Diene Polymers: Natural and Synthetic Rubbers
Natural rubber is formed from the isoprene monomer and has Z stereochemistry. The E polymer gutta-percha also occurs naturally, but is more brittle than rubber. Uses of this thermoplastic include dentistry, electrical insulators and the covering on golf balls.
Before 1839, the uses of natural rubber were somewhat limited. It became sticky in summer, hardened and cracked in winter, and was susceptible to attack by a variety of solvents. Charles Goodyear became interested in rubber in 1831, and bought the Eagle India Rubber Company of Woburn, Massachusetts, in 1838. In January of 1839, Goodyear accidentally placed a sample of rubber that had been mixed with sulfur and lead(II) oxide on a hot stove; the result was a product similar to charred leather, which did not melt below 138°C. Goodyear was granted a U.S. patent for his process (called vulcanization) in June of 1844. The story of vulcanization is an example of how major scientific and technological advances are often brought about as a result of an accidental discovery.
Notice that in the vulcanization process, the sulfur bridges are attached to allylic carbon atoms which connect the long Z polymer chains of rubber.
Vulcanized rubber
The amount of sulfur used in the vulcanization process will depend on the rigidity required in the product. For example, about 5% sulfur is used when producing rubber for rubber bands; about 30% sulfur is used when making rubber for use in battery casings. There are several characteristics of dienes and rubbers that you should recognize. First, be aware of the similarity between the polymerization of a diene and the 1,4-addition reactions of dienes. Second, recognize the similarity between a vulcanized rubber and a peptide containing cysteine cross-links. Third, be aware that as natural rubber contains double bonds, it will display some of the properties of simple alkenes.
The 1,4 polymerization of 1,3-butadiene shown in the reading produces the trans form of polybutadiene. However, it should be noted that the cis form shown here can also be formed.
cis- polbutadiene
