research communications
cis(S),trans(O,Nbpy)-(2,2′-bipyridyl-κ2N,N′)bis(dimethyl sulfoxide-κS)[phenyl(pyridin-2-yl)methanone-κ2N,O]ruthenium(II) bis(trifluoromethanesulfonate)
ofaDepartment of Engineering Science, Faculty of Engineering, Osaka, Electro-Communication University, 18-8 Hatsucho, Neyagawa, Osaka 572-8530, Japan, and bDepartment of Applied Chemistry, School of Science and Engineering, Meiji, University, 1-1-1 Higashimita, Tama, Kanagawa 214-8571, Japan
*Correspondence e-mail: m-toyama@osakac.ac.jp
The molecular and crystal structures of the title complex, [Ru(C10H8N2)(C12H9NO)(C2H6OS)2](CF3O3S)2 or cis(S),trans(O,Nbpy)-[Ru(bpy)(ppk)(dmso-S)2](OTf)2 {bpy = 2,2′-bipyridine, ppk = phenyl-2-pyridyl ketone [IUPAC nomenclature: phenyl(pyridine-2-yl)methanone], dmso = dimethyl sulfoxide, and OTf− = trifluoromethanesulfonate}, are reported. The Ru2+ ion has a distorted octahedral geometry with two bpy N atoms, the N and O atoms of ppk, and two S atoms of two cis dmso-S ligands. The carbonyl O atom of ppk is trans to bpy, and the N atom of pyridyl is trans to the dmso-S ligand [trans(O,Nbpy) geometry]. One of the trifluoromethanesulfonate anions is disordered over three positions, with occupancies of 0.4, 0.4, and 0.2, respectively, in the refined model. The original disordered and SQUEEZE [Spek (2015). Acta Cryst. C71, 9–18] models were found to be almost equivalent, indicating that both the SQUEEZE and the original disordered model are satisfactory.
1. Chemical context
Polypyridyl ruthenium(II) complexes have gained interest because of their unique photochemical and photophysical properties. Many homoleptic and bis-heteroleptic polypyridyl ruthenium(II) complexes have been synthesized, and their properties have been investigated (Gao et al., 2008; Patra et al., 2021). However, there are fewer studies on trisheteroleptic complexes, i.e. [Ru(L1-L1)(L2-L2)(L3-L3)]2+, than on bisheteroleptic complexes, i.e. [Ru(L-L1)2(L2-L2)]2+, (Spiccia et al., 2004). The difference can be traced to the limited suitable precursors for the trisheteroleptic complexes, such as cis-[Ru(L1-L1)(L2-L2)(X)2]2+ (X = labile monodentate ligand) complexes. We have reported the synthesis, and of trans(O,S)-[Ru(bpy)(dmso-S)2(dmso-O)2](OTf)2 (bpy = 2,2′-bipyridine, dmso = dimethyl sulfoxide, and OTf− = trifluoromethanesulfonate), in which two dmso-O ligands were easily substituted by another bidentate ligand, e.g., 1,10-phenanthroline (phen), to form cis-[Ru(bpy)(phen)(dmso-S)2](OTf)2 (Toyama et al., 2018). To investigate the potential synthetic utility of trans(O,S)-[Ru(bpy)(dmso-S)2(dmso-O)2](OTf)2 as a precursor, further complexes with different types of ligands must be synthesized. To this end, we became interested in unsymmetrical bidentate κ2N,O-pyridyl ligands because of the selectivity and reactivity of the resulting geometrical isomers. We have previously reported the syntheses and structures of heteroleptic ruthenium(II) complexes with picolinate (pic−) (Toyama et al., 2017) and 2-picolinamide (H2pia) (Toyama et al., 2019), which are coordinated to the Ru2+ ion via a pyridyl N and a carbonic O− or a carbonyl O atom. In our current work, phenyl-2-pyridyl ketone [ppk, IUPAC nomenclature : phenyl(pyridine-2-yl)methanone] has been chosen as a κ2N,O-pyridyl ligand. Herein, we report the of cis(S),trans(O,Nbpy)-[Ru(bpy)(ppk)(dmso-S)2](OTf)2. Notably, ppk is an analog of di-2-pyridyl ketone (dpk), which has three coordination modes: dpk–κ2N,O, dpk–κ2N,N′, and dpk–OH-κ3N,O,N′ (Toyama et al., 2007) and has attracted significant research attention. However, it is difficult to synthesize and control the stereoselectivity of complexes with dpk ligands. The ppk ligand is known to be analogous to the dpk ligand in the κ2N,O coordination mode and hence has been used in our current synthesis to ease the complexity of syntheses with the dpk ligand.
2. Structural commentary
An ORTEP view of cis(S),trans(O,Nbpy)-[Ru(bpy)(ppk)(dmso-S)2](OTf)2 is shown in Fig. 1. The Ru2+ ion has a distorted octahedral geometry with two bpy N atoms, the N and O atoms of ppk, and the S atoms of the two dmso-S ligands, which are cis to each other. The O atom of the carbonyl group of the ppk ligand is trans to the bpy ligand, and the N atom of the pyridyl group is trans to the dmso-S ligand, i.e., the trans(O,Nbpy)-isomer. Three isomers of [Ru(bpy)(ppk)(dmso)2]2+ are possible depending on the geometry of the two dmso ligands and the orientation of the ppk ligand: trans(dmso)-, cis(dmso),trans(O,Nbpy)-, and cis(dmso),trans(N,Nbpy)-isomers. The starting complex, trans(O,S)-[Ru(bpy)(dmso-S)2(dmso-O)2](OTf)2 has two inert cis dmso-S ligands and two labile cis dmso-O ligands. The inert dmso-S ligands in the starting complex were retained during the reaction to afford an isomer with cis(dmso)-geometry, that is, the cis(S)-geometry. The bpy ligand is located in the equatorial plane. The dmso-O ligand at the axial site is more labile than that at the equatorial site (Toyama et al., 2018). Hence, the pyridyl N atom of the ppk ligand attacks the labile axial dmso-O atom first, followed by the equatorial dmso-O, resulting in a trans(O,Nbpy)-geometry.
Selected bond lengths and angles are listed in Table 1. For Ru—N(bpy), the Ru1—N1 bond trans to S1 [2.0905 (16) Å] is slightly longer than the Ru1—N2 bond trans to O1 [2.0705 (16) Å]. Both these bonds are slightly longer than the previously reported Ru—N bonds in [Ru(bpy)2(N-O)]2+ [N-O = pic− or H2pia, which are the N,O bidentate ligands; 2.031–2.059 Å; Toyama et al., 2017, 2019], but are similar to those in [Ru(bpy)(phen)(dmso-S)2]2+ (2.092 and 2.087 Å; Toyama et al., 2018). These elongations are due to the electronic and steric effects of the two dmso ligands.
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The H10 atom of pyridyl-N2 of bpy shows hydrogen-bonding interactions with the O2 atom of dmso-S1 [H10⋯O2 = 2.33 Å, Fig. 2]. The torsion angle N2—Ru1—S1—O2 is 47.01 (6)°. The O2 atom of dmso-S1 orients toward the dmso-S2 ligand to reduce the with the pyridyl-N2 atom of the bpy ligand. The rotation of the dmso-S1 ligand is restricted by the pyridyl-N2 group of the bpy ligand. Moreover, hydrogen-bonding interactions can be observed between the neighboring methyl H atoms and the O atoms of the dmso-S1 and dmso-S2 ligands (H24A⋯O3 = 2.45 Å and H25A⋯O2 = 2.62 Å, Fig. 2). The rotation of the dmso-S2 ligand is also restricted by the dmso-S1 ligand. Hence, the two dmso-S ligands are cis to each other. A similar conformation in which the two dmso ligands are in the cis position has also been observed in [Ru(bpy)(phen)(dmso-S)2]2+ (Toyama et al., 2018).
The Ru1—S1 bond length [2.2845 (8) Å] is similar to the corresponding bond length in the starting complex [2.2723 (5) Å; Toyama et al., 2018]. However, the Ru1—S2 bond [2.2790 (6) Å] is longer than that of the starting complex [2.2063 (5) Å; Toyama et al., 2018] because of the trans influence (π-backdonation) of the pyridyl-N3 group in ppk. In this complex, both dmso-S ligands are trans to the pyridine rings, implying that the Ru1—S1 and Ru1—S2 bond lengths are similar. Therefore, the trans influences of pyridyl groups of ppk and bpy are comparable. For the Ru-ppk moiety, the Ru1—N3 [2.105 (2) Å] and Ru1—O1 bond lengths [2.0898 (14) Å] are similar to the corresponding lengths in trans(Cl)-[RuCl2(dpk-κ2N,O)(dmso-S)2] [2.113 (2) and 2.089 (2) Å, respectively; Toyama et al., 2007]. Moreover, the O1—C16 bond length [1.254 (3) Å] in the ketone group is comparable to the corresponding bond length in the Ru-dpk complex [1.243 (3) Å; Toyama et al., 2007], indicating that the former is also a double bond, C=O. The dihedral angle between pyridyl-N3 and the phenyl group is 129.26 (13)°, and the ortho proton (H22) in the phenyl group is in contact with the 3-position proton (H12) in the pyridyl-N3 group (H12⋯H22 = 2.32 Å, Fig. 2).
One of the trifluoromethanesulfonate anions is disordered over three positions, referred to as A, B, and C, with occupancies of 0.4, 0.4, and 0.2, respectively, in the refined model. To confirm the validity of the application of SQUEEZE (Spek, 2015), a region of the disordered OTf− anion was corrected using the SQUEEZE (Spek, 2015) routine in the PLATON program (Spek, 2020). The SQUEEZE model converged at R1[F2 > 2σ (F2)] = 0.0315, wR(F2) = 0.0712, GOF = 1.05, mean s (C-C) = 0.0037 Å, and rmax = 0.84 eÅ−3. The SQUEEZE model is an alternative to the original disordered model, with R1[F2 > 2s (F2)] = 0.0348, wR(F2) = 0.0806, GOF = 1.08, mean σ(C—C) = 0.0041 Å, and rmax = 0.86 eÅ−3. However, both the models are nearly equivalent, indicating that both the SQUEEZE and the original disordered model are satisfactory.
