Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand Full article
| Journal | Molecules , E-ISSN: 1420-3049 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Output data | Year: 2019, Volume: 24, Number: 6, Article number : 1176, Pages count : DOI: 10.3390/molecules24061176 | ||||||||||
| Tags | highly linear polyethylene; vinyl-end polyethylene; cobalt precatalyst; thermo-stable and efficient catalysis; correlation between structure and activity | ||||||||||
| Authors |  | ||||||||||
| Affiliations | 
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                            Abstract:
                            Six examples of 2-(1-arylimino)ethyl-9-arylimino-5,6,7,8-tetrahydrocycloheptapyridine-cobalt(II) chloride complexes, [2-(1-ArN)C2H3-9-ArN-5,6,7,8-C5H8C5H3N]CoCl2, (Ar = 2-(C5H9)-6-MeC6H3 Co1, 2-(C6H11)-6-MeC6H3 Co2, 2-(C8H15)-6-MeC6H3 Co3, 2-(C5H9)-4,6-Me2C6H2 Co4, 2-(C6H11)-4,6-Me2C6H2 Co5, and 2-(C8H15)-4,6-Me2C6H2 Co6), were synthesized by the direct reaction of the corresponding ortho-cycloalkyl substituted carbocyclic-fused bis(arylimino)pyridines (L1-L6) and cobalt(II) chloride in ethanol with good yields. All the synthesized ligands (L1-L6) and their corresponding cobalt complexes (Co1-Co6) were fully characterized by FT-IR, H-1/C-13-NMR spectroscopy and elemental analysis. The crystal structure of Co2 and Co3 revealed that the ring puckering of both the ortho-cyclohexyl/cyclooctyl substituents and the one pyridine-fused seven-membered ring; a square-based pyramidal geometry is conferred around the metal center. On treatment with either methylaluminoxane (MAO) or modified methylaluminoxane (MMAO), all the six complexes showed high activities (up to 4.09 x 10(6) g of PE mol(-1) (Co) h(-1)) toward ethylene polymerization at temperatures between 20 degrees C and 70 degrees C with the catalytic activities correlating with the type of ortho-cycloalkyl substituent: Cyclopentyl (Co1 and Co4) > cyclohexyl (Co2 and Co5) > cyclooctyl (Co3 and Co6) for either R = H or Me and afforded strictly linear polyethylene (T-m > 130 degrees C). The narrow unimodal distributions of the resulting polymers are consistent with single-site active species for the precatalyst. Furthermore, compared to the previously reported cobalt analogues, the titled precatalysts exhibited good thermo-stability (up to 70 degrees C) and possessed longer lifetime along with a higher molecular weight of PE (M-w: 9.2 similar to 25.3 kg mol(-1)).
                        
                    
                
                        Cite:
                                Guo J.
    ,        Wang Z.
    ,        Zhang W.
    ,        Oleynik I.I.
    ,        Vignesh A.
    ,        Oleynik I.V.
    ,        Hu X.
    ,        Sun Y.
    ,        Sun W-H.
    
Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
                         Molecules. 2019.
        V.24.     N6.     1176
        .    DOI: 10.3390/molecules24061176
            WOS
        
            Scopus
        
            РИНЦ
        
            OpenAlex
                Molecules. 2019.
        V.24.     N6.     1176
        .    DOI: 10.3390/molecules24061176
            WOS
        
            Scopus
        
            РИНЦ
        
            OpenAlex
        
                    
                    
                                            Highly Linear Polyethylenes Achieved Using Thermo-Stable and Efficient Cobalt Precatalysts Bearing Carbocyclic-Fused NNN-Pincer Ligand
 Molecules. 2019.
        V.24.     N6.     1176
        .    DOI: 10.3390/molecules24061176
            WOS
        
            Scopus
        
            РИНЦ
        
            OpenAlex
                Molecules. 2019.
        V.24.     N6.     1176
        .    DOI: 10.3390/molecules24061176
            WOS
        
            Scopus
        
            РИНЦ
        
            OpenAlex
        
                    
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                    | Published online: | Mar 25, 2019 | 
                        Identifiers:
                            
                    
                    
                                            
                    
                                            
                    
                | Web of science: | WOS:000465503800138 | 
| Scopus: | 2-s2.0-85063582348 | 
| Elibrary: | 41792401 | 
| OpenAlex: | W2923015664 |