(η6-Benzene){2-[2-(tert-butyl­sulfan­yl)phenyl]pyridine-κ2N,S}chlorido­ruthenium(II) hexa­fluorido­phosphate

Hirotsu, M.; Yogi, A.; Kinoshita, I.

doi:10.1107/S1600536810049810

metal-organic compounds

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ISSN: 2056-9890

Volume 67| Part 1| January 2011| Page m63

https://doi.org/10.1107/S1600536810049810

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(η⁶-Benzene){2-[2-(tert-butylsulfanyl)phenyl]pyridine-κ²N,S}chloridoruthenium(II) hexafluoridophosphate

Masakazu Hirotsu,^a ^* Akira Yogi ^a and Isamu Kinoshita ^a

^aGraduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan
^*Correspondence e-mail: mhiro@sci.osaka-cu.ac.jp

(Received 10 November 2010; accepted 29 November 2010; online 11 December 2010)

In the title compound, [RuCl(C₆H₆)(C₁₅H₁₇NS)]PF₆, the cation adopts a three-legged piano-stool structure around the Ru(II) atom with an η⁶-benzene ligand, a chloride ligand and a 2-[2-(tert-butylsulfanyl)phenyl]pyridine (btppy) ligand. The btppy ligand acts as a N,S-bidentate ligand, forming a six-membered ring, which has an envelope conformation. The S—Ru—N bite angle is 86.76 (9)°, and the dihedral angle between the pyridine and benzene rings in btppy is 39.8 (2)°. The unit cell contains two pairs of racemic diastereomers with (S_Ru,S_S) and (R_Ru,R_S) configurations, in which the tert-butyl group on the coordinated S atom is distant from the η⁶-benzene ligand.

Related literature

For general background to the use of chiral N,S-bidentate ligands in asymmetric allylic substitution reactions, see: Mellah et al. (2007 ). For the synthesis of 2-(2′-(tert-butylthio)phenyl)pyridine, see: Clavier et al. (2003 ). For related structures, see: Shibue et al. (2008 ); Sau et al. (2010 ).

Experimental

Crystal data

[RuCl(C₆H₆)(C₁₅H₁₇NS)]PF₆
M_r = 602.97
Monoclinic, C c
a = 16.638 (4) Å
b = 10.5589 (19) Å
c = 14.327 (3) Å
β = 110.758 (4)°
V = 2353.6 (8) Å³
Z = 4
Mo Kα radiation
μ = 0.99 mm⁻¹
T = 193 K
0.24 × 0.17 × 0.09 mm

Data collection

Rigaku Mercury diffractometer
Absorption correction: multi-scan (REQAB; Jacobson, 1998 ) T_min = 0.725, T_max = 0.914
11123 measured reflections
4474 independent reflections
4165 reflections with I > 2σ(I)
R_int = 0.034

Refinement

R[F² > 2σ(F²)] = 0.037
wR(F²) = 0.078
S = 1.03
4474 reflections
291 parameters
2 restraints
H-atom parameters constrained
Δρ_max = 0.52 e Å⁻³
Δρ_min = −0.39 e Å⁻³
Absolute structure: Flack (1983 ), 1824 Friedel pairs
Flack parameter: 0.03 (3)

Table 1
Selected geometric parameters (Å, °)

Ru1—Cl1	2.3970 (14)
Ru1—S1	2.3671 (10)
Ru1—N1	2.122 (3)
Ru1—C16	2.183 (6)
Ru1—C17	2.187 (6)
Ru1—C18	2.178 (6)
Ru1—C19	2.199 (6)
Ru1—C20	2.172 (7)
Ru1—C21	2.161 (5)

Cl1—Ru1—S1	93.84 (4)
Cl1—Ru1—N1	86.89 (14)
S1—Ru1—N1	86.76 (9)
Ru1—S1—C11	98.00 (15)
Ru1—S1—C12	123.42 (13)
C11—S1—C12	106.9 (2)
Ru1—N1—C1	116.1 (3)
Ru1—N1—C5	125.4 (3)

Data collection: CrystalClear (Rigaku, 1999 ); cell refinement: CrystalClear; data reduction: CrystalStructure (Rigaku/MSC, 2006 ); program(s) used to solve structure: SIR97 (Altomare et al., 1999 ); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008 ); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997 ); software used to prepare material for publication: CrystalStructure.

Supporting information

Crystal structure: contains datablocks global, I. DOI: https://doi.org/10.1107/S1600536810049810/fj2364sup1.cif

Structure factors: contains datablock I. DOI: https://doi.org/10.1107/S1600536810049810/fj2364Isup2.hkl

checkCIF report

Comment top

Coordination of bidentate ligands bearing thioether sulfur atoms generates chirality at the sulfur center. The chirality of the coordinated S atoms in catalysts would be important in improving enantioselectivities for asymmetric reactions. A variety of chiral N,S-bidentate ligands have been developed and used for asymmetric allylic substitution reactions (Mellah et al., 2007). We previously reported the structurally characterized ruthenium(II) arene complex with 4-(2'-pyridyl)dibenzothiophene (PyDBT), [RuCl(PyDBT)(η⁶-C₆H₆)]CF₃SO₃ (Shibue et al., 2008). In this complex, PyDBT acts as a N,S-bidentate ligand to form chiral centers at Ru and S atoms. The pyridine and dibenzothiophene planes in PyDBT are twisted with respect to each other, and the dibenzothiophene moiety is in close proximity to the η⁶-benzene ligand. To clarify the steric interactions around the coordinated S atom, we present here the crystal structure of the title ruthenium(II) arene complex of 2-(2'-(t-butylthio)phenyl)pyridine (btppy).

The asymmetric unit of the title compound (I) consists of a [RuCl(btppy)(η⁶-C₆H₆)]⁺ cation and a hexafluorophosphate anion (Fig. 1). The Ru center of the complex cation is surrounded by a benzene, a btppy and a chloride ligand to form a three-legged piano-stool structure. The btppy ligand acts as a N,S-bidentate ligand to form a six-membered ring. The chelate ring adopts an envelope conformation, which is similar to that in the previously reported ruthenium(II) complex [RuCl(PyDBT)(η⁶-C₆H₆)]CF₃SO₃, (II) (Shibue et al., 2008). The S—Ru—N bite angle (86.76 (9)°) is larger than that of (II) (79.20 (7)°, 80.00 (7)°, two independent molecules), which is due to the longer C—S bond in the btppy chelate ring (1.820 (5) Å) compared with the PyDBT chelate ring in (II) (C—S = 1.762 (5), 1.760 (4) Å). The Ru—S (2.3671 (10) Å) and Ru—N (2.122 (3) Å) bond lengths in (I) are slightly shorter than those in (II) (Ru—S, 2.3821 (9), 2.3901 (8) Å; Ru—N, 2.161 (3), 2.164 (3) Å), indicating the higher coordinating ability of btppy. The dihedral angle between the pyridine and benzene rings in btppy (39.8 (2)°) is similar to that in PyDBT of (II) (37.7 (2)°).

