SUBSTITUENT EFFECTS ON THE ALKYL MIGRATION REACTION IN BENZYL MANGANESE(I) AND IRON(II) SYSTEMS

Citation
Jam. Andersen et Jr. Moss, SUBSTITUENT EFFECTS ON THE ALKYL MIGRATION REACTION IN BENZYL MANGANESE(I) AND IRON(II) SYSTEMS, South African Journal of Chemistry, 50(3), 1997, pp. 144-152
Citations number
30
ISSN journal
03794350
Volume
50
Issue
3
Year of publication
1997
Pages
144 - 152
Database
ISI
SICI code
0379-4350(1997)50:3<144:SEOTAM>2.0.ZU;2-C
Abstract
Several new benzyl compounds of the types [Mn(CH2C6H4X)(CO)(5)] and [C pFe{(CH2)(n)C6H4X}(CO)(2)] have been synthesised. The manganese deriva tives underwent a facile alkyl migration upon reaction with triphenylp hosphine to form cis-tetracarbonyl acyl compounds. A linear free energ y relationship was found to exist for this reaction and a value of -0. 94 was obtained for rho, the sensitivity parameter. The iron derivativ es were generally much less reactive, although the phenylethyl (n = 2, X = H) and phenylpropyl (n = 3, X = H) species did react with triphen ylphosphine to give phosphine substituted acyl compounds.