Probing the Reactivity of Redox-Active 2-Aminophenolates on Iron Complexes of a Carbanionic N3C Donor Ligand

2014 ◽  
Vol 640 (6) ◽  
pp. 1168-1176 ◽  
Author(s):  
Sridhar Banerjee ◽  
Partha Halder ◽  
Tapan Kanti Paine
Keyword(s):  
Iron Complexes ◽  
Donor Ligand ◽  
Redox Active

Synthesis and Catalysis of Redox-Active Bis(imino)acenaphthene (BIAN) Iron Complexes

ChemCatChem ◽  
2017 ◽  
Vol 9 (16) ◽  
pp. 3203-3209 ◽  
Author(s):  
Matteo Villa ◽  
Dominique Miesel ◽  
Alexander Hildebrandt ◽  
Fabio Ragaini ◽  
Dieter Schaarschmidt ◽  
...  
Keyword(s):  
Iron Complexes ◽  
Redox Active

Electrochemical water oxidation by a copper complex with N4-donor ligand at neutral condition

2021 ◽  
Author(s):  
Junqi Lin ◽  
Xin Chen ◽  
Nini Wang ◽  
Shanshan Liu ◽  
Zhijun Ruan ◽  
...  
Keyword(s):  
Oxygen Evolution ◽  
Copper Complex ◽  
Water Oxidation ◽  
Neutral Condition ◽  
Turnover Frequency ◽  
High Turnover ◽  
Donor Ligand ◽  
Redox Active

Herein, electrochemical water oxidation catalyzed by a copper(II) complex [CuII(H2L)](NO3)2 with redox-active salophen-like N4-donor ligand N,N′-bis-(1H-imidazol-4-yl)methylidene-o-phenylenediamine is demonstrated. Oxygen evolution with high turnover frequency of 11.09 s-1 and low onset...

Di- and trivalent iron complexes with redox-active 1-(2-pyridylazo)-2-phenanthrol (papl)

Polyhedron ◽  
2017 ◽  
Vol 123 ◽  
pp. 462-469 ◽  
Author(s):  
Robin A. Taylor ◽  
Alan J. Lough ◽  
Takele Seda ◽  
Prashanth K. Poddutoori ◽  
Martin T. Lemaire
Keyword(s):  
Iron Complexes ◽  
Trivalent Iron ◽  
Redox Active

Reversible C–C Bond Formation between Redox-Active Pyridine Ligands in Iron Complexes

2012 ◽  
Vol 134 (50) ◽  
pp. 20352-20364 ◽  
Author(s):  
Thomas R. Dugan ◽  
Eckhard Bill ◽  
K. Cory MacLeod ◽  
Gemma J. Christian ◽  
Ryan E. Cowley ◽  
...  
Keyword(s):  
Bond Formation ◽  
Iron Complexes ◽  
Pyridine Ligands ◽  
Redox Active

scholarly journals An Iron Pyridyl-Carbene Catalyst for Low Overpotential CO2 reduction to CO: Mechanistic Comparisons with the Ruthenium Analogue and Photochemical Promotion

2020 ◽  
Author(s):  
Sergio Gonell ◽  
Julio Lloret ◽  
Alexander Miller
Keyword(s):  
Co2 Reduction ◽  
Iron Complexes ◽  
Transition Metal Ions ◽  
Ruthenium Catalysts ◽  
Computational Studies ◽  
Chelating Ligands ◽  
Faradaic Efficiency ◽  
Mechanistic Insight ◽  
Redox Active ◽  
Improved Performance

<div><div><div><p>Electrocatalysts for CO2 reduction based on first row transition metal ions have attracted attention as abundant and affordable candidates for energy conversion applications. We hypothesized that a successful strategy in ruthenium electrocatalyst design, featuring two chelating ligands that can be individually tuned to adjust the overpotential and catalytic activity, could be equally applicable in the analogous iron complexes. New iron complexes supported by a redox-active 2,2':6',2''-terpyridine (tpy) ligand and strong trans effect pyridyl- N-heterocyclic carbene ligand (1-methyl-benzimidazol-2-ylidene-3-(2-pyridine)) were synthesized, and these isostructural analogues to leading ruthenium catalysts were also found to be active CO2 reduction electrocatalysts. Electrochemical and computational studies reveal completely distinct mechanisms for the iron and ruthenium complexes, with hemilability in the iron system enabling electrocatalysis at overpotentials as low as 150 mV (ca. 500 mV lower than the ruthenium analogue). Cyclic voltammetry studies elucidated the mechanism of the net 4e–/2H+ process that occurs within the single reductive feature, with an iron solvento complex undergoing reduction, CO2 activation, and further reduction to an iron carbonyl. The mechanistic insight guided development of photoelectrocatalytic conditions under a continuous flow of CO2 that exhibited improved performance, with Faradaic efficiency up to 99%.</p></div></div></div>

Redox-Active, Boron-Based Ligands in Iron Complexes with Inverted Hydride Reactivity in Dehydrogenation Catalysis

ACS Catalysis ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 7300-7309 ◽  
Author(s):  
Andreas Bäcker ◽  
Yinwu Li ◽  
Maximilian Fritz ◽  
Maik Grätz ◽  
Zhuofeng Ke ◽  
...  
Keyword(s):  
Iron Complexes ◽  
Redox Active

Structural and Electronic Variations of sp/sp2 Carbon-Based Bridges in Di- and Trinuclear Redox-Active Iron Complexes Bearing Fe(diphosphine)2X (X = I, NCS) Moieties

2015 ◽  
Vol 34 (2) ◽  
pp. 408-418 ◽  
Author(s):  
Franziska Lissel ◽  
Olivier Blacque ◽  
Koushik Venkatesan ◽  
Heinz Berke
Keyword(s):  
Iron Complexes ◽  
Active Iron ◽  
Redox Active ◽  
Carbon Based

Electron Density Distributions of Redox Active Mixed Valence Carboxylate Bridged Trinuclear Iron Complexes

2003 ◽  
Vol 125 (36) ◽  
pp. 11088-11099 ◽  
Author(s):  
Jacob Overgaard ◽  
Finn K. Larsen ◽  
Birgit Schiøtt ◽  
Bo B. Iversen
Keyword(s):  
Electron Density ◽  
Mixed Valence ◽  
Iron Complexes ◽  
Density Distributions ◽  
Redox Active

scholarly journals Long range charge transfer in trimetallic mixed-valence iron complexes mediated by redox non-innocent cyanoacetylide ligands

2014 ◽  
Vol 43 (17) ◽  
pp. 6291-6294 ◽  
Author(s):  
Josef B. G. Gluyas ◽  
Andrew J. Boden ◽  
Samantha G. Eaves ◽  
Herrick Yu ◽  
Paul J. Low
Keyword(s):  
Electron Transfer ◽  
Charge Transfer ◽  
Long Range ◽  
Mixed Valence ◽  
Iron Complexes ◽  
Redox Active

A redox active 9-atom, 10-bond –CC–CN{Fe(dppx)2}NC–CC– bridge is shown to be effective at promoting electron transfer between metal centres separated by some 15 Å.

Sign in / Sign up

Export Citation Format

Share Document