metal-organic compounds\(\def\hfill{\hskip 5em}\def\hfil{\hskip 3em}\def\eqno#1{\hfil {#1}}\)

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ISSN: 2414-3146

μ-Carbonyl-bis­­(carbon­yl{η5-[tri­carbon­yl(η6-2-meth­yl­inden­yl)­chromium(0)]rhodium(III)})(RhRh)

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aInstitut de Chimie de Strasbourg, UMR 7177 CNRS Universite de Strasbourg, 4 rue Blaise Pascal, F-67000 Strasbourg, France, and bFédération de Chimie "Le Bel" FR 2010, Service de Radiocristallographie, 1 rue Blaise Pascal, F-67000 Strasbourg, France
*Correspondence e-mail: djukic@unistra.fr

Edited by M. Nieger, University of Helsinki, Finland (Received 7 January 2019; accepted 26 April 2019; online 10 May 2019)

The structure of the title complex, [Cr2Rh2(C10H9)2(CO)9], was solved by single-crystal X-ray diffraction analysis in the P21/c space group. The crystal shows two units of the tetra­metallic complex in the asymmetric unit. The most remarkable features of this new compound are the asymmetric bonding of the RhIII atom to the indenyl ligand, which can be formulated in terms of an η2;η3 coordination rather than η5, and the Rh—Rh distances of 2.6756 (6) and 2.6737 (6) Å that are characteristic of an inter­metallic inter­action supported by a bridging carbonyl ligand. The infrared spectroscopic signature informs of its clear bridging feature characterized by a significantly elongated C=O bond length compared to those in the two Rh-bound `terminal' carbonyl ligands.

3D view (loading...)
[Scheme 3D1]
Chemical scheme
[Scheme 1]

Structure description

Benzylic-type anions of tricarbon­yl(η6-inden­yl)chromium complexes (Ceccon et al., 1988[Ceccon, A., Gambaro, A., Venzo, A., Lucchini, V., Bitterwolf, T. E. & Shade, J. (1988). J. Organomet. Chem. 349, 315-322.]) are known to behave as efficient `hemichelating' (Werlé et al., 2013[Werlé, C., Bailly, C., Karmazin-Brelot, L., Le Goff, X.-F., Ricard, L. & Djukic, J.-P. (2013). J. Am. Chem. Soc. 135, 17839-17852.]) ligands of transition metal atoms such as PdII (Werlé et al., 2013[Werlé, C., Bailly, C., Karmazin-Brelot, L., Le Goff, X.-F., Ricard, L. & Djukic, J.-P. (2013). J. Am. Chem. Soc. 135, 17839-17852.], 2016[Werlé, C., Anstine, D. M., Karmazin, L., Bailly, C., Ricard, L. & Djukic, J.-P. (2016). Dalton Trans. 45, 607-617.], 2017[Werlé, C., Dohm, S., Bailly, C., Karmazin, L., Ricard, L., Sieffert, N., Pfeffer, M., Hansen, A., Grimme, S. & Djukic, J.-P. (2017). Dalton Trans. 46, 8125-8137.]), PdI (Werlé et al., 2015[Werlé, C., Karmazin, L., Bailly, C., Ricard, L. & Djukic, J.-P. (2015). Organometallics, 34, 3055-3064.]) and PtII (Werlé et al., 2013[Werlé, C., Bailly, C., Karmazin-Brelot, L., Le Goff, X.-F., Ricard, L. & Djukic, J.-P. (2013). J. Am. Chem. Soc. 135, 17839-17852.]). It has been shown that the Cr(CO)3 moiety contributes to the stabilization by establishing attractive dynamic and mostly non-covalent inter­actions (dispersion, electron correlation and electrostatic) with the hemichelated metal atom, the latter being bonded to the ligand in an η1 fashion, thus displaying formal electronic unsaturation in terms of valence electron bookkeeping. We have found out (Werlé et al., 2014[Werlé, C., Bailly, C., Karmazin-Brelot, L., Le Goff, X.-F., Pfeffer, M. & Djukic, J.-P. (2014). Angew. Chem. Int. Ed. 53, 9827-9831.]) that the typical hemichelation of the metal atom could not be achieved for RhI atoms with indenyl-based anions but rather with fluorenyl-based anions, the reason being that with indenyl-based anions the Rh atom prefers, according to Ceccon and co-workers (Ceccon et al., 1989[Ceccon, A., Gambaro, A., Santi, S., Valle, G. & Venzo, A. (1989). J. Chem. Soc. Chem. Commun. pp. 51-53.],1993[Ceccon, A., Elsevier, C. J., Ernsting, J. M., Gambaro, A., Santi, S. & Venzo, A. (1993). Inorg. Chim. Acta, 204, 15-26.]; Bellomo et al., 1993[Bellomo, S., Ceccon, A., Gambaro, A., Santi, S. & Venzo, A. (1993). J. Organomet. Chem. 453, C4-C6.]; Bonifaci et al., 1993[Bonifaci, C., Ceccon, A., Gambaro, A., Ganis, P., Santi, S., Valle, G. & Venzo, A. (1993). Organometallics, 12, 4211-4214.], 1995[Bonifaci, C., Ceccon, A., Santi, S., Mealli, C. & Zoellner, R. W. (1995). Inorg. Chim. Acta, 240, 541-549.], 1996[Bonifaci, C., Carta, G., Ceccon, A., Gambaro, A., Santi, S. & Venzo, A. (1996). Organometallics, 15, 1630-1636.]; Cecchetto et al., 1998[Cecchetto, P., Ceccon, A., Gambaro, A., Santi, S., Ganis, P., Gobetto, R., Valle, G. & Venzo, A. (1998). Organometallics, 17, 752-762.]) and us (Werlé et al., 2014[Werlé, C., Bailly, C., Karmazin-Brelot, L., Le Goff, X.-F., Pfeffer, M. & Djukic, J.-P. (2014). Angew. Chem. Int. Ed. 53, 9827-9831.]), to reach electron saturation by coord­inating to the indenyl ligand in an η3-fashion, either in a syn or anti-facial manner, the former syn geometry being thermodynamically favored over the anti one due to attractive dispersion force.

In the course of our investigations we have focused on the use of the anion derived from tricarbon­yl(η6:2-methyl­indene)chromium, i.e 1 (Fig. 1[link]). This ligand was applied to the coord­ination of the RhI atom with [L2RhX]2 dimers (Werlé et al., 2014[Werlé, C., Bailly, C., Karmazin-Brelot, L., Le Goff, X.-F., Pfeffer, M. & Djukic, J.-P. (2014). Angew. Chem. Int. Ed. 53, 9827-9831.]). In the case where L2 = two carbonyls, norbornadiene or cyclo­octa­diene, the results of syntheses carried out in tetra­hydro­furane disclosed the formation of well-defined syn and anti-facial RhI complexes (Werlé et al., 2014[Werlé, C., Bailly, C., Karmazin-Brelot, L., Le Goff, X.-F., Pfeffer, M. & Djukic, J.-P. (2014). Angew. Chem. Int. Ed. 53, 9827-9831.]). In the case where L = CO, we observed that the outcome of the reaction depended on the nature of the solvent used in the reaction of the indenylic anion with [Rh(μ-Cl)(CO)]2. This report discloses that when the reaction is carried out in diethyl ether (Fig. 1[link]), also at a sub-ambient temperature, the main product is not a Cr0,RhI complex such as 2a or 2b but rather a tetra­nuclear Cr0,RhIII complex formulated as μ-carbonyl-bis{carbon­yl{η5:[tricarbon­yl(η6:2-methyl­inden­yl)chromium]rhodium(III)}}, i.e 3, obtained in ca 27% yield (Fig. 1[link]). Although the reason for the formal oxidation of Rh in this reaction is not clear, this new compound arises from the loss of one carbonyl ligand at the Rh atom and the establishment of an Rh—Rh inter­action supported by a bridging CO ligand (Fig. 1[link]), which according to FT–IR data is characterized by a typical stretching mode at 1712 cm−1 that contrasts with those of terminal carbonyl ligands.

[Figure 1]
Figure 1
Reaction scheme.

Fig. 2[link] shows the structure of the two independent mol­ecules of 3 present in the asymmetric unit, namely 3a, and 3b. This structure contains two η6-bonded Cr(CO)3 moieties bonded to the benzo moieties of the 2-methyl­indenyl ligand. In both mol­ecules, the Rh atoms are bonded to the five-membered ring of the indenyl ligand in an anti fashion with respect to the Cr(CO)3 moiety in a distorted η5 way better described as η2;η3. Considering mol­ecule 3a, the latter composite hapticity is evident from the significant difference of inter­atomic distances existing between Rh1 (or Rh2) and atoms C1 and C6 of 2.371 (6) and 2.404 (6) Å [or C16 with C16—Rh2 = 2.342 (6) and C21 with C21—Rh2 2.353 (6) Å], and atoms C7, C8, C9 [or C22 with C22—Rh2 = 2.254 (5), C23 with C23—Rh2 = 2.290 (5), C24 with C24—Rh2 = 2.223 (5) Å] of 2.242 (5), 2.243 (5) and 2.213 (5) Å respectively. In 3a, Rh atoms are connected to each other by a bridging carbonyl ligand at C15 and by a direct metal–metal inter­action characterized by an Rh1—Rh2 distance of 2.6756 (6) Å, which lies in the range encountered in other carbonyl-bridged Rh clusters (Faraone et al., 1983[Faraone, F., Lo Schiavo, S., Bruno, G., Piraino, P. & Bombieri, G. (1983). J. Chem. Soc. Dalton Trans. pp. 1813-1817.]; Enders et al., 2004[Enders, M., Kohl, G. & Pritzkow, H. (2004). J. Organomet. Chem. 689, 3024-3030.]).

[Figure 2]
Figure 2
The asymmetric unit of 3 with displacement ellipsoid at the 30% probability level, showing the two independent mol­ecules, i.e. 3a (left) and 3b (right).

Mol­ecules 3a and 3b have an overall C2 axis of symmetry aligned with the C15—O5 (3a) and C44—O14 (3 b) vectors. The C15—O15 bond [1.174 (7) Å] of the μ-bridging carbonyl is consistently elongated as compared to the two Rh-bound terminal carbonyl ligands embodied by C29—O9 [1.142 (7) Å] and C14—O4 [1.132 (7) Å] moieties. The structure of 3b contains two η6-bonded Cr(CO)3 moieties bonded to the benzo moieties of the 2-methyl­indenyl ligand. Again, the Rh atoms are bonded to the five-membered ring of the indenyl ligand in an anti fashion with respect to the Cr(CO)3 moiety in a distorted η5 way, better described as η2;η3 owing to the significant difference of inter­atomic distances existing between Rh3 (or Rh4) and atoms C35 and C30 of 2.343 (5) and 2.398 (5) Å [or C50 2.379 (5) and C45 2.410 (6) Å], and atoms C36, C37, C38 [or C51 with C51—Rh4 = 2.217 (5), C52 with C52—Rh4 = 2.262 (5), C53 with C53—Rh4 = 2.240 (5) Å] of 2.202 (5), 2.258 (5) and 2.263 (5) Å, respectively. The Rh atoms are connected to each other by a bridging carbonyl ligand at C44 and by a direct metal–metal inter­action characterized by a Rh3—Rh4 distance of 2.6737 (6) Å, which also lies in the range encountered in other carbonyl-bridged Rh clusters (Faraone et al., 1983[Faraone, F., Lo Schiavo, S., Bruno, G., Piraino, P. & Bombieri, G. (1983). J. Chem. Soc. Dalton Trans. pp. 1813-1817.]; Enders et al., 2004[Enders, M., Kohl, G. & Pritzkow, H. (2004). J. Organomet. Chem. 689, 3024-3030.]). The C44—O14 bond [1.162 (7) Å] of the μ-bridging carbonyl is consistently elongated as compared to the two Rh-bound terminal carbonyl ligands embodied by C43—O13 [1.142 (7) Å] and C58—O18 [1.138 (6) Å] moieties.

Fig. 3[link] shows the unit cell and the weak C—H⋯H hydrogen-bond network that connects the mol­ecules in the crystal lattice (cf. Table 1[link]).

Table 1
Hydrogen-bond geometry (Å, °)

D—H⋯A D—H H⋯A DA D—H⋯A
C2—H2⋯O7i 0.95 2.52 3.403 (8) 155
C32—H32⋯O6i 0.95 2.72 3.632 (8) 162
C5—H5⋯O4ii 0.95 2.23 3.108 (7) 153
C7—H7⋯O10ii 0.95 2.61 3.432 (8) 144
C17—H17⋯O2iii 0.95 2.55 3.399 (8) 149
C34—H34⋯O17iii 0.95 2.67 3.510 (7) 148
C10—H10C⋯O14iv 0.98 2.53 3.441 (8) 155
C25—H25A⋯O14v 0.98 2.68 3.346 (8) 125
C20—H20⋯O9vi 0.95 2.42 3.306 (7) 156
C51—H51⋯O5vii 0.95 2.55 3.313 (8) 137
C54—H54C⋯O5vii 0.98 2.72 3.336 (8) 122
C39—H39B⋯O5viii 0.98 2.53 3.374 (8) 145
C38—H38⋯O6ix 0.95 2.58 3.521 (8) 170
C22—H22⋯O15x 0.95 2.69 3.554 (7) 152
C46—H46⋯O13xi 0.95 2.47 3.262 (7) 141
C31—H31⋯O18xii 0.95 2.51 3.144 (7) 124
C49—H49⋯O11xii 0.95 2.66 3.411 (8) 136
Symmetry codes: (i) x-1, y, z; (ii) [x, -y+{\script{3\over 2}}, z-{\script{1\over 2}}]; (iii) x+1, y, z; (iv) [-x+1, y-{\script{1\over 2}}, -z+{\script{1\over 2}}]; (v) [-x+2, y-{\script{1\over 2}}, -z+{\script{1\over 2}}]; (vi) [x, -y+{\script{3\over 2}}, z+{\script{1\over 2}}]; (vii) [-x+1, y+{\script{1\over 2}}, -z+{\script{1\over 2}}]; (viii) [-x+2, y+{\script{1\over 2}}, -z+{\script{1\over 2}}]; (ix) -x+2, -y+2, -z+1; (x) [x+1, -y+{\script{3\over 2}}, z+{\script{1\over 2}}]; (xi) -x+1, -y+2, -z; (xii) -x+1, -y+2, -z+1.
[Figure 3]
Figure 3
View of the weak C—H⋯O hydrogen-bond network (Table 1[link]).

Synthesis and crystallization

A solution of 1 (0.200 g, 0.75 mmol) in diethyl ether (5 ml) was treated with 1.1 equivalent of n-BuLi (0.52 ml, 0.83 mmol) at −40°C. The solution of the anion was transferred after 30 min at −40°C via cannula transfer to an ether solution (5 ml) containing 0.51 equivalents of [Rh(μ-Cl)(CO)]2 (0.149 g, 0.38 mmol). After stirring for 2 h whilst the temperature was slowly raised to −15°C, the solvent was removed under reduced pressure and the residue extracted with cold cyclo­hexane. After filtration through Celite, the solvent was pumped off and the residue was crystallized by slow diffusion of pentane into a di­chloro­methane solution of 3 placed in a 5 mm-wide glass tube at ca 20°C to afford dark-red crystals (0.167 g, 0.20 mmol, 27%). Elemental analysis calculated for C29H18Cr2O9Rh2: C, 42.46; H, 2.21. Found: C, 42.16; H, 2.51. HRMS-ESI (m/z): [M +1H]+ calculated for C29H18Cr2O9Rh2, 820.7944; found, 820.7869. IR (cm−1) ν(CO): 2046(s), 2000(s), 1941(s), 1892(s), 1833(vs), 1712(s).1H NMR (500 MHz, CDCl3, 293 K) δ 5.70 (dd, J = 5, 3 Hz, 4H, H21, H18, H4, H7), 5.53 (s, 4H, H15, H17, H3, H1), 5.06 (dd, J = 5, 3 Hz, 4H, H19, H20, H6, H5), 2.20 (s, 3H, H8), 2.20 (s, 3H, H22). 13C NMR (126 MHz, CDCl3, 293 K) δ 233.73 (C10, C9, C11, C24, C23, C25), 211.63 (bs, C14), 187.57 (d, J = 86.0 Hz, C12, C13), 129.70 (d, J = 6.6 Hz, C16, C2), 91.14 (bs, C21′, C17′, C3′, C7′), 90.12 (C19, C20, C6, C5), 83.77 (C21, C18, C4, C7), 74.52 (C15, C17, C3, C1), 17.28 (C22, C8).

Refinement

Crystal data, data collection and structure refinement details are summarized in Table 2[link].

