- PII
- 10.31857/S0044460X24020072-1
- DOI
- 10.31857/S0044460X24020072
- Publication type
- Article
- Status
- Published
- Authors
- Volume/ Edition
- Volume 94 / Issue number 2
- Pages
- 216-224
- Abstract
- Using the reaction of 2,4-di-(tert-butyl)-12-(4-methoxyphenyl)-10-methoxy-12H-quinoxalino[2,3-b]phenoxazine with π-electron acceptors such as tetracyanoquinodimethane and 3,6-di-(tert-butyl)-o-quinone) as an example it was shown that derivatives of this N,O-pentaheterocyclic system are effective electron donors that, under mild conditions, carry out electron transfer reactions with the formation of stable cation and anion radical structures.
- Keywords
- хиноксалино[2,3-b]феноксазины ион-радикалы тетрацианохинодиметан спектроскопия ЭПР молекулярная структура
- Date of publication
- 15.02.2024
- Year of publication
- 2024
- Number of purchasers
- 0
- Views
- 32
References
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