There are two pair of racemic diastereomers with (S_Ru, S_S) and (R_Ru, R_S) configurations in the unit cell. The t-butyl group on the coordinated S atom is placed far from the η⁶-benzene ligand. An average Ru—C distance of 2.180 (6) Å in (I) is comparable to that in (II) (2.192 (4), 2.180 (4) Å). The Cl—Ru—S angle (93.84 (4)°) in (I) is larger than that in (II) (82.84 (3)°, 84.87 (3)°), and no significant interaction was observed between the t-butyl group and the chloro ligand. Molecular modeling analysis suggests that the other diastereomers with configurations of (S_Ru, R_S) and (R_Ru, S_S) cause a severe repulsive interaction between the t-butyl group and the benzene ligand. The ¹H NMR spectrum of (I) in CDCl₃ revealed the presence of a single diastereomer. This suggests that the (S_Ru, S_S) and (R_Ru, R_S) isomers observed in the crystal are retained in solution. Similar stereoselectivity was recently reported for the iridium(III) complex [(η⁵-C₅Me₅)Ir(η²-ppy-S-p-tol)(H₂O)](OTf)₂ (Sau et al., 2010), in which the structure of the chelate ring is analogous to that for btppy in (I).

Related literature top

For general background to the use of chiral N,S-bidentate ligands in asymmetric allylic substitution reactions, see: Mellah et al. (2007). For the synthesis of 2-(2'-(tert-butylthio)phenyl)pyridine, see: Clavier et al. (2003). For related structures, see: Shibue et al. (2008); Sau et al. (2010).

Experimental top

The btppy ligand was prepared according to a literature procedure (Clavier et al., 2003). For the synthesis of the title compound (I), [RuCl₂(C₆H₆)]₂ (51 mg, 0.10 mmol) was added to a deoxygenated solution of btppy (50 mg, 0.21 mmol) in methanol (10 ml). The reaction mixture was refluxed for 6 h under an argon atmosphere. After cooling to room temperature, KPF₆ (60 mg, 0.33 mmol) was added. The resulting orange solution was concentrated under reduced pressure. The residue was dissolved in chloroform (10 ml), and the insoluble white solid was removed by filtration. The filtrate was concentrated under reduced pressure, and the resulting brown residue was recrystallized by vapor diffusion of diethyl ether into a dichloromethane solution to afford yellow crystals (19 mg, 15%). Anal. Calcd for C₂₁H₂₃ClF₆NPRuS: C, 41.83; H, 3.84; N, 2.32%. Found: C, 41.78; H, 3.82; N, 2.35%. ¹H NMR (300 MHz, CDCl₃): δ 1.00 (s, 9H, t-Bu), 5.62 (s, 6H, C₆H₆), 7.51 (ddd, J = 7.5, 6.0, 1.4 Hz, 1H), 7.62 (td, J = 7.6, 1.2 Hz, 1H), 7.77 (td, J = 7.7, 1.2 Hz, 1H), 7.82 (dd, J = 7.9, 1.0 Hz, 1H), 7.84 (dd, J = 7.6, 1.2 Hz, 1H), 8.02 (m, 2H), 9.39 (dd, J = 5.9, 1.2 Hz, 1H).

Structure description top

Computing details top

Data collection: CrystalClear (Rigaku, 1999); cell refinement: CrystalClear (Rigaku, 1999); data reduction: CrystalStructure (Rigaku/MSC, 2006); program(s) used to solve structure: SIR97 (Altomare et al., 1999); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997); software used to prepare material for publication: CrystalStructure (Rigaku/MSC, 2006).

Figures top

Fig. 1. The molecular structure of (I) with numbering scheme. Displacement ellipsoids are drawn at the 40% probability level.

(η⁶-Benzene){2-[2-(tert-butylsulfanyl)phenyl]pyridine- κ²N,S}chloridoruthenium(II) hexafluoridophosphate top

Crystal data top

[RuCl(C₆H₆)(C₁₅H₁₇NS)]PF₆	F(000) = 1208.00
M_r = 602.97	D_x = 1.702 Mg m⁻³
Monoclinic, Cc	Mo Kα radiation, λ = 0.71070 Å
Hall symbol: C -2yc	Cell parameters from 5146 reflections
a = 16.638 (4) Å	θ = 4.2–27.5°
b = 10.5589 (19) Å	µ = 0.99 mm⁻¹
c = 14.327 (3) Å	T = 193 K
β = 110.758 (4)°	Prism, yellow
V = 2353.6 (8) Å³	0.24 × 0.17 × 0.09 mm
Z = 4

Data collection top

Rigaku Mercury diffractometer	4474 independent reflections
Radiation source: rotating anode X-ray tube	4165 reflections with F² > 2σ(F²)
Graphite monochromator	R_int = 0.034
Detector resolution: 7.31 pixels mm^-1	θ_max = 27.5°, θ_min = 4.2°
ω scans	h = −21→21
Absorption correction: multi-scan (REQAB; Jacobson, 1998)	k = −13→12
T_min = 0.725, T_max = 0.914	l = −18→18
11123 measured reflections

Refinement top

Refinement on F²	H-atom parameters constrained
Least-squares matrix: full	w = 1/[σ²(F_o²) + (0.0317P)² + 6.2745P] where P = (F_o² + 2F_c²)/3
R[F² > 2σ(F²)] = 0.037	(Δ/σ)_max < 0.001
wR(F²) = 0.078	Δρ_max = 0.52 e Å⁻³
S = 1.03	Δρ_min = −0.39 e Å⁻³
4474 reflections	Absolute structure: Flack (1983), 1824 Friedel pairs
291 parameters	Absolute structure parameter: 0.03 (3)
2 restraints

Crystal data top

[RuCl(C₆H₆)(C₁₅H₁₇NS)]PF₆	V = 2353.6 (8) Å³
M_r = 602.97	Z = 4
Monoclinic, Cc	Mo Kα radiation
a = 16.638 (4) Å	µ = 0.99 mm⁻¹
b = 10.5589 (19) Å	T = 193 K
c = 14.327 (3) Å	0.24 × 0.17 × 0.09 mm
β = 110.758 (4)°

Data collection top

Rigaku Mercury diffractometer	4474 independent reflections
Absorption correction: multi-scan (REQAB; Jacobson, 1998)	4165 reflections with F² > 2σ(F²)
T_min = 0.725, T_max = 0.914	R_int = 0.034
11123 measured reflections

Refinement top

R[F² > 2σ(F²)] = 0.037	H-atom parameters constrained
wR(F²) = 0.078	Δρ_max = 0.52 e Å⁻³
S = 1.03	Δρ_min = −0.39 e Å⁻³
4474 reflections	Absolute structure: Flack (1983), 1824 Friedel pairs
291 parameters	Absolute structure parameter: 0.03 (3)
2 restraints

Special details top

Refinement. Refinement was performed using all reflections. The weighted R-factor (wR) and goodness of fit (S) are based on F². R-factor (gt) are based on F. The threshold expression of F² > 2.0 σ(F²) is used only for calculating R-factor (gt).

