Novel Approach to the Synthesis of Bithiophenesilane Dendrimers with Efficient Intramolecular Energy Transfer

M. S. Skorotetskii; Скоротецкий М. С.; O. V. Borshchev; Борщев О. В.; E. A. Kleimyuk; Клеймюк Е. А.; E. A. Svidchenko; Свидченко Е. А.; N. M. Surin; Сурин Н. М.; S. A. Ponomarenko; Пономаренко С. А.

doi:10.31857/S2308114723700425

Novel Approach to the Synthesis of Bithiophenesilane Dendrimers with Efficient Intramolecular Energy Transfer

Authors: Skorotetskii M.S.¹, Borshchev O.V.¹, Kleimyuk E.A.¹, Svidchenko E.A.¹, Surin N.M.¹, Ponomarenko S.A.¹^,2
Affiliations:
1. Enikolopov Institute of Synthetic Polymeric Materials, Russian Academy of Sciences
2. Department of Chemistry, Moscow State University
Issue: Vol 65, No 2 (2023)
Pages: 235-244
Section:
URL: https://journals.rcsi.science/2308-1147/article/view/232919
DOI: https://doi.org/10.31857/S2308114723700425
EDN: https://elibrary.ru/GCMGQJ
ID: 232919

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Abstract

A synthetic scheme allowing the preparation of nanostructured organosilicon luminophores of branched or dendritic structure with up to 18 bithiophenesilane donor fragments and one central acceptor fragment has been elaborated. This universal scheme has been successfully upscaled to 20 g of the product, and its efficiency has been verified by the synthesis of two earlier unknown bithiophenesilane dendrimers with dense molecular shell and the central acceptor fragment, 1,4-bis(5-phenylthienyl-2-yl)benzene. The synthesis of more branched dendrimers under the Suzuki reaction conditions has led to the formation of the side products with the rupture of the Si–C(thiophene) bond, not typical of the synthesis of analogous compounds with lower branching degree under the same conditions.

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