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dc.contributor.authorSuhonen, Aku
dc.contributor.authorKortelainen, Minna
dc.contributor.authorNauha, Elisa
dc.contributor.authorYliniemelä-Sipari, Sanna
dc.contributor.authorPihko, Petri
dc.contributor.authorNissinen, Maija
dc.date.accessioned2016-03-16T07:23:56Z
dc.date.available2017-02-19T22:45:04Z
dc.date.issued2016
dc.identifier.citationSuhonen, A., Kortelainen, M., Nauha, E., Yliniemelä-Sipari, S., Pihko, P., & Nissinen, M. (2016). Conformational properties and folding analysis of a series of seven oligoamide foldamers. <i>CrystEngComm</i>, <i>18</i>(11), 2005-2013. <a href="https://doi.org/10.1039/C5CE02458G" target="_blank">https://doi.org/10.1039/C5CE02458G</a>
dc.identifier.otherCONVID_25592531
dc.identifier.otherTUTKAID_69427
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/49062
dc.description.abstract33 crystal structures (11 unsolvated and 22 solvates) of a series of seven oligoamide foldamers were analysed. The crystal structures revealed that despite the structural and environmental differences the series of foldamers prefer only two general conformations, a protohelical @-conformation and a sigmoidal S-conformation. Both conformations also have preferred crystal packing motifs and solvate forming tendencies. Hydrogen bonding was found to be the most decisive factor in conformational preference, but steric properties, the type of the peripheral substituents, as well as solvent and aromatic interactions were also found to have an effect on the conformational details and crystal form.
dc.language.isoeng
dc.publisherRoyal Society of Chemistry
dc.relation.ispartofseriesCrystEngComm
dc.subject.otherconformational properties
dc.subject.otherfolding analysis
dc.subject.otheroligoamide foldamers
dc.titleConformational properties and folding analysis of a series of seven oligoamide foldamers
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201603111827
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.updated2016-03-11T10:15:07Z
dc.type.coarjournal article
dc.description.reviewstatuspeerReviewed
dc.format.pagerange2005-2013
dc.relation.issn1466-8033
dc.relation.numberinseries11
dc.relation.volume18
dc.type.versionacceptedVersion
dc.rights.copyright© The Royal Society of Chemistry 2016. 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.relation.doi10.1039/C5CE02458G


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