Bis(phenolate)amine-supported lanthanide borohydride complexes for styrene and trans-1,4-isoprene (co-)polymerisations

被引:26
作者
Bonnet, Fanny [1 ]
Dyer, Hellen E. [2 ]
El Kinani, Yassine [1 ]
Dietz, Carin [3 ]
Roussel, Pascal [1 ]
Bria, Marc [4 ]
Visseaux, Marc [1 ]
Zinck, Philippe [1 ]
Mountford, Philip [2 ]
机构
[1] Univ Lille 1, CNRS, Unite Catalyse & Chim Solide, Sci & Technol, F-59655 Villeneuve Dascq, France
[2] Univ Oxford, Chem Res Lab, Oxford OX1 3TA, England
[3] Eindhoven Univ Technol, Dept Chem Engn & Chem, Lab Polymer Chem, NL-5600 MB Eindhoven, Netherlands
[4] Univ Lille 1, Ctr Commun Mesure RMN, Sci & Technol, F-59655 Villeneuve Dascq, France
关键词
OLEFIN POLYMERIZATION CATALYSTS; CHAIN TRANSFER POLYMERIZATION; RING-OPENING POLYMERIZATION; RARE-EARTH BOROHYDRIDES; STEREOSPECIFIC POLYMERIZATION; ISOPRENE POLYMERIZATION; GRIGNARD-REAGENTS; ALKYL COMPLEXES; METAL-CATALYSTS; LIGANDS;
D O I
10.1039/c5dt00252d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
New bis(phenolate) amine-supported neodymium borohydride complexes and their previously reported samarium analogues were tested as catalysts for the polymerisation of styrene and isoprene. Reaction of Na2O2NL (L = py, OMe, NMe2) with Nd(BH4)(3)(THF)(3) afforded the borohydride complexes Nd(O2NL)(BH4)(THF) (L = py (1-Nd), OMe (2-Nd), NMe2 (3-Nd)). Complex 1-Nd has shown a propensity to form phenolate-O-bridged dimer [Nd(mu-O2Npy)(BH4)](2) (1'-Nd) as previously observed with the samarium analogues Sm(O2NL)(BH4)(THF) (L = py or Pr). X-ray structures of 1'-Nd and 2-Nd were determined and are presented. The neodymium borohydride complexes 1-Nd to 3-Nd and their samarium analogues Sm((ONL)-N-2) (BH4)(THF)(x) (L = py (1-Sm), OMe (2-Sm), NMe2 (3-Sm), Pr (4-Sm)) were tested as catalysts for the polymerisation of isoprene and styrene in the presence of n-butylethylmagnesium (Mg(Bu-n)(Et)). All complexes were found to be active for the polymerisation of isoprene in these conditions, leading to polyisoprene up to 95.1% trans-1,4 stereoregular. They were also found to be active for the polymerisation of styrene leading to atactic polystyrene in all cases. Interestingly, samarium-based complexes were found to be more active than the neodymium ones toward this latter monomer, in sharp contrast to what is usually observed with rare earth borohydride complexes. The structure of both trans-polyisoprenes and poly-styrenes obtained were studied in detail by MALDI-ToF analysis in order to better understand the polymerisation mechanisms. The coordinative chain transfer polymerisation (CCTP) of both monomers was further conducted using Mg(nBu)(Et) as transfer agent. Finally, the statistical copolymerisation of isoprene and styrene was examined using these catalytic systems, leading to the formation of poly[(trans-1,4-isoprene)-co-styrene] with up to 39% of styrene moieties inserted in a highly trans-1,4-stereoregular polyisoprene.
引用
收藏
页码:12312 / 12325
页数:14
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