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21.
Jinting Zhou Wei Lu Fangyu Hu Mengyu Zhang Liming Jiang Zhiquan Shen 《Journal of polymer science. Part A, Polymer chemistry》2014,52(16):2248-2257
A novel AB type of clickable monomer, (S)‐2‐[(2‐azido‐1‐phenylethylimino)methyl]‐5‐propargyloxyphenol (AMPP) was designed and polymerized to yield a class of main‐chain chiral poly(imine‐triazole)s through the metal‐free click reaction. With the thermally induced polymerization, the desired polytriazoles can be easily prepared in high yields by a stepwise heating‐up process and have the number‐average molecular masses ranging from 5.1 × 103 to 58.1 × 103 (polydispersity indices = 1.38?1.68). The polymers were characterized by Fourier Transform Infrared spectroscopy (FTIR), 1H Nuclear Magnetic Resonance (NMR), and gel permeation chromatography, and their optical properties were studied by fluorescence and circular dichroism (CD) spectroscopies. As a chemosensor, these polymers exhibited a selective “turn‐on” fluorescence enhancement response toward Zn2+ ion over other cations such as Na+, K+, Mg2+, Ca2+, Ag+, Pb2+, Cd2+, Hg2+, Mn2+, and Ni2+ in dimethyl sulfoxide. However, the Zn2+‐induced fluorescence signal was subject to serious interference by Al3+, Cu2+, Cr3+, and Fe3+ ions. Interestingly, the chiral polymer showed distinctive changes in the CD spectra on complexation with Zn2+, which allowed for the discrimination of this ion in the presence of other species tested including those interfering ions observed in the fluorescent detection. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 2248–2257 相似文献
22.
Electrospun Nanofibers from a Tricyanofuran‐Based Molecular Switch for Colorimetric Recognition of Ammonia Gas 下载免费PDF全文
Dr. Tawfik A. Khattab Dr. Sherif Abdelmoez Prof. Dr. Thomas M. Klapötke 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(12):4157-4163
A chromophore based on tricyanofuran (TCF) with a hydrazone (H) recognition moiety was developed. Its molecular‐switching performance is reversible and has differential sensitivity towards aqueous ammonia at comparable concentrations. Nanofibers were fabricated from the TCF–H chromophore by electrospinning. The film fabricated from these nanofibers functions as a solid‐state optical chemosensor for probing ammonia vapor. Recognition of ammonia vapor occurs by proton transfer from the hydrazone fragment of the chromophore to the ammonia nitrogen atom and is facilitated by the strongly electron withdrawing TCF fragment. The TCF–H chromophore was added to a solution of poly(acrylic acid), which was electrospun to obtain a nanofibrous sensor device. The morphology of the nanofibrous sensor was determined by SEM, which showed that nanofibers with a diameter range of 200–450 nm formed a nonwoven mat. The resultant nanofibrous sensor showed very good sensitivity in ammonia‐vapor detection. Furthermore, very good reversibility and short response time were also observed. 相似文献
23.
An Easy Access to Organic Salt‐Based Stimuli‐Responsive and Multifunctional Supramolecular Hydrogels 下载免费PDF全文
Dr. Joydeb Majumder Prof. Dr. Parthasarathi Dastidar 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(27):9267-9276
By exploiting orthogonal hydrogen bonding involving supramolecular synthons and hydrophobic/hydrophilic interactions, a new series of simple organic salt based hydrogelators derived from pyrene butyric acid and its β‐alanine amide derivative, and various primary amines has been achieved. The hydrogels were characterised by microscopy, table‐top rheology and dynamic rheology. FTIR, variable‐temperature 1H NMR and emission spectroscopy established the role of various supramolecular interactions such as hydrogen bonding and π–π stacking in hydrogelation. Single‐crystal X‐ray diffraction (SXRD) studies supported the conclusion that orthogonal hydrogen bonding involving amide–amide and primary ammonium monocarboxylate (PAM) synthons indeed played a crucial role in hydrogelation. The hydrogels were found to be stimuli‐responsive and were capable of sensing ammonia and adsorbing water‐soluble dye (methylene blue). All the hydrogelators were biocompatible (MTT assay in RAW 264.7 cells), indicating their suitability for use in drug delivery. 相似文献
24.
