Benzothiazole‐Pyimidine‐Based BF2 Complex for Selective Detection of Cysteine

Due to the similar structure and reactivity of cysteine (Cys), homocysteine (Hcy) and glutathione (GSH), the simultaneous discrimination of Cys over Hcy and GSH by a single fluorescent sensor is still a great challenge. In this work, a benzothiazole‐pyimidine‐based boron difluoride complex ( BPB ) was developed as a new fluorescent sensor for Cys. The sensor exhibits a highly selective “turn‐on” response to cysteine over Hcy, GSH and other amino acids in aqueous solution at physiological pH. The observed pseudo‐first‐order rate constant for the reaction of BPB with Cys was calculated to be about 0.062 min⁻¹. The detection limit of this sensor for Cys was determined to be 332 nm, and bioimaging of exogenous Cys by this sensor was successfully applied in living cells, thus indicating that this sensor holds great potential for biological applications.     

Electrochemical Label‐Free Nucleotide Sensors

Numerous researchers have devoted a great deal of effort over the last few decades to the development of electrochemical oligonucleotide detection techniques, owing to their advantages of simple design, inherently small dimensions, and low power requirements. Their simplicity and rapidity of detection makes label‐free oligonucleotide sensors of great potential use as first‐aid screening tools in the analytical field of environmental measurements and healthcare management. This review article covers label‐free oligonucleotide sensors, focusing specifically on topical electrochemical techniques, including intrinsic redox reaction of bases, conductive polymers, the use of electrochemical indicators, and highly ordered probe structures.     

A Reusable DNA Single‐Walled Carbon‐Nanotube‐Based Fluorescent Sensor for Highly Sensitive and Selective Detection of Ag+ and Cysteine in Aqueous Solutions

Here we report a reusable DNA single‐walled carbon nanotube (SWNT)‐based fluorescent sensor for highly sensitive and selective detection of Ag⁺ and cysteine (Cys) in aqueous solution. SWNTs can effectively quench the fluorescence of dye‐labeled single‐stranded DNA due to their strong π–π stacking interactions. However, upon incubation with Ag⁺, Ag⁺ can induce stable duplex formation mediated by C–Ag⁺–C (C=cytosine) coordination chemistry, which has been further confirmed by DNA melting studies. This weakens the interactions between DNA and SWNTs, and thus activates the sensor fluorescence. On the other hand, because Cys is a strong Ag⁺ binder, it can remove Ag⁺ from C–Ag⁺–C base pairs and deactivates the sensor fluorescence by rewrapping the dye‐labeled oligonucleotides around the SWNT. In this way, the fluorescence signal‐on and signal‐off of a DNA/SWNT sensor can be used to detect aqueous Ag⁺ and Cys, respectively. This sensing platform exhibits high sensitivity and selectivity toward Ag⁺ and Cys versus other metal ions and the other 19 natural amino acids, with a limit of detection of 1 nM for Ag⁺ and 9.5 nM for Cys. Based on these results, we have constructed a reusable fluorescent sensor by using the covalent‐linked SWNT–DNA conjugates according to the same sensing mechanism. There is no report on the use of SWNT–DNA assays for the detection of Ag⁺ and Cys. This assay is simple, effective, and reusable, and can in principle be used to detect other metal ions by substituting C–C base pairs with other native or artificial bases that selectively bind to other metal ions.     

Coordination Polymer Nanobelts as an Effective Sensing Platform for Fluorescence‐enhanced Nucleic Acid Detection

In this communication, the application of coordination polymer nanobelts (CPNs) assembled from H₂PtCl₆ and 3,3′,5,5′‐tetramethylbenzidine (TMB) are explored as an effective fluorescent sensing platform for nucleic acid detection for the first time. The suggested method has a high selectivity down to single‐base mismatch. DNA detection is accomplished by the following two steps: (1) CPN binds fluorecent dye‐labeled single‐stranded DNA (ssDNA) probe via both electrostatic attraction and π‐π stacking interactions between unpaired DNA bases and CPN. As a result, the fluorescent dye is brought into close proximity to CPN and substantial fluorescence quenching occurs due to photoinduced electron transfer from the nitrogen atom in CPN to the excited fluorophore. (2) The hybridization of adsorbed ssDNA probe with its target generates a double stranded DNA (dsDNA). The duplex cannot be adsorbed by CPN due to its rigid conformation and the absence of unpaired DNA bases, leading to an obvious fluorescence enhancement.

