Cleavage Alkylation Coupling with Versatile Amide-Based Eutectic Catalytic Systems

This study introduces amide-based eutectic solvents (ESs) as a versatile and high-efficiency catalytic system for converting polyolefin waste into liquid alkanes in coupled cracking–alkylation. Owing to the rich variety of molecular active species (i.e., [AlCl 3 (Acetamide) n ] and AlCl 3 ) and ionic active species (i.e., [Al 2 Cl 7 ] − and [AlCl 2 (Acetamide) n ] + ) present in the catalytic system, carbocation intermediates can be stably generated, thereby facilitating hydride transfer and cleaving polyethylene C–C bonds during the cracking cycle. For the first time, we establish a direct and quantitative correlation between Al species diversity and carbocation concentration, validated by Et 3 SiH chemical trapping combined with multinuclear NMR and operando IR spectroscopy. We demonstrate tunable selectivity to either light gasoline (C 4 –C 10 ) or aviation kerosene (C 7 –C 18 ) with isopentane or isopentene as alkylation reactants. Time-resolved product analysis together with isotopic labeling clearly confirms that aviation kerosene-range hydrocarbons (C 7 –C 18 ) are primarily derived from polyethylene fragments and chain-extended by iC 5 = alkylation. Ab initio molecular dynamics simulations reveal that cooperative dissociation of diverse Al species sustains a stable tert -butyl and chloromethyl carbocations population, rationalizing the superior catalytic efficiency of Acetamide-1.5AlCl 3 . These advances provide both mechanistic clarity and a broadly applicable strategy for selective production of gasoline- and kerosene-range hydrocarbons from plastic waste, offering new opportunities for premium-grade fuel generation.