[N,N-Bis(2-hy-droxy-eth-yl)di-thio-carbamato-κ2S,S']bis-(tri-phenyl-phosphane-κP)copper(I) chloro-form monosolvate: crystal structure, Hirshfeld surface analysis and solution NMR measurements.

The title compound, [Cu(C5H5NO2S2)(C18H15P)2]·CHCl3, features a tetra-hedrally coordinated CuI atom within a P2S2 donor set defined by two phosphane P atoms and by two S atoms derived from a symmetrically coordinating di-thio-carbamate ligand. Both intra- and inter-molecular hy-droxy-O-H⋯O(hydroxy) hydrogen bonding is observed: the former closes an eight-membered {⋯HOC2NC2O} ring, whereas the latter connects centrosymmetrically related mol-ecules into dimeric aggregates via eight-membered {⋯H-O⋯H-O}2 synthons. The complex mol-ecules are arranged to form channels along the c axis in which reside the chloro-form mol-ecules, being connected by Cl⋯π(arene) and short S⋯Cl [3.3488 (9) Å] inter-actions. The inter-molecular inter-actions have been investigated further by Hirshfeld surface analysis, which shows the conventional hydrogen bonding to be very localized with the main contributors to the surface, at nearly 60%, being H⋯H contacts. Solution NMR studies indicate that whilst the same basic mol-ecular structure is retained in solution, the tri-phenyl-phosphane ligands are highly labile, exchanging rapidly with free Ph3P at room temperature.

Chemical context

The motivation to prepare bis­(phosphane)copper(I) di­thio­carbamates of general formula (R 3P)2Cu(S2CNR′R′′) (R, R′, R′′ = alkyl, ar­yl) largely stems from the versatile biological properties exhibited by these types of compounds (Skrott & Cvek, 2012 ▸; Biersack et al., 2012 ▸) and metal di­thio­carbamates in general, as summarized in a recent review (Hogarth, 2012 ▸). At present, research continues to develop promising anti-microbial agents in light of the growing prevalence of bacterial infections and threats associated with drug-resistant bacteria (Verma & Singh, 2015 ▸; Onwudiwe et al., 2016 ▸). In our recent efforts to develop anti-microbial agents, phosphanegold(I) di­thio­carbamates, R 3PAu[S2CN(iPr)CH2CH2OH], were prepared and these compounds demonstrated prominent and distinctive anti-microbial activity against a broad range of Gram-positive and Gram-negative bacteria, dependent on the type of P-bound substituent employed (Sim et al., 2014 ▸). A distinct structure–activity relationship was noted in that when R = Et, the compound was potent against a broad range of Gram-positive and Gram-negative bacteria, whereas the R = Ph and Cy compounds showed specific activity against Gram-positive bacteria. Even greater, broad-range activity is apparent in tri­ethyl­phosphanegold(I) di­alkyl­dithio­carbamates (Chen et al., 2016 ▸). The above prompted an exploration of the anti-bacterial activity of related copper(I) and silver(I) deriv­atives, as these metals are known to possess noteworthy potential as anti-microbial agents (Losasso et al., 2014 ▸). Thus, a series of phosphanecopper(I) and silver(I) compounds of general formula (Ph3P)2 M[S2CN(R)CH2CH2OH] for M = Cu and Ag, and R = Me, iPr and CH2CH2OH, were prepared and evaluated for their anti-microbial activities (Jamaludin et al., 2016 ▸). While none of the studied compounds exhibited activity against Gram-negative bacteria, they were found to be selectively potent against Gram-positive bacteria. Following new syntheses to evaluate further the potential of this class of compounds, crystals became available for the title complex, (Ph3P)2Cu[S2CN(CH2CH2OH)2] (I), as its 1:1 chloro­form solvate. Herein, the crystal and mol­ecular structures of (I)·CHCl3 are described along with an analysis of its Hirshfeld surface. Finally, some non-standard, e.g. variable temperature, NMR measurements are presented in order to gain insight into the solution structure.

Structural commentary

The mol­ecular structure of the complex in (I)·CHCl3 is shown in Fig. 1 ▸ and selected geometric parameters are collected in Table 1 ▸. The copper atom is bound by two di­thio­carbamate-S atoms and two phosphane-P atoms. The di­thio­carbamate ligand is coordinating in a symmetric mode with Δ(Cu—S) = 0.042 Å, being the difference between the Cu—Slong and Cu—Sshort bond lengths. This near equivalence in Cu—S bond lengths is reflected in the experimental equivalence of the associated C1—S1, S2 bond lengths. A small disparity, i.e. 0.02 Å, is noted in the Cu—P bond lengths. The resulting P2S2 donor set defines an approximate tetra­hedral geometry. A measure of tetra­hedral vs square-planar geometry is the value of τ4 (Yang et al., 2007 ▸) with values of 1.0 and 0.0° corres­ponding to ideal tetra­hedral and square planar geometries, respectively. In the case of the complex in (I)·CHCl3, the value computes to 0.80. Distortions from the ideal tetra­hedral geometry are clearly related to the acute angle subtended by the di­thio­carbamate ligand and the wide angle subtended by the bulky tri­phenyl­phosphane ligands, Table 1 ▸.

Figure 1

The mol­ecular structure of the complex in (I)·CHCl3, showing the atom-labelling scheme and displacement ellipsoids at the 70% probability level. The solvent CHCl3 mol­ecule is omitted.

Table 1

Geometric data (Å, °) for (I) in (I)·CHCl3 and (I) in its 1:1 Ph3P co-crystal

Parameter	(I) in (I)·CHCl3	(I) in (I)·PPh3 a
Cu—S1	2.3791 (6)	2.3948 (12)
Cu—S2	2.4213 (5)	2.4288 (12)
Cu—P1	2.2602 (6)	2.2849 (12)
Cu—P2	2.2380 (5)	2.2594 (12)
C1—S1	1.714 (2)	1.709 (4)
C1—S2	1.717 (2)	1.702 (4)
S1—Cu—S2	75.264 (18)	74.76 (4)
S1—Cu—P1	110.96 (2)	109.85 (5)
S1—Cu—P2	109.81 (2)	112.35 (4)
S2—Cu—P1	103.74 (2)	102.50 (4)
S2—Cu—P2	123.17 (2)	122.04 (5)
P1—Cu—P2	123.65 (2)	124.52 (4)

Note: (a) Jian et al. (2000 ▸).

The structure of (I) has also been determined in its 1:1 co-crystal with PPh3 (Jian et al., 2000 ▸), hereafter (I)·Ph3P, and key geometric parameters for this structure are also included in Table 1 ▸. Inter­estingly, within pairs of comparable bond lengths, those in (I)·PPh3 are systematically longer. However, the value of Δ(Cu—S) is slightly less at 0.034 Å. The value of τ4 is identical at 0.80. An overlay diagram for (I) in each of (I)·CHCl3 and (I)·PPh3 is shown in Fig. 2 ▸ which confirms the very similar conformations adopted for (I) in both structures.

Figure 2

Overlay diagram of (I)·CHCl3 (red image) and (I)·Ph3P (blue). The mol­ecules have been overlapped so the chelate rings are coincident. The CHCl3 and Ph3P mol­ecules have been omitted.