     

液相爆炸物荧光化学传感器研究进展

溶液中爆炸物的快速灵敏检测对于防恐、反恐和环境质量监测等都具有十分重要的意义。本文在介绍液相爆炸物探测用均相荧光传感器、薄膜荧光传感器和颗粒荧光传感器的基础上,简要评述了各种方法的优缺点,指出新型化学薄膜荧光传感器的开发和基于这些薄膜的低成本、多功能和高品质液相专用爆炸物探测仪的研制将成为未来液相爆炸物探测研究的一个重...     

Novel Hydrazone‐Based Tripodal Sensors: Single Selective Colorimetric Chemosensor for Acetate in Aqueous Solution

A series of novel tripodal colorimetric anion sensors based on hydrazone CHN NH groups have been synthesized and their recognition behavior with anionic guests has been studied. In DMSO solutions, sensors 1 and 2 show colorimetric responses for F⁻, H₂PO⁻₄ and AcO⁻, while in DMSO/H₂O (9:1, V/V) solutions, sensor 1 shows single selectivity for AcO⁻. ¹H NMR titration confirms that the tripodal sensors could bind anions through the collaboration of three hydrazone groups and anions residing in the central cavity of the sensors.     

Highly Selective Fluorescence Detection for Mercury (II) Ions in Aqueous Solution Using Water Soluble Conjugated Polyelectrolytes

A highly selective assay method has been developed to detect mercury (II) (Hg²⁺) ions using cationic conjugated polymer (CCP). The transduction mechanism is based on a Hg²⁺ promoted reaction. In the absence of Hg²⁺ ions, the CCP can form the complex with an anionic 1,3‐dithiole‐2‐thione derivative through electrostatic interactions. The fluorescence of CCP is efficiently quenched by 1,3‐dithiole‐2‐thione derivative via an electron transfer process. Upon adding Hg²⁺ ions, the transformation of 1,3‐dithiole‐2‐thione into 1,3‐dithiole‐2‐one inhibits the quenching, and the fluorescence of CCP is recovered. Distinguishing aspects of this assay include the signal amplification of CCPs and a specific Hg²⁺ promoted reaction. By triggering the change in the emission intensity of CCP, it is possible to detect Hg²⁺ ions in aqueous solution.

     

Naphthyl End‐Capped Terthiophene‐Based Chemiresistive Sensors for Biogenic Amine Detection and Meat Spoilage Monitoring

A reliable and sensitive detection of biogenic amines (BAs) is essential to ensure food safety and maintain public health. In this study, two naphthyl end‐capped terthiophene derivatives, namely, 5‐(naphthalen‐1‐yl)‐2,2′:5′,2′′‐terthiophene ( NA‐3T ) and 5,5′′‐di(naphthalen‐1‐yl)‐2,2′:5′,2′′‐terthiophene ( NA‐3T‐NA ), were employed to develop chemiresistive sensors for detecting gaseous BAs. In contrast to NA‐3T , the NA‐3T‐NA ‐based sensor showed a higher sensitivity for trimethylamine (TMA) with an experimental detection limit lower than 22 ppm, and for aromatic BAs, including dopamine, histamine, tryptamine, and tyramine. Additionally, the recovery time for TMA was found to be shorter than 23 s. In addition, both sensors were successfully used for an in situ evaluation of meat freshness by monitoring the concentration of relevant volatile BAs. The difference in the sensing performances of the two chemiresistive sensors was tentatively ascribed to different packing structures of the derivatives and the adlayer structures of the films developed with the compounds.     

