Forster Resonance Energy Transfer across interpolymer complexes of poly(acrylic acid) and poly(acrylamide)

被引:10
|
作者
Swift, Thomas [1 ,2 ]
Paul, Natalie [2 ]
Swanson, Linda [2 ]
Katsikogianni, Maria [1 ]
Rimmer, Stephen [1 ,2 ]
机构
[1] Univ Bradford, Sch Chem & Biosci, Polymer Labs, Richmond Rd, Bradford BD7 1DP, S Yorkshire, England
[2] Univ Sheffield, Dept Chem, Polymer & Biomat Chem Labs, Brook Hill, Sheffield S3 7HD, S Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
Interpolymer complexation; poly(acrylic acid); Smart materials; Fluorescence; POLY(METHACRYLIC ACID); AQUEOUS-SOLUTION; HYDROLYZED POLY(ACRYLAMIDE); POLYMER NANOPARTICLES; CONJUGATED POLYMERS; FLUORESCENCE; PH; ANTHRACENE; FRET; POLY(N-ISOPROPYLACRYLAMIDE);
D O I
10.1016/j.polymer.2017.06.069
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Interpolymer complexes of homopolymer macromolecules are often described as 'laddered' or 'ribbon' type structures. The proposition of the existence of these ladder structures seems to us not reasonable and here we examine this hypothesis. To address this we have used polymers enabled for Forster Energy Transfer (FRET). Chromophores bound to a macromolecular backbone can transfer energy across short distances via FRET. The close binding of poly(acrylamide) and poly(acrylic acid) interpolymer complex formation at low pH forms a structure compact enough for significant energy transfer to occur between different chains containing naphthalene and anthracene labels. In the context of the proposition that ladder polymers can form it was surprising that the distance between labels on the same polymer backbone was equivalent regardless of whether the polymer was complexed or not. The data indicated that the bicomponent structure may be more compact than previously supposed: I.e. the complexes are not ladders composed of extended chains. This evidence suggests formation not of ordered 'ladder' systems but colloidal 'co-globules'. Crown Copyright (C) 2017 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:10 / 20
页数:11
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