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

	x	y	z	U_iso*/U_eq
Ru1	0.440889 (18)	0.11432 (3)	0.376620 (19)	0.02598 (8)
Cl1	0.45796 (9)	0.16185 (16)	0.22110 (9)	0.0513 (3)
S1	0.58842 (7)	0.14331 (10)	0.47160 (8)	0.0254 (2)
P1	0.69584 (11)	0.73747 (15)	0.57967 (11)	0.0475 (3)
F1	0.6579 (3)	0.6607 (5)	0.6493 (3)	0.0999 (15)
F2	0.7309 (4)	0.8098 (5)	0.5069 (4)	0.1156 (18)
F3	0.7809 (3)	0.7558 (4)	0.6683 (4)	0.131 (2)
F4	0.6641 (4)	0.8656 (4)	0.6080 (4)	0.120 (2)
F5	0.6079 (3)	0.7164 (7)	0.4899 (4)	0.138 (2)
F6	0.7296 (3)	0.6079 (4)	0.5553 (4)	0.1003 (16)
N1	0.4267 (2)	0.3121 (3)	0.3922 (3)	0.0329 (9)
C1	0.3753 (3)	0.3726 (5)	0.3113 (4)	0.0462 (12)
C2	0.3601 (4)	0.5007 (6)	0.3073 (6)	0.0675 (19)
C3	0.4025 (4)	0.5699 (5)	0.3912 (6)	0.066 (2)
C4	0.4540 (3)	0.5107 (4)	0.4763 (5)	0.0516 (14)
C5	0.4655 (3)	0.3802 (4)	0.4765 (3)	0.0336 (10)
C6	0.5200 (3)	0.3164 (4)	0.5718 (3)	0.0369 (11)
C7	0.5125 (4)	0.3609 (5)	0.6596 (4)	0.0549 (15)
C8	0.5601 (5)	0.3089 (7)	0.7504 (4)	0.0643 (18)
C9	0.6163 (4)	0.2118 (6)	0.7564 (4)	0.0589 (18)
C10	0.6249 (3)	0.1659 (5)	0.6696 (3)	0.0452 (12)
C11	0.5760 (3)	0.2207 (4)	0.5792 (3)	0.0306 (10)
C12	0.6615 (2)	0.2452 (4)	0.4304 (3)	0.0346 (10)
C13	0.6198 (3)	0.3698 (4)	0.3827 (4)	0.0450 (13)
C14	0.6825 (3)	0.1590 (6)	0.3568 (4)	0.0515 (14)
C15	0.7403 (3)	0.2697 (7)	0.5230 (4)	0.0566 (17)
C16	0.4470 (3)	−0.0321 (5)	0.4865 (4)	0.0507 (15)
C17	0.3813 (3)	0.0508 (5)	0.4822 (4)	0.0457 (13)
C18	0.3169 (3)	0.0775 (5)	0.3907 (5)	0.0519 (15)
C19	0.3172 (4)	0.0179 (7)	0.3037 (4)	0.069 (2)
C20	0.3868 (5)	−0.0664 (7)	0.3120 (6)	0.076 (2)
C21	0.4492 (6)	−0.0882 (5)	0.4002 (7)	0.068 (2)
H1	0.3474	0.3241	0.2528	0.055*
H2	0.3218	0.5398	0.2487	0.081*
H3	0.3961	0.6593	0.3903	0.079*
H4	0.4818	0.5585	0.5351	0.062*
H7	0.4739	0.4283	0.6569	0.066*
H8	0.5538	0.3406	0.8095	0.077*
H9	0.6491	0.1763	0.8193	0.071*
H10	0.6634	0.0984	0.6720	0.054*
H13A	0.5695	0.3517	0.3231	0.054*
H13B	0.6614	0.4197	0.3638	0.054*
H13C	0.6020	0.4178	0.4306	0.054*
H14A	0.6306	0.1453	0.2980	0.062*
H14B	0.7037	0.0775	0.3887	0.062*
H14C	0.7268	0.1989	0.3362	0.062*
H15A	0.7247	0.3251	0.5687	0.068*
H15B	0.7849	0.3106	0.5036	0.068*
H15C	0.7622	0.1891	0.5563	0.068*
H16	0.4907	−0.0505	0.5488	0.061*
H17	0.3800	0.0896	0.5415	0.055*
H18	0.2728	0.1363	0.3876	0.062*
H19	0.2728	0.0329	0.2413	0.083*
H20	0.3888	−0.1077	0.2539	0.091*
H21	0.4955	−0.1428	0.4034	0.082*