Table 2
Experimental details

Crystal data
Chemical formula [Cr2Rh2(C10H9)2(CO)9]
Mr 820.25
Crystal system, space group Monoclinic, P21/c
Temperature (K) 173
a, b, c (Å) 11.3335 (2), 32.6839 (9), 15.9743 (4)
β (°) 105.876 (1)
V3) 5691.5 (2)
Z 8
Radiation type Mo Kα
μ (mm−1) 1.94
Crystal size (mm) 0.20 × 0.15 × 0.12
 
Data collection
Diffractometer KappaCCD
Absorption correction Multi-scan (MULABS in PLATON; Spek, 2009[Spek, A. L. (2009). Acta Cryst. D65, 148-155.])
Tmin, Tmax 0.718, 0.796
No. of measured, independent and observed [I > 2σ(I)] reflections 37459, 12891, 8387
Rint 0.071
(sin θ/λ)max−1) 0.649
 
Refinement
R[F2 > 2σ(F2)], wR(F2), S 0.057, 0.112, 1.03
No. of reflections 12891
No. of parameters 761
H-atom treatment H-atom parameters constrained
Δρmax, Δρmin (e Å−3) 0.94, −1.03
Computer programs: COLLECT (Nonius, 1998[Nonius (1998). COLLECT. Nonius BV, Delft, The Netherlands .]), DENZO and SCALEPACK (Otwinowski & Minor, 1997[Otwinowski, Z. & Minor, W. (1997). Methods in Enzymology, Vol. 276, Macromolecular Crystallography, Part A, edited by C. W. Carter Jr & R. M. Sweet, pp. 307-326. New York: Academic Press.]), SHELXS2013 (Sheldrick, 2008[Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.]), SHELXL2014 (Sheldrick, 2015[Sheldrick, G. M. (2015). Acta Cryst. C71, 3-8.]) and Mercury (Macrae et al., 2008[Macrae, C. F., Bruno, I. J., Chisholm, J. A., Edgington, P. R., McCabe, P., Pidcock, E., Rodriguez-Monge, L., Taylor, R., van de Streek, J. & Wood, P. A. (2008). J. Appl. Cryst. 41, 466-470.]).

Structural data


Computing details top

Data collection: COLLECT (Nonius, 1998); cell refinement: SCALEPACK (Otwinowski & Minor, 1997); data reduction: DENZO and SCALEPACK (Otwinowski & Minor, 1997); program(s) used to solve structure: SHELXS2013 (Sheldrick, 2008); program(s) used to refine structure: SHELXL2014 (Sheldrick, 2015); molecular graphics: Mercury (Macrae et al., 2008); software used to prepare material for publication: SHELXL2014 (Sheldrick, 2015).

µ-Carbonyl-2:3κ2C:C-octacarbonyl-1κ3C, 2κC,3κC,4κ3C-bis[1:2µ-(η6:η5);3:4µ-(η5:η6)-2-methylindenyl]-1,4-dichromium(0)-2,3-dirhodium(III)}(RhRh) top
Crystal data top
[Cr2Rh2(C10H9)2(CO)9]F(000) = 3216
Mr = 820.25Dx = 1.915 Mg m3
Monoclinic, P21/cMo Kα radiation, λ = 0.71073 Å
a = 11.3335 (2) ÅCell parameters from 55124 reflections
b = 32.6839 (9) Åθ = 1.0–27.5°
c = 15.9743 (4) ŵ = 1.94 mm1
β = 105.876 (1)°T = 173 K
V = 5691.5 (2) Å3Prism, red
Z = 80.20 × 0.15 × 0.12 mm
Data collection top
KappaCCD
diffractometer
8387 reflections with I > 2σ(I)
Radiation source: sealed tubeRint = 0.071
phi and ω scansθmax = 27.5°, θmin = 1.3°
Absorption correction: multi-scan
(MULABS in PLATON; Spek, 2009)
h = 1314
Tmin = 0.718, Tmax = 0.796k = 3942
37459 measured reflectionsl = 2014
12891 independent reflections
Refinement top
Refinement on F2Primary atom site location: structure-invariant direct methods
Least-squares matrix: fullSecondary atom site location: difference Fourier map
R[F2 > 2σ(F2)] = 0.057Hydrogen site location: inferred from neighbouring sites
wR(F2) = 0.112H-atom parameters constrained
S = 1.03 w = 1/[σ2(Fo2) + (0.0268P)2 + 16.631P]
where P = (Fo2 + 2Fc2)/3
12891 reflections(Δ/σ)max = 0.002
761 parametersΔρmax = 0.94 e Å3
0 restraintsΔρmin = 1.03 e Å3
Special details top

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.

