Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Matthew T. Figgins"'
Autor:
Leigh Anna Hunt, Sanjit Das, Robert W. Lamb, Dinesh Nugegoda, Christine Curiac, Matthew T. Figgins, Ethan C. Lambert, Fengrui Qu, Nathan I. Hammer, Jared H. Delcamp, Charles Edwin Webster, Elizabeth T. Papish
Publikováno v:
ACS Catalysis. 13:5986-5999
Selective multi-electron aggregation at a hypervalent iodine center by sequential disproportionation
Autor:
Phong Thai, Brandon L. Frey, Matthew T. Figgins, Richard R. Thompson, Raanan Carmieli, David C. Powers
Publikováno v:
Chemical Communications. 59:4308-4311
We report a strategy to aggregate two- or four interfacial electron transfers at an iodine center as an approach to multi-electron electrosynthesis. The intermediates are characterized via UV-vis spectroscopy and single crystal X-ray crystallography.
Publikováno v:
J Am Chem Soc
Small molecule redox mediators convey interfacial electron transfer events into bulk solution and can enable diverse substrate activation mechanisms in synthetic electrocatalysis. Here we report that 1,2-diiodo-4,5-dimethoxybenzene is an efficient el
Autor:
Elizabeth T. Papish, Hunter Shirley, Chance M. Boudreaux, Matthew T. Figgins, Jared H. Delcamp, Robert W. Lamb, Nalaka P. Liyanage, Charles Edwin Webster
Publikováno v:
ChemCatChem. 12:4879-4885
Autor:
Dinesh Nugegoda, Charles Edwin Webster, Phillip E. Burrow, Robert W. Lamb, Sanjit Das, Matthew T. Figgins, Elizabeth T. Papish, Jared H. Delcamp, Chance M. Boudreaux, Fengrui Qu
Publikováno v:
European Journal of Inorganic Chemistry. 2020:2709-2717
Autor:
Sanjit Das, Dinesh Nugegoda, Wenzhi Yao, Fengrui Qu, Matthew T. Figgins, Robert W. Lamb, Charles Edwin Webster, Jared H. Delcamp, Elizabeth T. Papish
Publikováno v:
European Journal of Inorganic Chemistry. 2022
Autor:
Andrew Ozarowski, David C. Powers, Anuvab Das, Nattamai Bhuvanesh, Kaleb A. Reid, Joshua Telser, Gerard P. Van Trieste, Madeline H. Hicks, Matthew T. Figgins
Publikováno v:
Angewandte Chemie (International ed. in English). 60(51)
Manganese complexes supported by macrocyclic tetrapyrrole ligands represent an important platform for nitrene transfer catalysis and have been applied to both C-H amination and olefin aziridination catalysis. The reactivity of the transient high-vale