Supra­molecular features

Geometric parameters describing the salient inter­molecular inter­actions in the crystal of (I)·CHCl3 are collated in Table 2 ▸. There are two types of hy­droxy-O—H⋯O(hy­droxy) hydrogen bonding in the mol­ecular packing, one intra­molecular and the other inter­molecular. The former has hy­droxy-O2—H as the donor and the hy­droxy-O1 as the acceptor, and closes an eight-membered {⋯HOC2NC2O} ring. The key feature of the mol­ecular packing is the presence of hy­droxy-O—H⋯O(hy­droxy) hydrogen bonding which connects centrosymmetriclly-related mol­ecules into dimeric aggregates via eight-membered {⋯H—O⋯H—O}2 synthons, encompassing the intra­molecular hy­droxy-O—H⋯O(hydroxy) hydrogen bonds, Fig. 3 ▸ a. The only other identifiable directional inter­actions within standard distance criteria (Spek, 2009 ▸) involve the chloro­form mol­ecule. Thus, a chloro­form-Cl3⋯π(arene) inter­action is noted, Table 2 ▸. In addition, there is evidence for a close S1⋯Cl3 contact, i.e. involving the same chlorine atom as in the just mentioned Cl⋯π(arene) inter­action. The separation of 3.3488 (9) Å is about 0.2 Å less than the sum of their van der Waals radii (Spek, 2009 ▸). In a very recent and exhaustive review of halogen bonding (Cavallo et al., 2016 ▸), it was mentioned that sulfur is well known to function as an acceptor in R—X⋯S synthons. The inter­actions involving the chloro­form mol­ecule are highlighted in Fig. 3 ▸ b. Globally, mol­ecules of the copper(I) complex pack to define channels parallel to the c axis in which reside the solvent mol­ecules, Fig. 3 ▸ c. Given the presence of Ph3P ligands in (I)·CHCl3, evidence was sought for phenyl-embraces (Dance & Scudder, 1995 ▸). While none was apparent for the P1-phosphane, centrosymmetrically related P2-phosphane ligands approach each other in this manner to generate a sixfold phenyl-embrace. The closest inter­actions between the phosphane residues in this embrace is a pair of edge-to-face-phen­yl—H⋯π(arene) inter­actions, i.e. C63—H63⋯π(C51–C56)i = 3.25 Å with an angle at H62 of 133°; symmetry operation (i): 1 − x, 1 − y, 1 − z.

Table 2

Hydrogen-bond geometry (Å, °)

Cg1 is the ring centroid of (C51–C56).

D—H⋯A	D—H	H⋯A	D⋯A	D—H⋯A
O2—H2O⋯O1	0.84	1.95	2.710 (3)	150
O1—H1O⋯O2i	0.86	1.97	2.697 (3)	142
C6—Cl3⋯Cg1	1.77 (1)	3.81 (1)	3.798 (3)	76 (1)

Symmetry code: (i) .

Figure 3

Mol­ecular packing in (I)·CHCl3: (a) supra­molecular dimer sustained by hy­droxy-O—H⋯O(hy­droxy) hydrogen bonding shown as orange dashed lines, (b) a view of the inter­actions between the complex and solvent mol­ecules with the Cl⋯π(arene) and Cl⋯S inter­actions shown as purple and blue dashed lines, respectively, and (c) a view of the unit-cell contents in projection down the c axis, with chloro­form mol­ecules occupying one channel highlighted in space-filling mode.

Hirshfeld surface analysis

The protocols for the Hirshfeld surface analysis were as described recently (Yeo et al., 2016 ▸). In the present study, analyses were conducted on the following three species: (I) in (I)·CHCl3, (I)·CHCl3 and CHCl3 alone. Hirshfeld surface analysis provides visualization on the existence of any inter­molecular inter­actions within close proximity in a crystal structure, for which contact distances shorter than the sum of the respective van der Waals radii appear red while at distances equal or longer than this would be white and blue in appearance, respectively. Figs. 4 ▸ a and b show Hirshfeld surfaces mapped over d norm for (I) and CHCl3, respectively. The former image exhibits intense red spots on the surface near the hy­droxy­ethyl substituents which are correlated with the strong O—H⋯O hydrogen bonding. Apart from these dominant inter­actions, several other red spots attributed to the close contacts between the complex and chloro­form mol­ecules, i.e. C⋯H/H⋯C, S⋯Cl/Cl⋯S and H⋯Cl/Cl⋯H, are evident in Fig. 4 ▸ a and b.

Figure 4

Comparison of the Hirshfeld surfaces of (a) mol­ecule (I) in (I)·CHCl3 and (b) CHCl3 in (I)·CHCl3, highlighting inter­molecular inter­actions formed with the other component of the structure. The Hirshfeld surfaces were mapped over d norm within the range −0.572 to 1.457 Å.

The combination of d i and d e distances resulted in two-dimensional cuttlefish- and chicken wing-like fingerprint plots for (I), (I)·CHCl3 and CHCl3, Fig. 5 ▸ a, which may be decomposed into several essential close contacts as shown in Fig. 5 ▸ b–d. In general, complex (I) and its chloro­form solvate exhibit almost identical profiles except that the pincer form of (I) in its decomposed fingerprint plot delineated into C⋯H/H⋯C contacts shows two different tips at d e + d i ∼ 2.5 Å and ∼2.7  Å in contrast to the pincer form of (I)·CHCl3 with a pair of symmetrical tips at d e + d i ∼ 2.7 Å when the solvate is considered as a single entity. The close contact distance (d e + d i ∼ 2.5 Å), which is shorter than the sum of van der Waals radii of 2.9 Å (Spek, 2009 ▸), is also reflected in the lancet blade-like fingerprint plot of the solvent mol­ecule corres­ponding to the Cl—H⋯C(π) inter­action. The H⋯Cl/Cl⋯H contact, on the other hand, contributes to the half-pincer form in the decomposed fingerprint plot of (I) and develops into the full pincer form in (I)·CHCl3, both with d e + d i ∼ 2.9 Å that is very close to the sum of van der Waals radii (2.95 Å). As expected, O⋯H/H⋯O contacts constitute the strongest among all inter­actions with d e + d i ∼ 1.9 Å (cf. the sum of van der Waals radii of 2.75 Å) in the forceps form of both decomposed fingerprint plots of (I) and (I)·CHCl3, Fig. 5 ▸ d. Based on the asymmetric fingerprint patterns of the C⋯H/H⋯C and Cl⋯H/H⋯Cl contacts, Fig. 5 ▸ b and c, and the symmetric pattern of the O⋯H/H⋯O contacts, Fig. 5 ▸ d, it may be concluded that two complex mol­ecules are very closely associated, as shown in Fig. 3 ▸ a, and these are flanked by two CHCl3 mol­ecules, highlighted in Fig. 3 ▸ b.

Figure 5

Comparison between (I) in (I)·CHCl3, (I)·CHCl3 and CHCl3 of the (a) full two-dimensional fingerprint plots, and the plots delineated into (b) C⋯H/H⋯C, (c) Cl⋯H/H⋯Cl and (d) O⋯H/H⋯O contacts.

The qu­anti­fication on the distribution of each of the contacts to the Hirshfeld surface reveals that H⋯H, C⋯H/H⋯C and H⋯Cl/Cl⋯H are the three main components for (I) in (I)·CHCl3, with the corresponding contributions of ca 59.4, 20.2 and 8.9%, respectively, Fig. 6 ▸. Despite this, not all of these contacts result in meaningful inter­actions based on the comparison between d e + d i contact distances and the sum of the van der Waals radii. This sequence is followed by O⋯H/ H⋯O contacts which form the fourth most dominant inter­actions with a contribution of approximately 4.6% to the overall Hirshfeld surface. In general, there is not much deviation of the topological distribution between (I) and (I)·CHCl3 except that the contribution from H⋯Cl/Cl⋯H increases by nearly twofold upon the inclusion of the solvent mol­ecule in (I)·CHCl3. As for the chloro­form mol­ecule, H⋯Cl/Cl⋯H makes the major contribution at 74.4%, followed by 8.9% from H⋯H and 8.4% from H⋯Cl/Cl⋯H; the remaining contributions from other minor contacts.