Fractional atomic coordinates and isotropic or equivalent isotropic displacement parameters (Å2) top
xyzUiso*/Ueq
C10.7229 (5)0.7700 (2)0.2219 (4)0.0275 (14)
C20.7325 (5)0.8079 (2)0.2692 (4)0.0332 (16)
H20.68630.81210.30990.040*
C30.8096 (5)0.8378 (2)0.2545 (4)0.0346 (15)
H30.82090.86200.28900.041*
C40.8725 (5)0.8340 (2)0.1902 (4)0.0313 (15)
H40.92340.85570.18110.038*
C50.8611 (5)0.7986 (2)0.1395 (4)0.0267 (14)
H50.90120.79660.09470.032*
C60.7886 (5)0.76542 (19)0.1559 (3)0.0253 (13)
C70.7678 (5)0.7237 (2)0.1234 (4)0.0275 (14)
H70.80560.71120.08370.033*
C80.6810 (5)0.7048 (2)0.1613 (4)0.0305 (15)
C90.6619 (5)0.7319 (2)0.2258 (4)0.0303 (15)
H90.61560.72570.26560.036*
C100.6280 (6)0.6629 (2)0.1388 (5)0.0478 (19)
H10A0.68590.64600.11830.072*
H10B0.55050.66500.09300.072*
H10C0.61290.65030.19060.072*
C110.6412 (5)0.8781 (2)0.0972 (4)0.0307 (14)
C120.5134 (6)0.8211 (2)0.1302 (4)0.0367 (16)
C130.6270 (5)0.8122 (2)0.0106 (4)0.0366 (16)
C140.8903 (5)0.7148 (2)0.3863 (4)0.0383 (17)
C150.9546 (5)0.6631 (2)0.2650 (4)0.0306 (14)
C161.2562 (5)0.7467 (2)0.3233 (4)0.0280 (14)
C171.2705 (6)0.7829 (2)0.2769 (4)0.0344 (15)
H171.32450.78310.24080.041*
C181.2052 (6)0.8174 (2)0.2851 (4)0.0374 (16)
H181.20890.84070.25040.045*
C191.1326 (5)0.8188 (2)0.3445 (4)0.0358 (16)
H191.08970.84330.34930.043*
C201.1222 (5)0.7852 (2)0.3962 (4)0.0296 (15)
H201.07720.78710.43820.036*
C211.1811 (5)0.7481 (2)0.3840 (4)0.0253 (13)
C221.1803 (5)0.70680 (19)0.4176 (3)0.0264 (14)
H221.13430.69800.45590.032*
C231.2594 (5)0.6816 (2)0.3841 (4)0.0284 (14)
C241.2965 (5)0.7048 (2)0.3220 (4)0.0312 (15)
H241.34150.69440.28440.037*
C251.2920 (6)0.6381 (2)0.4108 (4)0.0412 (17)
H25A1.29640.62210.35980.062*
H25B1.22920.62640.43530.062*
H25C1.37180.63730.45450.062*
C261.3496 (6)0.8543 (2)0.4480 (4)0.0393 (17)
C271.4818 (6)0.7941 (2)0.4219 (4)0.0415 (18)
C281.3476 (5)0.7873 (2)0.5332 (4)0.0398 (17)
C291.0636 (5)0.6995 (2)0.1535 (4)0.0322 (15)
C300.6917 (5)1.00118 (19)0.3747 (3)0.0245 (13)
C310.6171 (5)0.9736 (2)0.4072 (4)0.0281 (14)
H310.58360.98180.45300.034*
C320.5938 (5)0.9347 (2)0.3713 (4)0.0292 (14)
H320.54000.91690.39030.035*
C330.6492 (5)0.9212 (2)0.3069 (4)0.0315 (15)
H330.63030.89480.28230.038*
C340.7318 (5)0.9462 (2)0.2788 (4)0.0314 (15)
H340.77350.93610.23890.038*
C350.7516 (5)0.98697 (18)0.3113 (3)0.0231 (13)
C360.8185 (5)1.0217 (2)0.2900 (4)0.0286 (15)
H360.86321.02180.24760.034*
C370.8058 (5)1.0552 (2)0.3432 (4)0.0326 (15)
C380.7196 (5)1.0443 (2)0.3890 (3)0.0279 (14)
H380.68581.06220.42320.033*
C390.8683 (6)1.0960 (2)0.3501 (5)0.049 (2)
H39A0.81111.11750.35620.074*
H39B0.89471.10100.29740.074*
H39C0.94001.09620.40100.074*
C400.8086 (6)0.8885 (2)0.4692 (4)0.0402 (17)
C410.8517 (6)0.9605 (2)0.5338 (4)0.0397 (17)
C420.9521 (6)0.9344 (2)0.4137 (4)0.0372 (16)
C430.6001 (5)1.0341 (2)0.1258 (4)0.0316 (15)
C440.5136 (5)1.0899 (2)0.2262 (4)0.0289 (14)
C450.2980 (4)0.99265 (19)0.1372 (3)0.0218 (13)
C460.3559 (5)0.95396 (19)0.1342 (4)0.0263 (13)
H460.39990.94880.09250.032*
C470.3458 (5)0.92417 (19)0.1940 (4)0.0291 (14)
H470.38720.89880.19500.035*
C480.2746 (5)0.9309 (2)0.2538 (4)0.0299 (14)
H480.27100.91020.29480.036*
C490.2108 (5)0.9671 (2)0.2531 (3)0.0280 (14)
H490.15760.97020.28950.034*
C500.2258 (5)0.99931 (18)0.1974 (3)0.0227 (13)
C510.1842 (5)1.04197 (19)0.1871 (4)0.0273 (14)
H510.13981.05540.22170.033*
C520.2201 (5)1.05984 (19)0.1181 (3)0.0261 (13)
C530.2998 (5)1.03163 (19)0.0928 (3)0.0247 (13)
H530.34681.03730.05320.030*
C540.1888 (5)1.1019 (2)0.0797 (4)0.0383 (17)
H54A0.10161.10290.04790.057*
H54B0.23851.10790.03970.057*
H54C0.20581.12230.12650.057*
C550.1197 (5)0.8872 (2)0.0947 (4)0.0291 (14)
C560.1199 (5)0.9496 (2)0.0013 (4)0.0318 (15)
C570.0034 (6)0.9482 (2)0.1201 (4)0.0369 (16)
C580.4135 (5)1.05808 (19)0.3504 (4)0.0280 (14)
O10.6166 (4)0.91143 (16)0.0748 (3)0.0475 (13)
O20.4114 (4)0.82046 (18)0.1308 (3)0.0591 (15)
O30.5982 (4)0.80494 (18)0.0629 (3)0.0586 (15)
O40.9075 (5)0.7174 (2)0.4593 (3)0.074 (2)
O50.9335 (4)0.62782 (15)0.2601 (3)0.0490 (13)
O61.3691 (5)0.88869 (16)0.4667 (3)0.0560 (14)
O71.5839 (4)0.79062 (18)0.4244 (3)0.0609 (16)
O81.3622 (4)0.77926 (18)0.6060 (3)0.0576 (15)
O91.0472 (4)0.69946 (19)0.0797 (3)0.0604 (16)
O100.8184 (5)0.85594 (17)0.4977 (4)0.0661 (16)
O110.8849 (5)0.97218 (18)0.6046 (3)0.0622 (16)
O121.0509 (4)0.92897 (18)0.4079 (3)0.0622 (16)
O130.5912 (4)1.02920 (17)0.0536 (3)0.0502 (14)
O140.5195 (4)1.12497 (15)0.2158 (3)0.0463 (12)
O150.0934 (4)0.85293 (15)0.0770 (3)0.0409 (11)
O160.0970 (4)0.95460 (17)0.0730 (3)0.0509 (14)
O170.1037 (4)0.95229 (17)0.1223 (3)0.0544 (14)
O180.4283 (4)1.06366 (15)0.4228 (3)0.0442 (13)
Cr10.67385 (8)0.82458 (3)0.12840 (6)0.0286 (2)
Cr21.31816 (8)0.80118 (3)0.41678 (6)0.0304 (2)
Cr30.79485 (8)0.94023 (3)0.42231 (6)0.0269 (2)
Cr40.15766 (8)0.94055 (3)0.11995 (6)0.0263 (2)
Rh10.85746 (4)0.71371 (2)0.26546 (3)0.02481 (12)
Rh21.09339 (4)0.70083 (2)0.27332 (3)0.02341 (12)
Rh30.62563 (4)1.04127 (2)0.24455 (3)0.02471 (12)
Rh40.38643 (4)1.04859 (2)0.23193 (3)0.02289 (12)
Atomic displacement parameters (Å2) top
U11U22U33U12U13U23
C10.021 (3)0.035 (4)0.026 (3)0.008 (3)0.006 (2)0.008 (3)
C20.032 (3)0.046 (5)0.022 (3)0.012 (3)0.008 (3)0.001 (3)
C30.031 (3)0.034 (4)0.033 (4)0.001 (3)0.001 (3)0.006 (3)
C40.021 (3)0.037 (4)0.032 (3)0.002 (3)0.001 (3)0.002 (3)
C50.023 (3)0.039 (4)0.020 (3)0.005 (3)0.010 (2)0.005 (3)
C60.023 (3)0.030 (4)0.022 (3)0.006 (3)0.004 (2)0.003 (3)
C70.027 (3)0.031 (4)0.021 (3)0.005 (3)0.001 (2)0.004 (3)
C80.023 (3)0.024 (4)0.036 (4)0.001 (3)0.005 (3)0.004 (3)
C90.024 (3)0.030 (4)0.035 (4)0.001 (3)0.005 (3)0.007 (3)
C100.039 (4)0.038 (5)0.058 (5)0.007 (3)0.000 (3)0.008 (4)
C110.028 (3)0.030 (4)0.031 (4)0.002 (3)0.003 (3)0.003 (3)
C120.032 (3)0.040 (4)0.039 (4)0.007 (3)0.011 (3)0.017 (3)
C130.032 (3)0.037 (4)0.040 (4)0.007 (3)0.008 (3)0.002 (3)
C140.034 (3)0.051 (5)0.033 (4)0.005 (3)0.012 (3)0.013 (3)
C150.030 (3)0.026 (4)0.036 (4)0.001 (3)0.009 (3)0.002 (3)
C160.029 (3)0.029 (4)0.023 (3)0.007 (3)0.001 (3)0.001 (3)
C170.043 (4)0.037 (4)0.023 (3)0.012 (3)0.008 (3)0.002 (3)
C180.049 (4)0.031 (4)0.022 (3)0.008 (3)0.006 (3)0.006 (3)
C190.033 (3)0.025 (4)0.039 (4)0.000 (3)0.009 (3)0.006 (3)
C200.023 (3)0.039 (4)0.023 (3)0.003 (3)0.001 (2)0.007 (3)
C210.020 (3)0.030 (4)0.024 (3)0.002 (3)0.002 (2)0.005 (3)
C220.029 (3)0.034 (4)0.016 (3)0.004 (3)0.005 (2)0.003 (3)
C230.024 (3)0.031 (4)0.027 (3)0.004 (3)0.000 (3)0.001 (3)
C240.024 (3)0.037 (4)0.030 (3)0.003 (3)0.005 (3)0.006 (3)
C250.047 (4)0.029 (4)0.044 (4)0.005 (3)0.007 (3)0.012 (3)
C260.040 (4)0.038 (5)0.034 (4)0.002 (3)0.000 (3)0.002 (3)
C270.043 (4)0.051 (5)0.027 (4)0.015 (4)0.004 (3)0.002 (3)
C280.030 (3)0.053 (5)0.031 (4)0.006 (3)0.000 (3)0.006 (3)
C290.027 (3)0.041 (4)0.029 (4)0.005 (3)0.009 (3)0.002 (3)
C300.026 (3)0.026 (4)0.018 (3)0.004 (3)0.001 (2)0.010 (3)
C310.027 (3)0.032 (4)0.025 (3)0.006 (3)0.006 (3)0.005 (3)
C320.022 (3)0.030 (4)0.035 (3)0.001 (3)0.007 (3)0.006 (3)
C330.027 (3)0.028 (4)0.034 (4)0.003 (3)0.002 (3)0.003 (3)
C340.024 (3)0.036 (4)0.031 (3)0.006 (3)0.003 (3)0.004 (3)
C350.023 (3)0.024 (4)0.021 (3)0.005 (3)0.003 (2)0.007 (3)
C360.019 (3)0.040 (4)0.024 (3)0.003 (3)0.002 (2)0.008 (3)
C370.020 (3)0.031 (4)0.038 (4)0.005 (3)0.008 (3)0.010 (3)
C380.031 (3)0.028 (4)0.019 (3)0.000 (3)0.001 (2)0.002 (3)
C390.037 (4)0.040 (5)0.060 (5)0.012 (3)0.005 (3)0.007 (4)
C400.031 (3)0.038 (5)0.046 (4)0.004 (3)0.000 (3)0.008 (4)
C410.033 (3)0.036 (5)0.045 (4)0.007 (3)0.003 (3)0.002 (4)
C420.034 (3)0.044 (5)0.030 (4)0.006 (3)0.002 (3)0.009 (3)
C430.023 (3)0.035 (4)0.036 (4)0.003 (3)0.007 (3)0.008 (3)
C440.028 (3)0.026 (4)0.032 (3)0.002 (3)0.006 (3)0.002 (3)
C450.017 (3)0.031 (4)0.015 (3)0.001 (2)0.001 (2)0.004 (3)
C460.019 (3)0.028 (4)0.029 (3)0.003 (3)0.000 (2)0.006 (3)
C470.020 (3)0.024 (4)0.036 (4)0.002 (3)0.006 (3)0.003 (3)
C480.035 (3)0.026 (4)0.022 (3)0.008 (3)0.004 (3)0.001 (3)
C490.032 (3)0.032 (4)0.018 (3)0.007 (3)0.006 (2)0.005 (3)
C500.022 (3)0.024 (4)0.019 (3)0.003 (2)0.001 (2)0.003 (3)
C510.023 (3)0.029 (4)0.027 (3)0.002 (3)0.003 (2)0.009 (3)
C520.024 (3)0.029 (4)0.020 (3)0.001 (3)0.003 (2)0.002 (3)
C530.020 (3)0.037 (4)0.016 (3)0.000 (3)0.003 (2)0.002 (3)
C540.037 (3)0.041 (5)0.032 (4)0.009 (3)0.001 (3)0.004 (3)
C550.028 (3)0.034 (4)0.023 (3)0.002 (3)0.004 (3)0.001 (3)
C560.025 (3)0.031 (4)0.038 (4)0.002 (3)0.005 (3)0.000 (3)
C570.030 (3)0.040 (5)0.036 (4)0.007 (3)0.002 (3)0.007 (3)
C580.026 (3)0.027 (4)0.030 (4)0.003 (3)0.009 (3)0.004 (3)
O10.048 (3)0.042 (3)0.048 (3)0.007 (3)0.007 (2)0.010 (3)
O20.036 (3)0.073 (4)0.070 (4)0.005 (3)0.017 (3)0.014 (3)
O30.064 (3)0.071 (4)0.032 (3)0.012 (3)0.000 (2)0.007 (3)
O40.064 (3)0.141 (6)0.018 (3)0.003 (4)0.014 (2)0.011 (3)
O50.051 (3)0.025 (3)0.076 (4)0.005 (2)0.026 (3)0.001 (3)
O60.066 (3)0.036 (3)0.055 (3)0.013 (3)0.004 (3)0.008 (3)
O70.038 (3)0.091 (5)0.051 (3)0.013 (3)0.008 (2)0.007 (3)
O80.056 (3)0.081 (5)0.031 (3)0.014 (3)0.004 (2)0.010 (3)
O90.053 (3)0.105 (5)0.025 (3)0.011 (3)0.015 (2)0.003 (3)
O100.067 (3)0.037 (4)0.084 (4)0.004 (3)0.004 (3)0.027 (3)
O110.064 (3)0.073 (4)0.036 (3)0.015 (3)0.010 (3)0.016 (3)
O120.032 (3)0.082 (5)0.075 (4)0.015 (3)0.019 (3)0.020 (3)
O130.051 (3)0.080 (4)0.019 (2)0.002 (3)0.011 (2)0.001 (2)
O140.052 (3)0.025 (3)0.065 (3)0.002 (2)0.021 (3)0.006 (3)
O150.050 (3)0.033 (3)0.037 (3)0.004 (2)0.008 (2)0.005 (2)
O160.046 (3)0.072 (4)0.028 (3)0.002 (3)0.001 (2)0.005 (3)
O170.033 (3)0.071 (4)0.060 (3)0.002 (3)0.015 (2)0.013 (3)
O180.054 (3)0.058 (4)0.022 (2)0.013 (3)0.013 (2)0.007 (2)
Cr10.0266 (5)0.0309 (6)0.0265 (5)0.0041 (4)0.0044 (4)0.0039 (5)
Cr20.0319 (5)0.0283 (6)0.0259 (5)0.0044 (5)0.0009 (4)0.0025 (5)
Cr30.0240 (5)0.0260 (6)0.0272 (5)0.0010 (4)0.0012 (4)0.0030 (4)
Cr40.0239 (5)0.0271 (6)0.0249 (5)0.0014 (4)0.0017 (4)0.0045 (4)
Rh10.0233 (2)0.0280 (3)0.0221 (2)0.0003 (2)0.00445 (19)0.0026 (2)
Rh20.0236 (2)0.0239 (3)0.0222 (2)0.0008 (2)0.00524 (19)0.0002 (2)
Rh30.0225 (2)0.0272 (3)0.0220 (2)0.0015 (2)0.00185 (18)0.0039 (2)
Rh40.0227 (2)0.0237 (3)0.0198 (2)0.0002 (2)0.00184 (18)0.0002 (2)
Geometric parameters (Å, º) top
C1—C91.435 (8)C26—Cr21.816 (8)
C1—C21.438 (9)C27—O71.153 (7)
C1—C61.455 (7)C27—Cr21.848 (7)
C1—Cr12.294 (6)C28—O81.158 (7)
C1—Rh12.371 (6)C28—Cr21.854 (7)
C2—C31.375 (9)C29—O91.142 (7)
C2—Cr12.232 (6)C29—Rh21.851 (6)
C2—H20.9500C34—Cr32.216 (6)
C3—C41.407 (8)C35—C361.455 (8)
C3—Cr12.218 (6)C35—Cr32.290 (5)
C3—H30.9500C35—Rh32.343 (5)
C4—C51.397 (8)C36—C371.418 (9)
C4—Cr12.219 (5)C36—Rh32.202 (5)
C4—H40.9500C36—H360.9500
C5—C61.426 (8)C37—C381.417 (8)
C5—Cr12.248 (5)C37—C391.501 (9)
C5—H50.9500C37—Rh32.258 (5)
C6—C71.454 (8)C38—Rh32.263 (5)
