No description available.

Thesis (Ph. D.)--University of Chicago, 1942. / Reproduced from type-written copy. Description based on print version record. Bibliographical foot-notes.

published_or_final_version / Chemistry / Master / Master of Science

Thesis (M. Sc.)--University of Hong Kong, 1955. / Type-written copy. Includes bibliographical references (p. 54-55).

A series of photochromic dithienylethene-containing triarylboranes has been synthesized and characterized. The X-ray crystal structure of (4,5-bis(2,5-dimethylthiophen-3-yl)-thiophen-2-yl)dimesitylborane has been determined. An intense electronic absorption band was observed in all the triarylborane-containing compounds, corresponding to the intramolecular charge-transfer transition from the π-conjugated thiophene / fused thiophene / bithiophene to the vacant pπorbital of boron. This class of compounds was also found to bind fluoride ion such that the trigonal planar geometry of the boron center would be changed to tetrahedral, leading to a significant perturbation in the photophysical properties. Upon photo-excitation into the transition band, (4,5-bis(2,5-dimethylthiophen-3-yl)-thiophen-2-yl)dimesityl- borane and (4,5-bis-(2,5-dimethylthiophen-3-yl)-thieno[3,2-b]thiophen-2-yl)- dimesitylborane displayed multi-addressable photochromic reactivities upon addition of fluoride, in which a green solution was found in the closed form of the unbound compounds, while they changed to a purple color upon fluoride binding. Interestingly, both (4',5'-bis(2,5-dimethyl-thiophen-3-yl)-2,2'- bithiophen-5-yl)dimesitylborane and (4',5'-bis(2,5-dimethyl-thiophen-3-yl)-2,2'- bithiophen-3-yl)dimesitylborane displayed gated photochromic reactivities upon addition of fluoride, while only typical photochromic reactivity was observed in (4',5'-bis(2,5-dimethyl-thiophen-3-yl)-2,2'-bithiophen-4-yl)- dimesitylborane, indicative of a strong influence of the substituent effect on the photochromic reactivity upon incorporation of the -BMes2 group. A series of photochromic dithienylethene-containing β-diketones and the corresponding boron(III) compounds, appended with -BF2, -B(C6F5)2 and -BPh2, have been designed and synthesized. Upon photo-excitation into the transition band, typical photochromism was observed in all the dithienylethene- containing β-diketone ligands with the color changed from pale yellow to green in degassed benzene solution. Upon incorporation of the -BF2 and -B(C6F5)2 groups, near-infrared responsive photochromic behavior was observed, in which the absorption of the closed form was found to be at ca. 758-863 nm, suggesting that a pronounced perturbation of the dithienylethene was achieved by coordination of the boron(III) center. Moreover, a significant reduction in luminescence intensity of over 90 % was observed upon photocyclization, indicative of their potential application as photoswitchable luminescence materials. The thermal stability of the closed form and the activation energy for the thermal cycloreversion have also been studied on the representative compounds, 1-(4,5-bis(2,5-dimethylthiophen-3-yl)thiophen-2- yl)-butane-1,3-dione and difluoroboryl(1-(4,5-bis(2,5-dimethylthiophen-3-yl)- thiophen-2-yl)butane-1,3-dionate). A series of photochromic dithienylethene-containing BODIPY has been successfully prepared and characterized. The electronic absorption properties have been studied. These compounds showed an intense visible absorption band, corresponding to the 0-0 band of a strong S0→S1 transition of the BODIPY core, with a weak and broad absorption band at higher energy, corresponding to the S0→ S2 transition of the BODIPY core. An absorption band in the UV region was also observed in 2,3-bis(2,5-dimethyl- thiophen-3-yl)thiophene-containing derivatives, corresponding to the π→π* transitions of the dithienylethene moiety. The photochromic reactivities have also been studied such that the photostationary state was found to be reached upon irradiation in the UV region for over eight hours, while no observable changes would be obtained upon photo-excitation in the visible region. The slow conversion rate has been suggested to be attributed to the fact that a rapid excitation energy transfer could occur from the excited Th-DTE to the BODIPY moiety, rendering the suppression of the photocyclization. / published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy

