作者：Dongtao Liu and Dongmei Cui
关键字：aluminium alkyl，copolymerization ，butadiene ， isoprenewas，catalytic activities
论文来源：期刊
具体来源：http://pubs.rsc.org/en/content/articlepdf/2011/dt/c1dt10100e
发表时间：2011年

The N-R-quinolinyl-8-amino ligands HL1–3 (R = 2,6-iPr2C6H3 (HL1), 2,6-Et2C6H3 (HL2), 2,6-Me2C6H3 (HL3)) have been prepared, which reacted readily with one equiv. of rare earth metal tris(alkyl)s to afford the corresponding bis(alkyl) complexes L1Y(CH2SiMe3)2(THF) (1) and L1–3Lu(CH2SiMe3)2(THF) (2–4) viaalkane elimination. Contrastingly, treatment of the in situ generated neodymium tri(alkyl)s with HL1 afforded a mono(alkyl) neodymium complex (5). Complexes 1, 2 and 5 in combination with aluminium alkyls and organoborates established homogenous ternary systems that exhibited versatile catalytic activities and trans-1,4 selectivities for the polymerization ofbutadiene, depending on the types of aluminium alkyl, organoborate and rare earth metalused. Furthermore, the trans-1,4 selective copolymerization of butadiene and isoprenewas achieved by using the ternary system of 1/AlMe3/[Ph3C][B(C6F5)4]. Both the kinetics of copolymerization and the thermal behavior of the copolymers were investigated.