C6—Cr12.305 (6)C38—H380.9500
C6—Rh12.404 (6)C39—H39A0.9800
C7—C81.429 (8)C39—H39B0.9800
C7—Rh12.242 (5)C39—H39C0.9800
C7—H70.9500C40—O101.150 (8)
C8—C91.420 (8)C40—Cr31.839 (7)
C8—C101.499 (9)C41—O111.155 (7)
C8—Rh12.243 (5)C41—Cr31.843 (7)
C9—Rh12.213 (5)C42—O121.163 (7)
C9—H90.9500C42—Cr31.835 (6)
C10—H10A0.9800C43—O131.142 (7)
C10—H10B0.9800C43—Rh31.854 (6)
C10—H10C0.9800C44—O141.162 (7)
C11—O11.156 (7)C44—Rh41.996 (6)
C11—Cr11.829 (7)C44—Rh32.006 (6)
C12—O21.158 (7)C45—C461.431 (8)
C12—Cr11.830 (6)C45—C501.440 (7)
C13—O31.154 (7)C45—C531.461 (8)
C13—Cr11.855 (7)C45—Cr42.295 (6)
C14—O41.132 (7)C45—Rh42.410 (6)
C14—Rh11.863 (6)C46—C471.391 (8)
C15—O51.174 (7)C46—Cr42.239 (5)
C15—Rh21.975 (6)C46—H460.9500
C15—Rh11.989 (6)C47—C481.426 (8)
C16—C171.428 (8)C47—Cr42.203 (5)
C16—C241.447 (9)C47—H470.9500
C16—C211.455 (8)C48—C491.385 (8)
C16—Cr22.306 (6)C48—Cr42.208 (6)
C16—Rh22.342 (6)C48—H480.9500
C17—C181.374 (9)C49—C501.420 (8)
C17—Cr22.231 (6)C49—Cr42.222 (5)
C17—H170.9500C49—H490.9500
C18—C191.416 (9)C50—C511.467 (8)
C18—Cr22.206 (6)C50—Cr42.301 (6)
C18—H180.9500C50—Rh42.379 (5)
C19—C201.398 (9)C51—C521.403 (8)
C19—Cr22.182 (6)C51—Rh42.217 (5)
C19—H190.9500C51—H510.9500
C20—C211.424 (8)C52—C531.424 (8)
C20—Cr22.216 (5)C52—C541.508 (8)
C20—H200.9500C52—Rh42.262 (5)
C21—C221.453 (8)C53—Rh42.240 (5)
C21—Cr22.292 (6)C53—H530.9500
C21—Rh22.353 (6)C54—H54A0.9800
C22—C231.425 (8)C54—H54B0.9800
C22—Rh22.254 (5)C54—H54C0.9800
C22—H220.9500C55—O151.174 (7)
C23—C241.401 (8)C55—Cr41.815 (7)
C23—C251.503 (9)C56—O161.155 (7)
C23—Rh22.290 (5)C56—Cr41.850 (7)
C24—Rh22.223 (5)C57—O171.154 (7)
C24—H240.9500C57—Cr41.843 (6)
C25—H25A0.9800C58—O181.138 (6)
C25—H25B0.9800Rh1—Rh22.6756 (6)
C25—H25C0.9800Rh3—Rh42.6737 (6)
C26—O61.167 (8)
C9—C1—C2133.8 (5)C51—C52—Rh470.0 (3)
C9—C1—C6106.8 (6)C53—C52—Rh470.7 (3)
C2—C1—C6119.3 (6)C54—C52—Rh4121.8 (4)
C9—C1—Cr1132.0 (4)C52—C53—C45109.4 (5)
C2—C1—Cr169.1 (3)C52—C53—Rh472.4 (3)
C6—C1—Cr171.9 (3)C45—C53—Rh478.1 (3)
C9—C1—Rh165.9 (3)C52—C53—H53125.3
C2—C1—Rh1124.3 (4)C45—C53—H53125.3
C6—C1—Rh173.5 (3)Rh4—C53—H53116.1
Cr1—C1—Rh1144.7 (2)C52—C54—H54A109.5
C3—C2—C1118.9 (5)C52—C54—H54B109.5
C3—C2—Cr171.4 (4)H54A—C54—H54B109.5
C1—C2—Cr173.8 (3)C52—C54—H54C109.5
C3—C2—H2120.6H54A—C54—H54C109.5
C1—C2—H2120.6H54B—C54—H54C109.5
Cr1—C2—H2125.9O15—C55—Cr4178.8 (6)
C2—C3—C4122.2 (6)O16—C56—Cr4179.0 (6)
C2—C3—Cr172.6 (3)O17—C57—Cr4178.2 (7)
C4—C3—Cr171.5 (3)O18—C58—Rh4178.9 (6)
C2—C3—H3118.9C11—Cr1—C1286.4 (3)
C4—C3—H3118.9C11—Cr1—C1387.2 (3)
Cr1—C3—H3129.6C12—Cr1—C1389.6 (3)
C5—C4—C3120.8 (6)C11—Cr1—C395.7 (3)
C5—C4—Cr172.9 (3)C12—Cr1—C3116.3 (3)
C3—C4—Cr171.5 (3)C13—Cr1—C3154.1 (2)
C5—C4—H4119.6C11—Cr1—C495.4 (3)
C3—C4—H4119.6C12—Cr1—C4153.3 (3)
Cr1—C4—H4128.3C13—Cr1—C4117.1 (2)
C4—C5—C6119.3 (5)C3—Cr1—C437.0 (2)
C4—C5—Cr170.6 (3)C11—Cr1—C2119.4 (3)
C6—C5—Cr173.9 (3)C12—Cr1—C289.5 (2)
C4—C5—H5120.4C13—Cr1—C2153.3 (3)
C6—C5—H5120.4C3—Cr1—C236.0 (2)
Cr1—C5—H5127.0C4—Cr1—C266.4 (2)
C5—C6—C7133.7 (5)C11—Cr1—C5120.0 (2)
C5—C6—C1119.3 (6)C12—Cr1—C5153.6 (3)
C7—C6—C1106.9 (5)C13—Cr1—C590.0 (2)
C5—C6—Cr169.6 (3)C3—Cr1—C566.2 (2)
C7—C6—Cr1133.6 (4)C4—Cr1—C536.5 (2)
C1—C6—Cr171.2 (3)C2—Cr1—C579.2 (2)
C5—C6—Rh1125.4 (4)C11—Cr1—C1156.3 (3)
C7—C6—Rh165.8 (3)C12—Cr1—C190.3 (2)
C1—C6—Rh171.0 (3)C13—Cr1—C1116.3 (3)
Cr1—C6—Rh1141.5 (2)C3—Cr1—C164.9 (2)
C8—C7—C6108.5 (5)C4—Cr1—C177.4 (2)
C8—C7—Rh171.5 (3)C2—Cr1—C137.0 (2)
C6—C7—Rh177.9 (3)C5—Cr1—C166.4 (2)
C8—C7—H7125.7C11—Cr1—C6156.3 (2)
C6—C7—H7125.7C12—Cr1—C6117.1 (3)
Rh1—C7—H7116.8C13—Cr1—C690.0 (2)
C9—C8—C7107.2 (5)C3—Cr1—C677.0 (2)
C9—C8—C10127.8 (6)C4—Cr1—C665.1 (2)
C7—C8—C10124.9 (6)C2—Cr1—C666.8 (2)
C9—C8—Rh170.3 (3)C5—Cr1—C636.5 (2)
C7—C8—Rh171.4 (3)C1—Cr1—C636.89 (19)
C10—C8—Rh1120.9 (4)C26—Cr2—C2789.4 (3)
C8—C9—C1109.9 (5)C26—Cr2—C2889.4 (3)
C8—C9—Rh172.6 (3)C27—Cr2—C2891.3 (3)
C1—C9—Rh177.8 (3)C26—Cr2—C1988.9 (3)
C8—C9—H9125.1C27—Cr2—C19150.1 (3)
C1—C9—H9125.1C28—Cr2—C19118.6 (3)
Rh1—C9—H9116.4C26—Cr2—C1892.9 (3)
C8—C10—H10A109.5C27—Cr2—C18112.7 (3)
C8—C10—H10B109.5C28—Cr2—C18155.9 (3)
H10A—C10—H10B109.5C19—Cr2—C1837.6 (2)
C8—C10—H10C109.5C26—Cr2—C20112.3 (3)
H10A—C10—H10C109.5C27—Cr2—C20158.4 (3)
H10B—C10—H10C109.5C28—Cr2—C2089.4 (2)
O1—C11—Cr1177.2 (6)C19—Cr2—C2037.1 (2)
O2—C12—Cr1177.3 (6)C18—Cr2—C2067.6 (2)
O3—C13—Cr1179.3 (7)C26—Cr2—C17120.5 (3)
O4—C14—Rh1176.4 (7)C27—Cr2—C1788.6 (3)
O5—C15—Rh2139.6 (5)C28—Cr2—C17150.1 (3)
O5—C15—Rh1135.5 (5)C19—Cr2—C1766.8 (2)
Rh2—C15—Rh184.9 (3)C18—Cr2—C1736.1 (2)
C17—C16—C24134.1 (6)C20—Cr2—C1780.2 (2)
C17—C16—C21119.3 (6)C26—Cr2—C21149.0 (3)
C24—C16—C21106.5 (5)C27—Cr2—C21121.6 (3)
C17—C16—Cr268.8 (4)C28—Cr2—C2188.2 (3)
C24—C16—Cr2134.4 (4)C19—Cr2—C2165.4 (2)
C21—C16—Cr271.0 (3)C18—Cr2—C2177.5 (2)
C17—C16—Rh2122.9 (4)C20—Cr2—C2136.8 (2)
C24—C16—Rh267.1 (3)C17—Cr2—C2166.7 (2)
C21—C16—Rh272.3 (3)C26—Cr2—C16156.7 (3)
Cr2—C16—Rh2141.9 (3)C27—Cr2—C1693.2 (3)
C18—C17—C16119.3 (6)C28—Cr2—C16113.6 (3)
C18—C17—Cr271.0 (4)C19—Cr2—C1677.5 (2)
C16—C17—Cr274.5 (3)C18—Cr2—C1664.8 (2)
C18—C17—H17120.3C20—Cr2—C1666.9 (2)
C16—C17—H17120.3C17—Cr2—C1636.6 (2)
Cr2—C17—H17125.9C21—Cr2—C1636.90 (19)
C17—C18—C19121.2 (6)C42—Cr3—C4087.7 (3)
C17—C18—Cr273.0 (4)C42—Cr3—C4191.1 (3)
C19—C18—Cr270.2 (3)C40—Cr3—C4188.2 (3)
C17—C18—H18119.4C42—Cr3—C33115.4 (3)
C19—C18—H18119.4C40—Cr3—C3392.4 (3)
Cr2—C18—H18130.0C41—Cr3—C33153.4 (3)
C20—C19—C18121.9 (6)C42—Cr3—C32152.9 (3)
C20—C19—Cr272.8 (3)C40—Cr3—C3292.2 (3)
C18—C19—Cr272.1 (3)C41—Cr3—C32116.0 (3)
C20—C19—H19119.1C33—Cr3—C3237.4 (2)
C18—C19—H19119.1C42—Cr3—C3488.7 (2)
Cr2—C19—H19128.3C40—Cr3—C34118.0 (3)
C19—C20—C21118.1 (5)C41—Cr3—C34153.7 (3)
C19—C20—Cr270.1 (3)C33—Cr3—C3437.1 (2)
C21—C20—Cr274.5 (3)C32—Cr3—C3467.5 (2)
C19—C20—H20121.0C42—Cr3—C31154.7 (3)
C21—C20—H20121.0C40—Cr3—C31117.6 (3)
Cr2—C20—H20126.1C41—Cr3—C3189.7 (2)
C20—C21—C22133.7 (5)C33—Cr3—C3166.5 (2)
C20—C21—C16119.9 (6)C32—Cr3—C3136.4 (2)
C22—C21—C16106.4 (5)C34—Cr3—C3179.6 (2)
C20—C21—Cr268.7 (3)C42—Cr3—C3591.0 (2)
C22—C21—Cr2133.7 (4)C40—Cr3—C35154.9 (3)
C16—C21—Cr272.1 (3)C41—Cr3—C35116.9 (3)
C20—C21—Rh2123.0 (4)C33—Cr3—C3565.6 (2)
C22—C21—Rh267.9 (3)C32—Cr3—C3577.8 (2)
C16—C21—Rh271.5 (3)C34—Cr3—C3536.8 (2)
Cr2—C21—Rh2142.1 (3)C31—Cr3—C3566.2 (2)
C23—C22—C21109.2 (5)C42—Cr3—C30118.3 (3)
C23—C22—Rh273.1 (3)C40—Cr3—C30154.0 (2)
C21—C22—Rh275.4 (3)C41—Cr3—C3091.1 (3)
C23—C22—H22125.4C33—Cr3—C3076.9 (2)
C21—C22—H22125.4C32—Cr3—C3064.8 (2)
Rh2—C22—H22117.9C34—Cr3—C3066.2 (2)
C24—C23—C22107.3 (6)C31—Cr3—C3036.3 (2)
C24—C23—C25127.9 (6)C35—Cr3—C3036.36 (19)
C22—C23—C25124.8 (5)C55—Cr4—C5787.4 (3)
C24—C23—Rh269.3 (3)C55—Cr4—C5687.2 (3)
C22—C23—Rh270.4 (3)C57—Cr4—C5691.7 (3)
C25—C23—Rh2124.4 (4)C55—Cr4—C4791.3 (2)
C23—C24—C16110.1 (5)C57—Cr4—C47147.7 (3)
C23—C24—Rh274.6 (3)C56—Cr4—C47120.5 (2)
C16—C24—Rh276.1 (3)C55—Cr4—C4897.0 (2)
C23—C24—H24124.9C57—Cr4—C48110.5 (3)
C16—C24—H24124.9C56—Cr4—C48157.6 (2)
Rh2—C24—H24116.2C47—Cr4—C4837.7 (2)
C23—C25—H25A109.5C55—Cr4—C49125.0 (2)
C23—C25—H25B109.5C57—Cr4—C4987.4 (2)
H25A—C25—H25B109.5C56—Cr4—C49147.7 (3)
C23—C25—H25C109.5C47—Cr4—C4967.2 (2)
H25A—C25—H25C109.5C48—Cr4—C4936.4 (2)
H25B—C25—H25C109.5C55—Cr4—C46112.4 (2)
O6—C26—Cr2178.8 (6)C57—Cr4—C46160.1 (3)
O7—C27—Cr2178.3 (7)C56—Cr4—C4691.0 (2)
O8—C28—Cr2177.7 (6)C47—Cr4—C4636.5 (2)
O9—C29—Rh2178.4 (6)C48—Cr4—C4667.0 (2)
C31—C30—C35119.4 (6)C49—Cr4—C4679.9 (2)
C31—C30—C38133.1 (5)C55—Cr4—C45148.7 (2)
C35—C30—C38107.4 (5)C57—Cr4—C45123.6 (3)
C31—C30—Cr368.6 (3)C56—Cr4—C4587.9 (2)
C35—C30—Cr370.3 (3)C47—Cr4—C4565.1 (2)
C38—C30—Cr3135.4 (4)C48—Cr4—C4577.1 (2)
C31—C30—Rh3125.8 (4)C49—Cr4—C4566.3 (2)
C35—C30—Rh370.2 (3)C46—Cr4—C4536.8 (2)
C38—C30—Rh366.9 (3)C55—Cr4—C50161.1 (2)
Cr3—C30—Rh3139.5 (3)C57—Cr4—C5094.2 (2)
C32—C31—C30119.5 (5)C56—Cr4—C50111.6 (3)
C32—C31—Cr370.3 (3)C47—Cr4—C5077.3 (2)
C30—C31—Cr375.1 (3)C48—Cr4—C5064.8 (2)
C32—C31—H31120.2C49—Cr4—C5036.5 (2)
C30—C31—H31120.2C46—Cr4—C5066.5 (2)
Cr3—C31—H31126.1C45—Cr4—C5036.51 (18)
C31—C32—C33120.9 (6)C14—Rh1—C1593.7 (3)
C31—C32—Cr373.3 (3)C14—Rh1—C9101.1 (2)
C33—C32—Cr371.0 (3)C15—Rh1—C9137.3 (2)
C31—C32—H32119.6C14—Rh1—C7162.3 (2)
C33—C32—H32119.6C15—Rh1—C7102.5 (2)
Cr3—C32—H32128.3C9—Rh1—C762.0 (2)
C34—C33—C32121.2 (6)C14—Rh1—C8131.0 (2)
C34—C33—Cr372.0 (3)C15—Rh1—C8105.7 (2)
C32—C33—Cr371.5 (3)C9—Rh1—C837.1 (2)
C34—C33—H33119.4C7—Rh1—C837.2 (2)
C32—C33—H33119.4C14—Rh1—C1102.7 (3)
Cr3—C33—H33129.6C15—Rh1—C1163.3 (2)
C33—C34—C35118.6 (6)C9—Rh1—C136.3 (2)
C33—C34—Cr370.9 (3)C7—Rh1—C160.8 (2)
C35—C34—Cr374.4 (3)C8—Rh1—C160.8 (2)
C33—C34—H34120.7C14—Rh1—C6132.4 (3)
C35—C34—H34120.7C15—Rh1—C6130.7 (2)
Cr3—C34—H34125.8C9—Rh1—C660.2 (2)
C34—C35—C30120.0 (5)C7—Rh1—C636.3 (2)
C34—C35—C36133.1 (5)C8—Rh1—C660.4 (2)
C30—C35—C36106.8 (5)C1—Rh1—C635.48 (18)
C34—C35—Cr368.7 (3)C14—Rh1—Rh292.31 (18)
C30—C35—Cr373.3 (3)C15—Rh1—Rh247.33 (18)
C36—C35—Cr3133.3 (4)C9—Rh1—Rh2164.86 (16)
C34—C35—Rh3121.8 (4)C7—Rh1—Rh2103.94 (14)
C30—C35—Rh374.4 (3)C8—Rh1—Rh2133.71 (16)
C36—C35—Rh366.1 (3)C1—Rh1—Rh2133.67 (14)
Cr3—C35—Rh3146.3 (2)C6—Rh1—Rh2105.43 (13)
C37—C36—C35108.5 (5)C29—Rh2—C1590.0 (3)
C37—C36—Rh373.6 (3)C29—Rh2—C24104.0 (2)
C35—C36—Rh376.7 (3)C15—Rh2—C24142.1 (3)
C37—C36—H36125.8C29—Rh2—C22164.7 (2)
C35—C36—H36125.8C15—Rh2—C22103.9 (2)
Rh3—C36—H36116.0C24—Rh2—C2261.1 (2)
C38—C37—C36108.2 (5)C29—Rh2—C23132.2 (2)
C38—C37—C39124.4 (6)C15—Rh2—C23110.6 (2)
C36—C37—C39127.4 (6)C24—Rh2—C2336.1 (2)
C38—C37—Rh371.9 (3)C22—Rh2—C2336.5 (2)
C36—C37—Rh369.3 (3)C29—Rh2—C16105.7 (2)
C39—C37—Rh3123.3 (4)C15—Rh2—C16164.1 (2)
C37—C38—C30108.4 (5)C24—Rh2—C1636.8 (2)
C37—C38—Rh371.6 (3)C22—Rh2—C1660.8 (2)
C30—C38—Rh377.1 (3)C23—Rh2—C1660.5 (2)
C37—C38—H38125.8C29—Rh2—C21135.4 (3)
C30—C38—H38125.8C15—Rh2—C21128.7 (2)
Rh3—C38—H38117.5C24—Rh2—C2161.0 (2)
C37—C39—H39A109.5C22—Rh2—C2136.7 (2)
C37—C39—H39B109.5C23—Rh2—C2160.7 (2)
H39A—C39—H39B109.5C16—Rh2—C2136.11 (19)
C37—C39—H39C109.5C29—Rh2—Rh193.30 (17)
H39A—C39—H39C109.5C15—Rh2—Rh147.78 (18)
H39B—C39—H39C109.5C24—Rh2—Rh1158.97 (16)
O10—C40—Cr3178.9 (7)C22—Rh2—Rh1100.71 (14)
O11—C41—Cr3177.6 (7)C23—Rh2—Rh1132.75 (14)
O12—C42—Cr3177.0 (7)C16—Rh2—Rh1126.83 (15)
O13—C43—Rh3176.1 (5)C21—Rh2—Rh198.25 (13)
O14—C44—Rh4138.1 (5)C43—Rh3—C4492.0 (3)
O14—C44—Rh3138.1 (5)C43—Rh3—C3699.4 (2)
Rh4—C44—Rh383.8 (3)C44—Rh3—C36144.1 (2)
C46—C45—C50120.4 (5)C43—Rh3—C37126.7 (2)
C46—C45—C53133.4 (5)C44—Rh3—C37110.9 (2)
C50—C45—C53106.2 (5)C36—Rh3—C3737.0 (2)
C46—C45—Cr469.5 (3)C43—Rh3—C38161.2 (2)
C50—C45—Cr472.0 (3)C44—Rh3—C38102.5 (2)
C53—C45—Cr4133.6 (4)C36—Rh3—C3861.9 (2)
C46—C45—Rh4125.1 (4)C37—Rh3—C3836.5 (2)
C50—C45—Rh471.4 (3)C43—Rh3—C35106.0 (2)
