Electrochemical Preparation of Chiral Polyaniline Nanofibers

被引:5
作者
Weng Shao-Huang [2 ]
Zhou Jian-Zhang [1 ]
Lin Zhong-Hua [1 ]
Lin Xin-Hua [2 ]
机构
[1] Xiamen Univ, Dept Chem, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surface, Xiamen 361005, Peoples R China
[2] Fujian Med Univ, Fac Pharm, Dept Pharmaceut Anal, Fuzhou 350004, Peoples R China
来源
CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE | 2012年 / 33卷 / 11期
关键词
Electropolymerization; Polyaniline (PANI) nanofiber; Chiral; Circular dichroism spectrum; Stereochemical selectivity; CHIROPTICAL PROPERTIES; ACID; NANOWIRES; NANOTUBES; POLYMERS; FILMS;
D O I
10.7503/cjcu20120239
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chiral polyaniline(PANI) nanofibers were synthesized via facilely potentiostatic electropolymerization method without template in the presence of (1S)-(+)-camphor-10-sulfonic acid(D-CSA) or (1R)-(-)-camphor-10-sulfonic acid(L-CSA) as the dopant. The morphology and optical property of chiral PANI nanofibers were characterized with scanning electron microscopy(SEM), transmission electron microscopy(TEM), UV-Vis spectrum(UV-Vis) and circular dichroism(CD). Combined with the average diameter of micelles and zeta-potential of different deposition solutions, the formation mechanism and the enhanced optical activity of the optical PANI nanofibers were studied. The morphology of PANI nanofibers without the helical structure was consistent with the change of the concentration of aniline in the deposition solution when the concerntion of CSA was 1 mol/L. Furthermore, the chiral PANI nanofibers induced by different chiral CSA exhibited mirror-imaged circular dichroism spectra with high ellipticity, indicating the stereochemical selectivity of the molecular structure of PANI chain in the electrodeposited process. The colors and optical activities of the chiral PANI nanofibers not only can be kept with the chemical dedoping/redoping treatment, but also can reversibly varied with the different oxidized forms which were controlled via electrochemical route.
引用
收藏
页码:2501 / 2508
页数:8
相关论文
共 25 条
[1]   Molecular imprinted polypyrrole nanowires for chiral amino acid recognition [J].
Huang, Jiyong ;
Wei, Zhixiang ;
Chen, Jinchun .
SENSORS AND ACTUATORS B-CHEMICAL, 2008, 134 (02) :573-578
[2]   Enantioselective discrimination of D- and L-phenylalanine by chiral polyaniline thin films [J].
Huang, JX ;
Egan, VM ;
Guo, HL ;
Yoon, JY ;
Briseno, AL ;
Rauda, IE ;
Garrell, RL ;
Knobler, CM ;
Zhou, FM ;
Kaner, RB .
ADVANCED MATERIALS, 2003, 15 (14) :1158-+
[3]   Shape and aggregation control of nanoparticles: Not shaken, not stirred [J].
Department of Chemistry and Biochemistry, California NanoSystems Institute, University of California, Los Angeles, Los Angeles, CA 90095-1569, United States .
J. Am. Chem. Soc., 2006, 3 (968-975)
[4]   Polyaniline Nanofibers: A Unique Polymer Nanostructure for Versatile Applications [J].
Li, Dan ;
Huang, Jiaxing ;
Kaner, Richard B. .
ACCOUNTS OF CHEMICAL RESEARCH, 2009, 42 (01) :135-145
[5]   Electrochemical synthesis of optically active polyaniline films [J].
Li, WG ;
Wang, HL .
ADVANCED FUNCTIONAL MATERIALS, 2005, 15 (11) :1793-1798
[6]   Oligomer-assisted synthesis of chiral polyaniline nanofibers [J].
Li, WG ;
Wang, HL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (08) :2278-2279
[7]   TEMPLATE-SYNTHESIZED POLYACETYLENE FIBRILS SHOW ENHANCED SUPERMOLECULAR ORDER [J].
LIANG, WB ;
MARTIN, CR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1990, 112 (26) :9666-9668
[8]   ENANTIOSELECTIVE ELECTROPOLYMERIZATION OF ANILINE IN THE PRESENCE OF (+)-CAMPHORSULFONATE OR (-)-CAMPHORSULFONATE ION - A FACILE ROUTE TO CONDUCTING POLYMERS WITH PREFERRED ONE-SCREW-SENSE HELICITY [J].
MAJIDI, MR ;
KANEMAGUIRE, LAP ;
WALLACE, GG .
POLYMER, 1994, 35 (14) :3113-3115
[9]   THERMOCHROMISM IN THE INSULATING FORMS OF POLYANILINE - ROLE OF RING-TORSIONAL CONFORMATION [J].
MASTERS, JG ;
GINDER, JM ;
MACDIARMID, AG ;
EPSTEIN, AJ .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (06) :4768-4778
[10]   SPECTROSCOPY AND DEFECT STATES IN POLYANILINE [J].
MCCALL, RP ;
GINDER, JM ;
LENG, JM ;
YE, HJ ;
MANOHAR, SK ;
MASTERS, JG ;
ASTURIAS, GE ;
MACDIARMID, AG ;
EPSTEIN, AJ .
PHYSICAL REVIEW B, 1990, 41 (08) :5202-5213