2011
DOI: 10.1016/j.poly.2011.06.040
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The crystal structure, infrared, Raman and density functional studies of bis(2-aminophenyl) diselenide

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Cited by 29 publications
(19 citation statements)
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“…4C). Two new peaks at 523 cm À1 and 438 cm À1 appeared in the FT-IR spectroscopy of Se@CNFs-CNT, which are correspondences to the torsion of ring in which a CeSe bond is contained and the bending vibration of CeSe bond, respectively [43,44,46].…”
Section: Resultsmentioning
confidence: 91%
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“…4C). Two new peaks at 523 cm À1 and 438 cm À1 appeared in the FT-IR spectroscopy of Se@CNFs-CNT, which are correspondences to the torsion of ring in which a CeSe bond is contained and the bending vibration of CeSe bond, respectively [43,44,46].…”
Section: Resultsmentioning
confidence: 91%
“…After heating at high temperature with CNFs-CNT (or CNFs), three characteristic peaks at 198, 231 and 288 cm À1 were obtained for both Se@CNFs-CNT and Se@CNFs. The peaks at 198 and 288 cm À1 can be ascribed to CeSe stretching vibration and the CeSeeSe group vibration [43,44]. Fig.…”
Section: Resultsmentioning
confidence: 95%
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“…4c displays the FT-IR spectra of the CPAN and CPAN/Se. 50 Both the CPAN and the CPAN/Se exhibit peaks at 1590, 1295, and 833 cm -1 corresponding to the C=C bond, C=N bond, and C-N bond, respectively, [16][17][18][19] suggesting the formation of a heterocyclic compound in the carbonization process. The new peak at 523 cm -1 corresponds to torsion of rings in which a C-Se 55 bond is contained, 20 and the peak located at 438 cm -1 could be also attributed to the C-Se bending vibration, 19 indicating the formation of C-Se bonds after the dehydrogenation and cyclization process.…”
Section: Resultsmentioning
confidence: 99%
“…25 Its mono-substituted derivatives, viz. 27 The 1 H and 13 C{ 1 H} NMR spectra exhibited expected resonances and peak multiplicities. The absence of a broad absorption at 3400 cm À1 in 2b, 3b, and 4b is indicative of substitution of both the OH groups in DHS(OH) 2 .…”
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confidence: 94%