Organic materials for nonlinear optics / by Peter D. Turner.
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Date
1999
Authors
Turner, Peter D. (Peter David)
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Thesis
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Abstract
The preparation of a series of conjugated cyclophanes is described. Molecular modelling studies were performed on the bis-coupled systems and the cyclophanes to investigate steric interactions between the constrained and unconstrained aromatic systems. A new catalytic protocol was discovered and developed for the palladium catalysed coupling of terminal alkynes to aryl-halides using zinc co-catalysts.
School/Discipline
Dept. of Chemistry
Dissertation Note
Thesis (Ph.D.)--University of Adelaide, Dept. of Chemistry, 1999
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Copyright material removed from digital thesis. See print copy in University of Adelaide Library for full text.
This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exception. If you are the author of this thesis and do not wish it to be made publicly available or If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals
This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exception. If you are the author of this thesis and do not wish it to be made publicly available or If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals
Description
Copies of author's previously published articles inserted.
Bibliography: leaves 190-204.
vii, 205 leaves : ill. ; 30 cm.
Bibliography: leaves 190-204.
vii, 205 leaves : ill. ; 30 cm.