Vinyl halides properties

In contrast to this, very little is known about the ozonolysis of olefins which bear halogen substituents at the double bond. This is somewhat surprising since compounds containing vinyl halide moieties are important technical products whose properties could be adversely affected by ozone degradation. A case in point is neoprene rubber, whose performance as an elastomer could suffer considerably by ozone attack and concurrent crack formation (1). 

The coupling of vinyl stannanes with vinyl halides is a useful route for making dienes, as, in general, the stereochemistry of the double bonds of the coupling partners is retained. This property of the reaction was exploited in a synthesis of coriolic acid (Scheme 2.59). ... 

On the other hand, the introduction of halide substituents at the C-2 and C-6 position decreases fluorescence quantum yields and gives a bathochromic shift of emission maxima. For example, bromine at the C-2 and C-6 position in compound 14b deteriorates fluorescence quantum yields from 0.95 (14a) to 0.45 and the emission maximum is red-shifted by 42 nm. Moreover, iodine at the C-2,6 position in compound 14d gives the similar bathochromic shift to bromine (14b, 44 nm) and more dramatic reduction in quantum yields (almost nonfluorescent, photophysical properties were interpreted as the heavy atom effect of halides on a BODIPY core skeleton. The bathochromic shift of BODIPY dyes without dramatic decrease in quantum yield was observed by the introduction of vinyl substituents at the C-2 and C-6 position. The extension of conjugation... 

Most of the conformational properties of the acyl derivatives originate in the high polarity of the C=0 bond. Comparative studies have been reported between several chemical functionalities containing the C=0 moiety, i.e., besides heterocyclic aldehydes and ketones, acyl halides, esters, amides, and urethanes, which have different electronic character. Furthermore, the behavior of the C=0 group has been compared, with regard to its conformational properties, to C=C and C=N double bonds in vinyl derivatives, oximes, and azomethines. Most of the results relative to five-membered aromatic heterocycles have been discussed previously (81RCR336 84KGS579). 

ZIEGLER-NATTA POLYMERIZATION. Polymerization of vinyl monomers under mild conditions using aluminum alkyls and TiCL lor other transition element halide) catalyst to give a stereoregulated, or tactic, polymer. These polymers, in which the stereochemistry of the chain is not random have very useful physical properties. 

CdO is used in connection with the stabilization of poly(vinyl chloride). This is discussed below in more detail. It also finds application in modifying the thermal properties of teflon and some rubbers. CdS is used in some smoke detectors, in lasers and in phosphors. The cadmium(II) halides are important as catalysts and are also used in pyrotechnics. Cadmium borates of the general type (Cd0)x(B203), are also used as phosphors. CdS04 is employed in the Weston cell, which is important as a voltage standard.137... 

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