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Fluorescence Quenching Studies of Ethyl 2-(chloromethyl)-4-phenyl-quinoline-3-carboxylate in the Presence of Nitro-explosives
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Southwest University of Science and Technology,Institute of Chemical Materials, CAEP,Institute of Chemical Materials, CAEP,Institute of Chemical Materials, CAEP,Institute of Chemical Materials, CAEP,Institute of Chemical Materials, CAEP

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    Abstract:

    In order to find sensing materials used for explosives detecting, fluorescence analysis technique was used to study the fluorescence response of the fluorescence of conjugated compounds with small molecular weight and fluorescent property ethyl 2-(chloromethyl)-4-phenyl-quinoline-3-carboxylate (ECMPQC) to trace nitro-explosives in practice, and fluorescence quenching efficiency with various concentration of nitro-explosives. Electron transfer occurs when ECMPQC with nitro-explosives (such as TNT, HNS and HMX) which are lack of electrons in their molecular structures. As a result, the fluorescence intensity decreases in this system and the fluorescence intensity decreases with the concentration of TNT increasing. ECMPQC has potential application in nitro-explosives detection. The fluorescence property of ECMPQC was investigated in chloroform, acetone and ethanol. Results show that with the increase of solvent polarity, the bathochromic shift of the emission maximum wavelength becomes more remarkable. In ethanol, a new emissive band which is assigned to the formation of the exciplex is appeared in the region of 365~450 nm in fluorescence spectrum between ECMPQC and nitro-explosives.

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何娜,钟发春,舒远杰,等.硝基爆炸物对2-(氯甲基)-4-苯基喹啉-3-甲酸乙酯的荧光猝灭研究[J].含能材料,2012,20(1):44-48.
HE Na, ZHONG Fa-chun, SHU Yuan-jie, et al. Fluorescence Quenching Studies of Ethyl 2-(chloromethyl)-4-phenyl-quinoline-3-carboxylate in the Presence of Nitro-explosives[J]. Chinese Journal of Energetic Materials,2012,20(1):44-48.

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History
  • Received:August 15,2011
  • Revised:September 10,2011
  • Adopted:September 26,2011
  • Online: February 23,2012
  • Published: