Molecular Approach to Supramolecular Polymer Assembly by Small Angle Neutron Scattering

被引:25
作者
Bras, Ana R. [1 ]
Hoevelmann, Claas H. [1 ]
Antonius, Wiebke [1 ]
Teixeira, Jose [2 ]
Radulescu, Aurel [3 ]
Allgaier, Juergen [1 ]
Pyckhout-Hintzen, Wim [1 ]
Wischnewski, Andreas [1 ]
Richter, Dieter [1 ]
机构
[1] Forschungszentrum Julich, JCNS ICS 1 1, D-52425 Julich, Germany
[2] CEA Saclay, CEA CNRS, Lab Leon Brillouin, F-91191 Gif Sur Yvette, France
[3] Forschungszentrum Julich, JCNS 1, Outstn FRM 2, D-85747 Garching, Germany
关键词
HYDROGEN-BONDING INTERACTIONS; RING-OPENING POLYMERIZATION; RANDOM-PHASE-APPROXIMATION; DYNAMIC LIGHT-SCATTERING; MICROPHASE SEPARATION; THERMOPLASTIC ELASTOMERS; TELECHELIC POLYMERS; DIBLOCK COPOLYMERS; CHAIN EXTENSION; ORDER;
D O I
10.1021/ma401714r
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We present a small angle neutron scattering (SANS) study of the association of heterocomplementary telechelic polypropylene glycol (PPG) polymers, bearing either diaminotriazine (DAT) or thymine (Thy) stickers as end-groups, both in the melt and in dilute solution. The SANS data are critically examined for the architecture and morphology as well as relative extent of linear assembly in the apolar solvent toluene. A random phase approximation (RPA) approach, adapted for a supramolecularly assembled multiblock copolymer is presented, which allows to extract the interaction parameters between the constituents and the medium. From the proposed approach, which describes very well heterocomplementary hydrogen-bonding telechelic polymers in both diluted toluene solution and in the melt, we conclude that linear association prevails.
引用
收藏
页码:9446 / 9454
页数:9
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