3. Supramolecular features
As shown in Fig. 3, the O5 atom of OTf-S3 forms hydrogen-bonding interactions (Table 2) with the H5 atom of the bpy ligand and the H26A atom of dmso-S2. As shown in Fig. 4, the O4 atom of OTf-S3 forms hydrogen-bonding interactions with the H4 and H5 atoms of bpy and H9 atom of bpy in a neighboring complex cation to form chains along the b-axis direction. Moreover, the F2 atom of OTf-S3 interacts with the H25A atom of dmso-S2 in the neighboring complex cation, and the rotation of the CF3 moiety of OTf-S3 is restricted by hydrogen-bonding interactions in the chain. In addition, the O6 atom of OTf-S3 interacts with atoms H25C and H26B of dmso-S2 in a neighboring complex cation in another chain to cross-link two neighboring chains and form a ladder-like double-chain structure. Consequently, the OTf-S3 anions are located inside the double chains and properly accommodated between the bpy ligand in the cation and phenyl group of the ppk ligand in the other cation. In contrast, the OTf-S4 anions are located between the double chains but are disordered and not properly accommodated in the void between the double chains.
4. Synthesis and crystallization
The title complex was prepared by the same procedure used for cis-[Ru(bpy)(phen)(dmso-S)2](OTf)2 (Toyama et al., 2018). The reaction of trans(O,S)-[Ru(bpy)(dmso-S)2(dmso-O)2](OTf)2 with ppk in acetone at room temperature afforded cis(S),trans(O,Nbpy)-[Ru(bpy)(ppk)(dmso-S)2](OTf)2. Single crystals suitable for X-ray structural analysis were obtained by the vapor diffusion of diethyl ether into a mixed solution of DMSO and ethanol (1:3) of cis(S),trans(O,Nbpy)-[Ru(bpy)(ppk)(dmso-S)2](OTf)2.
5. Refinement
Crystal data, data collection and structure . Hydrogen atoms attached to the carbon were included as riding contributions to the idealized positions [C—H = 0.95 Å (CH) or 0.98 Å (CH3)]. The isotropic displacement parameters were fixed at Uiso(H) = 1.2Ueq(C) for CH, and 1.5Ueq(C) for CH3. One of the trifluoromethanesulfonate anions is disordered over three positions (referred to as A, B, and C) with occupancies of 0.4, 0.4, and 0.2, respectively, in the refined model. Restraints (DFIX, DANG, and DELU) were used to correct the geometry and displacement parameters of the disordered OTf− ions. To confirm the validity of the disordered model, the SQUEEZE (Spek, 2015) routine in the PLATON program (Spek, 2020) was used to generate a modified dataset in which the contribution of the disordered OTf− anion to the structure amplitudes was discarded. The void volume of 511 Å3 occupied by the disordered OTf− anion (14.8% of the unit-cell volume) contains 298 electrons, corresponding to approximately four OTf− anions (296 electrons).
details are summarized in Table 3
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Supporting information
https://doi.org/10.1107/S2056989022010258/zn2022sup1.cif
contains datablocks global, disordered_model, Squeezed_model. DOI:Structure factors: contains datablock disordered_model. DOI: https://doi.org/10.1107/S2056989022010258/zn2022disordered_modelsup2.hkl
Structure factors: contains datablock Squeezed_model. DOI: https://doi.org/10.1107/S2056989022010258/zn2022Squeezed_modelsup3.hkl
Data collection: CrystalClear-SM Expert (Rigaku, 2016) for disordered_model. For both structures, cell
CrysAlis PRO (Rigaku OD, 2018); data reduction: CrysAlis PRO (Rigaku OD, 2018); program(s) used to solve structure: SIR2014 (Burla et al., 2015); program(s) used to refine structure: SHELXL2014/7 (Sheldrick, 2015); molecular graphics: ORTEP-3 for Windows (Farrugia, 2012) and Mercury (Macrae et al., 2020); software used to prepare material for publication: CrystalStructure (Rigaku, 2019), publCIF (Westrip, 2010).[Ru(C10H8N2)(C12H9NO)(C2H6OS)2](CF3O3S)2 | F(000) = 1808.00 |
Mr = 894.85 | Dx = 1.723 Mg m−3 |
Monoclinic, P21/c | Mo Kα radiation, λ = 0.71073 Å |
a = 17.3772 (4) Å | Cell parameters from 31997 reflections |
b = 12.2931 (2) Å | θ = 2.2–30.5° |
c = 16.3443 (4) Å | µ = 0.79 mm−1 |
β = 98.895 (2)° | T = 173 K |
V = 3449.47 (13) Å3 | Block, orange |
Z = 4 | 0.10 × 0.05 × 0.05 mm |
Rigaku Mercury70 diffractometer | 8290 reflections with F2 > 2.0σ(F2) |
Detector resolution: 14.629 pixels mm-1 | Rint = 0.019 |
ω scans | θmax = 30.4°, θmin = 2.0° |
Absorption correction: multi-scan (CrysAlisPro; Rigaku OD, 2018) | h = −23→23 |
Tmin = 0.921, Tmax = 0.962 | k = −16→16 |
42165 measured reflections | l = −23→22 |
9317 independent reflections |
Refinement on F2 | Secondary atom site location: difference Fourier map |
R[F2 > 2σ(F2)] = 0.035 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.081 | H-atom parameters constrained |
S = 1.08 | w = 1/[σ2(Fo2) + (0.0283P)2 + 3.9158P] where P = (Fo2 + 2Fc2)/3 |
9317 reflections | (Δ/σ)max = 0.001 |
608 parameters | Δρmax = 0.86 e Å−3 |
29 restraints | Δρmin = −0.87 e Å−3 |
Primary atom site location: structure-invariant direct methods |
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. |
Refinement. Refinement was performed using all reflections. The weighted R-factor (wR) and goodness of fit (S) are based on F2. R-factor (gt) are based on F. The threshold expression of F2 > 2.0 sigma(F2) is used only for calculating R-factor (gt). |
x | y | z | Uiso*/Ueq | Occ. (<1) | |
Ru1 | 0.21892 (2) | 0.05017 (2) | 0.20103 (2) | 0.02633 (5) | |
S1 | 0.27377 (5) | −0.04295 (5) | 0.10369 (4) | 0.04978 (18) | |
S2 | 0.10233 (3) | 0.03559 (4) | 0.11611 (3) | 0.02870 (10) | |
S3 | 0.07625 (4) | 0.46067 (4) | 0.18347 (3) | 0.03402 (12) | |
F1 | 0.03511 (10) | 0.58328 (12) | 0.05158 (8) | 0.0487 (4) | |
F2 | 0.04294 (10) | 0.66781 (10) | 0.16804 (9) | 0.0480 (4) | |
F3 | 0.14701 (9) | 0.62211 (12) | 0.12006 (9) | 0.0489 (4) | |
O1 | 0.24410 (9) | 0.19932 (12) | 0.14980 (9) | 0.0332 (3) | |
O2 | 0.23265 (16) | −0.14256 (15) | 0.07013 (12) | 0.0683 (7) | |
O3 | 0.10620 (11) | 0.06064 (13) | 0.02803 (9) | 0.0403 (4) | |
O4 | 0.12551 (12) | 0.48455 (14) | 0.26074 (10) | 0.0484 (4) | |
O5 | 0.10877 (12) | 0.38520 (13) | 0.13067 (11) | 0.0479 (4) | |
