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Photoinduced charge separation is crucial for converting solar energy to electrical and chemical energy. In this work, to improve the photoinduced charge separation efficiency at the photosensitizing dye–semiconductor interface, we synthesized two dual ...
Atsushi Kobayashi, Satoshi Odagiri
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Metalloporphyrin Catalyzed Oxidation of Thiophene Derivatives
Color poster with text, graphs, and diagrams.The oxidation of dibensothiphene and related compounds is an important reaction in oxidative desulfurization treatment of diesel and other fuels.
Swedien, Daniel +3 more
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Lawson L. Rosenberg, W. Mansfield Clark
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Electropolymerized metalloporphyrins
The electrocatalytic activities of electropolymerized metalloporphyrins and their applications in the development of nitric oxide (NO)-microsensors and as oxygen reduction catalysts were investigated. By means of a locally developed electrochemical robotic system, the optimization of the functional parameters which determine the sensor properties of Ni-
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A Metalloporphyrin-Based Colimetric Nose: "smell-Seeing
261 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2001.To reduce response times, the "Smell-Seeing" array was miniaturized. Deposition of plasticized metalloporphyrin/polymer films on Teflon posts gave microarrays with faster response ...
Rakow, Neal Anthony
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Nitric Oxide Insertion into a Metalloporphyrin–Carbon Bond
Jennifer Londoño-Salazar +8 more
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Metalloporphyrin phototoxicity
Journal of Photochemistry and Photobiology B: Biology, 1990The phototoxicities of six metalloporphyrin dimethylesters (i.e. cobalt (Co), copper (Cu), manganese (Mn), nickel (Ni), tin (Sn) and zinc (Zn) were investigated. Hemolysis of human erythrocytes and inactivation of two enzymes (acetylcholinesterase and beta-galactosidase) were used to assess the phototoxic efficacy of these metal chelates.
J, Scott +4 more
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Halogenation of metalloporphyrins
Russian Journal of Bioorganic Chemistry, 2000We found that thionyl chloride can chlorinate porphyrin complexes with transient metals (Pd, Ni, or Cu) at the free β andmeso-positions of the porphyrin macrocycle. A more prolonged or rigorous treatment also causes the chlorination of side alkyl substituents, mainly, methyl groups.
V. D. Rumyantseva +3 more
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Spectroelectrochemistry of metalloporphyrins
Pure and Applied Chemistry, 1990Abstract
K. M. Kadish, X. Mu
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