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Acta Crystallogr Sect E Struct Rep Online. 2010 February 1; 66(Pt 2): m178–m179.
Published online 2010 January 16. doi:  10.1107/S1600536809055287
PMCID: PMC2979922

[μ-Bis(diphenyl­arsino)methane-1:2κ2 As:As′][(4-bromo­phen­yl)diphenyl­phosphine-3κP]nona­carbonyl-1κ3 C,2κ3 C,3κ3 C-triangulo-tri­ruthenium(0) chloro­form 0.3-solvate

Abstract

The asymmetric unit of the title triangulo-triruthenium compound, [Ru3(C25H22As2)(C18H14BrP)(CO)9]·0.3CHCl3, contains one mol­ecule of the triangulo-triruthenium complex and one partially occupied disordered chloro­form solvent mol­ecule. The bis­(diphenyl­arsino)methane ligand bridges an Ru—Ru bond and the monodentate phosphine ligand bonds to the third Ru atom. Both the arsine and phosphine ligands are equatorial with respect to the Ru3 triangle. In addition, each Ru atom carries one equatorial and two axial terminal carbonyl ligands. The phosphine-substituted benzene rings make dihedral angles of 67.5 (3), 76.1 (3) and 78.1 (3)° with each other. The dihedral angles between the two benzene rings are 79.0 (4) and 81.4 (3)° for the two diphenyl­arsino groups. In the crystal packing, the mol­ecules are linked into chains along the a axis by inter­molecular C—H(...)O hydrogen bonds.

Related literature

For general background to triangulo-triruthenium derivatives, see: Bruce et al. (1985 [triangle], 1988a [triangle],b [triangle]). For related structures, see: Shawkataly et al. (1998 [triangle], 2004 [triangle], 2009 [triangle]). For the synthesis of μ-bis­(diphenyl­arsino)methane­deca­carbonyl­triruthenium(0), see: Bruce et al. (1983 [triangle]).

An external file that holds a picture, illustration, etc.
Object name is e-66-0m178-scheme1.jpg

Experimental

Crystal data

  • [Ru3(C25H22As2)(C18H14BrP)(CO)9]·0.3CHCl3
  • M r = 1404.55
  • Monoclinic, An external file that holds a picture, illustration, etc.
Object name is e-66-0m178-efi1.jpg
  • a = 13.2415 (2) Å
  • b = 16.9463 (3) Å
  • c = 25.2224 (4) Å
  • β = 91.831 (1)°
  • V = 5656.88 (16) Å3
  • Z = 4
  • Mo Kα radiation
  • μ = 2.78 mm−1
  • T = 296 K
  • 0.26 × 0.26 × 0.16 mm

Data collection

  • Bruker SMART APEXII CCD area-detector diffractometer
  • Absorption correction: multi-scan (SADABS; Bruker, 2005 [triangle]) T min = 0.537, T max = 0.673
  • 63188 measured reflections
  • 16521 independent reflections
  • 10783 reflections with I > 2σ(I)
  • R int = 0.042

Refinement

  • R[F 2 > 2σ(F 2)] = 0.048
  • wR(F 2) = 0.169
  • S = 1.08
  • 16521 reflections
  • 677 parameters
  • 6 restraints
  • H-atom parameters constrained
  • Δρmax = 1.41 e Å−3
  • Δρmin = −1.35 e Å−3

Data collection: APEX2 (Bruker, 2005 [triangle]); cell refinement: SAINT (Bruker, 2005 [triangle]); data reduction: SAINT; program(s) used to solve structure: SHELXTL (Sheldrick, 2008 [triangle]); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL and PLATON (Spek, 2009 [triangle]).

Table 1
Hydrogen-bond geometry (Å, °)

Supplementary Material

Crystal structure: contains datablocks global, I. DOI: 10.1107/S1600536809055287/rz2406sup1.cif

Structure factors: contains datablocks I. DOI: 10.1107/S1600536809055287/rz2406Isup2.hkl

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

Acknowledgments

The authors would like to thank the Malaysian Government and Universiti Sains Malaysia (USM) for the Research grant 1001/PJJAUH/811115. IAK is grateful to USM for a Postdoctoral Fellowship and to Gokhale Centenary College, Ankola, Karnataka, India, for postdoctoral study leave. HKF thanks USM for the Research University Golden Goose grant 1001/PFIZIK/811012. CSY thanks USM for the award of a USM Fellowship.

supplementary crystallographic information

Comment

Triangulo-triruthenium clusters are known for their interesting structural variations and related catalytic activity. A large number of substituted derivatives, Ru3(CO)12-nLn (L = group 15 ligand) have been reported (Bruce et al., 1985, 1988a,b). As part of our study on the substitution of transition metal-carbonyl clusters with mixed-ligand complexes, we have published several structures of triangulo-triruthenium-carbonyl clusters containing mixed P/As and P/Sb ligands (Shawkataly et al., 1998, 2004, 2009). Herein we report the synthesis and structure of title compound.

The asymmetric unit consists of one molecule of the triangulo-triruthenium complex and a 30% partially occupied molecule of disordered chloroform solvent (Fig. 1). The bond lengths and angles of title compound are comparable to those found in its related structure (Shawkataly et al., 2009). The bis(diphenylarsino)methane ligand bridges the Ru1—Ru2 bond and the monodentate phosphine ligand bonds to the Ru3 atom. Both the phosphine and arsine ligands are equatorial with respect to the Ru3 triangle. Additionally, each Ru atom carries one equatorial and two axial terminal carbonyl ligands. The phosphine-substituted benzene rings make dihedral angles (C26–C31/C32–C37, C26–C31/C38–C43 and C32–C37/C38–C43) of 67.5 (3), 76.1 (3) and 78.1 (3)° with each other respectively. The dihedral angles between the two benzene rings (C1–C6/C7–C12 and C14–C19/C20–C25) are 79.0 (4) and 81.4 (3)° for the two diphenylarsino groups respectively.

In the crystal packing (Fig. 2), the molecules are linked into chains along the a axis by intermolecular C23—H23A···O2 hydrogen bonds (Table 1).

