2004
DOI: 10.1002/polb.20328
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Theoretical and experimental studies on the Raman spectra of electrosynthesized polynaphthalene

Abstract: Polynaphthalene (Pnap) was electrosynthesized through the direct oxidation of naphthalene in boron trifluoride diethyl etherate and was characterized with IR and Raman spectroscopy, matrix-assisted laser desorption/ionization time-of-flight mass spectroscopy, and thermogravimetric analysis. Raman spectra of oligonaphthalene were calculated with Gaussian 98 at the B3LYP/6-31G* level. Combining the computational and experimental results, we assigned the Raman bands of pristine Pnap. The Raman bands related to th… Show more

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Cited by 14 publications
(8 citation statements)
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“…Rylenes also show large hyperpolarizabilities making them more similar to polyenes than phenylenes since the planar geometry forces delocalization of electrons in the plane of the molecule . This may be the reason why Raman spectra of PAz show fewer bands than similar spectra of, for examle, polynaphthtalene and polyparaphenylene. , …”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Rylenes also show large hyperpolarizabilities making them more similar to polyenes than phenylenes since the planar geometry forces delocalization of electrons in the plane of the molecule . This may be the reason why Raman spectra of PAz show fewer bands than similar spectra of, for examle, polynaphthtalene and polyparaphenylene. , …”
Section: Discussionmentioning
confidence: 99%
“…9 This may be the reason why Raman spectra of PAz show fewer bands than similar spectra of, for examle, polynaphthtalene and polyparaphenylene. 34,35…”
Section: Discussionmentioning
confidence: 99%
“…This also contributed to the band broadening of IR spectra. 40 In addition, the new sharp peaks appearing at around 839 cm À1 and 558 cm À1 indicate the presence of PF 6 À .…”
Section: Structural Characterisationmentioning
confidence: 97%
“…As can be seen, the absorption bands in the spectrum of the dedoped polymer were obviously broadened in comparison with those of monomer. This was not only attributable to the wide conjugated chain length distribution of the polymer but also the chemical defects on the polymer chain resulting from the over oxidation of the polymer [38].…”
Section: Structural Characterizationmentioning
confidence: 99%