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Andrew B. Holmes
Researcher at University of Melbourne
Publications - 547
Citations - 43432
Andrew B. Holmes is an academic researcher from University of Melbourne. The author has contributed to research in topics: Polymer & Supercritical carbon dioxide. The author has an hindex of 75, co-authored 524 publications receiving 42062 citations. Previous affiliations of Andrew B. Holmes include University of Washington & Clare College.
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Journal ArticleDOI
Cyclopolymerisation of an oriented 4,6-bis(4-vinylbenzyl)-myo-inositol orthoformate
TL;DR: Free radical-promoted cyclopolymerisation of a 4,6-bis(4-vinylbenzyl)-myo-inositol orthoformate was studied and the first formed intermediate was trapped using (tetramethylpiperidine N-oxyl) as mentioned in this paper.
Journal ArticleDOI
Optical spectroscopy of field-induced charge in poly(2.5-dimethoxy-p-phenylene vinylene) metal-insulator-semiconductor structures
TL;DR: In this paper, the authors investigated metal-insulator-semiconductor structures fabricated with poly(2,5-dimethoxy-p-phenylene vinylene) as the active semiconductor.
Book ChapterDOI
Poly(dibenzosilole)s
TL;DR: In this article, an emerging class of polymers with similar optoelectronic properties to polyfluorenes, such as poly(dibenzosilole)s, have been shown to be suitable hosts for blue triplet emitters in electrophosphorescent devices.
Journal ArticleDOI
Blue-Shifted Electroluminescence From a Stable Precursor to Poly(p-Phenylene Vinylene)
Adam R. Brown,Paul L. Burn,Donal D. C. Bradley,Richard H. Friend,Arno Kraft,Andrew B. Holmes +5 more
TL;DR: In this paper, a partially conjugated polymer precursor to poly(p-phenylene vinylene) (PPV) was used to produce stable electroluminescence which enhanced efficiency over PPV in a simple device configuration with a blue-shift in both the electrolumeinescence and photolumine emission spectra.
Journal ArticleDOI
Synthesis of 5-Aryloxazolidines via 1,3-Dipolar Cycloaddition Reaction of a Non-Stabilized Azomethine Ylide with Aromatic Aldehydes
TL;DR: The 1,3-dipolar cycloaddition reaction of a non-stabilized azomethine ylide 4a, formed in situ from N-(methoxymethyl)-N-(trimethylsilylmethyl)benzylamine 5 and a catalytic amount of trifluoroacetic acid, with aromatic aldehydes 3 gives rise to N-benzyl-5-aryloxazolidines 1.