CN107778196A - 一种芘衍生物及其合成方法和应用 - Google Patents

一种芘衍生物及其合成方法和应用 Download PDF

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CN107778196A
CN107778196A CN201711089648.0A CN201711089648A CN107778196A CN 107778196 A CN107778196 A CN 107778196A CN 201711089648 A CN201711089648 A CN 201711089648A CN 107778196 A CN107778196 A CN 107778196A
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于春伟
张军
傅琼瑶
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Hainan Medical College
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Abstract

本发明涉及铜离子的检测,具体的说是一种芘衍生物及其合成方法和应用。芘衍生物P如式一。本发明通过有效的合成手段得到的苯甲酰肼衍生物P,对铜离子表现出较好的选择性,在优化实验条件基础上,可以实现对铜离子的检测。

Description

一种芘衍生物及其合成方法和应用
技术领域
本发明涉及铜离子的检测,具体的说是一种芘衍生物及其合成方法和应用。
背景技术
在已报道的荧光分子探针中,多为同种识别机理实现特定目标物质的检测[1-3]。同一种探针,采用不同机理检测不同金属离子也有报道[4]。但是,同一种探针,不同机理识别同一种金属离子的报道较为少见。
芘衍生物具有优良的光学性质、合成简单,在金属离子荧光探针中有着广泛的应用。基于芘衍生物的荧光探针已被应用到汞离子、铅离子、铁离子、铬离子以及铜离子的检测中。但是基于一种探针,利用两种机理识别铜离子未见报道。
发明内容
本发明的目的是提供一种芘衍生物及其合成方法和应用。
为实现上述目的,本发明所采用的技术方案为:
一种芘衍生物,芘衍生物P如式一,
一种芘衍生物P的制备方法,将邻羟基苯甲酸乙酯与水合肼在无水乙醇中,75-80℃回流4-6h,冷却至室温后,析出固体在无水乙醇中,75-80℃下与芘甲醛反应4-6h,冷却后将析出固体抽滤,得淡黄色固体式一纯品P,反应式为:
所述邻羟基苯甲酸乙酯与水合肼以摩尔比1︰3-5反应;
析出固体与芘甲醛以摩尔比1︰1-1.2反应。
一种芘衍生物P的应用,所述芘衍生物P在作为荧光探针中的应用。
所述芘衍生物P在作为荧光探针在检测铜离子中的应用。
本发明所具有的优点:
本发明通过有效的合成手段得到芘衍生物P,合成步骤简单,成本低,易于提纯、产率高(85%)。该化合物对铜离子具有好的选择性,通过在低浓度荧光猝灭、在高浓度荧光增强两种不同识别机理检测铜离子,在实际测试中检出限低。
附图说明
图1为本发明实施例提供的芘衍生物P的质谱图。
图2为本发明实施例提供的芘衍生物P的核磁谱图。
图3为本发明实施例提供的铜离子低浓度时与芘衍生物P的络合质谱图。
图4为本发明实施例提供的铜离子高浓度时与芘衍生物P的络合质谱图。
图5为本发明实施例提供的化合物P(10μM)与Cu2+(0—10.0μM)在乙醇/水(v/v,7:3)中,pH6.8条件下的荧光滴定光谱。
具体实施方式
下面结合附图和实施例对本发明作进一步的解释说明。
实施例
芘衍生物P为式1所示的化合物。
芘衍生物P的制备:将1mM邻羟基苯甲酸乙酯与其5倍摩尔量的水合肼在30mL的无水乙醇中,75-80℃回流4h,冷却至室温后,析出固体过滤,固体再经无水乙醇洗涤,干燥后所得中间体化合物直接用于下一步。1mM中间体在无水乙醇中,75-80℃下与芘甲醛以摩尔比1︰1反应4h,冷却后将析出固体抽滤,依次用大量水和无水乙醇洗涤,干燥,得淡黄色固体纯品P,产率85%(参见图1和图2)。
由图1和2中可见分子离子峰和H的化学位移可知芘衍生物P的生成。
应用例
芘衍生物P对铜离子的光学识别
1)光学测定条件:在乙醇/水(7/3,v/v)介质中,用HEPES缓冲溶液控制体系pH为6.8。
2)实验方法:5mL比色管中,加入不同浓度的Cu2+标准溶液,而后加入50μL含上述作为探针分子的纯品P(1mM)的DMSO标准溶液,以乙醇/水(7/3,v/v,20mM HEPES,pH 6.8)稀释至刻度,摇匀。测试时,激发/发射狭缝=10/10nm,激发波长为349nm(参见图5)。
由图3Cu2+的荧光滴定谱图可见,P(10μM)的乙醇/水(7/3,v/v,20mM HEPES,pH6.8)溶液,荧光很弱,说明体系中P自身无荧光;加入低浓度的Cu2+后,441nm处的荧光峰强度逐渐降低并红移,说明两个探针P与Cu2+以摩尔比2:1络合(MS:m/z 792.16[2P+Cu2++Cl-]+)(图3和图5),形成激基缔合物,造成荧光猝灭;随着Cu2+浓度的增加,451nm处的荧光强度随之增强,该识别机理主要是分子内电子转移机理(MS:m/z 427.06[P+Cu2++Cl-]+)(图4和图5)。
参考文献:
1.Y.T.Li and C.M.Yang,Chem.Commun.,2003,2884-2885.
2.L.Fabbrizzi,M.Licchelli,P.Pallavicini,A.Perotti,A.Taglietti andD.Sacchi,Chem.Eur.J.,1996,2,75-82.
3.M.N.Elizabeth,J.L.Stephen,J.Mater.Chem.,2005,15,2778-2783.
4.张灯青.化学进展,2009,21,715-723。