O6 | −0.00431 (11) | 0.44379 (14) | 0.19017 (12) | 0.0484 (4) | |
N2 | 0.19998 (10) | −0.08308 (13) | 0.27279 (10) | 0.0272 (3) | |
N1 | 0.17314 (10) | 0.12390 (12) | 0.29825 (9) | 0.0247 (3) | |
N3 | 0.32656 (11) | 0.09263 (17) | 0.27151 (13) | 0.0406 (4) | |
C1 | 0.16540 (12) | 0.05711 (15) | 0.36240 (12) | 0.0279 (4) | |
C2 | 0.14501 (15) | 0.09718 (18) | 0.43554 (13) | 0.0369 (5) | |
H2 | 0.1394 | 0.0492 | 0.4798 | 0.044* | |
C3 | 0.13286 (16) | 0.20791 (18) | 0.44327 (14) | 0.0399 (5) | |
H3 | 0.1196 | 0.2368 | 0.4932 | 0.048* | |
C4 | 0.14022 (14) | 0.27586 (17) | 0.37750 (13) | 0.0350 (5) | |
H4 | 0.1316 | 0.3519 | 0.3813 | 0.042* | |
C5 | 0.16033 (12) | 0.23126 (15) | 0.30602 (13) | 0.0292 (4) | |
H5 | 0.1653 | 0.2780 | 0.2608 | 0.035* | |
C6 | 0.17955 (13) | −0.05890 (15) | 0.34785 (12) | 0.0282 (4) | |
C7 | 0.17177 (15) | −0.13966 (17) | 0.40547 (13) | 0.0384 (5) | |
H7 | 0.1584 | −0.1210 | 0.4579 | 0.046* | |
C8 | 0.18351 (16) | −0.24741 (18) | 0.38621 (14) | 0.0414 (5) | |
H8 | 0.1792 | −0.3032 | 0.4254 | 0.050* | |
C9 | 0.20155 (15) | −0.27232 (17) | 0.30936 (13) | 0.0381 (5) | |
H9 | 0.2082 | −0.3459 | 0.2940 | 0.046* | |
C10 | 0.20990 (14) | −0.18875 (16) | 0.25483 (13) | 0.0349 (5) | |
H10 | 0.2233 | −0.2066 | 0.2022 | 0.042* | |
C11 | 0.35019 (15) | 0.1962 (2) | 0.2582 (2) | 0.0520 (7) | |
C12 | 0.41884 (19) | 0.2382 (3) | 0.3007 (3) | 0.0886 (14) | |
H12 | 0.4351 | 0.3099 | 0.2899 | 0.106* | |
C13 | 0.4634 (2) | 0.1735 (4) | 0.3591 (4) | 0.121 (2) | |
H13 | 0.5106 | 0.2008 | 0.3891 | 0.145* | |
C14 | 0.4398 (2) | 0.0708 (4) | 0.3737 (3) | 0.0983 (16) | |
H14 | 0.4704 | 0.0255 | 0.4131 | 0.118* | |
C15 | 0.37045 (17) | 0.0340 (3) | 0.3300 (2) | 0.0649 (9) | |
H15 | 0.3530 | −0.0366 | 0.3420 | 0.078* | |
C16 | 0.29958 (14) | 0.25231 (19) | 0.18898 (16) | 0.0400 (5) | |
C17 | 0.31305 (14) | 0.3652 (2) | 0.16364 (17) | 0.0436 (5) | |
C18 | 0.30673 (18) | 0.3877 (2) | 0.07992 (19) | 0.0540 (7) | |
H18 | 0.2956 | 0.3310 | 0.0404 | 0.065* | |
C19 | 0.3167 (2) | 0.4937 (2) | 0.0537 (2) | 0.0652 (9) | |
H19 | 0.3140 | 0.5086 | −0.0037 | 0.078* | |
C20 | 0.33044 (19) | 0.5763 (2) | 0.1095 (3) | 0.0703 (10) | |
H20 | 0.3362 | 0.6486 | 0.0909 | 0.084* | |
C21 | 0.3360 (2) | 0.5550 (3) | 0.1929 (3) | 0.0716 (10) | |
H21 | 0.3453 | 0.6128 | 0.2318 | 0.086* | |
C22 | 0.32810 (18) | 0.4488 (2) | 0.2206 (2) | 0.0585 (7) | |
H22 | 0.3330 | 0.4339 | 0.2782 | 0.070* | |
C23 | 0.3719 (2) | −0.0815 (3) | 0.1403 (2) | 0.0880 (14) | |
H23A | 0.3733 | −0.1297 | 0.1882 | 0.106* | |
H23B | 0.4030 | −0.0163 | 0.1566 | 0.106* | |
H23C | 0.3933 | −0.1195 | 0.0962 | 0.106* | |
C24 | 0.2881 (2) | 0.0413 (2) | 0.01819 (18) | 0.0623 (9) | |
H24A | 0.2379 | 0.0715 | −0.0076 | 0.075* | |
H24B | 0.3104 | −0.0022 | −0.0226 | 0.075* | |
H24C | 0.3237 | 0.1008 | 0.0378 | 0.075* | |
C25 | 0.05597 (16) | −0.09281 (17) | 0.11911 (13) | 0.0384 (5) | |
H25A | 0.0906 | −0.1501 | 0.1043 | 0.046* | |
H25B | 0.0074 | −0.0931 | 0.0796 | 0.046* | |
H25C | 0.0444 | −0.1061 | 0.1751 | 0.046* | |
C26 | 0.02969 (14) | 0.12177 (18) | 0.14662 (15) | 0.0371 (5) | |
H26A | 0.0464 | 0.1978 | 0.1448 | 0.045* | |
H26B | 0.0219 | 0.1033 | 0.2031 | 0.045* | |
H26C | −0.0193 | 0.1117 | 0.1088 | 0.045* | |
C27 | 0.07521 (15) | 0.58964 (17) | 0.12770 (13) | 0.0353 (5) | |
S4A | 0.48251 (10) | −0.24864 (15) | 0.37611 (11) | 0.0429 (4) | 0.4 |
F4A | 0.4352 (6) | −0.4487 (7) | 0.3753 (8) | 0.126 (5) | 0.4 |
F5A | 0.3693 (6) | −0.3243 (13) | 0.4437 (10) | 0.173 (8) | 0.4 |
F6A | 0.4788 (6) | −0.3941 (10) | 0.4918 (6) | 0.113 (5) | 0.4 |
O7A | 0.5571 (5) | −0.2950 (10) | 0.3698 (7) | 0.068 (2) | 0.4 |
O8A | 0.4295 (10) | −0.2279 (15) | 0.2996 (9) | 0.067 (4) | 0.4 |
O9A | 0.4780 (12) | −0.1661 (11) | 0.4350 (7) | 0.125 (6) | 0.4 |
C28A | 0.4392 (8) | −0.3598 (9) | 0.4252 (8) | 0.090 (4) | 0.4 |
S4B | 0.4632 (3) | −0.3128 (5) | 0.3742 (4) | 0.0781 (13) | 0.2 |
F4B | 0.5073 (15) | −0.1612 (13) | 0.4572 (16) | 0.125 (10) | 0.2 |
F5B | 0.3966 (12) | −0.214 (2) | 0.4748 (17) | 0.124 (10) | 0.2 |
F6B | 0.5118 (12) | −0.3220 (14) | 0.5283 (8) | 0.089 (5) | 0.2 |
O7B | 0.4210 (10) | −0.4114 (9) | 0.3856 (10) | 0.063 (5) | 0.2 |
O8B | 0.5444 (5) | −0.3400 (14) | 0.380 (2) | 0.098 (9) | 0.2 |
O9B | 0.441 (2) | −0.2190 (19) | 0.323 (2) | 0.094 (10) | 0.2 |
C28B | 0.4695 (12) | −0.2511 (13) | 0.4737 (10) | 0.131 (13) | 0.2 |
S4C | 0.41337 (10) | −0.26601 (16) | 0.40330 (12) | 0.0500 (4) | 0.4 |
F4C | 0.5126 (9) | −0.4124 (11) | 0.3749 (7) | 0.187 (6) | 0.4 |
F5C | 0.5622 (4) | −0.2694 (12) | 0.4263 (10) | 0.169 (6) | 0.4 |
F6C | 0.5134 (7) | −0.3747 (11) | 0.5027 (8) | 0.107 (4) | 0.4 |
O7C | 0.3645 (5) | −0.3697 (9) | 0.3964 (6) | 0.080 (3) | 0.4 |
O8C | 0.4107 (9) | −0.2271 (13) | 0.3201 (8) | 0.057 (3) | 0.4 |
O9C | 0.4163 (13) | −0.1813 (12) | 0.4598 (8) | 0.146 (9) | 0.4 |
C28C | 0.4981 (4) | −0.3400 (5) | 0.4304 (4) | 0.0430 (15) | 0.4 |
U11 | U22 | U33 | U12 | U13 | U23 | |
Ru1 | 0.03761 (9) | 0.02047 (7) | 0.02264 (8) | 0.00535 (6) | 0.01015 (6) | 0.00556 (6) |
S1 | 0.0815 (5) | 0.0380 (3) | 0.0382 (3) | 0.0272 (3) | 0.0356 (3) | 0.0154 (2) |
S2 | 0.0468 (3) | 0.0203 (2) | 0.0192 (2) | −0.00074 (19) | 0.00577 (19) | 0.00434 (16) |
S3 | 0.0545 (3) | 0.0198 (2) | 0.0293 (2) | 0.0034 (2) | 0.0115 (2) | 0.00168 (18) |
F1 | 0.0732 (10) | 0.0421 (8) | 0.0295 (7) | 0.0040 (7) | 0.0041 (7) | 0.0053 (6) |
F2 | 0.0813 (11) | 0.0224 (6) | 0.0434 (8) | 0.0104 (6) | 0.0190 (7) | 0.0012 (5) |
F3 | 0.0626 (9) | 0.0412 (8) | 0.0459 (8) | −0.0064 (7) | 0.0174 (7) | 0.0077 (6) |
O1 | 0.0419 (8) | 0.0264 (7) | 0.0339 (8) | 0.0030 (6) | 0.0139 (6) | 0.0078 (6) |
O2 | 0.143 (2) | 0.0320 (9) | 0.0398 (10) | 0.0161 (11) | 0.0446 (12) | −0.0018 (8) |
O3 | 0.0635 (11) | 0.0365 (8) | 0.0208 (7) | −0.0041 (8) | 0.0063 (7) | 0.0096 (6) |
O4 | 0.0784 (13) | 0.0313 (8) | 0.0331 (8) | −0.0002 (8) | 0.0009 (8) | 0.0052 (7) |
O5 | 0.0773 (13) | 0.0265 (8) | 0.0434 (9) | 0.0104 (8) | 0.0202 (9) | −0.0021 (7) |
O6 | 0.0581 (11) | 0.0397 (9) | 0.0506 (10) | −0.0023 (8) | 0.0190 (9) | 0.0084 (8) |
N2 | 0.0413 (9) | 0.0198 (7) | 0.0212 (7) | 0.0039 (6) | 0.0073 (7) | 0.0035 (6) |
