906666-43-1Relevant articles and documents
Imido titanium ethylene polymerization catalysts containing triazacyclic ligands
Adams, Nico,Arts, Henricus J.,Bolton, Paul D.,Cowell, Dan,Dubberley, Stuart R.,Friederichs,Grant, Craig M.,Kranenburg, Mirko,Sealey, Andrew J.,Wang, Bing,Wilson, Paul J.,Zuideveld, Martin,Blake, Alexander J.,Schroeder, Martin,Mountford, Philip
, p. 3888 - 3903 (2008/10/09)
A comprehensive account of the synthesis, properties, and evaluation of a wide range of ethylene homopolymerization catalysts derived from imido titanium compounds supported by the triazacyclic ligands Me3[9]aneN 3 and R3[6]aneN3 is described (Me 3[9]aneN2 -1,4,7-trimethyltriazacyclononane; R 3[6]aneN3 = 1,3,5-trimethyl- or 1,3,5-tris(n-dodecyl) triazacyclohexane). Conventional preparative-scale reactions afforded the triazacycle-supported imido titanium compounds Ti(NR)(Me3[9]aneN 3)Cl2 (R = tBu (1), 2,6-C6H 3Me2, 2,6-C6H3iPr 2, Ph, C6F5, or CH2Ph (6)). Solid phase-supported analogues of 1 and 6 (linked by either the macrocycle or imido ligand to a 1% cross-linked polystyrene support) and representative Me 3[6]aneN3 solution phase systems Ti(NR)(R 3[6]aneN3)Cl2 (R = Me or n-dodecyl) were also synthesized. At ambient temperature, solution phase Me3[9]aneN 3 catalyst systems were more active for ethylene polymerization (methyl aluminoxane (MAO) cocatalyst) than their solid phase-supported or Me3[6]aneN3 analogues. A library of 41 other triazacyclononane-supported catalysts was prepared by the semiautomated, sequential treatment of Ti(NMe2)2Cl2 with RNH2 and Me3[9]aneN3. The ethylene polymerization capabilities of 46 compounds of the type Ti(NR)(Me 3[9]aneN3)Cl2 were evaluated at 100°C (MAO cocatalyst) and compared in representative cases to the corresponding productivities at ambient temperature. Whereas either bulky N-alkyl or N-aryl imido substituents in the compounds Ti(NR)(Me3[9]aneN 3)Cl2 were sufficient to give highly active catalysts at ambient temperature, only those with bulky N-alkyl groups excelled at 100°C. Polymer end group analysis indicated that polymeryl chain transfer to both AlMe3 and ethylene monomer is an active mechanism in these systems. The use of MAO pretreated with BHT-H (BHT-H = 2,6-di-tert-butyl-4-methylphenol) led to higher productivites, increased polymer molecular weights, and more polymer chain unsaturations, but productivity decreased when a large excess of BHT-H was used. The reactions of the well-defined alkyl species Ti(N tBu)(Me3[9]aneN3)Me2, [Ti(N tBu)(Me3[9]aneN3)-Cu-Me)2AlMe 2]+, and [Ti(NtBu)(Me3[9]aneN 3)Me]+ with BHT-H were examined, and the aryloxide compound [Ti(NtBu)(Me3[9]aneN3)(BHT)][BAr 4F] was isolated (ArF = C6F 5). The X-ray structures of Ti(NR)(Me3[9]aneN 3)Cl2 (R = tBu, 2,6-C6H 3Me2, 2,6-C6H3Pr2, Ph, C6F5) and Ti(NR)(Me3[6]aneN3)Cl 2 (R = 2,6-C6H3iPr2, Ph, C6F5) are reported. The perfluorophenyl imido titanium compounds both exhibit well-defined supramolecular structures based on C...F intermolecular interactions.
