共查询到20条相似文献,搜索用时 218 毫秒
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通过5,17-二氨基杯[4]芳烃衍生物与7-羟基-8-甲酰基-4-甲基香豆素缩合,得到了一种以亚胺基团为离子载体、香豆素为荧光基团的新型杯芳烃荧光识别试剂。 采用IR、1H NMR、13C NMR和MS测试技术表征了合成化合物的结构。 通过紫外光谱和荧光光谱,研究了其对过渡金属和重金属离子的识别性能。 结果表明,该化合物对Fe3+和Cr3+离子具有选择识别能力,与Fe3+和Cr3+配合的化学计量比为1∶1,配合生成常数分别为4.1×105和1.07×105 L/mol。 相似文献
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以9-蒽醛为荧光基团,吡唑和吗啉为识别基团,合成了一种荧光分子探针4-((3-(1-苯基-5-吡啶基-4,5-二氢-1H-吡唑-3-基)蒽-9-基)甲基)吗啉(L)。其结构经1H NMR、13C NMR表征,利用荧光发射光谱和紫外吸收光谱研究其离子识别性能。结果表明,探针L对Fe~(3+)和Cu~(2+)具有较强的选择性识别性能,荧光量子产率分别从0.47降到0.21和0.14;探针L的溶液颜色分别从淡黄色变为棕褐色和蓝色,裸眼可判断探针L选择性识别Fe~(3+)和Cu~(2+)。另外,根据Fe~(3+)、Cu~(2+)和H+不同组合时探针L的量子产率构建了分子水平上的三输入"NOR"逻辑门电路。 相似文献
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设计合成了8个1,5-二芳基-3-(2-羟基-4,6-二甲氧基苯基)-2-吡唑啉化合物4a~4h. 它们的结构经由IR、1H NMR、MS和元素分析确认. 测定了它们的紫外光谱和荧光光谱, 研究了它们对氟离子的选择性识别作用, 发现化合物4a,4c和4d均可选择性地识别氟离子, 其中4a和4c作为识别氟离子的荧光探针, 受常见离子干扰较小, 选择性较高. 相似文献
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以卟啉为荧光发色团,4-氯-7-硝基苯并-2-氧杂-1,3-二唑为识别基团,设计合成了一种具有较高选择性、高灵敏度的近红外硫离子荧光探针,其结构经~1H NMR,IR和HR-MS(ESI)表征。该合成路线简短,后处理简单。以荧光光谱为检测手段,测试了该探针分子对硫离子的识别效果。结果表明,此探针不仅具有高选择性和灵敏度,且在1. 0×10~(-6)~7. 0×10~(-6)mol·L~(-1)的浓度范围内呈现良好的线性关系,其检出限为78 nm。 相似文献
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设计合成了四个含有氢蒽基团的新型有机硒化合物1,8-二-(2-苄硒基)丙氧基-9,10-二氢蒽(L_1)、1,8-氧双(亚乙硒基丙氧基)-9,10-二氢蒽(L_2)、1,8-二-(2-苄硒基)乙氧基-9,10-二氢蒽(L_3)、1,8-氧双(亚乙硒基亚乙氧基)-9,10-二氢蒽(L_4),利用~1H NMR、~(13)C NMR对化合物进行了结构表征,采用荧光光谱法测定了主体对客体阳离子的识别性能。研究结果发现只有化合物L_1对Ag~+具有选择识别能力,且对Ag~+表现出"off-on"开关性能。化合物L_2与Ag~+和K~+络合后荧光略有增强。 相似文献
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通过Sonogashira偶联等反应,合成了三嵌段化合物9,10-双-(对-(甲氧基二缩三乙二醇基)苯基乙炔基)蒽,通过1H NMR和基质辅助激光解吸电离时间飞行质谱(MALDI-TOF-MS)对其结构进行了表征。利用差示扫描量热仪(DSC)、偏光显微镜(POM)及小角X射线散射仪(SAXS)等技术手段对其本体自组装行为进行了研究,结果表明,化合物在固态相自组装成近晶A相(SmA相)。光谱分析表明,该化合物继承了二取代蒽类发光材料具有高荧光量子产率(Φf)的特点,是一种性能良好的光致发光材料。 相似文献
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A fluorescent chemosensor 1 with different amide moieties as recognition elements has been designed and synthesised. The recognition behaviour of the chemosensor towards various monocarboxylates and their conjugate acids has been evaluated. Although the sensor 1 shows significant quenching of emission of anthracene in CH3CN, it shows an increase in emission in CHCl3 containing 2% CH3CN upon complexation of aliphatic monocarboxylates. Receptor 1 shows selectivity for acetate, propanoate and dihydrogen phosphate over the other anions studied under different conditions. The binding features have been established by 1H NMR, UV–vis and fluorescence spectroscopic methods. 相似文献
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The adenine-based fluorescent receptor 1 was designed and synthesized for the selective recognition of dicarboxylic acids in CH3CN. The recognition takes place through the Hoogsteen binding site of adenine with concomitant PET quenching of the anthracene moiety. The carboxylic acid binding to 1 was investigated by 1H NMR, X-ray, UV-vis, and fluorescence spectroscopic methods. The Hoogsteen (HG) cleft of receptor 1 is found to be selective for glutaric acid. 相似文献
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Fluorescence Sensor with A New ON1–OFF–ON2 Switching Mechanism Using the Excited State Intermolecular Proton Transfer Reaction of An Anthracene‐diurea Compound 下载免费PDF全文
Hisato Matsumoto Yoshinobu Nishimura Tatsuo Arai 《Photochemistry and photobiology》2017,93(5):1187-1192
A new photoreaction mechanism of “Three‐state molecular switch” fluorescence sensor based on ON1‐OFF‐ON2 sequence was achieved by anthracene‐diurea compound, which was designed using two phenylurea groups and one anthracene, 9,10BtDSPUA. Photochemical properties of 9,10BtDSPUA and interaction between 9,10BtDSPUA and anion were investigated in detail by absorption, 1H NMR, fluorescence, and fluorescence decay measurements. While the fluorescence of 9,10BtDSPUA in DMSO (ON1) was quenched in the presence of low concentration of acetate anion (OFF), fluorescence enhancement occurred by the addition of high concentration of acetate anion (ON2). This compound forms complex with acetate anion through hydrogen bonding interaction in the ground state resulted in tautomer formation by excited state intermolecular proton transfer (ESIPT) on irradiation. Whereas single coordination of acetate anion to anthracene‐diurea compound may cause fluorescence quenching, full coordination may cause fluorescence enhancement due to suppressing ESIPT. This suppressing ESIPT was occurred by electron‐donating resonance effect between two urea moieties. This study is the first example of ON1‐OFF‐ON2 fluorescence sensor for concentration detection of acetate anion. 相似文献
