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dc.contributor.authorPan, Fangfang
dc.contributor.authorChen, Yingchun
dc.contributor.authorLi, Siyu
dc.contributor.authorJiang, Minzhi
dc.contributor.authorRissanen, Kari
dc.date.accessioned2019-06-10T10:02:10Z
dc.date.available2020-04-19T21:35:14Z
dc.date.issued2019
dc.identifier.citationPan, F., Chen, Y., Li, S., Jiang, M., & Rissanen, K. (2019). Iodine Clathrated : A Solid-State Analog of the Iodine-Starch Complex. <i>Chemistry: A European Journal</i>, <i>25</i>(31), 7485-7488. <a href="https://doi.org/10.1002/chem.201901734" target="_blank">https://doi.org/10.1002/chem.201901734</a>
dc.identifier.otherCONVID_30123659
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/64481
dc.description.abstractCo-crystallizing iodine with a simple dicationic salt (1,8- diammoniumoctane chloride) results in the clathration of the iodine (I2) molecules inside trigonal and hexagonal helical channels of the crystal lattice with 72 wt% overall I2 loading. The I2 inside the bigger trigonal channel forms a I-I•••I-I•••I-I halogen-bonded infinite helical chain, while the I2 in the smaller hexagonal channel is disordered. In both channels the I2 interaction with the channel wall happens through I-I•••Cl- halogen bonds. The helical channels in the crystal lattice are constructed via the strong charge-assisted H2N+ -H•••Cl- hydrogen bonds between the dications and the chloride anions. The structure shows a marked similarity with the well-known starch-I2 system, and thus may provide insight for the yet unresolved structure of the I2 in the helical starch channel.fi
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherWiley - VCH Verlag GmbH & Co. KGaA
dc.relation.ispartofseriesChemistry: A European Journal
dc.rightsIn Copyright
dc.subject.otherclathrate
dc.subject.otherhalogen bonding
dc.subject.otherhydrogen bonding
dc.titleIodine Clathrated : A Solid-State Analog of the Iodine-Starch Complex
dc.typeresearch article
dc.identifier.urnURN:NBN:fi:jyu-201906073077
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineOrganic Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2019-06-07T15:15:40Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange7485-7488
dc.relation.issn0947-6539
dc.relation.numberinseries31
dc.relation.volume25
dc.type.versionacceptedVersion
dc.rights.copyright© 2019 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.rights.accesslevelopenAccessfi
dc.type.publicationarticle
dc.subject.ysojodi
dc.subject.ysosupramolekulaarinen kemia
dc.subject.ysokemialliset sidokset
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p18902
jyx.subject.urihttp://www.yso.fi/onto/yso/p37759
jyx.subject.urihttp://www.yso.fi/onto/yso/p10130
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1002/chem.201901734
dc.type.okmA1


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