4.3 Article

Synthesis and characteristics of silica-supported N-heterocyclic carbene catalyst for ring-opening polymerization of D-lactide to produce polylactide

期刊

MACROMOLECULAR RESEARCH
卷 22, 期 8, 页码 864-869

出版社

POLYMER SOC KOREA
DOI: 10.1007/s13233-014-2110-1

关键词

organocatalysts; N-heterocyclic carbene; silica; polylactide; ring-opening polymerization; D-lactide

资金

  1. Industrial Strategic Technology Development Program - Ministry of Knowledge Economy, Republic of Korea [10031756]
  2. Korea Evaluation Institute of Industrial Technology (KEIT) [10031756] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Homogeneous N-heterocyclic carbene (H-NHC) catalyst was synthesized by the reaction of 3-chloropropyl trimethoxysilane with 1-methyl imidazole and followed by carbene generation with potassium tert-butoxide. A silica-supported N-heterocyclic carbene (S-NHC) catalyst was obtained by immobilizing 1-methyl-3-(3-trimethoxysilylpropyl) imidazolium chloride on the calcined silica, followed by carbene generation. A series of solution polymerizations of D-lactide were conducted with the H-NHC and S-NHC catalyst to compare the characteristics of the catalysts and resulting polylactide (PLA). The PLA produced with S-NHC catalyst showed higher polymer bulk density and better morphology than that produced with H-NHC catalyst. However, the catalytic activity and the molecular weight of the PLA produced with S-NHC catalyst were a little lower than those of PLA prepared with H-NHC catalyst. The molecular weight distribution of PLAs produced with S-NHC catalyst was narrower than that of PLAs produced with H-NHC catalyst. This can be attributed to the formation of a similar environment for the active sites as a result of immobilization. The molecular weights of PLAs produced by both H-NHC and S-NHC catalyst increased with an increase in the D-lactide/catalyst molar ratio. However, the changes in the molecular weight distribution of PLA with increasing D-lactide/catalyst molar ratios were different with the different catalyst systems.

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