2017
DOI: 10.1080/00150193.2017.1360685
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Dielectric and FTIR studies on the hydrogen bonded binary system of ester and alcohol

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Cited by 17 publications
(4 citation statements)
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“…This shift can be attributed to weak hydrogen bonding between the sulfoxide group and hydroxyl group 22 . Previous literature reports have also observed a characteristic hydrogen bond peak around 3360 cm −1 between n-butanol and carbonyl groups 23 . Based on these findings, we analyzed the hydrogen bond characteristic peaks in modified PBFDO solution through fitting processing (see Fig.…”
Section: Resultsmentioning
confidence: 70%
“…This shift can be attributed to weak hydrogen bonding between the sulfoxide group and hydroxyl group 22 . Previous literature reports have also observed a characteristic hydrogen bond peak around 3360 cm −1 between n-butanol and carbonyl groups 23 . Based on these findings, we analyzed the hydrogen bond characteristic peaks in modified PBFDO solution through fitting processing (see Fig.…”
Section: Resultsmentioning
confidence: 70%
“…This higher relaxation time of MCS is due to the formation of multimers. Yaseen et al, 30 reported that the co-operative process of multimers O−H...O linkage give rise to high relaxation time. So, the relaxation time can be used to investigate the size of the rotating molecular unit and not for identifying the specific H-bond interaction sites of the solution constituents.…”
Section: Resultsmentioning
confidence: 99%
“…The absorption peaks that experienced changes in intensity and shift were the absorption peaks of the proton donor and acceptor groups of hydrogen bonds in the molecules of atorvastatin calcium and dipicolinic acid. Based on the results of the FTIR analysis it has been indicated that the atorvastatin calcium and dipicolinic acid molecules in the solids have formed intermolecular interactions, especially hydrogen bonds (Yaseen et al, 2017;Vemuri & Lankalapalli, 2021).…”
Section: Dsc Thermogrammentioning
confidence: 99%