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    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/3661

    Title: 2-甲基;Study on the synthesis of 2-methylpyridine cyanice compounds
    Authors: 鄭仲宏;Juen-Hung Jeng
    Contributors: 化學工程與材料工程研究所
    Keywords: 縮合反應;芳香醛;花青染料;2-甲基;塞安寧;aromatic aldehydes;2-methylpyridine;cyanin
    Date: 2001-06-26
    Issue Date: 2009-09-21 12:19:34 (UTC+8)
    Publisher: 國立中央大學圖書館
    Abstract: 2-甲基 Alkyl halides undergo nucleophilic substitution with heterocylic compounds such as 2-methylquinoline and 4-methylquinoline, and form the stabile quaternary ammonium salt. Because of strong withdrawal electrons effects at the nitrogen atom on quaternary ammonium salt, the methyl group out of aromatic ring becomes an active nucleophile, witch can react with aromatic aldehydes to form cyanine compounds. The blue dye “cyanine”was first prepared by Greville Williams in 1856, in which two heterocyclic nuclei containing nitrogen are linked through an odd numbered methane chain in such a way that resonance occurs through the conjugated system between tertiary and quaternary nitrogen atoms, that make the red shift of ultraviolet-visible spectra of the cyanine compounds. The study takes 2-methylpyridine to be the reactant and synthesizes cyanine compounds with aromatic aldehydes. By changing the number of methane chain, we hope to synthesize the compounds which have the maximum absorbance of ultraviolet-visible spectra more than 600nm, and study on the property of ultraviolet-visible and infrared spectra.
    Appears in Collections:[化學工程與材料工程研究所] 博碩士論文

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