Homo- and Heterobinuclear Cu and Pd Complexes with a Bridging Redox-Active Bisguanidino-Substituted Dioxolene Ligand: Electronic Structure and Metal-Ligand Electron-Transfer

2017 ◽  
Vol 23 (48) ◽  
pp. 11636-11648 ◽  
Author(s):  
David Fridolin Schrempp ◽  
Elisa Schneider ◽  
Elisabeth Kaifer ◽  
Hubert Wadepohl ◽  
Hans-Jörg Himmel
Keyword(s):  
Electron Transfer ◽  
Electronic Structure ◽  
Redox Active ◽  
Pd Complexes ◽  
Metal Ligand

Intramolecular metal–ligand electron transfer triggered by co-ligand substitution

2018 ◽  
Vol 47 (28) ◽  
pp. 9430-9441 ◽  
Author(s):  
Alexandra Ziesak ◽  
Lena Steuer ◽  
Elisabeth Kaifer ◽  
Norbert Wagner ◽  
Johannes Beck ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Ligand Substitution ◽  
Dinuclear Copper ◽  
Redox Active ◽  
Metal Ligand

Labile co-ligands are attached to a dinuclear copper(i) complex with a redox-active bridging guanidine ligand. Their substitution triggers electron-transfer from the copper atoms to the guanidine.

scholarly journals Insight to Microbial Fe(III) Reduction Mediated by Redox-Active Humic Acids with Varied Redox Potentials

2021 ◽  
Vol 18 (13) ◽  
pp. 6807
Author(s):  
Jingtao Duan ◽  
Zhiyuan Xu ◽  
Zhen Yang ◽  
Jie Jiang
Keyword(s):  
Molecular Weight ◽  
Electron Transfer ◽  
Humic Acids ◽  
Weight Fraction ◽  
Electrochemical Analysis ◽  
Microbial Reduction ◽  
Redox Potentials ◽  
Groundwater Environment ◽  
Redox Active ◽  
Different Molecular Weight

Redox-active humic acids (HA) are ubiquitous in terrestrial and aquatic systems and are involved in numerous electron transfer reactions affecting biogeochemical processes and fates of pollutants in soil environments. Redox-active contaminants are trapped in soil micropores (<2 nm) that have limited access to microbes and HA. Therefore, the contaminants whose molecular structure and properties are not damaged accumulate in the soil micropores and become potential pollution sources. Electron transfer capacities (ETC) of HA reflecting redox activities of low molecular weight fraction (LMWF, <2.5) HA can be detected by an electrochemical method, which is related to redox potentials (Eh) in soil and aquatic environments. Nevertheless, electron accepting capacities (EAC) and electron donating capacities (EDC) of these LMWF HA at different Eh are still unknown. EDC and EAC of different molecular weight HA at different Eh were analyzed using electrochemical methods. EAC of LMWF at −0.59 V was 12 times higher than that at −0.49 V, while EAC increased to 2.6 times when the Eh decreased from −0.59 V to −0.69 V. Afterward, LMWF can act as a shuttle to stimulate microbial Fe(III) reduction processes in microbial reduction experiments. Additionally, EAC by electrochemical analysis at a range of −0.49–−0.59 V was comparable to total calculated ETC of different molecular weight fractions of HA by microbial reduction. Therefore, it is indicated that redox-active functional groups that can be reduced at Eh range of −0.49–−0.59 are available to microbial reduction. This finding contributes to a novel perspective in the protection and remediation of the groundwater environment in the biogeochemistry process.

Revealing the Relationship between Semiconductor Electronic Structure and Electron Transfer Dynamics at Metal Oxide–Chromophore Interfaces

2013 ◽  
Vol 117 (48) ◽  
pp. 25259-25268 ◽  
Author(s):  
Robin R. Knauf ◽  
M. Kyle Brennaman ◽  
Leila Alibabaei ◽  
Michael R. Norris ◽  
Jillian L. Dempsey
Keyword(s):  
Electron Transfer ◽  
Electronic Structure ◽  
Metal Oxide ◽  
Semiconductor Electronic ◽  
The Relationship

Hydroquinone/quinone electro- and photochemical interconversion in isolable polypyridylruthenium(II) complexes

2021 ◽  
Author(s):  
Dai Oyama ◽  
Takatoshi Kanno ◽  
Tsugiko Takase
Keyword(s):  
Electron Transfer ◽  
Metal Complexes ◽  
Transfer Reactions ◽  
Electron Transfer Reactions ◽  
Fundamental Knowledge ◽  
Redox Active ◽  
Quinone Complexes

Quinone derivatives and their metal complexes are well-known molecules that participate in electron-transfer reactions relevant to diverse fields. However, the fundamental knowledge on the unique reactivity of redox-active quinone complexes...

A semi-empirical molecular orbital scheme to study electron transfer in iron–sulphur proteins

2005 ◽  
Vol 33 (1) ◽  
pp. 20-21 ◽  
Author(s):  
M. Sundararajan ◽  
J.P. McNamara ◽  
M. Mohr ◽  
I.H. Hillier ◽  
H. Wang
Keyword(s):  
Electron Transfer ◽  
Electronic Structure ◽  
Molecular Orbital ◽  
Parametric Method ◽  
Orbital Method ◽  
Molecular Orbital Method ◽  
Semi Empirical

We describe the use of the semi-empirical molecular orbital method PM3 (parametric method 3) to study the electronic structure of iron–sulphur proteins. We first develop appropriate parameters to describe models of the redox site of rubredoxins, followed by some preliminary calculations of multinuclear iron systems of relevance to hydrogenases.

Sulfur in humin as a redox-active element for extracellular electron transfer

Geoderma ◽  
2022 ◽  
Vol 408 ◽  
pp. 115580
Author(s):  
Duyen Minh Pham ◽  
Hiroshi Oji ◽  
Shinya Yagi ◽  
Satoshi Ogawa ◽  
Arata Katayama
Keyword(s):  
Electron Transfer ◽  
Active Element ◽  
Extracellular Electron Transfer ◽  
Redox Active
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