National Changhua University of Education Institutional Repository : Item 987654321/10075
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 6507/11669
Visitors : 29966093      Online Users : 383
RC Version 3.2 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Adv. Search
LoginUploadHelpAboutAdminister

Please use this identifier to cite or link to this item: http://ir.ncue.edu.tw/ir/handle/987654321/10075

Title: Hafnium Chloride and Hafnium Methyl Complexes Bearing Substituted Pyrrolyl Ligands: Synthesis, Characterization, and Ethylene Polymerization
Authors: Hsieh, K. C.;Chang, J. C.;Lee, M. T.;Hu, Ching-Han;Hung, J. H.;Lee, H. M.;Huang, J. H.;Wang, M. H.;Lee, T. Y.
Contributors: 化學系
Date: 2004-09
Issue Date: 2012-05-03T06:17:47Z
Publisher: Elsevier
Abstract: Reactions of HfCl4 with 2 and 3 equiv. of Li[C4H3N(CH2NMe2)-2] in toluene afford HfCl2[C4H3N(CH2NMe2)-2]2 (1) and HfCl[C4H3N(CH2NMe2)-2]3 (2), respectively. Transmetallation reaction of 1 with 2 equiv. of MeLi results in a hafnium dimethyl compound HfMe2[C4H3N(CH2NMe2)-2]2 (3). A variable-temperature 1H NMR spectroscopic study shows that the activation energy for the dissociation/association of the NMe2 units of compound 2 in solution is ca. 13.6 kcal/mol. Compounds 1–3 are characterized by NMR spectroscopy and single crystal X-ray diffraction. A polymerization study shows that compounds 1 and 3 exhibit moderate activity toward ethylene in the presence of TIBA and MAO.
The reactions of HfCl4 with 2 and 3 equiv. of Li[C4H3N(CH2NMe2)-2] afford HfCl2[C4H3N(CH2NMe2)-2]2 (1) and HfCl[C4H3N(CH2NMe2)-2]3 (2), respectively. Further reaction of 1 with MeLi results in a hafnium dimethyl compound HfMe2[C4H3N(CH2NMe2)-2]2 (3). A polymerization study shows that compounds 1 and 3 exhibit moderate activity toward ethylene in the presence of TIBA and MAO.
Relation: Inorganica Chimica Acta, 357(12): 3517-3524
Appears in Collections:[Department of Chemistry] Periodical Articles

Files in This Item:

File SizeFormat
index.html0KbHTML812View/Open


All items in NCUEIR are protected by copyright, with all rights reserved.

 


DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback