metal-organic compounds
(5,10,15,20-Tetraphenylporphyrinato-κ4N)(2,2,2-trifluoro-1-phenylethylidene-κC1)ruthenium(II): a stable fluorinated alkylidene complex of a ruthenium(II) porphyrin
aDepartment of Chemistry, School of Science, Kitasato University, Kitasato, Sagamihara, Kanagawa 228-8555, Japan
*Correspondence e-mail: orgnmtl@kitasato-u.ac.jp
In the title compound, [Ru(C44H28N4)(C8H5F3)], the fluorinated alkylidene group is bound to a five-coordinate Ru atom, which is located toward the carbene C atom, 0.3301 (5)Å from the least-squares plane of the C20N4 porphyrin core. The Ru=C bond is tilted slightly from the normal to the C20N4 least-squares plane due to steric repulsion between the porphyrinate ligand and the bulky trifluoromethyl group. The Ru=C bond length of 1.838 (2) Å is comparable with those in bis(subsituted phenyl)carbene analogs.
Related literature
For background on fluorine chemistry, see: Seebach (1990). For the preparation of the precursor of the 1-phenyl-2,2,2-trifluoroethylidene ligand, see: Shepard & Wentworth (1967). For related structures, see: Che & Huang (2002); Li et al. (2004); Wada et al. (2008). For C—H⋯π interactions, see: Hunter et al. (2001).
Experimental
Crystal data
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Data collection
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Refinement
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Data collection: MSC/AFC Diffractometer Control Software (Molecular Structure Corporation, 1993); cell MSC/AFC Diffractometer Control Software; data reduction: CrystalStructure (Rigaku/MSC, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997); software used to prepare material for publication: SHELXL97.
Supporting information
10.1107/S1600536808023374/lx2062sup1.cif
contains datablocks I, global. DOI:Structure factors: contains datablock I. DOI: 10.1107/S1600536808023374/lx2062Isup2.hkl
The carbene precursor, 1-phenyl-2,2,2-trifluorodiazoethane, was prepared according to lit. (Shepard & Wentworth, 1967). To an octane solution (50 ml) of [Ru(tpp)(CO)] (204 mg, 0.275 mmol) added an octane solution (10 ml) of 1-phenyl-2,2,2-trifluorodiazoethane (62 mg, 0.333 mmol) under nitrogen atmosphere with refluxing for 4 h. After removal of the volatiles in vacuo, the residue was chromatographed on a silica-gel column with dichloromethane/hexane mixture (v/v, 1/1). An intense red band was collected and evaporated to dryness. Recrystallization from a dichloromethane/hexane solution gave air-stable dark red crystals of (I) (yield, 133 mg, 0.153 mmol, 55%). Up to 450 K the compound [Ru(tpp){═C(CF3)Ph}] blackened and decomposed in air, but under reduced pressure (ca 10 Pa) it sublimed above 510 K. Spectroscopic analysis: 1H NMR (CDCl3, 500 MHz, δ, p.p.m.): 8.52 (s, 8H), 8.06–7.98 (m, 8H), 7.75–7.66 (m, 12H), 6.62 (t, J = 7.8, 1H), 6.21 (t, J = 7.8 Hz, 2H), 2.99 (d, J = 7.8 Hz, 2H), 19F{1H} NMR (CDCl3, 470 MHz, δ, p.p.m.): -69.1 (s); SIMS: m/z = 872 [M]+, UV/Vis (CH2Cl2): λmax (log ε) 403 (5.15), 536 (3.93) nm.
All H atoms were placed in geometrically idealized positions and constrained to ride on their parent atoms, with C—H = 0.93 Å and Uiso(H) = 1.2Ueq.
Data collection: MSC/AFC Diffractometer Control Software (Molecular Structure Corporation, 1993); cell
MSC/AFC Diffractometer Control Software (Molecular Structure Corporation, 1993); data reduction: CrystalStructure (Rigaku/MSC, 2007); program(s) used to solve structure: SHELXS97 (Sheldrick, 2008); program(s) used to refine structure: SHELXL97 (Sheldrick, 2008); molecular graphics: ORTEP-3 for Windows (Farrugia, 1997); software used to prepare material for publication: SHELXL97 (Sheldrick, 2008).[Ru(C44H28N4)(C8H5F3)] | Z = 2 |
Mr = 871.89 | F(000) = 888 |
Triclinic, P1 | Dx = 1.493 Mg m−3 |
Hall symbol: -P 1 | Mo Kα radiation, λ = 0.71069 Å |
a = 11.131 (1) Å | Cell parameters from 25 reflections |
b = 12.634 (2) Å | θ = 14.9–15.0° |
c = 15.749 (2) Å | µ = 0.46 mm−1 |
α = 101.713 (9)° | T = 296 K |
β = 110.133 (8)° | Prism, dark red |
γ = 102.15 (1)° | 0.20 × 0.20 × 0.20 mm |
V = 1939.2 (5) Å3 |
