A Stable (Amino)(phosphino)carbene as Bidentate Ligand for Palladium and Nickel Complexes: Synthesis, Structure, and Catalytic Activity.

ChemInform ◽  
2006 ◽  
Vol 37 (29) ◽  
Author(s):  
Emmanuelle Teuma ◽  
Celine Lyon-Saunier ◽  
Heinz Gornitzka ◽  
Gerard Mignani ◽  
Antoine Baceiredo ◽  
...  
2005 ◽  
Vol 690 (24-25) ◽  
pp. 5541-5545 ◽  
Author(s):  
Emmanuelle Teuma ◽  
Céline Lyon-Saunier ◽  
Heinz Gornitzka ◽  
Gérard Mignani ◽  
Antoine Baceiredo ◽  
...  

2013 ◽  
Vol 729 ◽  
pp. 40-45 ◽  
Author(s):  
Haibin Song ◽  
Dongna Fan ◽  
Yuqiao Liu ◽  
Guohua Hou ◽  
Guofu Zi

2014 ◽  
Vol 10 (2) ◽  
pp. 2234-2245
Author(s):  
Safaa N. Abdou ◽  
Abeer A. Faheim ◽  
Abdel-Nasser M. A. Alaghaz

Complexes of cobalt(II), nickel(II), copper(II), zinc(II) and Hafnium(II) of general composition [M(L)2(Cl)2] have been synthesized [L = 4-(phenylphosphinylideneamino-N-thiazolylbenzenesulfonamide]. The elemental analysis, molar conductance measurements, magnetic susceptibility measurements, mass, IR, UV, NMR, SEM, EDX, thermal and EPR spectral studies of the compounds led to the conclusion that the ligand acts as a bidentate manner. The molar conductance of the complexes in fresh solution of DMSO lies in the range of 7.46–9.13 Ω-1 cm2mol‒1 indicating their non-electrolytic behavior. On the basis of analytical and spectroscopic techniques, octahedral geometry of the complexes was proposed. The ligand acts as bidentate ligand, coordinated through sulfonamide oxygen and thiazole nitrogen atoms. The ligand field parameters were calculated for Co(II), Ni(II) and Cu(II) complexes and their values were found in the range reported for a octahedral structure. The catalytic activities of the divalent metal complexes have been studied in the oxidation of cyclohexane, using environmental friendly oxidant, hydrogen peroxide. Complex with rough surface has shown higher catalytic activity compared to the other complexes. The molecular parameters of the ligand and its Co(II) and Hf(II) complexes have been calculated. 


2008 ◽  
Vol 62 (3) ◽  
Author(s):  
Iwona Rykowska ◽  
Włodzimierz Urbaniak

AbstractTransition metal complexes bonded to silica via silanes with β-diketonate groups can be used as packings for complexation gas chromatography or as immobilized homogenous metal complex catalysts. On basis of elemental analysis and the determination of surface area, possible structures of the complexes formed on the silica surface have been proposed. The possibility of using the immobilized complexes as catalysts has been indicated. Especially nickel complexes were taken into consideration. These immobilized complexes were used previously as packings for complexation gas chromatography.


1995 ◽  
Vol 73 (7) ◽  
pp. 1175-1180 ◽  
Author(s):  
Michael D. Fryzuk ◽  
Xiaoliang Gao ◽  
Steven J. Rettig

The preparation of a mixed donor ligand consisting of an enolate and neutral phosphine is described and its coordination chemistry with nickel reported. The phosphino ketones R2PCH2COPh (R = Cy or Pri) are prepared by the reaction of the corresponding secondary phosphines with bromoacetophenone to form the corresponding phosphonium salts [R2P(H)CH2COPh]+Br− (R = Cy or Pri); subsequent deprotonation leads to the neutral ketones. The enolates are formed by addition of NaN(SiMe3)2 to the neutral ketone. The crystal structure of the sodium enolate having isopropyl substituents at phosphorus displays a tetrameric structure in the solid state and there is an interaction of the phosphorus donor with the sodium anion: Na—P, 2.852(2) Å. The preparation of a series of nickel complexes was achieved by addition of the sodium enolate to the appropriate Ni(II) starting material. The structures of the nickel derivatives are reported. The catalytic behaviour of one of these complexes in the polymerization and oligomerization of ethylene is briefly described. Crystals of {Na[Pri2PC(H)=C(O)Ph]}4, 2b, are tetragonal, a = b = 20.790(2) Å, c = 13.539(7) Å, Z = 4, space group I41/a1; those of [Cy2PC(H)=C(O)Ph](PPh3)NiPh, 3a, are triclinic, a = 10.742(2) Å, b = 19.811(3) Å, c = 10.621(2) Å, α = 101.88(1)°, β = 119.24(1)°, γ = 91.08(1)°, Z = 2, space group [Formula: see text] and those of [Pri2PC(H)=C(O)Ph](PPh3)NiPh, 3b, are triclinic, a = 10.219(1) Å, b = 17.432(3) Å, c = 9.788(1) Å, α = 101.18(1)°, β = 100.19(1)°, γ = 85.32(1)°, Z = 2, space group [Formula: see text] The structures were solved by direct (2b) and Patterson (3a and 3b) methods and were refined by full-matrix least-squares procedures to R = 0.045, 0.044, and 0.032 (Rw = 0.038, 0.041, and 0.030) for 965, 4483, and 5085 reflections with I > 3σ(I) respectively. Keywords: nickel, sodium enolate, homogeneous catalyst, oligomerization.


2016 ◽  
Vol 32 (5) ◽  
pp. 2509-2516
Author(s):  
R. Suresh ◽  
M. Deepa ◽  
P. Moganavally ◽  
P. Sudha

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