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The Solvatochromism and Electronic Structure of (e)-2

dc.authorid Gumus, Selcuk/0000-0002-8628-8943
dc.authorid Gumus, Aysegul/0000-0002-1613-7074
dc.authorscopusid 6603208702
dc.authorscopusid 35204095900
dc.authorscopusid 25655631500
dc.authorscopusid 6602962437
dc.contributor.author Gumus, Aysegul
dc.contributor.author Gulseven Sidir, Yadigar
dc.contributor.author Sidir, Isa
dc.contributor.author Gumus, Selcuk
dc.date.accessioned 2025-05-10T17:45:51Z
dc.date.available 2025-05-10T17:45:51Z
dc.date.issued 2019
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Gumus, Aysegul; Gumus, Selcuk] Van Yuzuncu Yil Univ, Fac Sci, Dept Chem, Van, Turkey; [Gulseven Sidir, Yadigar; Sidir, Isa] Bitlis Eren Univ, Fac Arts & Sci, Dept Phys, Bitlis, Turkey en_US
dc.description Gumus, Selcuk/0000-0002-8628-8943; Gumus, Aysegul/0000-0002-1613-7074 en_US
dc.description.abstract The (E)-2-(2-hydroxystyryl)quinolin-8-ol (abbreviated as HSQ) molecule was synthesized and characterized. The ESIPT, solvatochromism properties, electronic structure, and ground and excited electric dipole moments of this molecule were measured using absorption and fluorescence spectra recorded in 13 different solvents. Its electronic structure via electronic transitions was investigated to find the quantitative values of solvatochromism properties by LSER calculations. The ESIPT mechanism was clarified; ground and excited dipole moments were determined using solvatochromic shift methods. The DFT (B3LYP)/6-311 ++ G(d,p) method and basis set with potential energy surface (PES) calculations of proton transfer were used to explain the ESIPT mechanism. NBO analysis, NLO properties, and behavior under an electric field were also determined. en_US
dc.description.sponsorship Presidency of Scientific Research Projects of Van Yuzuncu Yil University [2015-FEN-B326]; Bitlis Eren University Scientific and Technological Application and Research Center en_US
dc.description.sponsorship We are grateful to the Presidency of Scientific Research Projects of Van Yuzuncu Yil University for its financial support (2015-FEN-B326). The authors greatly acknowledge the support of Bitlis Eren University Scientific and Technological Application and Research Center. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.3906/kim-1903-36
dc.identifier.endpage 1521 en_US
dc.identifier.issn 1300-0527
dc.identifier.issue 6 en_US
dc.identifier.scopus 2-s2.0-85077213758
dc.identifier.scopusquality Q3
dc.identifier.startpage 1503 en_US
dc.identifier.trdizinid 336085
dc.identifier.uri https://doi.org/10.3906/kim-1903-36
dc.identifier.uri https://hdl.handle.net/20.500.14720/16483
dc.identifier.volume 43 en_US
dc.identifier.wos WOS:000501598500001
dc.identifier.wosquality Q4
dc.language.iso en en_US
dc.publisher Tubitak Scientific & Technological Research Council Turkey en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject 8-Hydroxyquinoline en_US
dc.subject 2-Styrylquinoline en_US
dc.subject Solvatochromism en_US
dc.subject Electric Dipole Moment en_US
dc.subject Electronic Structure en_US
dc.title The Solvatochromism and Electronic Structure of (e)-2 en_US
dc.type Article en_US

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