2017
DOI: 10.1007/s00289-017-1924-3
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Synthesis and application of fluorinated α-diimine nickel catalyst for ethylene polymerization: deactivation mechanism

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Cited by 15 publications
(14 citation statements)
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“…10) possessing various backbone structures. 89,90 The acenaphthoquinone-based catalyst in ethylene polymerization exhibited a moderate activity of 1.4 × 10 4 g PE (mol Ni h) −1 (30°C, 30 min). 89 Despite the steric openness of these ligands, molecular weights of up to 2.48 × 10 5 g mol −1 with good crystallinity (58%) were generated.…”
Section: Fig 17mentioning
confidence: 99%
See 1 more Smart Citation
“…10) possessing various backbone structures. 89,90 The acenaphthoquinone-based catalyst in ethylene polymerization exhibited a moderate activity of 1.4 × 10 4 g PE (mol Ni h) −1 (30°C, 30 min). 89 Despite the steric openness of these ligands, molecular weights of up to 2.48 × 10 5 g mol −1 with good crystallinity (58%) were generated.…”
Section: Fig 17mentioning
confidence: 99%
“…Structures of the CF 3 , methoxy substituted and fluorinated α-diimine-based Pd and Ni complexes [88][89][90]. Fig.…”
mentioning
confidence: 99%
“…This behaviour is mainly due to higher concentration of the monomer close to the active centre which has an effect on diffusion, site activation and also propagation rate . A nonlinear relationship between monomer pressure and activity was previously reported . However, higher pressure can cause a reverse effect on the catalyst activity especially by formation of latent sites or dormant sites…”
Section: Resultsmentioning
confidence: 88%
“…[39,40] A nonlinear relationship between monomer pressure and activity was previously reported. [41][42][43] However, higher pressure can cause a reverse effect on the catalyst activity especially by formation of latent sites or dormant sites. [42]…”
Section: Ethylene Polymerization Using Nickel-based Catalystmentioning
confidence: 99%
“…1). 29,30 A series of unsymmetrical α-diimine nickel complexes with an acenaphthene backbone and with one fluorinated N-aryl ring was synthesized (IV, Fig. 1).…”
Section: Introductionmentioning
confidence: 99%