Issue 15, 2019

Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties

Abstract

The reaction of several azulenylalkynes having an aryl substituent with elemental sulfur afforded the corresponding azuleno[2,1-b]thiophenes in moderate to good yields. Decarboxylation of an azuleno[2,1-b]thiophene derivative with an ester function was also achieved by treatment with 100% H3PO4. The structural features of the azuleno[2,1-b]thiophene derivatives were revealed by X-ray single-crystal analysis. The optical and electrochemical properties of the azuleno[2,1-b]thiophene derivatives were investigated by UV/Vis spectroscopy, voltammetry experiments and theoretical calculations.

Graphical abstract: Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties

Supplementary files

Article information

Article type
Research Article
Submitted
03 May 2019
Accepted
20 Jun 2019
First published
20 Jun 2019

Org. Chem. Front., 2019,6, 2801-2811

Synthesis of azuleno[2,1-b]thiophenes by cycloaddition of azulenylalkynes with elemental sulfur and their structural, optical and electrochemical properties

T. Shoji, K. Miura, A. Ohta, R. Sekiguchi, S. Ito, Y. Endo, T. Nagahata, S. Mori and T. Okujima, Org. Chem. Front., 2019, 6, 2801 DOI: 10.1039/C9QO00593E

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