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• W2044725935 abstract "The mixed ligand P2CuN2 copper(I) complexes [Cu(PPh3)2(MeCN)2]X have been studied by one- and two-dimensional 31P CP MAS NMR spectroscopy for X = PF6, BF4 or ClO4 and single crystal X-ray diffraction for X = PF6 and ClO4, completing availability of precise structural data for this isomorphous series. The compounds crystallise as discrete cations and anions in space group P21/n with a ≈ 15, b ≈ 27, c ≈ 9 Å, β = 95°, Z = 4. The anion is located ca. 6 Å from the copper atom and adjacent to a cleft formed between the acetonitrile ligands and phosphine ligand 2 while the crystallographically independent PPh3 ligands adopt staggered three-bladed propeller-type conformations of opposite chirality. The geometric symmetry of the P2CuN2 co-ordination sphere is low with Cu–P(1) 2.276(4)–2.287(2), Cu–P(2) 2.258(4)–2.269(1) Å, Cu–N 2.023(9)–2.053(3) Å, P–Cu–P 126.82(4)–127.73(5), N–Cu–N 99.5(4)–100.3(1), P(1)–Cu–N 100.87(8)–102.34(9) and P(2)–Cu–N 110.4(1)–111.9(3)°. One- and two-dimensional solid state 31P CP MAS NMR spectra of the compounds at 9.40 T show chemical shift differences of 6 ppm between the signals arising from the two P sites which form part of an ABX spin system with 1J[31P(1)–63Cu] 1.13–1.14 kHz, 1J[31P(2)–63Cu] 1.30 kHz and 2J(31P–31P) 75 Hz. The copper quadrupolar induced distortion of the line spacings is different for the two sites and is postulated to be a consequence of variation in the angle between the Cu–P vectors and the z axis of the electric field gradient tensor. The magnitude of the distortion is relatively small and consistent with small copper quadrupolar coupling constants for the compounds and a balanced electronic charge distribution about the copper(I) site in spite of the low geometric symmetry of the P2CuN2 co-ordination sphere." @default.
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• W2044725935 date "1998-01-01" @default.
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• W2044725935 title "Structural and 31P CP MAS NMR spectroscopic studies of the P2CuN2 copper(I) complexes [Cu(PPh3)2(MeCN)2]X for X = PF6, BF4 and ClO4" @default.
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• W2044725935 doi "https://doi.org/10.1039/a802383b" @default.
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