Experimental

All manipulations were performed under a dry, oxygen-free dinitrogen atmosphere using standard Schlenk techniques, all solvents were dried over sodium and distilled from sodium benzophenone ketyl under nitrogen. (4-Bromophenyl)diphenylphosphine (Maybridge) was used as received and µ-bis(diphenylarsino)methane-decacarbonyl-triruthenium(0) (Bruce et al., 1983) were prepared by a reported procedure. The title compound was obtained by refluxing equimolar quantities of Ru3(CO)10(µ-Ph2AsCH2AsPh2) (105.5 mg, 0.1 mmol) and (4-bromophenyl)diphenylphosphine (34.12 mg, 0.1 mmol) in hexane under nitrogen atmosphere. Crystals suitable for X-ray diffraction were grown by slow solvent / solvent diffusion of CH3OH into CH2Cl2.

Refinement

All hydrogen atoms were positioned geometrically and refined using a riding model with C—H = 0.93–0.97 Å and Uiso(H) = 1.2 Ueq(C). The chloroform molecule is disordered over two positions with the site occupancies fixed to 0.15 for both components and with SADI command for the final refinement. The C53A and C53B atoms were refined isotropically. The maximum and minimum residual electron density peaks of 1.41 and -1.35 e Å-3, respectively, were located 0.56 Å and 0.96 Å from the Cl2B and Br1 atoms, respectively.

Figures

Fig. 1.
The molecular structure of the title compound with 20% probability ellipsoids for non-H atoms. All disordered components are shown.
Fig. 2.
The crystal packing of the title compound, viewed down the a axis, showing the molecules linked into chains along a axis. Hydrogen atoms not involved in the hydrogen-bonding (dashed lines) and the solvent molecules have been omitted for clarity.

Crystal data

[Ru3(C25H22As2)(C18H14BrP)(CO)9]·0.3CHCl3F(000) = 2742
Mr = 1404.55Dx = 1.649 Mg m3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
Hall symbol: -P 2ybcCell parameters from 9923 reflections
a = 13.2415 (2) Åθ = 2.2–27.8°
b = 16.9463 (3) ŵ = 2.78 mm1
c = 25.2224 (4) ÅT = 296 K
β = 91.831 (1)°Block, purple
V = 5656.88 (16) Å30.26 × 0.26 × 0.16 mm
Z = 4

Data collection

Bruker SMART APEXII CCD area-detector diffractometer16521 independent reflections
Radiation source: fine-focus sealed tube10783 reflections with I > 2σ(I)
graphiteRint = 0.042
[var phi] and ω scansθmax = 30.1°, θmin = 1.5°
Absorption correction: multi-scan (SADABS; Bruker, 2005)h = −15→18
Tmin = 0.537, Tmax = 0.673k = −23→23
63188 measured reflectionsl = −34→35

Refinement

Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.048Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.169H-atom parameters constrained
S = 1.08w = 1/[σ2(Fo2) + (0.0909P)2 + 1.7904P] where P = (Fo2 + 2Fc2)/3
16521 reflections(Δ/σ)max < 0.001
677 parametersΔρmax = 1.41 e Å3
6 restraintsΔρmin = −1.35 e Å3

Special details

Geometry. All e.s.d.'s (except the e.s.d. in the dihedral angle between two l.s. planes) are estimated using the full covariance matrix. The cell e.s.d.'s are taken into account individually in the estimation of e.s.d.'s in distances, angles and torsion angles; correlations between e.s.d.'s in cell parameters are only used when they are defined by crystal symmetry. An approximate (isotropic) treatment of cell e.s.d.'s is used for estimating e.s.d.'s involving l.s. planes.
Refinement. Refinement of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > σ(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger.

