클로로벤젠 설포네이트 음이온에 기반을 둔 비선형 광학 퀴놀리니움 결정

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dc.contributor.advisor권오필-
dc.contributor.author이승준-
dc.date.accessioned2018-11-08T08:10:40Z-
dc.date.available2018-11-08T08:10:40Z-
dc.date.issued2017-02-
dc.identifier.other24100-
dc.identifier.urihttps://dspace.ajou.ac.kr/handle/2018.oak/11202-
dc.description학위논문(석사)--아주대학교 일반대학원 :분자과학기술학과,2017. 2-
dc.description.tableofcontentsΙ. Introduction 1 II. Experiments 5 II.1. Chemical Structures 5 II.2. Synthesis 6 II.2.1. Materials 6 II.2.2. Synthesis of OHQ-CBS 7 II.3. General Characterization 8 II.3.1. 1H-NMR Analysis 8 II.3.1.1. 1H-NMR Analysis of Intermediate 8 II.3.1.2. 1H-NMR Analysis of Chromophore 10 III. Results and Discussion 12 III.1. Thermal Analysis 12 III.2. Optical Properties 14 III.2.1 UV-vis Absorption, FL Spectra 14 III.3. Second Harmonic Generation (SHG) Test 17 III.4. Crystal Growth and Structure Analysis 18 III.5. Growth of OHQ-CBS, OHQ-T Co-crystals 27 III.6. 1H-NMR Analysis of OHQ-CBS, OHQ-T Co-crystals 29 III.7. XRD Analysis of OHQ-CBS, OHQ-T Co-crystals 30 III.8. Thermal Analysis of OHQ-CBS, OHQ-T Co-crystals 32 III.9. Photophysical Property of OHQ-CBS, OHQ-T Co-crystals 33 III.10. IR spectroscopy in THz region of OHQ-CBS, OHQ-T Co-crystals 34 IV. Conclusions 35 V. References 36-
dc.language.isoeng-
dc.publisherThe Graduate School, Ajou University-
dc.rights아주대학교 논문은 저작권에 의해 보호받습니다.-
dc.title클로로벤젠 설포네이트 음이온에 기반을 둔 비선형 광학 퀴놀리니움 결정-
dc.typeThesis-
dc.contributor.affiliation아주대학교 일반대학원-
dc.contributor.department일반대학원 분자과학기술학과-
dc.date.awarded2017. 2-
dc.description.degreeMaster-
dc.identifier.localId770562-
dc.identifier.urlhttp://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000024100-
dc.subject.keywordCo-crystals-
dc.subject.keywordChlorobenzenesulfonate-
dc.subject.keywordCrystals-
dc.description.alternativeAbstractWe designed and synthesized the acentric core structure OHQ (2-(4-hydroxystyryl)-1-methylquinolinium) cation with 4-chlorobenzenesulfonate counter anions, named OHQ-CBS. OHQ-CBS single crystals were obtained by the various solution growth methods. We assured the non-centrosymmetric molecular arrangement by the second harmonic generation (SHG) test and X-ray diffraction analysis. In addition, we investigated the physical properties, such as thermal stability, absorbance, fluorescence, and optical nonlinearity. OHQ-CBS crystals maintained advantage of previously reported OHQ-T (2-(4-hydroxystyryl)-1-methylquinolinium 4-methylbenzenesulfonate) crystals such as thermal stability, high order parameter and large area of crystals. OHQ-CBS crystals exhibit strong SHG intensity more than OHQ-T crystals, which is indicating enhanced molecular nonlinearity. Accordingly, compared to OHQ-T crystals, OHQ-CBS crystals are highly red shift at absorbance, fluorecence in crystalline state. In order to discover differences of intermolecular interaction of OHQ-T crystals and OHQ-CBS crystals, we performed a hirshfeld analysis. Furthermore, we demonstrated co-crystallization of OHQ-T, OHQ-CBS crystals with different feeding ratio in solution. Physical property such as absorbance, photoluminescence, thermal stability, high frequency IR region was linearly changed by mole percentage of OHQ-T in crystal. It indicated that feeding ratio of counter anions in solution controlled physical property of co-crystals.-
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Graduate School of Ajou University > Department of Molecular Science and Technology > 3. Theses(Master)
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