The electrochemical behaviour of the title complex shows two reversible le oxidations centred on the ferrocenyl moieties, indicating a moderate electronic communication between such redox units through the organic chain and the Pt binge. Moreover, two irreversible le reductions are detected, and assigned to the stepwise Pt-II-->Pt-0 process. The transient Pt-I intermediate is somewhat stabilized by the electronic delocalization over the external ferrocenyl units. The assignment of the redox processes is carried out by comparison of the electrochemical behaviour of several model complexes, which represent the building blocks of the overall molecule.
ELECTRON-TRANSFER IN TRANS-[PT(PPH(3))(2)(-C-C-FC)(2)] AND RELATED-COMPOUNDS / D., Osella; O., Gambino; C., Nervi; M., Ravera; Russo, Maria Vittoria; G., Infante. - In: INORGANICA CHIMICA ACTA. - ISSN 0020-1693. - 225:(1994), pp. 35-40. [10.1016/0020-1693(94)04026-5]
ELECTRON-TRANSFER IN TRANS-[PT(PPH(3))(2)(-C-C-FC)(2)] AND RELATED-COMPOUNDS
RUSSO, Maria Vittoria;
1994
Abstract
The electrochemical behaviour of the title complex shows two reversible le oxidations centred on the ferrocenyl moieties, indicating a moderate electronic communication between such redox units through the organic chain and the Pt binge. Moreover, two irreversible le reductions are detected, and assigned to the stepwise Pt-II-->Pt-0 process. The transient Pt-I intermediate is somewhat stabilized by the electronic delocalization over the external ferrocenyl units. The assignment of the redox processes is carried out by comparison of the electrochemical behaviour of several model complexes, which represent the building blocks of the overall molecule.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
