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dc.contributor.authorRissanen, Kari
dc.date.accessioned2018-02-01T07:01:39Z
dc.date.available2018-04-05T21:45:14Z
dc.date.issued2017
dc.identifier.citationRissanen, K. (2017). Crystallography of encapsulated molecules. <i>Chemical Society Reviews</i>, <i>46</i>(9), 2638-2648. <a href="https://doi.org/10.1039/C7CS00090A" target="_blank">https://doi.org/10.1039/C7CS00090A</a>
dc.identifier.otherCONVID_26947919
dc.identifier.otherTUTKAID_73484
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/56970
dc.description.abstractThe crystallography of supramolecular host–guest complexes is reviewed and discussed as a part of small molecule crystallography. In these complexes, the host binds the guests through weak supramolecular interactions, such as hydrogen and halogen bonding, cation–π, anion–π, C–H–π, π–π, C–H–anion interactions and the hydrophobic effect. As the guest often shows severe disorder, large thermal motion and low occupancies, the reliable crystallographic determination of the guest can be very demanding. The analysis of host–guest interactions using tools such as Hirshfeld and cavity volume surface analysis will help to look closely at the most important host–guest interactions. The jewel in the crown of utilizing host–guest interactions in the solid-state is the recently developed Crystalline Sponge Method (CSM) by Makoto Fujita. This method, when successful, gives an accurate and unambiguous 3-D structure of the structurally unknown guest molecule from only micro- or nanogram amounts of the guest molecule. In the case of an optically pure enantiomer, its absolute configuration can be determined.
dc.language.isoeng
dc.publisherRoyal Society of Chemistry
dc.relation.ispartofseriesChemical Society Reviews
dc.subject.othersupramolecular host-guest complexes
dc.subject.otherhost-guest interactions
dc.titleCrystallography of encapsulated molecules
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201801311395
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineNanoscience Centerfi
dc.contributor.oppiaineOrganic Chemistryen
dc.contributor.oppiaineNanoscience Centeren
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2018-01-31T13:15:22Z
dc.type.coarjournal article
dc.description.reviewstatuspeerReviewed
dc.format.pagerange2638-2648
dc.relation.issn0306-0012
dc.relation.numberinseries9
dc.relation.volume46
dc.type.versionacceptedVersion
dc.rights.copyright© The Royal Society of Chemistry 2017. This is a final draft version of an article whose final and definitive form has been published by RSC. Published in this repository with the kind permission of the publisher.
dc.rights.accesslevelopenAccessfi
dc.subject.ysokidetiede
jyx.subject.urihttp://www.yso.fi/onto/yso/p643
dc.relation.doi10.1039/C7CS00090A


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