{"id":{"repo_id":"uiuc","oai_identifier":"oai:www.ideals.illinois.edu:2142/77257"},"canonical_url":"https://search.dev.ndltd.org/etd/uiuc/oai:www.ideals.illinois.edu:2142/77257","repository":{"repo_id":"uiuc","name":"University of Illinois - Urbana-Champaign","base_url":"https://www.ideals.illinois.edu/oai-pmh"},"display":{"title":"Multi-Method Investigation of the Mechanism of Surfactant-Induced Chromatotropism of Metal-Chelometric Dye Complexes","abstract":"The mechanism by which certain surfactants change the ultraviolet-visible (UV-vis) spectroscopic properties of certain metal-dye complexes has been largely ignored in the chemical literature. In this manuscript a model is developed to describe this mechanism. Intramolecular forces among surfactant molecules and host molecules are described to emphasize the importance of specific interactions to the mechanism. A review of the theoretical basis of UV-vis spectroscopic changes in dyes (chromatotropism) is given followed by application to the dyes of interest in this study. UV-vis spectra of the dyes, metal-dye complexes, and metal-dye-surfactant systems are analysed and a relationship between the symmetry of the chromophore and the UV-vis spectroscopic properties is described. This is the basis of the mechanistic model which postulates that the metal ion of the complex migrates from an asymmetric binding site to a symmetric binding site of the dye upon interaction with surfactant. Evidence in support of the molecular structures of the metal-dye complexes and metal-dye-surfactant systems proposed by the model is given in the analysis of infrared (IR) and Raman (R) spectra of these species. Structures of two metal-dye surfactant systems are proposed on the basis of the vibrational data. Thermodynamics of the rearrangements proposed by the model are investigated using ab-initio Hartree-Fock molecular orbital calculations.","abstract_html":"The mechanism by which certain surfactants change the ultraviolet-visible (UV-vis) spectroscopic properties of certain metal-dye complexes has been largely ignored in the chemical literature. In this manuscript a model is developed to describe this mechanism. Intramolecular forces among surfactant molecules and host molecules are described to emphasize the importance of specific interactions to the mechanism. A review of the theoretical basis of UV-vis spectroscopic changes in dyes (chromatotropism) is given followed by application to the dyes of interest in this study. UV-vis spectra of the dyes, metal-dye complexes, and metal-dye-surfactant systems are analysed and a relationship between the symmetry of the chromophore and the UV-vis spectroscopic properties is described. This is the basis of the mechanistic model which postulates that the metal ion of the complex migrates from an asymmetric binding site to a symmetric binding site of the dye upon interaction with surfactant. Evidence in support of the molecular structures of the metal-dye complexes and metal-dye-surfactant systems proposed by the model is given in the analysis of infrared (IR) and Raman (R) spectra of these species. Structures of two metal-dye surfactant systems are proposed on the basis of the vibrational data. Thermodynamics of the rearrangements proposed by the model are investigated using ab-initio Hartree-Fock molecular orbital calculations.","abstract_has_math":false,"creators":["Ogawa, Mark Kenneth"],"institution":"University of Illinois at Urbana-Champaign","degree_name":"Ph.D.","degree_level":"Dissertation","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2015,"date_issued":"2015-05-13T15:37:25Z","date_published":"2015-05-13T15:37:25Z","updated_at":"2026-07-22T22:26:10Z","subjects":["Chemistry, Analytical"],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["(UMI)AAI8803159"],"render_values":[{"text":"(UMI)AAI8803159","href":null,"code":true}]}]},"links":{"outbound_url":"http://hdl.handle.net/2142/77257","outbound_label":"Handle","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Ogawa, Mark Kenneth"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2015-05-13T15:37:25Z","10000-01-01","1987"]},{"key":"dc:type","label":"Dc Type","values":["text"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Ph.D."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Illinois at Urbana-Champaign"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Chemistry, Analytical"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["http://hdl.handle.net/2142/77257","(UMI)AAI8803159"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["The mechanism by which certain surfactants change the ultraviolet-visible (UV-vis) spectroscopic properties of certain metal-dye complexes has been largely ignored in the chemical literature. In this manuscript a model is developed to describe this mechanism. Intramolecular forces among surfactant molecules and host molecules are described to emphasize the importance of specific interactions to the mechanism. A review of the theoretical basis of UV-vis spectroscopic changes in dyes (chromatotropism) is given followed by application to the dyes of interest in this study. UV-vis spectra of the dyes, metal-dye complexes, and metal-dye-surfactant systems are analysed and a relationship between the symmetry of the chromophore and the UV-vis spectroscopic properties is described. This is the basis of the mechanistic model which postulates that the metal ion of the complex migrates from an asymmetric binding site to a symmetric binding site of the dye upon interaction with surfactant. Evidence in support of the molecular structures of the metal-dye complexes and metal-dye-surfactant systems proposed by the model is given in the analysis of infrared (IR) and Raman (R) spectra of these species. Structures of two metal-dye surfactant systems are proposed on the basis of the vibrational data. Thermodynamics of the rearrangements proposed by the model are investigated using ab-initio Hartree-Fock molecular orbital calculations.","Made available in DSpace on 2015-05-13T15:37:25Z (GMT). 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In this manuscript a model is developed to describe this mechanism. Intramolecular forces among surfactant molecules and host molecules are described to emphasize the importance of specific interactions to the mechanism. A review of the theoretical basis of UV-vis spectroscopic changes in dyes (chromatotropism) is given followed by application to the dyes of interest in this study. UV-vis spectra of the dyes, metal-dye complexes, and metal-dye-surfactant systems are analysed and a relationship between the symmetry of the chromophore and the UV-vis spectroscopic properties is described. This is the basis of the mechanistic model which postulates that the metal ion of the complex migrates from an asymmetric binding site to a symmetric binding site of the dye upon interaction with surfactant. Evidence in support of the molecular structures of the metal-dye complexes and metal-dye-surfactant systems proposed by the model is given in the analysis of infrared (IR) and Raman (R) spectra of these species. Structures of two metal-dye surfactant systems are proposed on the basis of the vibrational data. Thermodynamics of the rearrangements proposed by the model are investigated using ab-initio Hartree-Fock molecular orbital calculations.","Made available in DSpace on 2015-05-13T15:37:25Z (GMT). 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