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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Electrochemical behavior of phthalocyanines containing high oxidation state central metals: Titanium(IV), vanadium(IV), and tantalum(V)
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Electrochemical behavior of phthalocyanines containing high oxidation state central metals: Titanium(IV), vanadium(IV), and tantalum(V)

机译:包含高氧化态中心金属的酞菁的电化学行为:钛(IV),钒(IV)和钽(V)

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摘要

The syntheses of 2,(3)-(peripheral) and 1,(4)-(non-peripheral) (2-mercaptopyridine)phthalocyanine complexes of titanium(IV) oxide (5a and 6a, respectively), vanadium(IV) oxide (7a and 8a, respectively) and tantalum(V) hydroxide (9a, peripheral only) and their electrochemical characterization are presented in this report. Their electrochemistry is compared to that of thiophenyl and thiobenzyl substituted derivatives. The non-peripherally substituted complexes are more difficult to reduce than peripherally substituted derivatives. In addition, the mercaptopyridine substituted derivatives are more difficult to reduce compared to benzylmercapto and phenylmercapto derivatives, and aryl easier reduce than alkyl substitution. Spectroelectrochemistry of the complexes confirmed metal and ring redox processes for TaPc and TiPc derivatives and ring based processes only for VPc complexes.
机译:氧化钛(IV)(分别为5a和6a),氧化钒(IV)的2,(3)-(外围)和1,(4)-(非外围)(2-巯基吡啶)酞菁配合物的合成本报告介绍了分别为7a和8a的氢氧化钽和氢氧化钒(9a,仅用于外围设备)及其电化学特性。将它们的电化学与硫代苯基和硫代苄基取代的衍生物进行了比较。非外围取代的配合物比外围取代的衍生物更难还原。另外,与苄基巯基和苯基巯基衍生物相比,巯基吡啶取代的衍生物更难以还原,并且芳基比烷基取代更容易还原。配合物的光谱电化学证实了TaPc和TiPc衍生物的金属和环氧化还原过程以及仅VPc配合物的基于环的过程。

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