Kinetics and mechanism of the reactions on di-.mu.-carbonyl-bis(cyclopentadienyl)dinickel(0) with monodentate ligands

1971 ◽  
Vol 10 (2) ◽  
pp. 232-239 ◽  
Author(s):  
Paul C. Ellgen
1988 ◽  
Vol 13 (5) ◽  
pp. 336-339 ◽  
Author(s):  
Andreas Roodt ◽  
Johann G. Leipoldt ◽  
Stephen S. Basson ◽  
Izak M. Potgieter

10.1002/kin.7 ◽  
1996 ◽  
Vol 28 (9) ◽  
pp. 687-691 ◽  
Author(s):  
M. Calzadilla ◽  
A. Malpica ◽  
P. M. Diaz

1973 ◽  
Vol 70 ◽  
pp. 918-922 ◽  
Author(s):  
R. K. Srivastava ◽  
V. K. Srivastava ◽  
M. N. Srivastava ◽  
B. B. L. Saxena

2016 ◽  
Vol 2 (4) ◽  
pp. 39-45 ◽  
Author(s):  
J.D Chaplanova ◽  
S.N. Larykava ◽  
V.E Agabekov ◽  
I.N. Kukhta

2012 ◽  
Vol 3 (2) ◽  
pp. 131-133
Author(s):  
ANNAPURNA NOWDURI ◽  
◽  
Apparao Babu Duggada ◽  
Vijaya Raju Kurimella

2016 ◽  
Vol 10 (3) ◽  
pp. 259-270
Author(s):  
Ludmila Matienko ◽  
◽  
Larisa Mosolova ◽  
Vladimir Binyukov ◽  
Gennady Zaikov ◽  
...  

Mechanism of catalysis with binary and triple catalytic systems based on redox inactive metal (lithium) compound {LiSt+L2} and {LiSt+L2+PhOH} (L2=DMF or HMPA), in the selective ethylbenzene oxidation by dioxygen into -phenylethyl hydroperoxide is researched. The results are compared with catalysis by nickel-lithium triple system {NiII(acac)2+LiSt+PhOH} in selective ethylbenzene oxidation to PEH. The role of H-bonding in mechanism of catalysis is discussed. The possibility of the stable supramolecular nanostructures formation on the basis of triple systems, {LiSt+L2+PhOH}, due to intermolecular H-bonds, is researched with the AFM method.


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