C53—C45—Rh465.5 (3)C44—Rh3—C35161.7 (2)
Cr4—C45—Rh4142.5 (2)C36—Rh3—C3537.2 (2)
C47—C46—C45118.1 (5)C37—Rh3—C3560.9 (2)
C47—C46—Cr470.4 (3)C38—Rh3—C3560.7 (2)
C45—C46—Cr473.7 (3)C43—Rh3—C30138.0 (3)
C47—C46—H46121.0C44—Rh3—C30126.5 (2)
C45—C46—H46121.0C36—Rh3—C3060.6 (2)
Cr4—C46—H46126.8C37—Rh3—C3059.8 (2)
C46—C47—C48121.4 (6)C38—Rh3—C3036.0 (2)
C46—C47—Cr473.2 (3)C35—Rh3—C3035.39 (18)
C48—C47—Cr471.4 (3)C43—Rh3—Rh493.60 (17)
C46—C47—H47119.3C44—Rh3—Rh447.92 (17)
C48—C47—H47119.3C36—Rh3—Rh4161.03 (15)
Cr4—C47—H47128.5C37—Rh3—Rh4137.68 (17)
C49—C48—C47121.1 (6)C38—Rh3—Rh4104.93 (15)
C49—C48—Cr472.3 (3)C35—Rh3—Rh4125.53 (13)
C47—C48—Cr470.9 (3)C30—Rh3—Rh4100.62 (13)
C49—C48—H48119.4C58—Rh4—C4490.7 (2)
C47—C48—H48119.4C58—Rh4—C51102.3 (2)
Cr4—C48—H48129.9C44—Rh4—C51138.3 (2)
C48—C49—C50119.1 (5)C58—Rh4—C53163.2 (2)
C48—C49—Cr471.3 (3)C44—Rh4—C53104.4 (2)
C50—C49—Cr474.8 (3)C51—Rh4—C5361.4 (2)
C48—C49—H49120.4C58—Rh4—C52131.3 (2)
C50—C49—H49120.4C44—Rh4—C52107.9 (2)
Cr4—C49—H49125.2C51—Rh4—C5236.5 (2)
C49—C50—C45119.6 (5)C53—Rh4—C5236.9 (2)
C49—C50—C51133.3 (5)C58—Rh4—C50104.6 (2)
C45—C50—C51107.1 (5)C44—Rh4—C50164.6 (2)
C49—C50—Cr468.7 (3)C51—Rh4—C5037.0 (2)
C45—C50—Cr471.5 (3)C53—Rh4—C5060.18 (19)
C51—C50—Cr4133.1 (4)C52—Rh4—C5060.5 (2)
C49—C50—Rh4125.0 (4)C58—Rh4—C45133.7 (2)
C45—C50—Rh473.7 (3)C44—Rh4—C45131.8 (2)
C51—C50—Rh465.5 (3)C51—Rh4—C4560.51 (19)
Cr4—C50—Rh4144.4 (2)C53—Rh4—C4536.4 (2)
C52—C51—C50109.2 (5)C52—Rh4—C4560.4 (2)
C52—C51—Rh473.5 (3)C50—Rh4—C4534.98 (17)
C50—C51—Rh477.5 (3)C58—Rh4—Rh393.23 (17)
C52—C51—H51125.4C44—Rh4—Rh348.24 (18)
C50—C51—H51125.4C51—Rh4—Rh3162.38 (15)
Rh4—C51—H51115.6C53—Rh4—Rh3102.29 (13)
C51—C52—C53107.3 (5)C52—Rh4—Rh3132.83 (14)
C51—C52—C54127.8 (5)C50—Rh4—Rh3130.72 (14)
C53—C52—C54124.8 (5)C45—Rh4—Rh3102.61 (12)
C9—C1—C2—C3173.7 (6)C49—C48—Cr4—C5030.9 (3)
C6—C1—C2—C33.9 (8)C47—C48—Cr4—C50102.3 (4)
Cr1—C1—C2—C357.4 (5)C48—C49—Cr4—C5545.6 (4)
Rh1—C1—C2—C385.5 (6)C50—C49—Cr4—C55174.3 (3)
C9—C1—C2—Cr1128.9 (7)C48—C49—Cr4—C57130.7 (4)
C6—C1—C2—Cr153.5 (5)C50—C49—Cr4—C57100.6 (4)
Rh1—C1—C2—Cr1142.9 (4)C48—C49—Cr4—C56140.3 (5)
C1—C2—C3—C44.8 (9)C50—C49—Cr4—C5611.6 (6)
Cr1—C2—C3—C453.8 (5)C48—C49—Cr4—C4729.0 (3)
C1—C2—C3—Cr158.6 (5)C50—C49—Cr4—C4799.7 (4)
C2—C3—C4—C51.6 (9)C50—C49—Cr4—C48128.7 (5)
Cr1—C3—C4—C555.9 (5)C48—C49—Cr4—C4664.7 (4)
C2—C3—C4—Cr154.3 (5)C50—C49—Cr4—C4664.0 (3)
C3—C4—C5—C62.6 (8)C48—C49—Cr4—C45100.6 (4)
Cr1—C4—C5—C657.8 (5)C50—C49—Cr4—C4528.1 (3)
C3—C4—C5—Cr155.2 (5)C48—C49—Cr4—C50128.7 (5)
C4—C5—C6—C7172.3 (6)C47—C46—Cr4—C5558.8 (4)
Cr1—C5—C6—C7131.5 (6)C45—C46—Cr4—C55172.5 (3)
C4—C5—C6—C13.3 (8)C47—C46—Cr4—C57116.2 (8)
Cr1—C5—C6—C152.9 (4)C45—C46—Cr4—C5712.4 (9)
C4—C5—C6—Cr156.1 (5)C47—C46—Cr4—C56146.2 (4)
C4—C5—C6—Rh183.3 (6)C45—C46—Cr4—C5685.2 (4)
Cr1—C5—C6—Rh1139.4 (4)C45—C46—Cr4—C47128.7 (5)
C9—C1—C6—C5178.3 (5)C47—C46—Cr4—C4829.3 (4)
C2—C1—C6—C50.1 (8)C45—C46—Cr4—C4899.4 (4)
Cr1—C1—C6—C552.1 (5)C47—C46—Cr4—C4965.0 (4)
Rh1—C1—C6—C5120.6 (5)C45—C46—Cr4—C4963.7 (3)
C9—C1—C6—C71.6 (6)C47—C46—Cr4—C45128.7 (5)
C2—C1—C6—C7176.6 (5)C47—C46—Cr4—C50100.7 (4)
Cr1—C1—C6—C7131.2 (4)C45—C46—Cr4—C5028.0 (3)
Rh1—C1—C6—C756.1 (4)C46—C45—Cr4—C5513.4 (6)
C9—C1—C6—Cr1129.6 (4)C50—C45—Cr4—C55147.0 (4)
C2—C1—C6—Cr152.2 (5)C53—C45—Cr4—C55117.6 (6)
Rh1—C1—C6—Cr1172.7 (2)Rh4—C45—Cr4—C55134.9 (5)
C9—C1—C6—Rh157.7 (4)C46—C45—Cr4—C57174.9 (4)
C2—C1—C6—Rh1120.5 (5)C50—C45—Cr4—C5741.4 (4)
Cr1—C1—C6—Rh1172.7 (2)C53—C45—Cr4—C5754.0 (6)
C5—C6—C7—C8177.9 (6)Rh4—C45—Cr4—C5753.5 (5)
C1—C6—C7—C86.1 (6)C46—C45—Cr4—C5694.5 (4)
Cr1—C6—C7—C873.7 (6)C50—C45—Cr4—C56131.9 (4)
Rh1—C6—C7—C865.5 (4)C53—C45—Cr4—C5636.5 (5)
C5—C6—C7—Rh1116.6 (6)Rh4—C45—Cr4—C56144.1 (4)
C1—C6—C7—Rh159.4 (4)C46—C45—Cr4—C4730.8 (3)
Cr1—C6—C7—Rh1139.2 (5)C50—C45—Cr4—C47102.8 (4)
C6—C7—C8—C98.3 (6)C53—C45—Cr4—C47161.8 (6)
Rh1—C7—C8—C961.5 (4)Rh4—C45—Cr4—C4790.7 (4)
C6—C7—C8—C10174.9 (5)C46—C45—Cr4—C4868.7 (3)
Rh1—C7—C8—C10115.2 (6)C50—C45—Cr4—C4864.9 (3)
C6—C7—C8—Rh169.8 (4)C53—C45—Cr4—C48160.3 (6)
C7—C8—C9—C17.4 (6)Rh4—C45—Cr4—C4852.7 (4)
C10—C8—C9—C1176.0 (6)C46—C45—Cr4—C49105.5 (4)
Rh1—C8—C9—C169.6 (4)C50—C45—Cr4—C4928.1 (3)
C7—C8—C9—Rh162.2 (4)C53—C45—Cr4—C49123.5 (6)
C10—C8—C9—Rh1114.4 (6)Rh4—C45—Cr4—C4916.0 (4)
C2—C1—C9—C8178.6 (6)C50—C45—Cr4—C46133.6 (5)
C6—C1—C9—C83.6 (6)C53—C45—Cr4—C46131.0 (7)
Cr1—C1—C9—C877.0 (6)Rh4—C45—Cr4—C46121.5 (6)
Rh1—C1—C9—C866.2 (4)C46—C45—Cr4—C50133.6 (5)
C2—C1—C9—Rh1115.2 (7)C53—C45—Cr4—C5095.4 (6)
C6—C1—C9—Rh162.6 (4)Rh4—C45—Cr4—C5012.1 (3)
Cr1—C1—C9—Rh1143.2 (5)C49—C50—Cr4—C5514.5 (8)
C24—C16—C17—C18170.9 (6)C45—C50—Cr4—C55119.1 (7)
C21—C16—C17—C185.2 (8)C51—C50—Cr4—C55144.5 (7)
Cr2—C16—C17—C1857.1 (5)Rh4—C50—Cr4—C55106.3 (7)
Rh2—C16—C17—C1881.9 (7)C49—C50—Cr4—C5779.9 (4)
C24—C16—C17—Cr2132.1 (7)C45—C50—Cr4—C57146.5 (4)
C21—C16—C17—Cr251.9 (5)C51—C50—Cr4—C5750.1 (6)
Rh2—C16—C17—Cr2139.0 (4)Rh4—C50—Cr4—C57159.3 (5)
C16—C17—C18—C195.6 (9)C49—C50—Cr4—C56173.3 (3)
Cr2—C17—C18—C1953.2 (5)C45—C50—Cr4—C5653.1 (4)
C16—C17—C18—Cr258.8 (5)C51—C50—Cr4—C5643.3 (6)
C17—C18—C19—C201.1 (9)Rh4—C50—Cr4—C5665.9 (5)
Cr2—C18—C19—C2055.5 (5)C49—C50—Cr4—C4768.6 (4)
C17—C18—C19—Cr254.5 (5)C45—C50—Cr4—C4765.0 (3)
C18—C19—C20—C213.8 (8)C51—C50—Cr4—C47161.4 (6)
Cr2—C19—C20—C2159.0 (5)Rh4—C50—Cr4—C4752.2 (4)
C18—C19—C20—Cr255.2 (5)C49—C50—Cr4—C4830.8 (3)
C19—C20—C21—C22172.4 (6)C45—C50—Cr4—C48102.8 (4)
Cr2—C20—C21—C22130.8 (6)C51—C50—Cr4—C48160.8 (6)
C19—C20—C21—C164.1 (8)Rh4—C50—Cr4—C4890.0 (5)
Cr2—C20—C21—C1652.7 (5)C45—C50—Cr4—C49133.6 (5)
C19—C20—C21—Cr256.8 (5)C51—C50—Cr4—C49130.0 (7)
C19—C20—C21—Rh282.4 (6)Rh4—C50—Cr4—C49120.8 (6)
Cr2—C20—C21—Rh2139.2 (4)C49—C50—Cr4—C46105.4 (4)
C17—C16—C21—C200.3 (8)C45—C50—Cr4—C4628.2 (3)
C24—C16—C21—C20176.7 (5)C51—C50—Cr4—C46124.6 (6)
Cr2—C16—C21—C2051.2 (5)Rh4—C50—Cr4—C4615.4 (4)
Rh2—C16—C21—C20118.1 (5)C49—C50—Cr4—C45133.6 (5)
C17—C16—C21—C22177.7 (5)C51—C50—Cr4—C4596.4 (6)
C24—C16—C21—C220.6 (6)Rh4—C50—Cr4—C4512.8 (3)
Cr2—C16—C21—C22131.4 (4)O5—C15—Rh1—C1491.7 (8)
Rh2—C16—C21—C2259.3 (4)Rh2—C15—Rh1—C1489.7 (3)
C17—C16—C21—Cr250.9 (5)O5—C15—Rh1—C919.1 (9)
C24—C16—C21—Cr2132.1 (4)Rh2—C15—Rh1—C9159.5 (2)
Rh2—C16—C21—Cr2169.3 (2)O5—C15—Rh1—C781.0 (7)
C17—C16—C21—Rh2118.4 (5)Rh2—C15—Rh1—C797.6 (2)
C24—C16—C21—Rh258.7 (4)O5—C15—Rh1—C842.8 (8)
Cr2—C16—C21—Rh2169.3 (2)Rh2—C15—Rh1—C8135.8 (2)
C20—C21—C22—C23178.9 (6)O5—C15—Rh1—C177.3 (11)
C16—C21—C22—C234.2 (6)Rh2—C15—Rh1—C1101.3 (8)
Cr2—C21—C22—C2376.4 (6)O5—C15—Rh1—C6107.0 (7)
Rh2—C21—C22—C2365.9 (4)Rh2—C15—Rh1—C671.6 (3)
C20—C21—C22—Rh2115.2 (6)O5—C15—Rh1—Rh2178.6 (9)
C16—C21—C22—Rh261.6 (4)C8—C9—Rh1—C14148.0 (4)
Cr2—C21—C22—Rh2142.2 (5)C1—C9—Rh1—C1496.4 (4)
C21—C22—C23—C247.6 (6)C8—C9—Rh1—C1539.9 (5)
Rh2—C22—C23—C2459.8 (4)C1—C9—Rh1—C15155.5 (4)
C21—C22—C23—C25173.8 (5)C8—C9—Rh1—C737.6 (4)
Rh2—C22—C23—C25118.8 (6)C1—C9—Rh1—C778.0 (4)
C21—C22—C23—Rh267.4 (4)C1—C9—Rh1—C8115.6 (5)
C22—C23—C24—C168.1 (6)C8—C9—Rh1—C1115.6 (5)
C25—C23—C24—C16173.4 (6)C8—C9—Rh1—C679.2 (4)
Rh2—C23—C24—C1668.5 (4)C1—C9—Rh1—C636.4 (3)
C22—C23—C24—Rh260.4 (4)C8—C9—Rh1—Rh260.2 (8)
C25—C23—C24—Rh2118.1 (6)C1—C9—Rh1—Rh255.4 (8)
C17—C16—C24—C23178.2 (6)C8—C7—Rh1—C1455.8 (10)
C21—C16—C24—C235.4 (6)C6—C7—Rh1—C1458.7 (10)
Cr2—C16—C24—C2373.9 (7)C8—C7—Rh1—C1599.7 (4)
Rh2—C16—C24—C2367.5 (4)C6—C7—Rh1—C15145.9 (3)
C17—C16—C24—Rh2114.3 (7)C8—C7—Rh1—C937.6 (4)
C21—C16—C24—Rh262.1 (4)C6—C7—Rh1—C976.9 (3)
Cr2—C16—C24—Rh2141.4 (5)C6—C7—Rh1—C8114.5 (5)
C35—C30—C31—C326.0 (8)C8—C7—Rh1—C179.1 (4)
C38—C30—C31—C32170.5 (6)C6—C7—Rh1—C135.4 (3)
Cr3—C30—C31—C3256.6 (5)C8—C7—Rh1—C6114.5 (5)
Rh3—C30—C31—C3279.8 (7)C8—C7—Rh1—Rh2148.3 (3)
C35—C30—C31—Cr350.5 (4)C6—C7—Rh1—Rh297.2 (3)
C38—C30—C31—Cr3133.0 (6)C9—C8—Rh1—C1443.6 (5)
Rh3—C30—C31—Cr3136.4 (4)C7—C8—Rh1—C14160.5 (4)
C30—C31—C32—C334.0 (8)C10—C8—Rh1—C1479.4 (6)
Cr3—C31—C32—C3354.9 (5)C9—C8—Rh1—C15153.1 (4)
C30—C31—C32—Cr358.9 (5)C7—C8—Rh1—C1590.0 (4)
C31—C32—C33—C341.6 (9)C10—C8—Rh1—C1530.1 (6)
Cr3—C32—C33—C3454.4 (5)C7—C8—Rh1—C9116.9 (5)
C31—C32—C33—Cr356.0 (5)C10—C8—Rh1—C9123.0 (7)
C32—C33—C34—C355.0 (8)C9—C8—Rh1—C7116.9 (5)
Cr3—C33—C34—C3559.1 (5)C10—C8—Rh1—C7120.1 (7)
C32—C33—C34—Cr354.1 (5)C9—C8—Rh1—C137.7 (3)
C33—C34—C35—C302.8 (8)C7—C8—Rh1—C179.2 (4)
Cr3—C34—C35—C3054.5 (5)C10—C8—Rh1—C1160.7 (6)
C33—C34—C35—C36172.6 (6)C9—C8—Rh1—C678.6 (4)
Cr3—C34—C35—C36130.1 (6)C7—C8—Rh1—C638.3 (3)
C33—C34—C35—Cr357.3 (5)C10—C8—Rh1—C6158.4 (6)
C33—C34—C35—Rh386.7 (6)C9—C8—Rh1—Rh2161.7 (3)
Cr3—C34—C35—Rh3144.0 (3)C7—C8—Rh1—Rh244.8 (4)
C31—C30—C35—C342.7 (8)C10—C8—Rh1—Rh275.3 (6)
C38—C30—C35—C34174.7 (5)C9—C1—Rh1—C1491.5 (4)
Cr3—C30—C35—C3452.4 (5)C2—C1—Rh1—C1436.3 (5)
Rh3—C30—C35—C34118.0 (5)C6—C1—Rh1—C14150.9 (4)
C31—C30—C35—C36179.1 (5)Cr1—C1—Rh1—C14138.9 (5)
C38—C30—C35—C361.8 (6)C9—C1—Rh1—C1577.3 (9)
Cr3—C30—C35—C36131.1 (4)C2—C1—Rh1—C15154.9 (7)
Rh3—C30—C35—C3658.4 (3)C6—C1—Rh1—C1540.3 (9)
C31—C30—C35—Cr349.7 (4)Cr1—C1—Rh1—C1552.4 (11)
C38—C30—C35—Cr3132.9 (4)C2—C1—Rh1—C9127.8 (6)
Rh3—C30—C35—Cr3170.4 (2)C6—C1—Rh1—C9117.6 (5)
C31—C30—C35—Rh3120.7 (5)Cr1—C1—Rh1—C9129.6 (7)
C38—C30—C35—Rh356.6 (4)C9—C1—Rh1—C781.4 (4)
Cr3—C30—C35—Rh3170.4 (2)C2—C1—Rh1—C7150.8 (6)
C34—C35—C36—C37179.4 (6)C6—C1—Rh1—C736.2 (3)
C30—C35—C36—C373.6 (6)Cr1—C1—Rh1—C748.2 (5)
Cr3—C35—C36—C3779.1 (6)C9—C1—Rh1—C838.6 (3)
Rh3—C35—C36—C3767.4 (4)C2—C1—Rh1—C8166.4 (6)
C34—C35—C36—Rh3112.0 (6)C6—C1—Rh1—C879.0 (4)
C30—C35—C36—Rh363.8 (4)Cr1—C1—Rh1—C891.0 (5)
Cr3—C35—C36—Rh3146.5 (5)C9—C1—Rh1—C6117.6 (5)
C35—C36—C37—C387.7 (6)C2—C1—Rh1—C6114.6 (6)
Rh3—C36—C37—C3861.8 (4)Cr1—C1—Rh1—C612.0 (4)
C35—C36—C37—C39173.8 (5)C9—C1—Rh1—Rh2162.7 (3)
Rh3—C36—C37—C39116.8 (6)C2—C1—Rh1—Rh269.5 (5)
C35—C36—C37—Rh369.4 (4)C6—C1—Rh1—Rh245.1 (4)
C36—C37—C38—C308.8 (6)Cr1—C1—Rh1—Rh233.1 (6)
C39—C37—C38—C30172.6 (5)C5—C6—Rh1—C1473.0 (6)
Rh3—C37—C38—C3068.9 (4)C7—C6—Rh1—C14159.4 (4)
C36—C37—C38—Rh360.1 (4)C1—C6—Rh1—C1439.9 (5)
C39—C37—C38—Rh3118.4 (6)Cr1—C6—Rh1—C1428.8 (6)
C31—C30—C38—C37176.6 (6)C5—C6—Rh1—C1581.3 (6)
C35—C30—C38—C376.5 (6)C7—C6—Rh1—C1546.3 (4)
Cr3—C30—C38—C3772.9 (6)C1—C6—Rh1—C15165.8 (4)
Rh3—C30—C38—C3765.3 (4)Cr1—C6—Rh1—C15176.8 (4)
C31—C30—C38—Rh3118.1 (6)C5—C6—Rh1—C9150.1 (6)
C35—C30—C38—Rh358.7 (4)C7—C6—Rh1—C982.3 (4)
Cr3—C30—C38—Rh3138.1 (5)C1—C6—Rh1—C937.2 (3)
C50—C45—C46—C473.5 (8)Cr1—C6—Rh1—C948.3 (4)
C53—C45—C46—C47172.2 (6)C5—C6—Rh1—C7127.6 (6)
Cr4—C45—C46—C4756.5 (4)C1—C6—Rh1—C7119.5 (5)
Rh4—C45—C46—C4784.2 (6)Cr1—C6—Rh1—C7130.5 (6)
C50—C45—C46—Cr453.0 (4)C5—C6—Rh1—C8166.8 (6)
C53—C45—C46—Cr4131.3 (6)C7—C6—Rh1—C839.2 (3)
Rh4—C45—C46—Cr4140.6 (4)C1—C6—Rh1—C880.2 (4)
C45—C46—C47—C483.3 (8)Cr1—C6—Rh1—C891.3 (4)
Cr4—C46—C47—C4854.9 (5)C5—C6—Rh1—C1112.9 (6)
