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621.
A one step process for simultaneous reduction and functionalization of graphene oxide using tetrathiafulvalene (TTF) is described. Chemical oxidation of TTF to TTF(2+) using an aqueous solution of Fe(ClO(4))(3) expels the charged molecule from the graphene nanosheets, while subsequent immersion in neutral TTF solution allows the capture of the TTF molecules.  相似文献   
622.
A molecular engineering strategy based on rational variations of the bromine substitution pattern in two-photon absorbing singlet oxygen sensitizers allows studying the relations that exist between the positioning of an inter-system crossing promoter on the charge-transfer chromophore and its ability to generate singlet oxygen.  相似文献   
623.
The flavonoid quercetin is known to reduce the α-tocopheroxyl radical (˙TocO) and reconstitute α-tocopherol (TocOH). Structurally related polyphenolic compounds, hydroxy-2,3-diarylxanthones (XH), exhibit antioxidant activity which exceeds that of quercetin in biological systems. In the present study repair of ˙TocO by a series of these XH has been evaluated using pulse radiolysis. It has been shown that, among the studied XH, only 2,3-bis(3,4-dihydroxyphenyl)-9H-xanthen-9-one (XH9) reduces ˙TocO, though repair depends strongly on the micro-environment. In cationic cetyltrimethylammonium bromide (CTAB) micelles, 30% of ˙TocO radicals are repaired at a rate constant of ~7.4 × 10(6) M(-1) s(-1) by XH9 compared to 1.7 × 10(7) M(-1) s(-1) by ascorbate. Water-soluble Trolox (TrOH) radicals (˙TrO) are restored by XH9 in CTAB (rate constant ~3 × 10(4) M(-1) s(-1)) but not in neutral TX100 micelles where only 15% of ˙TocO are repaired (rate constant ~4.5 × 10(5) M(-1) s(-1)). In basic aqueous solutions ˙TrO is readily reduced by deprotonated XH9 species leading to ionized XH9 radical species (radical pK(a) ~10). An equilibrium is observed (K = 130) yielding an estimate of 130 mV for the reduction potential of the [˙X9,H(+)/XH9] couple at pH 11, lower than the 250 mV for the [˙TrO,H(+)/TrOH] couple. A comparable value (100 mV) has been determined by cyclic voltammetry measurements.  相似文献   
624.
The construction of a spatio-temporal wavelet and its tuning to speed was first realized in the 90s on the Morlet wavelet by Duval-Destin (1991, 1993) [14], [15]. This enabled to demonstrate the capacities of the speed-tuned Morlet for psychovisual analysis. This construction was also used very efficiently in a powerful aerial target tracking algorithm by Mujica et al. (1999, 2000) [20], [21]. In the last decade, this tool was proposed as an elegant and efficient alternative framework to the Optical Flow (OF), the Block Matching (BM) or the phase difference, for the study of motion estimation in image sequences. Nevertheless, the aperture selectivity of the 2D + T Morlet wavelet presents some difficulties. Here we propose to replace the 2D Morlet wavelet by a Gaussian-Conical (GC) wavelet for the spatial part of the spatio-temporal wavelet, since the GC wavelet has a better aperture selectivity and allows a very simple adjustment of the aperture. Therefore we build a new, highly directional, speed-tuned wavelet called Gaussian-Conical–Morlet (GCM) wavelet. Like the speed-tuned 2D + T Morlet, the new wavelet presents very good characteristics in motion estimation and tracking, namely long temporal dependence, robustness to noise and to occlusions, and supersedes the OF (Optical Flow) and BM (Block Matching) techniques. However, for aperture selectivity, directional speed-capture and spectral recognition and tracking, GCM easily outperforms Morlet. This paper describes the GCM construction, utilization and aperture performances.  相似文献   
625.
A method has been developed for the analysis and characterization in equine urine and plasma of iridoid glycosides: harpagide, harpagoside and 8-para-coumaroyl harpagide, which are the main active principles of Harpagophytum, a plant with antiinflammatory properties. The method involves liquid chromatography coupled with positive electrospray ionization mass spectrometry. The addition of sodium or lithium chloride instead of formic acid in the eluting solvent has been studied in order to enhance the signal and to modify the ion's internal energy. Fragmentation pathways and associated patterns are proposed for each analyte. A comparison of three types of mass spectrometer: a 3D ion trap, a triple quadrupole and a linear ion trap, has been conducted. The 3D ion trap was selected for drug screening analysis whereas the linear ion trap was retained for identification and quantitation analysis.  相似文献   
626.
The combined use of an automatic solid-phase extraction (SPE) apparatus with Oasis MCX cartridges and gas chromatography/mass spectrometry (GC/MS) to rapidly quantify quinine in biological samples with cyproheptadine as the internal standard is described. The selected ion monitoring mode, with the quantification ions m/z 136 and 287 (qualifier ions: m/z 261, 381 and 215, 96), allows the estimation of quinine levels, respectively. Separation was completed within 12.7 min. Excellent linearity was found up to 10 000 microg/L of plasma. The limit of detection (LOD) was 12.2 microg/L and the limit of quantification (LOQ) was 40.6 microg/L. High reproducibility (intra-assay CV range 1.9-4.3%, inter-assay CV range 2.2-11.3%) and accuracy values (intra-assay range 83.2-103.7%, inter-assay range 86.8-103.7%) were obtained. Recoveries were concentration-independent (97.2% and 89.8% for 4000 and 10 000 microg/L, respectively). This sensitive, simple assay for quinine in various matrices meets the current requirements for bioanalytical assays and may be used to monitor quinine levels in patients developing severe malaria with acute renal failure during hemofiltration. The optimal quinine dose in this situation is not really established and to improve clinical care, quinine concentrations might be explored to improve efficacy and minimise potential toxicity.  相似文献   
627.
Mixed monolayer protected gold nanoparticles have been fabricated incorporating 1,5-dialkyloxynaphthalene moieties that are capable of forming complexes with the tetracationic cyclophane cyclobis(paraquat-p-phenylene); electrochemical reduction of the cyclophane or the addition of tetrathiafulvalene results in disassembly of the complexes.  相似文献   
628.
629.
[structure: see text] A convergent and rapid stereoselective synthesis of (-)-spongidepsin has been achieved from the Roche ester in 14 steps with an overall yield of 13%.  相似文献   
630.
[reaction: see text] A new self-complexing donor-acceptor system has been synthesized that has the propensity to undergo intramolecular decomplexation under thermal and electrochemical perturbation and upon addition of a competitive guest for the cyclophane's cavity.  相似文献   
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