1-butyl-2-3-dimethylimidazolium has been researched along with 1-2-4-trichlorobenzene* in 1 studies
1 other study(ies) available for 1-butyl-2-3-dimethylimidazolium and 1-2-4-trichlorobenzene
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First acyclic diene metathesis polymerization under biphasic conditions using a dicationic ruthenium alkylidene: access to high-molecular-weight polymers with very low ruthenium contamination.
The acyclic diene metathesis (ADMET) polymerization of 6-hydroxy-1,10-undecadiene (M1) and 6-acetoxy-1,10-undecadiene (M2) by the action of two different catalysts, i.e., the second-generation Grubbs-Hoveyda system ([RuCl2(IMesH2)(CH-2-(2-PrO-C6H4)]) (1) and the dicationic ruthenium alkylidene [Ru(DMF)3(IMesH2)(CH-2-(2-PrO-C6H4)] (2, IMesH2 = 1,3-dimesitylimidazolin-2-ylidene) is reported. Biphasic conditions using 1-butyl-2,3-dimethylimidazolium tetrafluoroborate ([BDMIM(+)BF4(-)]) and 1,2,4-trichlorobenzene (TCB) are applied. Under the chosen conditions (T = 75 °C, 20 mbar), the use of catalyst 1 results only in the formation of low-molecular-weight polymers (Mn ≤ 10,000 g mol(-1)), while catalyst 2 allows for the high yield synthesis of high-molecular-weight polymers (Mn ≤ 40,000 g mol(-1), yields ≤ 99%). Irrespective of the catalyst used, all polymers display a high trans-content (>95%). Notably, Ru-contamination of the target polymers without any additional purification is as low as 1.2 ppm with catalyst 2. Together with the high yields and high molecular weights, the low Ru-contaminations clearly illustrate the advantages of the biphasic setup. Topics: Borates; Boric Acids; Catalysis; Cations; Chlorobenzenes; Hydrocarbons, Acyclic; Imidazoles; Magnetic Resonance Spectroscopy; Models, Chemical; Molecular Structure; Molecular Weight; Polyenes; Polymerization; Polymers; Ruthenium; Spectrophotometry, Infrared | 2015 |