Rigaku AFC-7R diffractometer | Rint = 0.017 |
Radiation source: rotating Mo anode | θmax = 27.5°, θmin = 2.6° |
Graphite monochromator | h = −14→0 |
ω/2θ scans | k = −16→16 |
9374 measured reflections | l = −19→20 |
8916 independent reflections | 3 standard reflections every 150 reflections |
7578 reflections with I > 2σ(I) | intensity decay: 3.5% |
Refinement on F2 | Primary atom site location: structure-invariant direct methods |
Least-squares matrix: full | Secondary atom site location: difference Fourier map |
R[F2 > 2σ(F2)] = 0.031 | Hydrogen site location: inferred from neighbouring sites |
wR(F2) = 0.077 | H-atom parameters constrained |
S = 1.03 | w = 1/[σ2(Fo2) + (0.0315P)2 + P] where P = (Fo2 + 2Fc2)/3 |
8916 reflections | (Δ/σ)max = 0.001 |
541 parameters | Δρmax = 0.37 e Å−3 |
0 restraints | Δρmin = −0.46 e Å−3 |
[Ru(C44H28N4)(C8H5F3)] | γ = 102.15 (1)° |
Mr = 871.89 | V = 1939.2 (5) Å3 |
Triclinic, P1 | Z = 2 |
a = 11.131 (1) Å | Mo Kα radiation |
b = 12.634 (2) Å | µ = 0.46 mm−1 |
c = 15.749 (2) Å | T = 296 K |
α = 101.713 (9)° | 0.20 × 0.20 × 0.20 mm |
β = 110.133 (8)° |
Rigaku AFC-7R diffractometer | Rint = 0.017 |
9374 measured reflections | 3 standard reflections every 150 reflections |
8916 independent reflections | intensity decay: 3.5% |
7578 reflections with I > 2σ(I) |
R[F2 > 2σ(F2)] = 0.031 | 0 restraints |
wR(F2) = 0.077 | H-atom parameters constrained |
S = 1.03 | Δρmax = 0.37 e Å−3 |
8916 reflections | Δρmin = −0.46 e Å−3 |
541 parameters |
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 of F2 against ALL reflections. The weighted R-factor wR and goodness of fit S are based on F2, conventional R-factors R are based on F, with F set to zero for negative F2. The threshold expression of F2 > 2sigma(F2) is used only for calculating R-factors(gt) etc. and is not relevant to the choice of reflections for refinement. R-factors based on F2 are statistically about twice as large as those based on F, and R- factors based on ALL data will be even larger. |
x | y | z | Uiso*/Ueq | ||
Ru | 0.471753 (17) | 0.400275 (13) | 0.271619 (12) | 0.02657 (5) | |
F1 | 0.3640 (2) | 0.24901 (18) | 0.04049 (12) | 0.0786 (6) | |
F2 | 0.22719 (18) | 0.18331 (13) | 0.09802 (13) | 0.0689 (5) | |
F3 | 0.1734 (2) | 0.27779 (16) | 0.00105 (12) | 0.0851 (7) | |
N1 | 0.48801 (17) | 0.23935 (14) | 0.24134 (12) | 0.0294 (4) | |
N2 | 0.63417 (17) | 0.45653 (14) | 0.24213 (12) | 0.0299 (4) | |
N3 | 0.48445 (17) | 0.56603 (14) | 0.32700 (12) | 0.0298 (4) | |
N4 | 0.35981 (17) | 0.35415 (14) | 0.34439 (12) | 0.0298 (4) | |
C1 | 0.4225 (2) | 0.14717 (17) | 0.26053 (15) | 0.0316 (4) | |
C2 | 0.4644 (2) | 0.05090 (18) | 0.23099 (17) | 0.0377 (5) | |
H2 | 0.4345 | −0.0213 | 0.2357 | 0.045* | |
C3 | 0.5547 (2) | 0.08434 (18) | 0.19533 (16) | 0.0361 (5) | |
H3 | 0.5985 | 0.0395 | 0.1708 | 0.043* | |
C4 | 0.5711 (2) | 0.20292 (17) | 0.20232 (15) | 0.0307 (4) | |
C5 | 0.6656 (2) | 0.27158 (17) | 0.18138 (15) | 0.0315 (4) | |
C6 | 0.6940 (2) | 0.38916 (18) | 0.19976 (15) | 0.0319 (4) | |
C7 | 0.7891 (2) | 0.45943 (19) | 0.17640 (17) | 0.0387 (5) | |
H7 | 0.8423 | 0.4352 | 0.1470 | 0.046* | |
C8 | 0.7876 (2) | 0.56714 (19) | 0.20473 (17) | 0.0395 (5) | |
H8 | 0.8404 | 0.6306 | 0.1990 | 0.047* | |
C9 | 0.6906 (2) | 0.56663 (17) | 0.24508 (15) | 0.0321 (4) | |
C10 | 0.6577 (2) | 0.66209 (17) | 0.28066 (15) | 0.0324 (4) | |
C11 | 0.5596 (2) | 0.66036 (17) | 0.31677 (15) | 0.0322 (4) | |
C12 | 0.5197 (2) | 0.75756 (18) | 0.34796 (17) | 0.0399 (5) | |
H12 | 0.5536 | 0.8309 | 0.3469 | 0.048* | |
C13 | 0.4246 (2) | 0.72243 (18) | 0.37877 (17) | 0.0396 (5) | |
H13 | 0.3797 | 0.7669 | 0.4024 | 0.048* | |
C14 | 0.4047 (2) | 0.60352 (17) | 0.36877 (15) | 0.0323 (4) | |
C15 | 0.3193 (2) | 0.53684 (18) | 0.39806 (15) | 0.0318 (4) | |
C16 | 0.3048 (2) | 0.42202 (18) | 0.39022 (15) | 0.0325 (4) | |
C17 | 0.2271 (2) | 0.3562 (2) | 0.42782 (18) | 0.0414 (5) | |
H17 | 0.1823 | 0.3827 | 0.4636 | 0.050* | |
C18 | 0.2304 (2) | 0.2485 (2) | 0.40216 (18) | 0.0417 (5) | |
H18 | 0.1872 | 0.1872 | 0.4162 | 0.050* | |
C19 | 0.3125 (2) | 0.24602 (18) | 0.34939 (16) | 0.0326 (4) | |
