Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/67496
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dc.titleMolecular orientation in mixed LB films containing photochromic molecules
dc.contributor.authorSrinivasan, M.P.
dc.contributor.authorLau, K.K.S.
dc.date.accessioned2014-06-17T10:01:55Z
dc.date.available2014-06-17T10:01:55Z
dc.date.issued1997-10-10
dc.identifier.citationSrinivasan, M.P., Lau, K.K.S. (1997-10-10). Molecular orientation in mixed LB films containing photochromic molecules. Thin Solid Films 307 (1-2) : 266-273. ScholarBank@NUS Repository.
dc.identifier.issn00406090
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/67496
dc.description.abstractOrientation of photochromic molecules in mixed Langmuir-Blodgett (LB) films that were subjected to ultraviolet irradiation has been investigated by polarised spectroscopy. The photochromic molecules (spiropyran (SP) and spirooxazine (SO)) were incorporated as guests in matrices of arachidic acid (AA), poly (methyl methacrylate) (PMMA) and poly (isobutyl methacrylate) (PIBM). The films were deposited in the dark (dark-deposited) and also while the Langmuir film on the water surface was subjected to ultraviolet irradiation (UV-deposited). Orientation of the open form of the chromophores was strongly influenced by the nature of the matrix and by the presence or absence of ultraviolet irradiation. In the case of LB films formed from either chromophore and PIBM, the dipole moments of the open forms exhibited large tilt angles relative to the substrate normal for both the dark-deposited and UV-deposited films. With AA or PMMA as the matrix, the tilt angles were large for the dark-deposited films, but the UV-deposited films displayed considerably smaller tilt angles. The nature of the matrix species and its Langmuir film is suggested as the basis for inteipreting the observations. © 1997 Elsevier Science S.A.
dc.sourceScopus
dc.subjectFTIR spectroscopy
dc.subjectLangmuir-Blodgett (LB) films
dc.subjectOptical properties
dc.subjectOptical spectroscopy
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.sourcetitleThin Solid Films
dc.description.volume307
dc.description.issue1-2
dc.description.page266-273
dc.description.codenTHSFA
dc.identifier.isiutNOT_IN_WOS
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