The Role of Solvent Hydroxyl Functional Groups on the Interaction Energy and Growth of Form i Paracetamol Crystal Facets

The morphology of a crystal grown in a solvent can change depending on the solvent used during the crystallization process. Modification of the morphology of a crystal can be engineered based on information conferred by the functional groups of the facets of interest and the functional groups of the...

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Published in:Organic Process Research and Development
Main Author: Shahrir N.; Anuar N.; Abdul Muttalib N.A.; Yusop S.N.; Abu Bakar M.R.; Adam F.; Ibrahim S.F.
Format: Article
Language:English
Published: American Chemical Society 2022
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85143682869&doi=10.1021%2facs.oprd.2c00151&partnerID=40&md5=711ef0b2bc3d494f9eac71d93d3268bc
id 2-s2.0-85143682869
spelling 2-s2.0-85143682869
Shahrir N.; Anuar N.; Abdul Muttalib N.A.; Yusop S.N.; Abu Bakar M.R.; Adam F.; Ibrahim S.F.
The Role of Solvent Hydroxyl Functional Groups on the Interaction Energy and Growth of Form i Paracetamol Crystal Facets
2022
Organic Process Research and Development
26
12
10.1021/acs.oprd.2c00151
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85143682869&doi=10.1021%2facs.oprd.2c00151&partnerID=40&md5=711ef0b2bc3d494f9eac71d93d3268bc
The morphology of a crystal grown in a solvent can change depending on the solvent used during the crystallization process. Modification of the morphology of a crystal can be engineered based on information conferred by the functional groups of the facets of interest and the functional groups of the solvent. This study aims to predict the effect of the alcoholic functional group of amyl alcohol, benzyl alcohol, and phenol on the {002}, {011}, and {110} facets of Form I paracetamol. Prediction and simulation studies were carried out using an embedded tool available in Material Studio. The interaction between the solvents (phenol, benzyl alcohol, and amyl alcohol) and the surfaces used in this study revealed that the {011} facet had the most negative nonbonded energy, followed by the {110} and {002} facets. Overall, the nonbonded interactions between the solvents and the facets were dominated by Coulombic interactions, accounting for more than 90% of the energies, which is within the range from -2566 to -3613 kcal/mol. The binding energy for amyl and benzyl alcohols on the facets of the crystal, ranked from the strongest to the weakest, was in the order {002} > {110} > {011}, while for phenol, the rank was {002} > {011} > {110}. This result is in line with the observed crystal morphology of Form I paracetamol crystallized in a polar protic solvent, in which the most favorable solvent binding on the {002} facets delayed the growth of the elongated hexagonal morphology along the c-axis and formed prismatic-like morphology. Using benzyl alcohol as a case study, an assessment of synthon formation on facets {002} and {011} showed that synthon B is an important synthon for the growth of units of these facets, while synthon F is an important building block synthon for the {110} facet. © 2022 American Chemical Society.
American Chemical Society
10836160
English
Article
All Open Access; Green Open Access
author Shahrir N.; Anuar N.; Abdul Muttalib N.A.; Yusop S.N.; Abu Bakar M.R.; Adam F.; Ibrahim S.F.
spellingShingle Shahrir N.; Anuar N.; Abdul Muttalib N.A.; Yusop S.N.; Abu Bakar M.R.; Adam F.; Ibrahim S.F.
The Role of Solvent Hydroxyl Functional Groups on the Interaction Energy and Growth of Form i Paracetamol Crystal Facets
author_facet Shahrir N.; Anuar N.; Abdul Muttalib N.A.; Yusop S.N.; Abu Bakar M.R.; Adam F.; Ibrahim S.F.
author_sort Shahrir N.; Anuar N.; Abdul Muttalib N.A.; Yusop S.N.; Abu Bakar M.R.; Adam F.; Ibrahim S.F.
title The Role of Solvent Hydroxyl Functional Groups on the Interaction Energy and Growth of Form i Paracetamol Crystal Facets
title_short The Role of Solvent Hydroxyl Functional Groups on the Interaction Energy and Growth of Form i Paracetamol Crystal Facets
title_full The Role of Solvent Hydroxyl Functional Groups on the Interaction Energy and Growth of Form i Paracetamol Crystal Facets
title_fullStr The Role of Solvent Hydroxyl Functional Groups on the Interaction Energy and Growth of Form i Paracetamol Crystal Facets
title_full_unstemmed The Role of Solvent Hydroxyl Functional Groups on the Interaction Energy and Growth of Form i Paracetamol Crystal Facets
title_sort The Role of Solvent Hydroxyl Functional Groups on the Interaction Energy and Growth of Form i Paracetamol Crystal Facets
publishDate 2022
container_title Organic Process Research and Development
container_volume 26
container_issue 12
doi_str_mv 10.1021/acs.oprd.2c00151
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85143682869&doi=10.1021%2facs.oprd.2c00151&partnerID=40&md5=711ef0b2bc3d494f9eac71d93d3268bc
description The morphology of a crystal grown in a solvent can change depending on the solvent used during the crystallization process. Modification of the morphology of a crystal can be engineered based on information conferred by the functional groups of the facets of interest and the functional groups of the solvent. This study aims to predict the effect of the alcoholic functional group of amyl alcohol, benzyl alcohol, and phenol on the {002}, {011}, and {110} facets of Form I paracetamol. Prediction and simulation studies were carried out using an embedded tool available in Material Studio. The interaction between the solvents (phenol, benzyl alcohol, and amyl alcohol) and the surfaces used in this study revealed that the {011} facet had the most negative nonbonded energy, followed by the {110} and {002} facets. Overall, the nonbonded interactions between the solvents and the facets were dominated by Coulombic interactions, accounting for more than 90% of the energies, which is within the range from -2566 to -3613 kcal/mol. The binding energy for amyl and benzyl alcohols on the facets of the crystal, ranked from the strongest to the weakest, was in the order {002} > {110} > {011}, while for phenol, the rank was {002} > {011} > {110}. This result is in line with the observed crystal morphology of Form I paracetamol crystallized in a polar protic solvent, in which the most favorable solvent binding on the {002} facets delayed the growth of the elongated hexagonal morphology along the c-axis and formed prismatic-like morphology. Using benzyl alcohol as a case study, an assessment of synthon formation on facets {002} and {011} showed that synthon B is an important synthon for the growth of units of these facets, while synthon F is an important building block synthon for the {110} facet. © 2022 American Chemical Society.
publisher American Chemical Society
issn 10836160
language English
format Article
accesstype All Open Access; Green Open Access
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