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1 Ergebnisse
1
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/dataset/Redox_Activity_of_Iron_Diazine-Diimine_Carbonyl_and_Dinitrogen_Complexes_A_Comparative_Study_of_the_Influence_of_the_Heterocyclic_Ring/17213219. , 2021
Link:
https://doi.org/10.1021/acs.inorgchem.1c03212.s002
RT Journal T1
Redox Activity of Iron Diazine-Diimine Carbonyl and Dinitrogen Complexes: A Comparative Study of the Influence of the Heterocyclic Ring
UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_17213219&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/dataset/Redox_Activity_of_Iron_Diazine-Diimine_Carbonyl_and_Dinitrogen_Complexes_A_Comparative_Study_of_the_Influence_of_the_Heterocyclic_Ring/17213219 LK http://dx.doi.org/https://doi.org/10.1021/acs.inorgchem.1c03212.s002 DO https://doi.org/10.1021/acs.inorgchem.1c03212.s002 SF ELIB - SuUB Bremen
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