C20 | 0.3387 (2) | 0.14895 (17) | 0.30846 (15) | 0.0324 (4) | |
C21 | 0.7482 (2) | 0.21607 (17) | 0.14047 (16) | 0.0326 (4) | |
C22 | 0.6894 (2) | 0.1358 (2) | 0.05146 (17) | 0.0408 (5) | |
H22 | 0.5974 | 0.1164 | 0.0161 | 0.049* | |
C23 | 0.7674 (3) | 0.0847 (2) | 0.01522 (19) | 0.0500 (6) | |
H23 | 0.7273 | 0.0308 | −0.0442 | 0.060* | |
C24 | 0.9036 (3) | 0.1132 (2) | 0.0667 (2) | 0.0520 (7) | |
H24 | 0.9555 | 0.0792 | 0.0418 | 0.062* | |
C25 | 0.9633 (3) | 0.1925 (2) | 0.1554 (2) | 0.0489 (6) | |
H25 | 1.0554 | 0.2119 | 0.1903 | 0.059* | |
C26 | 0.8858 (2) | 0.2429 (2) | 0.19212 (17) | 0.0400 (5) | |
H26 | 0.9262 | 0.2955 | 0.2522 | 0.048* | |
C27 | 0.7324 (2) | 0.77578 (18) | 0.28066 (17) | 0.0356 (5) | |
C28 | 0.7179 (3) | 0.8016 (2) | 0.19709 (19) | 0.0444 (6) | |
H28 | 0.6628 | 0.7469 | 0.1393 | 0.053* | |
C29 | 0.7850 (3) | 0.9086 (2) | 0.1989 (2) | 0.0539 (7) | |
H29 | 0.7758 | 0.9248 | 0.1424 | 0.065* | |
C30 | 0.8646 (3) | 0.9902 (2) | 0.2837 (2) | 0.0583 (8) | |
H30 | 0.9086 | 1.0620 | 0.2848 | 0.070* | |
C31 | 0.8792 (3) | 0.9664 (2) | 0.3666 (2) | 0.0583 (7) | |
H31 | 0.9328 | 1.0223 | 0.4241 | 0.070* | |
C32 | 0.8145 (3) | 0.8591 (2) | 0.36579 (19) | 0.0481 (6) | |
H32 | 0.8263 | 0.8432 | 0.4227 | 0.058* | |
C33 | 0.2382 (2) | 0.59080 (18) | 0.44118 (15) | 0.0323 (4) | |
C34 | 0.0990 (2) | 0.5541 (2) | 0.39707 (18) | 0.0408 (5) | |
H34 | 0.0564 | 0.4958 | 0.3401 | 0.049* | |
C35 | 0.0225 (2) | 0.6028 (2) | 0.43629 (19) | 0.0460 (6) | |
H35 | −0.0708 | 0.5762 | 0.4063 | 0.055* | |
C36 | 0.0845 (3) | 0.6905 (2) | 0.51967 (19) | 0.0451 (6) | |
H36 | 0.0333 | 0.7239 | 0.5458 | 0.054* | |
C37 | 0.2227 (3) | 0.7289 (2) | 0.56426 (18) | 0.0444 (6) | |
H37 | 0.2647 | 0.7883 | 0.6206 | 0.053* | |
C38 | 0.2992 (2) | 0.6791 (2) | 0.52544 (16) | 0.0391 (5) | |
H38 | 0.3924 | 0.7051 | 0.5562 | 0.047* | |
C39 | 0.2704 (2) | 0.03916 (18) | 0.31815 (18) | 0.0381 (5) | |
C40 | 0.1691 (3) | −0.0434 (2) | 0.2397 (2) | 0.0515 (6) | |
H40 | 0.1457 | −0.0323 | 0.1802 | 0.062* | |
C41 | 0.1022 (3) | −0.1432 (2) | 0.2495 (3) | 0.0689 (9) | |
H41 | 0.0344 | −0.1987 | 0.1965 | 0.083* | |
C42 | 0.1356 (4) | −0.1602 (3) | 0.3369 (3) | 0.0776 (11) | |
H42 | 0.0902 | −0.2270 | 0.3431 | 0.093* | |
C43 | 0.2352 (4) | −0.0792 (3) | 0.4144 (3) | 0.0702 (10) | |
H43 | 0.2571 | −0.0907 | 0.4737 | 0.084* | |
C44 | 0.3045 (3) | 0.0206 (2) | 0.4057 (2) | 0.0542 (7) | |
H44 | 0.3737 | 0.0749 | 0.4589 | 0.065* | |
C45 | 0.3393 (2) | 0.38402 (18) | 0.15662 (15) | 0.0330 (4) | |
C46 | 0.2869 (3) | 0.4779 (2) | 0.13103 (17) | 0.0445 (6) | |
C47 | 0.3502 (4) | 0.5498 (3) | 0.0933 (2) | 0.0684 (9) | |
H47 | 0.4251 | 0.5396 | 0.0832 | 0.082* | |
C48 | 0.3010 (5) | 0.6381 (3) | 0.0703 (3) | 0.0933 (14) | |
H48 | 0.3441 | 0.6874 | 0.0458 | 0.112* | |
C49 | 0.1903 (6) | 0.6521 (4) | 0.0837 (3) | 0.1069 (17) | |
H49 | 0.1581 | 0.7109 | 0.0683 | 0.128* | |
C50 | 0.1267 (5) | 0.5808 (4) | 0.1193 (3) | 0.1007 (14) | |
H50 | 0.0504 | 0.5905 | 0.1273 | 0.121* | |
C51 | 0.1739 (3) | 0.4937 (3) | 0.1439 (3) | 0.0708 (9) | |
H51 | 0.1301 | 0.4458 | 0.1690 | 0.085* | |
C52 | 0.2759 (3) | 0.2741 (2) | 0.07449 (18) | 0.0488 (6) |
U11 | U22 | U33 | U12 | U13 | U23 | |
Ru | 0.02924 (9) | 0.02307 (8) | 0.02976 (9) | 0.00762 (6) | 0.01476 (6) | 0.00812 (6) |
F1 | 0.0846 (13) | 0.1001 (15) | 0.0493 (10) | 0.0397 (12) | 0.0318 (10) | −0.0019 (9) |
F2 | 0.0632 (11) | 0.0388 (8) | 0.0758 (12) | 0.0029 (8) | 0.0093 (9) | 0.0041 (8) |
F3 | 0.0862 (13) | 0.0716 (12) | 0.0522 (10) | 0.0363 (11) | −0.0189 (9) | −0.0045 (9) |
N1 | 0.0312 (9) | 0.0255 (8) | 0.0343 (9) | 0.0092 (7) | 0.0158 (7) | 0.0096 (7) |
N2 | 0.0329 (9) | 0.0259 (8) | 0.0350 (9) | 0.0086 (7) | 0.0183 (8) | 0.0095 (7) |
N3 | 0.0331 (9) | 0.0254 (8) | 0.0338 (9) | 0.0083 (7) | 0.0175 (8) | 0.0087 (7) |
N4 | 0.0324 (9) | 0.0260 (8) | 0.0355 (9) | 0.0094 (7) | 0.0179 (8) | 0.0105 (7) |
C1 | 0.0344 (11) | 0.0248 (10) | 0.0360 (11) | 0.0079 (8) | 0.0151 (9) | 0.0093 (8) |
C2 | 0.0447 (13) | 0.0232 (10) | 0.0484 (13) | 0.0106 (9) | 0.0222 (11) | 0.0113 (9) |
