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发明领域
本发明一方面介绍一些荧光单体,另一方面还提供了含有这些荧光单体的标记处理聚合物。同时还介绍了在工业水处理中使用这些标记处理聚合物的方法。 相似文献
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水溶性荧光聚合物的合成和应用 总被引:1,自引:0,他引:1
综述了丙烯酰胺类水溶性荧光聚合物的合成方法,应用,理论研究及最新进展。这类聚合物可通过可参与聚合的荧光染料及其标记的单体与丙烯酰胺类水溶性单体共聚,或荧光染料与丙烯酰胺类水溶性聚合物及其衍生物反应制得。这类聚合物的荧光检测下限已达到0.1×10^_6-0.01×10^-6g/g。 相似文献
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先以丙烯腈和丙烯酸为单体合成聚合物(Polymer-1),用荧光染料对聚合物进行接枝改性后得到聚合物(Polymer-2);然后将这两种聚合物通过静电纺丝法制备出纳米纤维毡。研究了单体配比对Polymer-1共聚物粘均分子质量的影响;用DSC和IR测试手段对聚合物结构进行表征,用SEM和荧光光谱分析(FS)测试手段对纳... 相似文献
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含氟丙烯酸酯聚合物的特性与应用 总被引:7,自引:0,他引:7
1前言含氟丙烯酸酯和通常的非氟系丙烯酸酯单体一样有优良的均聚合性和与其他单体的共聚合性,并且用各种丙烯酸或丙烯酰卤与多种不同醇合成多种多样结构的单体。合成方法简单,所以是可以合成有氟或氟烷基的功能性聚合物的极有用的单体。这些含氟聚合物有独特的表面特性,故广泛用作纤维的憎水、增油处理剂,利用其光、电等其他功能性的用途也很多。本文介绍主要的含氟丙烯酸酯聚合物最近的物性研究与应用动向。2主要的含氟丙烯酸酯聚合物含氟丙烯酸酯聚合物中有酯部分的醇是含氟的和/或主链中含氟或氟烷基的(图1)。最常用的是聚(甲基… 相似文献
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采用合成的Eu-NTA和对二氨基联苯(ODA)为单体,亚磷酸三苯酯(TPP)和吡啶(Py)为浓缩剂,用溶液聚合的方法制备出具有荧光性能的聚合物Eu-NTA-co-ODA。对所合成聚合物利用红外光谱、溶解性能测试、XRD、紫外光谱与荧光光谱等手段进行了表征。通过红外光谱分析表明,聚合物Eu-NTA-co-ODA成功合成,Eu3+与聚合物体系中羰基发生了作用。通过荧光光谱分析表明Eu-NTA-co-ODA与Eu-NTA的荧光谱带的位置和形状基本相同,都反映了Eu3+的特征发射,位于592nm处的荧光发射为Eu3+的5D0→7F1磁偶极跃迁峰,出现在618nm处的跃迁为Eu3+的5D0→7F2电偶极跃迁峰,强度高于磁偶极跃迁峰,表现出红色荧光。 相似文献
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Ashootosh Vasant Ambade Britto Selvaraj Sandanaraj Akamol Klaikherd S Thayumanavan 《Polymer International》2007,56(4):474-481
This review discusses recent advances in protein sensing using fluorescent polyelectrolytes that are mainly water‐soluble conjugated polymers. A quencher‐labeled substrate or fluorophore‐labeled substrate is generally used as a probe. In the presence of an enzyme, the linker between substrate and quencher/fluorophore is cleaved and fluorescence of the polymer is either ‘turned on’ or ‘turned off’. Fluorescence behavior of these conjugated polymers is highly sensitive to conformation of the polymeric chains. Since upon binding with proteins the conformation is perturbed and fluorescence is affected, these polyelectrolytes have been used to study conformational changes in proteins. The conformation‐dependent fluorescence is also a limitation for these sensors in some cases and non‐conjugated polyelectrolytes have been shown to provide an alternative. Copyright © 2006 Society of Chemical Industry 相似文献
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Four novel hyperbranched polymers with 4 or 5 ring-closed rhodamine units in each were achieved through RAFT polymerization followed by modification with rhodamine moieties. The solubility, thermostability, and photophysical properties of the polymers were studied. The polymers showed high selectivity and sensitivity to Fe3+ among various metal ions in CH3CN/H2O (75/25, v/v) and could signal Fe3+ through multichannels: emerging a new absorption around 558 nm, over 30 nm fluorescence redshift and significant fluorescence enhancement (including 33–37 folds in intensity and 8.3–12.8 folds in quantum yield), accompanied by visual and fluorescent color changes. The polymers could be applied in the analysis of Fe3+ in real water samples. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48933. 相似文献
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苯乙烯马来酸酐共聚物(SMA)化学改性制备荧光聚合物及其荧光性能研究 总被引:4,自引:0,他引:4
用自行合成的2-氨基噻唑(1),2-氨基-4-苯基噻唑(2),2-氨基苯并噻唑(3)等荧光小分子化合物,与商品化的苯乙烯马来酸酐共聚物(SMA)中的酸酐基团反应,制成聚苯乙烯马来酰亚胺(SMI),实现了SMA化学改性,在获得荧光聚合物的同时,不仅保持了原SMA的可溶性,成膜性等优点,其热性能也得到了改善,通过示差扫描量热(DSC),凝胶色谱(GPC),红外,紫外及荧光光谱等手段表征了荧光聚合物的玻璃化转变温度,分子量及结构与荧光性能关系。 相似文献
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Facile enzymatic preparation of fluorescent conjugated polymers of phenols and their application in sensing
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Weeradech Kiratitanavit Ferdinando F. Bruno Jayant Kumar Ramaswamy Nagarajan 《应用聚合物科学杂志》2018,135(30)
The recognized drawback of utilizing metal catalysts for the synthesis of fluorescent conjugated polymers (CP) is the requirement for extensive purification to ensure complete removal of residual catalyst that would otherwise quench the fluorescence. In addition, typical synthesis of fluorescent CP involves multiple steps, monomers and solvents with varying levels of toxicity. This work demonstrates the possibility of utilizing oxidoreductase enzymes as the catalyst, for the one step polymerization of naturally occurring phenols to yield fluorescent conjugated polyphenols. The metal in the active site of the enzyme remains chelated during the synthesis allowing the polymers to be fluorescent as synthesized without the need for extensive purification. Three natural phenols, 4‐hydroxyphenylacetic acid, hydroxytyrosol, and chlorogenic acid were polymerized using Horseradish peroxidase as the biocatalyst. Spectroscopic techniques, UV–vis, Fourier transform infrared Spectroscopy–Attenuated Total Reflectance, and fluorescence, are used to characterize chemical structure and photoluminescence of these polymers. The polyphenols exhibit fluorescence with significant stokes shift in the range 30–100 nm rendering them useful in fluorescence quenching‐based sensors. Preliminary studies on use of these polymers, in the detection of nitro‐aromatic compounds in solution through using fluorescence‐quenching are also presented. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46496. 相似文献
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Norman C. Billingham Paul D. Calvert Jeremy B. Knight Timothy G. Ryan 《Polymer International》1979,11(3):155-159
The experimental requirements for ultraviolet and fluorescence microscopy are briefly discussed. The application of these techniques to polymers usually depends upon the use of some form of staining reagent to develop contrast within the polymer and three variations of this principle are described. In the first, ultraviolet absorbing or fluorescent additives are monitored during spherulitic crystallisation of a polymer with quantitative results which demonstrate rejection of the additive by the crystalline polymer and allow the diffusion coefficient for the additive in the molten polymer to be estimated. In the second application, the equilibrium distribution of absorbing additives after crystallisation is used to reveal crystallinity variations within the sample and to study the influence of non-crystallisable fractions upon these variations. Finally, reaction of carbonyl groups, with fluorescent or absorbing reagents, in oxidised polymers, has been investigated as a way of revealing uneven oxidation in polypropylene. 相似文献
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Fu‐Mian Li Qing‐Yu Gao Fu‐Sheng Du Geng‐Xu Yang Fu‐Lian Zhang Ju‐Xian Zhang Zi‐Chen Li 《应用聚合物科学杂志》2000,76(1):19-28
Two acrylic monomers bearing a pyrimidinyl moiety, N‐acryloyl‐N′‐2‐pyrimidinylpiperazine (APMP) and N‐methacryloyl‐N′‐2‐pyrimidinylpiperazine (MPMP), are prepared by reactions of N‐2‐pyrimidinylpiperazine with corresponding acryloyl chlorides in the presence of triethylamine. APMP and MPMP can be polymerized either by using radical initiators such as azobisisobutylonitrile or potassium persulfate (KPS) or by UV light irradiation without any sensitizer. APMP, MPMP, and their polymers are water soluble and liposoluble. They can act as sensitizers to initiate the photopolymerizations of acrylonitrile (AN) in DMF and acrylamide (AAm) or N‐acryloylmorpholine (AMPL) in an aqueous medium. They can also act as one component of a redox initiation system by combining with KPS to initiate the polymerization of AAm in an aqueous medium, and a superhigh molecular weight up to 106–107 for P(AAm) or 105–106 for P(AMPL) is obtained. The above polymerizations are pursued kinetically. The mechanism of the photopolymerizations initiated by MPMP or P(MPMP) are confirmed by an electron spin resonance study. By the fluorescent analysis of PAN and P(AAm) initiated by MPMP, APMP, or their polymers we confirm that they not only initiate the polymerization but also enter the polymer chains. The fluorescence spectra of MPMP, APMP, and their polymers are recorded. A fluorescence structural self‐quenching effect is also observed. The fluorescence of P(MPMP) can be quenched by adding electron‐deficient unsaturated compounds such as methacrylonitrile, AN, fumaronitrile, tetracyanoethylene, methyl acrylate, and methyl methacrylate and the correlation between the Stern–Volmer constants and the electron deficiency of the quenchers is described. The fluorescence quenching of P(MPMP) by a water‐soluble C60 derivative is also demonstrated. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 76: 19–28, 2000 相似文献
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Six new fluorescent monomers were synthesized by reaction of 2‐(5′‐amino‐2′‐hydroxyphenyl)benzazole derivatives with acryloyl chloride and allyl bromide. UV–vis and steady‐state fluorescence in solution were used to characterize its photophysical behavior. The monomers are fluorescent in the blue, green, yellow, and red region, with a large Stokes shift between 92 and 226 nm. A dual fluorescence ascribed to a conformational equilibrium in solution in the ground state dependent on the solvent polarity could be observed in the fluorescence emission spectra of the monomers. The radical polymerization of the monomers with methyl(methacrylate) allowed the production of fluorescent polymers in the blue–green region, with good optical and thermal properties. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci, 2006 相似文献