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A delocalized cobaltoviologen with seven reversibly accessible redox states and highly tunable electrochromic behaviour
Co II mediates electronic coupling between two N -Me-pyridinium-terpyridine ligands that are related to redox-active N , N -dialkyl-4,4′-bipyridinium dications (viologens). Borderline Class II/III electronic delocalization imparts the cobaltoviologen complex with distinct electronic properties ( e.g...
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Published in: | Chemical communications (Cambridge, England) England), 2020-11, Vol.56 (89), p.13864-13867 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Co
II
mediates electronic coupling between two
N
-Me-pyridinium-terpyridine ligands that are related to redox-active
N
,
N
-dialkyl-4,4′-bipyridinium dications (viologens). Borderline Class II/III electronic delocalization imparts the cobaltoviologen complex with distinct electronic properties (
e.g.
, 7 accessible redox states) relative to those of viologens, leading to enhanced electrochromism.
Cobalt was found to mediate strong electronic coupling between two viologen-like redox-active ligands, providing electrochromic properties that are easily tuned by the applied redox potential. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d0cc05627h |