화학공학소재연구정보센터
홈 로그인 로그아웃 연락처 사이트맵
Polymer(Korea), Vol.40, No.3, 347-354, May, 2016
DOI10.7317/pk.2016.40.3.347  Export Citation
(Benzoimidazolylmethyl)amine Zinc(II) 착화합물에 의해 촉매화된 락타이드의 개환 중합: 반응속도, 메커니즘, 그리고 고분자 입체규칙성 연구
Ring-opening Polymerization of Lactides Catalyzed by (Benzoimidazolylmethyl)amine Zinc(II) Complexes: Kinetics, Mechanism and Polymer Tacticity Studies
Nelson W. Attandoh, and Stephen O. Ojwach†
  • School of Chemistry and Physics, University of KwaZulu-Natal, Pietermaritzburg Campus, Private Bag X01 Scottsville, 3209, South Africa
E-mail:
Zinc(II) complexes of (benzoimidazolyl)amine ligands, N-(1H-benzoimidazol-2-ylmethyl)aniline (L1) and N-(1H-benzoimidazol-2-ylmethyl)-2-bromoaniline (L2), [Zn2(L1)2(OBz)4] (1), [Zn2(L2)2(OBz)4] (2) and [Zn(L1)2(OAc)2] (3) have been employed in the ring-opening polymerization of lactides. The complexes were found to form active catalysts in the polymerization of the D,L-lactide (D,L-LA) and L-lactide (L-LA) monomers. The polymerization kinetics proceeded via pseudo-first order mechanism with respect to the monomer. Low molecular weight polymers were obtained with relatively narrow molecular weight distribution of 1.30-1.50. The ligand architecture, the nature of the carboxylate anion and solvent system influenced the rate of lactide polymerization reactions. Polymerization reactions performed in methanol exhibited higher rates of reaction than those in toluene. The activation parameters measured for lactide polymerization using 3 were obtained as ΔH°=38.4±0.7 kJmol-1, ΔS°=-167.2±1.8 JK-1mol-1 and are consistent with a highly ordered transition state. The polymers produced were mainly atactic and isotactic.
Keywords:ring-opening polymerization;lactides;kinetics;tacticity
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