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    Please use this identifier to cite or link to this item: https://ir.lib.ncu.edu.tw/handle/987654321/101596


    Title: Convenient synthesis of organic-electronics-oriented building blocks via on-water and under-air homocoupling of (hetero)aryl iodides
    Authors: 劉青原;Chen, Yi-An;Liu, Ching-Yuan
    Contributors: 工學院化學工程與材料工程學系
    Date: 2015-08-25
    Issue Date: 2026-04-21 14:38:37 (UTC+8)
    Publisher: Royal Society of Chemistry
    Abstract: 摘要: We report herein an operationally simple homocoupling reaction that targets the convenient synthesis of organic-electronically important building blocks. A variety of synthetically useful bithiophene derivatives and functionalized biphenyls are efficiently prepared by an on-water and under-air protocol using Pd/C as catalyst. We find that Pd/C gives generally higher and cleaner homocoupling conversions than using Pd(OAc) 2 in the cases of (hetero)aryl iodides since Pd(OAc) 2 triggers more side reactions including dehalogenations and oligomerizations. Under the optimum conditions, a broad range of functional groups such as ester, ketone, aldehyde, nitrile, nitro, chloride, and bromide are well tolerated. We expect the present methodology would make a valuable synthetic contribution towards bridging green chemistry with thiophene-based organic materials. An on-water homocoupling reaction is developed for the alternative synthesis of various organic-electronically versatile bi(hetero)aryls. These multi-function building blocks are indispensable to polymer chemistry and modern organic electronics.
    出版日期: 2015-09-02
    資源來源: Royal Society of Chemistry
    識別號: EISSN: 2046-2069
    識別號: DOI: 10.1039/c5ra13517f
    Appears in Collections:[化學工程與材料工程學系 ] 期刊論文

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