N1 | 0.0340 (8) | 0.0191 (7) | 0.0211 (7) | 0.0013 (6) | 0.0047 (6) | 0.0011 (6) |
N3 | 0.0321 (9) | 0.0406 (10) | 0.0487 (11) | 0.0054 (8) | 0.0056 (8) | 0.0151 (9) |
C1 | 0.0415 (11) | 0.0215 (8) | 0.0209 (8) | 0.0006 (8) | 0.0052 (7) | 0.0002 (7) |
C2 | 0.0604 (14) | 0.0281 (10) | 0.0241 (9) | 0.0014 (10) | 0.0120 (9) | 0.0001 (8) |
C3 | 0.0633 (15) | 0.0301 (11) | 0.0283 (10) | 0.0045 (10) | 0.0132 (10) | −0.0059 (8) |
C4 | 0.0491 (13) | 0.0234 (9) | 0.0324 (10) | 0.0030 (9) | 0.0065 (9) | −0.0042 (8) |
C5 | 0.0383 (11) | 0.0203 (8) | 0.0290 (9) | 0.0014 (8) | 0.0049 (8) | 0.0011 (7) |
C6 | 0.0432 (11) | 0.0211 (8) | 0.0205 (8) | 0.0017 (8) | 0.0055 (8) | 0.0016 (7) |
C7 | 0.0678 (15) | 0.0262 (10) | 0.0227 (9) | 0.0023 (10) | 0.0117 (10) | 0.0049 (8) |
C8 | 0.0709 (16) | 0.0246 (10) | 0.0295 (10) | 0.0003 (10) | 0.0097 (11) | 0.0090 (8) |
C9 | 0.0637 (15) | 0.0196 (9) | 0.0304 (10) | 0.0041 (9) | 0.0057 (10) | 0.0031 (8) |
C10 | 0.0594 (14) | 0.0221 (9) | 0.0242 (9) | 0.0069 (9) | 0.0097 (9) | 0.0011 (7) |
C11 | 0.0337 (12) | 0.0491 (15) | 0.0728 (19) | −0.0020 (11) | 0.0065 (12) | 0.0237 (14) |
C12 | 0.0450 (17) | 0.077 (2) | 0.134 (4) | −0.0191 (16) | −0.0167 (19) | 0.049 (2) |
C13 | 0.053 (2) | 0.113 (4) | 0.176 (5) | −0.028 (2) | −0.046 (3) | 0.074 (4) |
C14 | 0.054 (2) | 0.093 (3) | 0.133 (4) | −0.0064 (19) | −0.032 (2) | 0.059 (3) |
C15 | 0.0400 (14) | 0.0660 (19) | 0.084 (2) | 0.0024 (13) | −0.0056 (14) | 0.0409 (17) |
C16 | 0.0376 (12) | 0.0347 (11) | 0.0505 (13) | 0.0034 (9) | 0.0153 (10) | 0.0105 (10) |
C17 | 0.0386 (12) | 0.0330 (11) | 0.0601 (15) | 0.0006 (9) | 0.0103 (11) | 0.0093 (11) |
C18 | 0.0654 (18) | 0.0359 (13) | 0.0605 (17) | −0.0002 (12) | 0.0093 (14) | 0.0126 (12) |
C19 | 0.073 (2) | 0.0428 (15) | 0.077 (2) | −0.0031 (14) | 0.0023 (17) | 0.0248 (15) |
C20 | 0.0601 (18) | 0.0333 (14) | 0.110 (3) | −0.0073 (12) | −0.0098 (18) | 0.0211 (16) |
C21 | 0.0611 (19) | 0.0404 (15) | 0.109 (3) | −0.0063 (14) | 0.0001 (19) | −0.0076 (17) |
C22 | 0.0545 (16) | 0.0459 (15) | 0.074 (2) | −0.0077 (13) | 0.0051 (14) | 0.0002 (14) |
C23 | 0.095 (3) | 0.097 (3) | 0.086 (2) | 0.068 (2) | 0.058 (2) | 0.051 (2) |
C24 | 0.093 (2) | 0.0563 (17) | 0.0492 (15) | 0.0332 (16) | 0.0482 (16) | 0.0272 (13) |
C25 | 0.0630 (15) | 0.0239 (9) | 0.0275 (10) | −0.0093 (10) | 0.0048 (10) | 0.0036 (8) |
C26 | 0.0410 (12) | 0.0303 (10) | 0.0391 (12) | 0.0040 (9) | 0.0037 (9) | 0.0028 (9) |
C27 | 0.0539 (13) | 0.0249 (9) | 0.0286 (10) | 0.0024 (9) | 0.0113 (9) | 0.0023 (8) |
S4A | 0.0488 (9) | 0.0355 (8) | 0.0449 (9) | −0.0039 (7) | 0.0086 (7) | 0.0100 (7) |
F4A | 0.099 (7) | 0.060 (5) | 0.195 (11) | −0.037 (5) | −0.055 (6) | 0.042 (5) |
F5A | 0.079 (7) | 0.223 (16) | 0.242 (15) | 0.054 (8) | 0.105 (9) | 0.159 (13) |
F6A | 0.143 (9) | 0.109 (8) | 0.101 (6) | 0.056 (7) | 0.071 (6) | 0.088 (7) |
O7A | 0.051 (4) | 0.067 (5) | 0.093 (5) | 0.011 (4) | 0.035 (4) | 0.026 (5) |
O8A | 0.069 (9) | 0.059 (5) | 0.061 (7) | −0.015 (5) | −0.033 (6) | 0.024 (6) |
O9A | 0.184 (15) | 0.118 (11) | 0.075 (6) | 0.094 (10) | 0.029 (8) | 0.025 (6) |
C28A | 0.119 (11) | 0.071 (7) | 0.087 (8) | 0.036 (7) | 0.040 (7) | 0.053 (7) |
S4B | 0.076 (3) | 0.077 (4) | 0.086 (4) | 0.011 (3) | 0.026 (3) | 0.008 (3) |
F4B | 0.15 (2) | 0.053 (9) | 0.18 (2) | −0.068 (13) | 0.049 (15) | −0.023 (10) |
F5B | 0.099 (11) | 0.112 (17) | 0.18 (2) | 0.006 (11) | 0.095 (13) | −0.061 (15) |
F6B | 0.113 (11) | 0.103 (12) | 0.048 (6) | 0.000 (11) | 0.003 (7) | 0.028 (7) |
O7B | 0.092 (13) | 0.052 (10) | 0.050 (7) | 0.021 (9) | 0.028 (8) | 0.007 (6) |
O8B | 0.064 (11) | 0.043 (9) | 0.21 (3) | 0.022 (8) | 0.080 (15) | 0.022 (14) |
O9B | 0.085 (16) | 0.080 (14) | 0.094 (18) | 0.043 (12) | −0.057 (14) | 0.007 (12) |
C28B | 0.23 (4) | 0.074 (16) | 0.083 (16) | −0.07 (2) | 0.00 (2) | 0.005 (14) |
S4C | 0.0421 (8) | 0.0549 (10) | 0.0551 (10) | 0.0193 (7) | 0.0142 (7) | 0.0171 (8) |
F4C | 0.246 (15) | 0.152 (9) | 0.185 (10) | 0.155 (11) | 0.099 (11) | 0.035 (10) |
F5C | 0.041 (3) | 0.233 (17) | 0.234 (15) | −0.027 (6) | 0.024 (6) | 0.112 (12) |
F6C | 0.079 (6) | 0.085 (7) | 0.150 (10) | 0.029 (6) | −0.006 (6) | 0.013 (6) |
O7C | 0.043 (4) | 0.100 (7) | 0.098 (6) | −0.026 (4) | 0.014 (4) | 0.045 (5) |
O8C | 0.080 (8) | 0.041 (4) | 0.051 (6) | −0.002 (5) | 0.007 (4) | 0.021 (4) |
O9C | 0.25 (2) | 0.092 (10) | 0.085 (8) | 0.089 (14) | −0.019 (11) | 0.008 (6) |
C28C | 0.039 (3) | 0.050 (4) | 0.040 (3) | 0.032 (3) | 0.004 (3) | 0.022 (3) |
Ru1—N2 | 2.0705 (16) | C14—C15 | 1.378 (5) |
Ru1—O1 | 2.0898 (14) | C14—H14 | 0.9500 |
Ru1—N1 | 2.0905 (16) | C15—H15 | 0.9500 |
Ru1—N3 | 2.105 (2) | C16—C17 | 1.477 (3) |
Ru1—S2 | 2.2789 (6) | C17—C18 | 1.384 (4) |
Ru1—S1 | 2.2845 (6) | C17—C22 | 1.384 (4) |
S1—O2 | 1.480 (2) | C18—C19 | 1.391 (4) |
S1—C23 | 1.781 (4) | C18—H18 | 0.9500 |
S1—C24 | 1.787 (2) | C19—C20 | 1.360 (5) |
S2—O3 | 1.4839 (15) | C19—H19 | 0.9500 |
S2—C25 | 1.776 (2) | C20—C21 | 1.377 (5) |
S2—C26 | 1.777 (2) | C20—H20 | 0.9500 |
S3—O6 | 1.436 (2) | C21—C22 | 1.396 (4) |
S3—O5 | 1.4407 (17) | C21—H21 | 0.9500 |
S3—O4 | 1.4421 (18) | C22—H22 | 0.9500 |
S3—C27 | 1.827 (2) | C23—H23A | 0.9800 |
F1—C27 | 1.331 (3) | C23—H23B | 0.9800 |
F2—C27 | 1.337 (2) | C23—H23C | 0.9800 |
F3—C27 | 1.334 (3) | C24—H24A | 0.9800 |
O1—C16 | 1.254 (3) | C24—H24B | 0.9800 |
N2—C10 | 1.349 (2) | C24—H24C | 0.9800 |
N2—C6 | 1.362 (2) | C25—H25A | 0.9800 |
N1—C5 | 1.348 (2) | C25—H25B | 0.9800 |
N1—C1 | 1.355 (2) | C25—H25C | 0.9800 |
N3—C15 | 1.338 (3) | C26—H26A | 0.9800 |
N3—C11 | 1.366 (3) | C26—H26B | 0.9800 |
C1—C2 | 1.389 (3) | C26—H26C | 0.9800 |
C1—C6 | 1.473 (3) | S4A—O9A | 1.409 (12) |
C2—C3 | 1.386 (3) | S4A—O7A | 1.435 (8) |
C2—H2 | 0.9500 | S4A—O8A | 1.456 (11) |
C3—C4 | 1.383 (3) | S4A—C28A | 1.806 (10) |
C3—H3 | 0.9500 | F4A—C28A | 1.359 (13) |
C4—C5 | 1.383 (3) | F5A—C28A | 1.367 (11) |
C4—H4 | 0.9500 | F6A—C28A | 1.267 (15) |
C5—H5 | 0.9500 | S4B—O8B | 1.438 (5) |
C6—C7 | 1.389 (3) | S4B—O9B | 1.439 (5) |
C7—C8 | 1.384 (3) | S4B—O7B | 1.444 (5) |
C7—H7 | 0.9500 | S4B—C28B | 1.784 (16) |
C8—C9 | 1.375 (3) | F4B—C28B | 1.335 (16) |