C3 | 0.0416 (12) | 0.0276 (10) | 0.0450 (12) | 0.0143 (9) | 0.0229 (10) | 0.0095 (9) |
C4 | 0.0327 (10) | 0.0276 (10) | 0.0323 (10) | 0.0105 (8) | 0.0136 (9) | 0.0078 (8) |
C5 | 0.0338 (11) | 0.0296 (10) | 0.0338 (11) | 0.0120 (8) | 0.0163 (9) | 0.0079 (8) |
C6 | 0.0327 (11) | 0.0317 (10) | 0.0340 (11) | 0.0093 (9) | 0.0171 (9) | 0.0098 (9) |
C7 | 0.0414 (12) | 0.0357 (11) | 0.0495 (13) | 0.0131 (10) | 0.0293 (11) | 0.0137 (10) |
C8 | 0.0416 (12) | 0.0322 (11) | 0.0532 (14) | 0.0082 (9) | 0.0301 (11) | 0.0141 (10) |
C9 | 0.0342 (11) | 0.0284 (10) | 0.0361 (11) | 0.0075 (8) | 0.0176 (9) | 0.0106 (9) |
C10 | 0.0381 (11) | 0.0271 (10) | 0.0351 (11) | 0.0085 (9) | 0.0183 (9) | 0.0110 (8) |
C11 | 0.0386 (11) | 0.0247 (10) | 0.0344 (11) | 0.0078 (8) | 0.0175 (9) | 0.0083 (8) |
C12 | 0.0506 (14) | 0.0245 (10) | 0.0512 (14) | 0.0107 (10) | 0.0290 (12) | 0.0106 (9) |
C13 | 0.0474 (13) | 0.0283 (11) | 0.0514 (14) | 0.0150 (10) | 0.0283 (11) | 0.0104 (10) |
C14 | 0.0344 (11) | 0.0274 (10) | 0.0377 (11) | 0.0100 (8) | 0.0184 (9) | 0.0076 (8) |
C15 | 0.0314 (10) | 0.0309 (10) | 0.0343 (11) | 0.0093 (8) | 0.0160 (9) | 0.0077 (8) |
C16 | 0.0342 (11) | 0.0320 (11) | 0.0367 (11) | 0.0111 (9) | 0.0195 (9) | 0.0111 (9) |
C17 | 0.0489 (14) | 0.0381 (12) | 0.0531 (14) | 0.0154 (10) | 0.0354 (12) | 0.0182 (11) |
C18 | 0.0482 (14) | 0.0349 (12) | 0.0563 (15) | 0.0128 (10) | 0.0343 (12) | 0.0196 (11) |
C19 | 0.0331 (11) | 0.0300 (10) | 0.0393 (11) | 0.0087 (8) | 0.0188 (9) | 0.0134 (9) |
C20 | 0.0363 (11) | 0.0272 (10) | 0.0356 (11) | 0.0079 (8) | 0.0162 (9) | 0.0120 (8) |
C21 | 0.0372 (11) | 0.0276 (10) | 0.0392 (11) | 0.0110 (9) | 0.0210 (10) | 0.0117 (9) |
C22 | 0.0422 (13) | 0.0399 (12) | 0.0407 (12) | 0.0142 (10) | 0.0178 (11) | 0.0093 (10) |
C23 | 0.0616 (17) | 0.0457 (14) | 0.0445 (14) | 0.0198 (13) | 0.0267 (13) | 0.0045 (11) |
C24 | 0.0590 (16) | 0.0535 (15) | 0.0626 (17) | 0.0301 (13) | 0.0393 (15) | 0.0171 (13) |
C25 | 0.0396 (13) | 0.0533 (15) | 0.0624 (17) | 0.0205 (12) | 0.0256 (12) | 0.0198 (13) |
C26 | 0.0391 (12) | 0.0368 (12) | 0.0433 (13) | 0.0114 (10) | 0.0183 (10) | 0.0075 (10) |
C27 | 0.0404 (12) | 0.0284 (10) | 0.0456 (12) | 0.0106 (9) | 0.0249 (10) | 0.0135 (9) |
C28 | 0.0563 (15) | 0.0386 (13) | 0.0490 (14) | 0.0159 (11) | 0.0298 (12) | 0.0186 (11) |
C29 | 0.0720 (19) | 0.0478 (15) | 0.0694 (18) | 0.0261 (14) | 0.0449 (16) | 0.0372 (14) |
C30 | 0.0627 (18) | 0.0360 (13) | 0.093 (2) | 0.0142 (13) | 0.0442 (17) | 0.0323 (15) |
C31 | 0.0586 (17) | 0.0326 (13) | 0.0690 (19) | −0.0003 (12) | 0.0201 (15) | 0.0102 (12) |
C32 | 0.0553 (15) | 0.0366 (13) | 0.0484 (14) | 0.0045 (11) | 0.0211 (12) | 0.0141 (11) |
C33 | 0.0338 (11) | 0.0309 (10) | 0.0382 (11) | 0.0118 (9) | 0.0198 (9) | 0.0114 (9) |
C34 | 0.0374 (12) | 0.0358 (12) | 0.0467 (13) | 0.0083 (10) | 0.0198 (11) | 0.0054 (10) |
C35 | 0.0333 (12) | 0.0520 (15) | 0.0566 (15) | 0.0133 (11) | 0.0226 (11) | 0.0163 (12) |
C36 | 0.0513 (14) | 0.0486 (14) | 0.0538 (15) | 0.0249 (12) | 0.0351 (13) | 0.0185 (12) |
C37 | 0.0533 (15) | 0.0452 (13) | 0.0389 (12) | 0.0176 (11) | 0.0247 (11) | 0.0077 (10) |
C38 | 0.0362 (12) | 0.0424 (13) | 0.0380 (12) | 0.0132 (10) | 0.0155 (10) | 0.0086 (10) |
C39 | 0.0440 (13) | 0.0278 (10) | 0.0543 (14) | 0.0130 (9) | 0.0296 (11) | 0.0171 (10) |
C40 | 0.0497 (15) | 0.0358 (13) | 0.0686 (18) | 0.0077 (11) | 0.0285 (14) | 0.0125 (12) |
C41 | 0.0570 (18) | 0.0348 (14) | 0.115 (3) | 0.0056 (13) | 0.0444 (19) | 0.0157 (16) |
C42 | 0.087 (2) | 0.0402 (16) | 0.150 (4) | 0.0267 (17) | 0.083 (3) | 0.048 (2) |
C43 | 0.105 (3) | 0.0600 (19) | 0.100 (3) | 0.046 (2) | 0.075 (2) | 0.054 (2) |
C44 | 0.0735 (19) | 0.0410 (14) | 0.0622 (17) | 0.0212 (13) | 0.0368 (15) | 0.0242 (13) |
C45 | 0.0350 (11) | 0.0344 (11) | 0.0320 (11) | 0.0102 (9) | 0.0159 (9) | 0.0110 (9) |
C46 | 0.0549 (15) | 0.0376 (12) | 0.0338 (12) | 0.0156 (11) | 0.0078 (11) | 0.0124 (10) |
C47 | 0.084 (2) | 0.0602 (18) | 0.0561 (18) | 0.0131 (17) | 0.0190 (16) | 0.0321 (15) |
C48 | 0.132 (4) | 0.060 (2) | 0.068 (2) | 0.019 (2) | 0.012 (2) | 0.0407 (18) |
C49 | 0.141 (4) | 0.064 (2) | 0.094 (3) | 0.053 (3) | 0.006 (3) | 0.029 (2) |
