Thesis (M.S. in Chemistry)--University of California, Berkeley, Sept. 1960. / "UCRL-9265." TID-4500 (15th ed.). Bibliography: leaf 33.

Thesis (Ph.D.)--Lehigh University, 1996. / Source: Dissertation Abstracts International, Volume: 57-09, Section: B, page: 5645. Adviser: John W. Larsen.

Thesis (Ph.D)--Chemical Engineering, Georgia Institute of Technology, 2010. / Committee Chair: Ronald Rousseau; Committee Co-Chair: Athanassios Sambanis; Committee Member: Amyn Teja; Committee Member: Athanasios Nenes; Committee Member: Ingeborg Schmidt-Krey. Part of the SMARTech Electronic Thesis and Dissertation Collection.

Thesis (Ph.D.) - University of St Andrews, October 2008.

Thesis (Ph. D.)--University of Wisconsin--Madison, 1984. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 227-240).

Thesis (M.S.)--University of Wisconsin--Madison, 1968. / eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.

Th.--Pharm.--Paris 5, 1984. N°: 104.

This dissertation presents the synthesis and characterization of a variety of neutral and cationic complexes featuring Group 13-15 element centres stabilized by N-, P-, and O-based donors. Unique aluminum and gallium cationic complexes are obtained from equimolar reactions of the metal halide with the chelating alkyl phosphine dmpe. However, using the analogous amine donor tmeda, neutral adducts are preferred for aluminum as well as for GaCl3, while cations are obtained for GaBr3 and GaI3. New cations of Ge(II) and Sn(II) were also discovered, featuring the coordination of either bipyridine ligands or dmpe. Utilizing bipyridine led to the expected mono and dicationic chelate complexes, however, using dmpe led to the formation of unprecedented tetracationic molecules. The reactivities of the bipyridine complexes were investigated with a variety of substrates which showcased their Lewis acidity as well as their ability to be oxidized. Finally, a new series of high oxidation-state main group cations have been synthesized using a variety of ligands. The ligand choice was found to be an important role in compound isolation as ligand degradation occurred for some of the compounds due to their high electrophilicity. Additionally, the Lewis acidity of some of the complexes leads to interesting reaction chemistry including sp3 C-H activation. Overall, the results presented herein represent new coordination chemistry for the main group elements and opens the door towards new reactivity pathways including small molecule activation and catalysis. / Graduate

Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências Físicas e Matemáticas. Programa de Pós-Graduação em Química / Made available in DSpace on 2012-10-26T09:52:39Z (GMT). No. of bitstreams: 0

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