Atomic displacement parameters (Å²) top

	U¹¹	U²²	U³³	U¹²	U¹³	U²³
Ru1	0.02434 (16)	0.02938 (15)	0.02221 (15)	−0.00544 (19)	0.00577 (12)	−0.00200 (19)
Cl1	0.0469 (7)	0.0825 (10)	0.0235 (5)	−0.0105 (7)	0.0113 (5)	−0.0022 (6)
S1	0.0239 (5)	0.0271 (5)	0.0237 (5)	−0.0005 (4)	0.0065 (4)	0.0003 (4)
P1	0.0524 (9)	0.0479 (8)	0.0337 (7)	0.0149 (7)	0.0047 (6)	−0.0053 (6)
F1	0.124 (4)	0.100 (3)	0.094 (3)	0.014 (3)	0.062 (3)	0.023 (2)
F2	0.148 (5)	0.094 (3)	0.114 (4)	−0.026 (3)	0.060 (3)	−0.005 (3)
F3	0.113 (4)	0.062 (2)	0.125 (4)	0.001 (2)	−0.071 (3)	0.003 (2)
F4	0.196 (6)	0.076 (3)	0.098 (3)	0.084 (3)	0.064 (4)	0.020 (2)
F5	0.093 (3)	0.205 (6)	0.073 (3)	−0.024 (4)	−0.025 (3)	0.027 (3)
F6	0.120 (3)	0.070 (2)	0.139 (4)	0.001 (2)	0.079 (3)	−0.043 (2)
N1	0.020 (2)	0.036 (2)	0.041 (2)	0.0042 (16)	0.0090 (17)	0.0089 (19)
C1	0.033 (2)	0.043 (3)	0.056 (3)	0.006 (2)	0.009 (2)	0.015 (2)
C2	0.046 (3)	0.058 (4)	0.090 (5)	0.013 (3)	0.014 (3)	0.037 (3)
C3	0.056 (4)	0.027 (2)	0.116 (6)	0.012 (2)	0.031 (4)	0.022 (3)
C4	0.046 (3)	0.028 (2)	0.082 (4)	0.003 (2)	0.025 (3)	−0.002 (2)
C5	0.026 (2)	0.032 (2)	0.042 (2)	−0.0003 (19)	0.012 (2)	0.002 (2)
C6	0.037 (2)	0.038 (2)	0.038 (2)	−0.013 (2)	0.016 (2)	−0.016 (2)
C7	0.066 (4)	0.053 (3)	0.051 (3)	−0.008 (2)	0.027 (3)	−0.025 (2)
C8	0.081 (4)	0.080 (4)	0.036 (3)	−0.025 (3)	0.026 (3)	−0.025 (3)
C9	0.074 (4)	0.074 (4)	0.020 (2)	−0.021 (3)	0.004 (3)	0.000 (2)
C10	0.050 (3)	0.050 (3)	0.029 (2)	−0.003 (2)	0.006 (2)	0.002 (2)
C11	0.035 (2)	0.025 (2)	0.021 (2)	−0.0133 (18)	−0.004 (2)	0.0025 (17)
C12	0.022 (2)	0.048 (2)	0.033 (2)	−0.006 (2)	0.010 (2)	0.005 (2)
C13	0.042 (3)	0.042 (2)	0.051 (3)	−0.008 (2)	0.016 (2)	0.015 (2)
C14	0.046 (3)	0.071 (4)	0.047 (3)	0.001 (2)	0.028 (2)	−0.001 (2)
C15	0.033 (3)	0.079 (4)	0.053 (4)	−0.017 (2)	0.008 (2)	0.008 (3)
C16	0.047 (3)	0.043 (3)	0.055 (3)	−0.017 (2)	0.008 (2)	0.022 (2)
C17	0.052 (3)	0.051 (3)	0.043 (3)	−0.020 (2)	0.027 (2)	0.001 (2)
C18	0.030 (2)	0.047 (3)	0.078 (4)	−0.005 (2)	0.019 (3)	0.018 (3)
C19	0.052 (4)	0.085 (5)	0.044 (3)	−0.049 (3)	−0.014 (3)	0.015 (3)
C20	0.096 (6)	0.066 (4)	0.088 (5)	−0.050 (4)	0.062 (5)	−0.052 (4)
C21	0.062 (5)	0.027 (2)	0.123 (9)	−0.009 (3)	0.042 (6)	0.000 (3)

Geometric parameters (Å, º) top

Ru1—Cl1	2.3970 (14)	C12—C14	1.524 (8)
Ru1—S1	2.3671 (10)	C12—C15	1.521 (6)
Ru1—N1	2.122 (3)	C16—C17	1.386 (8)
Ru1—C16	2.183 (6)	C16—C21	1.383 (12)
Ru1—C17	2.187 (6)	C17—C18	1.396 (7)
Ru1—C18	2.178 (6)	C18—C19	1.398 (10)
Ru1—C19	2.199 (6)	C19—C20	1.432 (12)
Ru1—C20	2.172 (7)	C20—C21	1.340 (11)
Ru1—C21	2.161 (5)	C1—H1	0.950
S1—C11	1.820 (5)	C2—H2	0.950
S1—C12	1.869 (5)	C3—H3	0.950
P1—F1	1.580 (6)	C4—H4	0.950
P1—F2	1.563 (7)	C7—H7	0.950
P1—F3	1.542 (5)	C8—H8	0.950
P1—F4	1.558 (6)	C9—H9	0.950
P1—F5	1.585 (5)	C10—H10	0.950
P1—F6	1.565 (5)	C13—H13A	0.980
N1—C1	1.335 (6)	C13—H13B	0.980
N1—C5	1.357 (6)	C13—H13C	0.980
C1—C2	1.374 (8)	C14—H14A	0.980
C2—C3	1.369 (10)	C14—H14B	0.980
C3—C4	1.368 (9)	C14—H14C	0.980
C4—C5	1.391 (7)	C15—H15A	0.980
C5—C6	1.505 (6)	C15—H15B	0.980
C6—C7	1.389 (9)	C15—H15C	0.980
C6—C11	1.353 (7)	C16—H16	0.950
C7—C8	1.374 (8)	C17—H17	0.950
C8—C9	1.370 (11)	C18—H18	0.950
C9—C10	1.389 (9)	C19—H19	0.950
C10—C11	1.388 (6)	C20—H20	0.950
C12—C13	1.531 (7)	C21—H21	0.950

