Cocrystal trimorphism as a consequence of the orthogonality of halogen- and hydrogen-bonds synthons

Topić, Filip; Lisac, Katarina; Arhangelskis, Mihails; Rissanen, Kari; Cinčić, Dominik; Friščić, Tomislav

doi:10.1039/C9CC06735C

dc.contributor.author	Topić, Filip
dc.contributor.author	Lisac, Katarina
dc.contributor.author	Arhangelskis, Mihails
dc.contributor.author	Rissanen, Kari
dc.contributor.author	Cinčić, Dominik
dc.contributor.author	Friščić, Tomislav
dc.date.accessioned	2020-01-20T11:37:25Z
dc.date.available	2020-01-20T11:37:25Z
dc.date.issued	2019
dc.identifier.citation	Topić, F., Lisac, K., Arhangelskis, M., Rissanen, K., Cinčić, D., & Friščić, T. (2019). Cocrystal trimorphism as a consequence of the orthogonality of halogen- and hydrogen-bonds synthons. <i>Chemical Communications</i>, <i>55</i>(93), 14066-14069. <a href="https://doi.org/10.1039/C9CC06735C" target="_blank">https://doi.org/10.1039/C9CC06735C</a>
dc.identifier.other	CONVID_33557939
dc.identifier.uri	https://jyx.jyu.fi/handle/123456789/67393
dc.description.abstract	True trimorphic cocrystals, i.e. multi-component molecular crystals of identical composition that exhibit three polymorphic structures, are exceedingly rare and so far no halogen-bonded cocrystal system has been reported to exhibit trimorphism. Here we describe a unique example of a trimorphic cocrystal exhibiting both hydrogen and halogen bonds in which the differences between polymorphs reveal their orthogonality, evident by the apparently independent variation of well-defined hydrogen- and halogen-bonded motifs.	en
dc.format.mimetype	application/pdf
dc.language	eng
dc.language.iso	eng
dc.publisher	Royal Society of Chemistry
dc.relation.ispartofseries	Chemical Communications
dc.rights	In Copyright
dc.title	Cocrystal trimorphism as a consequence of the orthogonality of halogen- and hydrogen-bonds synthons
dc.type	article
dc.identifier.urn	URN:NBN:fi:jyu-202001201334
dc.contributor.laitos	Kemian laitos	fi
dc.contributor.laitos	Department of Chemistry	en
dc.contributor.oppiaine	Orgaaninen kemia	fi
dc.contributor.oppiaine	Nanoscience Center	fi
dc.contributor.oppiaine	Organic Chemistry	en
dc.contributor.oppiaine	Nanoscience Center	en
dc.type.uri	http://purl.org/eprint/type/JournalArticle
dc.type.coar	http://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatus	peerReviewed
dc.format.pagerange	14066-14069
dc.relation.issn	1359-7345
dc.relation.numberinseries	93
dc.relation.volume	55
dc.type.version	acceptedVersion
dc.rights.copyright	© The Royal Society of Chemistry 2019
dc.rights.accesslevel	openAccess	fi
dc.subject.yso	kemialliset sidokset
dc.subject.yso	vetysidokset
dc.subject.yso	supramolekulaarinen kemia
dc.subject.yso	kiteet
dc.format.content	fulltext
jyx.subject.uri	http://www.yso.fi/onto/yso/p10130
jyx.subject.uri	http://www.yso.fi/onto/yso/p38131
jyx.subject.uri	http://www.yso.fi/onto/yso/p37759
jyx.subject.uri	http://www.yso.fi/onto/yso/p15440
dc.rights.url	http://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi	10.1039/C9CC06735C
jyx.fundinginformation	We thank the support of the Government of Canada Banting Fellowship (FT), University of Jyväskylä, NSERC Discovery Grant (RGPIN-2017-06467), E. W. R. Steacie Memorial Fellowship (SMFSU 507347-17), McGill University Herchel Smith Scholarship, Croatian Science Foundation (IP-2014-09-7367).
dc.type.okm	A1

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Cocrystal trimorphism as a consequence of the orthogonality of halogen- and hydrogen-bonds synthons

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