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作 者:董炎明[1] 郭振楚[2] 吴玉松[1] 阮永红[1] 童碧海[2] 赵雅青[1] 王惠武[1]
机构地区:[1]厦门大学材料科学与工程系,厦门361005 [2]湘潭师范学院化学系,湘潭411001
出 处:《高等学校化学学报》2003年第12期2330-2332,共3页Chemical Journal of Chinese Universities
基 金:国家自然科学基金 (批准号 :2 99740 2 3 )资助
摘 要:Chitin derivatives are difficult to be melten because of their very strong inter-molecular and intra-molecular hydrogen bonds. In this paper, N,O-benzyl chitosan was synthesized by means of phase-transfer method. The total degree of substitution for this derivative was 0 8 as determined with 1H NMR and the degree of substitution on nitrogen was 0 3 as determined with elemental analysis. This is a thermoplastic chitin derivative. Its melting point was 470 K as measured with DSC. A viscous isotropic melt occurred at the temperatures between the melting point and the decomposition temperature(513 K) while N,O-benzyl chitosan was heated on a hot stage. DSC results agreed with the results of microscopy observation. The benzyl group can not form hydrogen bonds. It is also non-polar and has larger volume. These factors weaken the interactions between chitosan chains, and therefore decrease the melting point, which was lower than the decomposition temperature. As a result, N,O-benzyl chitosan was able to melt.Chitin derivatives are difficult to be melten because of their very strong inter-molecular and intra-molecular hydrogen bonds. In this paper, N,O-benzyl chitosan was synthesized by means of phase-transfer method. The total degree of substitution for this derivative was 0 8 as determined with 1H NMR and the degree of substitution on nitrogen was 0 3 as determined with elemental analysis. This is a thermoplastic chitin derivative. Its melting point was 470 K as measured with DSC. A viscous isotropic melt occurred at the temperatures between the melting point and the decomposition temperature(513 K) while N,O-benzyl chitosan was heated on a hot stage. DSC results agreed with the results of microscopy observation. The benzyl group can not form hydrogen bonds. It is also non-polar and has larger volume. These factors weaken the interactions between chitosan chains, and therefore decrease the melting point, which was lower than the decomposition temperature. As a result, N,O-benzyl chitosan was able to melt.
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