Cl1···C16ⁱ	3.574 (6)	H2···H14B^xiii	3.292
S1···F4ⁱⁱ	3.502 (5)	H2···H14C^xiii	2.880
F1···C14ⁱⁱⁱ	3.430 (8)	H2···H15C^xii	3.534
F1···C19^iv	3.365 (8)	H3···F3^ix	3.206
F2···C9^v	3.423 (7)	H3···F5	3.354
F2···C18^vi	3.538 (9)	H3···C14^xiii	3.414
F3···C2^vii	3.233 (8)	H3···C16^viii	3.522
F3···C19^iv	3.414 (8)	H3···C20^viii	3.090
F3···C20^iv	2.962 (9)	H3···C21^viii	2.797
F4···S1^viii	3.502 (5)	H3···H8^v	3.222
F4···C10^viii	3.415 (8)	H3···H20^viii	3.117
F4···C14ⁱⁱⁱ	3.476 (9)	H3···H21^viii	2.630
F4···C16^viii	3.575 (8)	H3···H14B^xiii	3.308
F5···C3	3.556 (9)	H3···H14C^xiii	2.677
F5···C4	3.310 (9)	H3···H15B^xiii	3.277
F5···C8^v	3.247 (8)	H4···F1	3.005
F5···C9^v	3.481 (9)	H4···F5	2.926
F5···C21^viii	3.236 (10)	H7···C2ⁱⁱⁱ	3.418
F6···C13	3.545 (6)	H7···H2ⁱⁱⁱ	3.258
F6···C17^vi	3.116 (9)	H7···H13Aⁱⁱⁱ	3.303
F6···C18^vi	3.194 (10)	H8···F5ⁱⁱⁱ	2.490
F6···C19^iv	3.589 (8)	H8···C3ⁱⁱⁱ	3.270
C2···F3^ix	3.233 (8)	H8···C13ⁱⁱⁱ	3.292
C3···F5	3.556 (9)	H8···H3ⁱⁱⁱ	3.222
C4···F5	3.310 (9)	H8···H18^iv	3.419
C8···F5ⁱⁱⁱ	3.247 (8)	H8···H20^x	3.560
C9···F2ⁱⁱⁱ	3.423 (7)	H8···H21^x	2.836
C9···F5ⁱⁱⁱ	3.481 (9)	H8···H13Aⁱⁱⁱ	3.259
C10···F4ⁱⁱ	3.415 (8)	H8···H13Bⁱⁱⁱ	3.037
C13···F6	3.545 (6)	H8···H13Cⁱⁱⁱ	3.028
C14···F1^v	3.430 (8)	H9···F2ⁱⁱⁱ	2.550
C14···F4^v	3.476 (9)	H9···F5ⁱⁱⁱ	2.986
C16···Cl1^x	3.574 (6)	H9···C14^x	3.595
C16···F4ⁱⁱ	3.575 (8)	H9···H18^iv	2.772
C17···F6^xi	3.116 (9)	H9···H21^x	3.207
C18···F2^xi	3.538 (9)	H9···H14A^x	3.413
C18···F6^xi	3.194 (10)	H9···H14B^x	2.891
C19···F1^xii	3.365 (8)	H10···F4ⁱⁱ	2.626
C19···F3^xii	3.414 (8)	H10···C1^iv	3.394
C19···F6^xii	3.589 (8)	H10···C2^iv	3.328
C20···F3^xii	2.962 (9)	H10···H1^iv	2.979
C21···F5ⁱⁱ	3.236 (10)	H10···H2^iv	2.869
Cl1···H16ⁱ	2.954	H10···H14A^x	3.299
Cl1···H15B^xii	3.425	H10···H14B^x	3.474
P1···H2^vii	3.491	H16···Cl1^x	2.954
P1···H18^vi	3.584	H16···F4ⁱⁱ	2.845
P1···H20^iv	3.569	H16···F5ⁱⁱ	3.425
P1···H14Cⁱⁱⁱ	3.589	H16···H15B^xi	3.567
F1···H4	3.005	H17···F2^xi	3.307
F1···H19^iv	2.790	H17···F3^xi	3.351
F1···H13Aⁱⁱⁱ	3.313	H17···F6^xi	2.588
F1···H13Bⁱⁱⁱ	3.170	H17···H20^x	3.002
F1···H14Aⁱⁱⁱ	3.103	H17···H15B^xi	3.296
F1···H14Cⁱⁱⁱ	2.916	H18···P1^xi	3.584
F2···H9^v	2.550	H18···F2^xi	2.758
F2···H17^vi	3.307	H18···F6^xi	2.757
F2···H18^vi	2.758	H18···C8^xii	3.434
F2···H14B^viii	3.243	H18···C9^xii	3.068
F3···H2^vii	2.428	H18···H8^xii	3.419
F3···H3^vii	3.206	H18···H9^xii	2.772
F3···H17^vi	3.351	H18···H13B^xi	2.887
F3···H19^iv	3.241	H19···F1^xii	2.790
F3···H20^iv	2.369	H19···F3^xii	3.241
F3···H14Cⁱⁱⁱ	2.892	H19···F6^xii	2.910
F4···H2^vii	2.863	H19···H13B^xi	3.202
F4···H10^viii	2.626	H19···H15A^xii	2.757
F4···H16^viii	2.845	H20···P1^xii	3.569
F4···H21^viii	3.262	H20···F3^xii	2.369
F4···H14Aⁱⁱⁱ	2.968	H20···F6^xii	3.127
F4···H14Cⁱⁱⁱ	3.133	H20···C8ⁱ	3.569
F5···H3	3.354	H20···H3ⁱⁱ	3.117
F5···H4	2.926	H20···H8ⁱ	3.560
F5···H8^v	2.490	H20···H17ⁱ	3.002
F5···H9^v	2.986	H21···F4ⁱⁱ	3.262
F5···H16^viii	3.425	H21···F5ⁱⁱ	2.366
F5···H21^viii	2.366	H21···C3ⁱⁱ	3.382
F5···H13C	3.258	H21···C8ⁱ	3.272
F6···H17^vi	2.588	H21···C9ⁱ	3.465
F6···H18^vi	2.757	H21···H3ⁱⁱ	2.630
F6···H19^iv	2.910	H21···H8ⁱ	2.836
F6···H20^iv	3.127	H21···H9ⁱ	3.207
F6···H13B	3.249	H13A···F1^v	3.313
F6···H13C	3.006	H13A···H7^v	3.303
F6···H15A	2.996	H13A···H8^v	3.259
F6···H15B	3.425	H13B···F1^v	3.170
C1···H10^xii	3.394	H13B···F6	3.249
C1···H18	3.414	H13B···C8^v	3.428
C1···H13A	3.183	H13B···C18^vi	2.986
C1···H13C	3.579	H13B···C19^vi	3.181
C1···H15C^xii	3.527	H13B···H8^v	3.037
C2···H7^v	3.418	H13B···H18^vi	2.887
C2···H10^xii	3.328	H13B···H19^vi	3.202
C2···H14B^xiii	3.308	H13C···F5	3.258
C2···H14C^xiii	3.182	H13C···F6	3.006
C3···H8^v	3.270	H13C···H8^v	3.028
C3···H21^viii	3.382	H14A···F1^v	3.103
C3···H14B^xiii	3.296	H14A···F4^v	2.968
C3···H14C^xiii	3.065	H14A···H9ⁱ	3.413
C8···H18^iv	3.434	H14A···H10ⁱ	3.299
C8···H20^x	3.569	H14B···F2ⁱⁱ	3.243
C8···H21^x	3.272	H14B···C2^xiv	3.308
C8···H13Bⁱⁱⁱ	3.428	H14B···C3^xiv	3.296
C9···H18^iv	3.068	H14B···H2^xiv	3.292
C9···H21^x	3.465	H14B···H3^xiv	3.308
C10···H1^iv	3.466	H14B···H9ⁱ	2.891
C13···H8^v	3.292	H14B···H10ⁱ	3.474
C14···H2^xiv	3.449	H14C···P1^v	3.589
C14···H3^xiv	3.414	H14C···F1^v	2.916
C14···H9ⁱ	3.595	H14C···F3^v	2.892
C15···H1^iv	3.293	H14C···F4^v	3.133
C16···H3ⁱⁱ	3.522	H14C···C2^xiv	3.182
C16···H15B^xi	3.250	H14C···C3^xiv	3.065
C17···H15B^xi	3.074	H14C···H2^xiv	2.880
C18···H13B^xi	2.986	H14C···H3^xiv	2.677
C18···H15B^xi	3.384	H15A···F6	2.996
C19···H13B^xi	3.181	H15A···C19^iv	3.575
C19···H15A^xii	3.575	H15A···H1^iv	3.129
C20···H3ⁱⁱ	3.090	H15A···H19^iv	2.757
C21···H3ⁱⁱ	2.797	H15B···Cl1^iv	3.425
H1···C10^xii	3.466	H15B···F6	3.425
H1···C15^xii	3.293	H15B···C16^vi	3.250
H1···H10^xii	2.979	H15B···C17^vi	3.074
H1···H15A^xii	3.129	H15B···C18^vi	3.384
H1···H15C^xii	2.671	H15B···H3^xiv	3.277
H2···P1^ix	3.491	H15B···H16^vi	3.567
H2···F3^ix	2.428	H15B···H17^vi	3.296
H2···F4^ix	2.863	H15C···C1^iv	3.527
H2···C14^xiii	3.449	H15C···H1^iv	2.671
H2···H7^v	3.258	H15C···H2^iv	3.534
H2···H10^xii	2.869