Figure 6

Percentage contributions of the different close contacts to the Hirshfeld surface of (I) in (I)·CHCl3, (I)·CHCl3 and CHCl3.

As mentioned previously, Cl⋯π(arene) and S⋯Cl inter­actions are formed by the chloro­form mol­ecule. In order to gain insight into the charge distribution and rationalize these close contacts, the electrostatic potential (ESP) was mapped over the Hirshfeld surface by ab initio Hartree–Fock (HF) quantum modelling with the 6-31G(d) basis set, as this represents the best possible level of theory and basis set functions in this study so as to keep the accuracy and computational cost at manageable level.

As shown in Fig. 7 ▸ a, a phenyl ring of the complex mol­ecule exhibits mild electronegative character as evidenced from the pale-red spot on the ESP map in contrast to the strong electropositive character about CHCl3, being intense-blue. The electropositive character of the methine group extends slightly beyond the chloro atom approaching its equatorial ring of the negative charge region, hence establishing the weak Cl⋯π(arene) inter­action with d e + d i ∼ 3.3 Å being slightly less than the sum of van der Waals radii of 3.45 Å. The S⋯Cl halogen bond, on the other hand, is established through the highly directional inter­action between the electronegative sulfur of (I) and the σ-hole of the chloro atom of CHCl3 with weak electropositive character, Fig. 7 ▸ b. The electropositive character of the σ-hole results from the electron deficiency in the outer lobe of the p orbital (non-bonded) when a half-filled p orbital of a halogen participates in the formation of covalent bond (Clark et al., 2007 ▸).

Figure 7

Electrostatic potential (ESP) mapped over the Hirshfeld surfaces of the complex mol­ecule (I) (left) and CHCl3 (right), showing the attraction between the electronegative (red) and electropositive (blue) sites for (a) Cl⋯π(arene) and (b) S⋯Cl inter­actions, respectively. The ESP was mapped onto the Hirshfeld surface within the isocharge value of −0.119 to 0.164 a.u. by the ab initio Hartree–Fock (HF) quantum modelling approach with the 6-31G(d) basis set.

NMR Study

FT NMR spectra were recorded on a Bruker AVANCE III 400 MHz spectrometer, operating at 400.13, 100.61 and 161.98 MHz, respectively, for 1H, 13C and 31P. Spectra were indirectly referenced to the solvent deuterium lock shift; chemical shifts are quoted relative to TMS and 85% H3PO4. Probe temperatures were controlled by a standard variable temperature unit and are considered accurate to within ±1 K. Spectra were acquired on approximately 14 mmol solutions of (I) in each of CD2Cl2, d 6-DMSO and CDCl2CDCl2.

The ambient temperature (298 K) 1H NMR spectra of (I) display the expected signals due to the tri­phenyl­phosphine and di­thio­carbamate ligands. The spectra are qualitatively identical in all three solvents, with the only significant differences being the position of the –OH signal of the di­thio­carbamate ligand.

The aromatic region of the 1H spectrum in d 6-DMSO shows two multiplets at ca 7.39 ppm (6 H) and 7.28 ppm (24 H) attributable to Ph-H atoms of the tri­phenyl­phosphine ligands. A sharp singlet observed at 8.32 ppm (1 H) was assigned to CHCl3, as seen in the X-ray crystal structure analysis. The di­thio­carbamate moiety displays a single set of resonances, indicating the two –CH2CH2OH groups are chemically equivalent. The –OH groups display a triplet at 4.80 ppm (3 J HH = 5.3 Hz), which disappears on the addition of D2O. The methyl­ene hydrogen atoms display a triplet at 3.96 ppm (3 J HH = 6.4 Hz) and a pseudo quartet at 3.65 ppm, assignable to NCH2– and –CH2OH, respectively. On the addition of D2O, the quartet collapses to a triplet.

The 13C{1H} spectra in each of the solvents are also qualitatively identical. In d 6-DMSO solution, the carbon atoms of the tri­phenyl­phospine ligands give rise to four resonances at 134.6 ppm (very weak, d, 1 J PC ∼22 Hz, C), 133.6 ppm (d, 2 J PC = 12 Hz, C), 130.1 ppm (s, C) and 128.9 ppm (d, 3 J PC = 5.70 Hz, C). The di­thio­carbamate ligand shows two signals due to the methyl­ene carbon atoms at 58.7 ppm (NCH2—) and 56.0 ppm (—CH2OH), respectively. The quaternary carbon atom of the di­thio­carbamate was not observed.

The ambient temperature 31P{1H} spectrum in CD2Cl2 displays as single, broad resonance at −1.55 ppm (Δv1/2 = 280 Hz). The line broadening is attributed to rapid relaxation of Cu via the quadrupole relaxation (QR) mechanism. Quadrupole relaxation is strongly temperature dependent: the rate of relaxation increases as the temperature decreases. On cooling, the signal sharpens progressively: Δv1/2 (203 K) ∼35 Hz. The sharpening presumably arises because of the effective ‘decoupling’ of the 65Cu–31P and 63Cu–31P scalar couplings as the rate of (Cu) relaxation increases (Grace et al., 1970 ▸). The addition of ca 2 mg (0.9 equivalents) of tri­phenyl­phosphine at ambient temperature, to putatively give (I)·PPh3, gives a single, broad peak at ca −3 ppm, which is between the chemical shifts of pure (I) and free PPh3 (ca −6 ppm), indicating rapid exchange of the tri­phenyl­phosphine ligands.

In an attempt to resolve the Cu-P J couplings, 31P{1H} spectra were recorded in CDCl2CDCl2 solution at elevated temperatures (to reduce the rate of QR). However, no significant changes were observed in the line widths on elevating the temperature to 328 K, and any Cu–P coupling, if not lost through reversible ligand dissociation, remained unresolved. There was no evidence of decomposition at higher temperatures in this solvent.

There are two key conclusions from the foregoing. Firstly, the experiments with D2O proving exchange of the hy­droxy-H atom indicates that this atom is labile, suggesting functionalization at this group should, in principle, be feasible. Secondly, the presence of additional Ph3P in solution does not result in displacement of the di­thio­carbamate ligand nor force a monodentate mode of coordination proving the stability of complex (I) in each of (I)·CHCl3 and (I)·PPh3, and in solution.

