Chain transfer constants in the radical telomerization of vinyl chloride, propylene, and ethylene with carbon tetrachloride and chloroform; sensitivity of substitution reactions with cleavage of C-H and C-C1 bonds to polar effects

Author(s):  
B. A. �nglin ◽  
T. A. Onishchenko
Author(s):  
T. T. Vasil'eva ◽  
V. A. Kochetkova ◽  
B. V. Nelyubin ◽  
B. I. Dostovalova ◽  
R. Kh. Freidlina

1964 ◽  
Vol 42 (10) ◽  
pp. 2262-2274 ◽  
Author(s):  
Pierre C. Roberge ◽  
Jan A. Herman

The photolysis of vinyl iodide in carbon tetrachloride solutions gives several products among which the most important are: acetylene, hydrogen iodide, iodine, ethylene, and vinyl chloride. A mechanism based on diffusion-controlled disproportionation of geminate radicals, as first proposed by Hamill, agrees well with the observed phenomena. To explain the diminishing production of ethylene and iodine with increasing concentration of the monomer, it is necessary to postulate a telomerization of the vinyl iodide.


1983 ◽  
Vol 16 (5) ◽  
pp. 790-807 ◽  
Author(s):  
W. H. Starnes ◽  
Frederic C. Schilling ◽  
I. M. Plitz ◽  
Rudolf E. Cais ◽  
D. J. Freed ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (9) ◽  
pp. 7495-7503 ◽  
Author(s):  
Carlos M. R. Abreu ◽  
Pedro Maximiano ◽  
Tamaz Guliashvili ◽  
Julien Nicolas ◽  
Arménio C. Serra ◽  
...  

Cyclopentyl methyl ether (CPME) was successfully used as an environmentally friendly alternative to regularly employed organic solvents (e.g., THF, DMSO, DCM and DMF) for the RAFT and NMP polymerizations of vinyl chloride (VC) and styrene (S).


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