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Luminescent charge-transfer complexes of 4,4′-bipyridinium ion with tetrakis[3,5-bis(trifluoromethyl)phenyl]borate anion

✍ Scribed by Toshihiko Nagamura; Kenkichi Sakai


Publisher
Elsevier Science
Year
1987
Tongue
English
Weight
416 KB
Volume
141
Category
Article
ISSN
0009-2614

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✦ Synopsis


4,4'-bipyridinium ions form ion-pair charge-transfer (CT) complexes with tetrakis[3,5-bis(trifluoromethyl)phenyl]borate anion with a discrete absorption maximum at 420 nm in methanol and at 475 nm in 1,2-dimethoxyethane. These CT complexes in 1,2_dimethoxyethane at 20°C show broad structureless luminescence with a maximum at 553 nm, almost a mirror image of the CT absorption spectrum. The luminescence could not be observed for CT complexes in methanol. This is the first observation of luminescence from excited ion-pair CT complexes in solutions at room temperature.


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## Abstract Four iridium complexes with achiral phosphino‐oxazoline (PHOX) ligands were readily prepared in two steps starting from commercially available phenyloxazolines. The air‐stable complexes with tetrakis[3,5‐bis(trifluoromethyl)phenyl]borate (BAr~F~) as counterion showed high reactivity in