C8—H8 | 0.9500 | F5B—C28B | 1.350 (18) |
C9—C10 | 1.382 (3) | F6B—C28B | 1.375 (16) |
C9—H9 | 0.9500 | S4C—O9C | 1.387 (13) |
C10—H10 | 0.9500 | S4C—O8C | 1.435 (11) |
C11—C12 | 1.384 (4) | S4C—O7C | 1.526 (9) |
C11—C16 | 1.490 (4) | S4C—C28C | 1.730 (6) |
C12—C13 | 1.384 (5) | F4C—C28C | 1.323 (11) |
C12—H12 | 0.9500 | F5C—C28C | 1.421 (11) |
C13—C14 | 1.359 (6) | F6C—C28C | 1.245 (11) |
C13—H13 | 0.9500 | ||
N2—Ru1—O1 | 169.28 (6) | O1—C16—C17 | 119.2 (2) |
N2—Ru1—N1 | 78.46 (6) | O1—C16—C11 | 117.7 (2) |
O1—Ru1—N1 | 92.98 (6) | C17—C16—C11 | 123.2 (2) |
N2—Ru1—N3 | 95.27 (7) | C18—C17—C22 | 119.6 (3) |
O1—Ru1—N3 | 77.20 (7) | C18—C17—C16 | 118.3 (2) |
N1—Ru1—N3 | 83.51 (7) | C22—C17—C16 | 122.0 (3) |
N2—Ru1—S2 | 94.50 (5) | C17—C18—C19 | 119.8 (3) |
O1—Ru1—S2 | 92.67 (5) | C17—C18—H18 | 120.1 |
N1—Ru1—S2 | 95.17 (5) | C19—C18—H18 | 120.1 |
N3—Ru1—S2 | 169.66 (5) | C20—C19—C18 | 120.7 (3) |
N2—Ru1—S1 | 96.77 (5) | C20—C19—H19 | 119.7 |
O1—Ru1—S1 | 91.43 (4) | C18—C19—H19 | 119.7 |
N1—Ru1—S1 | 174.49 (5) | C19—C20—C21 | 120.0 (3) |
N3—Ru1—S1 | 94.26 (6) | C19—C20—H20 | 120.0 |
S2—Ru1—S1 | 87.93 (3) | C21—C20—H20 | 120.0 |
O2—S1—C23 | 106.67 (18) | C20—C21—C22 | 120.2 (3) |
O2—S1—C24 | 107.89 (15) | C20—C21—H21 | 119.9 |
C23—S1—C24 | 100.07 (16) | C22—C21—H21 | 119.9 |
O2—S1—Ru1 | 116.32 (9) | C17—C22—C21 | 119.6 (3) |
C23—S1—Ru1 | 112.34 (14) | C17—C22—H22 | 120.2 |
C24—S1—Ru1 | 112.18 (9) | C21—C22—H22 | 120.2 |
O3—S2—C25 | 107.45 (10) | S1—C23—H23A | 109.5 |
O3—S2—C26 | 106.81 (11) | S1—C23—H23B | 109.5 |
C25—S2—C26 | 100.20 (12) | H23A—C23—H23B | 109.5 |
O3—S2—Ru1 | 113.90 (8) | S1—C23—H23C | 109.5 |
C25—S2—Ru1 | 114.67 (8) | H23A—C23—H23C | 109.5 |
C26—S2—Ru1 | 112.67 (8) | H23B—C23—H23C | 109.5 |
O6—S3—O5 | 115.46 (12) | S1—C24—H24A | 109.5 |
O6—S3—O4 | 114.59 (12) | S1—C24—H24B | 109.5 |
O5—S3—O4 | 114.90 (12) | H24A—C24—H24B | 109.5 |
O6—S3—C27 | 103.23 (11) | S1—C24—H24C | 109.5 |
O5—S3—C27 | 103.57 (10) | H24A—C24—H24C | 109.5 |
O4—S3—C27 | 102.65 (10) | H24B—C24—H24C | 109.5 |
C16—O1—Ru1 | 116.30 (14) | S2—C25—H25A | 109.5 |
C10—N2—C6 | 117.79 (16) | S2—C25—H25B | 109.5 |
C10—N2—Ru1 | 127.01 (13) | H25A—C25—H25B | 109.5 |
C6—N2—Ru1 | 115.09 (13) | S2—C25—H25C | 109.5 |
C5—N1—C1 | 118.88 (17) | H25A—C25—H25C | 109.5 |
C5—N1—Ru1 | 125.73 (13) | H25B—C25—H25C | 109.5 |
C1—N1—Ru1 | 114.87 (12) | S2—C26—H26A | 109.5 |
C15—N3—C11 | 117.6 (2) | S2—C26—H26B | 109.5 |
C15—N3—Ru1 | 128.15 (19) | H26A—C26—H26B | 109.5 |
C11—N3—Ru1 | 114.06 (16) | S2—C26—H26C | 109.5 |
N1—C1—C2 | 121.35 (18) | H26A—C26—H26C | 109.5 |
N1—C1—C6 | 115.02 (16) | H26B—C26—H26C | 109.5 |
C2—C1—C6 | 123.63 (18) | F1—C27—F3 | 106.99 (18) |
C3—C2—C1 | 119.3 (2) | F1—C27—F2 | 107.71 (19) |
C3—C2—H2 | 120.3 | F3—C27—F2 | 107.51 (18) |
C1—C2—H2 | 120.3 | F1—C27—S3 | 112.25 (15) |
C4—C3—C2 | 119.3 (2) | F3—C27—S3 | 111.65 (16) |
C4—C3—H3 | 120.4 | F2—C27—S3 | 110.50 (14) |
C2—C3—H3 | 120.4 | O9A—S4A—O7A | 118.8 (9) |
C3—C4—C5 | 118.88 (19) | O9A—S4A—O8A | 111.5 (10) |
C3—C4—H4 | 120.6 | O7A—S4A—O8A | 117.8 (9) |
C5—C4—H4 | 120.6 | O9A—S4A—C28A | 99.8 (8) |
N1—C5—C4 | 122.32 (19) | O7A—S4A—C28A | 100.1 (5) |
N1—C5—H5 | 118.8 | O8A—S4A—C28A | 105.2 (8) |
C4—C5—H5 | 118.8 | F6A—C28A—F4A | 102.6 (10) |
N2—C6—C7 | 121.39 (18) | F6A—C28A—F5A | 107.5 (10) |
N2—C6—C1 | 115.48 (16) | F4A—C28A—F5A | 115.1 (15) |
C7—C6—C1 | 123.12 (18) | F6A—C28A—S4A | 115.1 (11) |
C8—C7—C6 | 119.78 (19) | F4A—C28A—S4A | 109.1 (8) |
C8—C7—H7 | 120.1 | F5A—C28A—S4A | 107.6 (7) |
C6—C7—H7 | 120.1 | O8B—S4B—O9B | 113.5 (17) |
C9—C8—C7 | 118.90 (19) | O8B—S4B—O7B | 108.0 (11) |
C9—C8—H8 | 120.6 | O9B—S4B—O7B | 130.5 (15) |
C7—C8—H8 | 120.6 | O8B—S4B—C28B | 96.7 (14) |
C8—C9—C10 | 119.0 (2) | O9B—S4B—C28B | 99.2 (19) |
C8—C9—H9 | 120.5 | O7B—S4B—C28B | 101.5 (9) |
C10—C9—H9 | 120.5 | F4B—C28B—F5B | 102 (2) |
N2—C10—C9 | 123.08 (19) | F4B—C28B—F6B | 115 (2) |
N2—C10—H10 | 118.5 | F5B—C28B—F6B | 128 (2) |
C9—C10—H10 | 118.5 | F4B—C28B—S4B | 97.4 (14) |
N3—C11—C12 | 121.7 (3) | F5B—C28B—S4B | 103.3 (14) |
N3—C11—C16 | 113.3 (2) | F6B—C28B—S4B | 105.8 (12) |
C12—C11—C16 | 124.7 (3) | O9C—S4C—O8C | 111.9 (9) |
C11—C12—C13 | 118.5 (3) | O9C—S4C—O7C | 129.7 (10) |
C11—C12—H12 | 120.7 | O8C—S4C—O7C | 105.8 (8) |
C13—C12—H12 | 120.7 | O9C—S4C—C28C | 106.4 (7) |
C14—C13—C12 | 120.2 (4) | O8C—S4C—C28C | 108.6 (7) |
C14—C13—H13 | 119.9 | O7C—S4C—C28C | 91.3 (5) |
C12—C13—H13 | 119.9 | F6C—C28C—F4C | 112.7 (9) |
C13—C14—C15 | 118.5 (3) | F6C—C28C—F5C | 101.6 (10) |
C13—C14—H14 | 120.7 | F4C—C28C—F5C | 98.4 (10) |
C15—C14—H14 | 120.7 | F6C—C28C—S4C | 118.1 (7) |
N3—C15—C14 | 123.3 (3) | F4C—C28C—S4C | 115.0 (7) |
N3—C15—H15 | 118.3 | F5C—C28C—S4C | 108.0 (6) |
C14—C15—H15 | 118.3 | ||
C5—N1—C1—C2 | −0.3 (3) | C11—C16—C17—C22 | −46.8 (4) |
Ru1—N1—C1—C2 | 171.93 (17) | C22—C17—C18—C19 | 1.0 (4) |
C5—N1—C1—C6 | 179.25 (19) | C16—C17—C18—C19 | 178.1 (3) |
Ru1—N1—C1—C6 | −8.5 (2) | C17—C18—C19—C20 | −1.9 (5) |
N1—C1—C2—C3 | −0.5 (4) | C18—C19—C20—C21 | 1.3 (5) |
C6—C1—C2—C3 | −180.0 (2) | C19—C20—C21—C22 | 0.3 (5) |
C1—C2—C3—C4 | 0.9 (4) | C18—C17—C22—C21 | 0.6 (4) |
C2—C3—C4—C5 | −0.7 (4) | C16—C17—C22—C21 | −176.4 (3) |
C1—N1—C5—C4 | 0.6 (3) | C20—C21—C22—C17 | −1.3 (5) |
Ru1—N1—C5—C4 | −170.71 (16) | O6—S3—C27—F1 | −63.67 (19) |
C3—C4—C5—N1 | −0.1 (3) | O5—S3—C27—F1 | 57.06 (19) |
C10—N2—C6—C7 | 2.2 (3) | O4—S3—C27—F1 | 176.93 (17) |
Ru1—N2—C6—C7 | −174.22 (18) | O6—S3—C27—F3 | 176.19 (15) |
C10—N2—C6—C1 | −176.9 (2) | O5—S3—C27—F3 | −63.08 (18) |
Ru1—N2—C6—C1 | 6.7 (2) | O4—S3—C27—F3 | 56.79 (18) |
N1—C1—C6—N2 | 1.3 (3) | O6—S3—C27—F2 | 56.59 (19) |
C2—C1—C6—N2 | −179.2 (2) | O5—S3—C27—F2 | 177.32 (17) |
N1—C1—C6—C7 | −177.8 (2) | O4—S3—C27—F2 | −62.81 (19) |
C2—C1—C6—C7 | 1.7 (4) | O9A—S4A—C28A—F6A | −67.7 (12) |
N2—C6—C7—C8 | −1.2 (4) | O7A—S4A—C28A—F6A | 54.1 (11) |
C1—C6—C7—C8 | 177.8 (2) | O8A—S4A—C28A—F6A | 176.8 (13) |
C6—C7—C8—C9 | −1.0 (4) | O9A—S4A—C28A—F4A | 177.6 (10) |
C7—C8—C9—C10 | 2.1 (4) | O7A—S4A—C28A—F4A | −60.6 (10) |
C6—N2—C10—C9 | −1.1 (4) | O8A—S4A—C28A—F4A | 62.1 (12) |
Ru1—N2—C10—C9 | 174.88 (18) | O9A—S4A—C28A—F5A | 52.1 (14) |
