245
Views
1
CrossRef citations to date
0
Altmetric
Articles

Functionalized amphiphilic polyethylene via direct copolymerizations of ethylene with α-olefin containing amino functionalization

, , , , , , & show all
Pages 202-210 | Received 30 Sep 2021, Accepted 11 Dec 2021, Published online: 05 Jan 2022
 

Abstract

Transition metal-catalyzed copolymerization of olefins with polar monomers signifies a challenge because transition metal catalysts usually easily get poisoned by heteroatoms. Novel amino-containing polyethylene with high molecular weight, fluorescent functionality was synthesized by direct copolymerization of ethylene and amino-olefin containing shielding groups. The highly efficient non-metallocene catalyst system with high tolerance to polar monomers [N, P] complexes [silicon bridged diphenyl phosphorus-phenyl-amine multi chelated] can effectively promote the copolymerization of ethylene and amino-olefins containing considerable group protection, in which the catalysts very high catalytic activity (up to 6.56 × 104 g mol−1 h−1) was achieved. The functional copolymer exhibited high molecular weight (up to 2.87 × 105 g mol–1) and amino-olefin comonomer incorporation (up to 2.43 mol%). Remarkably, the copolymer showed a high melting point (Tm around 138.7 °C) and thermal stability. The incorporated amino acid ester unit changes the surface characteristics of the polyolefin, making it have excellent hydrophilicity and fluorescence. Furthermore, as the content of functional copolymer increases, the properties both have significantly increased.

Graphical Abstract

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.