Expedient Synthesis of Substituted Thieno[3,2-b]thiophenes and Selenopheno[3,2-b]selenophenes Through Cascade Cyclization of Alkynyl Diol Derivatives

Thieno[3,2-<i>b</i>]thiophenes are used as key components in optoelectronic materials, porous hydrogen-storage hosts, organic solar cells, and polymer semiconductors. A step-efficient synthetic protocol was proposed herein for obtaining multisubstituted thieno[3,2-<i>b</i>]thiophene and selenopheno[3,2-<i>b</i>]selenophenes in moderate to good yields via the bisulfur/biselenium cyclization of alkynyl diols with I<sub>2</sub>/Na<sub>2</sub>S<sub>2</sub>O<sub>3</sub> or selenium. Using this strategy, substitution patterns were obtained for backbone modification in functional materials.

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Publication Details

Journal
Molecules
Published
2024-11-21
DOI
https://doi.org/10.3390/molecules29235507
Citations
1
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.25

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article

Expedient Synthesis of Substituted Thieno[3,2-b]thiophenes and Selenopheno[3,2-b]selenophenes Through Cascade Cyclization of Alkynyl Diol Derivatives

Ziqing He, Yibiao Li, Xiai Luo, Mengying Zhao et al.
1 citations
Molecules
Sulfur-Based Synthesis Techniques
0.25
article

Expedient Synthesis of Substituted Thieno[3,2-b]thiophenes and Selenopheno[3,2-b]selenophenes Through Cascade Cyclization of Alkynyl Diol Derivatives

Ziqing He, Yibiao Li, Xiai Luo, Mengying Zhao, Lu Chen, Xuelin Zhang, Yingqi Feng
article en
1 citations

Abstract

Thieno[3,2-<i>b</i>]thiophenes are used as key components in optoelectronic materials, porous hydrogen-storage hosts, organic solar cells, and polymer semiconductors. A step-efficient synthetic protocol was proposed herein for obtaining multisubstituted thieno[3,2-<i>b</i>]thiophene and selenopheno[3,2-<i>b</i>]selenophenes in moderate to good yields via the bisulfur/biselenium cyclization of alkynyl diols with I<sub>2</sub>/Na<sub>2</sub>S<sub>2</sub>O<sub>3</sub> or selenium. Using this strategy, substitution patterns were obtained for backbone modification in functional materials.

MoleculesVol. 29(23)
Hunan University of Traditional Chinese Medicine (CN), Wuyi University (CN)
Department of Education of Guangdong Province
Openalex Percentile: Top 46%
Sulfur-Based Synthesis Techniques
0.25
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