Reaction‐Based Colorimetric and Ratiometric Fluorescence Sensor for Detection of Cyanide in Aqueous Media

A stilbene‐based compound ( 1 ) has been prepared and was highly selective for the detection of cyanide anion in aqueous media even in the presence of other anions, such as F^?, Cl^?, Br^?, I^?, ClO₄^?, H₂PO₄^?, HSO₄^?, NO₃^?, and CH₃CO₂^?. A noticeable change in the color of the solution, along with a prominent fluorescence enhancement, was observed upon the addition of cyanide. The color change was observed upon the nucleophilic addition of the cyanide anion to the electron‐deficient cyanoacrylate group of 1 . The spectral changes induced by the reaction were analyzed by comparison with two model compounds, such as compound 2 with dimethyl substituents and compound 3 without a cyanoacrylate group. An intramolecular charge‐transfer (ICT) mechanism played a key role in the sensing properties, and the mechanism was supported by DFT/TDDFT calculations.     

水合铵硼氧酸盐及其饱和溶液的FTIR和Raman光谱研究

研究了NH₄B₅O₈·4H₂O和(NH₄)₂B₈O₁₃·6H₂O及其饱和溶液于20℃的FTIR和Raman光谱,对振动频率进行了归属.根据振动光谱特征,预测(NH₄)₂B₈O₁₃·6H₂O中所含基本结构单元为[B₇O ₁₁(OH)·B(OH)₃]^2-.首次将Raman光谱中516cm^-1处的强散射峰归属为这一多聚硼氧配阴离子的对称脉冲振动峰,并对以上2种铵硼氧酸盐饱和溶液中硼氧配阴离子的存在形式{B(OH)₃,[B₃O₃(OH)₄]^-和[B₅O₆(OH)₄]^-}和相互作用机理进行了探讨.     

A pH‐Neutral,Metal‐Free Aqueous Organic Redox Flow Battery Employing an Ammonium Anthraquinone Anolyte

Redox‐active anthraquinone molecules represent promising anolyte materials in aqueous organic redox flow batteries (AORFBs). However, the chemical stability issue and corrosion nature of anthraquinone‐based anolytes in reported acidic and alkaline AORFBs constitute a roadblock for their practical applications in energy storage. A feasible strategy to overcome these issues is migrating to pH‐neutral conditions and employing soluble AQDS salts. Herein, we report the 9,10‐anthraquinone‐2,7‐disulfonic diammonium salt AQDS(NH₄)₂ , as an anolyte material for pH‐neutral AORFBs with solubility of 1.9 m in water, which is more than 3 times that of the corresponding sodium salt. Paired with an NH₄I catholyte, the resulting pH‐neutral AORFB with an energy density of 12.5 Wh L^?1 displayed outstanding cycling stability over 300 cycles. Even at the pH‐neutral condition, the AQDS(NH₄)₂ /NH₄I AORFB delivered an impressive energy efficiency of 70.6 % at 60 mA cm^?2 and a high power density of 91.5 mW cm^?2 at 100 % SOC. The present AQDS(NH₄)₂ flow battery chemistry opens a new avenue to apply anthraquinone molecules in developing low‐cost and benign pH‐neutral flow batteries for scalable energy storage.     

用于抗生素检测的纳米材料基电化学传感器研究进展

近年来,抗生素作为基本的治疗药物在医学、畜牧业、水产养殖业等方面被广泛应用,但其过量使用造成的抗生素残留问题也给生态环境、食品安全和人类健康造成严重的威胁.鉴于此,纳米电化学传感器在抗生素快速检测方面的研究成为热点,也取得了可观的进展.本文首先对抗生素进行了简单介绍,通过分析抗生素的电化学性质,综述了不同结构和类型的纳...     

A New Simple Chromo‐fluorogenic Probe for NO2 Detection in Air

A new chromo‐fluorogenic probe, consisting of a biphenyl derivative containing both a silylbenzyl ether and a N,N‐dimethylamino group, for NO₂ detection in the gas phase has been developed. A clear colour change from colourless to yellow together with an emission quenching was observed when the probe reacted with NO₂. A limit of detection to the naked eye of about 0.1 ppm was determined and the system was successfully applied to the detection of NO₂ in realistic atmospheric conditions.     