Database survey

The structural chemistry of (R 3P)2Cu(S2CNR′R′′) compounds was summarized very recently (Jamaludin et al., 2016 ▸). In all, there are eight examples now available in the literature, namely {(Ph3P)2Cu[S2CN(Me)(CH2CH2OH)]}·CH2Cl2 Jamaludin et al., 2016 ▸), [(Ph3P)2Cu{S2CN(CH2CH2OH)2}]·PPh3 (Jian et al., 2000 ▸), [(Ph3P)2Cu{S2CN(n-Pr)2}]·CH2Cl2 (Xu et al., 2001 ▸), [(Ph3P)2Cu{S2CN(CH2CH2)2S}]·CH2Cl2 (Gupta et al., 2013 ▸), [(Ph3P)2Cu{S2CN(CH2CH2)2NPh}] (Gupta et al., 2013 ▸), [(Ph3P)2Cu{S2CN(Me)CH2Ph}]·CH2Cl2 (Kumar et al., 2009 ▸) and [(Ph3P)2Cu{S2CN(CH2Ph)(CH2py-4)}]·2H2O (Rajput et al., 2012 ▸). Inter­estingly, all but one structure co-crystallizes with another mol­ecule, solvent or otherwise, perhaps indicating inefficient mol­ecular packing for these mol­ecules. The P2S2 donor sets all eight compounds approximate tetra­hedral angles with the range of τ4 values being a low 0.78 in {(Ph3P)2Cu[S2CN(Me)(CH2CH2OH)]}·CH2Cl2 (Jamaludin et al., 2016 ▸) to a high of 0.85 in [(Ph3P)2Cu{S2CN(CH2CH2)2S}]·CH2Cl2 (Gupta et al., 2013 ▸), the narrow range emphasizing the similarity in the mol­ecular structures/geometries.

Synthesis and crystallization

All chemicals and solvents were used as purchased without purification, and all reactions were carried out under ambient conditions. The melting point was determined on a Biobase automatic melting point apparatus MP450. The IR spectrum was obtained on a Perkin Elmer Spectrum 400 FT Mid-IR/Far-IR spectrophotometer from 4000 to 400 cm−1; abbreviations: br, broad; m, medium; s, strong.

Preparation of (I)·CHCl3: tri­phenyl­phosphine (Alfa Aesar, 2 mmol, 0.524 g) in aceto­nitrile (Merck, 10 ml) was added to copper(I) chloride (Sigma Aldrich, 1 mmol, 0.099 g) in aceto­nitrile (10 ml), followed by addition of a dispersion of potassium bis­(2-hy­droxy­eth­yl)di­thio­carbamate (1 mmol, 0.219 g) in aceto­nitrile (15 ml), prepared from the standard procedures (Jamaludin et al., 2016 ▸). The resulting mixture was stirred for 2 h at room temperature. Chloro­form (Merck, 35 ml) was added to the reaction mixture and it was left for slow evaporation at room temperature. Yellow blocks of (I)·CHCl3 were obtained after one day. Yield: 0.699 g (91%). M.p. 423.8–424.5 K. IR (cm−1): 3268 (br) (OH), 1433 (s) (C—N), 1168 (m), 990 (s) (C—S).

Refinement

Crystal data, data collection and structure refinement details are summarized in Table 3 ▸. Carbon-bound H atoms were placed in calculated positions (C—H = 0.95–1.00 Å) and were included in the refinement in the riding-model approximation, with U iso(H) set to 1.2U eq(C). Refinement of the O-bound H atoms proved unstable so these atoms were fixed in the model in the positions revealed by a difference Fourier map, with U iso(H) = 1.5U eq(O). The maximum and minimum residual electron density peaks of 1.97 and 1.93 e Å−3, respectively, were located 0.78 and 0.62 Å from the Cl1 atom. While this feature of the difference map might indicate disorder, additional peaks that might be anti­cipated for the other atoms in the disordered component of chloro­form mol­ecule were not evident. This, plus the observation that the anisotropic displacement parameters of the atoms comprising the chloro­form mol­ecule exhibited no unusual features, suggest the residual electron densities have limited chemical significance. Finally, owing to poor agreement, four reflections, i.e. (326), (15), (666) and (12) , were omitted from the final cycles of refinement.

Table 3

Experimental details

Crystal data
Chemical formula	[Cu(C5H5NO2S2)(C18H15P)2]·CHCl3
M r	887.71
Crystal system, space group	Triclinic, P
Temperature (K)	100
a, b, c (Å)	10.7271 (2), 13.5412 (2), 15.9361 (3)
α, β, γ (°)	67.747 (2), 87.126 (2), 72.826 (2)
V (Å3)	2041.92 (7)
Z	2
Radiation type	Mo Kα
μ (mm−1)	0.95
Crystal size (mm)	0.44 × 0.24 × 0.19
Data collection
Diffractometer	Rigaku SuperNova, Dual Mo at zero, AtlasS2
Absorption correction	Multi-scan (CrysAlis PRO; Rigaku Oxford Diffraction, 2015 ▸)
T min, T max	0.928, 1.000
No. of measured, independent and observed [I > 2σ(I)] reflections	78295, 11363, 10195
R int	0.029
(sin θ/λ)max (Å−1)	0.708
Refinement
R[F 2 > 2σ(F 2)], wR(F 2), S	0.045, 0.117, 1.03
No. of reflections	11363
No. of parameters	478
H-atom treatment	H-atom parameters constrained
Δρmax, Δρmin (e Å−3)	1.97, −1.93

Computer programs: CrysAlis PRO (Rigaku Oxford Diffraction, 2015 ▸), SHELXS (Sheldrick, 2008 ▸), SHELXL2014 (Sheldrick, 2015 ▸), ORTEP-3 for Windows (Farrugia, 2012 ▸), QMol (Gans & Shalloway, 2001 ▸), DIAMOND (Brandenburg, 2006 ▸) and publCIF (Westrip, 2010 ▸).

Crystal structure: contains datablock(s) I, global. DOI: 10.1107/S2056989016017837/hb7632sup1.cif

Structure factors: contains datablock(s) I. DOI: 10.1107/S2056989016017837/hb7632Isup2.hkl

CCDC reference: 1515483

Additional supporting information: crystallographic information; 3D view; checkCIF report

[Cu(C5H5NO2S2)(C18H15P)2]·CHCl3	Z = 2
Mr = 887.71	F(000) = 916
Triclinic, P1	Dx = 1.444 Mg m−3
a = 10.7271 (2) Å	Mo Kα radiation, λ = 0.71073 Å
b = 13.5412 (2) Å	Cell parameters from 38605 reflections
c = 15.9361 (3) Å	θ = 3.1–30.1°
α = 67.747 (2)°	µ = 0.95 mm−1
β = 87.126 (2)°	T = 100 K
γ = 72.826 (2)°	Prism, colourless
V = 2041.92 (7) Å3	0.44 × 0.24 × 0.19 mm

Rigaku SuperNova, Dual Mo at zero, AtlasS2 diffractometer	11363 independent reflections
Radiation source: micro-focus sealed X-ray tube, SuperNova (Mo) X-ray Source	10195 reflections with I > 2σ(I)
Mirror monochromator	Rint = 0.029
Detector resolution: 5.2303 pixels mm-1	θmax = 30.2°, θmin = 2.4°
ω scans	h = −14→14
Absorption correction: multi-scan (CrysAlis PRO; Rigaku Oxford Diffraction, 2015)	k = −19→18
Tmin = 0.928, Tmax = 1.000	l = −22→21
78295 measured reflections

Refinement on F2	0 restraints
Least-squares matrix: full	Hydrogen site location: mixed
R[F2 > 2σ(F2)] = 0.045	H-atom parameters constrained
wR(F2) = 0.117	w = 1/[σ2(Fo2) + (0.0542P)2 + 3.7972P] where P = (Fo2 + 2Fc2)/3
S = 1.03	(Δ/σ)max = 0.002
11363 reflections	Δρmax = 1.97 e Å−3
478 parameters	Δρmin = −1.93 e Å−3

