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Light bulbs play an indispensable role in our lives as they provide unhindered ability to see the world even during the night. Efficiency of light bulbs is becoming increasingly important, and through this experiment, light bulb efficiencies are analyzed from measurements of relative light intensity and power input of various bulbs. Furthermore, this report is aimed to increase awareness of the efficiency advantage in fluorescent bulbs and to encourage their usage in the interest of conserving energy.

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The objective of this thesis was to explore the chemistry of series of linear and star shaped compounds based on benzimidazolyl, 2-(2’-pyridyl)benzimidazolyl, and 2,2’-dipyridylamino functional groups. These groups all possess Lewis base sites suitable for metal coordination, and are all known fluorophores. The first compounds to be presented are the homo-substituted benzimidazolyl derivatives. Compounds 2.1-2.5 have been fully characterized and are all luminescent with emission energies in the UV region. While coordination complexes with these ligands have not been isolated, the effect of metal ion complexation on ligand luminescence has been explored via metal ion titration experiments. Furthermore, these compounds all have electron affinities greater than -3.0 eV and large optical bandgaps that range between 3.55 and 3.95 eV. These compounds also have high thermal and morphological stability. In light of this, compound 2.3 was selected as a representative example, and further characterized as an electron transport/hole blocking material for OLED applications. It has demonstrated a performance comparable to that of the well known electron transport material Alq3 (q = 8-hydroxyquinolinate). The second class of compounds, 3.2 and 3.3, represent a pair of hetero-substituted ligands with two different binding sites available for coordination chemistry. A copper (I) complex of 3.3 has been isolated and exhibits orange phosphorescence at room temperature and at 77 K. Furthermore, a series of metal titration experiments have been performed on 3.3 and 3.4, and have demonstrated the preference of different metal ions for either the 2,2’-dipyridylamino site, or the 2-(2’-pyridyl)benzimidazolyl binding site. The details of these explorations will be presented in the subsequent chapters. / Thesis (Master, Chemistry) -- Queen's University, 2007-07-31 12:17:06.011

Green algae have evolved several photo-protective responses to cope with high-light stress. The present study examines the metabolic changes during photoacclimation to high-light in Chlamydomonas reinhardtii using nuclear magnetic resonance and mass spectrometry. Using principal component analysis, a clear metabolic response to highlight intensity was observed on global metabolite pools in Chlamydomonas, with major changes in the levels of amino acids and related nitrogen metabolites. Amino acid biosynthesis was induced during short-term photoacclimation presumably to alleviate excess excitation pressure in the plastid. An increase in mitochondrial metabolism through downstream photorespiratory and glyoxylate metabolism, pathways thought to act in a photo-protective capacity, was also observed. Long-term light stress resulted in a significant increase in antioxidant metabolites, ascorbate and dehydroascorbate. These results suggest that metabolism plays a direct role in coping with the imbalance in the excess excitation pressure generated during high-light stress; however, this metabolomics survey has generated additional questions about the roles of nitrogen assimilation associated metabolites in photoacclimatory responses to high-light in Chlamydomonas.

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