Intensive Cycloalkyl-Fused Pyridines for Aminopyridyl-Zinc-Heteroimidazoles Achieving High Efficiency toward the Ring-Opening Polymerization of Lactides.

ABSTRACT: The model precatalyst sp³- and sp²-N dinitrogen-coordinated zinc-heteroimidazole has been used as an efficient catalyst for the ring-opening polymerization of cyclic esters. Subsequent to our exceptional active 5,6,7-trihydroquinolin-8-amine-zinc catalysts for the ring-opening polymerization (ROP) of ε-caprolactone, various pyridine-fused cycloalkanones (ring size from five to eight) are developed for the correspondent fused amine-pyridine derivatives and their zinc-heteroimidazole chloride complexes Zn1-Zn8 (LZnCl₂) bearing N-diphenylphosphinoethyl pendants. Activated with two equivalents of LiN(SiMe₃)₂, the title zinc complexes efficiently promote the ROP of L-lactide (L-

SUBMITTER: Wang Y 

PROVIDER: S-EPMC11397438 | biostudies-literature | 2024 Aug

REPOSITORIES: biostudies-literature