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

	x	y	z	Uiso*/Ueq
Cu	0.36192 (2)	0.77121 (2)	0.71076 (2)	0.01300 (7)
S1	0.19989 (5)	0.72501 (4)	0.81318 (3)	0.01687 (10)
S2	0.18227 (5)	0.94266 (4)	0.66887 (3)	0.01434 (10)
P1	0.51698 (5)	0.80568 (4)	0.77705 (3)	0.01311 (10)
P2	0.40667 (5)	0.66266 (4)	0.62988 (3)	0.01279 (10)
O1	−0.0657 (2)	1.09492 (18)	0.86819 (14)	0.0388 (5)
H1O	−0.0221	1.1248	0.8899	0.058*
O2	−0.0552 (2)	0.89051 (18)	0.99446 (14)	0.0379 (5)
H2O	−0.0317	0.9473	0.9646	0.057*
N1	0.00449 (17)	0.90924 (16)	0.79337 (12)	0.0179 (3)
C1	0.11675 (19)	0.86434 (16)	0.76152 (13)	0.0138 (3)
C2	−0.0662 (2)	1.02862 (19)	0.74859 (15)	0.0222 (4)
H2A	−0.1600	1.0404	0.7600	0.027*
H2B	−0.0588	1.0517	0.6822	0.027*
C3	−0.0154 (3)	1.1018 (2)	0.78121 (17)	0.0274 (5)
H3A	0.0814	1.0761	0.7870	0.033*
H3B	−0.0444	1.1802	0.7370	0.033*
C4	−0.0538 (2)	0.8356 (2)	0.86728 (15)	0.0244 (5)
H4A	−0.0415	0.7655	0.8574	0.029*
H4B	−0.1491	0.8725	0.8635	0.029*
C5	0.0018 (2)	0.8061 (2)	0.96199 (16)	0.0276 (5)
H5A	−0.0136	0.7356	1.0035	0.033*
H5B	0.0974	0.7937	0.9613	0.033*
C11	0.4522 (2)	0.90455 (17)	0.83239 (13)	0.0155 (4)
C12	0.3587 (2)	0.88068 (19)	0.89530 (15)	0.0193 (4)
H12	0.3316	0.8164	0.9064	0.023*
C13	0.3054 (2)	0.9506 (2)	0.94159 (15)	0.0223 (4)
H13	0.2421	0.9338	0.9842	0.027*
C14	0.3446 (2)	1.0450 (2)	0.92569 (16)	0.0239 (4)
H14	0.3080	1.0928	0.9572	0.029*
C15	0.4374 (3)	1.0687 (2)	0.86363 (16)	0.0264 (5)
H15	0.4645	1.1330	0.8528	0.032*
C16	0.4912 (2)	0.99887 (18)	0.81703 (15)	0.0214 (4)
H16	0.5547	1.0158	0.7746	0.026*
C21	0.6312 (2)	0.86383 (16)	0.69950 (13)	0.0140 (3)
C22	0.5816 (2)	0.96097 (17)	0.62185 (14)	0.0186 (4)
H22	0.4900	0.9973	0.6120	0.022*
C23	0.6653 (2)	1.00436 (18)	0.55932 (15)	0.0221 (4)
H23	0.6308	1.0706	0.5072	0.027*
C24	0.7997 (2)	0.95133 (19)	0.57246 (15)	0.0212 (4)
H24	0.8568	0.9818	0.5298	0.025*
C25	0.8497 (2)	0.85403 (19)	0.64806 (14)	0.0196 (4)
H25	0.9411	0.8171	0.6568	0.024*
C26	0.7660 (2)	0.81042 (18)	0.71115 (14)	0.0169 (4)
H26	0.8009	0.7436	0.7627	0.020*
C31	0.6275 (2)	0.68849 (17)	0.86749 (13)	0.0162 (4)
C32	0.6884 (2)	0.70275 (19)	0.93539 (15)	0.0218 (4)
H32	0.6666	0.7743	0.9389	0.026*
C33	0.7811 (2)	0.6126 (2)	0.99804 (16)	0.0268 (5)
H33	0.8220	0.6228	1.0444	0.032*
C34	0.8138 (3)	0.5084 (2)	0.99318 (17)	0.0300 (5)
H34	0.8781	0.4474	1.0356	0.036*
C35	0.7531 (3)	0.4929 (2)	0.9266 (2)	0.0347 (6)
H35	0.7752	0.4211	0.9236	0.042*
C36	0.6593 (2)	0.58267 (19)	0.86396 (18)	0.0267 (5)
H36	0.6170	0.5716	0.8187	0.032*
C41	0.48854 (19)	0.51623 (16)	0.69995 (14)	0.0156 (4)
C42	0.5952 (2)	0.45035 (19)	0.67222 (16)	0.0220 (4)
H42	0.6255	0.4805	0.6136	0.026*
C43	0.6577 (2)	0.3406 (2)	0.73001 (18)	0.0272 (5)
H43	0.7300	0.2961	0.7105	0.033*
C44	0.6151 (2)	0.29608 (19)	0.81547 (18)	0.0273 (5)
H44	0.6593	0.2219	0.8552	0.033*
C45	0.5079 (3)	0.3600 (2)	0.84291 (17)	0.0273 (5)
H45	0.4773	0.3288	0.9012	0.033*
C46	0.4446 (2)	0.46945 (18)	0.78592 (16)	0.0223 (4)
H46	0.3711	0.5127	0.8055	0.027*
C51	0.26885 (19)	0.65508 (16)	0.57220 (13)	0.0135 (3)
C52	0.2709 (2)	0.55962 (17)	0.55691 (14)	0.0169 (4)
H52	0.3427	0.4937	0.5812	0.020*
C53	0.1684 (2)	0.56083 (18)	0.50627 (15)	0.0196 (4)
H53	0.1702	0.4958	0.4960	0.024*
C54	0.0630 (2)	0.65717 (19)	0.47064 (15)	0.0207 (4)
H54	−0.0067	0.6581	0.4355	0.025*
C55	0.0595 (2)	0.75232 (18)	0.48645 (15)	0.0192 (4)
H55	−0.0125	0.8181	0.4622	0.023*
C56	0.16193 (19)	0.75072 (17)	0.53791 (14)	0.0158 (4)
H56	0.1588	0.8151	0.5496	0.019*
C61	0.51483 (19)	0.69669 (16)	0.53792 (14)	0.0150 (4)
C62	0.4884 (2)	0.70661 (17)	0.44993 (14)	0.0179 (4)
H62	0.4136	0.6900	0.4363	0.021*
C63	0.5711 (2)	0.74078 (18)	0.38150 (16)	0.0225 (4)
H63	0.5526	0.7468	0.3218	0.027*
C64	0.6801 (2)	0.7659 (2)	0.40050 (18)	0.0266 (5)
H64	0.7356	0.7901	0.3538	0.032*
C65	0.7076 (2)	0.7553 (2)	0.4883 (2)	0.0295 (5)
H65	0.7827	0.7716	0.5018	0.035*
C66	0.6258 (2)	0.7211 (2)	0.55654 (17)	0.0237 (5)
H66	0.6454	0.7141	0.6164	0.028*
C6	0.0552 (3)	0.4509 (2)	0.7262 (2)	0.0354 (6)
H6	0.0901	0.4682	0.6646	0.042*
Cl1	0.14649 (11)	0.31507 (7)	0.79474 (7)	0.0593 (3)
Cl2	−0.10822 (9)	0.46142 (12)	0.71310 (9)	0.0740 (4)
Cl3	0.07466 (6)	0.55046 (5)	0.76719 (4)	0.03169 (13)

