Electrochemical synthesis and characterization of 2-amino-3-cyano-4-phenylthiophene dimer and oligomers
The electrochemical dimerization of 2-amino-3-cyano-4-phenylthiophene (ACPT) has been studied in acetonitrile solutions by using Pt electrodes. The resulting dimer obtained after a preparative electrolysis was characterized by using FAB mass, 13 C and 1 H nuclear magnetic resonance ( 13 C -NMR and 1...
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Published in | European polymer journal Vol. 38; no. 9; pp. 1837 - 1843 |
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Language | English |
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01.09.2002
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Abstract | The electrochemical dimerization of 2-amino-3-cyano-4-phenylthiophene (ACPT) has been studied in acetonitrile solutions by using Pt electrodes. The resulting dimer obtained after a preparative electrolysis was characterized by using FAB mass,
13
C
and
1
H
nuclear magnetic resonance (
13
C
-NMR and
1
H
-NMR) and fourier transform infrared spectroscopic techniques. Voltammetric measurements showed that the dimer formed by the coupling of two cation radicals (CR–CR) is stable and has a reversible electrochemical behavior. The fast scan voltammetric experiments using microelectrodes revealed that the dimer formed by the coupling of a cation radical with a parent molecule (CR–PM) has a quasi-reversible electrochemistry and undergoes to further couplings resulting in oligomers. On the basis of voltammetric and spectroscopic data, it was found that dimerization of ACPT occurs mainly by the coupling of a neutral ACPT molecule with the cation radicals, which is very important in the formation of regioregular oligomers and polymers. |
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AbstractList | The electrochemical dimerization of 2-amino-3-cyano-4-phenylthiophene (ACPT) has been studied in acetonitrile solutions by using Pt electrodes. The resulting dimer obtained after a preparative electrolysis was characterized by using FAB mass,
13
C
and
1
H
nuclear magnetic resonance (
13
C
-NMR and
1
H
-NMR) and fourier transform infrared spectroscopic techniques. Voltammetric measurements showed that the dimer formed by the coupling of two cation radicals (CR–CR) is stable and has a reversible electrochemical behavior. The fast scan voltammetric experiments using microelectrodes revealed that the dimer formed by the coupling of a cation radical with a parent molecule (CR–PM) has a quasi-reversible electrochemistry and undergoes to further couplings resulting in oligomers. On the basis of voltammetric and spectroscopic data, it was found that dimerization of ACPT occurs mainly by the coupling of a neutral ACPT molecule with the cation radicals, which is very important in the formation of regioregular oligomers and polymers. The electrochemical dimerization of 2-amino-3-cyano-4-phenylthiophene (ACPT) has been studied in acetonitrile solutions by using Pt electrodes. The resulting dimer obtained after a preparative electrolysis was characterized by using FAB mass, super(13)C and super(1)H nuclear magnetic resonance ( super(13)C-NMR and super(1)H-NMR) and fourier transform infrared spectroscopic techniques. Voltammetric measurements showed that the dimer formed by the coupling of two cation radicals (CR-CR) is stable and has a reversible electrochemical behavior. The fast scan voltammetric experiments using microelectrodes revealed that the dimer formed by the coupling of a cation radical with a parent molecule (CR-PM) has a quasi-reversible electrochemistry and undergoes to further couplings resulting in oligomers. On the basis of voltammetric and spectroscopic data, it was found that dimerization of ACPT occurs mainly by the coupling of a neutral ACPT molecule with the cation radicals, which is very important in the formation of regioregular oligomers and polymers. copyright 2002 Elsevier Science Ltd. All rights reserved. |
Author | Ekinci, Duygu Demir, Ümit Tümer, Ferhan |
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Cites_doi | 10.1016/0013-4686(95)90399-N 10.1021/ac60210a007 10.1021/cr950257t 10.1016/0022-0728(87)85115-X 10.1021/jp9804289 10.1021/jp9706083 10.1016/S0013-4686(00)00509-0 10.1021/ma960946m 10.1002/cber.19650981120 10.1016/S0022-0728(81)80362-2 10.1016/0022-0728(89)87035-4 10.1016/0022-0728(92)80466-H 10.1021/cm960545l 10.1021/cr00012a009 10.1021/cm00031a006 10.1016/0022-0728(91)85224-D 10.1002/rcm.1290020107 10.1002/(SICI)1521-4095(199808)10:12<927::AID-ADMA927>3.0.CO;2-G 10.1016/S0379-6779(98)00356-7 10.1021/cm000232x 10.1021/cm000421f 10.1016/S0022-0728(00)00036-X 10.1063/1.453844 10.1016/S0022-0728(98)00100-4 |
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Keywords | Cyclic voltammetry 2-Amino-3-cyano-4-phenylthiophene Ultramicroelectrodes Electropolymerization Electrodimerization Conducting polymers Thiophene derivative polymer Amine polymer Preparation Reaction mechanism Dimer Oligomer Experimental study Electrochemical polymerization Dimerization Functional polymer |
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SubjectTerms | 2-Amino-3-cyano-4-phenylthiophene Acetonitrile Applied sciences Cyclic voltammetry Dimerization Electrochemistry Electrodimerization Electrolysis Electropolymerization Exact sciences and technology Fourier transform infrared spectroscopy Microelectrodes Nuclear magnetic resonance spectroscopy Physicochemistry of polymers Polymerization Polymers and radiations Positive ions Synthesis (chemical) Ultramicroelectrodes |
Title | Electrochemical synthesis and characterization of 2-amino-3-cyano-4-phenylthiophene dimer and oligomers |
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