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    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/70311

    Title: 偶氮苯溶液中的聚集行為對於順反異構化之影響
    Authors: 林晉逸,;Lin,Chin-Yi
    Contributors: 化學學系
    Keywords: 偶氮苯;離子液體
    Date: 2016-05-26
    Issue Date: 2016-06-04 12:26:35 (UTC+8)
    Publisher: 國立中央大學
    Abstract: 偶氮苯化合物具有光致異構化的性質,在10-3M 時有碳長鏈取代
    而當濃度低於10-2M 時,順式偶氮苯分率上升,而反式偶氮苯分率下
    反應速率常數與濃度有相當大的關係,當濃度大於10-2M 時,反應速
    子在10-2M 以上時,會聚集產生微胞,而使得反式偶氮苯不易轉變成
    順式偶氮苯,而在10-2M 以下時,反應速率常數會有急遽變化,這是
    化的反應。;The azobenzene compounds exhibit a photoisomerization property. For solution of azobenzene derivatives carrying an alkyl-chain (AZO-1,4,6,8,10) with concentration less than 10-3 M, there are coexistence of cis and trans isomers. The cis to trans isomer ratio of azobenzenes changes according to the concentration of azobenzene.
    When the concentration of azobenzene is lower than 10-2 M, we found that the population of cis isomer increases and that of trans isomer decreases. In our experiments relevant to the dynamical studies on isomerization between the cis and trans forms, we found that rate
    constants for the isomerization vary with the concentrations of azobenzene, indeed. When the concentration of azobenzene is greater than 10-2 M, the rate constants would not change much. The rationale to this observation is that azobenzene derivatives with an alkyl-chain would likely aggregate into micelles above 10-2 M. The trans form in micelles is more difficult to proceed with photoisomerization to become cis form. When the concentration of azobenzene is lower than 10-2 M, the rate constants change drastically, attributable to the fact that the azobenzene derivatives likely exist as monomeric units and are easier to isomerize photolytically.
    Appears in Collections:[化學研究所] 博碩士論文

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