Zobrazeno 1 - 10
of 47
pro vyhledávání: '"George E. Cutsail"'
Autor:
Iván Ayuso-Fernández, Tom Z. Emrich-Mills, Julia Haak, Ole Golten, Kelsi R. Hall, Lorenz Schwaiger, Trond S. Moe, Anton A. Stepnov, Roland Ludwig, George E. Cutsail III, Morten Sørlie, Åsmund Kjendseth Røhr, Vincent G. H. Eijsink
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-15 (2024)
Abstract Oxidoreductases have evolved tyrosine/tryptophan pathways that channel highly oxidizing holes away from the active site to avoid damage. Here we dissect such a pathway in a bacterial LPMO, member of a widespread family of C-H bond activating
Externí odkaz:
https://doaj.org/article/af35a6ac3afc4cd6b8384d682064752a
Autor:
Chelladurai Ganesamoorthy, Christoph Helling, Christoph Wölper, Walter Frank, Eckhard Bill, George E. Cutsail, Stephan Schulz
Publikováno v:
Nature Communications, Vol 9, Iss 1, Pp 1-8 (2018)
Radicals of heavy main-group elements represent important intermediates in chemical synthesis, yet few have been isolated. Here the authors stabilize neutral stibinyl and bismuthinyl radicals using gallium-based ligands, and reduce the former to affo
Externí odkaz:
https://doaj.org/article/d5140502220e4a1cb90d07b971497c8f
Autor:
George E. Cutsail, Blaise L. Geoghegan, Christoph Helling, Christoph Wölper, Gebhard Haberhauer, Stephan Schulz, Yannick Schulte
Publikováno v:
Journal of the American Chemical Society. 143:12658-12664
Single crystal X-ray (sc XRD) analyses of three symmetrically substituted cyclopentadienyl radicals (1, 2, 5) containing sterically demanding aryl groups showed that they crystallize as discrete valence tautomers (Jahn-Teller distortion) in the solid
Publikováno v:
ACS Omega, Vol 6, Iss 28, Pp 18325-18332 (2021)
ACS Omega
ACS Omega
We report on a systematical reactivity study of β-diketiminate zinc complexes with redox-active 2,2′-bipyridine (bpy). The reaction of LZnI (L = HC[C(Me)N(2,6-iPr2C6H3)]2) with NaB(C6F5)4 in the presence of bpy yielded [LZn(bpy)][B(C6F5)4] (1), wi
Autor:
Julia, Haak, Julia, Krüger, Nikolay V, Abrosimov, Christoph, Helling, Stephan, Schulz, George E, Cutsail Iii
Publikováno v:
Inorganic chemistry. 61(29)
The recent successes in the isolation and characterization of several bismuth radicals inspire the development of new spectroscopic approaches for the in-depth analysis of their electronic structure. Electron paramagnetic resonance (EPR) spectroscopy
Autor:
Hannah Rosenbach, George E. Cutsail, James A. Birrell, Serena DeBeer, Ingrid Span, Marina Pascual-Ortiz, Ursula Fleig, Eva Walla
Publikováno v:
JBIC Journal of Biological Inorganic Chemistry. 26:93-108
TheSchizosaccharomyces pombeAsp1 protein is a bifunctional kinase/pyrophosphatase that belongs to the highly conserved eukaryotic diphosphoinositol pentakisphosphate kinase PPIP5K/Vip1 family. The N-terminal Asp1 kinase domain generates specific high
Publikováno v:
Chemical Science
Cyclic voltammetry (CV) studies of two L(X)Ga-substituted dipnictenes [L(R2N)GaE]2 (E = Sb, R = Me 1; E = Bi; R = Et 2; L = HC[C(Me)NDipp]2; Dipp = 2,6-i-Pr2C6H3) showed reversible reduction events. Single electron reduction of 1 and 2 with KC8 in DM
Autor:
Peng‐Cheng Duan, Roland Alexander Schulz, Anton Römer, Benjamin E. Van Kuiken, Sebastian Dechert, Serhiy Demeshko, George E. Cutsail, Serena DeBeer, Ricardo A. Mata, Franc Meyer
Publikováno v:
Angewandte Chemie. 133:1919-1924
Autor:
Serena DeBeer, Peng‐Cheng Duan, Anton Römer, Sebastian Dechert, Benjamin E. Van Kuiken, Ricardo A. Mata, George E. Cutsail, Serhiy Demeshko, Roland A. Schulz, Franc Meyer
Publikováno v:
Angewandte Chemie (International Ed. in English)
The dinickel(II) dihydride complex (1K) of a pyrazolate‐based compartmental ligand with β‐diketiminato (nacnac) chelate arms (L−), providing two pincer‐type {N3} binding pockets, has been reported to readily eliminate H2 and to serve as a ma
Autor:
George E. Cutsail, Rahul Banerjee, Derek B. Rice, Olivia McCubbin Stepanic, John D. Lipscomb, Serena DeBeer
Publikováno v:
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry. 27(6)
Soluble methane monooxygenase (sMMO) facilitates the conversion of methane to methanol at a non-heme FeIV2 intermediate MMOHQ, which is formed in the active site of the sMMO hydroxylase component (MMOH) during the catalytic cycle. Other biological sy