Phosphine photolabilisation studies of (eta(5)-C5H5)Fe(PPH3)(CO)-COR (R = Me, Ph, 2,6-C6B3F2) and (eta(5)-C5Me5)Fe(PPh3)(CO)-COR (R = Me, 2,6-C6H3F2)utilising NMR, laser desorption FT ICR MS and photofragmentation voltammetry analysis

Citation
Rt. Aplin et al., Phosphine photolabilisation studies of (eta(5)-C5H5)Fe(PPH3)(CO)-COR (R = Me, Ph, 2,6-C6B3F2) and (eta(5)-C5Me5)Fe(PPh3)(CO)-COR (R = Me, 2,6-C6H3F2)utilising NMR, laser desorption FT ICR MS and photofragmentation voltammetry analysis, J CHEM S P2, (5), 1999, pp. 913-922
Citations number
32
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
ISSN journal
03009580 → ACNP
Issue
5
Year of publication
1999
Pages
913 - 922
Database
ISI
SICI code
0300-9580(199905):5<913:PPSO((>2.0.ZU;2-1
Abstract
Photolysis of (eta(5)-C5Me5)Fe(CO)(PPh3)COR (R = 2,6-C6H3F2Me) leads to pre ferential loss of the phosphine ligand to form the corresponding alkyl spec ies (eta(5)-C5Me5)Fe(CO)(PPh3)R, while photolysis of (eta(5)-C5H5)Fe(CO)(PP h3)COR (R = Me, Ph, 2,6-C6H3F2) leads to loss of CO to form (eta(5)-C5H5)Fe (CO)(PPh3)R which subsequently undergoes rapid phosphine exchange. A mechan ism for this process is proposed which is corroborated using photofragmenta tion voltammetry. Laser desorption mass spectrometry was also used as a too l to probe whether phosphine loss was the primary photochemical process.