EPR study of intramolecular dynamics in o-semiquinonic nickel complexes with PCP-pincer ligand in solution

2004 ◽  
pp. 2957 ◽  
Author(s):  
Konstantin A. Kozhanov ◽  
Michael P. Bubnov ◽  
Vladimir K. Cherkasov ◽  
Georgy K. Fukin ◽  
Gleb A. Abakumov
2004 ◽  
Vol 357 (10) ◽  
pp. 3014-3018 ◽  
Author(s):  
Xiawei Zhang ◽  
Thomas J Emge ◽  
Alan S Goldman

2019 ◽  
Vol 33 (6) ◽  
pp. e4932 ◽  
Author(s):  
Zijing Wang ◽  
Xiaoyan Li ◽  
Shangqing Xie ◽  
Tingting Zheng ◽  
Hongjian Sun

2005 ◽  
Vol 24 (19) ◽  
pp. 4553-4557 ◽  
Author(s):  
Marcella Gagliardo ◽  
Preston A. Chase ◽  
Martin Lutz ◽  
Anthony L. Spek ◽  
Frantisek Hartl ◽  
...  
Keyword(s):  

Author(s):  
Christian Reitsamer ◽  
Inge Schlapp-Hackl ◽  
Gabriel Partl ◽  
Walter Schuh ◽  
Holger Kopacka ◽  
...  

After the successful creation of the newly designed PCP carbodiphosphorane (CDP) ligand [Reitsamer et al. (2012). Dalton Trans. 41, 3503–3514; Stallinger et al. (2007). Chem. Commun. pp. 510–512], the treatment of this PCP pincer system with the transition metal iridium and further the analysis of the structures by single-crystal diffraction and by NMR spectroscopy were of major interest. Two different iridium complexes, namely (bis{[(diphenylphosphanyl)methyl]diphenylphosphanylidene}methane-κ3 P,C,P′)carbonylchloridohydridoiridium(III) chloride dichloromethane trisolvate, [IrIII(CO){C(dppm)2-κ3 P,C,P′}ClH]Cl·3CH2Cl2 (1) and the closely related (bis{[(diphenylphosphanyl)methyl]diphenylphosphanylidene}methanide(1+)-κ3 P,C,P′)carbonylchloridohydridoiridium(III) dichloride–hydrochloric acid–water (1/2/5.5), [IrIII(CO){CH(dppm)2-κ3 P,C,P′)ClH]Cl}2 (2), have been designed and both complexes show a slightly distorted octahedral coordinated IrIII centre. The PCP pincer ligand system is arranged in a meridional manner, the CO ligand is located trans to the central PCP carbon and a hydride and chloride are located perpendicular above and below the P2C2 plane. With an Ir—CCDP distance of 2.157 (5) Å, an Ir—CO distance of 1.891 (6) Å and a quite short C—O distance of 1.117 (7) Å, complex 1 presents a strong carbonyl bond. Complex 2, the corresponding CH acid of 1, shows an additionally attached proton at the carbodiphosphorane carbon atom located antiperiplanar to the hydride of the metal centre. In comparison with complex 1, the Ir—CCDP distance of 2.207 (3) Å is lengthened and the Ir—C—O values indicate a weaker trans influence of the central carbodiphosphorane carbon atom.


2008 ◽  
pp. 2849 ◽  
Author(s):  
Konstantin A. Kozhanov ◽  
Michael P. Bubnov ◽  
Vladimir K. Cherkasov ◽  
Nina N. Vavilina ◽  
Larisa Yu. Efremova ◽  
...  

2016 ◽  
Vol 128 (40) ◽  
pp. 12539-12543 ◽  
Author(s):  
Junpeng He ◽  
Nolan W. Waggoner ◽  
Samuel G. Dunning ◽  
Alexander Steiner ◽  
Vincent M. Lynch ◽  
...  

2016 ◽  
Vol 45 (5) ◽  
pp. 1918-1929 ◽  
Author(s):  
Deirdra A. Evers-McGregor ◽  
Mark W. Bezpalko ◽  
Bruce M. Foxman ◽  
Christine M. Thomas

A tridentate ligand framework containing a central N-heterocyclic phosphenium cation (NHP+) has been coordinated to nickel. Among the compounds reported is a series of [(PPP)Ni]20/+/2+ dimers in three different redox states.


2015 ◽  
Vol 44 (27) ◽  
pp. 12082-12085 ◽  
Author(s):  
J. Borau-Garcia ◽  
D. V. Gutsulyak ◽  
R. J. Burford ◽  
W. E. Piers

Nickel(ii) hydroxo compounds supported by an electron rich PCP pincer ligand are active catalysts for the selective hydration of a variety of nitriles at low catalyst loadings and mild conditions.


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