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- W2131801068 endingPage "443" @default.
- W2131801068 startingPage "435" @default.
- W2131801068 abstract "Abstract An analysis of the conjugative possibilities of dienes carrying two terminal heteroatom donors shows some generalizations of these as possible redox‐active (redox “noninnocent”) ligands. If the two E=C functionalities (E = O,S, NR, CHR) are connected by an odd number of sp 2 ‐hybridized atoms, full conjugation between the two terminal E donors is not possible, a situation which is found both in 2,6‐bis(imino)pyridine (BIMPY) and beta‐diketiminate ligands; the character of their redox noninnocence is thus altered, compared to 1,4‐diheterodienes. Some insight into the BIMPY ligand comes from the analog where one imino arm is absent. The traditional stereochemical relationships which govern conjugation in arenes are analyzed for their implications for different bis(imino)pyridine isomers, and also for 2,6‐dipyrimidyl‐ and dipyridazinyl‐pyridines, as generalizations of the classic terpyridyl ligands. Factors which favor oxidized vs. reduced ligand forms are discussed." @default.
- W2131801068 created "2016-06-24" @default.
- W2131801068 creator A5034052449 @default.
- W2131801068 date "2011-11-14" @default.
- W2131801068 modified "2023-10-07" @default.
- W2131801068 title "Systematics and Future Projections Concerning Redox‐Noninnocent Amide/Imine Ligands" @default.
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