Cross-Polymerization of Hard Blocks in Segmented Copoly(ether urea)s

被引:23
作者
Koevoets, Rolf A. [1 ]
Karthikeyan, S. [1 ]
Magusin, Pieter C. M. M. [2 ]
Meijer, E. W. [1 ]
Sijbesma, Rint P. [1 ]
机构
[1] Eindhoven Univ Technol, Lab Macrool & Organ Chem, NL-5600 MB Eindhoven, Netherlands
[2] Eindhoven Univ Technol, Schuit Inst Catalysis, NL-5600 MB Eindhoven, Netherlands
关键词
CHAIN ORIENTATIONAL BEHAVIOR; COLORIMETRIC DETECTION; POLYDIACETYLENE FILMS; MOLECULAR RECOGNITION; MECHANICAL-PROPERTIES; OPTICAL-PROPERTIES; COPOLYMERS; DIACETYLENE; STATE; SPECTROSCOPY;
D O I
10.1021/ma801220q
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Diacetylene-containing segmented copoly(ether urea) 1 was prepared via a polycondensation of 1,10-diisocyanato-deca-4,6-diyne with bis(3-aminopropyl)poly(tetrahydrofuran) (M-n approximate to 2300 g/mol). The reactive diacetylene spacer, which resides within the hard domains of the segmented elastomer, was cross-polymerized topochemically by means of UV radiation, without disrupting the flexible nature of the material, resulting in an intensely blue insoluble material. The extent of cross-polymerization was determined using solid-state C-13 NMR and was found to be similar to 10%. The optical properties of the cross-polymerized material could be modified mechanically and thermally as well as by changing the solvent. A study into the mechanochromic behavior-a color change from blue to yellow upon elongation-showed that the color changes are irreversible at strain levels greater than 80%. Polarized UV spectroscopy indicated that upon deformation the polydiacetylene chains orient parallel to the deformation axis. Thermochromic and solvatochromic behavior of 1 was completely irreversible.
引用
收藏
页码:2609 / 2617
页数:9
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