A 2,3-dialkoxynaphthalene-based naphthocage

Lu, Song-Bo; Chai, Hongxin; Ward, Jas S.; Quan, Mao; Zhang, Jin; Rissanen, Kari; Luo, Ray; Yang, Liu-Pan; Jiang, Wei

doi:10.1039/C9CC09585C

dc.contributor.author	Lu, Song-Bo
dc.contributor.author	Chai, Hongxin
dc.contributor.author	Ward, Jas S.
dc.contributor.author	Quan, Mao
dc.contributor.author	Zhang, Jin
dc.contributor.author	Rissanen, Kari
dc.contributor.author	Luo, Ray
dc.contributor.author	Yang, Liu-Pan
dc.contributor.author	Jiang, Wei
dc.date.accessioned	2020-12-22T12:01:07Z
dc.date.available	2020-12-22T12:01:07Z
dc.date.issued	2020
dc.identifier.citation	Lu, 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.other	CONVID_34060623
dc.identifier.uri	https://jyx.jyu.fi/handle/123456789/73396
dc.description.abstract	A 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.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	A 2,3-dialkoxynaphthalene-based naphthocage
dc.type	article
dc.identifier.urn	URN:NBN:fi:jyu-202012227338
dc.contributor.laitos	Kemian laitos	fi
dc.contributor.laitos	Department of Chemistry	en
dc.contributor.oppiaine	Orgaaninen kemia	fi
dc.contributor.oppiaine	Organic Chemistry	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	888-891
dc.relation.issn	1359-7345
dc.relation.numberinseries	6
dc.relation.volume	56
dc.type.version	acceptedVersion
dc.rights.copyright	© 2020 Royal Society of Chemistry
dc.rights.accesslevel	openAccess	fi
dc.subject.yso	supramolekulaarinen kemia
dc.subject.yso	kationit
dc.format.content	fulltext
jyx.subject.uri	http://www.yso.fi/onto/yso/p37759
jyx.subject.uri	http://www.yso.fi/onto/yso/p27230
dc.rights.url	http://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi	10.1039/C9CC09585C
jyx.fundinginformation	This 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.okm	A1