Synthesis and properties of isomeric pyridyl-containing chitosan derivatives

被引:23
作者
Bratskaya, S. Yu [1 ]
Azarova, Yu A. [1 ]
Portnyagin, A. S. [1 ]
Mechaev, A. V. [2 ]
Voit, A. V. [1 ]
Pestov, A. V. [2 ]
机构
[1] Russian Acad Sci, Inst Chem, Far East Branch, Vladivostok 690022, Russia
[2] RAS, IYa Postovsky Inst Organ Synth, Ural Branch, Ekaterinburg 620990, Russia
关键词
Chitosan; Pyridyl derivative; Physical-chemical properties; CROSS-LINKED CHITOSAN; CHITIN; COMPLEXATION; ADSORPTION; GEL; VISCOSITY; EFFICIENT; BINDING; METALS; CU(II);
D O I
10.1016/j.ijbiomac.2013.09.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Here we report on the method of synthesis in gel of a new heterocyclic aminopolymer-N-2-(4-pyridyl)ethylchitosan (4-PEC) via direct addition of 4-vinylpyridine to chitosan that yields a derivative with the substitution degree (DS) up to 0.8. The comparison of reactivity, thermal, spectroscopic, and sorption properties of a new derivative and its isomer N-2-(2-pyridyl)ethylchitosan (2-PEC) is presented. 2-PEC has higher sorption capacity and forms more stable chelates with [PdCl4](2-) and [PtCl6](2-) ions than 4-PEC, but the latter shows higher selectivity to noble metals ions in the presence of Cl- ions. A gradual increase of the sorption capacities and the affinity coefficient for Cu2+ and Ni2+ in the row chitosan < 4-PEC < 2-PEC was related to the increase of electron donor nitrogen atoms content and chelating properties of 2-PEC. A nearly negligible increase of the 4-PEC sorption capacity for Ag+, as compared to plain chitosan, was suggested to be dependent on the difference in complexation models for 2-PEC and 4-PEC derivatives. The density functional theory (DFT) calculations have shown that the "pendant" model of the complex with Ag(I) is energetically favorable only for 2-PEC derivative, while in cases of chitosan and 4-PEC only "bridge" complexes can be formed that results in lower sorption capacity. Crown Copyright (C) 2013 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:426 / 432
页数:7
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