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/).
引用
收藏
页数:4
相关论文
共 50 条
  • [1] Redox-Active Monopyrrolotetrathiafulvalene-Based Rotaxane Incorporating the Dihydroazulene/Vinylheptafulvene Photo/Thermoswitch
    Kilde, Martin Drohse
    Kristensen, Rikke
    Olsen, Gunnar
    Jeppesen, Jan O.
    Nielsen, Mogens Brondsted
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2019, 2019 (31-32) : 5532 - 5539
  • [2] Design of π-extended dipyranylidenes as redox-active materials
    Courte, Marc
    Ng, Yong Xiang
    Tang, Shasha
    Fichou, Denis
    DYES AND PIGMENTS, 2021, 194
  • [3] Redox-active 17- and 19-membered metallamacrocycles incorporating tetrathiafulvalene
    Gachot, Gregory
    Pellon, Pascal
    Roisnel, Thierry
    Lorcy, Dominique
    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2006, (13) : 2604 - 2611
  • [4] Redox-Active Organic Materials: From Energy Storage to Redox Catalysis
    Kim, Jaehwan
    Ling, Jianheng
    Lai, Yihuan
    Milner, Phillip J.
    ACS MATERIALS AU, 2024, 4 (03): : 258 - 273
  • [5] Synthesis of Covalently Linked Oligo(phenyleneethynylene) Wires Incorporating Dithiafulvene Units: Redox-Active "H-Cruciforms"
    Jorgensen, Frederik Praestholm
    Petersen, Johannes F.
    Andersen, Cecilie Lindholm
    Skov, Anders B.
    Jevric, Martyn
    Hammerich, Ole
    Nielsen, Mogens Brondsted
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2017, 2017 (09) : 1253 - 1261
  • [6] Redox-active tetraaryldibenzoquinodimethanes
    Ishigaki, Yusuke
    Sugawara, Kazuma
    Tadokoro, Tomoki
    Hayashi, Yuki
    Harimoto, Takashi
    Suzuki, Takanori
    CHEMICAL COMMUNICATIONS, 2021, 57 (59) : 7201 - 7214
  • [7] Cyclic Conductance Switching in Networks of Redox-Active Molecular Junctions
    Liao, Jianhui
    Agustsson, Jon S.
    Wu, Songmei
    Schoenenberger, Christian
    Calame, Michel
    Leroux, Yann
    Mayor, Marcel
    Jeannin, Olivier
    Ran, Ying-Fen
    Liu, Shi-Xia
    Decurtins, Silvio
    NANO LETTERS, 2010, 10 (03) : 759 - 764
  • [8] Redox-Active Boron Clusters
    Ready, Austin D.
    Nelson, Yessica A.
    Pomares, Daniel F. Torres
    Spokoyny, Alexander M.
    ACCOUNTS OF CHEMICAL RESEARCH, 2024, 57 (09) : 1310 - 1324
  • [9] Amino-Substituted Azoxybenzenes as Potential Redox-Active Catholyte Materials
    Schatz, Dominic
    Burdenski, Chris
    Schneider, Finn M.
    Hansmann, Max M.
    Wegner, Hermann A.
    CHEMISTRY-A EUROPEAN JOURNAL, 2025,
  • [10] A singly bonded gallanediyl with redox-active and redox-inert reactivity
    Schreiner, Simon H. F.
    Rueffer, Tobias
    Kretschmer, Robert
    NATURE SYNTHESIS, 2025, 4 (01): : 67 - 74