The Polarizability of Some Deuterated Hydrocarbons

1994 ◽  
Vol 98 (18) ◽  
pp. 4842-4844 ◽  
Author(s):  
D. G. LeGrand ◽  
G. L. Gaines
2010 ◽  
Vol 2 (3) ◽  
pp. 246-254
Author(s):  
L. V. Sineva ◽  
E. A. Kozyukov ◽  
V. S. Ermolaev ◽  
I. G. Solomonik ◽  
A. Yu. Krylova ◽  
...  

2008 ◽  
Vol 53 (7) ◽  
pp. 1545-1556 ◽  
Author(s):  
Hui Zhao ◽  
Patamaporn Unhannanant ◽  
William Hanshaw ◽  
James S. Chickos

1967 ◽  
Vol 45 (13) ◽  
pp. 1511-1518 ◽  
Author(s):  
J. G. Atkinson ◽  
M. O. Luke ◽  
R. S. Stuart

A novel system for the individual preparation of fully deuterated hydrocarbons with 10 to 36 carbon atoms is described. The system permits the use of unsaturated and saturated, cyclic and acyclic starting materials and results in the perdeuterated, saturated equivalent of the starting material. Exchange occurs between hydrocarbon liquid and deuterium gas over carbon-supported, fixed-bed catalysts of Rh, Pt, and Pd at 190–200 °C and results in perdeuterated products of high isotopic and chemical purity. No cracking or structural isomerization occurs under the conditions used, but epimerization of asymmetric carbon atoms does occur. Yields of 35–75% are obtained, the chief losses being due to volatilization and sample withdrawal. The deuterated hydrocarbons prepared by liquid-phase exchange include n-decane-d22, n-dodecane-d26, n-hexadecane-d34, n-octadecane-d38, n-tetracosane-d50, n-octacosane-d58, n-hexatriacontane-d74, pristane-d40, squalane-d62, cyclododecane-d24, 1,2-dicyclohexylethane-d26, and decalin-d18.


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