Covalent organic frameworks as supports for a molecular Ni based ethylene oligomerization catalyst for the synthesis of long chain olefins

• Published in: Journal of catalysis Vol. 345; pp. 270 - 280
• Main Authors: Rozhko, Elena, Bavykina, Anastasiya, Osadchii, Dmitrii, Makkee, Michiel, Gascon, Jorge
• Format: Journal Article
• Language: English
• Published: San Diego Elsevier Inc 01.01.2017; Elsevier BV
• Subjects: Catalysis; Catalysts; Covalent organic framework; Ethylene; Ethylene oligomerization; Ni catalyst; Polymers; Porous aromatic polymers; Porous aromatic polymers; Covalent organic framework; Ethylene oligomerization; Ni catalyst
• ISSN: 0021-9517; 1090-2694
• DOI: 10.1016/j.jcat.2016.11.030

[Display omitted] •Two different families of Covalent Organic Frameworks are used as supports for a molecular Ni catalyst.•The resulting catalysts show high selectivity for the formation of C6C20 olefins in the oligomerization of ethylene.•Catalytic results are rationalized on the basis of the textural properties of the different COFs. The use of two different classes of covalent organic frameworks (covalent triazine and imine linked frameworks) as supports for molecular Ni2+ catalysts is presented. For COFs, a large concentration of N heteroatoms, either in the form of quasi bipyridine or as diiminopyridine moieties, allows for the coordination of NiBr2 to the scaffold of the porous polymers. When applied as catalysts in the oligomerization of ethylene under mild reaction conditions (15bar, 50°C), these new catalysts display an activity comparable to those of their homogeneous counterpart and a fivefold higher selectivity to C6+ olefins. Accumulation of long chain hydrocarbons within the porosity of the COFs leads to reversible deactivation. Full activity and selectivity of the best catalysts can be recovered upon washing with dichlorobenzene.