Electrochemical behaviour of tropone diiron pentacarbonyl complexes, Fe2(CO)5[(RC2R)3CO] (R=Me, Et, n-Pr). Formation of a carbon-carbon bond upon reduction
摘要:
We herein describe the electrochemical behaviour of some tropone diiron pentacarbonyl complexes Fe2(CO)5[(RC2R)3CO] (R=Et, Me, n-Pr). All these compounds exhibit a cyclic voltammetric (CV) response consisting of an electrochemically and chemically reversible one-electron reduction process at moderate cathodic potentials and a totally irreversible further reduction at c. -2 V versus SCE. At-root temperature (in the long electrolysis time scale) the electrogenerated monoanion Fe2(CO)5[(RC2R)3CO]- smoothly but completely decomposes to Fe(CO)3[(RC2R)3CO]. In this process the organic chain rearranges, and a new C-C bond is formed.
Tricarbonylbis(.eta.2-cis-cyclooctene)iron: photochemical synthesis of a versatile tricarbonyliron source for olefin isomerization and preparative applications
作者:Helmut Fleckner、Friedrich Wilhelm Grevels、Dieter Hess
DOI:10.1021/ja00319a021
日期:1984.4
Preparation par reaction photochimique a −40°C. La reaction thermique avec le pentene-1 resulte en une isomerisation de l'alcene
制备标准反应photochimique a -40°C。La 反应热反应 戊烯-1 结果 en une isomerisation de l'alcene