Structure and reactivity in neutral organic electron donors derived from 4-dimethylaminopyridine
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The effects on the redox properties of modifying the molecular skeleton of neutral bis-2-(4-dimethylamino)pyridinylidene electron donors, derived from 4-dimethylaminopyridine (4-DMAP), have been explored, by varying two parameters: (i) the length of a polymethylene chain linking the two pyridine-derived rings and (ii) the nature of the nitrogen substituents on the 4 and 4′ positions of the precursor pyridines. Restricting the bridge length to two methylene units significantly altered the redox profile, while changes in the nitrogen-substituents at the 4 and 4′ positions led to only slight changes in the redox potentials.
2011 ◽
Vol 15
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pp. 883-889
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1998 ◽
Vol 269
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pp. 260-268
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2018 ◽
Vol 57
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pp. 3148-3153
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1999 ◽
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pp. 1771-1807
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1983 ◽
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pp. 1600-1603
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2015 ◽
Vol 54
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pp. 11236-11239
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2018 ◽
Vol 140
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pp. 11510-11518
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