Selective recognition of aromatic hydrocarbons by endo-functionalized molecular tubes via C/N-H⋅⋅⋅π interactions

Huang, Guo-bao; Liu, Wei-Er; Valkonen, Arto; Yao, Huan; Rissanen, Kari; Jiang, Wei

doi:10.1016/j.cclet.2017.07.005

dc.contributor.author	Huang, Guo-bao
dc.contributor.author	Liu, Wei-Er
dc.contributor.author	Valkonen, Arto
dc.contributor.author	Yao, Huan
dc.contributor.author	Rissanen, Kari
dc.contributor.author	Jiang, Wei
dc.date.accessioned	2018-01-17T10:33:31Z
dc.date.available	2020-01-01T22:35:25Z
dc.date.issued	2018
dc.identifier.citation	Huang, G.-B., Liu, W.-E., Valkonen, A., Yao, H., Rissanen, K., & Jiang, W. (2018). Selective recognition of aromatic hydrocarbons by endo-functionalized molecular tubes via C/N-H⋅⋅⋅π interactions. <i>Chinese Chemical Letters</i>, <i>29</i>(1), 91-94. <a href="https://doi.org/10.1016/j.cclet.2017.07.005" target="_blank">https://doi.org/10.1016/j.cclet.2017.07.005</a>
dc.identifier.other	CONVID_27110718
dc.identifier.uri	https://jyx.jyu.fi/handle/123456789/56768
dc.description.abstract	Molecular recognition of aromatic hydrocarbons by four endo-functionalized molecular tubes has been studied by 1H NMR spectroscopy, computational methods, and single crystal X-ray crystallography. The binding selectivity is rationalized by invoking shape complementarity and dipole alignment. The non-covalent interactions are proved to predominantly be C/N-H⋅⋅⋅π interactions.	en
dc.language	eng
dc.language.iso	eng
dc.publisher	Elsevier Ltd; Chinese Chemical Society
dc.relation.ispartofseries	Chinese Chemical Letters
dc.subject.other	macrocycles
dc.subject.other	aromatic hydrocarbon
dc.subject.other	molecular recognition
dc.subject.other	host-guest chemistry
dc.subject.other	hydrogen bond
dc.title	Selective recognition of aromatic hydrocarbons by endo-functionalized molecular tubes via C/N-H⋅⋅⋅π interactions
dc.type	research article
dc.identifier.urn	URN:NBN:fi:jyu-201801151206
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.date.updated	2018-01-15T16:51:44Z
dc.type.coar	http://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatus	peerReviewed
dc.format.pagerange	91-94
dc.relation.issn	1001-8417
dc.relation.numberinseries	1
dc.relation.volume	29
dc.type.version	acceptedVersion
dc.rights.copyright	© 2017 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. This is a final draft version of an article whose final and definitive form has been published by Elsevier. Published in this repository with the kind permission of the publisher.
dc.rights.accesslevel	openAccess	fi
dc.type.publication	article
dc.relation.grantnumber	292746
dc.relation.grantnumber	263256
dc.subject.yso	molekyylidynamiikka
dc.subject.yso	vety
dc.subject.yso	hiilivedyt
jyx.subject.uri	http://www.yso.fi/onto/yso/p29332
jyx.subject.uri	http://www.yso.fi/onto/yso/p16151
jyx.subject.uri	http://www.yso.fi/onto/yso/p1169
dc.relation.doi	10.1016/j.cclet.2017.07.005
dc.relation.funder	Suomen Akatemia	fi
dc.relation.funder	Suomen Akatemia	fi
dc.relation.funder	Research Council of Finland	en
dc.relation.funder	Research Council of Finland	en
jyx.fundingprogram	Akatemiaprofessorin tutkimuskulut, SA	fi
jyx.fundingprogram	Akatemiaprofessorin tehtävä, SA	fi
jyx.fundingprogram	Research costs of Academy Professor, AoF	en
jyx.fundingprogram	Research post as Academy Professor, AoF	en
jyx.fundinginformation	This research was financially supported by the National Natural Science Foundation of China (No. 21572097), Thousand Young Talents Program, South University of Science and Technology of China, the Shenzhen special funds for the development of biomedicine, internet, new energy, and new material industries (Nos. JCYJ20160226192118056, JCYJ20170307105848463), the Startup Program of Yulin Normal University (No. G20160002) and the Academy of Finland (Nos. 263256, 265328 and 292746).
dc.type.okm	A1

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