Dioxygen reactivity of biomimetic iron-catecholate and iron-o-aminophenolate complexes of a tris(2-pyridylthio)methanido ligand: aromatic C-C bond cleavage of catecholate versus o-iminobenzosemiquinonate radical formation.
about
Dioxygen reactivity of biomimetic Fe(II) complexes with noninnocent catecholate, o-aminophenolate, and o-phenylenediamine ligands.Electronic nature of zwitterionic alkali metal methanides, silanides and germanides - a combined experimental and computational approach.Iron-catalyzed hydrogenation for the in situ regeneration of an NAD(P)H model: biomimetic reduction of α-keto-/α-iminoesters.Iron(III) complexes of tripodal tetradentate 4N ligands as functional models for catechol dioxygenases: the electronic vs. steric effect on extradiol cleavage.Iron(ii) complexes of 2-mercaptopyridine as rubredoxin site analogues.Substrate-dependent aromatic ring fission of catechol and 2-aminophenol with O2 catalyzed by a nonheme iron complex of a tripodal N4 ligand.Catalytic and regiospecific extradiol cleavage of catechol by a biomimetic iron complex.Biocatalysis, DNA-protein interactions, cytotoxicity and molecular docking of Cu(II), Ni(II), Zn(II) and V(IV) Schiff base complexes
P2860
Q37721709-E83AD292-5CC0-4B96-BB72-F7634FBC0350Q42314946-E2A5B76A-EDBB-40AC-B68B-A81493A977C7Q44281759-F85CF78C-578B-46AB-980E-0355C478D03FQ44738450-B4C89280-612B-4B72-895B-8DAE292B4DEFQ49686707-DA9CE160-C769-4102-9A39-FB5C746B5253Q52871218-E689E206-4C9C-4F3B-9334-C2F1692BB4EDQ53089159-29CDF663-4CCB-4CD1-978D-B02D97FE8782Q57816439-FD314323-12B2-4719-AC6B-762DB339112B
P2860
Dioxygen reactivity of biomimetic iron-catecholate and iron-o-aminophenolate complexes of a tris(2-pyridylthio)methanido ligand: aromatic C-C bond cleavage of catecholate versus o-iminobenzosemiquinonate radical formation.
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh-hant
name
Dioxygen reactivity of biomime ...... ophenolate complexes of a tris
@nl
Dioxygen reactivity of biomime ...... miquinonate radical formation.
@en
type
label
Dioxygen reactivity of biomime ...... ophenolate complexes of a tris
@nl
Dioxygen reactivity of biomime ...... miquinonate radical formation.
@en
prefLabel
Dioxygen reactivity of biomime ...... ophenolate complexes of a tris
@nl
Dioxygen reactivity of biomime ...... miquinonate radical formation.
@en
P2093
P2860
P356
P1476
Dioxygen reactivity of biomime ...... miquinonate radical formation.
@en
P2093
Partha Halder
Sayantan Paria
Tapan Kanti Paine
P2860
P304
11778-11787
P356
10.1002/CHEM.201200886
P407
P577
2012-07-29T00:00:00Z