C8—C9—C10—N2 | −1.1 (4) | O7A—S4A—C28A—F5A | 173.9 (13) |
C15—N3—C11—C12 | 2.9 (5) | O8A—S4A—C28A—F5A | −63.5 (15) |
Ru1—N3—C11—C12 | 178.7 (3) | O8B—S4B—C28B—F4B | 71.2 (17) |
C15—N3—C11—C16 | 177.0 (3) | O9B—S4B—C28B—F4B | −44 (2) |
Ru1—N3—C11—C16 | −7.2 (3) | O7B—S4B—C28B—F4B | −178.8 (17) |
N3—C11—C12—C13 | −1.3 (7) | O8B—S4B—C28B—F5B | 175.8 (18) |
C16—C11—C12—C13 | −174.7 (4) | O9B—S4B—C28B—F5B | 61 (2) |
C11—C12—C13—C14 | 0.3 (9) | O7B—S4B—C28B—F5B | −74.2 (18) |
C12—C13—C14—C15 | −1.0 (9) | O8B—S4B—C28B—F6B | −47.7 (17) |
C11—N3—C15—C14 | −3.7 (6) | O9B—S4B—C28B—F6B | −162.9 (19) |
Ru1—N3—C15—C14 | −178.7 (3) | O7B—S4B—C28B—F6B | 62.3 (16) |
C13—C14—C15—N3 | 2.7 (8) | O9C—S4C—C28C—F6C | 54.8 (13) |
Ru1—O1—C16—C17 | −170.77 (17) | O8C—S4C—C28C—F6C | 175.4 (12) |
Ru1—O1—C16—C11 | 10.7 (3) | O7C—S4C—C28C—F6C | −77.4 (10) |
N3—C11—C16—O1 | −2.2 (4) | O9C—S4C—C28C—F4C | −168.2 (13) |
C12—C11—C16—O1 | 171.7 (3) | O8C—S4C—C28C—F4C | −47.6 (12) |
N3—C11—C16—C17 | 179.4 (2) | O7C—S4C—C28C—F4C | 59.5 (10) |
C12—C11—C16—C17 | −6.7 (5) | O9C—S4C—C28C—F5C | −59.5 (12) |
O1—C16—C17—C18 | −42.3 (3) | O8C—S4C—C28C—F5C | 61.0 (11) |
C11—C16—C17—C18 | 136.2 (3) | O7C—S4C—C28C—F5C | 168.2 (9) |
O1—C16—C17—C22 | 134.7 (3) |
D—H···A | D—H | H···A | D···A | D—H···A |
C5—H5···O5 | 0.95 | 2.56 | 3.436 (3) | 152 |
C26—H26A···O5 | 0.98 | 2.57 | 3.543 (3) | 171 |
C4—H4···O4 | 0.95 | 2.55 | 3.184 (3) | 125 |
C5—H5···O4 | 0.95 | 2.63 | 3.236 (3) | 122 |
C9—H9···O4i | 0.95 | 2.54 | 3.314 (3) | 139 |
C25—H25A···F2i | 0.98 | 2.65 | 3.067 (2) | 106 |
C25—H25C···O6ii | 0.98 | 2.49 | 3.404 (3) | 156 |
C26—H26B···O6ii | 0.98 | 2.67 | 3.530 (3) | 146 |
C25—H25C···O6ii | 0.98 | 2.49 | 3.404 (3) | 1556 |
C26—H26B···O6ii | 0.98 | 2.67 | 3.530 (3) | 146 |
Symmetry codes: (i) x, y−1, z; (ii) −x, y−1/2, −z+1/2. |
C28H29F6N3O9RuS4 | F(000) = 1808.00 |
Mr = 894.85 | Dx = 1.723 Mg m−3 |
Monoclinic, P21/c | Mo Kα radiation, λ = 0.71073 Å |
a = 17.3772 (4) Å | Cell parameters from 31997 reflections |
b = 12.2931 (2) Å | θ = 2.2–30.5° |
c = 16.3443 (4) Å | µ = 0.79 mm−1 |
β = 98.895 (2)° | T = 173 K |
V = 3449.47 (13) Å3 | Block, orange |
Z = 4 | 0.10 × 0.05 × 0.05 mm |
Rigaku Mercury70 diffractometer | 8290 reflections with F2 > 2.0σ(F2) |
Detector resolution: 14.629 pixels mm-1 | Rint = 0.019 |
ω scans | θmax = 30.4°, θmin = 2.0° |
Absorption correction: multi-scan (CrysAlisPro; Rigaku OD, 2018) | h = −23→23 |
Tmin = 0.921, Tmax = 0.962 | k = −16→16 |
42165 measured reflections | l = −23→22 |
9317 independent reflections |
Refinement on F2 | Secondary atom site location: difference Fourier map |
R[F2 > 2σ(F2)] = 0.032 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.071 | H-atom parameters constrained |
S = 1.05 | w = 1/[σ2(Fo2) + (0.0242P)2 + 3.2481P] where P = (Fo2 + 2Fc2)/3 |
9317 reflections | (Δ/σ)max < 0.001 |
392 parameters | Δρmax = 0.84 e Å−3 |
0 restraints | Δρmin = −0.88 e Å−3 |
Primary atom site location: structure-invariant direct methods |
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. |
Refinement. Refinement was performed using all reflections. The weighted R-factor (wR) and goodness of fit (S) are based on F2. R-factor (gt) are based on F. The threshold expression of F2 > 2.0 sigma(F2) is used only for calculating R-factor (gt). |
x | y | z | Uiso*/Ueq | ||
Ru1 | 0.21892 (2) | 0.05017 (2) | 0.20103 (2) | 0.02636 (4) | |
S1 | 0.27378 (4) | −0.04295 (4) | 0.10370 (3) | 0.04980 (16) | |
S2 | 0.10234 (3) | 0.03559 (3) | 0.11611 (3) | 0.02876 (9) | |
S3 | 0.07627 (3) | 0.46067 (4) | 0.18348 (3) | 0.03408 (10) | |
F1 | 0.03507 (9) | 0.58331 (11) | 0.05157 (7) | 0.0488 (3) | |
F2 | 0.04294 (9) | 0.66787 (9) | 0.16804 (8) | 0.0479 (3) | |
F3 | 0.14705 (8) | 0.62215 (11) | 0.12006 (8) | 0.0489 (3) | |
O1 | 0.24409 (8) | 0.19932 (10) | 0.14977 (8) | 0.0332 (3) | |
O2 | 0.23263 (14) | −0.14250 (13) | 0.07011 (10) | 0.0683 (6) | |
O3 | 0.10620 (9) | 0.06063 (12) | 0.02799 (8) | 0.0404 (3) | |
O4 | 0.12550 (11) | 0.48452 (12) | 0.26071 (9) | 0.0484 (4) | |
O5 | 0.10880 (11) | 0.38527 (12) | 0.13066 (10) | 0.0479 (4) | |
O6 | −0.00432 (10) | 0.44374 (13) | 0.19013 (10) | 0.0483 (4) | |
N2 | 0.20000 (9) | −0.08312 (11) | 0.27273 (9) | 0.0272 (3) | |
N1 | 0.17312 (9) | 0.12391 (11) | 0.29822 (8) | 0.0248 (3) | |
N3 | 0.32653 (10) | 0.09260 (15) | 0.27153 (12) | 0.0407 (4) | |
C1 | 0.16540 (11) | 0.05712 (14) | 0.36240 (10) | 0.0280 (3) | |
C2 | 0.14500 (13) | 0.09717 (16) | 0.43552 (11) | 0.0369 (4) | |
H2 | 0.1394 | 0.0492 | 0.4798 | 0.044* | |
C3 | 0.13283 (14) | 0.20795 (16) | 0.44327 (12) | 0.0399 (5) | |
H3 | 0.1196 | 0.2368 | 0.4932 | 0.048* | |
C4 | 0.14025 (12) | 0.27582 (15) | 0.37749 (12) | 0.0350 (4) | |
H4 | 0.1317 | 0.3518 | 0.3813 | 0.042* | |
C5 | 0.16035 (11) | 0.23127 (14) | 0.30601 (11) | 0.0293 (4) | |
H5 | 0.1653 | 0.2780 | 0.2608 | 0.035* | |
C6 | 0.17960 (11) | −0.05895 (14) | 0.34786 (10) | 0.0283 (3) | |
C7 | 0.17188 (14) | −0.13966 (15) | 0.40550 (11) | 0.0384 (4) | |
H7 | 0.1587 | −0.1210 | 0.4580 | 0.046* | |
C8 | 0.18354 (14) | −0.24735 (16) | 0.38619 (12) | 0.0415 (5) | |
H8 | 0.1792 | −0.3032 | 0.4254 | 0.050* | |
C9 | 0.20157 (13) | −0.27230 (15) | 0.30937 (12) | 0.0381 (4) | |
H9 | 0.2082 | −0.3458 | 0.2940 | 0.046* | |
C10 | 0.20995 (13) | −0.18874 (14) | 0.25485 (11) | 0.0347 (4) | |
H10 | 0.2233 | −0.2066 | 0.2023 | 0.042* | |
C11 | 0.35012 (13) | 0.1962 (2) | 0.25811 (17) | 0.0520 (6) | |
C12 | 0.41880 (17) | 0.2384 (3) | 0.3007 (2) | 0.0890 (12) | |
H12 | 0.4349 | 0.3101 | 0.2901 | 0.107* | |
C13 | 0.4635 (2) | 0.1735 (4) | 0.3593 (3) | 0.1220 (19) | |
H13 | 0.5106 | 0.2009 | 0.3894 | 0.146* | |
C14 | 0.43982 (19) | 0.0708 (3) | 0.3736 (3) | 0.0986 (14) | |
H14 | 0.4704 | 0.0253 | 0.4128 | 0.118* | |
C15 | 0.37040 (15) | 0.0341 (2) | 0.32992 (19) | 0.0651 (8) | |
H15 | 0.3529 | −0.0364 | 0.3420 | 0.078* | |
C16 | 0.29956 (12) | 0.25231 (17) | 0.18902 (14) | 0.0402 (5) | |
C17 | 0.31303 (13) | 0.36515 (17) | 0.16368 (15) | 0.0438 (5) | |
C18 | 0.30677 (16) | 0.3878 (2) | 0.07994 (17) | 0.0542 (6) | |
H18 | 0.2957 | 0.3310 | 0.0404 | 0.065* | |
