p-Diphenoquinone analogs extended by dihydrothiophenediylidene insertion. A novel amphoteric multistage redox system
K Takahashi, T Suzuki
Index: Takahashi, Kazuko; Suzuki, Tsuyoshi Journal of the American Chemical Society, 1989 , vol. 111, # 14 p. 5483 - 5485
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Citation Number: 31
Abstract
Chart 1 1: n= l 2: n= 2 10a: n= l lob: n= 2 3: n= 3 4: n= 4 1Oc: n= 3 10d: n= 4 rings of diphenoquinone, that is 2, 5-bis (4-oxo-2, 5-cyclo-hexadien-1-ylidene)-2, 5- dihydrothiophene and its oligodihydrothiophene analogues. In such a system, amphotericity can be enhanced by the conjugated sp2 carbon chain and the heteroaromatic stabilization of the corresponding radical ions and divalent ions created through the redox processes. ...
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