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Issue 48, 2020
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Influence of solvent on crystal nucleation of benzocaine

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The influence of the solvent in nucleation of a polymorphic organic molecule, benzocaine, has been explored by measuring nucleation induction times, probing solvent–solute interactions in solution with spectroscopy and modelling the strength of solvent–solute intermolecular interactions using density functional theory (DFT). Over 2640 induction time experiments were conducted to study the crystal nucleation of benzocaine FII in six different organic solvents. The nucleation driving force required to reach the same induction time is strongly solvent-dependent, increasing in the order: ethyl acetate < 1,4-dioxane < acetonitrile < methanol < n-butanol. Nucleation in toluene is reasonably easy but the exact position varies with the induction time. The order between the solvents overall corresponds to the order of increasing interfacial energy as determined within the classical nucleation theory. The shift of the FTIR carbonyl frequency reflecting the strength in the solvent–solute interaction decreases in the same order as the interfacial energy of benzocaine FII increases. This shift is corroborated by DFT calculated energies of binding one solvent molecule to the carboxyl group of benzocaine. An even better correlation of the influence of the solvent on the nucleation is provided by DFT calculated energy of binding the complete first solvation shell to the benzocaine molecule. The different methods reveal a consistent picture and suggest that the stronger the solvent binds to the benzocaine molecule in solution, the slower the nucleation becomes.

Graphical abstract: Influence of solvent on crystal nucleation of benzocaine

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Article information

08 Sep 2020
09 Nov 2020
First published
11 Nov 2020

CrystEngComm, 2020,22, 8330-8342
Article type

Influence of solvent on crystal nucleation of benzocaine

D. Cheuk, J. Zeglinski, R. Krishnaraj and Å. C. Rasmuson, CrystEngComm, 2020, 22, 8330
DOI: 10.1039/D0CE01306D

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