Cargando…
Supramolecular Similarity in Polymorphs: Use of Similarity Indices (I(X))
[Image: see text] A systematic investigation to assess the degree of similarity between polymorphs was carried out. A similarity indices (I(X)) approach was applied in ten series of polymorphs with different characteristics and number of molecules in the asymmetric unit. Geometric (I(D)), contact ar...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648757/ https://www.ncbi.nlm.nih.gov/pubmed/31460060 http://dx.doi.org/10.1021/acsomega.8b03660 |
_version_ | 1783437935921594368 |
---|---|
author | Salbego, Paulo R. S. Bender, Caroline R. Orlando, Tainára Moraes, Guilherme A. Copetti, João P. P. Weimer, Gustavo H. Bonacorso, Helio G. Zanatta, Nilo Hoerner, Manfredo Martins, Marcos A. P. |
author_facet | Salbego, Paulo R. S. Bender, Caroline R. Orlando, Tainára Moraes, Guilherme A. Copetti, João P. P. Weimer, Gustavo H. Bonacorso, Helio G. Zanatta, Nilo Hoerner, Manfredo Martins, Marcos A. P. |
author_sort | Salbego, Paulo R. S. |
collection | PubMed |
description | [Image: see text] A systematic investigation to assess the degree of similarity between polymorphs was carried out. A similarity indices (I(X)) approach was applied in ten series of polymorphs with different characteristics and number of molecules in the asymmetric unit. Geometric (I(D)), contact area (I(C)), and stabilization energy (I(G)) parameters were used. It was possible to situate each comparison in different regions of similarity within the polymorphism phenomenon and determine the boundaries between quasi-isostructural polymorphs and polymorphs of low similarity. The multiparameter I(DCG) index was used as a robust tool to determine the total similarity within the polymorphism phenomenon. The highest contribution of the stabilization energy parameter (45%) toward the final value of similarity (I(DCG)) was observed, followed by the contact area index (32%). The geometric index contributed approximately 23% to the final value of I(DCG). This information reinforces the importance of the contact area and stabilization energy in assessing the degree of similarity between crystalline structures. A new descriptor (I(Q)) based on the comparison of the energetic contribution of intermolecular interaction types present in each crystal structure is presented. I(Q) can be a versatile tool and applicable even for systems that do not share any similarity. |
format | Online Article Text |
id | pubmed-6648757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66487572019-08-27 Supramolecular Similarity in Polymorphs: Use of Similarity Indices (I(X)) Salbego, Paulo R. S. Bender, Caroline R. Orlando, Tainára Moraes, Guilherme A. Copetti, João P. P. Weimer, Gustavo H. Bonacorso, Helio G. Zanatta, Nilo Hoerner, Manfredo Martins, Marcos A. P. ACS Omega [Image: see text] A systematic investigation to assess the degree of similarity between polymorphs was carried out. A similarity indices (I(X)) approach was applied in ten series of polymorphs with different characteristics and number of molecules in the asymmetric unit. Geometric (I(D)), contact area (I(C)), and stabilization energy (I(G)) parameters were used. It was possible to situate each comparison in different regions of similarity within the polymorphism phenomenon and determine the boundaries between quasi-isostructural polymorphs and polymorphs of low similarity. The multiparameter I(DCG) index was used as a robust tool to determine the total similarity within the polymorphism phenomenon. The highest contribution of the stabilization energy parameter (45%) toward the final value of similarity (I(DCG)) was observed, followed by the contact area index (32%). The geometric index contributed approximately 23% to the final value of I(DCG). This information reinforces the importance of the contact area and stabilization energy in assessing the degree of similarity between crystalline structures. A new descriptor (I(Q)) based on the comparison of the energetic contribution of intermolecular interaction types present in each crystal structure is presented. I(Q) can be a versatile tool and applicable even for systems that do not share any similarity. American Chemical Society 2019-06-03 /pmc/articles/PMC6648757/ /pubmed/31460060 http://dx.doi.org/10.1021/acsomega.8b03660 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Salbego, Paulo R. S. Bender, Caroline R. Orlando, Tainára Moraes, Guilherme A. Copetti, João P. P. Weimer, Gustavo H. Bonacorso, Helio G. Zanatta, Nilo Hoerner, Manfredo Martins, Marcos A. P. Supramolecular Similarity in Polymorphs: Use of Similarity Indices (I(X)) |
title | Supramolecular Similarity in Polymorphs: Use of Similarity
Indices (I(X)) |
title_full | Supramolecular Similarity in Polymorphs: Use of Similarity
Indices (I(X)) |
title_fullStr | Supramolecular Similarity in Polymorphs: Use of Similarity
Indices (I(X)) |
title_full_unstemmed | Supramolecular Similarity in Polymorphs: Use of Similarity
Indices (I(X)) |
title_short | Supramolecular Similarity in Polymorphs: Use of Similarity
Indices (I(X)) |
title_sort | supramolecular similarity in polymorphs: use of similarity
indices (i(x)) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648757/ https://www.ncbi.nlm.nih.gov/pubmed/31460060 http://dx.doi.org/10.1021/acsomega.8b03660 |
work_keys_str_mv | AT salbegopaulors supramolecularsimilarityinpolymorphsuseofsimilarityindicesix AT bendercaroliner supramolecularsimilarityinpolymorphsuseofsimilarityindicesix AT orlandotainara supramolecularsimilarityinpolymorphsuseofsimilarityindicesix AT moraesguilhermea supramolecularsimilarityinpolymorphsuseofsimilarityindicesix AT copettijoaopp supramolecularsimilarityinpolymorphsuseofsimilarityindicesix AT weimergustavoh supramolecularsimilarityinpolymorphsuseofsimilarityindicesix AT bonacorsoheliog supramolecularsimilarityinpolymorphsuseofsimilarityindicesix AT zanattanilo supramolecularsimilarityinpolymorphsuseofsimilarityindicesix AT hoernermanfredo supramolecularsimilarityinpolymorphsuseofsimilarityindicesix AT martinsmarcosap supramolecularsimilarityinpolymorphsuseofsimilarityindicesix |