A remarkable inversion of structure-activity dependence on imido N-substituents with varying co-ligand topology and the synthesis of a new borate-free zwitterionic polymerisation catalyst

Chem Commun (Camb). 2006 Jan 28:(4):436-8. doi: 10.1039/b514467a.

Abstract

Ethylene polymerisation productivities of tris(pyrazolyl)methane-supported catalysts [Ti(NR){HC(Me2pz)3}Cl2] show a dramatically different dependence on the imido R-group compared to those of their TACN analogues, attributed to differences in fac-N3 donor topology; when treated with AliBu3, the zwitterionic tris(pyrazolyl)methide compound [Ti(N-2-C6H4tBu){C(Me2pz)3}Cl(THF)] also acts as a highly active, single site catalyst (TACN = 1,4,7-trimethyltriazacyclononane).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aza Compounds / chemical synthesis*
  • Borates / chemistry
  • Catalysis
  • Imides / chemistry*
  • Ligands
  • Molecular Structure
  • Organometallic Compounds / chemical synthesis*
  • Polymers / chemistry
  • Pyrazoles / chemical synthesis*
  • Titanium / chemistry*

Substances

  • 1,4,7-trimethyl-1,4,7-triazacyclononane
  • Aza Compounds
  • Borates
  • Imides
  • Ligands
  • Organometallic Compounds
  • Polymers
  • Pyrazoles
  • tris(pyrazolyl)methane
  • Titanium