2017
DOI: 10.1016/j.saa.2017.01.068
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Molecular interactions in ethyl acetate-chlorobenzene binary solution: Dielectric, spectroscopic studies and quantum chemical calculations

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Cited by 7 publications
(2 citation statements)
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“…38 Additionally, it is also capable of forming C−H•••π interactions with the benzoyl chloride π system through the ethyl group of the ester. 40 These ethyl acetate−IMC interactions might hinder the assembly of IMC molecules to form preassemblies leading to the formation of crystal nuclei. Hydrogen bonding of the acetone molecule with the carboxyl group of the IMC molecule is also shown in Figure 8.…”
Section: Induction Time Of Indomethacin Exemplary Results From Induct...mentioning
confidence: 99%
See 1 more Smart Citation
“…38 Additionally, it is also capable of forming C−H•••π interactions with the benzoyl chloride π system through the ethyl group of the ester. 40 These ethyl acetate−IMC interactions might hinder the assembly of IMC molecules to form preassemblies leading to the formation of crystal nuclei. Hydrogen bonding of the acetone molecule with the carboxyl group of the IMC molecule is also shown in Figure 8.…”
Section: Induction Time Of Indomethacin Exemplary Results From Induct...mentioning
confidence: 99%
“…Ethyl acetate, with two hydrogen-bond acceptors, is capable of forming a hydrogen bond only with the carboxylic group of IMC, as shown in Figure ; however, it has been reported to interact with the π system of the indole ring . Additionally, it is also capable of forming C–H···π interactions with the benzoyl chloride π system through the ethyl group of the ester . These ethyl acetate–IMC interactions might hinder the assembly of IMC molecules to form preassemblies leading to the formation of crystal nuclei.…”
Section: Results and Discussionmentioning
confidence: 99%