Synthesis, spectroscopic, and magnetic studies of new alkoxy and allied bimetallic derivatives of nickel(II) with aluminium

1984 ◽  
Vol 62 (6) ◽  
pp. 1003-1007 ◽  
Author(s):  
R. C. Mehrotra ◽  
Jagvir Singh

Nickel(II) tetraisopropoxyaluminate undergoes alcoholysis reactions with various alcohols and acetylacetone to yield products with the composition: Ni[Al(OR)4]2 (when ROH = methanol, ethanol, 2,2,2-trifluoroethanol, 2,2,2-trichloroethanol, n-butanol, and 1,3-dichloro-2-propanol); Ni[Al(O-i-Pr)(O-t-Bu)3]2 (with tertiary butyl alcohol); Ni[Al(O-i-Pr)2(O-t-Am)2]2 (with tertiary amyl alcohol); and Ni[Al(O-i-Pr)2(acac)2] (with acetylacetone). On the basis of their visible reflectance and infrared spectra along with molecular weights and magnetic susceptibilities, and octahedral geometry is tentatively suggested for these complexes in the solid state with indications of an equilibrium between tetrahedral and octahedral forms in solution. The alkoxy ligands have also been fitted into the spectrochemical and nephelauxetic series.


1868 ◽  
Vol 16 ◽  
pp. 367-372 ◽  

On the relation between Boiling-point and Chemical Structure . It is from researches published only during last year that we have obtained a more definite knowledge of the chemical structure of some of the hydrocarbons of the above series, so that we are enabled to explain the mode in which the carbon atoms are united. This has been achieved by obtaining these hydrocarbons by synthesis from other compounds, the structure of which is perfectly well known. Thus Friedel and Ladenburg* prepared, by acting upon methylchloracetol, C { CH 3 CH 3 Cl 2 , with zincethyl, the hydrocarbon C 7 H 16 , which they call carbdimethyldiethyl, and which has the structure C {CH 3 CH 3 C 2 H 5 C 2 H 5 . Butlerow replaced in tertiary butyl alcohol the group HO by hydrogen, and obtained an isomer of diethyl to which he gives the name trimethylformen, C { CH 3 CH 3 CH 3 H. In my last communication to the Society I described di-iso-propyl and amylisopropyl, and pointed out their constitution. Further, Erlenmeyer has shown that amyl alcohol and butyl alcohol formed by fermentation have the following structure:







1984 ◽  
Author(s):  
David J. Miller ◽  
David A. Drake ◽  
James M. DeJovine ◽  
George Yogis


2006 ◽  
Vol 312 (1-2) ◽  
pp. 131-136 ◽  
Author(s):  
JingXia Cui ◽  
ChunLei Li ◽  
YingJie Deng ◽  
YongLi Wang ◽  
Wei Wang




2010 ◽  
Vol 260 (1) ◽  
pp. 77-83 ◽  
Author(s):  
E.A. Cohen ◽  
B.J. Drouin ◽  
E.A. Valenzuela ◽  
R.C. Woods ◽  
W. Caminati ◽  
...  


AIChE Journal ◽  
1961 ◽  
Vol 7 (1) ◽  
pp. 172-172
Author(s):  
Frank Maslan


1961 ◽  
Vol 39 (7) ◽  
pp. 1424-1433 ◽  
Author(s):  
K. M. Bell ◽  
C. A. McDowell

The mercury-photosensitized oxidation of isobutane has been studied over a wide range of pressures of the hydrocarbon and oxygen, in a conventional static photochemical apparatus at the temperatures of 30 °C and 100 °C. The main products of the reaction are tertiary butyl hydroperoxide, together with tertiary butyl alcohol, acetone, and corresponding small quantities of formaldehyde and methyl alcohol. Isobutyraldehyde was also detected; ditertiary butyl peroxide being notably absent. Peroxide yields suggest that a reaction between an excited isobutane molecule and oxygen is important in the initiation processes and that peroxide is formed in the reaction[Formula: see text]



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