Bi Youan E Tra,Yujie Zhao,Andrew Molino,Yifu Ouyang,Chun-Lin Deng,Colleen McAloon,Noah D McMillion,Heechan Kim,Chonghe Zhang,Peter Müller,Robert G Griffin,Robert J Gilliard
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Diboron-Incorporated Indenofluorene: Isolation of Crystalline Neutral and Reduced States of 6,12-Diboraindeno[1,2-b]fluorene.
The synthesis and redox transformations of 6,12-diboraindeno[1,2-b]fluorene (DBIF)─a pentacyclic π-system with diboron incorporation─are reported. In notable contrast to the all-hydrocarbon indenofluorenes, a ligand coordination and reduction strategy allows tuning of the electronic structure across four redox states. Accordingly, we introduce an 18π e- neutral DBIF, a 20π e- diradical, a 21π e- radical anion, and a 22π e- dianion, all of which have been isolated and structurally authenticated. The diradicals exhibit diradical character of up to 77% and possess open-shell singlet ground states with thermally accessible triplet states.
期刊介绍:
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