Rourke, J.P. ![]() |
Abstract
The mechanism of formation of mer,trans-[(PMe3)3Rh(−C⋮C−R)2H] from [(PMe3)4Rh(Me)] and terminal alkyne has been studied. The initial step of the reaction is the elimination of methane and the formation of the trigonal bipyramidal complex [(PMe3)4Rh(−C⋮C−R)], a reaction that is complete in time of mixing at −78 °C. This intermediate undergoes an oxidative addition reaction with a second equivalent of alkyne to give fac-[(PMe3)3Rh(−C⋮C−R)2H] as the kinetic product. This fac isomer is not stable above −20 °C and isomerizes to the thermodynamic product mer,trans-[(PMe3)3Rh(−C⋮C−R)2H]. fac-[(PMe3)3Rh(−C⋮C−R)2H] will exchange alkynyl groups with free alkyne, a reaction that has a lower energetic barrier than the isomerization to mer,trans-[(PMe3)3Rh(−C⋮C−R)2H]. Density functional theory studies on all stages of the formation of mer,trans-[(PMe3)3Rh(−C⋮C−R)2H] have been carried out and give ground state energies in line with those experimentally observed. Once formed, mer,trans-[(PMe3)3Rh(−C⋮C−R)2H] is configurationally stable and not prone to scrambling, although it will react with chloroform, whereupon the hydride is replaced by chloride. The initial product of this reaction is mer,trans-[(PMe3)3Rh(−C⋮C−R)2Cl], and this compound has been studied by single-crystal X-ray diffraction. In solution mer,trans-[(PMe3)3Rh(−C⋮C−R)2Cl] isomerizes slowly to mer,cis-[(PMe3)3Rh(−C⋮C−R)2Cl].
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Schools > Chemistry |
Publisher: | American Chemical Society |
ISSN: | 0276-7333 |
Last Modified: | 05 Apr 2023 14:45 |
URI: | https://orca.cardiff.ac.uk/id/eprint/155208 |
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