C45—C46—C47—Cr458.2 (4)C7—C6—Rh1—C1119.5 (5)
C46—C47—C48—C491.4 (8)Cr1—C6—Rh1—C111.1 (3)
Cr4—C47—C48—C4954.3 (5)C5—C6—Rh1—Rh234.9 (5)
C46—C47—C48—Cr455.7 (5)C7—C6—Rh1—Rh292.7 (3)
C47—C48—C49—C505.9 (8)C1—C6—Rh1—Rh2147.9 (3)
Cr4—C48—C49—C5059.5 (5)Cr1—C6—Rh1—Rh2136.8 (4)
C47—C48—C49—Cr453.7 (5)O5—C15—Rh2—C2984.0 (8)
C48—C49—C50—C455.6 (8)Rh1—C15—Rh2—C2994.5 (3)
Cr4—C49—C50—C4552.2 (4)O5—C15—Rh2—C2429.1 (10)
C48—C49—C50—C51172.4 (6)Rh1—C15—Rh2—C24152.4 (3)
Cr4—C49—C50—C51129.8 (6)O5—C15—Rh2—C2289.5 (8)
C48—C49—C50—Cr457.8 (5)Rh1—C15—Rh2—C2292.0 (2)
C48—C49—C50—Rh484.6 (6)O5—C15—Rh2—C2351.8 (9)
Cr4—C49—C50—Rh4142.3 (4)Rh1—C15—Rh2—C23129.7 (2)
C46—C45—C50—C490.9 (8)O5—C15—Rh2—C16104.8 (11)
C53—C45—C50—C49177.7 (5)Rh1—C15—Rh2—C1676.7 (9)
Cr4—C45—C50—C4950.9 (4)O5—C15—Rh2—C21120.1 (8)
Rh4—C45—C50—C49121.3 (5)Rh1—C15—Rh2—C2161.4 (3)
C46—C45—C50—C51177.6 (5)O5—C15—Rh2—Rh1178.5 (9)
C53—C45—C50—C510.8 (6)C23—C24—Rh2—C29146.5 (4)
Cr4—C45—C50—C51130.6 (4)C16—C24—Rh2—C2997.7 (4)
Rh4—C45—C50—C5157.2 (4)C23—C24—Rh2—C1537.9 (6)
C46—C45—C50—Cr451.8 (4)C16—C24—Rh2—C15153.7 (4)
C53—C45—C50—Cr4131.4 (4)C23—C24—Rh2—C2236.8 (4)
Rh4—C45—C50—Cr4172.3 (2)C16—C24—Rh2—C2279.0 (4)
C46—C45—C50—Rh4120.4 (5)C16—C24—Rh2—C23115.8 (5)
C53—C45—C50—Rh456.3 (3)C23—C24—Rh2—C16115.8 (5)
Cr4—C45—C50—Rh4172.3 (2)C23—C24—Rh2—C2179.0 (4)
C49—C50—C51—C52176.9 (6)C16—C24—Rh2—C2136.8 (3)
C45—C50—C51—C524.9 (6)C23—C24—Rh2—Rh169.2 (6)
Cr4—C50—C51—C5275.5 (6)C16—C24—Rh2—Rh146.6 (6)
Rh4—C50—C51—C5267.3 (4)C23—C22—Rh2—C2948.7 (11)
C49—C50—C51—Rh4115.8 (6)C21—C22—Rh2—C2967.0 (11)
C45—C50—C51—Rh462.4 (4)C23—C22—Rh2—C15106.0 (4)
Cr4—C50—C51—Rh4142.8 (4)C21—C22—Rh2—C15138.3 (3)
C50—C51—C52—C538.7 (6)C23—C22—Rh2—C2436.4 (4)
Rh4—C51—C52—C5361.2 (4)C21—C22—Rh2—C2479.3 (3)
C50—C51—C52—C54174.7 (5)C21—C22—Rh2—C23115.7 (5)
Rh4—C51—C52—C54115.3 (6)C23—C22—Rh2—C1678.8 (4)
C50—C51—C52—Rh470.0 (4)C21—C22—Rh2—C1636.9 (3)
C51—C52—C53—C459.3 (6)C23—C22—Rh2—C21115.7 (5)
C54—C52—C53—C45174.0 (5)C23—C22—Rh2—Rh1154.8 (3)
Rh4—C52—C53—C4570.1 (4)C21—C22—Rh2—Rh189.5 (3)
C51—C52—C53—Rh460.8 (4)C24—C23—Rh2—C2946.4 (5)
C54—C52—C53—Rh4115.9 (6)C22—C23—Rh2—C29164.5 (4)
C46—C45—C53—C52177.6 (5)C25—C23—Rh2—C2976.1 (6)
C50—C45—C53—C526.2 (6)C24—C23—Rh2—C15156.3 (4)
Cr4—C45—C53—C5274.1 (6)C22—C23—Rh2—C1585.6 (4)
Rh4—C45—C53—C5266.3 (4)C25—C23—Rh2—C1533.8 (6)
C46—C45—C53—Rh4116.1 (6)C22—C23—Rh2—C24118.1 (5)
C50—C45—C53—Rh460.1 (4)C25—C23—Rh2—C24122.5 (7)
Cr4—C45—C53—Rh4140.4 (4)C24—C23—Rh2—C22118.1 (5)
C2—C3—Cr1—C11134.6 (4)C25—C23—Rh2—C22119.4 (6)
C4—C3—Cr1—C1191.4 (4)C24—C23—Rh2—C1638.3 (4)
C2—C3—Cr1—C1245.8 (5)C22—C23—Rh2—C1679.8 (4)
C4—C3—Cr1—C12179.8 (4)C25—C23—Rh2—C16160.8 (6)
C2—C3—Cr1—C13130.1 (6)C24—C23—Rh2—C2180.0 (4)
C4—C3—Cr1—C133.9 (8)C22—C23—Rh2—C2138.1 (3)
C2—C3—Cr1—C4133.9 (6)C25—C23—Rh2—C21157.5 (6)
C4—C3—Cr1—C2133.9 (6)C24—C23—Rh2—Rh1152.8 (3)
C2—C3—Cr1—C5105.1 (4)C22—C23—Rh2—Rh134.7 (4)
C4—C3—Cr1—C528.9 (4)C25—C23—Rh2—Rh184.7 (5)
C2—C3—Cr1—C131.2 (3)C17—C16—Rh2—C2936.4 (6)
C4—C3—Cr1—C1102.8 (4)C24—C16—Rh2—C2992.4 (4)
C2—C3—Cr1—C668.2 (4)C21—C16—Rh2—C29150.3 (4)
C4—C3—Cr1—C665.7 (4)Cr2—C16—Rh2—C29133.8 (4)
C5—C4—Cr1—C11135.8 (4)C17—C16—Rh2—C15134.4 (8)
C3—C4—Cr1—C1192.3 (4)C24—C16—Rh2—C1596.8 (9)
C5—C4—Cr1—C12131.5 (6)C21—C16—Rh2—C1520.5 (10)
C3—C4—Cr1—C120.4 (8)Cr2—C16—Rh2—C1537.0 (11)
C5—C4—Cr1—C1346.1 (5)C17—C16—Rh2—C24128.8 (7)
C3—C4—Cr1—C13178.1 (4)C21—C16—Rh2—C24117.2 (5)
C5—C4—Cr1—C3132.0 (6)Cr2—C16—Rh2—C24133.8 (6)
C5—C4—Cr1—C2104.4 (4)C17—C16—Rh2—C22151.5 (6)
C3—C4—Cr1—C227.5 (4)C24—C16—Rh2—C2279.7 (4)
C3—C4—Cr1—C5132.0 (6)C21—C16—Rh2—C2237.5 (3)
C5—C4—Cr1—C167.1 (4)Cr2—C16—Rh2—C2254.1 (4)
C3—C4—Cr1—C164.8 (4)C17—C16—Rh2—C23166.4 (6)
C5—C4—Cr1—C630.2 (3)C24—C16—Rh2—C2337.6 (3)
C3—C4—Cr1—C6101.7 (4)C21—C16—Rh2—C2379.7 (4)
C3—C2—Cr1—C1154.4 (4)Cr2—C16—Rh2—C2396.2 (5)
C1—C2—Cr1—C11176.7 (3)C17—C16—Rh2—C21114.0 (7)
C3—C2—Cr1—C12140.0 (4)C24—C16—Rh2—C21117.2 (5)
C1—C2—Cr1—C1291.1 (4)Cr2—C16—Rh2—C2116.6 (3)
C3—C2—Cr1—C13131.9 (6)C17—C16—Rh2—Rh170.2 (5)
C1—C2—Cr1—C133.0 (7)C24—C16—Rh2—Rh1161.0 (3)
C1—C2—Cr1—C3128.9 (5)C21—C16—Rh2—Rh143.7 (4)
C3—C2—Cr1—C428.2 (4)Cr2—C16—Rh2—Rh127.2 (5)
C1—C2—Cr1—C4100.7 (4)C20—C21—Rh2—C2971.5 (6)
C3—C2—Cr1—C564.1 (4)C22—C21—Rh2—C29159.8 (4)
C1—C2—Cr1—C564.8 (3)C16—C21—Rh2—C2942.7 (5)
C3—C2—Cr1—C1128.9 (5)Cr2—C21—Rh2—C2925.9 (6)
C3—C2—Cr1—C6100.1 (4)C20—C21—Rh2—C1572.9 (6)
C1—C2—Cr1—C628.8 (3)C22—C21—Rh2—C1555.8 (4)
C4—C5—Cr1—C1153.3 (4)C16—C21—Rh2—C15172.9 (4)
C6—C5—Cr1—C11176.9 (3)Cr2—C21—Rh2—C15170.3 (4)
C4—C5—Cr1—C12130.9 (6)C20—C21—Rh2—C24151.8 (6)
C6—C5—Cr1—C121.0 (7)C22—C21—Rh2—C2479.6 (4)
C4—C5—Cr1—C13140.1 (4)C16—C21—Rh2—C2437.6 (3)
C6—C5—Cr1—C1390.1 (4)Cr2—C21—Rh2—C2454.3 (4)
C4—C5—Cr1—C329.3 (4)C20—C21—Rh2—C22128.7 (6)
C6—C5—Cr1—C3100.6 (4)C16—C21—Rh2—C22117.1 (5)
C6—C5—Cr1—C4129.8 (5)Cr2—C21—Rh2—C22133.9 (6)
C4—C5—Cr1—C264.6 (4)C20—C21—Rh2—C23166.6 (6)
C6—C5—Cr1—C265.3 (3)C22—C21—Rh2—C2338.0 (3)
C4—C5—Cr1—C1101.1 (4)C16—C21—Rh2—C2379.1 (4)
C6—C5—Cr1—C128.8 (3)Cr2—C21—Rh2—C2395.9 (5)
C4—C5—Cr1—C6129.8 (5)C20—C21—Rh2—C16114.2 (6)
C9—C1—Cr1—C11123.7 (7)C22—C21—Rh2—C16117.1 (5)
C2—C1—Cr1—C117.1 (7)Cr2—C21—Rh2—C1616.8 (3)
C6—C1—Cr1—C11139.6 (6)C20—C21—Rh2—Rh131.8 (5)
Rh1—C1—Cr1—C11127.5 (6)C22—C21—Rh2—Rh196.9 (3)
C9—C1—Cr1—C1242.1 (6)C16—C21—Rh2—Rh1146.0 (3)
C2—C1—Cr1—C1288.8 (4)Cr2—C21—Rh2—Rh1129.2 (4)
C6—C1—Cr1—C12138.7 (4)C14—Rh1—Rh2—C29179.9 (3)
Rh1—C1—Cr1—C12150.9 (5)C15—Rh1—Rh2—C2987.0 (3)
C9—C1—Cr1—C1347.6 (6)C9—Rh1—Rh2—C2927.7 (7)
C2—C1—Cr1—C13178.5 (3)C7—Rh1—Rh2—C297.3 (3)
C6—C1—Cr1—C1349.0 (4)C8—Rh1—Rh2—C2918.7 (3)
Rh1—C1—Cr1—C1361.2 (6)C1—Rh1—Rh2—C2970.0 (3)
C9—C1—Cr1—C3161.2 (6)C6—Rh1—Rh2—C2944.8 (3)
C2—C1—Cr1—C330.3 (3)C14—Rh1—Rh2—C1592.9 (3)
C6—C1—Cr1—C3102.1 (4)C9—Rh1—Rh2—C15114.7 (7)
Rh1—C1—Cr1—C390.0 (5)C7—Rh1—Rh2—C1594.3 (3)
C9—C1—Cr1—C4161.9 (6)C8—Rh1—Rh2—C1568.2 (3)
C2—C1—Cr1—C467.3 (3)C1—Rh1—Rh2—C15157.0 (3)
C6—C1—Cr1—C465.2 (3)C6—Rh1—Rh2—C15131.8 (3)
Rh1—C1—Cr1—C453.1 (5)C14—Rh1—Rh2—C2434.6 (5)
C9—C1—Cr1—C2130.9 (7)C15—Rh1—Rh2—C24127.5 (5)
C6—C1—Cr1—C2132.5 (5)C9—Rh1—Rh2—C24117.8 (8)
Rh1—C1—Cr1—C2120.4 (6)C7—Rh1—Rh2—C24138.2 (5)
C9—C1—Cr1—C5125.2 (6)C8—Rh1—Rh2—C24164.2 (5)
C2—C1—Cr1—C5104.0 (4)C1—Rh1—Rh2—C2475.4 (5)
C6—C1—Cr1—C528.5 (3)C6—Rh1—Rh2—C24100.7 (5)
Rh1—C1—Cr1—C516.4 (4)C14—Rh1—Rh2—C226.2 (3)
C9—C1—Cr1—C696.7 (7)C15—Rh1—Rh2—C2299.1 (3)
C2—C1—Cr1—C6132.5 (5)C9—Rh1—Rh2—C22146.2 (7)
Rh1—C1—Cr1—C612.1 (4)C7—Rh1—Rh2—C22166.7 (2)
C5—C6—Cr1—C116.8 (7)C8—Rh1—Rh2—C22167.3 (3)
C7—C6—Cr1—C11124.8 (7)C1—Rh1—Rh2—C22103.9 (3)
C1—C6—Cr1—C11139.5 (6)C6—Rh1—Rh2—C22129.2 (2)
Rh1—C6—Cr1—C11128.4 (6)C14—Rh1—Rh2—C2314.0 (3)
C5—C6—Cr1—C12179.5 (4)C15—Rh1—Rh2—C2378.9 (3)
C7—C6—Cr1—C1247.9 (6)C9—Rh1—Rh2—C23166.4 (7)
C1—C6—Cr1—C1247.8 (4)C7—Rh1—Rh2—C23173.2 (3)
Rh1—C6—Cr1—C1258.9 (5)C8—Rh1—Rh2—C23147.2 (3)
C5—C6—Cr1—C1389.9 (4)C1—Rh1—Rh2—C23124.1 (3)
C7—C6—Cr1—C1341.7 (6)C6—Rh1—Rh2—C23149.3 (3)
C1—C6—Cr1—C13137.4 (4)C14—Rh1—Rh2—C1667.6 (3)
Rh1—C6—Cr1—C13148.4 (4)C15—Rh1—Rh2—C16160.5 (3)
C5—C6—Cr1—C367.4 (3)C9—Rh1—Rh2—C1684.8 (7)
C7—C6—Cr1—C3161.0 (6)C7—Rh1—Rh2—C16105.2 (2)
C1—C6—Cr1—C365.3 (3)C8—Rh1—Rh2—C16131.2 (3)
Rh1—C6—Cr1—C354.2 (4)C1—Rh1—Rh2—C1642.5 (3)
C5—C6—Cr1—C430.2 (3)C6—Rh1—Rh2—C1667.7 (2)
C7—C6—Cr1—C4161.8 (6)C14—Rh1—Rh2—C2143.3 (3)
C1—C6—Cr1—C4102.5 (4)C15—Rh1—Rh2—C21136.2 (3)
Rh1—C6—Cr1—C491.4 (4)C9—Rh1—Rh2—C21109.1 (7)
C5—C6—Cr1—C2103.8 (4)C7—Rh1—Rh2—C21129.5 (2)
C7—C6—Cr1—C2124.6 (6)C8—Rh1—Rh2—C21155.5 (3)
C1—C6—Cr1—C228.9 (3)C1—Rh1—Rh2—C2166.8 (3)
Rh1—C6—Cr1—C217.8 (4)C6—Rh1—Rh2—C2192.0 (2)
C7—C6—Cr1—C5131.6 (7)O14—C44—Rh3—C4385.7 (8)
C1—C6—Cr1—C5132.7 (5)Rh4—C44—Rh3—C4393.0 (2)
Rh1—C6—Cr1—C5121.6 (6)O14—C44—Rh3—C3623.4 (10)
C5—C6—Cr1—C1132.7 (5)Rh4—C44—Rh3—C36157.8 (3)
C7—C6—Cr1—C195.7 (6)O14—C44—Rh3—C3745.1 (8)
Rh1—C6—Cr1—C111.1 (3)Rh4—C44—Rh3—C37136.1 (2)
C20—C19—Cr2—C26130.9 (4)O14—C44—Rh3—C3882.3 (8)
C18—C19—Cr2—C2696.2 (4)Rh4—C44—Rh3—C3898.9 (2)
C20—C19—Cr2—C27142.3 (6)O14—C44—Rh3—C35104.9 (9)
C18—C19—Cr2—C279.4 (8)Rh4—C44—Rh3—C3576.4 (7)
C20—C19—Cr2—C2842.1 (5)O14—C44—Rh3—C30112.3 (7)
C18—C19—Cr2—C28175.0 (4)Rh4—C44—Rh3—C3068.9 (3)
C20—C19—Cr2—C18132.9 (6)O14—C44—Rh3—Rh4178.8 (9)
C18—C19—Cr2—C20132.9 (6)C37—C36—Rh3—C43141.8 (4)
C20—C19—Cr2—C17105.1 (4)C35—C36—Rh3—C43104.1 (4)
C18—C19—Cr2—C1727.8 (4)C37—C36—Rh3—C4434.9 (6)
C20—C19—Cr2—C2131.1 (3)C35—C36—Rh3—C44149.1 (4)
C18—C19—Cr2—C21101.7 (4)C35—C36—Rh3—C37114.1 (5)
C20—C19—Cr2—C1668.1 (4)C37—C36—Rh3—C3836.5 (3)
C18—C19—Cr2—C1664.8 (4)C35—C36—Rh3—C3877.7 (4)
C17—C18—Cr2—C26142.4 (4)C37—C36—Rh3—C35114.1 (5)
C19—C18—Cr2—C2684.4 (4)C37—C36—Rh3—C3077.8 (4)
C17—C18—Cr2—C2751.8 (5)C35—C36—Rh3—C3036.4 (3)
C19—C18—Cr2—C27174.9 (4)C37—C36—Rh3—Rh485.5 (6)
C17—C18—Cr2—C28122.4 (7)C35—C36—Rh3—Rh428.7 (7)
C19—C18—Cr2—C2810.9 (9)C38—C37—Rh3—C43167.9 (4)
C17—C18—Cr2—C19133.3 (6)C36—C37—Rh3—C4349.6 (5)
C17—C18—Cr2—C20104.7 (4)C39—C37—Rh3—C4372.4 (6)
C19—C18—Cr2—C2028.5 (4)C38—C37—Rh3—C4482.7 (4)
C19—C18—Cr2—C17133.3 (6)C36—C37—Rh3—C44159.0 (4)
C17—C18—Cr2—C2167.5 (4)C39—C37—Rh3—C4437.0 (6)
C19—C18—Cr2—C2165.8 (4)C38—C37—Rh3—C36118.3 (5)
C17—C18—Cr2—C1630.7 (4)C39—C37—Rh3—C36122.0 (7)
C19—C18—Cr2—C16102.5 (4)C36—C37—Rh3—C38118.3 (5)
C19—C20—Cr2—C2654.8 (4)C39—C37—Rh3—C38119.7 (7)
C21—C20—Cr2—C26177.0 (4)C38—C37—Rh3—C3579.1 (4)
C19—C20—Cr2—C27124.3 (7)C36—C37—Rh3—C3539.2 (3)
C21—C20—Cr2—C274.0 (8)C39—C37—Rh3—C35161.1 (6)
C19—C20—Cr2—C28143.9 (4)C38—C37—Rh3—C3038.2 (4)
C21—C20—Cr2—C2887.8 (4)C36—C37—Rh3—C3080.1 (4)
C21—C20—Cr2—C19128.3 (5)C39—C37—Rh3—C30157.9 (6)
C19—C20—Cr2—C1829.0 (4)C38—C37—Rh3—Rh432.9 (5)
C21—C20—Cr2—C1899.3 (4)C36—C37—Rh3—Rh4151.2 (3)
C19—C20—Cr2—C1764.3 (4)C39—C37—Rh3—Rh486.8 (6)
C21—C20—Cr2—C1764.0 (4)C37—C38—Rh3—C4331.6 (10)
C19—C20—Cr2—C21128.3 (5)C30—C38—Rh3—C4383.1 (9)
C19—C20—Cr2—C16100.0 (4)C37—C38—Rh3—C44108.4 (4)
C21—C20—Cr2—C1628.3 (3)C30—C38—Rh3—C44136.9 (3)
C18—C17—Cr2—C2645.0 (5)C37—C38—Rh3—C3637.0 (4)
C16—C17—Cr2—C26174.3 (4)C30—C38—Rh3—C3677.7 (4)
C18—C17—Cr2—C27133.5 (4)C30—C38—Rh3—C37114.7 (5)
C16—C17—Cr2—C2797.2 (4)C37—C38—Rh3—C3579.6 (4)
C18—C17—Cr2—C28136.4 (5)C30—C38—Rh3—C3535.1 (3)
C16—C17—Cr2—C287.1 (7)C37—C38—Rh3—C30114.7 (5)
C18—C17—Cr2—C1928.9 (4)C37—C38—Rh3—Rh4157.7 (3)
C16—C17—Cr2—C19100.3 (4)C30—C38—Rh3—Rh487.6 (3)
C16—C17—Cr2—C18129.3 (5)C34—C35—Rh3—C4342.7 (5)
C18—C17—Cr2—C2065.1 (4)C30—C35—Rh3—C43158.6 (3)
C16—C17—Cr2—C2064.2 (4)C36—C35—Rh3—C4384.5 (4)
C18—C17—Cr2—C21101.0 (4)Cr3—C35—Rh3—C43142.0 (5)
C16—C17—Cr2—C2128.3 (3)C34—C35—Rh3—C44126.2 (7)
C18—C17—Cr2—C16129.3 (5)C30—C35—Rh3—C4410.3 (9)
C20—C21—Cr2—C265.5 (6)C36—C35—Rh3—C44106.5 (7)
C22—C21—Cr2—C26125.3 (6)Cr3—C35—Rh3—C4427.0 (10)
