Incorporating sulfur into redox-active reagents and materials

被引:0
作者
Beil, Sebastian B. [1 ]
Wonink, Marco B. S. [1 ]
Feringa, Ben L. [1 ]
机构
[1] Univ Groningen, Stratingh Inst Chem, Nijenborgh 7, NL-9747 AG Groningen, Netherlands
关键词
Hianthrene; Tetrathiafulvalene; Redox chemistry; Synthesis; Materials; TETRATHIAFULVALENE; DERIVATIVES; REDUCTION; ALKENES;
D O I
10.1016/j.tet.2023.133262
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Small sulfur-containing heterocycles, like thianthrenes and tetrathiafulvalenes, together with their larger is-extended counterparts, represent a long-known structural motif and offer reversible redox chemistry at low potentials. Recently these motifs gained an increasing interest in a variety of fields circulating organic chemistry ranging from molecular switches and redox reagents in synthesis to supramolecular aggregates. We anticipate fruitful developments from these versatile building blocks in modern tech-nologies based on their reversible redox properties.(c) 2023 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
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页数:4
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