Cl1—Ru1—S1	93.84 (4)	S1—C12—C14	102.1 (3)
Cl1—Ru1—N1	86.89 (14)	S1—C12—C15	106.2 (4)
Cl1—Ru1—C16	145.87 (18)	C13—C12—C14	112.5 (4)
Cl1—Ru1—C17	159.90 (13)	C13—C12—C15	110.9 (4)
Cl1—Ru1—C18	123.49 (17)	C14—C12—C15	111.5 (4)
Cl1—Ru1—C19	93.14 (19)	Ru1—C16—C17	71.7 (3)
Cl1—Ru1—C20	87.4 (2)	Ru1—C16—C21	70.6 (4)
Cl1—Ru1—C21	109.3 (3)	C17—C16—C21	120.1 (5)
S1—Ru1—N1	86.76 (9)	Ru1—C17—C16	71.4 (4)
S1—Ru1—C16	84.44 (15)	Ru1—C17—C18	71.0 (4)
S1—Ru1—C17	105.91 (13)	C16—C17—C18	120.0 (5)
S1—Ru1—C18	142.48 (17)	Ru1—C18—C17	71.7 (3)
S1—Ru1—C19	159.70 (19)	Ru1—C18—C19	72.2 (4)
S1—Ru1—C20	123.2 (2)	C17—C18—C19	120.1 (5)
S1—Ru1—C21	92.4 (2)	Ru1—C19—C18	70.5 (3)
N1—Ru1—C16	126.9 (2)	Ru1—C19—C20	69.8 (4)
N1—Ru1—C17	97.7 (2)	C18—C19—C20	117.7 (5)
N1—Ru1—C18	91.25 (19)	Ru1—C20—C19	71.9 (4)
N1—Ru1—C19	112.7 (2)	Ru1—C20—C21	71.5 (4)
N1—Ru1—C20	149.9 (2)	C19—C20—C21	121.2 (8)
N1—Ru1—C21	163.8 (3)	Ru1—C21—C16	72.3 (3)
C16—Ru1—C17	37.0 (2)	Ru1—C21—C20	72.4 (4)
C16—Ru1—C18	67.1 (2)	C16—C21—C20	120.8 (8)
C16—Ru1—C19	79.1 (2)	N1—C1—H1	118.0
C16—Ru1—C20	65.9 (2)	C2—C1—H1	118.0
C16—Ru1—C21	37.1 (3)	C1—C2—H2	121.3
C17—Ru1—C18	37.3 (2)	C3—C2—H2	121.3
C17—Ru1—C19	67.0 (2)	C2—C3—H3	119.9
C17—Ru1—C20	78.7 (3)	C4—C3—H3	119.9
C17—Ru1—C21	67.0 (3)	C3—C4—H4	120.1
C18—Ru1—C19	37.2 (2)	C5—C4—H4	120.1
C18—Ru1—C20	67.7 (3)	C6—C7—H7	119.5
C18—Ru1—C21	79.6 (3)	C8—C7—H7	119.5
C19—Ru1—C20	38.2 (3)	C7—C8—H8	119.7
C19—Ru1—C21	67.3 (3)	C9—C8—H8	119.7
C20—Ru1—C21	36.0 (3)	C8—C9—H9	120.3
Ru1—S1—C11	98.00 (15)	C10—C9—H9	120.3
Ru1—S1—C12	123.42 (13)	C9—C10—H10	120.7
C11—S1—C12	106.9 (2)	C11—C10—H10	120.7
F1—P1—F2	177.5 (2)	C12—C13—H13A	109.5
F1—P1—F3	90.0 (3)	C12—C13—H13B	109.5
F1—P1—F4	91.8 (3)	C12—C13—H13C	109.5
F1—P1—F5	88.8 (3)	H13A—C13—H13B	109.5
F1—P1—F6	87.0 (3)	H13A—C13—H13C	109.5
F2—P1—F3	92.1 (3)	H13B—C13—H13C	109.5
F2—P1—F4	89.5 (3)	C12—C14—H14A	109.5
F2—P1—F5	89.0 (3)	C12—C14—H14B	109.5
F2—P1—F6	91.7 (3)	C12—C14—H14C	109.5
F3—P1—F4	88.5 (2)	H14A—C14—H14B	109.5
F3—P1—F5	178.8 (3)	H14A—C14—H14C	109.5
F3—P1—F6	89.8 (2)	H14B—C14—H14C	109.5
F4—P1—F5	91.8 (3)	C12—C15—H15A	109.5
F4—P1—F6	177.9 (2)	C12—C15—H15B	109.5
F5—P1—F6	89.8 (3)	C12—C15—H15C	109.5
Ru1—N1—C1	116.1 (3)	H15A—C15—H15B	109.5
Ru1—N1—C5	125.4 (3)	H15A—C15—H15C	109.5
C1—N1—C5	118.4 (4)	H15B—C15—H15C	109.5
N1—C1—C2	124.0 (5)	Ru1—C16—H16	130.3
C1—C2—C3	117.3 (6)	C17—C16—H16	120.0
C2—C3—C4	120.3 (5)	C21—C16—H16	120.0
C3—C4—C5	119.8 (5)	Ru1—C17—H17	130.2
N1—C5—C4	120.1 (4)	C16—C17—H17	120.0
N1—C5—C6	121.0 (4)	C18—C17—H17	120.0
C4—C5—C6	118.9 (4)	Ru1—C18—H18	128.4
C5—C6—C7	116.9 (4)	C17—C18—H18	119.9
C5—C6—C11	125.6 (5)	C19—C18—H18	119.9
C7—C6—C11	117.5 (4)	Ru1—C19—H19	130.9
C6—C7—C8	121.1 (6)	C18—C19—H19	121.2
C7—C8—C9	120.6 (6)	C20—C19—H19	121.2
C8—C9—C10	119.3 (5)	Ru1—C20—H20	129.7
C9—C10—C11	118.5 (5)	C19—C20—H20	119.4
S1—C11—C6	123.5 (3)	C21—C20—H20	119.4
S1—C11—C10	113.5 (3)	Ru1—C21—H21	127.9
C6—C11—C10	122.9 (5)	C16—C21—H21	119.6
S1—C12—C13	113.2 (3)	C20—C21—H21	119.6