C16—C21—Cr2—C26139.0 (5)C34—C35—Rh3—C36127.2 (6)
Rh2—C21—Cr2—C26122.3 (5)C30—C35—Rh3—C36116.9 (5)
C20—C21—Cr2—C27178.3 (4)Cr3—C35—Rh3—C36133.5 (7)
C22—C21—Cr2—C2751.0 (6)C34—C35—Rh3—C37166.2 (5)
C16—C21—Cr2—C2744.7 (4)C30—C35—Rh3—C3777.9 (4)
Rh2—C21—Cr2—C2761.5 (5)C36—C35—Rh3—C3739.0 (3)
C20—C21—Cr2—C2891.4 (4)Cr3—C35—Rh3—C3794.5 (5)
C22—C21—Cr2—C2839.3 (6)C34—C35—Rh3—C38151.7 (5)
C16—C21—Cr2—C28135.1 (4)C30—C35—Rh3—C3835.8 (3)
Rh2—C21—Cr2—C28151.8 (5)C36—C35—Rh3—C3881.1 (4)
C20—C21—Cr2—C1931.3 (3)Cr3—C35—Rh3—C3852.4 (5)
C22—C21—Cr2—C19162.1 (6)C34—C35—Rh3—C30115.9 (6)
C16—C21—Cr2—C19102.2 (4)C36—C35—Rh3—C30116.9 (5)
Rh2—C21—Cr2—C1985.5 (5)Cr3—C35—Rh3—C3016.7 (4)
C20—C21—Cr2—C1869.1 (4)C34—C35—Rh3—Rh463.8 (5)
C22—C21—Cr2—C18160.2 (6)C30—C35—Rh3—Rh452.1 (4)
C16—C21—Cr2—C1864.4 (4)C36—C35—Rh3—Rh4169.0 (3)
Rh2—C21—Cr2—C1847.7 (4)Cr3—C35—Rh3—Rh435.4 (6)
C22—C21—Cr2—C20130.7 (7)C31—C30—Rh3—C4381.1 (6)
C16—C21—Cr2—C20133.5 (5)C35—C30—Rh3—C4331.5 (5)
Rh2—C21—Cr2—C20116.8 (6)C38—C30—Rh3—C43151.5 (4)
C20—C21—Cr2—C17105.4 (4)Cr3—C30—Rh3—C4317.6 (6)
C22—C21—Cr2—C17123.9 (6)C31—C30—Rh3—C4471.4 (6)
C16—C21—Cr2—C1728.1 (3)C35—C30—Rh3—C44176.0 (3)
Rh2—C21—Cr2—C1711.4 (4)C38—C30—Rh3—C4456.0 (4)
C20—C21—Cr2—C16133.5 (5)Cr3—C30—Rh3—C44170.1 (3)
C22—C21—Cr2—C1695.8 (6)C31—C30—Rh3—C36150.9 (6)
Rh2—C21—Cr2—C1616.7 (3)C35—C30—Rh3—C3638.2 (3)
C17—C16—Cr2—C2612.5 (8)C38—C30—Rh3—C3681.7 (4)
C24—C16—Cr2—C26144.2 (7)Cr3—C30—Rh3—C3652.2 (4)
C21—C16—Cr2—C26121.0 (6)C31—C30—Rh3—C37166.2 (6)
Rh2—C16—Cr2—C26104.3 (7)C35—C30—Rh3—C3781.2 (4)
C17—C16—Cr2—C2783.4 (4)C38—C30—Rh3—C3738.8 (3)
C24—C16—Cr2—C2748.3 (6)Cr3—C30—Rh3—C3795.1 (4)
C21—C16—Cr2—C27143.1 (4)C31—C30—Rh3—C38127.4 (7)
Rh2—C16—Cr2—C27159.8 (5)C35—C30—Rh3—C38120.0 (5)
C17—C16—Cr2—C28176.2 (4)Cr3—C30—Rh3—C38133.9 (6)
C24—C16—Cr2—C2844.4 (6)C31—C30—Rh3—C35112.6 (7)
C21—C16—Cr2—C2850.3 (4)C38—C30—Rh3—C35120.0 (5)
Rh2—C16—Cr2—C2867.0 (5)Cr3—C30—Rh3—C3513.9 (3)
C17—C16—Cr2—C1967.9 (4)C31—C30—Rh3—Rh426.6 (5)
C24—C16—Cr2—C19160.4 (6)C35—C30—Rh3—Rh4139.2 (3)
C21—C16—Cr2—C1965.6 (4)C38—C30—Rh3—Rh4100.8 (3)
Rh2—C16—Cr2—C1948.9 (4)Cr3—C30—Rh3—Rh4125.3 (4)
C17—C16—Cr2—C1830.2 (4)O14—C44—Rh4—C5887.5 (8)
C24—C16—Cr2—C18162.0 (6)Rh3—C44—Rh4—C5893.7 (2)
C21—C16—Cr2—C18103.3 (4)O14—C44—Rh4—C5122.1 (9)
Rh2—C16—Cr2—C1886.5 (5)Rh3—C44—Rh4—C51156.7 (2)
C17—C16—Cr2—C20105.3 (4)O14—C44—Rh4—C5385.0 (8)
C24—C16—Cr2—C20122.9 (6)Rh3—C44—Rh4—C5393.8 (2)
C21—C16—Cr2—C2028.2 (3)O14—C44—Rh4—C5246.7 (8)
Rh2—C16—Cr2—C2011.5 (4)Rh3—C44—Rh4—C52132.0 (2)
C24—C16—Cr2—C17131.7 (7)O14—C44—Rh4—C5085.8 (12)
C21—C16—Cr2—C17133.5 (5)Rh3—C44—Rh4—C5093.0 (8)
Rh2—C16—Cr2—C17116.8 (6)O14—C44—Rh4—C45112.7 (7)
C17—C16—Cr2—C21133.5 (5)Rh3—C44—Rh4—C4566.1 (3)
C24—C16—Cr2—C2194.8 (7)O14—C44—Rh4—Rh3178.8 (9)
Rh2—C16—Cr2—C2116.7 (3)C52—C51—Rh4—C58147.3 (4)
C34—C33—Cr3—C4247.8 (5)C50—C51—Rh4—C5898.0 (4)
C32—C33—Cr3—C42179.1 (4)C52—C51—Rh4—C4441.9 (5)
C34—C33—Cr3—C40136.4 (4)C50—C51—Rh4—C44156.6 (3)
C32—C33—Cr3—C4090.5 (4)C52—C51—Rh4—C5337.3 (4)
C34—C33—Cr3—C41132.8 (6)C50—C51—Rh4—C5377.4 (3)
C32—C33—Cr3—C410.3 (8)C50—C51—Rh4—C52114.7 (5)
C34—C33—Cr3—C32133.1 (6)C52—C51—Rh4—C50114.7 (5)
C32—C33—Cr3—C34133.1 (6)C52—C51—Rh4—C4579.1 (4)
C34—C33—Cr3—C31104.4 (4)C50—C51—Rh4—C4535.6 (3)
C32—C33—Cr3—C3128.7 (4)C52—C51—Rh4—Rh361.3 (7)
C34—C33—Cr3—C3531.0 (3)C50—C51—Rh4—Rh353.4 (7)
C32—C33—Cr3—C35102.1 (4)C52—C53—Rh4—C5852.7 (10)
C34—C33—Cr3—C3067.6 (4)C45—C53—Rh4—C5862.3 (9)
C32—C33—Cr3—C3065.5 (4)C52—C53—Rh4—C44100.7 (4)
C31—C32—Cr3—C42133.8 (6)C45—C53—Rh4—C44144.3 (3)
C33—C32—Cr3—C421.7 (8)C52—C53—Rh4—C5136.9 (3)
C31—C32—Cr3—C40136.9 (4)C45—C53—Rh4—C5178.1 (3)
C33—C32—Cr3—C4091.0 (4)C45—C53—Rh4—C52115.0 (5)
C31—C32—Cr3—C4147.8 (4)C52—C53—Rh4—C5079.5 (4)
C33—C32—Cr3—C41179.9 (4)C45—C53—Rh4—C5035.5 (3)
C31—C32—Cr3—C33132.0 (5)C52—C53—Rh4—C45115.0 (5)
C31—C32—Cr3—C34103.5 (4)C52—C53—Rh4—Rh3150.3 (3)
C33—C32—Cr3—C3428.5 (4)C45—C53—Rh4—Rh394.6 (3)
C33—C32—Cr3—C31132.0 (5)C51—C52—Rh4—C5844.6 (5)
C31—C32—Cr3—C3566.4 (4)C53—C52—Rh4—C58162.1 (4)
C33—C32—Cr3—C3565.7 (4)C54—C52—Rh4—C5878.2 (5)
C31—C32—Cr3—C3030.3 (3)C51—C52—Rh4—C44152.2 (4)
C33—C32—Cr3—C30101.7 (4)C53—C52—Rh4—C4490.3 (4)
C33—C34—Cr3—C42138.0 (4)C54—C52—Rh4—C4429.4 (5)
C35—C34—Cr3—C4293.4 (4)C53—C52—Rh4—C51117.5 (5)
C33—C34—Cr3—C4051.3 (4)C54—C52—Rh4—C51122.8 (6)
C35—C34—Cr3—C40179.9 (3)C51—C52—Rh4—C53117.5 (5)
C33—C34—Cr3—C41132.2 (6)C54—C52—Rh4—C53119.7 (6)
C35—C34—Cr3—C413.6 (7)C51—C52—Rh4—C5038.9 (3)
C35—C34—Cr3—C33128.6 (5)C53—C52—Rh4—C5078.6 (4)
C33—C34—Cr3—C3228.7 (4)C54—C52—Rh4—C50161.7 (5)
C35—C34—Cr3—C3299.8 (4)C51—C52—Rh4—C4579.3 (4)
C33—C34—Cr3—C3164.6 (4)C53—C52—Rh4—C4538.2 (3)
C35—C34—Cr3—C3164.0 (3)C54—C52—Rh4—C45157.9 (5)
C33—C34—Cr3—C35128.6 (5)C51—C52—Rh4—Rh3158.8 (3)
C33—C34—Cr3—C30100.0 (4)C53—C52—Rh4—Rh341.2 (4)
C35—C34—Cr3—C3028.5 (3)C54—C52—Rh4—Rh378.4 (5)
C32—C31—Cr3—C42129.7 (6)C49—C50—Rh4—C5835.7 (5)
C30—C31—Cr3—C420.2 (7)C45—C50—Rh4—C58150.8 (3)
C32—C31—Cr3—C4050.4 (4)C51—C50—Rh4—C5891.2 (4)
C30—C31—Cr3—C40179.9 (4)Cr4—C50—Rh4—C58138.1 (4)
C32—C31—Cr3—C41138.2 (4)C49—C50—Rh4—C44151.2 (8)
C30—C31—Cr3—C4192.2 (4)C45—C50—Rh4—C4436.1 (10)
C32—C31—Cr3—C3329.5 (3)C51—C50—Rh4—C4481.9 (9)
C30—C31—Cr3—C33100.1 (4)Cr4—C50—Rh4—C4448.8 (11)
C30—C31—Cr3—C32129.5 (5)C49—C50—Rh4—C51126.9 (6)
C32—C31—Cr3—C3465.9 (4)C45—C50—Rh4—C51118.0 (5)
C30—C31—Cr3—C3463.6 (4)Cr4—C50—Rh4—C51130.7 (6)
C32—C31—Cr3—C35102.0 (4)C49—C50—Rh4—C53152.0 (6)
C30—C31—Cr3—C3527.5 (3)C45—C50—Rh4—C5336.9 (3)
C32—C31—Cr3—C30129.5 (5)C51—C50—Rh4—C5381.1 (3)
C34—C35—Cr3—C4286.4 (4)Cr4—C50—Rh4—C5349.6 (4)
C30—C35—Cr3—C42141.0 (4)C49—C50—Rh4—C52165.3 (6)
C36—C35—Cr3—C4243.4 (6)C45—C50—Rh4—C5279.6 (3)
Rh3—C35—Cr3—C42157.8 (5)C51—C50—Rh4—C5238.4 (3)
C34—C35—Cr3—C400.3 (7)Cr4—C50—Rh4—C5292.3 (5)
C30—C35—Cr3—C40132.3 (6)C49—C50—Rh4—C45115.1 (6)
C36—C35—Cr3—C40130.1 (7)C51—C50—Rh4—C45118.0 (5)
Rh3—C35—Cr3—C40115.5 (7)Cr4—C50—Rh4—C4512.7 (3)
C34—C35—Cr3—C41178.2 (3)C49—C50—Rh4—Rh371.8 (5)
C30—C35—Cr3—C4149.2 (4)C45—C50—Rh4—Rh343.3 (4)
C36—C35—Cr3—C4148.3 (6)C51—C50—Rh4—Rh3161.3 (3)
Rh3—C35—Cr3—C4166.0 (5)Cr4—C50—Rh4—Rh330.6 (5)
C34—C35—Cr3—C3331.2 (3)C46—C45—Rh4—C5873.7 (5)
C30—C35—Cr3—C33101.4 (4)C50—C45—Rh4—C5840.8 (5)
C36—C35—Cr3—C33161.1 (6)C53—C45—Rh4—C58159.3 (3)
Rh3—C35—Cr3—C3384.6 (5)Cr4—C45—Rh4—C5828.6 (6)
C34—C35—Cr3—C3268.6 (3)C46—C45—Rh4—C4477.6 (6)
C30—C35—Cr3—C3263.9 (3)C50—C45—Rh4—C44167.8 (3)
C36—C35—Cr3—C32161.5 (6)C53—C45—Rh4—C4449.4 (4)
Rh3—C35—Cr3—C3247.1 (5)Cr4—C45—Rh4—C44180.0 (4)
C30—C35—Cr3—C34132.5 (5)C46—C45—Rh4—C51152.1 (5)
C36—C35—Cr3—C34129.9 (7)C50—C45—Rh4—C5137.6 (3)
Rh3—C35—Cr3—C34115.8 (6)C53—C45—Rh4—C5180.9 (3)
C34—C35—Cr3—C31105.0 (4)Cr4—C45—Rh4—C5149.8 (4)
C30—C35—Cr3—C3127.5 (3)C46—C45—Rh4—C53127.0 (6)
C36—C35—Cr3—C31125.1 (6)C50—C45—Rh4—C53118.5 (5)
Rh3—C35—Cr3—C3110.8 (5)Cr4—C45—Rh4—C53130.7 (6)
C34—C35—Cr3—C30132.5 (5)C46—C45—Rh4—C52165.7 (5)
C36—C35—Cr3—C3097.6 (7)C50—C45—Rh4—C5279.8 (3)
Rh3—C35—Cr3—C3016.8 (4)C53—C45—Rh4—C5238.7 (3)
C31—C30—Cr3—C42179.9 (4)Cr4—C45—Rh4—C5292.0 (4)
C35—C30—Cr3—C4245.6 (4)C46—C45—Rh4—C50114.5 (6)
C38—C30—Cr3—C4249.6 (6)C53—C45—Rh4—C50118.5 (5)
Rh3—C30—Cr3—C4259.5 (5)Cr4—C45—Rh4—C5012.2 (3)
C31—C30—Cr3—C400.1 (7)C46—C45—Rh4—Rh333.3 (5)
C35—C30—Cr3—C40134.3 (6)C50—C45—Rh4—Rh3147.8 (3)
C38—C30—Cr3—C40130.5 (7)C53—C45—Rh4—Rh393.7 (3)
Rh3—C30—Cr3—C40120.4 (6)Cr4—C45—Rh4—Rh3135.7 (4)
C31—C30—Cr3—C4188.0 (4)C43—Rh3—Rh4—C58177.6 (3)
C35—C30—Cr3—C41137.5 (4)C44—Rh3—Rh4—C5888.1 (3)
C38—C30—Cr3—C4142.3 (6)C36—Rh3—Rh4—C5849.0 (6)
Rh3—C30—Cr3—C41151.4 (4)C37—Rh3—Rh4—C5814.2 (3)
C31—C30—Cr3—C3368.0 (4)C38—Rh3—Rh4—C585.4 (3)
C35—C30—Cr3—C3366.4 (3)C35—Rh3—Rh4—C5869.8 (3)
C38—C30—Cr3—C33161.7 (6)C30—Rh3—Rh4—C5842.1 (2)
Rh3—C30—Cr3—C3352.5 (4)C43—Rh3—Rh4—C4489.5 (3)
C31—C30—Cr3—C3230.3 (3)C36—Rh3—Rh4—C44137.1 (6)
C35—C30—Cr3—C32104.1 (4)C37—Rh3—Rh4—C4474.0 (3)
C38—C30—Cr3—C32160.7 (6)C38—Rh3—Rh4—C4493.5 (3)
Rh3—C30—Cr3—C3290.2 (4)C35—Rh3—Rh4—C44158.0 (3)
C31—C30—Cr3—C34105.6 (4)C30—Rh3—Rh4—C44130.3 (3)
C35—C30—Cr3—C3428.9 (3)C43—Rh3—Rh4—C5130.4 (6)
C38—C30—Cr3—C34124.1 (6)C44—Rh3—Rh4—C51119.9 (6)
Rh3—C30—Cr3—C3415.0 (4)C36—Rh3—Rh4—C51103.1 (7)
C35—C30—Cr3—C31134.5 (5)C37—Rh3—Rh4—C51166.2 (6)
C38—C30—Cr3—C31130.3 (7)C38—Rh3—Rh4—C51146.6 (6)
Rh3—C30—Cr3—C31120.5 (6)C35—Rh3—Rh4—C5182.2 (6)
C31—C30—Cr3—C35134.5 (5)C30—Rh3—Rh4—C51109.9 (6)
C38—C30—Cr3—C3595.2 (6)C43—Rh3—Rh4—C539.0 (3)
Rh3—C30—Cr3—C3513.9 (3)C44—Rh3—Rh4—C5398.4 (3)
C46—C47—Cr4—C55127.7 (4)C36—Rh3—Rh4—C53124.5 (6)
C48—C47—Cr4—C5599.8 (4)C37—Rh3—Rh4—C53172.4 (3)
C46—C47—Cr4—C57145.1 (5)C38—Rh3—Rh4—C53168.1 (2)
C48—C47—Cr4—C5712.6 (7)C35—Rh3—Rh4—C53103.6 (2)
C46—C47—Cr4—C5640.2 (5)C30—Rh3—Rh4—C53131.3 (2)
C48—C47—Cr4—C56172.8 (4)C43—Rh3—Rh4—C5214.9 (3)
C46—C47—Cr4—C48132.5 (5)C44—Rh3—Rh4—C5274.5 (3)
C46—C47—Cr4—C49104.5 (4)C36—Rh3—Rh4—C52148.4 (6)
C48—C47—Cr4—C4928.0 (4)C37—Rh3—Rh4—C52148.5 (3)
C48—C47—Cr4—C46132.5 (5)C38—Rh3—Rh4—C52168.1 (3)
C46—C47—Cr4—C4531.0 (3)C35—Rh3—Rh4—C52127.5 (3)
C48—C47—Cr4—C45101.5 (4)C30—Rh3—Rh4—C52155.2 (3)
C46—C47—Cr4—C5067.5 (4)C43—Rh3—Rh4—C5070.0 (3)
C48—C47—Cr4—C5065.0 (4)C44—Rh3—Rh4—C50159.5 (3)
C49—C48—Cr4—C55143.8 (4)C36—Rh3—Rh4—C5063.5 (6)
C47—C48—Cr4—C5583.0 (4)C37—Rh3—Rh4—C50126.6 (3)
C49—C48—Cr4—C5754.0 (4)C38—Rh3—Rh4—C50107.0 (2)
C47—C48—Cr4—C57172.9 (4)C35—Rh3—Rh4—C5042.6 (2)
C49—C48—Cr4—C56116.6 (7)C30—Rh3—Rh4—C5070.3 (2)
C47—C48—Cr4—C5616.5 (9)C43—Rh3—Rh4—C4546.3 (2)
C49—C48—Cr4—C47133.1 (5)C44—Rh3—Rh4—C45135.7 (3)
C47—C48—Cr4—C49133.1 (5)C36—Rh3—Rh4—C4587.2 (5)
C49—C48—Cr4—C46104.7 (4)C37—Rh3—Rh4—C45150.3 (3)
C47—C48—Cr4—C4628.4 (3)C38—Rh3—Rh4—C45130.8 (2)
C49—C48—Cr4—C4567.4 (4)C35—Rh3—Rh4—C4566.3 (2)
C47—C48—Cr4—C4565.7 (4)C30—Rh3—Rh4—C4594.0 (2)
Hydrogen-bond geometry (Å, º) top
D—H···AD—HH···AD···AD—H···A
C2—H2···O7i0.952.523.403 (8)155
C32—H32···O6i0.952.723.632 (8)162
C5—H5···O4ii0.952.233.108 (7)153
C7—H7···O10ii0.952.613.432 (8)144
C17—H17···O2iii0.952.553.399 (8)149
C34—H34···O17iii0.952.673.510 (7)148
C10—H10C···O14iv0.982.533.441 (8)155
C25—H25A···O14v0.982.683.346 (8)125
C20—H20···O9vi0.952.423.306 (7)156
C51—H51···O5vii0.952.553.313 (8)137
C54—H54C···O5vii0.982.723.336 (8)122
C39—H39B···O5viii0.982.533.374 (8)145
C38—H38···O6ix0.952.583.521 (8)170
C22—H22···O15x0.952.693.554 (7)152
C46—H46···O13xi0.952.473.262 (7)141
C31—H31···O18xii0.952.513.144 (7)124
C49—H49···O11xii0.952.663.411 (8)136
Symmetry codes: (i) x1, y, z; (ii) x, y+3/2, z1/2; (iii) x+1, y, z; (iv) x+1, y1/2, z+1/2; (v) x+2, y1/2, z+1/2; (vi) x, y+3/2, z+1/2; (vii) x+1, y+1/2, z+1/2; (viii) x+2, y+1/2, z+1/2; (ix) x+2, y+2, z+1; (x) x+1, y+3/2, z+1/2; (xi) x+1, y+2, z; (xii) x+1, y+2, z+1.
 

