scholarly journals Thermodynamics of Vinyl Ethers. XXXII. Thermodynamic Stability of Tri-alkoxy Substituted Derivatives of Ethylene.

1985 ◽  
Vol 39b ◽  
pp. 877-878 ◽  
Author(s):  
Esko Taskinen ◽  
Bertil Samuelsson ◽  
Eirik Stensvik ◽  
J. Chattopadhyaya
1994 ◽  
Vol 15 (3) ◽  
pp. 339-380 ◽  
Author(s):  
Nina A. Nedolya ◽  
Boris A. Trofimov
Keyword(s):  

1981 ◽  
Vol 59 (10) ◽  
pp. 1425-1432 ◽  
Author(s):  
Anu Mishra

Vinyl ethers, 1-olefins, and styrene were homo- and copolymerized by the use of catalyst derived from a mixture of lithium tetraalkylaluminate (LiAlR4), aluminum chloride (AlCl3), and titanium tetrachloride (TiCl4), in order to determine the nature of the active components present.It is postulated that the active catalyst in the stereospecific polymerization of vinyl ethers is ether-coordinated TiCl3•LiCl, while in the polymerization of 1-olefins and styrene, it is the alkylated derivatives of TiCl3•LiCl.For homo- and copolymerization of styrene, AlR3 seems to be the preferred alkylating agent. About 3 to 4 equivalents of AlR3 are needed for complete alkylation of TiCl3•LiCl, probably due to heterogeneity of the system.Highly isotactic polystyrene and copolymers of styrene with 1-olefins can be prepared in good yields by the use of this catalyst.


1991 ◽  
Vol 4 (12) ◽  
pp. 714-720 ◽  
Author(s):  
Lynne H. Reed ◽  
Keerthi Jayasuria ◽  
Sunil K. Koovakkat ◽  
Leland C. Allen

1981 ◽  
Vol 46 (6) ◽  
pp. 1495-1503 ◽  
Author(s):  
Jiří Svoboda ◽  
Oldřich Paleta ◽  
Václav Dědek

The vinylic nucleophilic substitution of methyl trifluoropropenoate (I) with potassium cyanide affords methyl 2,3-difluoro-3-cyanopropenoate (II) in the form of a mixture of cis- and trans-isomers in 95 : 5 ratio. Simultaneously the dimerization of propenoate I to dimethyl perfluoro-4-methyl-2-pentenedioate (III) also takes place to a lesser extent. On acid catalysed methanolysis of compound II dimethyl 2,3-difluoro-2-butenedioate (VI) is formed with the same content of configurational isomers. Diester VI with a relative cis : trans ratio of 35 : 65 was obtained on dehalogenation of dimethyl 2,3-dichloro-2,3-difluorobutanedioate (V), which was prepared by addition of chlorine to the cyano derivative II and subsequent acid catalyzed methanolysis. When reacting them with potassium fluoride in dimethyl sulfoxide compounds II and VIunderwent anionic cis-trans isomerization reaction. In the 0-80 °C interval the cis isomers prevail in the equilibrium mixture, and the conversion cis → trans is endothermic: in the 40-80 °C interval for IIa → IIb ΔH = 12.8 kJ mol-1, for VIa → VIb ΔH = 38.6 kJ mol-1. The influence of the cis-effect of the fluorine atoms on the thermodynamic stability of the configurational isomers of compounds II and VI is discussed.


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