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香豆素衍生物凝胶的制备及性质研究 被引量:2

Preparation and Properties of Coumarin Derivative Gel
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摘要 设计合成了香豆素衍生物凝胶因子1,该凝胶因子可以在乙腈和N,N-二甲基亚砜(DMSO)中形成有机凝胶.通过紫外可见光谱(UV-vis)、红外光谱(FTIR)、扫描电镜(SEM)、X-射线粉末衍射(XRD)和接触角(CA)等技术对该凝胶因子在乙腈和N,N-二甲基亚砜的自组装过程进行了详细表征.该凝胶体系在氢键和范德华力的驱动力下自组装成微米带结构,该结构表面展示了疏水性质,其接触角为136.5°和124°. Coumarin derivative gelator1 was designed and synthesized, which could form organic gels in acetonitrile and dimethylsulfoxide(DMSO).The self-assembly process of1 in acetonitrile and DMSO was characterized by UVvis spectra, fourier transform infrared spectroscopy(FTIR), scanning electron microscope(SEM), X-ray diffraction(XRD) and contacting angle(CA).The gelator1 was self-assembled into microbelts structure under the driving force of hydrogen bonding and van der Waals force.The structure surface showed the hydrophobic properties,and the contact angle were 136.5 ° and 124 °.
作者 高爱萍 李依冉 曹新华 GAO Aiping;LI Yiran;CAO Xinhua(College of Chemistry and Chemical Engineering/Henan Province Key Laboratory of Utilization of Non-metallic Mineral in the South of Henan,Xinyang Normal University,Xinyang 464000,China)
出处 《信阳师范学院学报(自然科学版)》 CAS 北大核心 2020年第1期129-133,共5页 Journal of Xinyang Normal University(Natural Science Edition)
基金 国家自然科学基金项目(U1704164) 河南省高校创新人才项目(17HASTIT005)
关键词 香豆素 凝胶 超分子自组装 疏水性 coumarin gel supramolecular self-assembly hydrophobicity
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  • 1祁刚,屠树滋,王秋娟,马琳.多取代香豆素磺酰脲类化合物的合成及其降血糖活性研究[J].中国药物化学杂志,2004,14(6):331-334. 被引量:3
  • 2Smyth T, Ramachandran V N, Smyth W F. A study of the antimicrobial activity of selected naturally occurring and synthetic coumarins [J]. International Journal of Antimicrobial Agents, 2009, 33: 421-426.
  • 3Basanagouda M, Shivashankar K, Kulkarni M V, et al. Synthesis and antimicrobial studies on novel sulfonamides containing 4-azidomethyl coumarin [J]. European Journal of Medicinal Chemistry, 2010, 45(3): 1 151-1 157.
  • 4Garazd Y L, Kornienko E M, Maloshtan N, et al. Modified coumarins 17. synthesis and anticoagulant activity of 3,4- cycloannelated coumarin D-glycopyranosides [J]. Chemistry of Natural Compounds, 2005, 41 (5): 508-512.
  • 5Kashman Y, Gustafson K R, Fuller R W, et al. The ealanolides, a novel HIV-Inhibitory class of eoumarin derivatives from the tropical rainforest tree, calophyllum lanigerum[J]. J Med Chem, 1992, 35 (15): 2 735-2 743.
  • 6Tummino P J, Ferguson D, Hupe D. Competitive inhibition of HIV-1 protease by warfarin derivatives[J]. Biochem Biophys Res Commun, 1994, 201 (1): 290-294.
  • 7Jimenez-Orozco F A, Moline-Guarneros J A, Mendoza-Patino N. Decrease of cyclin D1 in the humanlung adenocarcinoma cell line A-427 by 7-hydroxycoumarin[J]. Lung Cancer, 2001, 34 (2) : 185.
  • 8Lee K H, Chai H B, Tamez P A, et al. Biologically active allky latedcoumarins from kayeaassamica [J]. Phyto Chemistry, 2003, 64 (2): 535-541.
  • 9Guilt D, Helesbeux J J, Seraphin D, et al. Novelcytotoxic 42 phenyl Furanocoumarins from calophyllum dispar [J]. J Nat Prod, 2001, 64(5): 563-568.
  • 10Kawase M, Vsru B, Shah A. Antimicrobial activity of new coumarin derivatives[J]. Arzeneim Forsch, 2001, 51 (1): 67-71.

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