Cl1—Ru1—S1—C11	141.23 (14)	C18—Ru1—C17—C16	132.5 (5)
Cl1—Ru1—S1—C12	24.8 (2)	C17—Ru1—C19—C18	29.6 (3)
Cl1—Ru1—N1—C1	45.1 (4)	C17—Ru1—C19—C20	−101.3 (5)
Cl1—Ru1—N1—C5	−134.7 (4)	C19—Ru1—C17—C16	102.9 (3)
Cl1—Ru1—C16—C17	−145.4 (2)	C19—Ru1—C17—C18	−29.6 (3)
Cl1—Ru1—C16—C21	−12.8 (6)	C17—Ru1—C20—C19	67.0 (4)
Cl1—Ru1—C17—C16	112.0 (4)	C17—Ru1—C20—C21	−66.1 (6)
Cl1—Ru1—C17—C18	−20.4 (6)	C20—Ru1—C17—C16	64.7 (3)
Cl1—Ru1—C18—C17	171.7 (2)	C20—Ru1—C17—C18	−67.8 (3)
Cl1—Ru1—C18—C19	40.4 (4)	C17—Ru1—C21—C16	−28.8 (4)
Cl1—Ru1—C19—C18	−147.3 (3)	C17—Ru1—C21—C20	102.9 (6)
Cl1—Ru1—C19—C20	81.9 (4)	C21—Ru1—C17—C16	28.9 (3)
Cl1—Ru1—C20—C19	−98.3 (4)	C21—Ru1—C17—C18	−103.6 (4)
Cl1—Ru1—C20—C21	128.5 (6)	C18—Ru1—C19—C20	−130.9 (6)
Cl1—Ru1—C21—C16	172.4 (3)	C19—Ru1—C18—C17	131.4 (5)
Cl1—Ru1—C21—C20	−55.9 (7)	C18—Ru1—C20—C19	29.6 (4)
S1—Ru1—N1—C1	139.1 (4)	C18—Ru1—C20—C21	−103.5 (7)
S1—Ru1—N1—C5	−40.7 (4)	C20—Ru1—C18—C17	101.0 (4)
N1—Ru1—S1—C11	54.57 (19)	C20—Ru1—C18—C19	−30.4 (4)
N1—Ru1—S1—C12	−61.8 (2)	C18—Ru1—C21—C16	−65.6 (4)
S1—Ru1—C16—C17	126.0 (3)	C18—Ru1—C21—C20	66.1 (6)
S1—Ru1—C16—C21	−101.5 (4)	C21—Ru1—C18—C17	65.4 (4)
C16—Ru1—S1—C11	−73.0 (2)	C21—Ru1—C18—C19	−66.0 (4)
C16—Ru1—S1—C12	170.6 (2)	C19—Ru1—C20—C21	−133.1 (9)
S1—Ru1—C17—C16	−56.9 (3)	C20—Ru1—C19—C18	130.9 (6)
S1—Ru1—C17—C18	170.7 (3)	C19—Ru1—C21—C16	−102.4 (5)
C17—Ru1—S1—C11	−42.6 (2)	C19—Ru1—C21—C20	29.3 (6)
C17—Ru1—S1—C12	−159.0 (2)	C21—Ru1—C19—C18	103.2 (5)
S1—Ru1—C18—C17	−14.9 (4)	C21—Ru1—C19—C20	−27.7 (5)
S1—Ru1—C18—C19	−146.2 (3)	C20—Ru1—C21—C16	−131.7 (9)
C18—Ru1—S1—C11	−33.3 (3)	C21—Ru1—C20—C19	133.1 (9)
C18—Ru1—S1—C12	−149.7 (3)	Ru1—S1—C11—C6	−46.4 (4)
S1—Ru1—C19—C18	102.8 (6)	Ru1—S1—C11—C10	129.0 (3)
S1—Ru1—C19—C20	−28.1 (8)	Ru1—S1—C12—C13	41.4 (4)
C19—Ru1—S1—C11	−108.9 (6)	Ru1—S1—C12—C14	−79.8 (3)
C19—Ru1—S1—C12	134.6 (6)	Ru1—S1—C12—C15	163.3 (3)
S1—Ru1—C20—C19	168.7 (3)	C11—S1—C12—C13	−70.6 (3)
S1—Ru1—C20—C21	35.6 (7)	C11—S1—C12—C14	168.2 (2)
C20—Ru1—S1—C11	−129.3 (3)	C11—S1—C12—C15	51.3 (4)
C20—Ru1—S1—C12	114.3 (3)	C12—S1—C11—C6	82.3 (4)
S1—Ru1—C21—C16	77.5 (4)	C12—S1—C11—C10	−102.3 (4)
S1—Ru1—C21—C20	−150.8 (6)	Ru1—N1—C1—C2	−178.6 (6)
C21—Ru1—S1—C11	−109.3 (3)	Ru1—N1—C5—C4	177.3 (4)
C21—Ru1—S1—C12	134.3 (3)	Ru1—N1—C5—C6	−3.9 (7)
N1—Ru1—C16—C17	44.3 (3)	C1—N1—C5—C4	−2.5 (8)
N1—Ru1—C16—C21	176.8 (4)	C1—N1—C5—C6	176.3 (5)
C16—Ru1—N1—C1	−140.3 (4)	C5—N1—C1—C2	1.2 (10)
C16—Ru1—N1—C5	39.9 (5)	N1—C1—C2—C3	1.7 (12)
N1—Ru1—C17—C16	−145.7 (3)	C1—C2—C3—C4	−3.3 (12)
N1—Ru1—C17—C18	81.8 (3)	C2—C3—C4—C5	2.1 (12)
C17—Ru1—N1—C1	−115.3 (4)	C3—C4—C5—N1	0.9 (10)
C17—Ru1—N1—C5	64.9 (4)	C3—C4—C5—C6	−177.9 (6)
N1—Ru1—C18—C17	−101.2 (3)	N1—C5—C6—C7	−140.0 (5)
N1—Ru1—C18—C19	127.5 (3)	N1—C5—C6—C11	40.7 (8)
C18—Ru1—N1—C1	−78.4 (4)	C4—C5—C6—C7	38.8 (8)
C18—Ru1—N1—C5	101.8 (4)	C4—C5—C6—C11	−140.5 (6)
N1—Ru1—C19—C18	−59.3 (4)	C5—C6—C7—C8	−179.6 (6)
N1—Ru1—C19—C20	169.8 (4)	C5—C6—C11—S1	−5.3 (7)
C19—Ru1—N1—C1	−47.0 (5)	C5—C6—C11—C10	179.7 (5)
C19—Ru1—N1—C5	133.2 (4)	C7—C6—C11—S1	175.4 (4)
N1—Ru1—C20—C19	−19.0 (8)	C7—C6—C11—C10	0.5 (8)
N1—Ru1—C20—C21	−152.1 (6)	C11—C6—C7—C8	−0.3 (8)
C20—Ru1—N1—C1	−34.4 (8)	C6—C7—C8—C9	0.1 (8)
C20—Ru1—N1—C5	145.8 (6)	C7—C8—C9—C10	−0.1 (9)
N1—Ru1—C21—C16	−9.2 (12)	C8—C9—C10—C11	0.2 (7)
N1—Ru1—C21—C20	122.5 (8)	C9—C10—C11—S1	−175.8 (5)
C21—Ru1—N1—C1	−133.4 (9)	C9—C10—C11—C6	−0.4 (8)
C21—Ru1—N1—C5	46.8 (11)	Ru1—C16—C17—C18	53.7 (5)
C16—Ru1—C17—C18	−132.5 (5)	Ru1—C16—C21—C20	−56.0 (7)
C17—Ru1—C16—C21	132.6 (5)	C17—C16—C21—Ru1	53.9 (6)
C16—Ru1—C18—C17	28.8 (3)	C17—C16—C21—C20	−2.1 (11)
C16—Ru1—C18—C19	−102.6 (4)	C21—C16—C17—Ru1	−53.4 (6)
C18—Ru1—C16—C17	−29.0 (3)	C21—C16—C17—C18	0.3 (8)
C18—Ru1—C16—C21	103.5 (5)	Ru1—C17—C18—C19	55.7 (6)
C16—Ru1—C19—C18	66.3 (3)	C16—C17—C18—Ru1	−53.9 (5)
C16—Ru1—C19—C20	−64.6 (5)	C16—C17—C18—C19	1.8 (9)
C19—Ru1—C16—C17	−66.0 (3)	Ru1—C18—C19—C20	53.3 (6)
C19—Ru1—C16—C21	66.6 (5)	C17—C18—C19—Ru1	−55.4 (5)
C16—Ru1—C20—C19	103.6 (5)	C17—C18—C19—C20	−2.2 (10)
C16—Ru1—C20—C21	−29.6 (6)	Ru1—C19—C20—C21	54.0 (7)
C20—Ru1—C16—C17	−103.8 (4)	C18—C19—C20—Ru1	−53.6 (6)
C20—Ru1—C16—C21	28.8 (5)	C18—C19—C20—C21	0.4 (11)
C16—Ru1—C21—C20	131.7 (9)	Ru1—C20—C21—C16	55.9 (6)
C21—Ru1—C16—C17	−132.6 (5)	C19—C20—C21—Ru1	−54.2 (7)
C17—Ru1—C18—C19	−131.4 (5)	C19—C20—C21—C16	1.7 (13)

