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Ferrocenyl‐Capped p ‐Phenylenediamine as a Redox‐Switching System
Author(s) -
Moriuchi Toshiyuki,
Takagi Yoshihiro,
Hirao Toshikazu
Publication year - 2008
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200800072
Subject(s) - chemistry , redox , moiety , conjugated system , non innocent ligand , combinatorial chemistry , photochemistry , polymer chemistry , stereochemistry , organic chemistry , polymer
Terminal redox‐active ferrocenyl groups were introduced into the redox‐active p ‐phenylenediamine bridging spacer, which can be oxidized to the p ‐quinonediimine, to provide a redox‐switching system with electronic communication between the ferrocenyl groups through the redox‐active π‐conjugated bridging spacer. The communication was controlled by redox interconversion between the p ‐phenylenediamine and p ‐quinonediimine spacers. Furthermore, two palladium complexes were demonstrated to be introduced to the oxidized quinonediimine moiety, affording the multimetallic complex, in which the complexed quinonediimine serves as an electron sink. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

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