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Article: Phenyl-Linked Anthracene-Based Macrocycles with Geometrically Tunable Optical Properties

TitlePhenyl-Linked Anthracene-Based Macrocycles with Geometrically Tunable Optical Properties
Authors
Keywordsanthracene
macrocycles
geometrically
optical properties
fluorescence
Issue Date2020
PublisherThieme Open. The Journal's web site is located at https://www.thieme.de/en/thieme-chemistry/organic-materials-journal-information-136626.htm
Citation
Organic Materials, 2020, v. 02 n. 04, p. 336-341 How to Cite?
AbstractAnthracene has been widely explored because of its intrinsic photophysical and photochemical properties. Here, two novel anthracene-based macrocycles (1 and 2) were designed and synthesized with para- and meta-phenylene spacers. X-ray crystallographic analysis demonstrates that compound 1 with para-phenylene spacers adopts a nearly planar structure, while compound 2 with meta-phenylene spacers displays a V-shaped geometry. The photophysical properties of the resultant macrocycles, which are structural isomers, are well studied using photoluminescence spectra and time-resolved absorption spectra, which are further corroborated by density functional theory calculations. The optical properties of these two novel macrocycles can be finely tuned via their geometries.
Persistent Identifierhttp://hdl.handle.net/10722/305274
ISSN

 

DC FieldValueLanguage
dc.contributor.authorRong, MG-
dc.contributor.authorWANG, J-
dc.contributor.authorLow, KH-
dc.contributor.authorLiu, J-
dc.date.accessioned2021-10-20T10:07:06Z-
dc.date.available2021-10-20T10:07:06Z-
dc.date.issued2020-
dc.identifier.citationOrganic Materials, 2020, v. 02 n. 04, p. 336-341-
dc.identifier.issn2625-1825-
dc.identifier.urihttp://hdl.handle.net/10722/305274-
dc.description.abstractAnthracene has been widely explored because of its intrinsic photophysical and photochemical properties. Here, two novel anthracene-based macrocycles (1 and 2) were designed and synthesized with para- and meta-phenylene spacers. X-ray crystallographic analysis demonstrates that compound 1 with para-phenylene spacers adopts a nearly planar structure, while compound 2 with meta-phenylene spacers displays a V-shaped geometry. The photophysical properties of the resultant macrocycles, which are structural isomers, are well studied using photoluminescence spectra and time-resolved absorption spectra, which are further corroborated by density functional theory calculations. The optical properties of these two novel macrocycles can be finely tuned via their geometries.-
dc.languageeng-
dc.publisherThieme Open. The Journal's web site is located at https://www.thieme.de/en/thieme-chemistry/organic-materials-journal-information-136626.htm-
dc.relation.ispartofOrganic Materials-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectanthracene-
dc.subjectmacrocycles-
dc.subjectgeometrically-
dc.subjectoptical properties-
dc.subjectfluorescence-
dc.titlePhenyl-Linked Anthracene-Based Macrocycles with Geometrically Tunable Optical Properties-
dc.typeArticle-
dc.identifier.emailRong, MG: rongmg@hku.hk-
dc.identifier.emailLow, KH: khlow@hku.hk-
dc.identifier.emailLiu, J: juliu@hku.hk-
dc.identifier.authorityLiu, J=rp02584-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1055/s-0040-1721729-
dc.identifier.hkuros327172-
dc.identifier.volume02-
dc.identifier.issue04-
dc.identifier.spage336-
dc.identifier.epage341-
dc.publisher.placeGermany-

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