Studies in polymerization. XIII. The activated initiation of vinyl polymerization by metal carbonyls

It has been found that the hexaearbonyls of group VI metals in the presence of some organic halogen compounds are active initiators of vinyl polymerization. Molybdenum hexacarbonyl is the most active, and halogen compounds containing —CC1 3 , —CBr 3 are generally more effective than those with fewer halogen atoms joined to a single carbon. Fluorine and iodine compounds are inactive. A study has been made of the initiation of the polymerization of methyl methacrylate by the Cr(CO) 6 + CCl 4 system. The polymerization is markedly retarded by carbon monoxide. It is shown that the reaction proceeds through free-radical intermediates, and a kinetic mechanism for initiation is derived (equation (4)) leading to the expression (5) for the rate of chain starting. This quantity may be calculated from (5) with the aid of the numerical values in table 3. Kinetic observations are in satisfactory agreement with this mechanism. The nature of the participating reactions is discussed.

1962 ◽  
Vol 17 (12) ◽  
pp. 804-806 ◽  
Author(s):  
C. H. Bamford ◽  
C. A. Finch

The relative efficiencies of 26 organic halogen compounds when used with the carbonyls of Cr. Mo, W, Mn, Fe and Ni for initiating the free-radical polymerization of methyl methacrylate are assessed; many active systems are found. Previous observations suggesting that the presence of the — C(hal)3 group is especially favourable are confirmed, although fluorine and iodine derivatives show no special activity. Outstandingly effective halides for initiating with the carbonyls of the Group VI metals are CCl3CONH2, CCl3COOH, CCl3CN and those incorporating aromatic rings, with the exception of 3 — F·C6H4·CCl3 with Cr(CO)6.


2019 ◽  
Author(s):  
Marharyta V. Laktsevich-Iskryk ◽  
Nastassia A. Varabyeva ◽  
Volha V. Kazlova ◽  
Vladimir N. Zhabinskii ◽  
Vladimir A. Khripach ◽  
...  

In this article, we report a photocatalytic protocol for the isomerization of 1,2-disubstituted cyclopropanols to linear ketones. The reaction proceeds <i>via</i> radical intermediates and tolerates various functional groups.


2019 ◽  
Author(s):  
Marharyta V. Laktsevich-Iskryk ◽  
Nastassia A. Varabyeva ◽  
Volha V. Kazlova ◽  
Vladimir N. Zhabinskii ◽  
Vladimir A. Khripach ◽  
...  

In this article, we report a photocatalytic protocol for the isomerization of 1,2-disubstituted cyclopropanols to linear ketones. The reaction proceeds <i>via</i> radical intermediates and tolerates various functional groups.


2018 ◽  
Author(s):  
Patrick Moon ◽  
Zhongyu Wie ◽  
Rylan Lundgren

The stability and wide availability of carboxylic acids make them valuable reagents in chemical synthesis. Most transition metal catalyzed processes using carboxylic acid substrates are initiated by a decarboxylation event that generates reactive carbanion or radical intermediates. Developing enantioselective methodologies relying on these principles can be challenging, as highly reactive species tend to react indiscriminately without selectivity. Furthermore, anionic or radical intermediates generated from decarboxylation can be incompatible with protic and electrophilic functionality, or groups that undergo trapping with radicals. We demonstrate that metal-catalyzed enantioselective benzylation reactions of allylic electrophiles can occur directly from aryl acetic acids. The reaction proceeds via a pathway in which decarboxylation is the terminal event, occurring after stereoselective carbon–carbon bond formation. The mechanistic features of the process enable enantioselective benzylation without the generation of a highly basic nucleophile. Thus, the process has broad functional group compatibility that would not be possible employing established protocols.<br>


1979 ◽  
Vol 10 (17) ◽  
Author(s):  
S. C. TRIPATHI ◽  
S. C. SRIVASTAVA ◽  
D. P. PANDEY ◽  
R. P. CHATURVEDI

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