完整後設資料紀錄
DC 欄位語言
dc.contributor.authorHaupa, Karolina Annaen_US
dc.contributor.authorSzukalski, Adamen_US
dc.contributor.authorMysliwiec, Jaroslawen_US
dc.date.accessioned2019-04-02T06:00:29Z-
dc.date.available2019-04-02T06:00:29Z-
dc.date.issued2018-10-04en_US
dc.identifier.issn1089-5639en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.jpca.8b04814en_US
dc.identifier.urihttp://hdl.handle.net/11536/148271-
dc.description.abstractIntermolecular interactions between dyes and solvents are essential in understanding a number of phenomena. In this contribution, we focused on similarities and differences between two molecules belonging to the same pyrazoline derivatives group: the small and rigid- 3-(1,1-dicyanoethenyl)-1-phenyl-4,5-dihydro-1H-pyrazole (DCNP) molecule and the quite long and 3 flexible one of (4-(2-(1-phenyl-4,5-dihydro-1H-pyrazol-3-yl)vinyl)-benzylidene) malononitrile (PY-PhdiCN). We experimentally show and use theoretical calculations to prove that extension of pi-connector significantly changes the electrostatic potential distribution, which results in delocalization of negative charge along the whole donor group and increases potential surface of interaction with solvent molecules giving large spectral shifts. We also show that pyrazoline derivatives are very effective and sensitive solvent indicators with long-time stability.en_US
dc.language.isoen_USen_US
dc.titleLow-Molecular Push Pull Pyrazoline Derivatives: Solvatochromic Effect and Theoretical Insights into Dye-based Molecular Engineeringen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.jpca.8b04814en_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Aen_US
dc.citation.volume122en_US
dc.citation.spage7808en_US
dc.citation.epage7818en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000446925400005en_US
dc.citation.woscount1en_US
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