1979
DOI: 10.1007/bf01100269
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IR spectroscopic study of the decomposition of dimers of oleic and elaidic acids

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Cited by 3 publications
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“…The absorption band at 1711 cm −1 in both cases can be attributed to stretching vibrations of C=O in one of the types of (cyclic or acyclic) dimer binding observed for the majority of aliphatic carboxylic acids in nonpolar environments [32]. It is also confirmed the absence of the absorption band of the OH group at 3300-3500 cm −1 and the presence of the absorption band at 2677-2688 cm −1 , referring to -OH stretching oleic/undecylenic acids in dimer form in the spectra of OA and UA (see Figure S2, Figure S3, respectively, in Supporting Information File 1) [33]. In the reaction mixture spectra at the end of the first stage of the synthesis, the intensity of the band at 1711 cm −1 is reduced compared to that at the beginning of this stage (spectra S0 Stage1) due to the consumption of acid and formation of a complex with Fe(III).…”
Section: Resultssupporting
confidence: 70%
“…The absorption band at 1711 cm −1 in both cases can be attributed to stretching vibrations of C=O in one of the types of (cyclic or acyclic) dimer binding observed for the majority of aliphatic carboxylic acids in nonpolar environments [32]. It is also confirmed the absence of the absorption band of the OH group at 3300-3500 cm −1 and the presence of the absorption band at 2677-2688 cm −1 , referring to -OH stretching oleic/undecylenic acids in dimer form in the spectra of OA and UA (see Figure S2, Figure S3, respectively, in Supporting Information File 1) [33]. In the reaction mixture spectra at the end of the first stage of the synthesis, the intensity of the band at 1711 cm −1 is reduced compared to that at the beginning of this stage (spectra S0 Stage1) due to the consumption of acid and formation of a complex with Fe(III).…”
Section: Resultssupporting
confidence: 70%
“…The peak observed at 2989 cm À1 is associated with the CH 3 stretching vibration whereas the 1709 cm À1 peak is characteristic of the CQO bond of the carboxylic acid. [20][21][22] In addition to the peaks usually associated with oleic acid, a shoulder appears at 1544 cm À1 which may indicate the existence of a carboxylic acid salt. The continuing presence of the 1710 cm À1 band implies that only a proportion is electrostatically bonded as oleate on the PbO surface, and that free oleic acid appears to still be present in the nanocrystal sample.…”
mentioning
confidence: 99%
“…This was also seen here by the intense band at 1708 cm -1 (Figure 4c) for the carbonyl group (C=O), characteristic of the dimer form of oleic acid formed due to hydrogen bonding. However, with the increase in temperature, dimers may change (gradually) into the monomer form (Noskov et al 1980). The carbonyl group of the monomer appears at approximately around 1745 cm -1 Figure 4c).…”
Section: Resultsmentioning
confidence: 99%