1997
DOI: 10.1016/s0040-6090(97)00271-x
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Investigation of the plasma polymer deposited from pyrrole

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Cited by 56 publications
(55 citation statements)
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References 29 publications
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“…2) the previously reported absorption peaks were obtained. 11,12 The NH stretch and NH band modes were present at 3400 and 1140 cm Ϫ1 ; the bands were also present in the spectrum of polypyrrole at 3400 and 1120 cm Ϫ1 . This is a clear indication of the presence of the NH band in the polymer.…”
Section: Ir and Sem Studiesmentioning
confidence: 94%
See 1 more Smart Citation
“…2) the previously reported absorption peaks were obtained. 11,12 The NH stretch and NH band modes were present at 3400 and 1140 cm Ϫ1 ; the bands were also present in the spectrum of polypyrrole at 3400 and 1120 cm Ϫ1 . This is a clear indication of the presence of the NH band in the polymer.…”
Section: Ir and Sem Studiesmentioning
confidence: 94%
“…In addition, the presence of bands at 1450 and 1420 cm Ϫ1 in the polymer spectrum indicates that the ring structure is not affected by polymerization process, which was also previously reported. 12 The strong band, characteristic of a five-membered aromatic ring occurring between 700 and 800 cm Ϫ1 , was present in the spectra of both monomer and polymer. Again, this strongly suggests that the ring is not opened up in the polymerization process.…”
Section: Ir and Sem Studiesmentioning
confidence: 96%
“…The single charged dimer can then lose one protons to rearomatize and form a stable dimer, which is more easily protonation than the monomer and may participate in additional radical coupling reactions to form oligomers and eventually polymer. The synthesis of the polymerization of pyrrole is illustrated in Scheme 1. peak at 2923 cm −1 due to the stretching of C-H, and the band at 2357 cm −1 are attributed to the stretching of C N [29,30]. The N-H bending in amine is observed at 1634 cm −1 , it seems too broad, hence, includes the contributions from C N imines stretch and possibly C C alkenes stretching [31].…”
Section: The Mechanism About Formation Of Polypyrrole Oligomers (Ppo)mentioning
confidence: 99%
“…Previous work on conductive polymers for optical applications has typically used one of three material systems: aniline 12,14-15 , thiophene [16][17][18] (used in spin coating work) or pyrrole [9][10][19][20][21] . In addition to the spin coating effort, our work has used electrochemically deposited polypyrrole, doped to provide high conductivity.…”
Section: Figure 4 Sem Images Of Spin Coated Pedot After Lithographicmentioning
confidence: 99%