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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
来源:
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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