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Title: Bis(imino)pyridines fused with 6- and 7-membered carbocylic rings as N,N,N-scaffolds for cobalt ethylene polymerization catalysts
Authors: Wang, Z
Ma, Y
Guo, J
Liu, Q
Solan, GA
Liang, T
Sun, W-H
First Published: 10-Jan-2019
Publisher: Royal Society of Chemistry
Citation: Dalton Trans, 2019, 48, pp. 2582-2591
Abstract: The unsymmetrical diketone, 1,2,3,7,8,9,10-heptahydrocyclohepta[b]quinoline-4,6-dione, based on a central pyridine unit fused by both 6- and 7-membered rings, has been synthesized via a sequence of reactions including ruthenium-catalyzed coupling cyclization. Templating this diketone with a mixture of cobalt(ii) chloride hexahydrate and the corresponding aniline in acetic acid at reflux afforded five examples of carbocyclic-fused bis(arylimino)pyridine-cobalt(ii) chlorides (aryl = 2,6-Me2Ph Co1, 2,6-Et2Ph Co2, 2,6-i-Pr2Ph Co3, 2,4,6-Me3Ph Co4, 4-Me-2,6-Et2Ph Co5) in good yield. All cobalt complexes have been fully characterized including by 1H NMR spectroscopy which reveals broad but assignable paramagnetically shifted peaks. The molecular structures of Co1, Co3 and Co4 highlight the inequivalency of the two fused rings with the cobalt center adopting a distorted trigonal bipyramidal geometry. Treatment of Co1-Co5 with MAO gave highly active catalysts (up to 5.03 × 106 g PE mol-1 (Co) h-1 at 40 °C, with Co4 > Co5 > Co1 > Co2 > Co3) for ethylene polymerization generating strictly linear vinyl-terminated polymers with low molecular weights (Mw range: 1.53-22.77 kg mol-1). By comparison, polymerizations conducted using Co1-Co5/MMAO were less active and displayed a lower selectivity for unsaturated polymers. Common to both MAO and MMAO, the most sterically hindered precatalyst Co3 gave the highest molecular weight polymer of the series (up to 22.77 kg mol-1) but exhibited the lowest activity.
DOI Link: 10.1039/c8dt04892d
eISSN: 1477-9234
Embargo on file until: 10-Jan-2020
Version: Post-print
Status: Peer-reviewed
Type: Journal Article
Rights: Copyright © The Royal Society of Chemistry 2019. Deposited with reference to the publisher’s open access archiving policy. (
Description: The file associated with this record is under embargo until 12 months after publication, in accordance with the publisher's self-archiving policy. The full text may be available through the publisher links provided above.
Appears in Collections:Published Articles, Dept. of Chemistry

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