Selective oxidation of organic substrates by oxygen, where all 4 oxidizing equivalents are used productively, remains an unsolved problem in catalysis. In an idealized catalytic cycle that could solve this problem, three separate steps are involved: first oxygen must be rapidly bound, then the O-O bond must be cleaved, and finally each oxo ligand needs to react independently with the substrate regenerating the catalyst. The first and last steps were investigated in this research program. Molecular mechanics was used to study the O{sub 2} binding step and ab initio electronic structure tools were used to study M-O bonding and the reactivity of M{double_bond}O bonds with methane. Mn and Fe complexes are involved
A straight-forward way to learn how different complementary properties of a catalyst control a resul...
The reaction profile for sulfide oxidation by formally Mn(v)=O species depends critically on the ele...
Activation of non reactive C-H bonds and their transformation into C-OH alcohol groups without the o...
Inspired by oxidation enzymes such as P450 and TauD, several groups have based their research on the...
International audienceInspired by oxidation enzymes such as P450 and TauD, several groups have based...
Oxidation is a term used to cover a wide range of processes that are central to life. Although we as...
A simplified approach is described for the design of oxidation catalysts. It is based on three compo...
A simplified approach is described for the design of oxidation catalysts. It is based on three compo...
Transition metal oxide-based systems as catalysts for oxidative reactions are studied. Utilizing aer...
Transition metal oxide-based systems as catalysts for oxidative reactions are studied. Utilizing aer...
A simplified approach is described for the design of oxidation catalysts. It is based on three compo...
Transition metal oxide-based systems as catalysts for oxidative reactions are studied. Utilizing aer...
Reaction paths underlying the catalytic oxidation of methane with H2O2 over an Fe containing MIL-53(...
A simplified approach is described for the design of oxidation catalysts. It is based on three compo...
A straight-forward way to learn how different complementary properties of a catalyst control a resul...
A straight-forward way to learn how different complementary properties of a catalyst control a resul...
The reaction profile for sulfide oxidation by formally Mn(v)=O species depends critically on the ele...
Activation of non reactive C-H bonds and their transformation into C-OH alcohol groups without the o...
Inspired by oxidation enzymes such as P450 and TauD, several groups have based their research on the...
International audienceInspired by oxidation enzymes such as P450 and TauD, several groups have based...
Oxidation is a term used to cover a wide range of processes that are central to life. Although we as...
A simplified approach is described for the design of oxidation catalysts. It is based on three compo...
A simplified approach is described for the design of oxidation catalysts. It is based on three compo...
Transition metal oxide-based systems as catalysts for oxidative reactions are studied. Utilizing aer...
Transition metal oxide-based systems as catalysts for oxidative reactions are studied. Utilizing aer...
A simplified approach is described for the design of oxidation catalysts. It is based on three compo...
Transition metal oxide-based systems as catalysts for oxidative reactions are studied. Utilizing aer...
Reaction paths underlying the catalytic oxidation of methane with H2O2 over an Fe containing MIL-53(...
A simplified approach is described for the design of oxidation catalysts. It is based on three compo...
A straight-forward way to learn how different complementary properties of a catalyst control a resul...
A straight-forward way to learn how different complementary properties of a catalyst control a resul...
The reaction profile for sulfide oxidation by formally Mn(v)=O species depends critically on the ele...
Activation of non reactive C-H bonds and their transformation into C-OH alcohol groups without the o...