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
No coin nor oath required. For personal study only.
✦ 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 [
📜 SIMILAR VOLUMES
Tetra-tert-butyl-as-indaceno[1,2,3-cd:6,7,8-c%d%]diphenalene (TTB-as-IDPL) was prepared and found to behave as a four-stage amphoteric redox compound. The properties of its five redox states were investigated.