Bulletin of the Korean Chemical Society

  • 제34권2호
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  • Pages.489-494
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  • 2013
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Efficient One-Pot Three-Component Synthesis of Monomethine Cyanine Dyes with Quinoline Nucleus and Their Spectral Properties

  • Fu, Y.L. (Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), College of Chemistry and Materials Science, Northwest University) ;
  • Zhang, B.R. (Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), College of Chemistry and Materials Science, Northwest University) ;
  • Wang, S. (Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), College of Chemistry and Materials Science, Northwest University) ;
  • Gao, X.X. (Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), College of Chemistry and Materials Science, Northwest University) ;
  • Wang, L.Y. (Key Laboratory of Synthetic and Natural Functional Molecule Chemistry (Ministry of Education), College of Chemistry and Materials Science, Northwest University)
  • 투고 : 2012.10.19
  • 심사 : 2012.11.19
  • 발행 : 2013.02.20
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초록

An improved method for the preparation of monomethine cyanine dyes with quinoline nucleus by one-pot three-component using 1-methyl-2-quinolinethione, quaternized 2- or 4-methylheterocyclic compounds and methyl p-toluenesulfonate as starting materials was described. Compared with the traditional methods, the new synthetic method reduced the reaction steps, shortened the reaction time, avoided the separation and purification of the intermediate and reduced cost. The dyes absorbed in the region 478.0-563.0 nm and had molar extinction coefficients of $1.3{\times}10^4-9.4 {\times}10^4L\;mol^{-1}\;cm^{-1}$. Their fluorescence maxima and Stokes shifts were in the range of 525.2-594.4 nm and 16.2-80.6 nm in different solvents, respectively. From the spectral properties of the dyes in different solvents, it could be found that the ${\lambda}_{max}$ of the dyes were shorter in protonic solvents, and showed hypsochromic shifts with the increase of polarity of the solvents.

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피인용 문헌

  1. ChemInform Abstract: Efficient One-Pot Three-Component Synthesis of Monomethine Cyanine Dyes with Quinoline Nucleus and Their Spectral Properties. vol.44, pp.40, 2013, https://doi.org/10.1002/chin.201340199
  2. Facile Dearomatization of Nitroquinolines through [3+2] and [4+2] Cycloaddition Reactions vol.4, pp.2, 2015, https://doi.org/10.1002/ajoc.201402207
  3. Synthesis, crystal structures, and spectral properties of double N-alkylated dimethine cyanine dyes and their interactions with biomolecules and living cells vol.5, pp.6, 2015, https://doi.org/10.1039/C4RA10741A
  4. -Oxide vol.5, pp.5, 2016, https://doi.org/10.1002/ajoc.201600065
  5. Spontaneous Aerobic Oxidation of 1,1,2,2-Tetrakis(N-methylpyridin- 4-ium)ethane Iodide to the Alkene and the Epoxide vol.20, pp.5, 2018, https://doi.org/10.1021/acs.orglett.7b03995
  6. Cyanine Dyes Containing Quinoline Moieties: History, Synthesis, Optical Properties, and Applications vol.27, pp.13, 2013, https://doi.org/10.1002/chem.202003697