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

xyzUiso*/UeqOcc. (<1)
Ru10.23647 (3)0.31292 (2)0.159957 (17)0.03734 (11)
Ru20.04996 (3)0.23846 (2)0.182974 (15)0.03237 (10)
Ru30.19834 (3)0.15122 (2)0.129329 (15)0.03373 (11)
As10.16719 (4)0.44257 (3)0.18017 (2)0.03586 (13)
As2−0.01816 (3)0.34651 (3)0.234290 (19)0.03180 (12)
P10.31671 (10)0.08260 (8)0.07993 (5)0.0391 (3)
Br10.73998 (7)0.26067 (7)0.03555 (5)0.1197 (4)
O10.1908 (4)0.3326 (3)0.04092 (18)0.0692 (13)
O20.4533 (4)0.3563 (4)0.1392 (3)0.128 (3)
O30.2858 (4)0.2977 (3)0.2792 (2)0.0750 (14)
O40.1342 (4)0.1548 (3)0.28246 (18)0.0709 (13)
O5−0.1249 (4)0.1225 (3)0.1762 (2)0.0891 (17)
O6−0.0303 (3)0.3221 (3)0.08269 (17)0.0646 (12)
O70.0669 (4)0.1772 (3)0.02798 (19)0.0770 (14)
O80.0746 (3)0.0079 (3)0.15645 (19)0.0663 (12)
O90.3573 (3)0.1471 (2)0.21969 (19)0.0634 (12)
C10.2604 (4)0.5220 (3)0.2096 (2)0.0463 (13)
C20.2406 (5)0.6013 (4)0.2031 (3)0.0702 (19)
H2A0.18400.61750.18320.084*
C30.3065 (6)0.6578 (4)0.2265 (4)0.089 (3)
H3A0.29340.71140.22220.107*
C40.3881 (6)0.6337 (5)0.2549 (4)0.088 (3)
H4A0.43150.67090.27030.106*
C50.4079 (6)0.5570 (5)0.2613 (4)0.096 (3)
H5A0.46440.54160.28150.115*
C60.3448 (5)0.4995 (4)0.2380 (3)0.080 (2)
H6A0.36040.44630.24190.096*
C70.1009 (4)0.5021 (3)0.1233 (2)0.0451 (12)
C80.0047 (5)0.5283 (5)0.1246 (3)0.076 (2)
H8A−0.03450.51710.15350.091*
C9−0.0355 (7)0.5722 (6)0.0823 (4)0.105 (3)
H9A−0.10210.58940.08370.125*
C100.0150 (8)0.5901 (6)0.0414 (4)0.095 (3)
H10A−0.01500.61980.01410.115*
C110.1142 (8)0.5653 (5)0.0379 (3)0.093 (3)
H11A0.15170.57850.00860.111*
C120.1568 (5)0.5199 (4)0.0791 (3)0.0703 (19)
H12A0.22270.50150.07700.084*
C130.0693 (4)0.4407 (3)0.2370 (2)0.0373 (11)
H13A0.02730.48760.23430.045*
H13B0.10550.44230.27100.045*
C14−0.0395 (4)0.3275 (3)0.30969 (19)0.0376 (11)
C150.0424 (4)0.3164 (4)0.3438 (2)0.0564 (16)
H15A0.10770.31970.33150.068*
C160.0267 (5)0.3004 (5)0.3969 (2)0.069 (2)
H16A0.08200.29270.42000.083*
C17−0.0679 (6)0.2958 (4)0.4156 (3)0.0707 (19)
H17A−0.07700.28530.45130.085*
C18−0.1519 (5)0.3068 (5)0.3813 (3)0.0681 (19)
H18A−0.21710.30370.39380.082*
C19−0.1358 (4)0.3225 (4)0.3283 (2)0.0511 (14)
H19A−0.19090.32970.30500.061*
C20−0.1490 (3)0.3869 (3)0.21020 (19)0.0368 (11)
C21−0.2132 (4)0.3360 (4)0.1828 (3)0.0545 (15)
H21A−0.19240.28480.17550.065*
C22−0.3100 (4)0.3616 (4)0.1660 (3)0.069 (2)
H22A−0.35310.32770.14710.083*
C23−0.3408 (4)0.4376 (4)0.1778 (3)0.0614 (17)
H23A−0.40500.45480.16710.074*
C24−0.2765 (4)0.4878 (3)0.2054 (2)0.0501 (14)
H24A−0.29680.53890.21320.060*
C25−0.1817 (4)0.4617 (3)0.2214 (2)0.0428 (12)
H25A−0.13870.49580.24020.051*
C260.4375 (4)0.1316 (3)0.0694 (2)0.0433 (12)
C270.4367 (5)0.2075 (4)0.0496 (2)0.0574 (15)
H27A0.37550.23320.04280.069*
C280.5284 (5)0.2465 (4)0.0394 (3)0.0693 (19)
H28A0.52810.29680.02480.083*
C290.6169 (5)0.2092 (5)0.0514 (3)0.069 (2)
C300.6201 (5)0.1363 (5)0.0732 (3)0.077 (2)
H30A0.68170.11300.08270.092*
C310.5310 (4)0.0971 (4)0.0813 (3)0.0603 (16)
H31A0.53320.04610.09500.072*
C320.2688 (4)0.0565 (3)0.0135 (2)0.0468 (13)
C330.1857 (5)0.0077 (4)0.0086 (3)0.0665 (18)
H33A0.1581−0.01310.03900.080*
C340.1424 (5)−0.0111 (5)−0.0403 (4)0.086 (3)
H34A0.0866−0.0443−0.04280.103*
C350.1842 (7)0.0212 (5)−0.0873 (3)0.088 (3)
H35A0.15600.0090−0.12060.105*
C360.2638 (7)0.0686 (5)−0.0828 (3)0.084 (2)
H36A0.29100.0898−0.11320.101*
C370.3079 (5)0.0874 (4)−0.0327 (2)0.0645 (17)
H37A0.36360.1207−0.03050.077*
C380.3574 (4)−0.0136 (3)0.1050 (2)0.0433 (12)
C390.3556 (4)−0.0316 (4)0.1587 (2)0.0523 (14)
H39A0.32770.00440.18190.063*
C400.3944 (5)−0.1020 (4)0.1784 (3)0.0623 (17)
H40A0.3925−0.11310.21450.075*
C410.4354 (5)−0.1553 (4)0.1442 (3)0.0685 (19)
H41A0.4647−0.20150.15740.082*
C420.4335 (5)−0.1402 (4)0.0897 (3)0.071 (2)
H42A0.4572−0.17770.06630.085*
C430.3966 (5)−0.0703 (4)0.0715 (2)0.0571 (16)
H43A0.3974−0.06000.03530.069*
C440.2033 (4)0.3203 (3)0.0846 (3)0.0491 (14)
C450.3714 (4)0.3393 (4)0.1466 (3)0.0670 (19)
C460.2647 (5)0.2992 (3)0.2354 (3)0.0525 (14)
C470.1078 (4)0.1867 (3)0.2453 (2)0.0475 (13)
C48−0.0591 (4)0.1669 (3)0.1799 (3)0.0513 (14)
C490.0046 (4)0.2904 (3)0.1191 (2)0.0431 (12)
C500.1146 (4)0.1708 (4)0.0662 (2)0.0481 (13)
C510.1244 (4)0.0604 (3)0.1463 (2)0.0428 (12)
C520.2949 (4)0.1556 (3)0.1875 (2)0.0442 (12)
Cl1A0.3768 (15)0.4277 (14)−0.0348 (9)0.097 (6)0.15
Cl2A0.5082 (16)0.3887 (11)−0.1025 (9)0.118 (7)0.15
Cl3A0.326 (2)0.3053 (11)−0.0909 (11)0.102 (7)0.15
C53A0.393 (2)0.382 (2)−0.0880 (16)0.073 (13)*0.15
H53A0.35970.4163−0.11450.088*0.15
Cl1B0.3361 (12)0.4365 (13)−0.0503 (7)0.084 (5)0.15
Cl2B0.4565 (12)0.3670 (9)−0.1348 (7)0.085 (5)0.15
Cl3B0.3069 (15)0.2742 (9)−0.0856 (6)0.064 (4)0.15
C53B0.348 (2)0.3668 (12)−0.0994 (11)0.042 (8)*0.15
H53B0.29710.3845−0.12600.051*0.15

Atomic displacement parameters (Å2)

U11U22U33U12U13U23
Ru10.03017 (19)0.0334 (2)0.0485 (3)−0.00255 (15)0.00296 (16)−0.00460 (18)
Ru20.03149 (19)0.0291 (2)0.0367 (2)−0.00158 (14)0.00485 (15)−0.00434 (16)
Ru30.03338 (19)0.0313 (2)0.0368 (2)0.00096 (15)0.00430 (15)−0.00422 (16)
As10.0338 (2)0.0305 (3)0.0433 (3)−0.00346 (19)0.0004 (2)−0.0003 (2)
As20.0318 (2)0.0296 (3)0.0341 (3)0.00008 (18)0.00137 (19)−0.0033 (2)
P10.0365 (6)0.0405 (7)0.0407 (7)−0.0001 (5)0.0085 (5)−0.0065 (6)
Br10.0793 (6)0.1379 (9)0.1450 (9)−0.0582 (6)0.0501 (6)−0.0405 (7)
O10.082 (3)0.077 (3)0.049 (3)−0.009 (3)0.007 (2)0.007 (2)
O20.047 (3)0.155 (6)0.182 (7)−0.041 (3)0.029 (4)−0.067 (5)
O30.106 (4)0.060 (3)0.058 (3)0.003 (3)−0.017 (3)−0.005 (2)
O40.094 (4)0.061 (3)0.057 (3)0.022 (3)−0.002 (2)0.015 (2)
O50.062 (3)0.061 (3)0.147 (5)−0.029 (2)0.029 (3)−0.022 (3)
O60.054 (2)0.085 (3)0.054 (3)0.009 (2)−0.001 (2)0.010 (2)
O70.090 (3)0.082 (4)0.058 (3)0.016 (3)−0.022 (3)−0.008 (3)
O80.069 (3)0.046 (3)0.084 (3)−0.013 (2)0.006 (2)0.007 (2)
O90.060 (3)0.049 (3)0.080 (3)0.013 (2)−0.027 (2)−0.013 (2)
C10.039 (3)0.040 (3)0.059 (4)−0.010 (2)−0.001 (2)−0.005 (3)
C20.065 (4)0.042 (4)0.102 (6)−0.003 (3)−0.022 (4)−0.005 (4)
C30.077 (5)0.042 (4)0.146 (8)−0.015 (3)−0.027 (5)−0.014 (4)
C40.064 (4)0.060 (5)0.139 (8)−0.016 (4)−0.027 (5)−0.030 (5)
C50.083 (5)0.062 (5)0.138 (8)−0.008 (4)−0.059 (5)−0.002 (5)
C60.071 (4)0.040 (4)0.126 (7)−0.008 (3)−0.044 (4)0.002 (4)
C70.051 (3)0.038 (3)0.046 (3)−0.004 (2)−0.001 (2)0.004 (2)
C80.058 (4)0.095 (6)0.074 (5)0.013 (4)0.001 (3)0.038 (4)
C90.089 (6)0.122 (8)0.100 (7)0.030 (5)−0.021 (5)0.050 (6)
C100.111 (7)0.098 (7)0.075 (6)0.008 (6)−0.026 (5)0.043 (5)
C110.158 (9)0.073 (5)0.048 (4)−0.024 (6)0.005 (5)0.019 (4)
C120.075 (4)0.071 (5)0.065 (4)−0.006 (4)0.008 (3)0.018 (4)
C130.042 (3)0.036 (3)0.035 (3)−0.003 (2)0.002 (2)−0.004 (2)
C140.044 (3)0.033 (3)0.036 (3)−0.002 (2)0.005 (2)−0.003 (2)
C150.047 (3)0.082 (5)0.041 (3)0.008 (3)0.001 (2)−0.002 (3)
C160.062 (4)0.109 (6)0.037 (3)0.005 (4)−0.005 (3)0.009 (3)
C170.083 (5)0.082 (5)0.047 (4)−0.008 (4)0.013 (3)0.007 (4)
C180.064 (4)0.088 (5)0.053 (4)−0.008 (4)0.015 (3)0.005 (4)
C190.042 (3)0.064 (4)0.048 (3)−0.004 (3)0.001 (2)0.004 (3)
C200.034 (2)0.041 (3)0.036 (3)0.002 (2)−0.0006 (19)−0.003 (2)
C210.041 (3)0.049 (3)0.073 (4)0.003 (2)−0.007 (3)−0.019 (3)
C220.036 (3)0.073 (5)0.097 (5)0.004 (3)−0.017 (3)−0.028 (4)
C230.039 (3)0.072 (4)0.073 (4)0.017 (3)−0.009 (3)0.000 (3)
C240.046 (3)0.041 (3)0.063 (4)0.008 (2)−0.006 (3)−0.001 (3)
C250.040 (3)0.038 (3)0.049 (3)−0.001 (2)−0.004 (2)−0.005 (2)
C260.038 (3)0.053 (3)0.039 (3)−0.004 (2)0.005 (2)−0.009 (2)
C270.055 (3)0.055 (4)0.063 (4)−0.004 (3)0.013 (3)−0.002 (3)
C280.072 (4)0.063 (4)0.074 (5)−0.017 (3)0.026 (4)0.001 (3)
C290.045 (3)0.089 (5)0.075 (5)−0.028 (3)0.026 (3)−0.027 (4)
C300.044 (3)0.094 (6)0.094 (6)−0.013 (4)0.012 (3)−0.014 (5)
C310.046 (3)0.066 (4)0.070 (4)0.001 (3)0.001 (3)0.000 (3)
C320.043 (3)0.050 (3)0.047 (3)0.003 (2)0.000 (2)−0.015 (3)
C330.058 (4)0.069 (4)0.073 (5)−0.003 (3)0.002 (3)−0.020 (4)
C340.061 (4)0.085 (6)0.110 (7)−0.001 (4)−0.023 (4)−0.042 (5)
C350.108 (7)0.086 (6)0.068 (5)0.016 (5)−0.029 (5)−0.029 (5)
C360.108 (6)0.091 (6)0.051 (4)0.007 (5)−0.012 (4)−0.011 (4)
C370.065 (4)0.080 (5)0.049 (4)0.003 (3)0.002 (3)−0.010 (3)
C380.040 (3)0.039 (3)0.051 (3)0.003 (2)0.010 (2)−0.004 (2)
C390.057 (3)0.046 (3)0.054 (4)0.008 (3)0.008 (3)−0.008 (3)
C400.077 (4)0.050 (4)0.061 (4)0.011 (3)0.012 (3)0.003 (3)
C410.069 (4)0.044 (4)0.093 (5)0.017 (3)0.016 (4)0.004 (4)
C420.079 (5)0.049 (4)0.087 (5)0.016 (3)0.034 (4)−0.008 (4)
C430.070 (4)0.050 (4)0.053 (4)0.014 (3)0.018 (3)−0.007 (3)
C440.041 (3)0.048 (3)0.058 (4)−0.008 (2)0.011 (3)−0.004 (3)
C450.040 (3)0.069 (4)0.092 (5)−0.011 (3)0.007 (3)−0.020 (4)
C460.060 (4)0.037 (3)0.060 (4)0.006 (3)−0.004 (3)−0.001 (3)
C470.053 (3)0.037 (3)0.053 (4)0.008 (2)0.008 (3)−0.003 (3)
C480.043 (3)0.042 (3)0.070 (4)−0.005 (2)0.014 (3)−0.010 (3)
C490.035 (2)0.051 (3)0.044 (3)0.000 (2)0.001 (2)−0.001 (3)
C500.049 (3)0.051 (3)0.044 (3)0.007 (3)0.000 (3)−0.007 (3)
C510.041 (3)0.041 (3)0.046 (3)0.002 (2)0.001 (2)0.000 (2)
C520.047 (3)0.035 (3)0.051 (3)0.002 (2)−0.002 (2)−0.011 (2)
Cl1A0.087 (13)0.096 (12)0.106 (14)0.037 (11)−0.019 (10)0.010 (10)
Cl2A0.130 (16)0.092 (12)0.136 (17)0.018 (11)0.087 (13)0.028 (12)
Cl3A0.117 (16)0.054 (12)0.135 (17)0.003 (10)−0.007 (12)0.008 (11)
Cl1B0.062 (9)0.110 (13)0.081 (11)0.027 (9)0.012 (8)0.000 (9)
Cl2B0.098 (11)0.060 (8)0.099 (11)0.058 (8)0.034 (8)0.020 (8)
Cl3B0.090 (9)0.046 (9)0.054 (7)−0.010 (7)−0.012 (6)0.027 (7)

