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[三聚氯氰活化的氨基化合物修饰戊二醛交联壳聚糖树脂的制备及其傅里叶变换红外光谱特性]

[Preparation and FTIR properties of amino compounds modified glutaraldehyde crosslinked chitosan resin activated with cyanuric chloride].

作者信息

Feng Chang-gen, Bai Lin-shan, Ren Qi-sheng

机构信息

Center of Research and Development for New Pharmaceuticals, Beijing Institute of Technology, Beijing 100081, China.

出版信息

Guang Pu Xue Yu Guang Pu Fen Xi. 2004 Nov;24(11):1315-8.

Abstract

The preparation and IR properties of 1-butylamine, dimethylamine, trimethylamine, triethylamine, benzylamine, 4-methylaniline and 4-aminobenzenesulfonic acid modified glutaraldehyde crosslinked chitosan activated with cyanuric chloride were studied. The absorption of nu(O-H) and nu(N-H) at 3430-3440 cm(-1), nu(C-O-C) at 1155 cm(-1), nu(C-OH) at 1030 cm(-1) and nu(C-O) of beta-D-glucose at 899 cm(-1) were not shifted obviously. The absorption of delta(C-H) at 1400-1384 cm(-1) and nu(C-OH) at 1095 cm(-1) varied markedly. The nu(C=N) absorption of crosslinked chitosan was at 1640-1650 cm(-1). The skeleton vibration absorption of 1,3,5-triazine ring was at 803-812 cm(-1) and 1584-1590 cm(-1). With different deacetylation or substitution, the amide I, II, III absorption at 1650, 1600 and 1310 cm(-1) varied obviously. When modified with 1-butylamine, dimethylamine, benzylamine, 4-methylaniline and 4-aminobenzenesulfonic acid, strong absorption of delta(NH3+) appeared at 1517-1530 cm(-1), which was weakened or disappeared when modified with trimethylamine or triethylamine, but a series of new absorption of nu(C-N) appeared at 1400-1500 cm(-1).

摘要

研究了用三聚氯氰活化的1-丁胺、二甲胺、三甲胺、三乙胺、苄胺、4-甲基苯胺和4-氨基苯磺酸改性的戊二醛交联壳聚糖的制备及其红外性能。在3430 - 3440 cm⁻¹处的ν(O - H)和ν(N - H)、1155 cm⁻¹处的ν(C - O - C)、1030 cm⁻¹处的ν(C - OH)以及899 cm⁻¹处β - D - 葡萄糖的ν(C - O)吸收峰没有明显位移。在1400 - 1384 cm⁻¹处的δ(C - H)和1095 cm⁻¹处的ν(C - OH)吸收峰有明显变化。交联壳聚糖的ν(C = N)吸收峰在1640 - 1650 cm⁻¹处。1,3,5 - 三嗪环的骨架振动吸收峰在803 - 812 cm⁻¹和1584 - 1590 cm⁻¹处。随着脱乙酰度或取代度的不同,在1650、1600和1310 cm⁻¹处的酰胺I、II、III吸收峰有明显变化。用1-丁胺、二甲胺、苄胺、4-甲基苯胺和4-氨基苯磺酸改性时,在1517 - 1530 cm⁻¹处出现强的δ(NH₃⁺)吸收峰,用三甲胺或三乙胺改性时该吸收峰减弱或消失,但在1400 - 1500 cm⁻¹处出现一系列新的ν(C - N)吸收峰。

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