C50 | 0.100 (3) | 0.088 (3) | 0.122 (4) | 0.066 (3) | 0.030 (3) | 0.035 (3) |
C51 | 0.074 (2) | 0.065 (2) | 0.090 (2) | 0.0413 (18) | 0.0342 (19) | 0.0320 (18) |
C52 | 0.0496 (15) | 0.0482 (15) | 0.0396 (13) | 0.0197 (12) | 0.0091 (11) | 0.0055 (11) |
Ru—C45 | 1.838 (2) | C23—H23 | 0.9300 |
Ru—N1 | 2.053 (2) | C24—C25 | 1.382 (4) |
Ru—N2 | 2.040 (2) | C24—H24 | 0.9300 |
Ru—N3 | 2.053 (2) | C25—C26 | 1.382 (3) |
Ru—N4 | 2.038 (2) | C25—H25 | 0.9300 |
F1—C52 | 1.331 (3) | C26—H26 | 0.9300 |
F2—C52 | 1.341 (3) | C27—C28 | 1.384 (3) |
F3—C52 | 1.333 (3) | C27—C32 | 1.386 (3) |
N1—C4 | 1.378 (3) | C28—C29 | 1.390 (3) |
N1—C1 | 1.384 (3) | C28—H28 | 0.9300 |
N2—C9 | 1.385 (3) | C29—C30 | 1.369 (4) |
N2—C6 | 1.388 (3) | C29—H29 | 0.9300 |
N3—C11 | 1.377 (3) | C30—C31 | 1.362 (4) |
N3—C14 | 1.378 (3) | C30—H30 | 0.9300 |
N4—C16 | 1.380 (3) | C31—C32 | 1.390 (3) |
N4—C19 | 1.385 (3) | C31—H31 | 0.9300 |
C1—C20 | 1.388 (3) | C32—H32 | 0.9300 |
C1—C2 | 1.439 (3) | C33—C34 | 1.387 (3) |
C2—C3 | 1.346 (3) | C33—C38 | 1.388 (3) |
C2—H2 | 0.9300 | C34—C35 | 1.383 (3) |
C3—C4 | 1.447 (3) | C34—H34 | 0.9300 |
C3—H3 | 0.9300 | C35—C36 | 1.376 (4) |
C4—C5 | 1.393 (3) | C35—H35 | 0.9300 |
C5—C6 | 1.398 (3) | C36—C37 | 1.377 (4) |
C5—C21 | 1.499 (3) | C36—H36 | 0.9300 |
C6—C7 | 1.432 (3) | C37—C38 | 1.387 (3) |
C7—C8 | 1.349 (3) | C37—H37 | 0.9300 |
C7—H7 | 0.9300 | C38—H38 | 0.9300 |
C8—C9 | 1.428 (3) | C39—C40 | 1.382 (4) |
C8—H8 | 0.9300 | C39—C44 | 1.382 (4) |
C9—C10 | 1.398 (3) | C40—C41 | 1.390 (4) |
C10—C11 | 1.392 (3) | C40—H40 | 0.9300 |
C10—C27 | 1.501 (3) | C41—C42 | 1.370 (5) |
C11—C12 | 1.443 (3) | C41—H41 | 0.9300 |
C12—C13 | 1.340 (3) | C42—C43 | 1.360 (5) |
C12—H12 | 0.9300 | C42—H42 | 0.9300 |
C13—C14 | 1.439 (3) | C43—C44 | 1.392 (4) |
C13—H13 | 0.9300 | C43—H43 | 0.9300 |
C14—C15 | 1.396 (3) | C44—H44 | 0.9300 |
C15—C16 | 1.400 (3) | C45—C46 | 1.494 (3) |
C15—C33 | 1.495 (3) | C45—C52 | 1.526 (3) |
C16—C17 | 1.428 (3) | C46—C47 | 1.383 (4) |
C17—C18 | 1.350 (3) | C46—C51 | 1.389 (4) |
C17—H17 | 0.9300 | C47—C48 | 1.401 (5) |
C18—C19 | 1.433 (3) | C47—H47 | 0.9300 |
C18—H18 | 0.9300 | C48—C49 | 1.359 (6) |
C19—C20 | 1.401 (3) | C48—H48 | 0.9300 |
C20—C39 | 1.499 (3) | C49—C50 | 1.356 (7) |
C21—C22 | 1.390 (3) | C49—H49 | 0.9300 |
C21—C26 | 1.391 (3) | C50—C51 | 1.383 (5) |
C22—C23 | 1.387 (3) | C50—H50 | 0.9300 |
C22—H22 | 0.9300 | C51—H51 | 0.9300 |
C23—C24 | 1.376 (4) | ||
H37···C3i | 2.79 | H38···C1i | 2.86 |
H37···C4i | 2.72 | ||
C45—Ru—N4 | 100.99 (8) | C23—C24—C25 | 120.0 (2) |
C45—Ru—N2 | 98.27 (8) | C23—C24—H24 | 120.0 |
N4—Ru—N2 | 160.70 (7) | C25—C24—H24 | 120.0 |
C45—Ru—N1 | 97.70 (8) | C24—C25—C26 | 119.8 (2) |
N4—Ru—N1 | 89.42 (7) | C24—C25—H25 | 120.1 |
N2—Ru—N1 | 89.28 (7) | C26—C25—H25 | 120.1 |
C45—Ru—N3 | 93.42 (9) | C25—C26—C21 | 120.9 (2) |
N4—Ru—N3 | 88.58 (7) | C25—C26—H26 | 119.5 |
N2—Ru—N3 | 89.01 (7) | C21—C26—H26 | 119.5 |
N1—Ru—N3 | 168.88 (7) | C28—C27—C32 | 118.5 (2) |
C4—N1—C1 | 106.29 (17) | C28—C27—C10 | 121.5 (2) |
C4—N1—Ru | 126.95 (14) | C32—C27—C10 | 119.9 (2) |
C1—N1—Ru | 126.68 (14) | C27—C28—C29 | 120.5 (3) |
C9—N2—C6 | 106.62 (17) | C27—C28—H28 | 119.7 |
C9—N2—Ru | 126.37 (14) | C29—C28—H28 | 119.7 |
C6—N2—Ru | 126.16 (13) | C30—C29—C28 | 120.1 (3) |
C11—N3—C14 | 106.12 (17) | C30—C29—H29 | 119.9 |
C11—N3—Ru | 126.55 (14) | C28—C29—H29 | 119.9 |
C14—N3—Ru | 126.65 (14) | C31—C30—C29 | 120.1 (2) |
C16—N4—C19 | 106.40 (17) | C31—C30—H30 | 120.0 |
C16—N4—Ru | 126.59 (14) | C29—C30—H30 | 120.0 |
C19—N4—Ru | 126.71 (14) | C30—C31—C32 | 120.4 (3) |
N1—C1—C20 | 125.66 (19) | C30—C31—H31 | 119.8 |
N1—C1—C2 | 109.44 (18) | C32—C31—H31 | 119.8 |
C20—C1—C2 | 124.67 (19) | C27—C32—C31 | 120.4 (3) |
C3—C2—C1 | 107.56 (19) | C27—C32—H32 | 119.8 |
C3—C2—H2 | 126.2 | C31—C32—H32 | 119.8 |
C1—C2—H2 | 126.2 | C34—C33—C38 | 118.2 (2) |
C2—C3—C4 | 107.30 (19) | C34—C33—C15 | 120.5 (2) |
C2—C3—H3 | 126.3 | C38—C33—C15 | 121.36 (19) |
C4—C3—H3 | 126.3 | C35—C34—C33 | 121.2 (2) |
N1—C4—C5 | 125.50 (18) | C35—C34—H34 | 119.4 |
N1—C4—C3 | 109.39 (18) | C33—C34—H34 | 119.4 |
C5—C4—C3 | 124.84 (19) | C36—C35—C34 | 119.9 (2) |
