Polyisoprene

 ( Organic Polymers ) 

Polyisoprene is, strictly speaking, a collective name for that are produced by polymerization of isoprene. In practice polyisoprene is commonly used to refer to synthetic cis-1,4-polyisoprene, made by the industrial polymerisation of isoprene. Natural forms of polyisoprene are also used in substantial quantities, the most important being "natural rubber" (99.99% cis-1,4-polyisoprene), which is derived from the sap of trees. Both synthetic polyisoprene and natural rubber are highly elastic and consequently used to make tires and a variety of other applications.

The trans isomer, which is much harder than the cis isomer, has also seen significant use in the past. It too has been synthesised and extracted from plant sap, the latter resin being known as gutta-percha. These were widely used as an electrical insulator and as components of . Annual worldwide production of synthetic polyisoprene was 13 million tons in 2007Sebastian Koltzenburg, Michael Maskos, Oskar Nuyken, Polymere: Synthese, Eigenschaften und Anwendungen, Springer, Berlin, 2012, p. 424. and 16 million tons in 2020.

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Synthesis In principle, the polymerization of isoprene can result in four different . The relative amount of each isomer in the polymer is dependent on the mechanism of the polymerization reaction.

Anionic chain polymerization, which is initiated by n-Butyllithium, produces cis-1,4-polyisoprene dominant polyisoprene. 90–92% of repeating units are cis-1,4-, 2–3% trans-1,4- and 6–7% 3,4-units.Jürgen Falbe, Manfred Regitz (Hrsg.): CD Römpp Chemie Lexikon, Thieme, Stuttgart, 1995.

Coordinative chain polymerization: With Ziegler–Natta catalyst TiCl₄/Al( i-C₄H₉)₃, a more pure cis-1,4-polyisoprene similar to natural rubber is formed. With Ziegler–Natta catalyst VCl₃/Al( i-C₄H₉)₃, trans-dominant polyisoprene is formed.Bernd Tieke, Makromolekulare Chemie, 3. Auflage, Wiley-VCH, Weinheim, 2014, S. 149.

1,2 and 3,4 dominant polyisoprene is produced MoO₂Cl₂ catalyst supported by phosphorus ligand and Al(OPhCH₃)( i-Bu)₂ co-catalyst.

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History The first reported commercialisation of a stereoregular poly-1,4-isoprene with > 90% cis (90% to 92%) was in 1960 by the Shell Chemicals. Shell used an alkyl lithium catalyst. 90% cis-1,4 content proved insufficiently crystalline to be useful.

In 1962, Goodyear succeeded in making a 98.5% cis polymer using a Ziegler-Natta catalyst, and this went on to commercial success.

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Usage Natural rubber and synthetic polyisoprene are used primarily for tires. Other applications include latex products, footwear, belting, hoses, and .

Natural gutta-percha and synthetic trans-1,4-polyisoprene were used for .

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See also

• Synthetic rubber

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