Versatile sugar derivatives for the synthesis of potential degradable hydrophilic-hydrophobic polyurethanes and polyureas

被引:20
|
作者
Banez, M. Violante de Paz [1 ]
Moreno, Jose A. Aznar [1 ]
Galbis, Juan A. [1 ]
机构
[1] Univ Seville, Dept Organ & Pharmaceut Chem, Fac Pharm, Seville 41071, Spain
关键词
polyurethanes; polyureas; biodegradable polymers; O-benzylalditols; diaminosugars;
D O I
10.1080/07328300802030878
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Biodegradable polymers obtained from renewable natural sources are currently receiving increasing attention because they are an alternative to the traditional petroleum-based plastics. In the present communication we describe the synthesis of the diol monomers 2,3,4-tri-O-benzyl-L-arabinitol (ABnOH) and 2,3,4-tri-O-benzylxylitol (XBnOH), and the diamino monomers 1,5-diamino-1,5-dideoxy-2,3,4-tri-O-benzyl-L-arabinitol (ABnNH(2)) and 1,5-diamino-1,5-dideoxy-2,3,4-tri-O-benzylxylitol (XBnNH(2)), which can be used in the preparation of new potentially biodegradable sugar-based polymers. As an example, we describe the synthesis and characterization of a polyurethane [PU-(ABnOH-HMDI)] and a polyurea [PUR-(ABnNH(2)-HMDI)] by poly addition reaction of ABnOH and ABnNH(2) with 1,6-hexamethylene diisocyanate.
引用
收藏
页码:120 / 140
页数:21
相关论文
共 50 条
  • [11] Crystal structure model based on the analysis of hydrophilic-hydrophobic ratio in molecules. Isosteviol derivatives
    Gubaidullin, A. T.
    Beskrovnyj, D. V.
    Litvinov, I. A.
    JOURNAL OF STRUCTURAL CHEMISTRY, 2005, 46 (Suppl 1) : S195 - S201
  • [12] Interaction Principle Between Coagulation Factor X and Fullerene Derivatives with Different Hydrophilic-Hydrophobic Properties for Anticoagulation
    Liu, Jinke
    Liu, Ru
    Li, Lin
    Wang, Xiaofeng
    Gao, Xueyun
    Xing, Gengmei
    Jiang, Huaidong
    Zhao, Lina
    JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2019, 19 (08) : 4603 - 4610
  • [13] Synthesis and characterization of sulfonated-fluorinated, hydrophilic-hydrophobic multiblock copolymers for proton exchange membranes
    Yu, Xiang
    Roy, Abhishek
    Dunn, Stuart
    Yang, Juan
    McGrath, James E.
    MACROMOLECULAR SYMPOSIA, 2006, 245 : 439 - 449
  • [14] Synthesis and Characterization of Sulfonated-Fluorinated, Hydrophilic-Hydrophobic Multiblock Copolymers for Proton Exchange Membranes
    Yu, Xiang
    Roy, Abhishek
    Dunn, Stuart
    Badami, Anand S.
    Yang, Juan
    Good, Alec S.
    Mcgrath, James E.
    JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2009, 47 (04) : 1038 - 1051
  • [15] Synthesis of hydrophilic-hydrophobic AB and ABA block copolymers by atom transfer radical polymerization.
    Zhang, X
    Matyjaszewski, K
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1998, 216 : U45 - U45
  • [16] Synthesis of per-substituted hydrophilic and hydrophobic β-cyclodextrin derivatives
    Ba, O. -M.
    Lahiani-Skiba, M.
    Bouzbouz, S.
    Skiba, M.
    JOURNAL OF INCLUSION PHENOMENA AND MACROCYCLIC CHEMISTRY, 2011, 69 (3-4) : 333 - 337
  • [17] Synthesis of per-substituted hydrophilic and hydrophobic β-cyclodextrin derivatives
    O.-M. Ba
    M. Lahiani-Skiba
    S. Bouzbouz
    M. Skiba
    Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2011, 69 : 333 - 337
  • [18] Synthesis and properties of hydrophilic-hydrophobic diblock copolymer ionomers based on poly(p-phenylene)s
    Takeoka, Y.
    Umezawa, K.
    Oshima, T.
    Yoshida, M.
    Yoshizawa-Fujita, M.
    Rikukawa, M.
    POLYMER CHEMISTRY, 2014, 5 (13) : 4132 - 4140
  • [19] FUEL 98-Synthesis and characterization of multiblock copolymers with hydrophilic-hydrophobic sequences for proton exchange membranes
    Lee, Hae-Seung
    Lane, Ozma R.
    McGrath, James E.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2008, 236
  • [20] Synthesis of hydrophilic-hydrophobic diblock copolymers and surface properties evaluation on solid substrates: Evaluation of particle morphology
    Ayane, Morikawa
    Yoshizawa-Fujita, Masahiro
    Takeoka, Yuko
    Rikukawa, Masahiro
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2019, 258