Makoto Obata Ryo Asato Kazunori Mitsuo Shiho Hirohara 《Journal of polymer science. Part A, Polymer chemistry》2014,52(7):963-972
Three CF3‐substituted methyl methacrylates (MMAs), 2,2,2‐trifluoroethyl methacrylate (TFEMA), 1,1,1,3,3,3‐hexafluoroisopropyl methacrylate (HFIPMA) and nonafluoro‐tert‐butyl methacrylate (NFTBMA), were polymerized by conventional radical polymerization to give oxygen‐permeable polymers for application in pressure‐sensitive paint (PSP). The radical copolymerizations of styrene with TFEMA, HFIPMA, or NFTBMA were carried out to examine the effect of CF3 groups on the polymerizability. The e values increased in the order of MMA (0.40) < TFEMA (0.76) < HFIPMA (1.19) < NFTBMA (1.31). The homopolymers of TFEMA, HFIPMA and NFTBMA (PTFEMA, PHFIPMA, and PNFTBM, respectively) were examined as polymers for use in PSP using 5,10,15,20‐tetrakis(pentafluorophenyl)porphinato platinum(II) (PtTFPP). The PSP consisting of PNFTBMA and PtTFPP exerted very high pressure sensitivity and very low temperature sensitivity. In the absence of oxygen, the temperature sensitivity decreased in the order of PTFEMA > PHFIPMA > PNFTBMA = PMMA, which corresponds to the order of glass transition temperatures (Tg). However, the activation energies of the overall process of the luminescence quenching by oxygen were found to be 16.8 (PMMA), 13.0 (PTFEMA), 6.8 (PHFIPMA), and 4.3 kJ mol?1 (PNFTBMA). Therefore, the low temperature sensitivity of PNFTBMA was attributed to its high degree of substitution with CF3 groups and to its relatively high Tg value. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2014 , 52, 963–972 相似文献
25.
Photocatalytically Renewable Micro‐electrochemical Sensor for Real‐Time Monitoring of Cells 下载免费PDF全文
Jia‐Quan Xu Yan‐Ling Liu Qian Wang Huan‐Huan Duo Xin‐Wei Zhang Dr. Yu‐Tao Li Prof. Wei‐Hua Huang 《Angewandte Chemie (International ed. in English)》2015,54(48):14402-14406
Electrode fouling and passivation is a substantial and inevitable limitation in electrochemical biosensing, and it is a great challenge to efficiently remove the contaminant without changing the surface structure and electrochemical performance. Herein, we propose a versatile and efficient strategy based on photocatalytic cleaning to construct renewable electrochemical sensors for cell analysis. This kind of sensor was fabricated by controllable assembly of reduced graphene oxide (RGO) and TiO2 to form a sandwiching RGO@TiO2 structure, followed by deposition of Au nanoparticles (NPs) onto the RGO shell. The Au NPs‐RGO composite shell provides high electrochemical performance. Meanwhile, the encapsulated TiO2 ensures an excellent photocatalytic cleaning property. Application of this renewable microsensor for detection of nitric oxide (NO) release from cells demonstrates the great potential of this strategy in electrode regeneration and biosensing. 相似文献
26.
Jun‐Seok Lee Jae Wook Lee Namyoung Kang Hyung‐Ho Ha Young‐Tae Chang 《Chemical record (New York, N.Y.)》2015,15(2):495-510
Synthetic molecules that modulate and probe biological events are critical tools in chemical biology. Utilizing combinatorial and diversity‐oriented synthetic strategies, access to large numbers of small molecules is becoming more and more feasible, and research groups in this field can take advantage of the power of chemical diversity. Since the majority of early studies were focused on the discovery of compounds that perturb protein functions, diversity‐based approaches are often considered as therapeutic lead discovery tactics. However, the diversity‐oriented approach can also be applied to advance distinct aims, such as target protein identification, or the development of imaging probes and sensors. This review provides a personal perspective of the chemical‐diversity‐based approach and how this principle can be adapted to various chemical biology studies. 相似文献
27.
