Photooxidation of Cobalt-Bound Thiolato Ligands
Overview
Objectives/Goals This project studies the reaction of the complex bis(ethylenediamine)-(SO)(N,S-2-aminoethanethiolato)Cobalt chloride(III) with singlet oxygen. Similar sulfur- coordinated to transition metal complexes are found in many biological systems. Oxidation at a metal-sulfur site may lead to deactivation at that site. Methods/Materials Reaction rates in different solvents, dimethylformamide (DMF) and water will be attained. The rate-constants in this experiment were recorded through time-resolved Laser Spectroscopy. The compound#s consumption of 1O2 was monitored by the singlet oxygen decay at varying concentrations of quencher. Data was processed using Microsoft Excel and Origin 5.0 computer programs. Results It was found that polar solvents typically display a slower rate of quenching Co(SO)Cystamine. Conclusions/Discussion Solvents that were more nonpolar were supposed to show a faster rate of reaction. The increase in 1O2 quenching rate on the polar solvents is believed to occur because of added stabilization caused by intermolecular hydrogen bonding from the amino protons to the sulfur
Summary statement
Studying how solvent polarity affects the oxidation rate of reaction of Cobalt-Thiolato Complexes.
Help received
Professor Matthias Selke provided lab and guidance, Mentors Billy Hernandez and Cesar Galvez taught experimental techniques, concepts involved in experiment, and provided supervision, Dad bought the science fair board.
Competition history
- CSEF 2004
Resources
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