{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Zong K"],"funding":["Natural Science Foundation of Hebei Province","National Natural Science Foundation of China"],"pagination":["3684"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9459716"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["14(17)"],"pubmed_abstract":["Four supported α-diimine nickel(II) catalysts covalently linked to silica via hydroxyl functionality on α-diimine acenaphthequinone-backbone were prepared and used in slurry polymerizations of ethylene to produce branched polyethylenes. The catalytic activities of these still reached 10<sup>6</sup> g/molNi·h at 70 °C. The life of the supported catalyst is prolonged, as can be seen from the kinetic profile. The molecular weight of the polyethylene obtained by the 955 silica gel supported catalyst was higher than that obtained by the 2408D silica gel supported catalyst. The melting points of polyethylene obtained by the supported catalysts S-C1-a/b are all above 110 °C. Compared with the homogeneous catalyst, the branching numbers of the polyethylenes obtained by the supported catalysts S-C1"],"journal":["Polymers"],"pubmed_title":["Slurry Homopolymerization of Ethylene Using Thermostable α-Diimine Nickel Catalysts Covalently Linked to Silica Supports via Substituents on Acenaphthequinone-Backbone."],"pmcid":["PMC9459716"],"funding_grant_id":["B2015202049","No. 21004017, 21004043"],"pubmed_authors":["Yang M","Zong K","Liu B","Hou Y","Sun Y","Zhao X"],"additional_accession":[]},"is_claimable":false,"name":"Slurry Homopolymerization of Ethylene Using Thermostable α-Diimine Nickel Catalysts Covalently Linked to Silica Supports via Substituents on Acenaphthequinone-Backbone.","description":"Four supported α-diimine nickel(II) catalysts covalently linked to silica via hydroxyl functionality on α-diimine acenaphthequinone-backbone were prepared and used in slurry polymerizations of ethylene to produce branched polyethylenes. The catalytic activities of these still reached 10<sup>6</sup> g/molNi·h at 70 °C. The life of the supported catalyst is prolonged, as can be seen from the kinetic profile. The molecular weight of the polyethylene obtained by the 955 silica gel supported catalyst was higher than that obtained by the 2408D silica gel supported catalyst. The melting points of polyethylene obtained by the supported catalysts S-C1-a/b are all above 110 °C. Compared with the homogeneous catalyst, the branching numbers of the polyethylenes obtained by the supported catalysts S-C1","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Sep","modification":"2025-04-18T22:40:56.068Z","creation":"2025-04-07T10:25:07.186Z"},"accession":"S-EPMC9459716","cross_references":{"pubmed":["36080759"],"doi":["10.3390/polym14173684"]}}