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通过三嗪荧光探针的多氢键作用识别胸腺嘧啶 被引量:1

Recognition of Thymine by Triazinyl Fluorescence Probe Through the Formation of Intermolecular Multi-hydrogen Bonds
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摘要 In this work, a novel long-wavelength fluorescence probe, 3-(4-chloro-6-methylamino-1,3,5-triazinylamino)-7-dimethylamino-2-methylphenazine, was synthesized by the reaction of neutral red and methylamine subsequently with cyanuric chloride, and its recognition behavior for thymine together with its spectroscopic properties in different solvents was studied. The results show that the fluorescence probe can be selectively quenched by thymine instead of guanine, suggesting that the fully complementary hydrogen bonding plays a key role in such a recognition process. In this work, a novel long-wavelength fluorescence probe, 3-(4-chloro-6-methylamino-1,3,5-triazinylamino)-7-dimethylamino-2-methylphenazine, was synthesized by the reaction of neutral red and methylamine subsequently with cyanuric chloride, and its recognition behavior for thymine together with its spectroscopic properties in different solvents was studied. The results show that the fluorescence probe can be selectively quenched by thymine instead of guanine, suggesting that the fully complementary hydrogen bonding plays a key role in such a recognition process.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2003年第1期37-39,共3页 Chemical Journal of Chinese Universities
基金 国家自然科学基金 (批准号 :2 0 175 0 31 2 0 0 35 0 10 )资助
关键词 三嗪 分子间氢键 荧光探针 分子识别 胸腺嘧啶 核酸 碱基 Intermolecular hydrogen bond Fluorescence probe Molecular recognition Thymine
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  • 1程琼 彭图治.Chem. J. Chinese Universities(高等学校化学学报)[J],2002,23(9):1-1.

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