Zobrazeno 1 - 10
of 95
pro vyhledávání: '"Edward J, Reijerse"'
Publikováno v:
Journal of the American Chemical Society. 145:9988-9993
Autor:
Xiuxiu Yang, Edward J. Reijerse, Nils Nöthling, Daniel J. SantaLucia, Markus Leutzsch, Alexander Schnegg, Josep Cornella
Publikováno v:
Journal of the American Chemical Society. 145:5618-5623
Herein, we report the synthesis, isolation and characterization of two cationic organobismuth(II) compounds bearing N,C,N pincer frameworks, which are crucial intermediates in bismuth radical processes. X-ray crystallography uncovered a monomeric Bi(
Autor:
Nipa Chongdar, Patricia Rodríguez-Maciá, Edward J. Reijerse, Wolfgang Lubitz, Hideaki Ogata, James A. Birrell
Publikováno v:
Chemical Science. 14:3682-3692
Site-directed mutagenesis of the sensory [FeFe] hydrogenase from Thermotoga maritima reveals new insight into how the protein environment tunes the active site properties for its sensory role.
Autor:
Mahendra K. Sharma, Sonia Chabbra, Christoph Wölper, Hanns M. Weinert, Edward J. Reijerse, Alexander Schnegg, Stephan Schulz
Publikováno v:
Chemical Science. 13:12643-12650
Modulating the electronic structures of main group element compounds is crucial to control their chemical reactivity. Herein we report on the synthesis, frontier orbital modulation, and one-electron oxidation of two L(X)Ga-substituted diphosphenes [L
Publikováno v:
Journal of the American Chemical Society
In this article, we investigated the I2-promoted cyclic dialkyl ether formation from 6-membered oxanickelacycles originally reported by Hillhouse. A detailed mechanistic investigation based on spectroscopic and crystallographic analysis revealed that
Autor:
Stephen P. Cramer, Martin Kaupp, Wolfgang Lubitz, Edward J. Reijerse, James A. Birrell, Thomas B. Rauchfuss, Vladimir Pelmenschikov, Casseday P. Richers
Publikováno v:
The Journal of Physical Chemistry Letters
[FeFe] hydrogenases are very active enzymes that catalyze the reversible conversion of molecular hydrogen into protons and electrons. Their active site, the H-cluster, contains a unique binuclear iron complex, [2Fe]H, with CN– and CO ligands as wel
Autor:
James A. Birrell, Hongxin Wang, Stephen P. Cramer, Vladimir Pelmenschikov, Kenji Tamasaku, Lei Li, Leland B. Gee, Nakul Mishra, Simon Arragain, Yoshitaka Yoda, Wolfgang Lubitz, Casseday P. Richers, Edward J. Reijerse, Thomas B. Rauchfuss, Hiroaki Matsuura
Publikováno v:
J Am Chem Soc
[FeFe] hydrogenases are highly active catalysts for the interconversion of molecular hydrogen with protons and electrons. Here, we use a combination of isotopic labeling, (57)Fe nuclear resonance vibrational spectroscopy (NRVS), and density functiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b879477a9c54bc201ea0f6399acd396e
https://europepmc.org/articles/PMC8211414/
https://europepmc.org/articles/PMC8211414/
Autor:
Sarah M. Narehood, Edward J. Reijerse, James A. Birrell, Monica L. K. Sanchez, R. Brian Dyer, Sara E. Konecny, Wolfgang Lubitz
Publikováno v:
The journal of physical chemistry. B. 124(40)
Oxidoreductase enzymes often perform technologically useful chemical transformations using abundant metal cofactors with high efficiency under ambient conditions. The understanding of the catalytic mechanism of these enzymes is, however, highly depen
Autor:
Olaf Rüdiger, Patricia Rodríguez-Maciá, Maurice van Gastel, Edward J. Reijerse, Wolfgang Lubitz, James A. Birrell, Serena DeBeer
Publikováno v:
Journal of the American Chemical Society. 140:9346-9350
[FeFe] hydrogenases catalyze proton reduction and hydrogen oxidation with high rates and efficiency under physiological conditions, but are highly oxygen sensitive. The [FeFe] hydrogenase from Desulfovibrio desulfuricans (DdHydAB) can be purified und
Autor:
Heiko Bamberger, Christian Würtele, Edward J. Reijerse, Max C. Holthausen, Martin Diefenbach, Joris van Slageren, Sven Schneider, Christian Volkmann, Serhiy Demeshko, Markus Kinauer, Bas de Bruin
Publikováno v:
Chemical Science
Chemical Science, 9(18), 4325-4332. Royal Society of Chemistry
Chemical Science, 9(18), 4325-4332. Royal Society of Chemistry
An iridium(iii–v) imido series has been isolated that features an iridium complex with an unprecedented triplet ground state.
The iridium(iii/iv/v) imido redox series [Ir(NtBu){N(CHCHPtBu2)2}]0/+/2+ was synthesized and examined spectroscopical
The iridium(iii/iv/v) imido redox series [Ir(NtBu){N(CHCHPtBu2)2}]0/+/2+ was synthesized and examined spectroscopical