C4—C5—C6 | 125.03 (19) | C36—C35—H35 | 120.0 |
C4—C5—C21 | 117.48 (18) | C34—C35—H35 | 120.0 |
C6—C5—C21 | 117.42 (18) | C35—C36—C37 | 119.8 (2) |
N2—C6—C5 | 126.04 (19) | C35—C36—H36 | 120.1 |
N2—C6—C7 | 108.92 (18) | C37—C36—H36 | 120.1 |
C5—C6—C7 | 125.0 (2) | C36—C37—C38 | 120.2 (2) |
C8—C7—C6 | 107.54 (19) | C36—C37—H37 | 119.9 |
C8—C7—H7 | 126.2 | C38—C37—H37 | 119.9 |
C6—C7—H7 | 126.2 | C37—C38—C33 | 120.7 (2) |
C7—C8—C9 | 108.05 (19) | C37—C38—H38 | 119.6 |
C7—C8—H8 | 126.0 | C33—C38—H38 | 119.6 |
C9—C8—H8 | 126.0 | C40—C39—C44 | 119.1 (2) |
N2—C9—C10 | 125.95 (19) | C40—C39—C20 | 120.1 (2) |
N2—C9—C8 | 108.87 (18) | C44—C39—C20 | 120.7 (2) |
C10—C9—C8 | 125.18 (19) | C39—C40—C41 | 120.0 (3) |
C11—C10—C9 | 124.88 (19) | C39—C40—H40 | 120.0 |
C11—C10—C27 | 116.57 (19) | C41—C40—H40 | 120.0 |
C9—C10—C27 | 118.55 (19) | C42—C41—C40 | 120.4 (3) |
N3—C11—C10 | 125.57 (19) | C42—C41—H41 | 119.8 |
N3—C11—C12 | 109.51 (18) | C40—C41—H41 | 119.8 |
C10—C11—C12 | 124.92 (19) | C43—C42—C41 | 119.9 (3) |
C13—C12—C11 | 107.20 (19) | C43—C42—H42 | 120.1 |
C13—C12—H12 | 126.4 | C41—C42—H42 | 120.1 |
C11—C12—H12 | 126.4 | C42—C43—C44 | 120.5 (3) |
C12—C13—C14 | 107.6 (2) | C42—C43—H43 | 119.7 |
C12—C13—H13 | 126.2 | C44—C43—H43 | 119.7 |
C14—C13—H13 | 126.2 | C39—C44—C43 | 120.0 (3) |
N3—C14—C15 | 125.25 (19) | C39—C44—H44 | 120.0 |
N3—C14—C13 | 109.39 (18) | C43—C44—H44 | 120.0 |
C15—C14—C13 | 125.4 (2) | C46—C45—C52 | 112.38 (19) |
C14—C15—C16 | 124.24 (19) | C46—C45—Ru | 124.10 (16) |
C14—C15—C33 | 118.35 (19) | C52—C45—Ru | 123.44 (17) |
C16—C15—C33 | 117.40 (18) | C47—C46—C51 | 119.1 (3) |
N4—C16—C15 | 126.30 (19) | C47—C46—C45 | 120.2 (3) |
N4—C16—C17 | 109.27 (18) | C51—C46—C45 | 120.7 (2) |
C15—C16—C17 | 124.4 (2) | C46—C47—C48 | 119.7 (4) |
C18—C17—C16 | 107.7 (2) | C46—C47—H47 | 120.2 |
C18—C17—H17 | 126.1 | C48—C47—H47 | 120.2 |
C16—C17—H17 | 126.1 | C49—C48—C47 | 120.2 (4) |
C17—C18—C19 | 107.39 (19) | C49—C48—H48 | 119.9 |
C17—C18—H18 | 126.3 | C47—C48—H48 | 119.9 |
C19—C18—H18 | 126.3 | C50—C49—C48 | 120.3 (4) |
N4—C19—C20 | 125.80 (19) | C50—C49—H49 | 119.8 |
N4—C19—C18 | 109.13 (18) | C48—C49—H49 | 119.8 |
C20—C19—C18 | 125.06 (19) | C49—C50—C51 | 120.9 (4) |
C1—C20—C19 | 125.15 (19) | C49—C50—H50 | 119.5 |
C1—C20—C39 | 118.16 (19) | C51—C50—H50 | 119.5 |
C19—C20—C39 | 116.69 (19) | C50—C51—C46 | 119.8 (4) |
C22—C21—C26 | 118.6 (2) | C50—C51—H51 | 120.1 |
C22—C21—C5 | 121.1 (2) | C46—C51—H51 | 120.1 |
C26—C21—C5 | 120.2 (2) | F1—C52—F3 | 106.0 (2) |
C23—C22—C21 | 120.3 (2) | F1—C52—F2 | 106.0 (2) |
C23—C22—H22 | 119.9 | F3—C52—F2 | 105.4 (2) |
C21—C22—H22 | 119.9 | F1—C52—C45 | 111.8 (2) |
C24—C23—C22 | 120.4 (2) | F3—C52—C45 | 113.4 (2) |
C24—C23—H23 | 119.8 | F2—C52—C45 | 113.6 (2) |
C22—C23—H23 | 119.8 | ||
C45—Ru—N1—C4 | 89.58 (18) | C14—C15—C16—N4 | −7.3 (4) |
N4—Ru—N1—C4 | −169.41 (17) | C33—C15—C16—N4 | 173.1 (2) |
N2—Ru—N1—C4 | −8.66 (17) | C14—C15—C16—C17 | 174.0 (2) |
N3—Ru—N1—C4 | −89.8 (4) | C33—C15—C16—C17 | −5.6 (3) |
C45—Ru—N1—C1 | −93.94 (18) | N4—C16—C17—C18 | −2.3 (3) |
N4—Ru—N1—C1 | 7.07 (18) | C15—C16—C17—C18 | 176.6 (2) |
N2—Ru—N1—C1 | 167.82 (18) | C16—C17—C18—C19 | 1.0 (3) |
N3—Ru—N1—C1 | 86.7 (4) | C16—N4—C19—C20 | 177.2 (2) |
C45—Ru—N2—C9 | 81.26 (18) | Ru—N4—C19—C20 | 3.2 (3) |
N4—Ru—N2—C9 | −94.9 (3) | C16—N4—C19—C18 | −1.9 (2) |
N1—Ru—N2—C9 | 178.93 (18) | Ru—N4—C19—C18 | −175.98 (15) |
N3—Ru—N2—C9 | −12.06 (18) | C17—C18—C19—N4 | 0.6 (3) |
C45—Ru—N2—C6 | −86.67 (18) | C17—C18—C19—C20 | −178.6 (2) |
N4—Ru—N2—C6 | 97.2 (2) | N1—C1—C20—C19 | −3.5 (4) |
N1—Ru—N2—C6 | 11.00 (17) | C2—C1—C20—C19 | 170.4 (2) |
N3—Ru—N2—C6 | −179.99 (18) | N1—C1—C20—C39 | 176.8 (2) |
C45—Ru—N3—C11 | −84.89 (19) | C2—C1—C20—C39 | −9.4 (3) |
N4—Ru—N3—C11 | 174.18 (18) | N4—C19—C20—C1 | 3.7 (4) |
N2—Ru—N3—C11 | 13.33 (18) | C18—C19—C20—C1 | −177.3 (2) |
N1—Ru—N3—C11 | 94.5 (4) | N4—C19—C20—C39 | −176.6 (2) |
C45—Ru—N3—C14 | 84.30 (19) | C18—C19—C20—C39 | 2.5 (3) |
N4—Ru—N3—C14 | −16.63 (18) | C4—C5—C21—C22 | 65.4 (3) |
N2—Ru—N3—C14 | −177.48 (18) | C6—C5—C21—C22 | −117.6 (2) |
