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Dimerization and polymerization of butadiene with zero-valent nickel and protonic acids
Authors:Junji Furukawa  Jitsuo Kiji  Hisatoshi Konishi  Kazuyoshi Yamamoto  Shin-Ichi Mitani  Susumu Yoshikawa
Abstract:The behavior of hydridonickel coordination compounds as catalysts for the oligomerization and polymerization of butadiene in various solvents was studied. In the presence of alcohol bis(tricyclohexylphosphine)chlorohydridonickel ( 4 , X = Cl) (HNiClP(C6H11)3]2) catalyzes the linear dimerization. With hydridotetrakis(phosphite)nickel(1+) ( 2 ) (HNi{P(OR)3}4]+), which is prepared from tetrakis(phosphite)nickel ( 1 ) (NiP(OR)3]4) and trifluoroacetic acid, dimerization occurs in sec-alcohol but there is no reaction in tert-alcohol. The main product is 2-methylenevinylcyclopentane ( 8 ). The other products are 4-vinylcyclohexene ( 10 ), 1,5-cyclooctadiene ( 5 ), 1,3,7-octatriene ( 7 ) and 1,3,6-octatriene ( 9 ). The hydridonickel coordination compound, prepared with inorganic acids, does not afford the dimers but the 1,4-trans polymer.
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