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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >Synthesis and electrochemical properdties of pi-extended n-arylpyrrolo[3,4-d]tetrathia-fulvelenes
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Synthesis and electrochemical properdties of pi-extended n-arylpyrrolo[3,4-d]tetrathia-fulvelenes

机译:π-延伸的正芳基吡咯并[3,4-d]四硫代富勒烯的合成及电化学性质

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摘要

A series of pi-extended N-arylpyrrolo[3,4-d]tetrathiafulvalenes,N-aryl-2-[4,5-bis(ethylthio)-l,3-dithiole-2-ylidene]-(l,3)-dithiolo[4,5-c]pyrrole (3a-d) were prepared via cross-coupling of 4,5-bis(ethylthio)-l,3-dithiol-2-one (12) with N-aryl-(l,3)-dithiolo[4,5-c]pyrrole-2-thiones (lla-d).The latters were obtained by the reactions of 4,5-bis(bromomethyl)-l,3-dithiole-2-thione (8) with aromatic amines (9a-d).Electrochemical behavior of compounds (3a-d) was studied by means of cyclic voltammetry.It was found that all these compounds (3a-d) have comparable to or lower half-wave potentials than those of N-alkyl-pyrrolo[3,4-d]tetrathiafulvalenes (2a-c).
机译:一系列π-延伸的N-芳基吡咯并[3,4-d]四硫富瓦烯,N-芳基-2- [4,5-双(乙硫基)-1,3-二硫基-2-亚烷基]-(l,3)通过将4,5-双(乙硫基)-1,3-二硫基-2-酮(12)与N-芳基-(1)交叉偶联制备-二硫代[4,5-c]吡咯(3a-d)。 ,3)-二硫代[4,5-c]吡咯-2-硫酮(IIa-d)。后者是通过4,5-双(溴甲基)-1,3-二硫代-2-硫酮( 8)用芳香胺(9a-d),通过循环伏安法研究化合物(3a-d)的电化学行为,发现所有这些化合物(3a-d)的半波电势均低于或低于N-烷基-吡咯并[3,4-d]四硫富瓦烯(2a-c)的那些。

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