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手性离子液体修饰纳米金粒子用于酪氨酸对映体的手性识别 被引量:2

Application of Chiral Ionic Liquid Modified Gold Nanoparticles in the Chiral Recognition of Tyrosine Enantiomers
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摘要 本文以手性离子液体1-乙基-3-甲基咪唑L-酒石酸盐(EMIML-Tar)为修饰剂合成了EMIML-Tar修饰的金纳米粒子(EMIML-Tar-AuNPs)。采用透射电镜、紫外-可见分光光度计对EMIML-Tar-AuNPs进行了表征。合成的EMIML-Tar-AuNPs平均粒径约为6.5nm,其紫外-可见吸收光谱的最大吸收波长为520nm。进一步将EMIML-Tar-AuNPs用于酪氨酸(Tyr)对映体的手性识别,观察添加不同浓度D-Tyr和L-Tyr的EMIML-Tar-AuNPs的颜色变化及其紫外-可见吸收光谱。结果表明,经过D-Tyr和L-Tyr处理的EMIML-Tar-AuNPs胶体的颜色不同,而且紫外-可见光谱图也存在明显差异。对各浓度光谱图在650nm和520nm处的吸光度比值进行比较,结果发现各浓度D-Tyr的吸光度比值均较低且差别不大,而L-Tyr的吸光度比值均较高,且随着浓度的增大会出现大幅度增加。 Using the chiral ionic liquid(1-ethyl-3-methylimidazole L-tartrate,EMIML-Tar)as the modifier,EMIML-Tar modified gold nanoparticles(EMIML-Tar-AuNPs)were synthesized.Transmission electron microscope and UV-Vis spectrophotometer were used for the characterization of EMIML-TarAuNPs.The average particle size of the synthesized EMIML-Tar-AuNPs was about 6.5nm,and the maximum absorption wavelength was 520 nm.EMIML-Tar-AuNPs were further applied in the chiral recognition of tyrosine(Tyr)enantiomers.The changes in the color and UV-Vis absorption spectra of EMIML-Tar-AuNPs in the presence of D-Tyr and L-Tyr were observed.The ratios of absorption intensities at 650 nm and 520 nm were compared.It was found that the absorbance ratios of D-Tyr with different concentrations were lower and had no obvious change,while the absorbance ratios of L-Tyr were larger and had a substantial increase with the concentration increasing.
出处 《分析科学学报》 CAS CSCD 北大核心 2016年第3期381-384,共4页 Journal of Analytical Science
基金 国家自然科学基金(No.21405075) 福建省中青年教师教育科研项目(No.JA14248) 闽江学院科技项目(No.MYK14002) 福建省大学生创新创业训练计划项目(No.201410395042)
关键词 手性离子液体 手性识别 金纳米粒子 酪氨酸 Chiral ionic liquid Chiral recognition Gold nanoparticles Tyrosine
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  • 1Narayanan K B,Sakthivel N.Colloid Interf Sci[J],2010,156(1-2):1.
  • 2Shao P,Ji G,Chen P.J Membr Sci[J],2005,255(1-2):1.
  • 3Lu J Y,Ye F G,Zhang A Z,Wei Z,Peng Y,Zhao S L.J Sep Sci[J],2011,34(16-17):2329.
  • 4Li H F,Zeng H L,Chen Z F,Lin J M.Electrophoresis[J],2009,30(6):1022.
  • 5Li M,Tarawally M,Liu X,Liu X L,Guo L P,Yang L,Wang G.Talanta[J],2013,109:1.
  • 6Yang L,Chen C J,Liu X,Shi J,Wang G,Zhu L D,Guo L P,Glennon J D,Scully N M,Doherty B E.Electrophoresis[J],2010,31(10):1697.
  • 7Li M,Liu X,Jiang F Y,Guo L P,Yang L.J Chromatogr A[J],2011,1218(23):3725.
  • 8Su H Y,Zheng Q L,Li H B.J Mater Chem[J],2012,22(14):6546.
  • 9Lim I I S,Mort D,Engelhard M H,Pan Y,Kamodia S,Luo J,Njoki P N,Zhou S Q,Wang L C,Zhong C J.Anal Chem[J],2009,81(2):689.
  • 10Shukla N,Bartel M A,Gellman A J.J Am Chem Soc[J],2010,132(25):8575.

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