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L. Santana, M. Teijeira, E. Uriarte, C. Teran, B. Li?ares, R. Villar, R. Laguna and E. Cano, “AM1 Theoretical Study, Synthesis and Biological Evaluation of Some Benzofuran Analogues of Anti-Inflammatory Arylalkanoic Acids,” European Journal of Pharmaceutical Sciences, Vol. 7, No. 2, 1999, pp. 161-166.
doi:10.1016/S0928-0987(98)00019-0
has been cited by the following article:
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TITLE:
Synthesis and Characterization of Lactone Functional Macromonomers by End Group Deactivation and Their Use in Miktoarm Star Polymer
AUTHORS:
Kadir Demirelli, Feride Bezgin
KEYWORDS:
Miktoarm Star Polymer; Lacton; Ring Open Polymerization
JOURNAL NAME:
Open Journal of Polymer Chemistry,
Vol.2 No.2,
May
30,
2012
ABSTRACT: Newly designed miktoarm star-shaped copolymers made of poly[(benzyl methacrylate(BMA)-co-(ε-caprolacton)(CL)] and poly[(BMA-b-MMA-b-BMA)-co-ε-caprolacton)(CL)] were synthesized by combining ring-opening polymerization (ROP) of ε-caprolactone (CL) and poly(BMA) five membered lacton fuctionalized prepared via atom transfer radical polymerization (ATRP) of BMA, and ε-CL and P(BMA-b-MMA-b-BMA) dual functionalized diblock copolymer, in the presence of tin(II) bis(2-ethylhexanoate) (Sn(Oct)2). Although lactone ended poly(benzyl methacrylate) with ε-caprolactone monomer gave ring open polymerization by Sn(Oct)2, the macromonomer itself did not give any poly- merization The macromonomers, and the miktoarm star-shaped copolymers were analyzed by FT-IR and 1H-NMR spectroscopies and GPC (gel permeation chromatograph), Differential scanning calorimetry (DSC-50) and termo- gravimetric analysis (TGA-50). These copolymers exhibited the expected structure. The crystallization of star-shaped copolymers was studied by DSC. The results show that when the content of the BMA block increased, the Tm of the star-shaped block copolymer increased.