1988
DOI: 10.1016/0022-328x(88)89094-6
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Synthesis of complexes with tungstencobalt bonds via alkylidyne group coupling reactions; crystal structure of the compound [Wco{μ-C(C6H4Me-4)C(O)C(C6H4Me-4)}(CO)5(η-C5H5)]

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Cited by 14 publications
(7 citation statements)
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“…NMR spectral data (of the 11a,b mixture, acetone-de, <5, ppm) are as follows: 11a, 5.13 (Cp), 3.36 (OMe), 1.92, 1.84, 1.442, 1.435, 1.414, 1.382, 1.306, 0.712 (Me signals); lib, 5.08 (Cp), 3.34 (OMe), 2.17, 2.12,1.79, 1.60,1.34,1.25,1.11, 0.66 (Me signals). 13C NMR spectral data (of 11a,b mixture, acetone-dg, ó, ppm) 11a, 248.9 (CO), 246.3 (CO), 141.5, 132.7, 106.1, 104.6, 102.7, 101.8, 99.8, 91.5 (Cp), 60.2, 57.0, 32.3 (Me), 23.8 (Me), 23.4 (Me), 11.6 (Me), 10.8 (Me), 10.5 (Me), 8.0 (Me), 7.7 (Me); lib, 251.9 (CO), 246.8 (CO), 150.4, 133.4, 110.6, 104.7, 103.1, 101.2, 91.5 (Cp), 57.2, 55.0, 23.3 (Me), 22.2 (Me), 11.1 (Me), 11.0 (Me), 9.4 (Me), 8.5 (Me). 0)Cp]+BF4- (7).…”
Section: Methodsmentioning
confidence: 99%
“…NMR spectral data (of the 11a,b mixture, acetone-de, <5, ppm) are as follows: 11a, 5.13 (Cp), 3.36 (OMe), 1.92, 1.84, 1.442, 1.435, 1.414, 1.382, 1.306, 0.712 (Me signals); lib, 5.08 (Cp), 3.34 (OMe), 2.17, 2.12,1.79, 1.60,1.34,1.25,1.11, 0.66 (Me signals). 13C NMR spectral data (of 11a,b mixture, acetone-dg, ó, ppm) 11a, 248.9 (CO), 246.3 (CO), 141.5, 132.7, 106.1, 104.6, 102.7, 101.8, 99.8, 91.5 (Cp), 60.2, 57.0, 32.3 (Me), 23.8 (Me), 23.4 (Me), 11.6 (Me), 10.8 (Me), 10.5 (Me), 8.0 (Me), 7.7 (Me); lib, 251.9 (CO), 246.8 (CO), 150.4, 133.4, 110.6, 104.7, 103.1, 101.2, 91.5 (Cp), 57.2, 55.0, 23.3 (Me), 22.2 (Me), 11.1 (Me), 11.0 (Me), 9.4 (Me), 8.5 (Me). 0)Cp]+BF4- (7).…”
Section: Methodsmentioning
confidence: 99%
“…Two cobalt-tungsten heterobimetallic complexes are obtained: µ-RCtCR′ species 128 (for all combinations of 127 and 3 attempted) and complexes 129 (formed in the reactions of 127a with 3b and 3e only), in which there are bridging CTol-CO-CTol groups as summarized in the scheme. 138…”
Section: Carbyne−carbyne Couplingmentioning
confidence: 99%
“…The product is the µ-PhCtCPh complex 128m, shown in Scheme 149, which is believed to form by ring opening of the organic ligand and coordination of the resulting CPh-CPh-CO group onto the dimetal center, followed by decarbonylation. 138 The bridging organic ligand that spans the iron-platinum bond in 243 shown in Scheme 150 is formed by the coupling of allene with a carbonyl ligand (see Scheme 129). When refluxed in benzene, this molecule eliminates CO and forms the allene complex 271 of unusual geometry.…”
Section: Carbon−carbon Bond Cleavage By Other Decarbonylation Reactionsmentioning
confidence: 99%
“…401 Cyclopropenones are known to give some dinuclear metal complexes and complexes with a metal- containing cluster. When treated with Pt 3 (CNBu t ) 6 402 and WCo(CO) 7 (η-C 5 H 5 ), 403 diarylcyclopropenones underwent cleavage of the CdC bond, forming homoand heterodinuclear complexes 439 and 440, respectively. The reaction of diphenylcyclopropenethione with Fe 2 (CO) 9 gave a complex having a triafulvene structure 441 and a carbene complex 442.…”
Section: H Formation Of Metal Complexesmentioning
confidence: 99%