N1—Ru—N3—C14 | −96.3 (4) | C4—C5—C21—C26 | −113.5 (2) |
C45—Ru—N4—C16 | −82.03 (19) | C6—C5—C21—C26 | 63.5 (3) |
N2—Ru—N4—C16 | 94.1 (3) | C26—C21—C22—C23 | −0.5 (3) |
N1—Ru—N4—C16 | −179.75 (18) | C5—C21—C22—C23 | −179.4 (2) |
N3—Ru—N4—C16 | 11.18 (18) | C21—C22—C23—C24 | −0.4 (4) |
C45—Ru—N4—C19 | 90.84 (19) | C22—C23—C24—C25 | 0.6 (4) |
N2—Ru—N4—C19 | −93.0 (3) | C23—C24—C25—C26 | 0.0 (4) |
N1—Ru—N4—C19 | −6.89 (18) | C24—C25—C26—C21 | −0.8 (4) |
N3—Ru—N4—C19 | −175.96 (18) | C22—C21—C26—C25 | 1.0 (4) |
C4—N1—C1—C20 | 173.6 (2) | C5—C21—C26—C25 | 180.0 (2) |
Ru—N1—C1—C20 | −3.5 (3) | C11—C10—C27—C28 | −112.4 (3) |
C4—N1—C1—C2 | −1.1 (2) | C9—C10—C27—C28 | 67.6 (3) |
Ru—N1—C1—C2 | −178.15 (14) | C11—C10—C27—C32 | 65.2 (3) |
N1—C1—C2—C3 | 0.6 (3) | C9—C10—C27—C32 | −114.8 (3) |
C20—C1—C2—C3 | −174.1 (2) | C32—C27—C28—C29 | 0.4 (4) |
C1—C2—C3—C4 | 0.2 (3) | C10—C27—C28—C29 | 178.0 (2) |
C1—N1—C4—C5 | −173.0 (2) | C27—C28—C29—C30 | −1.1 (4) |
Ru—N1—C4—C5 | 4.0 (3) | C28—C29—C30—C31 | 0.7 (4) |
C1—N1—C4—C3 | 1.2 (2) | C29—C30—C31—C32 | 0.4 (5) |
Ru—N1—C4—C3 | 178.23 (14) | C28—C27—C32—C31 | 0.7 (4) |
C2—C3—C4—N1 | −0.8 (3) | C10—C27—C32—C31 | −177.0 (2) |
C2—C3—C4—C5 | 173.4 (2) | C30—C31—C32—C27 | −1.1 (5) |
N1—C4—C5—C6 | 2.3 (4) | C14—C15—C33—C34 | 116.4 (2) |
C3—C4—C5—C6 | −171.1 (2) | C16—C15—C33—C34 | −64.0 (3) |
N1—C4—C5—C21 | 179.02 (19) | C14—C15—C33—C38 | −63.1 (3) |
C3—C4—C5—C21 | 5.7 (3) | C16—C15—C33—C38 | 116.6 (2) |
C9—N2—C6—C5 | −179.2 (2) | C38—C33—C34—C35 | −0.9 (4) |
Ru—N2—C6—C5 | −9.3 (3) | C15—C33—C34—C35 | 179.7 (2) |
C9—N2—C6—C7 | 0.1 (2) | C33—C34—C35—C36 | 1.2 (4) |
Ru—N2—C6—C7 | 169.97 (15) | C34—C35—C36—C37 | −0.6 (4) |
C4—C5—C6—N2 | 0.6 (4) | C35—C36—C37—C38 | −0.1 (4) |
C21—C5—C6—N2 | −176.2 (2) | C36—C37—C38—C33 | 0.4 (4) |
C4—C5—C6—C7 | −178.6 (2) | C34—C33—C38—C37 | 0.1 (4) |
C21—C5—C6—C7 | 4.6 (3) | C15—C33—C38—C37 | 179.5 (2) |
N2—C6—C7—C8 | 0.4 (3) | C1—C20—C39—C40 | −70.2 (3) |
C5—C6—C7—C8 | 179.7 (2) | C19—C20—C39—C40 | 110.1 (3) |
C6—C7—C8—C9 | −0.8 (3) | C1—C20—C39—C44 | 112.1 (3) |
C6—N2—C9—C10 | 178.8 (2) | C19—C20—C39—C44 | −67.7 (3) |
Ru—N2—C9—C10 | 8.9 (3) | C44—C39—C40—C41 | 0.5 (4) |
C6—N2—C9—C8 | −0.6 (2) | C20—C39—C40—C41 | −177.3 (2) |
Ru—N2—C9—C8 | −170.43 (15) | C39—C40—C41—C42 | 0.3 (4) |
C7—C8—C9—N2 | 0.9 (3) | C40—C41—C42—C43 | −0.3 (5) |
C7—C8—C9—C10 | −178.5 (2) | C41—C42—C43—C44 | −0.5 (5) |
N2—C9—C10—C11 | −1.7 (4) | C40—C39—C44—C43 | −1.3 (4) |
C8—C9—C10—C11 | 177.6 (2) | C20—C39—C44—C43 | 176.5 (2) |
N2—C9—C10—C27 | 178.2 (2) | C42—C43—C44—C39 | 1.4 (5) |
C8—C9—C10—C27 | −2.5 (3) | N4—Ru—C45—C46 | 93.0 (2) |
C14—N3—C11—C10 | 177.5 (2) | N2—Ru—C45—C46 | −85.7 (2) |
Ru—N3—C11—C10 | −11.5 (3) | N1—Ru—C45—C46 | −176.11 (19) |
C14—N3—C11—C12 | −3.4 (2) | N3—Ru—C45—C46 | 3.8 (2) |
Ru—N3—C11—C12 | 167.60 (15) | N4—Ru—C45—C52 | −90.6 (2) |
C9—C10—C11—N3 | 3.1 (4) | N2—Ru—C45—C52 | 90.7 (2) |
C27—C10—C11—N3 | −176.9 (2) | N1—Ru—C45—C52 | 0.3 (2) |
C9—C10—C11—C12 | −175.9 (2) | N3—Ru—C45—C52 | −179.79 (19) |
C27—C10—C11—C12 | 4.1 (3) | C52—C45—C46—C47 | −90.1 (3) |
N3—C11—C12—C13 | 1.6 (3) | Ru—C45—C46—C47 | 86.7 (3) |
C10—C11—C12—C13 | −179.3 (2) | C52—C45—C46—C51 | 89.3 (3) |
C11—C12—C13—C14 | 0.8 (3) | Ru—C45—C46—C51 | −93.9 (3) |
C11—N3—C14—C15 | −175.3 (2) | C51—C46—C47—C48 | 1.1 (5) |
Ru—N3—C14—C15 | 13.8 (3) | C45—C46—C47—C48 | −179.5 (3) |
C11—N3—C14—C13 | 3.9 (2) | C46—C47—C48—C49 | −1.0 (6) |
Ru—N3—C14—C13 | −167.09 (15) | C47—C48—C49—C50 | 0.0 (7) |
C12—C13—C14—N3 | −3.0 (3) | C48—C49—C50—C51 | 0.9 (7) |
C12—C13—C14—C15 | 176.2 (2) | C49—C50—C51—C46 | −0.8 (6) |
N3—C14—C15—C16 | 1.1 (4) | C47—C46—C51—C50 | −0.3 (5) |
C13—C14—C15—C16 | −177.9 (2) | C45—C46—C51—C50 | −179.7 (3) |
N3—C14—C15—C33 | −179.2 (2) | C46—C45—C52—F1 | 110.7 (2) |
C13—C14—C15—C33 | 1.7 (3) | Ru—C45—C52—F1 | −66.1 (3) |
C19—N4—C16—C15 | −176.3 (2) | C46—C45—C52—F3 | −9.1 (3) |
Ru—N4—C16—C15 | −2.3 (3) | Ru—C45—C52—F3 | 174.08 (19) |
C19—N4—C16—C17 | 2.6 (2) | C46—C45—C52—F2 | −129.5 (2) |
Ru—N4—C16—C17 | 176.62 (15) | Ru—C45—C52—F2 | 53.7 (3) |
Symmetry code: (i) −x+1, −y+1, −z+1. |
Experimental details
