Electrogenerated chemiluminescence (ECL) studies were performed on several interesting compounds. A series of silole-based (silacyclopentadiene) chromophores was examined to understand the effects of their structure on the electrochemistry and spectroscopy of these compounds. A case was observed in which high steric hindrance improved ECL by inhibiting internal conversion and protecting radicals from secondary reactions. Another case was observed in which steric effects induced a rotation in the silole substituents, increasing secondary reactions and lowering quantum efficiency ([Phi subscript PL]). Spiro-FPA, which consists of two DPA centers, exhibits excimer formation despite high steric hindrance, due to its ability to form di-ions, which have a greater electrostatic attraction to one another than mono-ions. The compound (dppy)BTPA is a highly solvatochromic, boron-containing chromophore that was examined in a variety of solvents. Of note is the emission in pure acetonitrile, which is prominent in the ECL spectrum, but barely visible in the photoluminescence. Finally, B⁸ amide, a compound based on the laser dye, BODIPY, was examined. It exhibited unusual ECL characteristics. These include a strong, long-wavelength emission and transients that are clearly visible for 20 min or more, but display dramatically varying light intensities with each pulse. Evidence for the contribution of a film formed with the oxidation product is presented. Additionally, ECL simulations are performed using a general physics software package to better understand some of the observed phenomena.

Thesis (Ph. D.)--University of Texas at Austin, 2007. / Vita. Includes bibliographical references.

Thesis (M.S.)--University of Missouri, School of Mines and Metallurgy, 1933. / The entire thesis text is included in file. Typescript. Title from title screen of thesis/dissertation PDF file (viewed June 14, 2010) Includes bibliographical references (p. 68-62) and index (p. 63-64).

No description available.

We have reacted several derivatives of the anticancer drug cisplatin with N-acetyl-Lcysteine (N-AcCys) and N-acetyl-L-methionine (N-AcMet), which are two of the primary amino acid targets of platinum. NMR spectroscopy was used to monitor the reactions and determine the effect the different ligands would have on the platinum reactivity. Several of the platinum compounds were tested at pH of 4 and 7, and with platinum:amino acid ratios of 1:1, 2:1 and 1:2. Competition reactions between cysteine and methionine were done to confirm which would react with the platinum compound first. [Pt(dien)(NO3)]+ reacts faster with methionine than with cysteine at both pH 4 and 7 at a 1:1:1 ratio. [Pt(N,N,N',N',N"-pentamethyldiethylenetriamine)(NO3)]+ reacts with methionine faster at pH 4 but with cysteine faster at pH 7. This is most likely due to the thiol in the cysteine starting to deprotonate around pH 7. [Pt(Me4en)(NO3)2] (Me4en = N,N,N',N'-tetramethylethylenediamine) forms several products with N-AcCys at both pH 4 and 7, with the amounts of the products varying depending on the ratio of platinum and Cys. Mass spectrometry indicated one product as {[Pt(Me4en)(H2O)]2(N-AcCys)}2+, with two platinum compounds coordinated to a single cysteine. Lastly Pt[(en)(NO3)2] when reacting with N-AcCys at a ratio of 1:1 will coordinate with 2 different Cys molecules. With an excess of Pt the complex prefers to bind to only 1 Cys.

iv, 191 leaves : ill. (some in end pocket) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / Thesis (Ph.D.)--University of Adelaide, Dept. of Organic Chemistry, 1980

Thesis (Ph.D.) -- University of Adelaide, Dept. of Organic Chemistry, 1980.

Thesis (M.S.)--West Virginia University, 2004. / Title from document title page. Document formatted into pages; contains xi, 94 p. : ill. (some col.). Includes abstract. Includes bibliographical references and index.

Honors Project--Smith College, Northampton, Mass., 2010.

This thesis describes the effect of placing a phosphorus atom in a sterically strained environment with particular emphasis on the geminal disubstitution of two 2,4,6-tri-tert-butylphenyl (Mes*) groups on a single phosphorus centre and intramolecular sub-van der Waals interactions between peri-substituted atoms on naphthalene and acenaphthene. Chapter 2 outlines the reactive chemistry of a sterically encumbered phosphinic chloride (Mes*)₂P(=O)Cl, which was shown to have extremely low reactivity at the phosphorus centre. It has however, been demonstrated that synthetically significant transformations are possible. The phosphine oxide (Mes*)₂P(=O)H and a secondary phosphine Mes*(2,4-tBu₂C₆H₃)PH were obtained from the reduction of (Mes*)₂P(=O)Cl with hydridic reagents under forcing conditions. The corresponding phosphinite was acquired from the deprotonation of (Mes*)₂P(=O)H, which furnished very crowded tertiary phosphine oxides (Mes*)₂P(=O)R (R = Me and Et) on reactions with electrophiles. We have been unable to chlorinate or deprotonate Mes*(2,4-tBu₂C₆H₃)PH, however the reaction with elemental sulfur afforded the affiliated phosphine sulfide Mes*(2,4-[supercript(t)]Bu₂C₆H₃)P(=S)H, albeit under forcing conditions. Our computations (B3LYP and M06-2X level) show that strain energies of geminally substituted compounds are extremely high (180 to 250 kJ mol⁻¹), the majority of the strain is stored as boat distortions to the phenyl rings in Mes* substituents. Chapter 3 describes the strain inherent with non-bonding atomic distances shorter than the sum of their van der Waals radii, specifically heteroatom substitution of the peri-positions of naphthalene and acenaphthene. It also documents the importance of amine protecting groups in chlorophosphine chemistry. The preparation of Ace[P(Ph)N(ⁱPr)₂]Br (Ace = acenaphthene-5,6-diyl) and Ace[P(Ph)N(ⁱPr)₂]₂, plus the elucidation of the molecular structures of Mes*P[N(CH₃)₂]₂, Ace[P(Mes)N(ⁱPr)₂]Br (Mes = 2,4,6-tri-methylphenyl) and Ace[P([supercript(t)]Bu)N(Et)₂]Br sufficiently demonstrate the ring distorting characteristics of structurally encumbered molecules. The reaction of Ace[P(Ph)N(ⁱPr)₂]Br and Ace[P(Ph)N(ⁱPr)₂]₂ with a methylating agent was also investigated.