Font Size: a A A

Part one: Synthesis of carboranes and metallacarboranes for use as molecular building blocks and motors. Part two: The synthesis of self-assembling fullerenes for use in organic photovoltaic devices

Posted on:2010-02-19Degree:Ph.DType:Thesis
University:University of California, Los AngelesCandidate:Kennedy, Robert DanielFull Text:PDF
GTID:2441390002978841Subject:Chemistry
Abstract/Summary:
Chapter I begins with an introduction to modular chemistry and the iodination chemistry of orthocarborane. The synthesis and characterization of a new family of compounds derived from 8-I-closo-1,2-C2B 10H11 is then described. These compounds include the first examples of apically mono-substituted [1-X-nido-C2B 9H11]-- anions (X = I, Ph) and the first example of an axially disubstituted bis(dicarbollide) metal complex.;Chapter II begins with an introduction to chirality and hindered rotation in bis(dicarbollide) metal complexes. The chapter deals with the continuing approaches to molecular unidirectional rotation using bis(dicarbollide) nickel complexes. A combination of single-crystal X-ray diffraction analysis, variable-temperature NMR spectroscopy and computational methods are used to probe the rotational energy barriers of diastereomeric nickel bis(dicarbollide) complexes derived from the [nido-7-CH3-7,8-C2B9 H11]-- anion.;Chapter III begins with a general introduction to organic photovoltaic devices (OPVDs). The synthesis and single-crystal X-ray diffraction analysis of a large series of 6,9,12,15,18-pentaaryl-1-hydro[60]fullerenes, which have potential as acceptors in OPVDs, is then described. The performance of OPVDs fabricated using these derivatives is discussed.
Keywords/Search Tags:Synthesis
Related items
Green chemistry in pyrrole synthesis. I. Solvent effect in Barton-Zard pyrrole synthesis: An improved synthesis of 3,4-dialkyl-1H-pyrrole-2-carboxylates. II. A novel route for the synthesis of pharmaceutically important pyrrole derivatives
Part I: Design, synthesis, and reactivity of 1-hydrazinodienes for use in organic synthesis Part II: Studies toward a synthesis of the antibiotic platensimycin
Manganese(III)-based oxidative cyclizations: Formal synthesis of 15-acetoxypallescensin A. Synthesis of hindered guanidines. Completion of the total synthesis of martinellic acid
Synthesis, Characterization And Luminescence Properties Of Environmental Functional Material β-NaYF4 Doped With Rare Earth
Part I: The total synthesis of (+/-)-securinine and (+/-)-allosecurinine and synthetic strategies for a second generation synthesis of the securinega alkaloids and Part II: The use of (+)-K252a in the semi-synthesis of indolocarbazole natural products and
New methods and strategies for heterocycle synthesis: Progress toward the total synthesis of upenamide and the total synthesis of (+)-5-epiindolizidine 167B and indolizidine 223AB
Synthesis of side chain-modified iodothyronines. Synthesis and structure-activity relationships (SARS) of galanthamine derivatives. Total synthesis of (+)-valyldetoxinine. Synthesis and mechanism of cyclic acetal and ketal formation in pentono-1,4-lactone
The application of asymmetric catalysis to the synthesis of natural products: A total synthesis of (-)-tubulosine, progress towards a total synthesis of (+)-reserpine, and a total synthesis of (+)-peloruside A
Cyclobutanes in organic synthesis: Lewis acid-promoted ketene-alkene [2+2] cycloadditions, total synthesis of gracilioether F, and collaborative total synthesis of hippolachnin A
10 A ring-closing metathesis/Diels-Alder approach to the synthesis of the eunicellin diterpenes: Application to the total synthesis of ophirin B and partial synthesis of astrogorgin