Grafting Organic and Biomolecules on H-Terminated Porous Silicon from a Diazirine

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著者

    • WEI Shuai
    • State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University
    • WANG Jing
    • State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University
    • GUO Dong-Jie
    • State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University
    • CHEN Ya-Qing
    • State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University
    • XIAO Shou-Jun
    • State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University

抄録

A diazirine compound, 1,4-(1-azi-2,2,2-trifluoroethyl)benzoic acid, was used as a stable carbene precursor to react with Si–H terminated porous silicon (PSi) under microwave irradiation. After formation of a molecular monolayer, the end carboxyl group was converted to an amine-reactive crosslinker species, NHS ester, and finally to a Bovine Serum Albumin (BSA) monolayer on PSi.

収録刊行物

  • Chemistry letters  

    Chemistry letters 35(10), 1172-1173, 2006-10-05 

    The Chemical Society of Japan

参考文献:  18件

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各種コード

  • NII論文ID(NAID)
    10018323459
  • NII書誌ID(NCID)
    AA00603318
  • 本文言語コード
    ENG
  • 資料種別
    SHO
  • ISSN
    03667022
  • データ提供元
    CJP書誌  J-STAGE 
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