	U11	U22	U33	U12	U13	U23
Cu	0.01265 (12)	0.01232 (11)	0.01406 (12)	−0.00179 (8)	0.00184 (8)	−0.00664 (9)
S1	0.0200 (2)	0.0124 (2)	0.0169 (2)	−0.00543 (18)	0.00520 (18)	−0.00421 (17)
S2	0.0153 (2)	0.0118 (2)	0.0124 (2)	−0.00113 (16)	0.00266 (16)	−0.00311 (16)
P1	0.0136 (2)	0.0124 (2)	0.0123 (2)	−0.00270 (17)	0.00066 (17)	−0.00431 (17)
P2	0.0117 (2)	0.0117 (2)	0.0150 (2)	−0.00122 (17)	0.00111 (17)	−0.00678 (18)
O1	0.0411 (11)	0.0450 (12)	0.0303 (10)	0.0017 (9)	0.0000 (8)	−0.0252 (9)
O2	0.0432 (11)	0.0421 (11)	0.0300 (10)	−0.0052 (9)	0.0066 (8)	−0.0216 (9)
N1	0.0131 (8)	0.0227 (9)	0.0159 (8)	−0.0025 (7)	0.0033 (6)	−0.0078 (7)
C1	0.0134 (8)	0.0163 (9)	0.0125 (8)	−0.0043 (7)	0.0015 (7)	−0.0065 (7)
C2	0.0161 (9)	0.0255 (11)	0.0198 (10)	0.0043 (8)	−0.0011 (8)	−0.0107 (8)
C3	0.0300 (12)	0.0218 (11)	0.0257 (11)	0.0060 (9)	−0.0041 (9)	−0.0136 (9)
C4	0.0171 (10)	0.0363 (13)	0.0199 (10)	−0.0105 (9)	0.0076 (8)	−0.0097 (9)
C5	0.0244 (11)	0.0366 (13)	0.0182 (10)	−0.0062 (10)	0.0046 (8)	−0.0090 (9)
C11	0.0166 (9)	0.0161 (9)	0.0135 (9)	−0.0027 (7)	−0.0002 (7)	−0.0069 (7)
C12	0.0188 (10)	0.0219 (10)	0.0200 (10)	−0.0076 (8)	0.0039 (8)	−0.0103 (8)
C13	0.0220 (10)	0.0269 (11)	0.0194 (10)	−0.0055 (9)	0.0044 (8)	−0.0119 (9)
C14	0.0300 (12)	0.0234 (11)	0.0194 (10)	−0.0039 (9)	0.0027 (9)	−0.0126 (9)
C15	0.0400 (13)	0.0209 (10)	0.0233 (11)	−0.0130 (10)	0.0068 (10)	−0.0117 (9)
C16	0.0284 (11)	0.0194 (10)	0.0190 (10)	−0.0094 (8)	0.0055 (8)	−0.0090 (8)
C21	0.0178 (9)	0.0127 (8)	0.0120 (8)	−0.0049 (7)	0.0004 (7)	−0.0050 (7)
C22	0.0230 (10)	0.0134 (9)	0.0152 (9)	−0.0008 (7)	0.0012 (8)	−0.0046 (7)
C23	0.0335 (12)	0.0135 (9)	0.0153 (9)	−0.0054 (8)	0.0040 (8)	−0.0025 (7)
C24	0.0311 (11)	0.0200 (10)	0.0169 (10)	−0.0132 (9)	0.0084 (8)	−0.0083 (8)
C25	0.0191 (10)	0.0245 (10)	0.0171 (9)	−0.0087 (8)	0.0029 (8)	−0.0085 (8)
C26	0.0167 (9)	0.0187 (9)	0.0137 (9)	−0.0050 (7)	0.0002 (7)	−0.0047 (7)
C31	0.0153 (9)	0.0159 (9)	0.0132 (9)	−0.0052 (7)	0.0003 (7)	−0.0006 (7)
C32	0.0241 (11)	0.0226 (10)	0.0153 (9)	−0.0067 (8)	−0.0009 (8)	−0.0035 (8)
C33	0.0274 (12)	0.0311 (12)	0.0164 (10)	−0.0105 (10)	−0.0048 (8)	−0.0009 (9)
C34	0.0268 (12)	0.0241 (11)	0.0247 (12)	−0.0076 (9)	−0.0063 (9)	0.0073 (9)
C35	0.0373 (14)	0.0151 (10)	0.0410 (15)	−0.0023 (10)	−0.0130 (12)	−0.0012 (10)
C36	0.0292 (12)	0.0164 (10)	0.0299 (12)	−0.0050 (9)	−0.0087 (9)	−0.0038 (9)
C41	0.0146 (9)	0.0137 (8)	0.0183 (9)	−0.0020 (7)	−0.0018 (7)	−0.0072 (7)
C42	0.0199 (10)	0.0190 (10)	0.0232 (11)	0.0006 (8)	0.0000 (8)	−0.0085 (8)
C43	0.0213 (11)	0.0186 (10)	0.0339 (13)	0.0049 (8)	−0.0025 (9)	−0.0093 (9)
C44	0.0259 (11)	0.0158 (10)	0.0322 (12)	−0.0018 (8)	−0.0085 (9)	−0.0027 (9)
C45	0.0308 (12)	0.0188 (10)	0.0263 (12)	−0.0079 (9)	0.0009 (9)	−0.0017 (9)
C46	0.0218 (10)	0.0170 (10)	0.0249 (11)	−0.0042 (8)	0.0041 (8)	−0.0062 (8)
C51	0.0126 (8)	0.0146 (8)	0.0125 (8)	−0.0039 (7)	0.0032 (6)	−0.0049 (7)
C52	0.0156 (9)	0.0154 (9)	0.0198 (9)	−0.0023 (7)	0.0013 (7)	−0.0083 (7)
C53	0.0198 (10)	0.0201 (10)	0.0227 (10)	−0.0072 (8)	0.0031 (8)	−0.0116 (8)
C54	0.0156 (9)	0.0260 (11)	0.0214 (10)	−0.0068 (8)	0.0002 (8)	−0.0096 (8)
C55	0.0138 (9)	0.0177 (9)	0.0219 (10)	−0.0013 (7)	−0.0002 (7)	−0.0054 (8)
C56	0.0143 (9)	0.0137 (9)	0.0186 (9)	−0.0030 (7)	0.0035 (7)	−0.0064 (7)
C61	0.0131 (8)	0.0117 (8)	0.0209 (9)	−0.0018 (7)	0.0043 (7)	−0.0087 (7)
C62	0.0174 (9)	0.0152 (9)	0.0195 (10)	−0.0038 (7)	0.0037 (7)	−0.0060 (7)
C63	0.0245 (11)	0.0178 (10)	0.0205 (10)	−0.0044 (8)	0.0066 (8)	−0.0043 (8)
C64	0.0239 (11)	0.0217 (11)	0.0373 (13)	−0.0098 (9)	0.0165 (10)	−0.0142 (10)
C65	0.0198 (11)	0.0349 (13)	0.0484 (15)	−0.0146 (10)	0.0147 (10)	−0.0284 (12)
C66	0.0177 (10)	0.0309 (12)	0.0332 (12)	−0.0088 (9)	0.0075 (9)	−0.0231 (10)
C6	0.0351 (14)	0.0380 (14)	0.0356 (14)	−0.0135 (12)	−0.0031 (11)	−0.0143 (12)
Cl1	0.0739 (6)	0.0376 (4)	0.0688 (6)	−0.0043 (4)	−0.0159 (5)	−0.0297 (4)
Cl2	0.0320 (4)	0.1170 (9)	0.1089 (9)	−0.0168 (5)	−0.0041 (5)	−0.0847 (8)
Cl3	0.0340 (3)	0.0258 (3)	0.0323 (3)	−0.0095 (2)	−0.0041 (2)	−0.0067 (2)

