TY - JOUR
T1 - Synthesis, structure and catalytic activity of phosphine-substituted zirconium salicylaldiminato complexes
AU - Said, Musa
AU - Hughes, David L.
AU - Bochmann, Manfred
PY - 2006/8/1
Y1 - 2006/8/1
N2 - The reaction of the lithium iminophenolate LiOC6H3-2-But-6-CH==as m-dash" border="0">NAr, where Ar = 3-C6H4P{C6H3(CF3)2-3,5}2, [Li(O–NP)] with ZrCl4 affords ZrCl2(O–NP)2. Whereas previously reported zirconium bis(salicylaldiminato) complexes are typified by the trans orientation of the O-atoms, the molecular structure ZrCl2(O–NP)2 is unusual in adopting an all-cis arrangement of N, O and Cl donors. The crystal structure of the parent ligand, HOC6H3-2-But-6-CH==as m-dash" border="0">NC6H4PPh2-3, is reported for comparison. Upon activation with methylaluminoxane the complex is highly active for the polymerisation of ethylene to oligomers and low-molecular weight polymers. Notably, the catalytic activity is unaffected by the presence of phosphine donors.
AB - The reaction of the lithium iminophenolate LiOC6H3-2-But-6-CH==as m-dash" border="0">NAr, where Ar = 3-C6H4P{C6H3(CF3)2-3,5}2, [Li(O–NP)] with ZrCl4 affords ZrCl2(O–NP)2. Whereas previously reported zirconium bis(salicylaldiminato) complexes are typified by the trans orientation of the O-atoms, the molecular structure ZrCl2(O–NP)2 is unusual in adopting an all-cis arrangement of N, O and Cl donors. The crystal structure of the parent ligand, HOC6H3-2-But-6-CH==as m-dash" border="0">NC6H4PPh2-3, is reported for comparison. Upon activation with methylaluminoxane the complex is highly active for the polymerisation of ethylene to oligomers and low-molecular weight polymers. Notably, the catalytic activity is unaffected by the presence of phosphine donors.
U2 - 10.1016/j.ica.2005.10.041
DO - 10.1016/j.ica.2005.10.041
M3 - Article
VL - 359
SP - 3467
EP - 3473
JO - Inorganica Chimica Acta
JF - Inorganica Chimica Acta
SN - 0020-1693
IS - 11
ER -