Comparative Calculations of LCAO‐MOs of the Allyl Radical

1957 ◽  
Vol 26 (1) ◽  
pp. 151-156 ◽  
Author(s):  
Jiro Higuchi
Keyword(s):  
1979 ◽  
Vol 44 (7) ◽  
pp. 2009-2014 ◽  
Author(s):  
Jana Nováková ◽  
Zdeněk Dolejšek

Products of (a) allyl radical interaction with unheated Co3O4, (b) thermally activated 1,5-hexadiene or thermally activated allyl bromide with unheated Co3O4, (c) moderately heated Co3O4 with unheated 1,5-hexadiene or allyl bromide were studied under Knudsen flow conditions. Cobalt suboxide Co3O4, a typical catalyst of deep oxidations yielded acrolein in reaction with allyl radicals as early as at the room temperature of the catalyst. A similar acrolein formation was also observed in the allyl radical interaction with other oxides exhibiting different catalytic properties. It appears that acrolein is in general the primary product of the allyl radical interaction with the oxides. The results are discussed and compared with previous data obtained with MoO3.


1988 ◽  
Vol 31 (6) ◽  
pp. 478-484
Author(s):  
Daisuke NOHARA ◽  
Tomoya SAKAI
Keyword(s):  

2008 ◽  
Vol 112 (39) ◽  
pp. 9366-9373 ◽  
Author(s):  
Talitha M. Selby ◽  
Giovanni Meloni ◽  
Fabien Goulay ◽  
Stephen R. Leone ◽  
Askar Fahr ◽  
...  

1978 ◽  
Vol 16 (3) ◽  
pp. 467-484 ◽  
Author(s):  
V. M. Patel ◽  
G. N. Patel ◽  
N. Gvozdic ◽  
C. S. Hsu ◽  
Malcolm Dole

2002 ◽  
Vol 116 (15) ◽  
pp. 6505-6512 ◽  
Author(s):  
Jia-xiang Han ◽  
Yu. G. Utkin ◽  
Hong-bing Chen ◽  
Neil T. Hunt ◽  
R. F. Curl

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