Cross‐Reactive Sensor Arrays for the Detection of Peptides in Aqueous Solution by Fluorescence Spectroscopy

A simple but powerful method for the sensing of peptides in aqueous solution has been developed. The transition‐metal complexes [PdCl₂(en)], [{RhCl₂Cp*}₂], and [{RuCl₂(p‐cymene)}₂] were combined with six different fluorescent dyes to build a cross‐reactive sensor array. The fluorescence response of the individual sensor units was based on competitive complexation reactions between the peptide analytes and the fluorescent dyes. The collective response of the sensor array in a time‐resolved fashion was used as an input for multivariate analyses. A sensor array comprised of only six metal–dye combinations was able to differentiate ten different dipeptides in buffered aqueous solution at a concentration of 50 μM . Furthermore, the cross‐reactive sensor could be used to obtain information about the identity and the quantity of the pharmacologically interesting dipeptides carnosine and homocarnosine in a complex biological matrix, such as deproteinized human blood serum. The sensor array was also able to sense longer peptides, which was demonstrated by differentiating mixtures of the nonapeptide bradykinin and the decapeptide kallidin.     

Fluorescence Turn‐On Detection of Nitric Oxide in Aqueous Solution Using Cationic Conjugated Polyelectrolytes

A fluorescent turn‐on detection for nitric oxide in aqueous solution is developed using cationic conjugated polymers. The assay benefits from the sensitivity of optical signals from conjugated polymers and the simplicity of fluorescence measurement techniques. The assay contains three elements: a cationic conjugated polymer that contains imidazole moieties, Cu²⁺ ions, and the target nitric oxide. The highly fluorescent conjugated polymer coordinates to Cu²⁺ ions through weak N · · · Cu interactions, and its fluorescence is efficiently quenched by a photo‐induced electron transfer process (‘off’ state). In the presence of nitric oxide, the transformation of the paramagnetic Cu²⁺ ion into a diamagnetic Cu¹⁺ ion inhibits the quenching and, therefore, the fluorescence of the conjugate polymer is recovered (‘on’ state). Other biologically relevant reactive nitrogen species, such as NOBF₄, NaNO₂, and NaNO₃ don't exhibit the fluorescence recovery of the conjugated polymer under the same conditions as nitric oxide. The cationic conjugated polymer/Cu²⁺ complex can thus be used as a platform to detect nitric oxide in aqueous solution with high sensitivity and selectivity.

     

Bulk Aggregation Based Fluorescence Turn‐On Sensors for Selective Detection of Progesterone in Aqueous Solution

Steroids are polycyclic compounds that share tetracyclic ring as core scaffold, and selective detection of a steroid is challenging owing to their structural similarities. The discovery of chemosensors that recognize progesterone by alteration of self‐aggregation state is described, and these show significant fluorescence turn‐on. A self‐aggregated 48‐membered dansyl library was screened against a series of metabolites in aqueous buffer and discovered two compounds ( PG‐1 , PG‐2 ) exhibited exceptional selectivity for progesterone. Following studies of aggregation properties of probes using dynamic light scattering and transmission electron microscopy supports progesterone recognition lead to the generation of bulk aggregates that induce fluorescence enhancement. Though many fluorescence sensing mechanisms have been proposed, a sensing mode based on the bulk aggregate formation of fluorophore has never been reported, and this may open a new avenue of chemosensor design.     

Sensors Based on SNO2 As a Detector for CO Oxidation in Air

This work describes properties of sensors based on SnO₂ , which were used as detectors in the temperature-programmed surface reaction (TPSR) of CO oxidation. Usually, the detection in temperature-programmed processes is realized by using TCD (katharometer) or a mass spectrograph. In our work we present preliminary results which show that the sensors manufactured from SnO₂ can also be used to this aim.     

Ratiometric Single‐Nanoparticle Oxygen Sensors for Biological Imaging

It makes sense : Conjugated polymer nanoparticles doped with a platinum porphyrin dye exhibit bright phosphorescence that is highly sensitive to the concentration of molecular oxygen. The small size, extraordinary brightness, excellent sensitivity, and ratiometric emission, together with the demonstration of single‐particle sensing and cellular uptake, indicate the potential of the nanoparticle sensors for quantitative mapping of local molecular oxygen concentration.