Nonlinear optical properties of metal free thio alkyl and tert-butyl phenoxy phthalocyanine

dc.contributor.advisorKhene, Samson
dc.contributor.advisorBritton, Johnathan
dc.contributor.authorJoseph, Otto
dc.date.accessioned2026-03-04T08:42:40Z
dc.date.issued21-Oct
dc.description.abstractThis work reports on the nonlinear optical properties of tetra - and octa substituted phthalocyanines (Pcs) utilising pentane thiol and 4-tertbutyl phenol as substituents. Their nonlinear absorption coefficient (𠛽) and absorption cross sections were determined using the Z-scan technique with a 10 ns pulse laser at 532 nm. The molecular second order hyperpolarizability Im[γ] was observed and the following Im[γ] trend was obtained for 𠛼-H2Pc(SC5H11)4 isomers, 5.93 ×10−31 (Cs) 2.24×10−32(D2h) > 1.21×10−32(C4h) > 1.05×10−32 (C2v) esu, respectively, in chloroform. Symmetry was seen to have an effect on the observed reverse saturable absorption (RSA) response. Based on the five level model rate equation nonlinear fit of the RSA response curves and Real Time Time Dependant Density Functional Theory (RT-TDDFT) results, the singlet excited state population dynamics was found to play a significant role in producing the observed Im[γ] trend.
dc.description.degreeMaster's thesis
dc.description.degreeMSc
dc.format.extent126 pages
dc.format.mimetypeapplication/pdf
dc.identifier.otherhttp://hdl.handle.net/10962/190712
dc.identifier.urihttps://researchrepository.ru.ac.za/handle/123456789/6084
dc.languageEnglish
dc.publisherRhodes University, Faculty of Science, Department of Chemistry
dc.rightsJoseph, Otto
dc.subjectNonlinear optics
dc.subjectPhthalocyanines
dc.subjectTime-dependent density functional theory
dc.subjectMagnetic circular dichroism
dc.subjectReverse saturable absorption (RSA)
dc.subjectReal Time Dependent Density Functional Theory (RT-TDDFT)
dc.titleNonlinear optical properties of metal free thio alkyl and tert-butyl phenoxy phthalocyanine
dc.typeAcademic thesis

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