Preparation and Activation of Complexes of the Type [((mesityl)NCH2CH2)2NX]ZrMe2 (X = H, Me) with [Ph3C][B(C6F5)4] or [PhNMe2H][B(C6F5)4]
Author:
Affiliation:
1. Department of Chemistry, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om0004996
Reference65 articles.
1. NMR detection of living intermediates prepared from activated [NON]ZrMe2 ([NON]2−=[(t-Bu-d6-N-o-C6H4)2O]2−) and olefins
2. Synthesis of Titanium, Zirconium, and Hafnium Complexes that Contain Diamido Donor Ligands of the Type [(t-BuN-o-C6H4)2O]2- and an Evaluation of Activated Versions for the Polymerization of 1-Hexene
3. Synthesis of Titanium and Zirconium Complexes That Contain the Tridentate Diamido Ligand, [((t-Bu-d6)N-o-C6H4)2O]2- ([NON]2-) and the Living Polymerization of 1-Hexene by Activated [NON]ZrMe2
4. Synthesis of Group 4 Complexes that Contain the Diamidoamine Ligands, [(2,4,6-Me3C6H2NCH2CH2)2NR]2- ([Mes2N2NR]2-; R = H or CH3), and Polymerization of 1-Hexene by Activated [Mes2N2NR]ZrMe2 Complexes
5. Synthesis of group 4 complexes that contain the tridentate diamido ligands [(ArNCH2CH2)2O]2− (Ar = C6H3-Me2-2,6 or C6H3Pri2-2,6)
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