Journal article icon

Journal article

Trends in Structure and Ethylene Polymerization Reactivity of Transition-Metal Permethylindenyl-phenoxy (PHENI*) Complexes

Abstract:
A family of ansa-permethylindenyl-phenoxy (PHENI*) transition-metal chloride complexes has been synthesized and characterized (1-7; {(η5-C9Me6)Me(R″)Si(2-R-4-R'-C6H2O)}MCl2; R,R' = Me, tBu, Cumyl (CMe2Ph); R″ = Me, nPr, Ph; M = Ti, Zr, Hf). The ancillary chloride ligands could readily be exchanged with halides, alkyls, alkoxides, aryloxides, or amides to form PHENI* complexes [L]TiX2 (8-17; X = Br, I, Me, CH2SiMe3, CH2Ph, NMe2, OEt, ODipp). The solid-state crystal structures of these PHENI* complexes indicate that one of two conformations may be preferred, parametrized by a characteristic torsion angle (TA'), in which the η5 system is either disposed away from the metal center or toward it. Compared to indenyl PHENICS complexes, the permethylindenyl (I*) ligand appears to favor a conformation in which the metal center is more accessible. When heterogenized on solid polymethylaluminoxane (sMAO), titanium PHENI* complexes exhibit exceptional catalytic activity toward the polymerization of ethylene. Substantially greater activities are reported than for comparable PHENICS catalysts, along with the formation of ultrahigh-molecular-weight polyethylenes (UHMWPE). Catalyst-cocatalyst ion pairing effects are observed in cationization experiments and found to be significant in homogeneous catalytic regimes; these effects are also related to the influence of the ancillary ligand leaving groups in slurry-phase polymerizations. Catalytic efficiency and polyethylene molecular weight are found to increase with pressure, and PHENI* catalysts can be categorized as being among the most active for the controlled synthesis of UHMWPE.
Publication status:
Published
Peer review status:
Peer reviewed

Actions


Access Document


Files:
Publisher copy:
10.1021/acs.organomet.3c00503

Authors


More by this author
Institution:
University of Oxford
Division:
HUMS
Department:
Classics Faculty
Sub department:
Chemistry Research Laboratory
Role:
Author
ORCID:
0000-0001-5513-2412
More by this author
Institution:
University of Oxford
Division:
HUMS
Department:
Classics Faculty
Sub department:
Chemistry Research Laboratory
Role:
Author
ORCID:
0000-0003-3671-6839
More by this author
Institution:
University of Oxford
Division:
HUMS
Department:
Classics Faculty
Sub department:
Chemistry Research Laboratory
Role:
Author
More by this author
Institution:
University of Oxford
Division:
HUMS
Department:
Classics Faculty
Sub department:
Chemistry Research Laboratory
Role:
Author
ORCID:
0000-0003-2363-4498
More by this author
Institution:
University of Oxford
Division:
HUMS
Department:
Classics Faculty
Sub department:
Chemistry Research Laboratory
Role:
Author
ORCID:
0000-0003-2044-9203


Publisher:
American Chemical Society
Journal:
Organometallics More from this journal
Volume:
43
Issue:
4
Pages:
540-556
Publication date:
2024-02-14
DOI:
ISSN:
0276-7333
Pmid:
38425384


Language:
English
Source identifiers:
1815957
Deposit date:
2024-05-30
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

Terms of use



Views and Downloads






If you are the owner of this record, you can report an update to it here: Report update to this record

TO TOP