On the Formation and Electropolymerization of a Star Copolymer With Peripheral Carbazoles

被引:9
作者
Cao, Peng-Fei [1 ,2 ]
Felipe, Mary Jane [1 ,2 ]
Advincula, Rigoberto C. [1 ,2 ,3 ]
机构
[1] Univ Houston, Dept Chem, Houston, TX 77204 USA
[2] Univ Houston, Dept Chem Engn, Houston, TX 77204 USA
[3] Case Western Reserve Univ, Dept Macromol Sci & Engn, Cleveland, OH 44106 USA
基金
美国国家科学基金会;
关键词
conformational freedom; functionalization; polymeric films; ring-opening polymerization; steric limitation; CROSS-LINKING; GUEST ENCAPSULATION; DENDRIMERS; POLYMERS; DENDRON; FILMS; ELECTRODEPOSITION; NANOPARTICLES; TERTHIOPHENE; PRECURSORS;
D O I
10.1002/macp.201200344
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
Utilizing a hyperbranched cored ring-opening polymerization of caprolactone, carbazole peripheral groups are extended to afford electropolymerizable star-like copolymers. Different arm lengths are obtained on the basis of different degrees of polymerization from the polyethyleneimine core. This is confirmed by NMR and Fourier transform IR (FTIR) spectroscopy, size-exclusion chromatography (SEC), and quantitative spectral characterization. Atomic force microscopy (AFM) imaging shows two distinct particle aggregation characteristics, before and after functionalization with carbazole groups. Cyclic voltammetry verifies the electrochemical cross-linking properties. The results indicate that the conformational freedom of the electroactive peripheral functional groups can be controlled. Moreover, an interesting loop effect together with solid-state polymerization is observed.
引用
收藏
页码:386 / 395
页数:10
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