C19 | 0.31671 (18) | 0.4937 (2) | 0.0538 (2) | 0.0654 (8) | |
H19 | 0.3138 | 0.5086 | −0.0036 | 0.079* | |
C20 | 0.33052 (17) | 0.5763 (2) | 0.1096 (2) | 0.0704 (9) | |
H20 | 0.3363 | 0.6486 | 0.0909 | 0.084* | |
C21 | 0.33610 (17) | 0.5550 (2) | 0.1931 (2) | 0.0714 (9) | |
H21 | 0.3455 | 0.6127 | 0.2319 | 0.086* | |
C22 | 0.32804 (16) | 0.4488 (2) | 0.2206 (2) | 0.0585 (6) | |
H22 | 0.3328 | 0.4339 | 0.2782 | 0.070* | |
C23 | 0.3718 (2) | −0.0814 (3) | 0.1402 (2) | 0.0882 (13) | |
H23A | 0.3733 | −0.1289 | 0.1886 | 0.106* | |
H23B | 0.4031 | −0.0162 | 0.1558 | 0.106* | |
H23C | 0.3931 | −0.1203 | 0.0963 | 0.106* | |
C24 | 0.28800 (18) | 0.0412 (2) | 0.01821 (15) | 0.0621 (8) | |
H24A | 0.2379 | 0.0715 | −0.0075 | 0.075* | |
H24B | 0.3102 | −0.0023 | −0.0226 | 0.075* | |
H24C | 0.3237 | 0.1007 | 0.0378 | 0.075* | |
C25 | 0.05595 (14) | −0.09282 (15) | 0.11908 (12) | 0.0382 (4) | |
H25A | 0.0906 | −0.1501 | 0.1045 | 0.046* | |
H25B | 0.0075 | −0.0932 | 0.0794 | 0.046* | |
H25C | 0.0441 | −0.1060 | 0.1749 | 0.046* | |
C26 | 0.02972 (12) | 0.12184 (16) | 0.14662 (13) | 0.0371 (4) | |
H26A | 0.0462 | 0.1979 | 0.1442 | 0.045* | |
H26B | 0.0224 | 0.1040 | 0.2033 | 0.045* | |
H26C | −0.0194 | 0.1113 | 0.1091 | 0.045* | |
C27 | 0.07526 (13) | 0.58962 (15) | 0.12773 (12) | 0.0356 (4) |
U11 | U22 | U33 | U12 | U13 | U23 | |
Ru1 | 0.03765 (8) | 0.02051 (7) | 0.02267 (7) | 0.00532 (5) | 0.01014 (5) | 0.00555 (5) |
S1 | 0.0815 (4) | 0.0381 (3) | 0.0382 (3) | 0.0271 (3) | 0.0355 (3) | 0.0154 (2) |
S2 | 0.0468 (3) | 0.02038 (18) | 0.01935 (18) | −0.00077 (17) | 0.00577 (17) | 0.00437 (14) |
S3 | 0.0546 (3) | 0.01982 (19) | 0.0294 (2) | 0.00343 (18) | 0.0115 (2) | 0.00172 (16) |
F1 | 0.0737 (9) | 0.0423 (7) | 0.0292 (6) | 0.0041 (6) | 0.0038 (6) | 0.0052 (5) |
F2 | 0.0807 (9) | 0.0225 (5) | 0.0433 (7) | 0.0104 (6) | 0.0188 (6) | 0.0011 (5) |
F3 | 0.0626 (8) | 0.0413 (7) | 0.0456 (7) | −0.0065 (6) | 0.0172 (6) | 0.0078 (6) |
O1 | 0.0417 (7) | 0.0264 (6) | 0.0340 (7) | 0.0029 (5) | 0.0139 (6) | 0.0078 (5) |
O2 | 0.1423 (19) | 0.0322 (8) | 0.0403 (9) | 0.0156 (10) | 0.0448 (11) | −0.0021 (7) |
O3 | 0.0637 (9) | 0.0365 (7) | 0.0208 (6) | −0.0040 (7) | 0.0062 (6) | 0.0096 (5) |
O4 | 0.0786 (12) | 0.0312 (7) | 0.0331 (7) | −0.0002 (7) | 0.0007 (7) | 0.0051 (6) |
O5 | 0.0772 (11) | 0.0265 (7) | 0.0434 (8) | 0.0106 (7) | 0.0200 (8) | −0.0022 (6) |
O6 | 0.0577 (10) | 0.0394 (8) | 0.0512 (9) | −0.0023 (7) | 0.0191 (8) | 0.0080 (7) |
N2 | 0.0412 (8) | 0.0200 (6) | 0.0213 (7) | 0.0040 (6) | 0.0073 (6) | 0.0036 (5) |
N1 | 0.0344 (7) | 0.0190 (6) | 0.0211 (6) | 0.0014 (5) | 0.0049 (5) | 0.0010 (5) |
N3 | 0.0319 (8) | 0.0408 (9) | 0.0492 (10) | 0.0052 (7) | 0.0058 (7) | 0.0147 (8) |
C1 | 0.0417 (9) | 0.0216 (7) | 0.0209 (7) | 0.0005 (7) | 0.0052 (7) | 0.0003 (6) |
C2 | 0.0607 (13) | 0.0280 (9) | 0.0237 (8) | 0.0012 (8) | 0.0119 (8) | 0.0002 (7) |
C3 | 0.0631 (13) | 0.0302 (9) | 0.0283 (9) | 0.0046 (9) | 0.0133 (9) | −0.0057 (7) |
C4 | 0.0494 (11) | 0.0232 (8) | 0.0326 (9) | 0.0029 (8) | 0.0067 (8) | −0.0044 (7) |
C5 | 0.0382 (9) | 0.0203 (7) | 0.0294 (8) | 0.0013 (7) | 0.0049 (7) | 0.0010 (6) |
C6 | 0.0432 (10) | 0.0212 (7) | 0.0206 (7) | 0.0018 (7) | 0.0057 (7) | 0.0015 (6) |
C7 | 0.0675 (14) | 0.0266 (9) | 0.0225 (8) | 0.0022 (9) | 0.0119 (9) | 0.0048 (7) |
C8 | 0.0709 (15) | 0.0246 (9) | 0.0295 (9) | 0.0001 (9) | 0.0097 (9) | 0.0090 (7) |
C9 | 0.0634 (13) | 0.0197 (8) | 0.0306 (9) | 0.0043 (8) | 0.0056 (9) | 0.0030 (7) |
C10 | 0.0587 (12) | 0.0224 (8) | 0.0241 (8) | 0.0067 (8) | 0.0095 (8) | 0.0012 (7) |
C11 | 0.0338 (11) | 0.0485 (13) | 0.0732 (16) | −0.0016 (9) | 0.0066 (11) | 0.0239 (12) |
C12 | 0.0449 (15) | 0.078 (2) | 0.134 (3) | −0.0196 (14) | −0.0173 (17) | 0.050 (2) |
C13 | 0.0526 (18) | 0.114 (3) | 0.179 (4) | −0.027 (2) | −0.046 (2) | 0.076 (3) |
C14 | 0.0547 (17) | 0.092 (3) | 0.134 (3) | −0.0068 (17) | −0.0337 (19) | 0.058 (2) |
C15 | 0.0406 (12) | 0.0655 (17) | 0.084 (2) | 0.0029 (12) | −0.0055 (12) | 0.0411 (15) |
C16 | 0.0380 (10) | 0.0345 (10) | 0.0508 (12) | 0.0034 (8) | 0.0154 (9) | 0.0109 (9) |
C17 | 0.0386 (11) | 0.0330 (10) | 0.0607 (14) | 0.0006 (8) | 0.0106 (10) | 0.0094 (10) |
C18 | 0.0653 (16) | 0.0358 (11) | 0.0614 (15) | −0.0004 (11) | 0.0094 (12) | 0.0124 (11) |
C19 | 0.0731 (18) | 0.0432 (14) | 0.0769 (19) | −0.0032 (13) | 0.0022 (15) | 0.0248 (13) |
C20 | 0.0600 (16) | 0.0336 (12) | 0.110 (3) | −0.0071 (11) | −0.0093 (16) | 0.0202 (14) |
C21 | 0.0610 (17) | 0.0405 (13) | 0.108 (3) | −0.0067 (12) | −0.0001 (17) | −0.0079 (15) |
C22 | 0.0548 (15) | 0.0461 (13) | 0.0732 (18) | −0.0079 (11) | 0.0051 (13) | 0.0001 (12) |
C23 | 0.095 (2) | 0.098 (2) | 0.086 (2) | 0.068 (2) | 0.0578 (19) | 0.0509 (19) |
C24 | 0.093 (2) | 0.0563 (15) | 0.0486 (13) | 0.0328 (14) | 0.0476 (14) | 0.0269 (11) |
C25 | 0.0627 (13) | 0.0238 (8) | 0.0273 (9) | −0.0092 (8) | 0.0044 (9) | 0.0035 (7) |
C26 | 0.0411 (10) | 0.0304 (9) | 0.0390 (10) | 0.0041 (8) | 0.0037 (8) | 0.0028 (8) |
C27 | 0.0545 (12) | 0.0252 (8) | 0.0290 (9) | 0.0025 (8) | 0.0117 (8) | 0.0020 (7) |
Ru1—N2 | 2.0702 (14) | C8—C9 | 1.375 (3) |
Ru1—O1 | 2.0900 (12) | C8—H8 | 0.9500 |
Ru1—N1 | 2.0904 (14) | C9—C10 | 1.382 (3) |
Ru1—N3 | 2.1047 (18) | C9—H9 | 0.9500 |
Ru1—S2 | 2.2789 (5) | C10—H10 | 0.9500 |
Ru1—S1 | 2.2844 (5) | C11—C12 | 1.386 (4) |
S1—O2 | 1.480 (2) | C11—C16 | 1.489 (3) |
S1—C23 | 1.780 (3) | C12—C13 | 1.387 (4) |
S1—C24 | 1.786 (2) | C12—H12 | 0.9500 |
S2—O3 | 1.4843 (13) | C13—C14 | 1.359 (5) |
S2—C25 | 1.7765 (19) | C13—H13 | 0.9500 |
S2—C26 | 1.778 (2) | C14—C15 | 1.379 (4) |
S3—O6 | 1.4364 (17) | C14—H14 | 0.9500 |
S3—O5 | 1.4405 (15) | C15—H15 | 0.9500 |
S3—O4 | 1.4414 (16) | C16—C17 | 1.477 (3) |
S3—C27 | 1.8270 (19) | C17—C22 | 1.384 (4) |
F1—C27 | 1.332 (2) | C17—C18 | 1.384 (3) |
F2—C27 | 1.338 (2) | C18—C19 | 1.390 (3) |
F3—C27 | 1.334 (2) | C18—H18 | 0.9500 |
O1—C16 | 1.254 (3) | C19—C20 | 1.360 (4) |
N2—C10 | 1.348 (2) | C19—H19 | 0.9500 |
N2—C6 | 1.363 (2) | C20—C21 | 1.378 (5) |
N1—C5 | 1.348 (2) | C20—H20 | 0.9500 |
N1—C1 | 1.355 (2) | C21—C22 | 1.395 (4) |
N3—C15 | 1.336 (3) | C21—H21 | 0.9500 |