Geometric parameters (Å, °)

Ru1—C451.883 (6)C15—C161.388 (8)
Ru1—C441.940 (7)C15—H15A0.9300
Ru1—C461.942 (7)C16—C171.354 (9)
Ru1—As12.4410 (6)C16—H16A0.9300
Ru1—Ru22.8495 (5)C17—C181.400 (10)
Ru1—Ru32.8870 (6)C17—H17A0.9300
Ru2—C481.885 (6)C18—C191.386 (8)
Ru2—C491.915 (6)C18—H18A0.9300
Ru2—C471.935 (6)C19—H19A0.9300
Ru2—As22.4323 (6)C20—C251.371 (7)
Ru2—Ru32.8366 (5)C20—C211.382 (7)
Ru3—C511.880 (5)C21—C221.405 (8)
Ru3—C521.916 (6)C21—H21A0.9300
Ru3—C501.940 (6)C22—C231.388 (9)
Ru3—P12.3423 (13)C22—H22A0.9300
As1—C71.941 (5)C23—C241.376 (8)
As1—C11.957 (5)C23—H23A0.9300
As1—C131.964 (5)C24—C251.379 (7)
As2—C201.942 (5)C24—H24A0.9300
As2—C141.958 (5)C25—H25A0.9300
As2—C131.972 (5)C26—C271.381 (8)
P1—C381.823 (6)C26—C311.393 (8)
P1—C321.828 (6)C27—C281.412 (8)
P1—C261.828 (5)C27—H27A0.9300
Br1—C291.902 (6)C28—C291.358 (10)
O1—C441.129 (7)C28—H28A0.9300
O2—C451.143 (7)C29—C301.352 (11)
O3—C461.132 (7)C30—C311.375 (9)
O4—C471.130 (7)C30—H30A0.9300
O5—C481.153 (7)C31—H31A0.9300
O6—C491.149 (6)C32—C331.380 (8)
O7—C501.140 (7)C32—C371.390 (8)
O8—C511.142 (6)C33—C341.381 (10)
O9—C521.149 (6)C33—H33A0.9300
C1—C61.362 (8)C34—C351.433 (12)
C1—C21.378 (8)C34—H34A0.9300
C2—C31.412 (9)C35—C361.326 (11)
C2—H2A0.9300C35—H35A0.9300
C3—C41.342 (10)C36—C371.412 (9)
C3—H3A0.9300C36—H36A0.9300
C4—C51.333 (11)C37—H37A0.9300
C4—H4A0.9300C38—C391.390 (8)
C5—C61.401 (9)C38—C431.390 (7)
C5—H5A0.9300C39—C401.385 (8)
C6—H6A0.9300C39—H39A0.9300
C7—C81.349 (8)C40—C411.372 (9)
C7—C121.390 (8)C40—H40A0.9300
C8—C91.393 (10)C41—C421.397 (10)
C8—H8A0.9300C41—H41A0.9300
C9—C101.283 (12)C42—C431.356 (9)
C9—H9A0.9300C42—H42A0.9300
C10—C111.385 (12)C43—H43A0.9300
C10—H10A0.9300Cl1A—C53A1.57 (2)
C11—C121.398 (10)Cl2A—C53A1.58 (2)
C11—H11A0.9300Cl3A—C53A1.58 (2)
C12—H12A0.9300C53A—H53A0.9800
C13—H13A0.9700Cl1B—C53B1.721 (17)
C13—H13B0.9700Cl2B—C53B1.720 (16)
C14—C151.375 (7)Cl3B—C53B1.699 (16)
C14—C191.376 (7)C53B—H53B0.9800
C45—Ru1—C4489.8 (3)C14—C15—C16119.4 (6)
C45—Ru1—C4692.9 (3)C14—C15—H15A120.3
C44—Ru1—C46176.3 (2)C16—C15—H15A120.3
C45—Ru1—As1100.9 (2)C17—C16—C15121.0 (6)
C44—Ru1—As194.12 (17)C17—C16—H16A119.5
C46—Ru1—As187.98 (17)C15—C16—H16A119.5
C45—Ru1—Ru2167.2 (2)C16—C17—C18120.2 (6)
C44—Ru1—Ru293.30 (15)C16—C17—H17A119.9
C46—Ru1—Ru283.58 (18)C18—C17—H17A119.9
As1—Ru1—Ru291.263 (18)C19—C18—C17118.5 (6)
C45—Ru1—Ru3109.7 (2)C19—C18—H18A120.7
C44—Ru1—Ru376.52 (17)C17—C18—H18A120.7
C46—Ru1—Ru3100.10 (17)C14—C19—C18120.9 (6)
As1—Ru1—Ru3147.83 (2)C14—C19—H19A119.5
Ru2—Ru1—Ru359.268 (13)C18—C19—H19A119.5
C48—Ru2—C4992.4 (3)C25—C20—C21119.1 (5)
C48—Ru2—C4791.4 (3)C25—C20—As2123.1 (4)
C49—Ru2—C47175.0 (2)C21—C20—As2117.7 (4)
C48—Ru2—As2102.07 (17)C20—C21—C22119.9 (5)
C49—Ru2—As289.41 (16)C20—C21—H21A120.0
C47—Ru2—As293.03 (16)C22—C21—H21A120.0
C48—Ru2—Ru3100.77 (17)C23—C22—C21119.6 (6)
C49—Ru2—Ru392.41 (15)C23—C22—H22A120.2
C47—Ru2—Ru383.63 (15)C21—C22—H22A120.2
As2—Ru2—Ru3156.99 (2)C24—C23—C22120.1 (5)
