1986
DOI: 10.1016/0379-6779(86)90183-9
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Chemical vapour deposition (CVD) of conducting polymers: Polypyrrole

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Cited by 150 publications
(54 citation statements)
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“…Several research groups [25,[40][41][42][43][44] have made the assignments of vibration modes of PPy. The spectra e of Figure 3 (polypyrrole powder synthesized with FeCl 3 , so called PPy-Cl) contains bands at 1540 cm −1 (C-C stretching vibrations in pyrrole ring) [25], at 1459 cm -1 (C-N stretching vibration in the ring) [25]; from 1400 cm -1 to 1250 cm -1 (broad band, C-H or C-N in-plane deformation modes of secondary aromatic amines) [25,42], bands from 1250 to 1100 cm -1 (vibrations of the pyrrole ring) [25], characteristic for oxidized polypyrrole.…”
Section: Fourier-transform Infrared Spectroscopymentioning
confidence: 99%
“…Several research groups [25,[40][41][42][43][44] have made the assignments of vibration modes of PPy. The spectra e of Figure 3 (polypyrrole powder synthesized with FeCl 3 , so called PPy-Cl) contains bands at 1540 cm −1 (C-C stretching vibrations in pyrrole ring) [25], at 1459 cm -1 (C-N stretching vibration in the ring) [25]; from 1400 cm -1 to 1250 cm -1 (broad band, C-H or C-N in-plane deformation modes of secondary aromatic amines) [25,42], bands from 1250 to 1100 cm -1 (vibrations of the pyrrole ring) [25], characteristic for oxidized polypyrrole.…”
Section: Fourier-transform Infrared Spectroscopymentioning
confidence: 99%
“…Vapor phase polymerization (VPP) was first described by Mohamadi et al [20] as a CVD process using FeCl 3 as oxidants for polymerization of polypyrrole films. Then using Fe(III) tosylate as the oxidant has been reported an excellent route to form both smooth and highly conducting films [21].…”
Section: Introductionmentioning
confidence: 99%
“…This is supported by the infrared (IR) absorption spectra. The intensity of the IR absorption band at 1040 cm -1 , attributable to Cµ-H in-plane vibration, 16 decreases as the proportion of covalently bonded bromine increases. Furthermore, for samples with high covalent to ionic ratio, the hydrogen content decreases substantially from the theoretical C: H : N ratio of 4: 3 : 1 for a linear chain of disubstituted pyrrole rings.…”
Section: Conductivity Measurementsmentioning
confidence: 99%