N3—C11 | 1.366 (3) | C22—H22 | 0.9500 |
C1—C2 | 1.388 (2) | C23—H23A | 0.9800 |
C1—C6 | 1.474 (2) | C23—H23B | 0.9800 |
C2—C3 | 1.387 (3) | C23—H23C | 0.9800 |
C2—H2 | 0.9500 | C24—H24A | 0.9800 |
C3—C4 | 1.383 (3) | C24—H24B | 0.9800 |
C3—H3 | 0.9500 | C24—H24C | 0.9800 |
C4—C5 | 1.383 (3) | C25—H25A | 0.9800 |
C4—H4 | 0.9500 | C25—H25B | 0.9800 |
C5—H5 | 0.9500 | C25—H25C | 0.9800 |
C6—C7 | 1.389 (2) | C26—H26A | 0.9800 |
C7—C8 | 1.383 (3) | C26—H26B | 0.9800 |
C7—H7 | 0.9500 | C26—H26C | 0.9800 |
N2—Ru1—O1 | 169.32 (6) | N2—C10—C9 | 123.11 (17) |
N2—Ru1—N1 | 78.50 (5) | N2—C10—H10 | 118.4 |
O1—Ru1—N1 | 92.98 (5) | C9—C10—H10 | 118.4 |
N2—Ru1—N3 | 95.26 (6) | N3—C11—C12 | 121.6 (2) |
O1—Ru1—N3 | 77.22 (6) | N3—C11—C16 | 113.4 (2) |
N1—Ru1—N3 | 83.51 (7) | C12—C11—C16 | 124.7 (2) |
N2—Ru1—S2 | 94.50 (4) | C11—C12—C13 | 118.6 (3) |
O1—Ru1—S2 | 92.65 (4) | C11—C12—H12 | 120.7 |
N1—Ru1—S2 | 95.15 (4) | C13—C12—H12 | 120.7 |
N3—Ru1—S2 | 169.67 (5) | C14—C13—C12 | 120.1 (3) |
N2—Ru1—S1 | 96.74 (4) | C14—C13—H13 | 120.0 |
O1—Ru1—S1 | 91.42 (4) | C12—C13—H13 | 120.0 |
N1—Ru1—S1 | 174.50 (4) | C13—C14—C15 | 118.6 (3) |
N3—Ru1—S1 | 94.26 (6) | C13—C14—H14 | 120.7 |
S2—Ru1—S1 | 87.93 (2) | C15—C14—H14 | 120.7 |
O2—S1—C23 | 106.70 (16) | N3—C15—C14 | 123.4 (3) |
O2—S1—C24 | 107.83 (13) | N3—C15—H15 | 118.3 |
C23—S1—C24 | 100.07 (14) | C14—C15—H15 | 118.3 |
O2—S1—Ru1 | 116.31 (8) | O1—C16—C17 | 119.14 (19) |
C23—S1—Ru1 | 112.37 (12) | O1—C16—C11 | 117.65 (18) |
C24—S1—Ru1 | 112.18 (8) | C17—C16—C11 | 123.2 (2) |
O3—S2—C25 | 107.43 (9) | C22—C17—C18 | 119.5 (2) |
O3—S2—C26 | 106.80 (9) | C22—C17—C16 | 122.1 (2) |
C25—S2—C26 | 100.23 (10) | C18—C17—C16 | 118.3 (2) |
O3—S2—Ru1 | 113.91 (7) | C17—C18—C19 | 119.8 (3) |
C25—S2—Ru1 | 114.69 (7) | C17—C18—H18 | 120.1 |
C26—S2—Ru1 | 112.64 (7) | C19—C18—H18 | 120.1 |
O6—S3—O5 | 115.44 (10) | C20—C19—C18 | 120.7 (3) |
O6—S3—O4 | 114.63 (10) | C20—C19—H19 | 119.6 |
O5—S3—O4 | 114.90 (10) | C18—C19—H19 | 119.6 |
O6—S3—C27 | 103.25 (10) | C19—C20—C21 | 120.0 (3) |
O5—S3—C27 | 103.52 (9) | C19—C20—H20 | 120.0 |
O4—S3—C27 | 102.64 (9) | C21—C20—H20 | 120.0 |
C16—O1—Ru1 | 116.26 (12) | C20—C21—C22 | 120.1 (3) |
C10—N2—C6 | 117.74 (15) | C20—C21—H21 | 119.9 |
C10—N2—Ru1 | 127.07 (12) | C22—C21—H21 | 119.9 |
C6—N2—Ru1 | 115.07 (11) | C17—C22—C21 | 119.8 (3) |
C5—N1—C1 | 118.87 (15) | C17—C22—H22 | 120.1 |
C5—N1—Ru1 | 125.74 (12) | C21—C22—H22 | 120.1 |
C1—N1—Ru1 | 114.86 (11) | S1—C23—H23A | 109.5 |
C15—N3—C11 | 117.7 (2) | S1—C23—H23B | 109.5 |
C15—N3—Ru1 | 128.20 (17) | H23A—C23—H23B | 109.5 |
C11—N3—Ru1 | 113.98 (14) | S1—C23—H23C | 109.5 |
N1—C1—C2 | 121.36 (16) | H23A—C23—H23C | 109.5 |
N1—C1—C6 | 115.02 (14) | H23B—C23—H23C | 109.5 |
C2—C1—C6 | 123.62 (16) | S1—C24—H24A | 109.5 |
C3—C2—C1 | 119.32 (17) | S1—C24—H24B | 109.5 |
C3—C2—H2 | 120.3 | H24A—C24—H24B | 109.5 |
C1—C2—H2 | 120.3 | S1—C24—H24C | 109.5 |
C4—C3—C2 | 119.19 (17) | H24A—C24—H24C | 109.5 |
C4—C3—H3 | 120.4 | H24B—C24—H24C | 109.5 |
C2—C3—H3 | 120.4 | S2—C25—H25A | 109.5 |
C3—C4—C5 | 118.95 (17) | S2—C25—H25B | 109.5 |
C3—C4—H4 | 120.5 | H25A—C25—H25B | 109.5 |
C5—C4—H4 | 120.5 | S2—C25—H25C | 109.5 |
N1—C5—C4 | 122.31 (16) | H25A—C25—H25C | 109.5 |
N1—C5—H5 | 118.8 | H25B—C25—H25C | 109.5 |
C4—C5—H5 | 118.8 | S2—C26—H26A | 109.5 |
N2—C6—C7 | 121.42 (16) | S2—C26—H26B | 109.5 |
N2—C6—C1 | 115.46 (14) | H26A—C26—H26B | 109.5 |
C7—C6—C1 | 123.11 (16) | S2—C26—H26C | 109.5 |
C8—C7—C6 | 119.74 (17) | H26A—C26—H26C | 109.5 |
C8—C7—H7 | 120.1 | H26B—C26—H26C | 109.5 |
C6—C7—H7 | 120.1 | F1—C27—F3 | 106.99 (16) |
C9—C8—C7 | 118.95 (17) | F1—C27—F2 | 107.62 (17) |
C9—C8—H8 | 120.5 | F3—C27—F2 | 107.49 (16) |
C7—C8—H8 | 120.5 | F1—C27—S3 | 112.25 (14) |
C8—C9—C10 | 118.98 (17) | F3—C27—S3 | 111.71 (14) |
C8—C9—H9 | 120.5 | F2—C27—S3 | 110.53 (13) |
C10—C9—H9 | 120.5 | ||
C5—N1—C1—C2 | −0.2 (3) | C11—C12—C13—C14 | 0.3 (8) |
Ru1—N1—C1—C2 | 171.93 (15) | C12—C13—C14—C15 | −1.1 (8) |
C5—N1—C1—C6 | 179.31 (16) | C11—N3—C15—C14 | −3.7 (5) |
Ru1—N1—C1—C6 | −8.5 (2) | Ru1—N3—C15—C14 | −178.8 (3) |
N1—C1—C2—C3 | −0.5 (3) | C13—C14—C15—N3 | 2.9 (7) |
C6—C1—C2—C3 | −180.0 (2) | Ru1—O1—C16—C17 | −170.77 (15) |
C1—C2—C3—C4 | 0.9 (3) | Ru1—O1—C16—C11 | 10.8 (2) |
C2—C3—C4—C5 | −0.6 (3) | N3—C11—C16—O1 | −2.3 (3) |
C1—N1—C5—C4 | 0.5 (3) | C12—C11—C16—O1 | 171.8 (3) |
Ru1—N1—C5—C4 | −170.68 (14) | N3—C11—C16—C17 | 179.3 (2) |
C3—C4—C5—N1 | −0.1 (3) | C12—C11—C16—C17 | −6.5 (4) |
C10—N2—C6—C7 | 2.2 (3) | O1—C16—C17—C22 | 134.7 (2) |
Ru1—N2—C6—C7 | −174.17 (16) | C11—C16—C17—C22 | −46.9 (3) |
C10—N2—C6—C1 | −176.87 (17) | O1—C16—C17—C18 | −42.3 (3) |
Ru1—N2—C6—C1 | 6.7 (2) | C11—C16—C17—C18 | 136.0 (3) |
N1—C1—C6—N2 | 1.2 (2) | C22—C17—C18—C19 | 0.9 (4) |
C2—C1—C6—N2 | −179.24 (18) | C16—C17—C18—C19 | 178.0 (2) |
N1—C1—C6—C7 | −177.82 (19) | C17—C18—C19—C20 | −1.8 (4) |
C2—C1—C6—C7 | 1.7 (3) | C18—C19—C20—C21 | 1.1 (5) |
N2—C6—C7—C8 | −1.3 (3) | C19—C20—C21—C22 | 0.4 (5) |
C1—C6—C7—C8 | 177.7 (2) | C18—C17—C22—C21 | 0.5 (4) |
C6—C7—C8—C9 | −0.9 (4) | C16—C17—C22—C21 | −176.5 (2) |
C7—C8—C9—C10 | 2.1 (3) | C20—C21—C22—C17 | −1.2 (4) |
C6—N2—C10—C9 | −1.0 (3) | O6—S3—C27—F1 | −63.58 (16) |
Ru1—N2—C10—C9 | 174.89 (16) | O5—S3—C27—F1 | 57.13 (17) |
C8—C9—C10—N2 | −1.1 (3) | O4—S3—C27—F1 | 176.98 (15) |
C15—N3—C11—C12 | 2.7 (4) | O6—S3—C27—F3 | 176.23 (14) |
Ru1—N3—C11—C12 | 178.5 (3) | O5—S3—C27—F3 | −63.06 (16) |
C15—N3—C11—C16 | 177.1 (2) | O4—S3—C27—F3 | 56.79 (16) |
Ru1—N3—C11—C16 | −7.1 (3) | O6—S3—C27—F2 | 56.58 (17) |
N3—C11—C12—C13 | −1.1 (6) | O5—S3—C27—F2 | 177.29 (15) |
C16—C11—C12—C13 | −174.8 (4) | O4—S3—C27—F2 | −62.86 (17) |
Ru1—N1 | 2.0905 (16) | Ru1—N2 | 2.0705 (16) |
Ru1—N3 | 2.105 (2) | Ru1—O1 | 2.0898 (14) |
Ru1–S1 | 2.2845 (6) | Ru1—S2 | 2.2789 (6) |
O1—C16 | 1.254 (3) | ||
N1—Ru1—N2 | 78.46 (6) | N3—Ru1—O1 | 77.20 (7) |
S1—Ru1—S2 | 87.93 (3) |
Acknowledgements
We would like to thank Editage (www.editage.com) for English language editing.
Funding information
Funding for this research was provided by: JSPS KAKENHI (grant No. JP20K05589).
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