Cu—P2	2.2380 (5)	C26—H26	0.9500
Cu—P1	2.2602 (6)	C31—C32	1.392 (3)
Cu—S1	2.3791 (6)	C31—C36	1.394 (3)
Cu—S2	2.4213 (5)	C32—C33	1.391 (3)
S1—C1	1.714 (2)	C32—H32	0.9500
S2—C1	1.717 (2)	C33—C34	1.381 (4)
P1—C31	1.824 (2)	C33—H33	0.9500
P1—C21	1.825 (2)	C34—C35	1.383 (4)
P1—C11	1.827 (2)	C34—H34	0.9500
P2—C51	1.827 (2)	C35—C36	1.395 (3)
P2—C61	1.828 (2)	C35—H35	0.9500
P2—C41	1.828 (2)	C36—H36	0.9500
O1—C3	1.442 (3)	C41—C42	1.395 (3)
O1—H1O	0.8576	C41—C46	1.398 (3)
O2—C5	1.397 (3)	C42—C43	1.394 (3)
O2—H2O	0.8400	C42—H42	0.9500
N1—C1	1.348 (3)	C43—C44	1.380 (4)
N1—C2	1.468 (3)	C43—H43	0.9500
N1—C4	1.476 (3)	C44—C45	1.382 (4)
C2—C3	1.513 (3)	C44—H44	0.9500
C2—H2A	0.9900	C45—C46	1.390 (3)
C2—H2B	0.9900	C45—H45	0.9500
C3—H3A	0.9900	C46—H46	0.9500
C3—H3B	0.9900	C51—C56	1.393 (3)
C4—C5	1.512 (3)	C51—C52	1.397 (3)
C4—H4A	0.9900	C52—C53	1.389 (3)
C4—H4B	0.9900	C52—H52	0.9500
C5—H5A	0.9900	C53—C54	1.391 (3)
C5—H5B	0.9900	C53—H53	0.9500
C11—C16	1.391 (3)	C54—C55	1.393 (3)
C11—C12	1.400 (3)	C54—H54	0.9500
C12—C13	1.391 (3)	C55—C56	1.394 (3)
C12—H12	0.9500	C55—H55	0.9500
C13—C14	1.391 (3)	C56—H56	0.9500
C13—H13	0.9500	C61—C62	1.393 (3)
C14—C15	1.386 (3)	C61—C66	1.398 (3)
C14—H14	0.9500	C62—C63	1.397 (3)
C15—C16	1.395 (3)	C62—H62	0.9500
C15—H15	0.9500	C63—C64	1.387 (3)
C16—H16	0.9500	C63—H63	0.9500
C21—C26	1.399 (3)	C64—C65	1.390 (4)
C21—C22	1.402 (3)	C64—H64	0.9500
C22—C23	1.386 (3)	C65—C66	1.389 (3)
C22—H22	0.9500	C65—H65	0.9500
C23—C24	1.394 (3)	C66—H66	0.9500
C23—H23	0.9500	C6—Cl2	1.733 (3)
C24—C25	1.386 (3)	C6—Cl1	1.748 (3)
C24—H24	0.9500	C6—Cl3	1.771 (3)
C25—C26	1.392 (3)	C6—H6	1.0000
C25—H25	0.9500
P2—Cu—P1	123.65 (2)	C24—C25—H25	120.0
P2—Cu—S1	109.81 (2)	C26—C25—H25	120.0
P1—Cu—S1	110.96 (2)	C25—C26—C21	120.80 (19)
P2—Cu—S2	123.17 (2)	C25—C26—H26	119.6
P1—Cu—S2	103.74 (2)	C21—C26—H26	119.6
S1—Cu—S2	75.264 (18)	C32—C31—C36	119.2 (2)
C1—S1—Cu	84.12 (7)	C32—C31—P1	122.25 (16)
C1—S2—Cu	82.75 (7)	C36—C31—P1	118.39 (16)
C31—P1—C21	101.95 (9)	C33—C32—C31	120.2 (2)
C31—P1—C11	101.78 (9)	C33—C32—H32	119.9
C21—P1—C11	104.44 (9)	C31—C32—H32	119.9
C31—P1—Cu	118.06 (7)	C34—C33—C32	120.3 (2)
C21—P1—Cu	114.57 (7)	C34—C33—H33	119.9
C11—P1—Cu	114.16 (7)	C32—C33—H33	119.9
C51—P2—C61	102.10 (9)	C33—C34—C35	120.0 (2)
C51—P2—C41	103.13 (9)	C33—C34—H34	120.0
C61—P2—C41	103.77 (9)	C35—C34—H34	120.0
C51—P2—Cu	117.50 (6)	C34—C35—C36	120.0 (2)
C61—P2—Cu	116.28 (7)	C34—C35—H35	120.0
C41—P2—Cu	112.27 (7)	C36—C35—H35	120.0
C3—O1—H1O	105.7	C31—C36—C35	120.2 (2)
C5—O2—H2O	109.4	C31—C36—H36	119.9
C1—N1—C2	120.12 (18)	C35—C36—H36	119.9
C1—N1—C4	119.48 (18)	C42—C41—C46	118.73 (19)
C2—N1—C4	120.09 (18)	C42—C41—P2	122.71 (17)
N1—C1—S1	120.50 (15)	C46—C41—P2	118.53 (16)
N1—C1—S2	122.12 (15)	C41—C42—C43	120.4 (2)
S1—C1—S2	117.38 (11)	C41—C42—H42	119.8
N1—C2—C3	113.01 (18)	C43—C42—H42	119.8
N1—C2—H2A	109.0	C44—C43—C42	120.3 (2)
C3—C2—H2A	109.0	C44—C43—H43	119.8
N1—C2—H2B	109.0	C42—C43—H43	119.8
C3—C2—H2B	109.0	C43—C44—C45	119.7 (2)
H2A—C2—H2B	107.8	C43—C44—H44	120.1
O1—C3—C2	108.3 (2)	C45—C44—H44	120.1
O1—C3—H3A	110.0	C44—C45—C46	120.5 (2)
C2—C3—H3A	110.0	C44—C45—H45	119.7
O1—C3—H3B	110.0	C46—C45—H45	119.7
C2—C3—H3B	110.0	C45—C46—C41	120.3 (2)
H3A—C3—H3B	108.4	C45—C46—H46	119.8
N1—C4—C5	114.9 (2)	C41—C46—H46	119.8
N1—C4—H4A	108.5	C56—C51—C52	119.51 (18)
C5—C4—H4A	108.5	C56—C51—P2	118.08 (15)
N1—C4—H4B	108.5	C52—C51—P2	122.29 (15)
C5—C4—H4B	108.5	C53—C52—C51	120.22 (19)
H4A—C4—H4B	107.5	C53—C52—H52	119.9
O2—C5—C4	111.6 (2)	C51—C52—H52	119.9
O2—C5—H5A	109.3	C52—C53—C54	120.1 (2)
C4—C5—H5A	109.3	C52—C53—H53	119.9
O2—C5—H5B	109.3	C54—C53—H53	119.9
C4—C5—H5B	109.3	C53—C54—C55	120.0 (2)
H5A—C5—H5B	108.0	C53—C54—H54	120.0
C16—C11—C12	119.11 (19)	C55—C54—H54	120.0
C16—C11—P1	124.41 (16)	C54—C55—C56	119.85 (19)
C12—C11—P1	116.47 (16)	C54—C55—H55	120.1