C48—Ru2—Ru1160.77 (17)C24—C23—H23A120.0
C49—Ru2—Ru182.88 (15)C22—C23—H23A120.0
C47—Ru2—Ru192.46 (17)C23—C24—C25119.5 (5)
As2—Ru2—Ru196.525 (18)C23—C24—H24A120.2
Ru3—Ru2—Ru161.024 (13)C25—C24—H24A120.2
C51—Ru3—C52101.4 (2)C20—C25—C24121.8 (5)
C51—Ru3—C5092.2 (2)C20—C25—H25A119.1
C52—Ru3—C50166.3 (2)C24—C25—H25A119.1
C51—Ru3—P194.43 (16)C27—C26—C31117.7 (5)
C52—Ru3—P189.15 (16)C27—C26—P1118.6 (4)
C50—Ru3—P191.29 (16)C31—C26—P1123.6 (5)
C51—Ru3—Ru286.79 (16)C26—C27—C28120.3 (6)
C52—Ru3—Ru294.01 (15)C26—C27—H27A119.8
C50—Ru3—Ru285.20 (16)C28—C27—H27A119.8
P1—Ru3—Ru2176.33 (4)C29—C28—C27118.9 (7)
C51—Ru3—Ru1143.46 (16)C29—C28—H28A120.5
C52—Ru3—Ru169.60 (16)C27—C28—H28A120.5
C50—Ru3—Ru198.52 (18)C30—C29—C28122.1 (6)
P1—Ru3—Ru1119.95 (4)C30—C29—Br1119.3 (6)
Ru2—Ru3—Ru159.708 (13)C28—C29—Br1118.6 (6)
C7—As1—C1100.8 (2)C29—C30—C31119.1 (7)
C7—As1—C13104.7 (2)C29—C30—H30A120.4
C1—As1—C1399.0 (2)C31—C30—H30A120.4
C7—As1—Ru1118.55 (17)C30—C31—C26121.7 (7)
C1—As1—Ru1117.51 (16)C30—C31—H31A119.1
C13—As1—Ru1113.54 (15)C26—C31—H31A119.1
C20—As2—C14102.0 (2)C33—C32—C37117.9 (6)
C20—As2—C13104.0 (2)C33—C32—P1118.6 (5)
C14—As2—C13101.7 (2)C37—C32—P1123.3 (5)
C20—As2—Ru2116.18 (14)C32—C33—C34121.7 (7)
C14—As2—Ru2117.40 (15)C32—C33—H33A119.2
C13—As2—Ru2113.62 (14)C34—C33—H33A119.2
C38—P1—C32101.1 (3)C33—C34—C35119.4 (7)
C38—P1—C26101.9 (3)C33—C34—H34A120.3
C32—P1—C26104.9 (2)C35—C34—H34A120.3
C38—P1—Ru3117.08 (17)C36—C35—C34119.1 (7)
C32—P1—Ru3112.92 (17)C36—C35—H35A120.4
C26—P1—Ru3117.05 (18)C34—C35—H35A120.4
C6—C1—C2119.0 (5)C35—C36—C37121.2 (8)
C6—C1—As1120.3 (5)C35—C36—H36A119.4
C2—C1—As1120.7 (4)C37—C36—H36A119.4
C1—C2—C3119.9 (6)C32—C37—C36120.7 (7)
C1—C2—H2A120.0C32—C37—H37A119.7
C3—C2—H2A120.0C36—C37—H37A119.7
C4—C3—C2119.5 (7)C39—C38—C43117.3 (5)
C4—C3—H3A120.2C39—C38—P1121.3 (4)
C2—C3—H3A120.2C43—C38—P1121.3 (4)
C5—C4—C3120.9 (7)C40—C39—C38121.4 (5)
C5—C4—H4A119.6C40—C39—H39A119.3
C3—C4—H4A119.6C38—C39—H39A119.3
C4—C5—C6121.0 (7)C41—C40—C39119.4 (6)
C4—C5—H5A119.5C41—C40—H40A120.3
C6—C5—H5A119.5C39—C40—H40A120.3
C1—C6—C5119.6 (6)C40—C41—C42120.1 (6)
C1—C6—H6A120.2C40—C41—H41A119.9
C5—C6—H6A120.2C42—C41—H41A119.9
C8—C7—C12118.3 (6)C43—C42—C41119.3 (6)
C8—C7—As1123.9 (5)C43—C42—H42A120.4
C12—C7—As1117.7 (5)C41—C42—H42A120.4
C7—C8—C9119.7 (7)C42—C43—C38122.3 (6)
C7—C8—H8A120.1C42—C43—H43A118.8
C9—C8—H8A120.1C38—C43—H43A118.8
C10—C9—C8123.0 (9)O1—C44—Ru1171.8 (5)
C10—C9—H9A118.5O2—C45—Ru1178.8 (7)
C8—C9—H9A118.5O3—C46—Ru1173.6 (6)
C9—C10—C11119.9 (8)O4—C47—Ru2174.7 (5)
C9—C10—H10A120.0O5—C48—Ru2177.5 (6)
C11—C10—H10A120.0O6—C49—Ru2174.3 (5)
C10—C11—C12118.7 (7)O7—C50—Ru3175.4 (5)
C10—C11—H11A120.7O8—C51—Ru3176.1 (5)
C12—C11—H11A120.7O9—C52—Ru3169.5 (5)
C7—C12—C11120.2 (7)Cl1A—C53A—Cl3A111 (2)
C7—C12—H12A119.9Cl1A—C53A—Cl2A109 (2)
C11—C12—H12A119.9Cl3A—C53A—Cl2A127 (2)
As1—C13—As2112.8 (2)Cl1A—C53A—H53A102.5
As1—C13—H13A109.0Cl3A—C53A—H53A102.5
As2—C13—H13A109.0Cl2A—C53A—H53A102.5