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Hui Zhang Tianzhi Yu Yuling Zhao Duowang Fan Yangjun Xia Peng Zhang Yongqing Qiu Lili Chen 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2010,75(1):325-329
A new coumarin derivative, 3-(4-(anthracen-10-yl)phenyl)-benzo[5,6]coumarin, was synthesized and characterized by FT-IR, 1H NMR, element analysis and single crystal X-ray crystallography. The dihedral angle of benzo[5,6]coumarin ring and phenyl group is 36.15°, and the dihedral angle of phenyl group and anthracene skeleton is 89.37°. The UV–vis absorption and photoluminescence of the compound were discussed. The result shown that the compound exhibits high fluorescence quantum yield (ΦF), large Stokes shift and green emission (508 nm). The molecular structure of the compound was optimized using density functional theory (DFT) at B3LYP/6-31G(d) level, and the HOMO and LUMO levels of the compound were deduced. 相似文献
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Sook Kyung Kim Soo Jeong Kim Seung Hee Kim Kwang S. Kim Juyoung Yoon 《Tetrahedron》2005,61(19):4545-4550
For the recognition and sensing of anionic analytes, comparative studies were carried out on the anion bindings of pyrophosphate, H2PO4−, and dicarboxylates to the anthracene derivatives bearing two urea groups on the 1,8 and 9,10-positions as fluorescent chemosensors for anions. Their binding properties were compared using fluorescence and 1H NMR, and the results were rationalized with an ab initio study. 相似文献
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《Journal of Coordination Chemistry》2012,65(10):1847-1858
The synthesis and characterization of metal-free (H2-Pc) and metal-containing (Zn, Co, and Cu) derivatives of a symmetrically octa-substituted phthalocyanine derived from 4,5-bis[2-(phenylthio)ethoxy]phthalonitrile were carried out by microwave irradiation. The electrochemical properties of the metal-free phthalocyanine 4 and metallophthalocyanine complexes 5 and 6 were investigated by cyclic voltammetry and differential pulse voltammetry. We have previously investigated the electrochemical properties of the tetra substituted 2-(phenylthio)ethoxy phthalocyanines. The reduction potential of the octa-substituted metal-free phthalocyanine shifted to more negative potential as a result of the electron donating of the 2-(phenylthio)ethoxy groups on the periphery compared to those of tetra substituted. The H2Pc and ZnPc demonstrated ligand-based electron transfer processes, while CoPc complex has a metal-based reduction process. Similar aggregation behavior was observed for octa-substituted phthalocyanines. The compounds were characterized using IR, 1H NMR, 13C NMR, elemental analysis, and MS spectral data. 相似文献
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Xuefang Shang Wanli Li Xiaofang Wei Huanle Zhang Zhiyuan Fu Jinlian Zhang Xiufang Xu 《Heteroatom Chemistry》2015,26(2):142-149
Two new compounds ( 1 and 2 ) containing 2‐sulfydryl‐1,3,4‐thiodiazole have been synthesized and optimized. They both showed wide antibacterial activity for colon bacillus, Staphylococcus aureus, S. albus, dysentery bacillus and inferior activity for Bacillus subtilis. In addition, their binding properties were evaluated for biologically important anions (F–, Cl–, Br–, I–, AcO–, and H2PO4–) by theoretical investigation, UV–vis, fluorescence, and 1H NMR titration experiments, and they displayed strong binding ability for H2PO4– without the interference of other anions tested. Especially the binding ability of compound 2 containing anthracene with H2PO4– was 1000 times stronger than that of compound 1 containing nitrobenzene. Two compounds based on 2‐sulfydryl‐1,3,4‐thiodiazole have both properties of anion recognition and antibacterial activity. 相似文献
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An anthracene-based macrocyclic receptor has been designed and synthesized for selective recognition of 1,4-phenylenediacetate (Ka = 3.34 × 105 M?1). The macrocycle binds 1,4-phenylenediacetate selectively at the charged sites of the receptor with a concomitant increase in fluorescence of anthracene. The interaction properties of the macrocycle were evaluated by 1H NMR, UV–vis and fluorescence spectroscopic methods. 相似文献