Shuttling of Nickel Oxidation States in N4S2 Coordination Geometry versus Donor Strength of Tridentate N2S Donor Ligands

2012 ◽  
Vol 51 (14) ◽  
pp. 7625-7635 ◽  
Author(s):  
Sudip K. Chatterjee ◽  
Suprakash Roy ◽  
Suman Kumar Barman ◽  
Ram Chandra Maji ◽  
Marilyn M. Olmstead ◽  
...  

1991 ◽  
Vol 30 (23) ◽  
pp. 4354-4360 ◽  
Author(s):  
Suranjan Bhanja. Choudhury ◽  
Debashis. Ray ◽  
Animesh. Chakravorty


2015 ◽  
Vol 185 ◽  
pp. 87-104 ◽  
Author(s):  
Lianpeng Tong ◽  
Ruifa Zong ◽  
Rongwei Zhou ◽  
Nattawut Kaveevivitchai ◽  
Gang Zhang ◽  
...  

A series of RuII complexes that behave as water oxidation catalysts were prepared involving a tetradentate equatorial ligand and two 4-substituted pyridines as the axial ligands. Two of these complexes were derived from 2,9-di-(pyrid-2′-yl)-1,10-phenanthroline (dpp) and examine the effect of incorporating electron-donating amino and bulky t-butyl groups on catalytic activity. A third complex replaced the two distal pyridines with N-methylimidazoles that are more electron-donating than the pyridines of dpp and potentially stabilize higher oxidation states of the metal. The tetradentate ligand 2-(pyrid-2′-yl)-6-(1′′,10′′-phenanthrol-2′′-yl)pyridine (bpy–phen), possessing a bonding cavity similar to dpp, was also prepared. The RuII complex of this ligand does not have two rotatable pyridines in the equatorial plane and thus shows different flexibility from the [Ru(dpp)] complexes. All the complexes showed activity towards water oxidation. Investigation of their catalytic behavior and electrochemical properties suggests that they may follow the same catalytic pathway as the prototype [Ru(dpp)pic2]2+ involving a seven-coordinated [RuIV(O)] intermediate. The influence of coordination geometry on catalytic performance is analyzed and discussed.



Catalysts ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1016 ◽  
Author(s):  
Kotohiro Nomura

Solution V K-edge XANES (X-ray absorption near edge structure) and EXAFS (extended X-ray absorption fine structure) analysis of vanadium(V) complexes containing both imido ligands and anionic ancillary donor ligands (L) of type, V(NR)(L)X2 (R = Ar, Ad (1-adamantyl); Ar = 2,6-Me2C6H3; X = Cl, Me, L = 2-(ArNCH2)C5H4N, OAr, WCA-NHC, and 2-(2’-benzimidazolyl)pyridine; WCA-NHC = anionic NHCs containing weak coordinating B(C6F5)3), which catalyze ethylene dimerization and/or polymerization in the presence of Al cocatalysts, has been explored. Different catalytically actives species with different oxidation states were formed depending upon the Al cocatalyst (MAO, Me2AlCl, AliBu3, etc.) and the anionic ancillary donor ligand employed. The method is useful for obtainment of the direct information of the active species (oxidation state, basic framework around the centered metal) in solution, and for better understanding in catalysis mechanism and organometallic as well as coordination chemistry.



2000 ◽  
Vol 122 (1) ◽  
pp. 182-183 ◽  
Author(s):  
Joshua Telser ◽  
Yih-Chern Horng ◽  
Donald F. Becker ◽  
Brian M. Hoffman ◽  
Stephen W. Ragsdale


1998 ◽  
Vol 16 ◽  
pp. S169
Author(s):  
Suzan Artik ◽  
Christian von Vultée ◽  
Erkan Elieyioglu ◽  
Peter Griem ◽  
Ernst Gleichmann


2011 ◽  
Vol 98 (17) ◽  
pp. 173109 ◽  
Author(s):  
George J. Nelson ◽  
William M. Harris ◽  
John R. Izzo ◽  
Kyle N. Grew ◽  
Wilson K. S. Chiu ◽  
...  


2019 ◽  
Vol 35 (1) ◽  
pp. 1315-1321 ◽  
Author(s):  
George Nelson ◽  
William Harris ◽  
John Izzo ◽  
Kyle N. Grew ◽  
Wilson K. Chiu ◽  
...  


2004 ◽  
Vol 126 (13) ◽  
pp. 4068-4069 ◽  
Author(s):  
Jennifer L. Craft ◽  
Yih-Chern Horng ◽  
Stephen W. Ragsdale ◽  
Thomas C. Brunold


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