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Isobutylene (or 2-methylpropene) is a hydrocarbon with the chemical formula (CH 3) 2 C=CH 2. It is a four-carbon branched alkene (olefin), one of the four isomers of butylene . It is a colorless flammable gas, and is of considerable industrial value.
The reaction conditions for the synthesis of each type of isobutylene product vary depending on the desired molecular weight and what type(s) of monomer(s) is used. The conditions most commonly used to form low molecular weight (5–10 x 10 4 Da) polyisobutylene are initiation with AlCl 3 , BF 3 , or TiCl 4 at a temperature range of −40 to 10 ...
Living cationic polymerization is a living polymerization technique involving cationic propagating species. [1] [2] It enables the synthesis of very well defined polymers (low molar mass distribution) and of polymers with unusual architecture such as star polymers and block copolymers and living cationic polymerization is therefore as such of commercial and academic interest.
Isobutylene can be produced through a variety of methods. n-butane can be isomerized into isobutane which can be dehydrogenated to isobutylene. [7] In the Halcon process, t-Butyl hydroperoxide derived from isobutane oxygenation is treated with propylene to produce propylene oxide and t-butanol. The t-butanol can be dehydrated to isobutylene.
Hydroboration–oxidation reaction is a two-step hydration reaction that converts an alkene into an alcohol. [1] The process results in the syn addition of a hydrogen and a hydroxyl group where the double bond had been.
The synthesis of TiBA requires two steps; the first step produces diisobutylaluminium hydride (written as a monomer): 4 CH 2 =C(CH 3) 2 + 2 Al + 3 H 2 → 2 HAl(CH 2 CH(CH 3) 2) 2. In the second step isobutylene adds to the diisobutylaluminium to give TiBA: CH 2 =C(CH 3) 2 + HAl(CH 2 CH(CH 3) 2) 2 → Al(CH 2 CH(CH 3) 2) 3
The history of polyisobuteneamine dates back to the early development and study of polyisobutylene. The first synthesis of polyisobutylene was reported in 1931 by the German chemists Hermann Staudinger and Leonidas Zechmeister, who obtained the polymer through the cationic polymerization of isobutylene. [1]
In the context of butanol fuel, isobutyraldehyde is of interest as a precursor to isobutanol. E. coli as well as several other organisms has been genetically modified to produce isobutanol. α-Ketoisovalerate, derived from oxidative deamination of valine, is prone to decarboxylation to give isobutyraldehyde, which is susceptible to reduction to the alcohol: [3]