published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy

Haloalkenes were shown to react with cysteine, N-acetyl cysteine, or glutathione to form halogenated vinylthio (HVT) or saturated conjugates. When HVT were administered iv to rabbits, active transport in the renal tubules was inhibited 50% at doses as low as 20 mg/kg within 1 hr after dosing. There was sloughing of the renal brush border membrane with the injury progressing to a specific renal tubular necrosis of the S₃ segment. In vitro studies with renal tubules found that the HVT produced a dose-response related inhibition of acid/base transport, with complete inhibition of transport occurring at 1 mM. The cysteine conjugate synthesized from trichloroethylene, DCVC, inhibited tubular active transport 60 min after in vivo dosing (20-100 mg/kg), 45 min after exposure in the isolated perfused kidney (0.01-1 mM) and 15 min after incubation with isolated tubules (0.01-1 mM). All HVT conjugates had a similar potency with regard to transport inhibition in isolated tubules, with complete inhibition occurring at 1 mM within 15 min for cysteine conjugates compared to 45-60 min for the N-acetyl cysteine or glutathione conjugates. These latter conjugates are thought to be bioactivated to the cysteine conjugate prior to transport inhibition. Inhibition of tubular (gamma)-glutamyl transpeptidase by 1 mM AT-125 or 20 mM serine/borate prevented the inhibition of acid/base transport by the glutathione conjugate. In addition, the sequential formation of glutamate, glycine and the vinyl cysteine conjugate after tubule incubation with the glutathione conjugate provides further evidence for this bioactivation. The cysteine conjugates are thought to be further metabolized in tubules to a toxic intermediate by a brush border localized enzyme, C-S lyase. The inhibitor effect of this intermediate on acid/base transport is reversed in the presence of, or subsequent addition of, 6 mM exogenous glutathione. These studies provide further evidence for the nephrotoxicity of HVT, and formation of the nephrotoxic cysteine conjugates from glutathione and cysteine conjugates. The formation of saturated conjugates from CTFE was also demonstrated. These saturated and/or unsaturated conjugates may be responsible for haloalkene-induced nephrotoxicity.

Environmental factors such as chemical contamination can have immunomodulatory effects on the immune response of fish and may be contributing to the decline in salmonid populations by augmenting disease susceptibility. Xenobiotics can interfere with the immune system at several levels of complexity, and different immune cells and processes have variable sensitivity to pollutants. For this reason, a suite of tests is required to evaluate immunomodulatory mechanisms. In this thesis, I formulated and calibrated an assay for the detection of humoral immunity for chinook salmon (Oncorhynchus tshawvtscha). Subsequently, I used this technique in conjunction with other immune and endocrine assays to detect effects of embryonic exposure to o,p'-DDE, a known environmental estrogen. The technique combines exposure of whole animals or leukocyte cultures to immunomodulatory agents/conditions with in vitro mitogenic activation of B-lymphocytes. The proportion of leukocytes undergoing blastogenesis following in vitro stimulation with lipopolysaccaride (LPS) was quantified by flow cytometric analysis of forward and side scatter properties. In addition, I used a fluorescein isothiocyanate labeled anti-rainbow trout surface immunoglobin monoclonal antibody (anti-RBT SIgM-FITC) to determine the ability of the lymphoblasts to express surface immunoglobin (SIgM) through flow cytometry. I used the assay to evaluate the effects of short-term exposures to o,p'-DDE during early life history stages on the long-term immune competence of fall chinook salmon. Immersion of chinook salmon eggs in 10 ppm o,p'-DDE for 1 h at fertilization followed by 2 h at hatch caused significant reductions in the ability of splenic leukocytes to undergo blastogenesis and express SIgM upon in vitro stimulation with LPS one year after treatment (ANOVA, P<0.05). The concentration of o,p'-DDE in fry treated with 10 ppm o,p'-DDE was 0.92 ��g g����� lipid one month post first feeding. The chemical persisted through development and, one year after exposure, levels in juvenile muscle tissue were 0.94 ��g g����� lipid. Mortality rate, time to hatch, fish size, sex ratios, gonadal development, plasma estradiol and 11-ketotestosterone concentrations were not affected by treatment with o,p'-DDE. In addition, neither plasma lysozyme concentration, nor mitogenic response of splenic leukocytes to concanavallin A or polyinosinic-polycytidylic acid were influenced by the treatment. A short period of exposure to an estrogenic chemical during early periods of development induced long term effects on humoral immune competence of chinook salmon. I discuss the possibility that the xenobiotic is exerting its activity through steroid-mediated pathways. / Graduation date: 2002

Thesis (Ph. D.)--University of Hong Kong, 2009. / Includes bibliographical references (leaves 263-287) Also available in print.

Thesis (Ph. D.)--University of Hong Kong, 2009. / Includes bibliographical references (leaves 263-287) Also available online.