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Quantitative surface and Hirshfeld surface analysis of nicorandil molecule and further insight into its solubility in several aqueous protic and aprotic cosolvent solutions.

Authors :
Wang, Juan
Li, Shuguang
Li, Kang
Wang, Yakun
Li, Wentian
Source :
Journal of Molecular Liquids. Sep2022, Vol. 362, pN.PAG-N.PAG. 1p.
Publication Year :
2022

Abstract

[Display omitted] • Quantitative surface and Hirshfeld surface analysis of nicorandil molecules were studied. • Solubility data was analyzed by using extended Hildebrand solubility approach. • Preferential solvation were investigated via inverse Kirkwood–Buff integrals method. • Dissolution properties and enthalpy–entropy compensation were studied. The quantum-chemical quantities of highest negative surface electrostatic potential and lowest surface average local ionization energy as well as Hirshfeld surface were used herein to explain the electrostatic features of both basicity and acidity of nicorandil molecule. The primary electrophilic and nucleophilic sites are the -N and > NH groups, respectively. According to the nicorandil solubility in solutions of isopropanol (1) + water (2), ethanol (1) + water (2), DMF (1) + water (2), and methanol (1) + water (2), preferential solvation of nicorandil was investigated using the famous inverse Kirkwood-Buff integrals approach. In poor water composition areas, nicorandil was surrounded preferentially by organic solvent, showing the selective solvation of nicorandil by methanol/DMF/ethanol/isopropanol. This performance was due to high basicity of organic solvents compared with water, which favors interactions with nicorandil's acidic groups. The Hansen solubility parameter was used to evaluate the performance of nicorandil solubility in depth. The derived dissolution Gibbs energy change, enthalpy and entropy indicated that the solubilization capacity improved with increasing methanol/DMF/ethanol/isopropanol compositions. As the proportions of methanol/DMF/ethanol/isopropanol rose, analysis of enthalpy–entropy compensation revealed a shift in main dissolving mechanism from enthalpy-driven to entropy-driven (alcohol solutions) or from entropy-driven to enthalpy-driven (DMF solutions). [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01677322
Volume :
362
Database :
Academic Search Index
Journal :
Journal of Molecular Liquids
Publication Type :
Academic Journal
Accession number :
158209073
Full Text :
https://doi.org/10.1016/j.molliq.2022.119697