C13—C12—C11	120.4 (2)	C56—C55—H55	120.1
C13—C12—H12	119.8	C51—C56—C55	120.29 (19)
C11—C12—H12	119.8	C51—C56—H56	119.9
C14—C13—C12	120.2 (2)	C55—C56—H56	119.9
C14—C13—H13	119.9	C62—C61—C66	118.8 (2)
C12—C13—H13	119.9	C62—C61—P2	123.81 (16)
C15—C14—C13	119.6 (2)	C66—C61—P2	117.29 (16)
C15—C14—H14	120.2	C61—C62—C63	120.5 (2)
C13—C14—H14	120.2	C61—C62—H62	119.7
C14—C15—C16	120.4 (2)	C63—C62—H62	119.7
C14—C15—H15	119.8	C64—C63—C62	120.2 (2)
C16—C15—H15	119.8	C64—C63—H63	119.9
C11—C16—C15	120.3 (2)	C62—C63—H63	119.9
C11—C16—H16	119.9	C63—C64—C65	119.6 (2)
C15—C16—H16	119.9	C63—C64—H64	120.2
C26—C21—C22	118.63 (19)	C65—C64—H64	120.2
C26—C21—P1	122.28 (15)	C66—C65—C64	120.3 (2)
C22—C21—P1	118.91 (16)	C66—C65—H65	119.8
C23—C22—C21	120.4 (2)	C64—C65—H65	119.8
C23—C22—H22	119.8	C65—C66—C61	120.6 (2)
C21—C22—H22	119.8	C65—C66—H66	119.7
C22—C23—C24	120.4 (2)	C61—C66—H66	119.7
C22—C23—H23	119.8	Cl2—C6—Cl1	111.63 (17)
C24—C23—H23	119.8	Cl2—C6—Cl3	111.63 (17)
C25—C24—C23	119.7 (2)	Cl1—C6—Cl3	111.60 (15)
C25—C24—H24	120.1	Cl2—C6—H6	107.2
C23—C24—H24	120.1	Cl1—C6—H6	107.2
C24—C25—C26	120.0 (2)	Cl3—C6—H6	107.2
C2—N1—C1—S1	−179.88 (15)	P1—C31—C32—C33	−174.02 (18)
C4—N1—C1—S1	−6.2 (3)	C31—C32—C33—C34	0.3 (4)
C2—N1—C1—S2	0.1 (3)	C32—C33—C34—C35	−0.9 (4)
C4—N1—C1—S2	173.79 (16)	C33—C34—C35—C36	0.4 (4)
Cu—S1—C1—N1	−173.40 (17)	C32—C31—C36—C35	−1.3 (4)
Cu—S1—C1—S2	6.57 (10)	P1—C31—C36—C35	173.7 (2)
Cu—S2—C1—N1	173.49 (17)	C34—C35—C36—C31	0.7 (4)
Cu—S2—C1—S1	−6.48 (10)	C51—P2—C41—C42	96.01 (19)
C1—N1—C2—C3	−84.6 (2)	C61—P2—C41—C42	−10.2 (2)
C4—N1—C2—C3	101.8 (2)	Cu—P2—C41—C42	−136.55 (17)
N1—C2—C3—O1	−77.9 (2)	C51—P2—C41—C46	−85.86 (18)
C1—N1—C4—C5	83.8 (3)	C61—P2—C41—C46	167.95 (17)
C2—N1—C4—C5	−102.5 (2)	Cu—P2—C41—C46	41.58 (19)
N1—C4—C5—O2	82.1 (3)	C46—C41—C42—C43	−1.0 (3)
C31—P1—C11—C16	103.55 (19)	P2—C41—C42—C43	177.13 (18)
C21—P1—C11—C16	−2.2 (2)	C41—C42—C43—C44	−0.3 (4)
Cu—P1—C11—C16	−128.12 (17)	C42—C43—C44—C45	1.6 (4)
C31—P1—C11—C12	−75.31 (18)	C43—C44—C45—C46	−1.4 (4)
C21—P1—C11—C12	178.89 (16)	C44—C45—C46—C41	0.1 (4)
Cu—P1—C11—C12	53.01 (17)	C42—C41—C46—C45	1.1 (3)
C16—C11—C12—C13	0.2 (3)	P2—C41—C46—C45	−177.09 (19)
P1—C11—C12—C13	179.10 (17)	C61—P2—C51—C56	−94.07 (16)
C11—C12—C13—C14	0.0 (3)	C41—P2—C51—C56	158.48 (16)
C12—C13—C14—C15	−0.2 (4)	Cu—P2—C51—C56	34.40 (18)
C13—C14—C15—C16	0.2 (4)	C61—P2—C51—C52	82.03 (18)
C12—C11—C16—C15	−0.2 (3)	C41—P2—C51—C52	−25.42 (19)
P1—C11—C16—C15	−179.03 (18)	Cu—P2—C51—C52	−149.50 (15)
C14—C15—C16—C11	0.0 (4)	C56—C51—C52—C53	1.3 (3)
C31—P1—C21—C26	8.01 (19)	P2—C51—C52—C53	−174.71 (16)
C11—P1—C21—C26	113.67 (18)	C51—C52—C53—C54	−0.1 (3)
Cu—P1—C21—C26	−120.71 (16)	C52—C53—C54—C55	−0.6 (3)
C31—P1—C21—C22	−176.85 (16)	C53—C54—C55—C56	0.1 (3)
C11—P1—C21—C22	−71.19 (18)	C52—C51—C56—C55	−1.9 (3)
Cu—P1—C21—C22	54.43 (17)	P2—C51—C56—C55	174.34 (16)
C26—C21—C22—C23	−1.6 (3)	C54—C55—C56—C51	1.2 (3)
P1—C21—C22—C23	−176.94 (17)	C51—P2—C61—C62	−2.56 (19)
C21—C22—C23—C24	0.6 (3)	C41—P2—C61—C62	104.40 (18)
C22—C23—C24—C25	0.6 (3)	Cu—P2—C61—C62	−131.80 (16)
C23—C24—C25—C26	−0.9 (3)	C51—P2—C61—C66	173.12 (17)
C24—C25—C26—C21	−0.2 (3)	C41—P2—C61—C66	−79.91 (18)
C22—C21—C26—C25	1.4 (3)	Cu—P2—C61—C66	43.89 (18)
P1—C21—C26—C25	176.57 (16)	C66—C61—C62—C63	−0.3 (3)
C21—P1—C31—C32	79.67 (19)	P2—C61—C62—C63	175.35 (16)
C11—P1—C31—C32	−28.1 (2)	C61—C62—C63—C64	−0.4 (3)
Cu—P1—C31—C32	−153.85 (16)	C62—C63—C64—C65	0.9 (3)
C21—P1—C31—C36	−95.22 (19)	C63—C64—C65—C66	−0.7 (4)
C11—P1—C31—C36	157.05 (19)	C64—C65—C66—C61	0.0 (4)
Cu—P1—C31—C36	31.3 (2)	C62—C61—C66—C65	0.5 (3)
C36—C31—C32—C33	0.8 (3)	P2—C61—C66—C65	−175.44 (18)

D—H···A	D—H	H···A	D···A	D—H···A
O2—H2O···O1	0.84	1.95	2.710 (3)	150
O1—H1O···O2i	0.86	1.97	2.697 (3)	142
C6—Cl3···Cg1	1.77 (1)	3.81 (1)	3.798 (3)	76 (1)