Nickel atom – ligand reactions: evidence for an unstable η3-benzylnickel species from mixed-ligand cocondensations with nickel atoms

1982 ◽  
Vol 60 (21) ◽  
pp. 2654-2660 ◽  
Author(s):  
J. Stephen Hartman ◽  
Eric C. Kelusky

Detailed studies of nickel atom – benzyl halide cocondensation reactions, with and without a second organic ligand, have been carried out. Benzyl halides (X = Cl, Br) when cocondensed with nickel atoms at −196 °C give no isolable organonickel product but only bibenzyl and nickel(II) halide, indicative of an initial unstable benzylnickel compound. Allyl chloride/benzyl chloride mixtures do not give the stable η3-allylnickel chloride, but instead a highly-unstable sublimable yellow solid which apparently is the η3-benzylnickel chloride dimer. All of this work indicates complexities in the initial metal atom interactions with the ligands. A further case is reported in which the presence of aluminosilicate insulating wool drastically changes the products obtained.

2014 ◽  
Vol 50 (86) ◽  
pp. 13026-13029 ◽  
Author(s):  
Fareed Bhasha Sayyed ◽  
Shigeyoshi Sakaki

MgCl2 accelerates the CO2 insertion as a non-innocent additive and the one-electron reduction process as one reagent in the Ni-catalyzed carboxylation of benzyl chloride with CO2.


1972 ◽  
Vol 50 (16) ◽  
pp. 2557-2560 ◽  
Author(s):  
G. Marcotrigiano ◽  
R. Battistuzzi ◽  
G. C. Pellacani

The bis(β-ketoenolates)nickel(II) adducts of piperidine, piperazine, methylpiperazine, and morpholine are isolated in the solid state and investigated by magnetic measurements and electronic and i.r. spectra. Magnetic measurements and electronic spectra give evidence of trans-octahedral configuration while i.r. spectra show that the amines are coordinated to the nickel atom towards the nitrogen atom. The new band found in the range 385–300 cm−1 for all complexes can be assigned to Ni—N vibration. In the Ni(DBM)2•4B (B = methylpiperazine and morpholine) the two additional bases are not coordinated to the metal atom.


RSC Advances ◽  
2018 ◽  
Vol 8 (61) ◽  
pp. 35056-35061 ◽  
Author(s):  
Masato Ohsumi ◽  
Akitaka Ito ◽  
Nagatoshi Nishiwaki

Two reaction conditions were developed to accomplish the substrate switchable (benzyl esters vs. benzyl halides) Suzuki–Miyaura coupling.


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