As1—C13—H13B109.0Cl3B—C53B—Cl2B112.6 (15)
As2—C13—H13B109.0Cl3B—C53B—Cl1B116.8 (16)
H13A—C13—H13B107.8Cl2B—C53B—Cl1B117.9 (14)
C15—C14—C19119.9 (5)Cl3B—C53B—H53B102.0
C15—C14—As2119.7 (4)Cl2B—C53B—H53B102.0
C19—C14—As2120.4 (4)Cl1B—C53B—H53B102.0
C45—Ru1—Ru2—C48−51.6 (12)C13—As1—C1—C695.6 (6)
C44—Ru1—Ru2—C4852.1 (6)Ru1—As1—C1—C6−27.0 (6)
C46—Ru1—Ru2—C48−125.9 (6)C7—As1—C1—C224.0 (6)
As1—Ru1—Ru2—C48146.3 (6)C13—As1—C1—C2−83.0 (6)
Ru3—Ru1—Ru2—C48−20.1 (6)Ru1—As1—C1—C2154.4 (5)
C45—Ru1—Ru2—C49−128.2 (10)C6—C1—C2—C3−1.2 (11)
C44—Ru1—Ru2—C49−24.6 (2)As1—C1—C2—C3177.4 (6)
C46—Ru1—Ru2—C49157.5 (2)C1—C2—C3—C40.1 (13)
As1—Ru1—Ru2—C4969.63 (17)C2—C3—C4—C50.0 (15)
Ru3—Ru1—Ru2—C49−96.76 (17)C3—C4—C5—C60.8 (16)
C45—Ru1—Ru2—C4749.9 (10)C2—C1—C6—C52.1 (12)
C44—Ru1—Ru2—C47153.5 (2)As1—C1—C6—C5−176.5 (7)
C46—Ru1—Ru2—C47−24.5 (2)C4—C5—C6—C1−1.9 (15)
As1—Ru1—Ru2—C47−112.29 (16)C1—As1—C7—C8−107.4 (6)
Ru3—Ru1—Ru2—C4781.33 (16)C13—As1—C7—C8−5.0 (6)
C45—Ru1—Ru2—As2143.2 (10)Ru1—As1—C7—C8122.8 (6)
C44—Ru1—Ru2—As2−113.15 (17)C1—As1—C7—C1271.4 (5)
C46—Ru1—Ru2—As268.87 (17)C13—As1—C7—C12173.8 (5)
As1—Ru1—Ru2—As2−18.95 (2)Ru1—As1—C7—C12−58.3 (5)
Ru3—Ru1—Ru2—As2174.66 (2)C12—C7—C8—C9−0.3 (12)
C45—Ru1—Ru2—Ru3−31.5 (10)As1—C7—C8—C9178.5 (7)
C44—Ru1—Ru2—Ru372.19 (17)C7—C8—C9—C10−0.5 (16)
C46—Ru1—Ru2—Ru3−105.79 (17)C8—C9—C10—C110.3 (17)
As1—Ru1—Ru2—Ru3166.39 (2)C9—C10—C11—C120.8 (15)
C48—Ru2—Ru3—C51−21.9 (3)C8—C7—C12—C111.4 (10)
C49—Ru2—Ru3—C51−114.8 (2)As1—C7—C12—C11−177.5 (6)
C47—Ru2—Ru3—C5168.3 (2)C10—C11—C12—C7−1.6 (12)
As2—Ru2—Ru3—C51151.05 (17)C7—As1—C13—As292.9 (3)
Ru1—Ru2—Ru3—C51164.73 (17)C1—As1—C13—As2−163.3 (3)
C48—Ru2—Ru3—C52−123.1 (3)Ru1—As1—C13—As2−37.9 (3)
C49—Ru2—Ru3—C52144.0 (2)C20—As2—C13—As1−107.9 (3)
C47—Ru2—Ru3—C52−32.8 (2)C14—As2—C13—As1146.4 (3)
As2—Ru2—Ru3—C5249.86 (17)Ru2—As2—C13—As119.3 (3)
Ru1—Ru2—Ru3—C5263.54 (17)C20—As2—C14—C15−164.4 (5)
C48—Ru2—Ru3—C5070.6 (3)C13—As2—C14—C15−57.1 (5)
C49—Ru2—Ru3—C50−22.3 (2)Ru2—As2—C14—C1567.5 (5)
C47—Ru2—Ru3—C50160.8 (2)C20—As2—C14—C1917.8 (5)
As2—Ru2—Ru3—C50−116.46 (19)C13—As2—C14—C19125.1 (5)
Ru1—Ru2—Ru3—C50−102.79 (18)Ru2—As2—C14—C19−110.3 (4)
C48—Ru2—Ru3—Ru1173.4 (2)C19—C14—C15—C16−0.1 (10)
C49—Ru2—Ru3—Ru180.49 (16)As2—C14—C15—C16−177.9 (5)
C47—Ru2—Ru3—Ru1−96.39 (17)C14—C15—C16—C17−0.3 (11)
As2—Ru2—Ru3—Ru1−13.68 (5)C15—C16—C17—C180.4 (12)
C45—Ru1—Ru3—C51146.7 (4)C16—C17—C18—C19−0.1 (11)
C44—Ru1—Ru3—C51−128.4 (3)C15—C14—C19—C180.3 (9)
C46—Ru1—Ru3—C5150.0 (3)As2—C14—C19—C18178.2 (5)
As1—Ru1—Ru3—C51−52.4 (3)C17—C18—C19—C14−0.3 (10)
Ru2—Ru1—Ru3—C51−26.2 (3)C14—As2—C20—C2574.7 (5)
C45—Ru1—Ru3—C5265.3 (3)C13—As2—C20—C25−30.7 (5)
C44—Ru1—Ru3—C52150.1 (2)Ru2—As2—C20—C25−156.4 (4)
C46—Ru1—Ru3—C52−31.4 (3)C14—As2—C20—C21−102.1 (5)
As1—Ru1—Ru3—C52−133.90 (18)C13—As2—C20—C21152.5 (4)
Ru2—Ru1—Ru3—C52−107.67 (17)Ru2—As2—C20—C2126.8 (5)
C45—Ru1—Ru3—C50−107.7 (3)C25—C20—C21—C221.0 (9)
C44—Ru1—Ru3—C50−22.9 (2)As2—C20—C21—C22177.9 (5)
