Mono N,C,N-pincer complexes of titanium, vanadium and niobium. Synthesis, structure and catalytic activity in olefin polymerisation

被引:21
作者
Chuchuryukin, Alexey V. [2 ,4 ]
Huang, Rubin [3 ,4 ]
van Faassen, Ernst E.
van Klink, Gerard P. M. [2 ,4 ]
Lutz, Martin [1 ]
Chadwick, John C. [3 ,4 ]
Spek, Anthony L. [1 ]
van Koten, Gerard [2 ]
机构
[1] Univ Utrecht, Fac Sci, Bijvoet Ctr Biomol Res Crystal & Struct Chem, NL-3584 CH Utrecht, Netherlands
[2] Univ Utrecht, Fac Sci, Debye Inst Nanomat Res Organ Chem & Catalysis, NL-3584 CH Utrecht, Netherlands
[3] Eindhoven Univ Technol, Polymer Chem Lab, NL-5600 MB Eindhoven, Netherlands
[4] Dutch Polymer Inst, NL-5600 AX Eindhoven, Netherlands
关键词
ETHYLENE POLYMERIZATION; C-H; CRYSTAL-STRUCTURES; SINGLE-CENTER; POLYETHYLENE; ACTIVATION; LIGAND; REARRANGEMENT; SUPPORTS;
D O I
10.1039/c1dt10482a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Transmetallation of 4,4'-bis{(2,6-bis[(dimethylamino)methyl]phenylgold)diphenyl-phosphino}biphenyl (3) with MCl4 (M = Ti, NbCl, V) in benzene gave the corresponding transition metal pincer complexes (4) and insoluble 4,4'- bis[P-(chloro gold(I))diphenylphosphino]biphenyl (2), which can be quantitatively recovered and recycled. Interestingly, 3 did not react with TiCl3. However, reaction of 2,6-bis[(dimethylamino)methyl]phenyllithium (1) with TiCl3 resulted in formation of the novel diaryltitanium(IV) compound 5 (16% yield), comprising one N,C,N-mer bound NCN-pincer ligand and a second NCN-pincer ligand that is rearranged from a 1,2,6-isomer to a 1,2,4 one. The latter NCN-ligand is dianionic and is bidentate bonded; one of the CH2NMe2 substituents (para to C'(ipso)) is non-coordinated, while the second CH2NMe2 group, after C-H activation of one of the Me groups, is eta(2)-C,N-bonded to the titanium centre trans to C-ipso of the mer-NCN ligand. The new NCN-pincer metal complexes 2,6-bis[(dimethylamino)methyl]phenylTiCl(3) (4a) and 2,6-bis[(dimethylamino)methyl]phenylVCl(2) (4d) gave, after immobilization on MgCl2-based supports, very high activity in ethene polymerisation.
引用
收藏
页码:8887 / 8895
页数:9
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