6'B—C5'B	−1.1 (12)
C2'A—C1'A—C6'A—C5'A	−0.8 (11)	C1B—C1'B—C6'B—C5'B	179.2 (7)
C1A—C1'A—C6'A—C5'A	−177.8 (7)	C4'B—C5'B—C6'B—C1'B	0.5 (11)

Experimental details

Crystal data
Chemical formula	C₁₄H₈Cl₆O₄S
M_r	484.96
Crystal system, space group	Orthorhombic, Pca2₁
Temperature (K)	90
a, b, c (Å)	13.993 (3), 9.1890 (18), 28.778 (6)
V (Å³)	3700.3 (13)
Z	8
Radiation type	Cu Kα
µ (mm⁻¹)	9.71
Crystal size (mm)	0.17 × 0.09 × 0.02

Data collection
Diffractometer	Bruker X8 Proteum diffractometer
Absorption correction	Multi-scan (SADABS; Bruker, 2006)
T_min, T_max	0.504, 0.830
No. of measured, independent and observed [I > 2σ(I)] reflections	45894, 6651, 6238
R_int	0.062
(sin θ/λ)_max (Å⁻¹)	0.603

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.064, 0.161, 1.15
No. of reflections	6651
No. of parameters	302
No. of restraints	1
H-atom treatment	H-atom parameters constrained
	w = 1/[σ²(F_o²) + (0.0514P)² + 21.3733P] where P = (F_o² + 2F_c²)/3
Δρ_max, Δρ_min (e Å⁻³)	0.96, −0.85
Absolute structure	Flack (1983), 3176 Friedel pairs
Absolute structure parameter	0.15 (3)

Computer programs: APEX2 (Bruker, 2006), SAINT (Bruker, 2006), SHELXS97 (Sheldrick, 2008), XP in SHELXTL (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008) and local procedures.

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3,4',5-Trichloro­biphenyl-4-yl 2,2,2-trichloro­ethyl sulfate

Supporting information

Key indicators

checkCIF/PLATON results

3,4',5-Trichlorobiphenyl-4-yl 2,2,2-trichloroethyl sulfate