Issue 34, 2017

Heteroaryldisilenes: heteroaryl groups serve as electron acceptors for Si[double bond, length as m-dash]Si double bonds in intramolecular charge transfer transitions

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[double bond, length as m-dash]Si double bonds.

Graphical abstract: Heteroaryldisilenes: heteroaryl groups serve as electron acceptors for Si [[double bond, length as m-dash]] Si double bonds in intramolecular charge transfer transitions

Supplementary files

Article information

Article type
Paper
Submitted
30 Jun 2017
Accepted
26 Jul 2017
First published
11 Aug 2017

Dalton Trans., 2017,46, 11271-11281

Heteroaryldisilenes: heteroaryl groups serve as electron acceptors for Si[double bond, length as m-dash]Si double bonds in intramolecular charge transfer transitions

T. Kosai, S. Ishida and T. Iwamoto, Dalton Trans., 2017, 46, 11271 DOI: 10.1039/C7DT02357J

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