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A 2,3-dialkoxynaphthalene-based naphthocage

dc.contributor.authorLu, Song-Bo
dc.contributor.authorChai, Hongxin
dc.contributor.authorWard, Jas S.
dc.contributor.authorQuan, Mao
dc.contributor.authorZhang, Jin
dc.contributor.authorRissanen, Kari
dc.contributor.authorLuo, Ray
dc.contributor.authorYang, Liu-Pan
dc.contributor.authorJiang, Wei
dc.date.accessioned2020-12-22T12:01:07Z
dc.date.available2020-12-22T12:01:07Z
dc.date.issued2020
dc.identifier.citationLu, S.-B., Chai, H., Ward, J. S., Quan, M., Zhang, J., Rissanen, K., Luo, R., Yang, L.-P., & Jiang, W. (2020). A 2,3-dialkoxynaphthalene-based naphthocage. <i>Chemical Communications</i>, <i>56</i>(6), 888-891. <a href="https://doi.org/10.1039/C9CC09585C" target="_blank">https://doi.org/10.1039/C9CC09585C</a>
dc.identifier.otherCONVID_34060623
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/73396
dc.description.abstractA 2,3-dialkoxynaphthalene-based naphthocage has been synthesized. This naphthocage prefers to bind small organic cations with its low-symmetry conformation, which is in contrast to 2,6-dialkoxynaphthalene-based naphthocages. Self-sorting of these two naphthocages with two structurally similar guests tetramethylammonium and tetraethylammonium was achieved as well.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherRoyal Society of Chemistry
dc.relation.ispartofseriesChemical Communications
dc.rightsIn Copyright
dc.titleA 2,3-dialkoxynaphthalene-based naphthocage
dc.typeresearch article
dc.identifier.urnURN:NBN:fi:jyu-202012227338
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.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange888-891
dc.relation.issn1359-7345
dc.relation.numberinseries6
dc.relation.volume56
dc.type.versionacceptedVersion
dc.rights.copyright© 2020 Royal Society of Chemistry
dc.rights.accesslevelopenAccessfi
dc.type.publicationarticle
dc.subject.ysosupramolekulaarinen kemia
dc.subject.ysokationit
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p37759
jyx.subject.urihttp://www.yso.fi/onto/yso/p27230
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1039/C9CC09585C
jyx.fundinginformationThis research was financially supported by the National Natural Science Foundation of China (Grant No. 21822104, 21801125), China Postdoctoral Science Foundation (Grant No. 2019M652183), the Shenzhen Science and Technology Innovation Committee (Grant No. JCYJ20180504165810828 and KQJSCX 20170728162528382), the Shenzhen Nobel Prize Scientists Laboratory Project (C17783101), the Open Project of the State Key Laboratory of Molecular Engineering of Polymers (Fudan University, K2019-05) and the University of Jyväskylä. We thank SUSTech CRF and the Center for Computational Science and Engineering for the technical supports.
dc.type.okmA1


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