scholarly journals Rhodium, iridium and nickel complexes with a 1,3,5-triphenylbenzene tris-MIC ligand. Study of the electronic properties and catalytic activities

2015 ◽  
Vol 11 ◽  
pp. 2584-2590 ◽  
Author(s):  
Carmen Mejuto ◽  
Beatriz Royo ◽  
Gregorio Guisado-Barrios ◽  
Eduardo Peris

The coordination versatility of a 1,3,5-triphenylbenzene-tris-mesoionic carbene ligand is illustrated by the preparation of complexes with three different metals: rhodium, iridium and nickel. The rhodium and iridium complexes contained the [MCl(COD)] fragments, while the nickel compound contained [NiCpCl]. The preparation of the tris-MIC (MIC = mesoionic carbene) complex with three [IrCl(CO)2] fragments, allowed the estimation of the Tolman electronic parameter (TEP) for the ligand, which was compared with the TEP value for a related 1,3,5-triphenylbenzene-tris-NHC ligand. The electronic properties of the tris-MIC ligand were studied by cyclic voltammetry measurements. In all cases, the tris-MIC ligand showed a stronger electron-donating character than the corresponding NHC-based ligands. The catalytic activity of the tri-rhodium complex was tested in the addition reaction of arylboronic acids to α,β-unsaturated ketones.

2005 ◽  
Vol 34 (11) ◽  
pp. 1480-1481 ◽  
Author(s):  
Tamio Hayashi ◽  
Norihito Tokunaga ◽  
Kazuhiro Okamoto ◽  
Ryo Shintani

RSC Advances ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 6900-6918 ◽  
Author(s):  
Mouhieddinne Guergueb ◽  
Soumaya Nasri ◽  
Jihed Brahmi ◽  
Frédérique Loiseau ◽  
Florian Molton ◽  
...  

Preparation and UV/vis, IR, MS, 1H NMR, cyclic voltammetry and molecular structures of two new Co(ii) complexes with para-methoxy-phenyl and para-chloro meso-porphyrins and 4-cyanopyridine ligand (1–2). Catalytic oxidation data of MB dye using 1–2.


Author(s):  
Juan D. Villada ◽  
Álvaro Duarte-Ruiz ◽  
Manuel N. Chaur

We report a new methodology for the synthesis of two highly symmetric equatorial malonate hexaadducts of C60 fullerene. The synthetic methodology is based on a series of protection and deprotection steps that allow the preparation of a fullerene [60] functionalized with six symmetrical positioned malonate addends without using complicated and expensive separation techniques (highperformance liquid chromatography, HPLC) or long reaction times. This methodology allowed us to prepare the carboxylic adducts 6 (equatorial octacarboxylic tetraadduct of C60) and 8 (equatorial dodecacarboxylic hexakisadduct of C60). As far as we  now, compound 6 has not yet been reported. We also studied the electronic properties of the main compounds by UV-Vis spectroscopy and cyclic voltammetry (CV). The reported fullerene adducts exhibited several reversible reduction processes whose electron transfers are controlled by diffusion. 


2019 ◽  
Vol 48 (35) ◽  
pp. 13205-13211 ◽  
Author(s):  
Stefan S. Rohner ◽  
Niklas W. Kinzel ◽  
Christophe Werlé ◽  
Walter Leitner

Systematic series of iron(+iii) and manganese(+ii) complexes are investigated by cyclic voltammetry to elucidate how the electronic properties of the ligands influence overpotential and catalytic current in the context of water oxidation catalysis.


2005 ◽  
Vol 24 (16) ◽  
pp. 4003-4013 ◽  
Author(s):  
Daniel Gareau ◽  
Christine Sui-Seng ◽  
Laurent F. Groux ◽  
François Brisse ◽  
Davit Zargarian

ChemInform ◽  
2012 ◽  
Vol 43 (12) ◽  
pp. no-no
Author(s):  
Byron J. Truscott ◽  
George C. Fortman ◽  
Alexandra M. Z. Slawin ◽  
Steven P. Nolan

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