Claims (5)

1.一种芘衍生物,其特征在于:芘衍生物P如式一,
2.一种权利要求1所述的芘衍生物P的制备方法,其特征在于:将邻羟基苯甲酸乙酯与水合肼在无水乙醇中,75-80℃回流4-6h,冷却至室温后,析出固体在过量的无水乙醇中,75-80℃下与芘甲醛反应4-6h,冷却后将析出固体抽滤,得淡黄色固体式一纯品P。
3.按权利要求2所述的芘衍生物P的制备方法,其特征在于:所述邻羟基苯甲酸乙酯与水合肼以摩尔比1︰3-5反应;
析出固体与芘甲醛以摩尔比1︰1-1.2反应。
4.一种权利要求1所述的芘衍生物P的应用,其特征在于:所述芘衍生物P在作为荧光探针中的应用。
5.按权利要求4所述的芘衍生物P的应用,其特征在于:所述芘衍生物P在作为荧光探针在检测铜离子中的应用。
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109053487A (zh) * 2018-09-12 2018-12-21 西北师范大学 一种能单一选择荧光识别L-Arg的超分子传感器及其合成和应用
CN109516928A (zh) * 2018-10-12 2019-03-26 华南师范大学 一种化合物及其制备方法与应用

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3600383A (en) * 1967-08-15 1971-08-17 Ici Ltd Oxadiazole compounds

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3600383A (en) * 1967-08-15 1971-08-17 Ici Ltd Oxadiazole compounds

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACT: "RN:901644-93-7", 《STN ON THE WEB REG 数据库》 *
GHOSH, SOUMEN ETAL: "Binding mode dependent signaling for the detection of Cu2+: An experimental and theoretical approach with practical applications", 《SPECTROCHIMICA ACTA, PART A: MOLECULAR AND BIOMOLECULAR SPECTROSCOPY(2018)》 *
MARK A. SMITH ETAL: "Identification of the Binding Site of Brucella VirB8 Interaction Inhibitors", 《CHEMISTRY & BIOLOGY 》 *
文少白等: "基于萘酰亚胺为发光团的 Zn", 《化学试剂》 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109053487A (zh) * 2018-09-12 2018-12-21 西北师范大学 一种能单一选择荧光识别L-Arg的超分子传感器及其合成和应用
CN109516928A (zh) * 2018-10-12 2019-03-26 华南师范大学 一种化合物及其制备方法与应用
CN109516928B (zh) * 2018-10-12 2021-05-25 华南师范大学 一种化合物及其制备方法与应用

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