Crystal data | |
Chemical formula | [Ru(C44H28N4)(C8H5F3)] |
Mr | 871.89 |
Crystal system, space group | Triclinic, P1 |
Temperature (K) | 296 |
a, b, c (Å) | 11.131 (1), 12.634 (2), 15.749 (2) |
α, β, γ (°) | 101.713 (9), 110.133 (8), 102.15 (1) |
V (Å3) | 1939.2 (5) |
Z | 2 |
Radiation type | Mo Kα |
µ (mm−1) | 0.46 |
Crystal size (mm) | 0.20 × 0.20 × 0.20 |
Data collection | |
Diffractometer | Rigaku AFC-7R diffractometer |
Absorption correction | – |
No. of measured, independent and observed [I > 2σ(I)] reflections | 9374, 8916, 7578 |
Rint | 0.017 |
(sin θ/λ)max (Å−1) | 0.650 |
Refinement | |
R[F2 > 2σ(F2)], wR(F2), S | 0.031, 0.077, 1.03 |
No. of reflections | 8916 |
No. of parameters | 541 |
H-atom treatment | H-atom parameters constrained |
Δρmax, Δρmin (e Å−3) | 0.37, −0.46 |
Computer programs: MSC/AFC Diffractometer Control Software (Molecular Structure Corporation, 1993), CrystalStructure (Rigaku/MSC, 2007), SHELXS97 (Sheldrick, 2008), SHELXL97 (Sheldrick, 2008), ORTEP-3 for Windows (Farrugia, 1997).
H37···C3i | 2.79 | H38···C1i | 2.86 |
H37···C4i | 2.72 |
Symmetry code: (i) −x+1, −y+1, −z+1. |
References
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Ruthenium(II)-porphyrin-carbene complexes have been studied as effective and stereoselective catalysts for cyclopropanation or epoxidation of some alkenes (Che & Huang, 2002). In order to improve their robustness, activity or selectivity toward the reactions a number of compounds have been invented and applied for the reactions under different conditions (Li et al., 2004; Wada et al., 2008). It is important to introduce fluorine atom(s) for a tuning of the catalysts, taking advantage of its high electronegativity (Seebach, 1990). Surveying the carbene complexes of transition metals, few crystal structures of fluorinated alkylidene complexes have been known, especially in that fluorine atom(s) is attached to the β-carbon atom adjacent to the carbene carbon (α-carbon) atom. With ruthenium(II)-tetraphenylporphyrinate (tpp), we have prepared a highly stable fluorinated alkylidene complex [Ru(tpp){═C(CF3)Ph}] (I), and present here its X-ray structure that features the trifluoromethyl group attached to the carbene carbon atom directly.
As shown in Fig. 1, the five-coordinate ruthenium atom is bound to the carbene carbon atom to which the phenyl and trifluoromethyl groups are attached, lying in a distorted square-pyramidal geometry in (I). There seems to be no remarkable difference in the bond lengths and angles about the carbene carbon atom, compared with those for the five-coordinate ruthenium(II)-porphyrin analogs reported so far, in the ranges 1.82–1.87 Å and 111–118° (Li et al., 2004; Wada et al., 2008). The porphyrin core in (I) is deformed in domed conformation with maximum and minimum deviations from the C20N4 least-squares plane of 0.205 (2) and -0.209 (2) Å for N1 and C17, respectively. The trifluoromethyl group has so large van der Waals radius (2.7 Å) (Seebach, 1990) that the steric repulsion toward the porphyrin core would affect some structural features. The ruthenium atom is situated at 0.3301 (5) Å out of the C20N4 least-squares plane toward the carbene moiety in (I), while the displacements are 0.216 (2)–0.287 (1) Å in other tetraphenyl- or tetra(p-tolyl)porphyrin complexes (Wada et al., 2008). In addition, the Ru═C45 bond is slightly tilted from the normal to the C20N4 least-squares plane, as indicated by the larger C45═Ru—N1 angle [97.70 (8)°] than the C45═Ru—N3 [93.42 (8)°]. The projection of the phenyl and trifluoromethyl groups of the carbene ligand on to the porphyrin plane shows an eclipsed configuration with regard to the Ru—N bonds.
In the unit cell a pair of the porphyrin cores of [Ru(tpp){═C(CF3)Ph}] are arranged facing each other across an inversion center with a distance of ca 4.0 Å, which is too far for the face-to-face aromatic interaction. The closer distances might suggest CH···π interactions between the porphrin core and two H atoms of the phenyl group at meso-position of the neighboring porphyrin (Table 1; Hunter et al., 2001).