Symmetry codes: (i) x, −y, z−1/2; (ii) x, y−1, z; (iii) x, −y+1, z+1/2; (iv) x+1/2, −y+1/2, z+1/2; (v) x, −y+1, z−1/2; (vi) x+1/2, y+1/2, z; (vii) x+1/2, −y+3/2, z+1/2; (viii) x, y+1, z; (ix) x−1/2, −y+3/2, z−1/2; (x) x, −y, z+1/2; (xi) x−1/2, y−1/2, z; (xii) x−1/2, −y+1/2, z−1/2; (xiii) x−1/2, y+1/2, z; (xiv) x+1/2, y−1/2, z.

Experimental details

Crystal data
Chemical formula	[RuCl(C₆H₆)(C₁₅H₁₇NS)]PF₆
M_r	602.97
Crystal system, space group	Monoclinic, Cc
Temperature (K)	193
a, b, c (Å)	16.638 (4), 10.5589 (19), 14.327 (3)
β (°)	110.758 (4)
V (Å³)	2353.6 (8)
Z	4
Radiation type	Mo Kα
µ (mm⁻¹)	0.99
Crystal size (mm)	0.24 × 0.17 × 0.09

Data collection
Diffractometer	Rigaku Mercury
Absorption correction	Multi-scan (REQAB; Jacobson, 1998)
T_min, T_max	0.725, 0.914
No. of measured, independent and observed [F² > 2σ(F²)] reflections	11123, 4474, 4165
R_int	0.034
(sin θ/λ)_max (Å⁻¹)	0.649

Refinement
R[F² > 2σ(F²)], wR(F²), S	0.037, 0.078, 1.03
No. of reflections	4474
No. of parameters	291
No. of restraints	2
H-atom treatment	H-atom parameters constrained
Δρ_max, Δρ_min (e Å⁻³)	0.52, −0.39
Absolute structure	Flack (1983), 1824 Friedel pairs
Absolute structure parameter	0.03 (3)

Computer programs: CrystalClear (Rigaku, 1999), CrystalStructure (Rigaku/MSC, 2006), SIR97 (Altomare et al., 1999), SHELXL97 (Sheldrick, 2008), ORTEP-3 for Windows (Farrugia, 1997).

Selected geometric parameters (Å, º) top

Ru1—Cl1	2.3970 (14)	Ru1—C19	2.199 (6)
Ru1—S1	2.3671 (10)	Ru1—C20	2.172 (7)
Ru1—N1	2.122 (3)	Ru1—C21	2.161 (5)
Ru1—C16	2.183 (6)	S1—C11	1.820 (5)
Ru1—C17	2.187 (6)	S1—C12	1.869 (5)
Ru1—C18	2.178 (6)

Cl1—Ru1—S1	93.84 (4)	Ru1—S1—C12	123.42 (13)
Cl1—Ru1—N1	86.89 (14)	C11—S1—C12	106.9 (2)
S1—Ru1—N1	86.76 (9)	Ru1—N1—C1	116.1 (3)
Ru1—S1—C11	98.00 (15)	Ru1—N1—C5	125.4 (3)

References

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