Funding information

The authors gratefully acknowledge the ANR, the CNRS and the University of Strasbourg for financial support. CW thanks the Agence Nationale de la Recherche for PhD support.

References

First citationBellomo, S., Ceccon, A., Gambaro, A., Santi, S. & Venzo, A. (1993). J. Organomet. Chem. 453, C4–C6.  CrossRef CAS Web of Science Google Scholar
First citationBonifaci, C., Carta, G., Ceccon, A., Gambaro, A., Santi, S. & Venzo, A. (1996). Organometallics, 15, 1630–1636.  CrossRef CAS Web of Science Google Scholar
First citationBonifaci, C., Ceccon, A., Gambaro, A., Ganis, P., Santi, S., Valle, G. & Venzo, A. (1993). Organometallics, 12, 4211–4214.  CSD CrossRef CAS Web of Science Google Scholar
First citationBonifaci, C., Ceccon, A., Santi, S., Mealli, C. & Zoellner, R. W. (1995). Inorg. Chim. Acta, 240, 541–549.  CrossRef CAS Web of Science Google Scholar
First citationCecchetto, P., Ceccon, A., Gambaro, A., Santi, S., Ganis, P., Gobetto, R., Valle, G. & Venzo, A. (1998). Organometallics, 17, 752–762.  Web of Science CSD CrossRef CAS Google Scholar
First citationCeccon, A., Elsevier, C. J., Ernsting, J. M., Gambaro, A., Santi, S. & Venzo, A. (1993). Inorg. Chim. Acta, 204, 15–26.  CrossRef CAS Web of Science Google Scholar
First citationCeccon, A., Gambaro, A., Santi, S., Valle, G. & Venzo, A. (1989). J. Chem. Soc. Chem. Commun. pp. 51–53.  CrossRef Web of Science Google Scholar
First citationCeccon, A., Gambaro, A., Venzo, A., Lucchini, V., Bitterwolf, T. E. & Shade, J. (1988). J. Organomet. Chem. 349, 315–322.  CrossRef CAS Web of Science Google Scholar
First citationEnders, M., Kohl, G. & Pritzkow, H. (2004). J. Organomet. Chem. 689, 3024–3030.  Web of Science CSD CrossRef CAS Google Scholar
First citationFaraone, F., Lo Schiavo, S., Bruno, G., Piraino, P. & Bombieri, G. (1983). J. Chem. Soc. Dalton Trans. pp. 1813–1817.  CSD CrossRef Web of Science Google Scholar
First citationMacrae, C. F., Bruno, I. J., Chisholm, J. A., Edgington, P. R., McCabe, P., Pidcock, E., Rodriguez-Monge, L., Taylor, R., van de Streek, J. & Wood, P. A. (2008). J. Appl. Cryst. 41, 466–470.  Web of Science CrossRef CAS IUCr Journals Google Scholar
First citationNonius (1998). COLLECT. Nonius BV, Delft, The Netherlands .  Google Scholar
First citationOtwinowski, Z. & Minor, W. (1997). Methods in Enzymology, Vol. 276, Macromolecular Crystallography, Part A, edited by C. W. Carter Jr & R. M. Sweet, pp. 307–326. New York: Academic Press.  Google Scholar
First citationSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.  Web of Science CrossRef CAS IUCr Journals Google Scholar
First citationSheldrick, G. M. (2015). Acta Cryst. C71, 3–8.  Web of Science CrossRef IUCr Journals Google Scholar
First citationSpek, A. L. (2009). Acta Cryst. D65, 148–155.  Web of Science CrossRef CAS IUCr Journals Google Scholar
First citationWerlé, C., Anstine, D. M., Karmazin, L., Bailly, C., Ricard, L. & Djukic, J.-P. (2016). Dalton Trans. 45, 607–617.  Web of Science PubMed Google Scholar
First citationWerlé, C., Bailly, C., Karmazin-Brelot, L., Le Goff, X.-F., Pfeffer, M. & Djukic, J.-P. (2014). Angew. Chem. Int. Ed. 53, 9827–9831.  Google Scholar
First citationWerlé, C., Bailly, C., Karmazin-Brelot, L., Le Goff, X.-F., Ricard, L. & Djukic, J.-P. (2013). J. Am. Chem. Soc. 135, 17839–17852.  Web of Science PubMed Google Scholar
First citationWerlé, C., Dohm, S., Bailly, C., Karmazin, L., Ricard, L., Sieffert, N., Pfeffer, M., Hansen, A., Grimme, S. & Djukic, J.-P. (2017). Dalton Trans. 46, 8125–8137.  Web of Science PubMed Google Scholar
First citationWerlé, C., Karmazin, L., Bailly, C., Ricard, L. & Djukic, J.-P. (2015). Organometallics, 34, 3055–3064.  Google Scholar

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