作者: Stefan Mecking , Lynda K. Johnson , Lin Wang , Maurice Brookhart
DOI: 10.1021/JA964144I
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摘要: Mechanistic aspects of palladium-catalyzed insertion copolymerizations ethylene and α-olefins with methyl acrylate to give high molar mass polymers are described. Complexes [(N∧N)Pd(CH2)3C(O)OMe]BAr‘4 (2) or [(N∧N)Pd(CH3)(L)]BAr‘4 (1: L = OEt2; 3: ⋮ NCMe; 4: NCAr‘) (N∧N ≡ ArNC(R)−C(R)NAr, e.g., Ar 2,6-C6H3(i-Pr)2, R H (a), Me (b); Ar‘ 3,5-C6H3(CF3)2) bulky substituted α-diimine ligands were used as catalyst precursors. The copolymers highly branched, the comonomer being incorporated predominantly at ends branches −CH2CH2C(O)OMe groups. effects reaction conditions structure on copolymerization rationalized. Low-temperature NMR studies show that migratory in η2-methyl (MA) complex [(N∧N)PdMe{H2CCHC(O)OMe}]+ (5) occurs initially 2,1-insertion product [(N∧N)PdCH(CH2CH3)C(O)OMe]+ (6), which rearranges stepwise yield 2 final upon warming −20 °C. Activation parameters (ΔH⧧ ...