1989
DOI: 10.1016/0379-6779(89)90301-9
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A solid-state NMR investigation of the structure and dynamics of polyanilines

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Cited by 52 publications
(23 citation statements)
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“…Both spectra showed a spectrum of emeraldine base, which was described by Kaplan et al 24 Peak assignment corresponds to numbering scheme given in structure 2. The C = N quinoid resonance (C-7) was observed at 157 ppm, which is typical for emeraldine and can not be observed in leucoemeraldine.…”
Section: Resultsmentioning
confidence: 99%
“…Both spectra showed a spectrum of emeraldine base, which was described by Kaplan et al 24 Peak assignment corresponds to numbering scheme given in structure 2. The C = N quinoid resonance (C-7) was observed at 157 ppm, which is typical for emeraldine and can not be observed in leucoemeraldine.…”
Section: Resultsmentioning
confidence: 99%
“…The peaks for PAAMPSA-45 are assigned in Figure 1(e) in accordance to the chemical structure. 8,9 In addition to the polymer acid peaks between 10 and 70 ppm, as well as that at 175 ppm, a broad bump due to charge delocalization along the PANI backbone 10,11 appears between 100 and 160 ppm in the PANI-PAAMPSA spectra (Figure 1(a)-(d)), and its intensity increases with decreasing PAAMPSA content. This observation indicates that PANI content increases in PANI-PAAMPSA samples as the PAAMPSA content decreases.…”
mentioning
confidence: 99%
“…Kaplan et al employed 13 C and 2 H solid-state NMR spectroscopy to investigate PANI in emeraldine base (EB), leucoemeraldine (LEB), and emeraldine hydrochloride (ES) forms [42]. They confirmed the presence of alternating reduced and oxidized units in the EB structure by comparing the 13 C CP/MAS spectrum of EB to the spectra of the pristine and partly air-oxidized LEBs.…”
Section: The Structure and Molecular Dynamics Of Panimentioning
confidence: 99%
“…This motion became partly inhibited in the ES form due to the π-character of the ring-nitrogen bonds and steric interactions with the neighboring chloride counterions. At higher temperatures free volume in polymer increased, making rings sterically less constrained by neighboring chains so that the number of fast flipping rings increased [42].…”
Section: The Structure and Molecular Dynamics Of Panimentioning
confidence: 99%