Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Spencer A. Kerns"'
Autor:
Sean T. Goralski, Junhyeok Seo, Vincent M. Lynch, Jason Shearer, Michael J. Rose, Spencer A. Kerns, Eileen R. Sullivan
Publikováno v:
Chemical Science. 12:12838-12846
We report the synthesis and reactivity of a model of [Fe]-hydrogenase derived from an anthracene-based scaffold that includes the endogenous, organometallic acyl(methylene) donor. In comparison to other non-scaffolded acyl-containing complexes, the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f0e3cd88cf6e99c54dbd24d8b219db0
https://doi.org/10.1039/d0sc03154b
https://doi.org/10.1039/d0sc03154b
Autor:
Michael J. Rose, Spencer A. Kerns
Publikováno v:
Accounts of Chemical Research. 53:1637-1647
ConspectusThe well-known dinuclear [FeFe] and [NiFe] hydrogenase enzymes are redox-based proton reduction and H2 oxidation catalysts. In comparison, the structural and functional aspects of the mon...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93ae65dfa273a3b1e7c98e14ae54e428
https://doi.org/10.1021/acs.accounts.0c00315
https://doi.org/10.1021/acs.accounts.0c00315
Publikováno v:
Inorganic Chemistry. 59:2548-2561
A set of bioinspired carbamoyl CNP pincer complexes are reported that are relevant to [Fe]-hydrogenase (Hmd). The dicarbonyl species [(CNHNNHPR2)Fe(CO)2I] [R = Ph, 1; R = iPr, 2] undergoes ligand deprotonation, resulting in the dearomatized complexes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a2c9ccfa505931e70e71c715061d368
https://doi.org/10.1021/acs.inorgchem.9b03476
https://doi.org/10.1021/acs.inorgchem.9b03476
Publikováno v:
JACS Au, vol 2, iss 6
Artificial metalloproteins (ArMs) have recently gained significant interest due to their potential to address issues in a broad scope of applications, including biocatalysis, biotechnology, protein assembly, and model chemistry. ArMs are assembled by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e1ae0d1e4fb8de1c3a22185619d6737
https://pubmed.ncbi.nlm.nih.gov/35783165
https://pubmed.ncbi.nlm.nih.gov/35783165
Autor:
Spencer A, Kerns, Junhyeok, Seo, Vincent M, Lynch, Jason, Shearer, Sean T, Goralski, Eileen R, Sullivan, Michael J, Rose
Publikováno v:
Chemical Science
We report the synthesis and reactivity of a model of [Fe]-hydrogenase derived from an anthracene-based scaffold that includes the endogenous, organometallic acyl(methylene) donor. In comparison to other non-scaffolded acyl-containing complexes, the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bfa4fb0362a3d371f407424cf70dc371
https://pubmed.ncbi.nlm.nih.gov/34703571
https://pubmed.ncbi.nlm.nih.gov/34703571
Publikováno v:
Inorganic chemistry. 59(4)
A set of bioinspired carbamoyl CNP pincer complexes are reported that are relevant to [Fe]-hydrogenase (Hmd). The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::335c362f12b059b6b53ba4bca63095fb
https://pubmed.ncbi.nlm.nih.gov/32017541
https://pubmed.ncbi.nlm.nih.gov/32017541
Publikováno v:
Angewandte Chemie. 130:2905-2908
We report the synthesis, X-ray structure and functional biomimetic activity of a model complex of mono-iron hydrogenase (Hmd). To achieve the desired biomimetic fac-CNS(thiolate) ligation motif, an anthracene framework is used to provide the requisit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99555eb699a791e08381b174b58520c4
https://doi.org/10.1002/ange.201712948
https://doi.org/10.1002/ange.201712948
Publikováno v:
European Journal of Inorganic Chemistry. 2015:5708-5714
Quinoxalinol salen ligands have been characterized as selective ligands for the rapid identification of uranyl. The absorption maximum of ligand 1 presented a hypsochromic (blue) shift with the addition of UO22+ (as the acetate salt), and a bathochro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3788de3df1aa26c13f95b5ed4586230
https://doi.org/10.1002/ejic.201501033
https://doi.org/10.1002/ejic.201501033