The Role of Equatorial and Axial Ligands in Promoting the Activity of Non-Heme Oxidoiron(IV) Catalysts in Alkane Hydroxylation

2007 ◽  
Vol 2007 (19) ◽  
pp. 3023-3033 ◽  
Author(s):  
Leonardo Bernasconi ◽  
Manuel J. Louwerse ◽  
Evert Jan Baerends
1995 ◽  
Vol 59 (2-3) ◽  
pp. 490
Author(s):  
I.M.C.M. Rietjens ◽  
J. Spee ◽  
R. Weiss ◽  
A.X. Trautwein ◽  
W. Van Dongen ◽  
...  
Keyword(s):  

2020 ◽  
Vol 11 ◽  
pp. 1264-1271
Author(s):  
Thomas Habets ◽  
Sylvia Speller ◽  
Johannes A A W Elemans

In a liquid-STM setup environment, the redox behavior of manganese porphyrins was studied at various solid–liquid interfaces. In the presence of a solution of Mn(III)Cl porphyrins in 1-phenyloctane, which was placed at a conductive surface, large and constant additional currents relative to a set tunneling current were observed, which varied with the magnitude of the applied bias voltage. These currents occurred regardless of the type of surface (HOPG or Au(111)) or tip material (PtIr, Au or W). The additional currents were ascribed to the occurrence of redox reactions in which chloride is oxidized to chlorine and the Mn(III) center of the porphyrin moiety is reduced to Mn(II). The resulting Mn(II) porphyrin products were identified by UV–vis analysis of the liquid phase. For solutions of Mn(III) porphyrins with non-redox active acetate instead of chloride axial ligands, the currents remained absent.


1996 ◽  
Vol 256 (1) ◽  
pp. 172-186 ◽  
Author(s):  
Daizo Hamada ◽  
Yutaka Kuroda ◽  
Mikio Kataoka ◽  
Saburo Aimoto ◽  
Tetsuro Yoshimura ◽  
...  

2006 ◽  
Vol 12 (1) ◽  
pp. 49-61 ◽  
Author(s):  
Jimmy Heimdal ◽  
Kasper P. Jensen ◽  
Ajitha Devarajan ◽  
Ulf Ryde

Author(s):  
Reena Balhara ◽  
Ritwika Chatterjee ◽  
Garima Jindal

Engineered heme enzymes such as myoglobin and cytochrome P450s metalloproteins are gaining widespread importance due to their efficiency in catalyzing non-natural reactions. In a recent strategy, the naturally occurring Fe...


2004 ◽  
Vol 279 (50) ◽  
pp. 51981-51988 ◽  
Author(s):  
Takeshi Uchida ◽  
Julie M. Stevens ◽  
Oliver Daltrop ◽  
Edgar M. Harvat ◽  
Lin Hong ◽  
...  

The heme chaperone CcmE is a novel protein that binds heme covalently via a histidine residue as part of its essential function in the process of cytochromecbiogenesis in many bacteria as well as plant mitochondria. In the continued absence of a structure of the holoform of CcmE, identification of the heme ligands is an important step in understanding the molecular function of this protein and the role of covalent heme binding to CcmE during the maturation ofc-type cytochromes. In this work, we present spectroscopic data that provide insight into the ligation of the heme iron in the soluble domain of CcmE fromEscherichia coli. Resonance Raman spectra demonstrated that one of the heme axial ligands is a histidine residue and that the other is likely to be Tyr134. In addition, the properties of the heme resonances of the holo-protein as compared with those of a form of CcmE with non-covalently bound heme provide evidence for the modification of one of the heme vinyl side chains by the protein, most likely the 2-vinyl group.


2018 ◽  
Vol 96 (2) ◽  
pp. 110-118 ◽  
Author(s):  
Chen Zhang ◽  
Mathew Sutherland ◽  
Khrystyna Herasymchuk ◽  
Ryan M. Clarke ◽  
John R. Thompson ◽  
...  

A series of octahedral CoIII salen complexes (where salen represents a N2O2 bis-Schiff-base bis-phenolate framework) were prepared with axial imidazole ligating groups. When using 1-methylimidazole (1-MeIm) axial ligands, the CoIII/CoII reduction potential could be altered by 220 mV via variation of the electron-donating ability of the para-ring substituents (R = H (1), OMe (2), tBu (3), Br (4), NO2 (5), and CF3 (6)). In addition, the irreversibility of the reduction process suggested substantial geometrical changes and axial ligand exchange upon reduction to the more labile CoII oxidation state. Installing an imidazole-coumarin conjugate as the axial ligands resulted in fluorescence quenching when bound to the CoIII centre (R = H (7), OMe (8), and CF3 (9)). The redox properties and fluorescence increase upon ligand release for 7–9 were studied under reducing conditions and in the presence of excess competing ligand (1-MeIm). It was determined that the Lewis acidity of the CoIII centre was the dominant factor in controlling axial ligand exchange for this series of complexes.


2018 ◽  
Vol 42 (4) ◽  
pp. 2476-2482 ◽  
Author(s):  
Fanglin Cai ◽  
Wei Su ◽  
Hussein A. Younus ◽  
Kui Zhou ◽  
Cheng Chen ◽  
...  

The role of charged axial ligands in tuning the reactivity and stability of Ru WOCs is well-known, less is explored when axial ligands are neutral molecules.


2013 ◽  
Vol 288 (4) ◽  
pp. 2190-2190 ◽  
Author(s):  
Célia Caillet-Saguy ◽  
Mario Piccioli ◽  
Paola Turano ◽  
Gudrun Lukat-Rodgers ◽  
Nicolas Wolff ◽  
...  

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