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31.
Dilsat Ozkan‐Ariksoysal Ozlem Akgul Seyma Aydinlik Seda Nur Topkaya Nilay Aladag Mehmet Ozsoz 《Electroanalysis》2010,22(19):2225-2234
In this work, an electrochemical DNA‐based sensor was developed for the detection of the interaction between the anticonvulsant compounds 2‐phthalimido‐N‐substituted phenylethanesulfonamides (PMPES‐derivatives) and 24‐mer short DNA sequences by using differential pulse voltammetry (DPV) based on both compound and guanine oxidation signals at the renewable carbon graphite electrode (CGE) surface. The influence of compounds on DNA showed differences depending on the nature and position of the substituent on the N‐phenyl ring. Compounds bearing 3‐methoxy, 4‐chloro and 2,6‐dimethyl substituents bind to single stranded probe DNA more strongly than the other derivatives of PMPES. Thus, these compounds were evaluated for use as an electrochemical hybridization label (indicator). 相似文献
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Three novel donor-acceptor-donor type random copolymers based on benzothiadiazole (BTh) and benzoselenadiazole (BSe) were synthesized via Pd (0) catalyzed Suzuki polycondensation reaction. The two acceptor units were coupled with electron rich moieties which are carbazole (CZ), fluorene (FL) and silafluorene (SiFL). Monomers were characterized using 1H and 13C-NMR spectroscopy. The number and weight average molecular weights of the polymers were calculated using gel permeation chromatography (GPC). All three polymers were electrochemically and spectroelectrochemically characterized. PBThBSeCZ, PBThBSeFL and PBThBSeSiFL showed only p-dopable character and their doping/dedoping potentials were determined as 1.4 V/1.2 V, 1.53 V/1.27 V and 1.8 V/1.3 V, respectively. Corresponding HOMO energy levels were calculated as ?5.85 eV, ?6.05 eV and ?6.15 eV whereas LUMO energy levels were found to be ?3.67 eV, ?3.84 eV and ?3.77 eV, respectively. PBThBSeCZ had lower HOMO level and band gap than PBThBSeFL and PBThBSeSiFL due to its increased electron donating capability of nitrogen atom in carbazole unit. 相似文献
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Electrochemical Biosensors for Cancer Biomarkers Detection: Recent Advances and Challenges 下载免费PDF全文
Biomarkers are described as characteristics that provide information about biological conditions whether normal or pathological. Detection of biomarkers at the earliest stage of the cancer is of utmost importance for clinical diagnosis. Electrochemical biosensors allow detecting the low levels of specific analytes in blood, urine or saliva and providing a sensitive approach for direct measurement for cancer biomarker detection. Moreover, the integration of electrochemical devices with nanomaterials, such as carbon nanotubes, gold and magnetic particles offer amplification and multiplexing capabilities for simultaneous measurements of cancer biomarkers very sensitively. This review summarizes the recent developments of electrochemical biosensors systems for the detection of cancer biomarkers with emphasis on voltammetric, amperometric and impedimetric biosensors. A special attention is paid to aptamers and miRNAs that are very promising for the ultra‐sensitive and specific cancer biomarker detection. 相似文献
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In this work, using lacunary sequences and the notion of ideal convergence we define and examine new sequence spaces with respect to a sequence of modulus functions in n-normed linear spaces. Further, the definition of Iθ-convergence in n-normed linear spaces and some related results are given. 相似文献
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A new voltammetric method, based on the use of single‐use pencil graphite electrode, was developed for the quantitative determination of cefdinir by square wave voltammetry. Chemometric optimization strategy was used to select the suitable values for three experimental parameters (pH of the supporting electrolyte, frequency and square wave amplitude) by applying a 33 full factorial design model. The optimal voltammetric conditions were found to be pH 5.0 for supporting electrolyte (Britton‐Robinson buffer), 43 mV for square wave amplitude and 108 Hz for frequency. Square wave voltammograms of calibration, validation and unknown samples were recorded between 0.0–1400 mV under the optimized voltammetric conditions. Linear regression equation was computed in the linear working range of 0.5–20 μg/mL by using the relationship between the concentration and peak current at 600 mV. The optimized voltammetric method was validated by assessing the analysis results of validation samples. Then the proposed method was applied for the quantitative determination of cefdinir in three different pharmaceutical preparations, namely film‐coated tablets, effervescent tablets and powder for oral suspension. It was concluded that the proposed voltammetric method was suitable for the quantitative analysis of commercial pharmaceutical preparations containing cefdinir. 相似文献
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Metal–organic framework (MOF)/polymer mixed matrix membranes (MMMs) have received significant interest in the last decade. MOFs are incorporated into polymers to make MMMs that exhibit improved gas permeability and selectivity compared with pure polymer membranes. The fundamental challenge in this area is to choose the appropriate MOF/polymer combinations for a gas separation of interest. Even if a single polymer is considered, there are thousands of MOFs that could potentially be used as fillers in MMMs. As a result, there has been a large demand for computational studies that can accurately predict the gas separation performance of MOF/polymer MMMs prior to experiments. We have developed computational approaches to assess gas separation potentials of MOF/polymer MMMs and used them to identify the most promising MOF/polymer pairs. In this Personal Account, we aim to provide a critical overview of current computational methods for modeling MOF/polymer MMMs. We give our perspective on the background, successes, and failures that led to developments in this area and discuss the opportunities and challenges of using computational methods for MOF/polymer MMMs. 相似文献
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Spannhoff K Kehr G Kehr S Fröhlich R Erker G 《Dalton transactions (Cambridge, England : 2003)》2008,(25):3339-3344
Staudinger reaction of dppm-CN (5) gave the corresponding bis(N-phenylphosphinimino)acetonitrile system (6). Deprotonation with LDA furnished the corresponding anionic ligand 9. Its reaction with [(CO)(2)RhCl](2) gave the corresponding kappa(2)N,N'-chelate complex 11. X-Ray diffraction revealed a non-planar boat-like conformation of the six-membered chelate ring in the crystal. Treatment of 9 with [(nbd)RhCl](2) gave the six-membered chelate complex 12 which features a different twist-like structure in the solid state, as does 13, which was formed by reacting 9 with [(cod)IrCl](2). 相似文献