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dc.contributor.authorMoro, Artur J.
dc.contributor.authorRome, Bertrand
dc.contributor.authorAguiló, Elisabet
dc.contributor.authorArcau, Julià
dc.contributor.authorPuttreddy, Rakesh
dc.contributor.authorRissanen, Kari
dc.contributor.authorLima, João Carlos
dc.contributor.authorRodríguez, Laura
dc.date.accessioned2016-07-01T06:06:17Z
dc.date.available2016-07-01T06:06:17Z
dc.date.issued2015
dc.identifier.citationMoro, A. J., Rome, B., Aguiló, E., Arcau, J., Puttreddy, R., Rissanen, K., Lima, J. C., & Rodríguez, L. (2015). A coumarin based gold(I)-alkynyl complex: a new class of supramolecular hydrogelators. <i>Organic and biomolecular chemistry</i>, <i>13</i>(7), 2026-2033. <a href="https://doi.org/10.1039/C4OB02077D" target="_blank">https://doi.org/10.1039/C4OB02077D</a>
dc.identifier.otherCONVID_24534726
dc.identifier.otherTUTKAID_65144
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/50670
dc.description.abstractA phosphine-gold(I)-alkynyl-coumarin complex, [Au{7-(prop-2-ine-1-yloxy)-1-benzopyran-2-one}- (DAPTA)] (1), was synthesized and the formation of long luminescent fibers in solution was characterized via fluorescence microscopy and dynamic light scattering. The fibers presented strong blue and green luminescence, suggesting that the gold(I) in the complex increased intersystem crossing due to the heavy atom effect, resulting in a significant increase in triplet emission. The X-ray structure of the fibers indicates that both aurophilic, π–π interactions and hydrogen bonding contribute to their formation in aqueous solvents.
dc.language.isoeng
dc.publisherRSC Publications
dc.relation.ispartofseriesOrganic and biomolecular chemistry
dc.subject.othercoumarin based
dc.subject.othergold(I)-alkynyl complex
dc.subject.othersupramolecular
dc.subject.otherhydrogelators
dc.titleA coumarin based gold(I)-alkynyl complex: a new class of supramolecular hydrogelators
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201606303416
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineNanoscience Centerfi
dc.contributor.oppiaineOrganic Chemistryen
dc.contributor.oppiaineNanoscience Centeren
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2016-06-30T12:15:31Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange2026-2033
dc.relation.issn1477-0520
dc.relation.numberinseries7
dc.relation.volume13
dc.type.versionpublishedVersion
dc.rights.copyright© the Authors, 2015. The journal is © The Royal Society of Chemistry 2015. This is an open access article distributed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
dc.rights.accesslevelopenAccessfi
dc.rights.urlhttps://creativecommons.org/licenses/by-nc/3.0/
dc.relation.doi10.1039/C4OB02077D
dc.type.okmA1


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© the Authors, 2015. The journal is © The Royal Society of Chemistry 2015. This is an open access article distributed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.
Ellei muuten mainita, aineiston lisenssi on © the Authors, 2015. The journal is © The Royal Society of Chemistry 2015. This is an open access article distributed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence.