Introduction to Infrared and Raman Spectroscopy 1990
DOI: 10.1016/b978-0-08-091740-5.50012-0
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Carbonyl Compounds

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Cited by 129 publications
(184 citation statements)
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“…The low wavenumber domain of FTIR spectra (between 400 cm À1 and 1950 cm À1 ) may be considered as the ngerprint region that allows to differentiate between the hydrophilic and hydrophobic PDs fractions. In the case of hydrophilic PDs, the appearance of an intense band at 1576 cm À1 , 71,74,75 characteristic for enol form with intramolecular resonance, reveals that the carbonyl (C]O) groups are mostly coupled with -OH groups (weak signals at 2655 cm À1 , 2704 cm À1 , 2725 cm À1 , 2800 cm À1 , and 2839 cm À1 ) by hydrogen bonding (Fig. S7 †).…”
Section: Structural Characterizationsmentioning
confidence: 99%
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“…The low wavenumber domain of FTIR spectra (between 400 cm À1 and 1950 cm À1 ) may be considered as the ngerprint region that allows to differentiate between the hydrophilic and hydrophobic PDs fractions. In the case of hydrophilic PDs, the appearance of an intense band at 1576 cm À1 , 71,74,75 characteristic for enol form with intramolecular resonance, reveals that the carbonyl (C]O) groups are mostly coupled with -OH groups (weak signals at 2655 cm À1 , 2704 cm À1 , 2725 cm À1 , 2800 cm À1 , and 2839 cm À1 ) by hydrogen bonding (Fig. S7 †).…”
Section: Structural Characterizationsmentioning
confidence: 99%
“…71,[74][75][76][77] The strong peaks at 1620 cm À1 and 1656 cm À1 can be attributed to the unsaturated C]C bonds. 71,73,74,78 FTIR spectra of hydrophobic PDs are more complex. The characteristic peak of free C]O groups at 1703 cm À1 is more pronounced in the hydrophobic fraction.…”
Section: Structural Characterizationsmentioning
confidence: 99%
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“…The significantly higher frequency band at 1755 cm -1 suggests that the corresponding surface species contain C=O bonds, which are not conjugated to the C=C bonds. [14] The appearance of this vibration points to the formation of an oxopropyl surface species, resulting from the partial hydrogenation of acrolein molecules with only one H atom attached to the C=C bond. Figure 3 show a possible structure of the oxopropyl species.…”
Section: Figure 2 Acrolein Hydrogenation Over Pd(111) At 270 K (A) mentioning
confidence: 99%