Iron(III)‐Selective Chelation‐Enhanced Fluorescence Sensing for In Vivo Imaging Applications 下载免费PDF全文
Lin E. Guo Xin Yi Liu Huan Wang Qiu Ling Chen Guang Ke Wang Prof. Kaijun Luo Qi Li Mi Prof. Ying Zhou Jun Feng Zhang 《化学:亚洲杂志》2015,10(9):1898-1902
A “turn‐on” pattern Fe3+‐selective fluorescent sensor was synthesized and characterized that showed high fluorescence discrimination of Fe3+ over Fe2+ and other tested ions. With a 62‐fold fluorescence enhancement towards Fe3+, the probe was employed to detect Fe3+ in vivo in HeLa cells and Caenorhabditis elegans, and it was also successfully used to elucidate Fe3+ enrichment and exchange infected by innexin3 (Inx3) in hemichannel‐closed Sf9 cells. 相似文献
28.
The covalent boron–diol interaction enables elaborate design of boronic acid‐based saccharide sensors. Over the last decade, this research topic has been well developed thanks to the integration of boronic acid chemistry with a range of techniques, including supramolecular chemistry, materials chemistry, surface modification, and nanotechnology. New sensing strategies and platforms have been introduced and remarkable progress has been achieved to fully utilize the unique property of boron–diol interaction and to improve the binding affinity towards different targets, especially under physiological conditions. In this review, the latest progress over the past 30 months (from late 2012 to early 2015) is highlighted and discussed to shed light on this versatile and promising platform for saccharide sensing. 相似文献
29.
A Nanoscale Multiresponsive Luminescent Sensor Based on a Terbium(III) Metal–Organic Framework 下载免费PDF全文
Dr. Song Dang Dr. Ting Wang Dr. Feiyan Yi Dr. Qinghui Liu Dr. Weiting Yang Prof. Zhong‐Ming Sun 《化学:亚洲杂志》2015,10(8):1703-1709
A nanoscale terbium‐containing metal–organic framework ( nTbL ), with a layer‐like structure and [H2NMe2]+ cations located in the framework channels, was synthesized under hydrothermal conditions. The structure of the as‐prepared sample was systematically confirmed by powder XRD and elemental analysis; the morphology was characterized by field‐emission SEM and TEM. The photoluminescence studies revealed that rod‐like nTbL exhibited bright‐green emission, corresponding to 5D4→7FJ (J=6–3) transitions of the Tb3+ ion under excitation. Further sensing measurements revealed that as‐prepared nTbL could be utilized as a multiresponsive luminescent sensor, which showed significant and exclusive detection ability for Fe3+ ions and phenylmethanol. These results highlight the practical applications of lanthanide‐containing metal–organic frameworks as fluorescent probes. 相似文献
30.
Luminescent Nanofibers Fabricated from Phenanthroimidazole Derivatives by Organogelation: Fluorescence Response towards Acid with High Performance 下载免费PDF全文
Jiang Peng Dr. Jingbo Sun Peng Gong Dr. Pengchong Xue Zhenqi Zhang Gonghe Zhang Prof. Ran Lu 《化学:亚洲杂志》2015,10(8):1717-1724
Nanofibers based on phenanthroimidazole derivatives PCC , PDC , and PSC were fabricated by organogelation processes, and their fluorescence sensory properties towards acid were investigated. It was found that the emission of PCC in the nanofiber‐based film could be quenched significantly upon exposure to gaseous TFA due to the formation of protonated PCC , in which ICT (intramolecular charge transfer) would occur. On the other hand, TFA vapor led to the emitting colors of PDC and PSC in the nanofiber‐based films to turn to yellow and green from sky blue and blue, respectively. Additionally, we found that the decay times of PCC were 0.1 s and 1.9 s in probing the saturated vapor of TFA in nanofiber‐based film and in spin‐coated film, respectively. The results suggested that the high surface‐to‐volume ratio and large interspace in the nanofiber‐based networks favored the enhanced adsorption, accumulation, and diffusion of gaseous molecules, resulting in such a high performance. 相似文献