Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Matthew E. O'Reilly"'
Publikováno v:
ACS Central Science, Vol 3, Iss 11, Pp 1174-1179 (2017)
Externí odkaz:
https://doaj.org/article/aa89516ed6254a738f43091484dc5cb1
Autor:
Jeffrey T. Miller, Min Chieh Yang, R. Soyoung Kim, Christopher H. Hendon, Seokjoon Oh, Yogesh Surendranath, Evan C. Wegener, Matthew E. O'Reilly
Publikováno v:
Journal of the American Chemical Society. 142(49)
High-valent Pd complexes are potent agents for the oxidative functionalization of inert C-H bonds, and it was previously shown that rapid electrocatalytic methane monofunctionalization could be achieved by electro-oxidation of PdII to a critical dinu
Publikováno v:
ACS Central Science, Vol 3, Iss 11, Pp 1174-1179 (2017)
ACS Central Science
ACS central science, vol 3, iss 11
ACS Central Science, vol 3, iss 11
ACS Central Science
ACS central science, vol 3, iss 11
ACS Central Science, vol 3, iss 11
Electrophilic high-valent metal ions are potent intermediates for the catalytic functionalization of methane, but in many cases, their high redox potentials make these intermediates difficult or impossible to access using mild stoichiometric oxidants
Publikováno v:
Chemical Reviews. 116:8105-8145
This review describes organometallic compounds and materials that are capable of mediating a rarely encountered but fundamentally important reaction: β-alkyl elimination at the metal-Cα-Cβ-R moiety, in which an alkyl group attached to the Cβ atom
Autor:
Quanning Li, T. Brent Gunnoe, William A. Hubbard, Andrew M. Herring, Brian G. Trewyn, Vinh Nguyen, Chilan Ngo, Matthew E. O'Reilly, Tristan S. Gray, Madhura Joglekar, Svitlana Pylypenko
Publikováno v:
Journal of the American Chemical Society. 138:116-125
Low-temperature direct methane fuel cells (DMEFCs) offer the opportunity to substantially improve the efficiency of energy production from natural gas. This study focuses on the development of well-defined platinum organometallic complexes covalently
Publikováno v:
Angewandte Chemie. 127:15353-15357
A chemically non-innocent pyrrole-based trianionic (ONO)(3-) pincer ligand within [(pyr-ONO)TiCl(thf)2 ] (2) can access the dianionic [(3H-pyr-ONO)TiCl2 (thf)] (1-THF) and monoanionic [(3H,4H-pyr-ONO)TiCl2 (OEt2 )][B{3,5-(CF3 )2 C6 H3 }4 ] (3-Et2 O)
Publikováno v:
Organometallics. 33:6504-6510
The reductive functionalization of RhIII–Me bonds in acids is a key step for RhI/III-based catalysts for methane functionalization. Heating electronic-rich [tBu3terpy]Rh(Me)(Cl)I (1; tBu3terpy = 4,4′,4″-tri-tert-butylterpyridine) in H2O, AcOD,
Autor:
Robert J. Nielsen, Michal Sabat, Ross Fu, T. Brent Gunnoe, William A. Goddard, Matthew E. O'Reilly
Publikováno v:
Journal of the American Chemical Society. 136:14690-14693
Traditional C–H bond activation by a concerted metalation–deprotonation (CMD) mechanism involves precoordination of the C–H bond followed by deprotonation from an internal base. Reported herein is a “through-arene” activation of an uncoordi
Autor:
Matthew E. O'Reilly, Adam S. Veige
Publikováno v:
Chem. Soc. Rev.. 43:6325-6369
Trianionic pincer and pincer-type ligands are the focus of this review. Metal ions from across the periodic table, from main group elements, transition metals, and the rare earths, are combined with trianionic pincer ligands to produce some of the mo
Publikováno v:
Organometallics. 33:836-839
Synthetic protocols for a pyrrolide-centered ONO3– trianionic pincer-type ligand are presented. Treating (tBuO)3W≡CtBu with the proligand [pyr-ONO]H3 (2) results in the formation of the trianionic pincer alkylidene complex [pyr-ONO]W═CHtBu(OtBu