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Redox Activity of Iron Diazine-Diimine Carbonyl and Dinitro..:

Julianna S. Doll (10687522) ; Nicolas I. Regenauer (11845568) ; Viktoria P. Bothe (11845571)..
https://figshare.com/articles/journal_contribution/Redox_Activity_of_Iron_Diazine-Diimine_Carbonyl_and_Dinitrogen_Complexes_A_Comparative_Study_of_the_Influence_of_the_Heterocyclic_Ring/17213216. , 2021

Link: https://doi.org/10.1021/acs.inorgchem.1c03212.s001

RT Journal
T1 <Title>Redox Activity of Iron Diazine-Diimine Carbonyl and Dinitrogen Complexes: A Comparative Study of the Influence of the Heterocyclic Ring</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_17213216&Exemplar=1&LAN=DE
				
A1 Julianna S. Doll (10687522)
A1 Nicolas I. Regenauer (11845568)
A1 Viktoria P. Bothe (11845571)
A1 Hubert Wadepohl (1264056)
A1 Dragoş-Adrian Roşca (1371855)
YR 2021
K1 Biophysics
K1 Biochemistry
K1 Microbiology
K1 Cell Biology
K1 Chemical Sciences not elsewhere classified
K1 reversibly cleaved oxidatively
K1 ligands triggers changes
K1 c – c
K1 supporting chelate triggers
K1 pyrazine )
K1 supported
K1 electron density around
K1 2 </ sub
K1 pyrimidine  diimine
K1 diazinediimine iron complexes
K1 iron diazine
K1 diimine carbonyl
K1 yield either
K1 transfer processes
K1 supporting heterocycle
K1 redox potentials
K1 redox activity
K1 planar lfecl
K1 nitrogen complexes
K1 monoradical character
K1 heterocyclic ring
K1 field n
K1 en route
K1 employing weak
K1 electronic structure
K1 dinitrogen complexes
K1 detailed investigation
K1 dearomatized core
K1 comparative study
K1 centered radical
K1 carbonyl analogues
K1 bonded dimer
K1 asymmetric distribution
JF https://figshare.com/articles/journal_contribution/Redox_Activity_of_Iron_Diazine-Diimine_Carbonyl_and_Dinitrogen_Complexes_A_Comparative_Study_of_the_Influence_of_the_Heterocyclic_Ring/17213216
LK http://dx.doi.org/https://doi.org/10.1021/acs.inorgchem.1c03212.s001
DO https://doi.org/10.1021/acs.inorgchem.1c03212.s001
SF ELIB - SuUB Bremen

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