1988
DOI: 10.1016/0379-6779(88)90309-8
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Raman spectra of polypyrrole and its 2,5-13C-substituted and C-deuterated analogues in doped and undoped states

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Cited by 338 publications
(153 citation statements)
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“…The CAA/PPy spectrum shows bands at 1608 (s), 1500 (w), 1378 (s), 1315 (s), 1250 (m), 1213 (sh), 1076 (m), 1049 (m), 973 (m), 934 (s), 873 (sh), 695 (w) and 634 (w) cm -1 . These bands are in agreement with the spectrum previously described of polypyrrole in its oxidized form, which shows the presence of polarons and bipolarons 31,32 (bands at 1378, 1250, 1076 and 973 cm -1 ). These bands are not observed in the reduced polypyrrole spectrum and are attributed to the mobile species in polypyrrole 31,32 .…”
Section: Resultssupporting
confidence: 79%
“…The CAA/PPy spectrum shows bands at 1608 (s), 1500 (w), 1378 (s), 1315 (s), 1250 (m), 1213 (sh), 1076 (m), 1049 (m), 973 (m), 934 (s), 873 (sh), 695 (w) and 634 (w) cm -1 . These bands are in agreement with the spectrum previously described of polypyrrole in its oxidized form, which shows the presence of polarons and bipolarons 31,32 (bands at 1378, 1250, 1076 and 973 cm -1 ). These bands are not observed in the reduced polypyrrole spectrum and are attributed to the mobile species in polypyrrole 31,32 .…”
Section: Resultssupporting
confidence: 79%
“…The fact that Raman spectroscopy is based on scattering phenomena leads to the possibility of analysis of insoluble samples that require no sample preparation. inter-ring C-C str N-C and C-C str C-C str C-H def Ring def, sym Several Raman studies of polypyrrole have been published previously where the source used generally has a wavelength of 5 14.5 nm (14,15). A list of generally accepted assignments is provided in Table 1.…”
mentioning
confidence: 99%
“…This band is characteristic of the bipolaronic structure (quinoid form) in the oxidized state and is attributed to out-of-plane C-H deformation. Additionally, two bands characteristic of the polaronic structure (aromatic form), at 982 and 1047cm − 1 , assigned to ring deformation mode and CH in-plane deformation mode respectively, increased when the Fe 3 O 4 is present in the composite (Furukawa et al, 1988). Both the bands at 1500 and 982cm − 1 are assignable to aromatic segments but these are also present at the most oxidized state.…”
Section: Physical Chemical Interaction and Stabilization Of The Polymermentioning
confidence: 90%
“…The spectra present the characteristic bands already attributed to PPy vibrational modes located at 1592, 1382, 1320, 1252, 1082, 1047, 982 and 931cm −1 (Santos et al, 2007). By comparing with reported data by in-situ Raman studies (Furukawa et al, 1988;Santos et al, 2007), it is clear that the polymer is in the oxidized state where both aromatic and quinoid structures coexist indicating a pseudoequilibrium between polaronic and bipolaronic structures at the same oxidation level as already pointed out by Santos (Santos et al, 2007) and Furukawa (Furukawa et al, 1988). Figure 9 shows that the intensity of the band at 931cm − 1 decreases when the Fe 3 O 4 is in the film.…”
Section: Physical Chemical Interaction and Stabilization Of The Polymermentioning
confidence: 97%