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首页> 外文期刊>Polimery >INVESTIGATIONS OF ELECTROCHEMICAL AND SPECTROELECTROCHEMICAL PROPERTIES (UV-Vis, EPR) OF THIOPHENE TRIMER DERIVATIVES SUBSTITUTED WITH PHENYLVINYL GROUPS
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INVESTIGATIONS OF ELECTROCHEMICAL AND SPECTROELECTROCHEMICAL PROPERTIES (UV-Vis, EPR) OF THIOPHENE TRIMER DERIVATIVES SUBSTITUTED WITH PHENYLVINYL GROUPS

机译:取代乙烯基乙烯基的噻吩三聚体衍生物的电化学和光谱化学性质(UV-Vis,EPR)的研究

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摘要

The results of investigations concerning electrochemical properties of two thiophene trimers derivatives substituted with phenylvinyl groups {3'[(E)-2-phenylethenyl]-2,2':5',2"-thiophene (monomer A) and 4,4"-didecyloxy-3'[(E)-2-phenylethenyl]-2,2':5',2"-thiophene (monomer B)} and the products of their oxidation were discussed. Electropolymerizations of A and B monomers were carried out with use of cyclic voltammetry and electrochemical measurements were coupled in-situ with spectroscopic methods (UV-Vis, EPR). It was found that A monomer oxidized to oligomers soluble in dichloromethane (Fig. 1—4 and 7) while monomer B showed ability to form stable conductive polymer layers showing low-energy forbidden band (1.6 eV) (Fig. 1,5,6 and 8,9).
机译:关于两种被苯基乙烯基{3'[(E)-2-苯基乙烯基] -2,2':5',2“-噻吩(单体A)和4,4”取代的噻吩三聚体衍生物的电化学性质的研究结果讨论了-二癸氧基-3'[((E)-2-苯基乙烯基] -2,2':5',2“-噻吩(单体B)}及其氧化产物。进行了A和B单体的电聚合循环伏安法和电化学测量结合使用光谱法(UV-Vis,EPR)进行原位偶联,发现A单体被氧化成可溶于二氯甲烷的低聚物(图1-4和7),而单体B则显示出能力形成具有低能量禁带(1.6 eV)的稳定的导电聚合物层(图1,5,6和8,9)。

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