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烷基-β-D-吡喃葡萄糖苷的合成与性能 被引量:9

Syntheses and Properties of Alkyl β-D-Glucopyranosides
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摘要 以葡萄糖为原料,经乙酰化、选择性脱C1位乙酰基、转化成三氯乙酰亚胺酯、与受体醇偶联和脱保护5步反应合成了11种不同碳链长度的烷基-β-D-吡喃葡萄糖苷。利用核磁共振、偏光显微镜和热失重分析法对其进行结构表征和性能测试。结果表明,当烷基-β-D-吡喃葡萄糖苷疏水烷基链长n为6—10时,均具有发泡和乳化性能,特别是正壬基β-D-吡喃葡萄糖苷(rt=9)具有更加优异的发泡和乳化性能;当烷基-β-D-吡喃葡萄糖苷疏水链的长度n/〉7时,均具有热致液晶行为,特别是正十二烷基-β-D-吡喃葡萄糖苷(n=12)和十四烷基-β-D-吡喃葡萄糖苷(n=14)能够形成更加稳定的液晶态。 Using D-glucose as precursor, eleven alkyl β-D-glucopyranosides with different carbon chain length were synthesized, via five consecutive steps including acetylation, selective deacetylation at the C1 position, conversion to trichloroacetimidate, coupling with acceptors alcohols and deprotection. Their structures and properties were characterized by NMR, polarization microscope (POM) and thermogravimetry (TG). The results show that alkyl β-D-glucopyranosides possess foaming and emulsifying capacities for those with chain length of hydrophobic aglycon n = 6 - 10. Remarkably, n-nonyl β-D-glucopyranoside ( n = 9 ) shows even superior foaming and emulsifying capacities. Meanwhile, when the chain length of hydrophobic aglycon(n) is greater than 7, all alkyl β-D-glucopyranosides exhibit thermotropic liquid crystalline behavior. Among them, n-dodecyl β-D-glucopyranoside with n = 12 and n-tetradecyβ-D-glucopyranoside with n = 14 can form more stable liquid crystal state. Keywords glucose, alky β-D-glucopyranosides, foaming, emulsification, thermotropic liquid crystalline
出处 《应用化学》 CAS CSCD 北大核心 2013年第10期1120-1126,共7页 Chinese Journal of Applied Chemistry
基金 湖南省自然科学基金资助项目(10JJ6023 05JJ40054) 湘潭大学第八批大学生创新基金研究项目(30) 博士科研启动费(05QDZ09)
关键词 葡萄糖 烷基-β-D-吡喃葡萄糖苷 发泡 乳化 热致液晶 glucose, alkyl β-D-glucopyranosides, foaming, emulsification, thermotropic liquid crystalline
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参考文献16

  • 1Xu W,Osei-Prempeh C,Lema C,et al.Synthesis,Thermal Properties,and Cytotoxicity Evaluation of Hydrocarbon and Fluorocarbon Alkyl β-D-xylopyranoside Surfactants [J].Carbohydr Res,2012,349:12-23.
  • 2Yakimchuk O D,Kotomin A A,Petel'skii M B,et al.Cleaning Action and Surfactant Properties of Alkyl Glucosides[J].Russ J Appl Chem,2004,77 (12):2001-2005.
  • 3Persson C M,Claesson P M.Interfacial Behavior of n-Octyl β-D-glucopyranoside Compared to That of a Technical Mixture Consisting of Octyl Glucosides[J].Langmuir,2000,16:10227-10235.
  • 4Ogawa S,Asakura K,Osanai S.Freezing and Melting Behavior of an Octyl β-D-glucoside-water Binary System-inhibitoryEffect of Octyl β-D-glucoside on Ice Crystal Formation[J].Phys Chem Chem Phys,2012,14:16312-16320.
  • 5Akita H,Kawahara E,Kato K.Chemoenzymatic Synthesis of Rhodiooctanoside Isolated from Chinese Medicines,Rhodiolae Radix [J].Tetrahedron-Asymmetr,2004,15:1623-1629.
  • 6Richard G,Morel S,Willemot R-M,et al.Glucosylation of α-Butyl-and α-Octyl-D-glucopyranosides by Dextxansucrase andAltemansucrase from Leuconostoc Mesenteroides [J].Carbohydr Res,2003,338:855-864.
  • 7Ferlin N,Duchet L,Kovensky J,et al.Microwave-assited Synthesis of Long-chain Alkyl Glucopyranosides[J].Carbohydr2008,343:2819-2821.
  • 8Bomaghi L F,Poulsen S-A.Microwave-accelerated Fischer Glycosylation[J].Tetrahadron Lett,2005,46:3485-3488.
  • 9Adasch V,Hoffmann B,Milius Wfet al.Preparation of Alkyl α-and β-D-Glucopyranosides Thermotropic Properties andX-Ray Analysis [J].Carbohydr Res,1998,314:177-187.
  • 10Hashim R,Mirzadeh S M,Heidelberg T,et al.A Reevaluation of the Epimeric and Anomeric Relationship of Glucosidesand Galactosides in Thermotropic Liquid Crystal Self-assemblies [J].Carbohydr Revs,2011,346:2948-2956.

二级参考文献39

  • 1于珍祥,马菊瑛.烷基多苷的现状和未来[J].日用化学工业,1996,26(2):29-32. 被引量:30
  • 2宋启煌.精细化工工艺学[M].北京:化学工业出版社,1996.73.
  • 3宋照斌 宋启煌.“绿色”表面活性剂烷基糖苷的开发应用[J].精细化工,1999,16:9-12.
  • 4吕树祥.十二烷基葡萄糖苷合成工艺及反应动力学研究[M].河南:郑州工业大学,1997..
  • 5Podlasek CA, Wu J, Stripe WA, et al. [^13C] Enriched methyl aldopyranosides: structural interpretations of ^13C-^1H spin-coupling constants and ^1H chemical shifts [J]. J Am Chem Soc, 1995, 117: 8635-8644.
  • 6Shashkov AS. ^13C NMR spectra of parent hexopyranoses [J]. Russ Chem Bull, 1983, 32: 1200-1207.
  • 7Yu DQ, Yang JS. Analytical Chemistry Handbook(分析化学手册).Analysis of Nuclear Magnetic Resonance Spectroscopy(核磁共振波谱解析)[M].Beijing: Chemical Industry Press,2002: 492.
  • 8Snyder JR, Serianni AS. D-Idose: a one- and two-dimensional NMR investigation of solution composition and conformation [J]. J Org Chem, 1986, 51: 2694-2702.
  • 9Bock K, Pedersen C. Carbon-13 nuclear magnetic resonance spectroscopy of monosaccharides [J]. Adv Carbohydr Chem Biochem, 1983, 41: 27-66.
  • 10Gong YH, Ding LS. ^13C NMR Analysis of Natural Products(天然产物核磁共振碳谱分析)[M].Kunming: Yurman Science and Technology Press, 2006: 856.

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