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Four-Stage Amphoteric Redox Properties and Biradicaloid Character of Tetra-tert-butyldicyclopenta[b;d]thieno[1,2,3-cd;5,6,7-c′d′]diphenalene

✍ Scribed by Takashi Kubo; Maki Sakamoto; Minako Akabane; Yoshinori Fujiwara; Kagetoshi Yamamoto; Motoko Akita; Katsuya Inoue; Takeji Takui; Kazuhiro Nakasuji


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
347 KB
Volume
43
Category
Article
ISSN
0044-8249

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✦ Synopsis


Dedicated to Emeritus Professor Ichiro Murata on the occasion of his 75th birthday

Phenalenyl-based hydrocarbons possess highly amphoteric redox properties that give low oxidation and high reduction potentials and afford stable multivalent redox species. [1] These compounds have frontier orbitals with a nonbonding molecular orbital (NBMO) character that results from a weak perturbation between singly occupied molecular orbitals (SOMOs) of the phenalenyl radical and the frontier orbitals of a central conjugated system. This perturbation leads to a [


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