Abstract
Although many stable disilenes (silicon-silicon doubly-bonded compounds) containing organic π-electron systems have been reported, stable disilenes with heteroaromatic groups remain rare. Herein, we report the synthesis of monodisilenyl-substituted thiophene 1, anthracene 4, acridine 5, and mesitylene 7 and bis(disilenyl)-substituted thiophene 2, 2,2′-bithiophene 3, and anthracene 6via reactions of dialkylmesityldisilenide 8 with the corresponding haloarenes. Disilenes 1-7 show absorption bands with contributions of intramolecular charge transfer (ICT) transitions from π(disilene) to π∗(aryl). In the ICT transitions, (bi)thienyl groups as well as anthryl and acrydinyl groups serve as electron acceptors for the Si=Si double bonds.
Original language | English |
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Pages (from-to) | 11271-11281 |
Number of pages | 11 |
Journal | Dalton Transactions |
Volume | 46 |
Issue number | 34 |
DOIs | |
Publication status | Published - 2017 |