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职称:Associate Professor
所属学校:Illinois State University
所属院系:Biochemistry
所属专业:Biochemistry
联系方式:(309) 438-2118
Research interests in my group involve the chemistry of free radicals and radical anions, particularly those that are important to polymeric chemistry and biochemistry. We employ magnetic resonance techniques to explore the chemistry of these systems. My students and I have been very active in looking at the electron initiated cycloaddition of isocyanates that results in the formation of stable isocyanurate anion radicals; both isocyanates and isocyanurates are important in polyurethane chemistry (Organic Letters, 2008, 10, 4521-4524). We are currently exploring the reduction of a variety of aryl substituted isocyanates. My group is also interested in the reactivity between phenoxyl radicals with nitrogen oxide free radicals, both of which are important in many environmental and biological processes. We have just finished investigating the rearrangement mechanism of a stericly hindered nitrocyclohexadienone (2) under anaerobic conditions, see mechanism below (European Journal of Organic Chemistry. 2009, 35, 6104–6108). Notably, we discovered that a key step in this mechanism is the release of the free radical nitric oxide, which is an important biological messenger in numerous living organisms. This reaction is slow enough to observe the transformation of 2 to the final products using our new state-of-the-art Bruker nuclear magnetic resonance spectrometers.
Research interests in my group involve the chemistry of free radicals and radical anions, particularly those that are important to polymeric chemistry and biochemistry. We employ magnetic resonance techniques to explore the chemistry of these systems. My students and I have been very active in looking at the electron initiated cycloaddition of isocyanates that results in the formation of stable isocyanurate anion radicals; both isocyanates and isocyanurates are important in polyurethane chemistry (Organic Letters, 2008, 10, 4521-4524). We are currently exploring the reduction of a variety of aryl substituted isocyanates. My group is also interested in the reactivity between phenoxyl radicals with nitrogen oxide free radicals, both of which are important in many environmental and biological processes. We have just finished investigating the rearrangement mechanism of a stericly hindered nitrocyclohexadienone (2) under anaerobic conditions, see mechanism below (European Journal of Organic Chemistry. 2009, 35, 6104–6108). Notably, we discovered that a key step in this mechanism is the release of the free radical nitric oxide, which is an important biological messenger in numerous living organisms. This reaction is slow enough to observe the transformation of 2 to the final products using our new state-of-the-art Bruker nuclear magnetic resonance spectrometers.