1993
DOI: 10.1016/0022-328x(93)86085-v
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Metallorganische chemie in fester phase: Umlagerungs-, eliminierungs-und additionsreaktionen von organometallverbindungen ohne solvens

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Cited by 27 publications
(17 citation statements)
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“…An interesting case of ligand displacement, in as much as that cleavage of a dimer is occurring in the solid state, comes from the reaction shown in scheme 2 in which Werner and co-workers [ 45 ] reported that addition of CO or ethene to a chloride-bridged Rh(I) dimer resulted in the generation of monomeric species, where two dative Rh–Cl bonds had been cleaved by CO or ethene. Other examples of ligand of displacement in the solid state have been reported.…”
Section: Stoichiometric Solid–gas Reactionsmentioning
confidence: 99%
“…An interesting case of ligand displacement, in as much as that cleavage of a dimer is occurring in the solid state, comes from the reaction shown in scheme 2 in which Werner and co-workers [ 45 ] reported that addition of CO or ethene to a chloride-bridged Rh(I) dimer resulted in the generation of monomeric species, where two dative Rh–Cl bonds had been cleaved by CO or ethene. Other examples of ligand of displacement in the solid state have been reported.…”
Section: Stoichiometric Solid–gas Reactionsmentioning
confidence: 99%
“…These findings were pivotal in the development of the "oxidative-addition" pathway for the formation of metal vinylidene complexes. [25,[40][41][42][43][44][45][46] Despite the initial reports in this area being published over 25 years ago, the precise mechanism that connects the three compounds has been the subject of a considerable number of recent experimental and theoretical studies. Much of this work has been focused specifically on the conversion of the alkynyl hydride species to the corresponding vinylidene complexes.…”
Section: In a Series Of Pioneering Studies Werner Established That Tmentioning
confidence: 99%
“…Conversely, the corresponding h 3 -2,3,4-trans-butadienyl complexes are obtained in benzene solution at 50°C [136]. Furthermore, the quantitative rearrangement of the rhodium complex 426 to give 427 is stereoselective [137]. Further reactions of that type are reported [137].…”
Section: Cycloadditionmentioning
confidence: 99%
“…Furthermore, the quantitative rearrangement of the rhodium complex 426 to give 427 is stereoselective [137]. Further reactions of that type are reported [137].…”
Section: Cycloadditionmentioning
confidence: 99%