C46—Ru1—Ru3—C50155.5 (2)C20—C21—C22—C23−0.9 (11)
As1—Ru1—Ru3—C5053.08 (17)C21—C22—C23—C240.6 (11)
Ru2—Ru1—Ru3—C5079.31 (16)C22—C23—C24—C25−0.3 (10)
C45—Ru1—Ru3—P1−11.3 (3)C21—C20—C25—C24−0.8 (8)
C44—Ru1—Ru3—P173.58 (16)As2—C20—C25—C24−177.5 (4)
C46—Ru1—Ru3—P1−107.99 (19)C23—C24—C25—C200.5 (9)
As1—Ru1—Ru3—P1149.55 (6)C38—P1—C26—C27179.3 (5)
Ru2—Ru1—Ru3—P1175.78 (5)C32—P1—C26—C2774.3 (5)
C45—Ru1—Ru3—Ru2173.0 (3)Ru3—P1—C26—C27−51.7 (5)
C44—Ru1—Ru3—Ru2−102.20 (16)C38—P1—C26—C31−1.9 (5)
C46—Ru1—Ru3—Ru276.23 (18)C32—P1—C26—C31−106.8 (5)
As1—Ru1—Ru3—Ru2−26.23 (4)Ru3—P1—C26—C31127.2 (5)
C45—Ru1—As1—C794.2 (3)C31—C26—C27—C283.0 (9)
C44—Ru1—As1—C73.7 (2)P1—C26—C27—C28−178.1 (5)
C46—Ru1—As1—C7−173.3 (3)C26—C27—C28—C29−2.5 (10)
Ru2—Ru1—As1—C7−89.72 (18)C27—C28—C29—C30−0.6 (11)
Ru3—Ru1—As1—C7−67.39 (19)C27—C28—C29—Br1178.0 (5)
C45—Ru1—As1—C1−27.4 (3)C28—C29—C30—C313.1 (11)
C44—Ru1—As1—C1−118.0 (2)Br1—C29—C30—C31−175.5 (5)
C46—Ru1—As1—C165.1 (3)C29—C30—C31—C26−2.5 (11)
Ru2—Ru1—As1—C1148.64 (19)C27—C26—C31—C30−0.5 (9)
Ru3—Ru1—As1—C1170.97 (19)P1—C26—C31—C30−179.3 (5)
C45—Ru1—As1—C13−142.2 (3)C38—P1—C32—C3364.5 (5)
C44—Ru1—As1—C13127.2 (2)C26—P1—C32—C33170.1 (5)
C46—Ru1—As1—C13−49.7 (2)Ru3—P1—C32—C33−61.4 (5)
Ru2—Ru1—As1—C1333.83 (16)C38—P1—C32—C37−119.7 (5)
Ru3—Ru1—As1—C1356.16 (17)C26—P1—C32—C37−14.1 (6)
C48—Ru2—As2—C20−50.9 (3)Ru3—P1—C32—C37114.4 (5)
C49—Ru2—As2—C2041.4 (2)C37—C32—C33—C340.6 (10)
C47—Ru2—As2—C20−143.0 (2)P1—C32—C33—C34176.6 (5)
Ru3—Ru2—As2—C20136.14 (17)C32—C33—C34—C35−0.3 (11)
Ru1—Ru2—As2—C20124.12 (16)C33—C34—C35—C36−0.1 (12)
C48—Ru2—As2—C1470.0 (3)C34—C35—C36—C370.3 (13)
C49—Ru2—As2—C14162.3 (2)C33—C32—C37—C36−0.4 (10)
C47—Ru2—As2—C14−22.1 (2)P1—C32—C37—C36−176.2 (5)
Ru3—Ru2—As2—C14−102.88 (17)C35—C36—C37—C32−0.1 (12)
Ru1—Ru2—As2—C14−114.89 (17)C32—P1—C38—C39−149.9 (5)
C48—Ru2—As2—C13−171.6 (3)C26—P1—C38—C39102.2 (5)
C49—Ru2—As2—C13−79.3 (2)Ru3—P1—C38—C39−26.8 (5)
C47—Ru2—As2—C1396.3 (2)C32—P1—C38—C4333.6 (5)
Ru3—Ru2—As2—C1315.51 (18)C26—P1—C38—C43−74.4 (5)
Ru1—Ru2—As2—C133.49 (17)Ru3—P1—C38—C43156.6 (4)
C51—Ru3—P1—C38−38.5 (3)C43—C38—C39—C402.2 (9)
C52—Ru3—P1—C3862.9 (3)P1—C38—C39—C40−174.5 (5)
C50—Ru3—P1—C38−130.8 (3)C38—C39—C40—C410.0 (10)
Ru1—Ru3—P1—C38128.6 (2)C39—C40—C41—C42−3.2 (11)
C51—Ru3—P1—C3278.3 (3)C40—C41—C42—C434.2 (11)
C52—Ru3—P1—C32179.6 (3)C41—C42—C43—C38−2.0 (11)
C50—Ru3—P1—C32−14.1 (3)C39—C38—C43—C42−1.1 (9)
Ru1—Ru3—P1—C32−114.7 (2)P1—C38—C43—C42175.5 (5)
C51—Ru3—P1—C26−159.8 (3)C51—Ru3—C52—O960 (3)
C52—Ru3—P1—C26−58.5 (3)C50—Ru3—C52—O9−127 (3)
C50—Ru3—P1—C26107.8 (3)P1—Ru3—C52—O9−35 (3)
Ru1—Ru3—P1—C267.2 (2)Ru2—Ru3—C52—O9147 (3)
C7—As1—C1—C6−157.4 (6)Ru1—Ru3—C52—O9−157 (3)

Hydrogen-bond geometry (Å, °)

D—H···AD—HH···AD···AD—H···A
C23—H23A···O2i0.932.593.180 (8)122

Symmetry codes: (i) x−1, y, z.

Footnotes

Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: RZ2406).

References

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