Das gleiche Redoxverhalten — nur mit entgegengesetztem Vorzeichen — zeigen die lange bekannten p-Phenylendiamine 1, R  Alkyl, Aryl, und das neue B,B,B′,B′-Tetramesityl-p-phenylendiboran 2. Elektrochemische und ESR/ENDOR-Untersuchungen lassen erkennen, daß der Dimesitylboryl-Substituent in bezug auf die Acceptorstärke nur noch von der Nitrogruppe übertroffen wird.

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Volume96, Issue8

August 1984

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p-Phenylendiamine Spiegelbild der p-Phenylendiamine?

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p-Phenylendiamine Spiegelbild der p-Phenylendiamine?

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