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排序方式: 共有197条查询结果,搜索用时 31 毫秒
91.
The identification and application of (+)-(2R,3R)-1,1,4,4-tetraphenylbutane-1,2,3,4-tetrol (TETROL) as an efficient and selective host compound is described. Computational and single crystal X-ray diffraction analyses revealed that the butane backbone of TETROL adopts a relatively rigid anti-conformation, with the hydroxy groups oriented syn and connected through a cyclic, homodromic arrangement of their O–H bonds. This structure is stabilised through a pair of 1,3-hydrogen bonding interactions. TETROL forms inclusion complexes with pyridine and 3- and 4-methylpyridine, and does so selectively from mixtures of the pyridines. X-ray diffraction (single crystal and powder) and thermal analyses of the inclusion compounds are described. 相似文献
92.
MM Ottakam Thotiyl H Basit JA Sánchez C Goyer L Coche-Guerente P Dumy S Sampath P Labbé JC Moutet 《Journal of colloid and interface science》2012,383(1):130-139
Multilayers of poly(diallyldimethylammonium chloride) (PDDA) and citrate capped Au nanoparticles (AuNPs) anchored on sodium 3-mercapto-1-propanesulfonate modified gold electrode by electrostatic layer-by-layer assembly (LbL) technique are shown to be an excellent architecture for the direct electrochemical oxidation of As(III) species. The growth of successive layers in the proposed LbL architecture is followed by atomic force microscopy, UV-vis spectroscopy, quartz crystal microbalance with energy dissipation, and electrochemistry. The first bilayer is found to show rather different physico-chemical characteristics as compared to the subsequent bilayers, and this is attributed to the difference in the adsorption environments. The analytical utility of the architecture with five bilayers is exploited for arsenic sensing via the direct electrocatalytic oxidation of As(III), and the detection limit is found to be well below the WHO guidelines of 10ppb. When the non-redox active PDDA is replaced by the redox-active Os(2,2'-bipyridine)(2)Cl-poly(4-vinylpyridine) polyelectrolyte (PVPOs) in the LbL assembly, the performance is found to be inferior, demonstrating that the redox activity of the polyelectrolyte is futile as far as the direct electro-oxidation of As(III) is concerned. 相似文献
93.
Timothy J. Donohoe John F. Bower Lisa P. Fishlock Cedric K.A. Callens 《Tetrahedron》2009,65(44):8969-1328
Ring-closing olefin metathesis (RCM) has been applied to the efficient synthesis of densely and diversely substituted pyridine and pyridazine frameworks. Routes to suitable metathesis precursors have been investigated and the scope of the metathesis step has been probed. The metathesis products function as precursors to the target heteroaromatic structures via elimination of a suitable leaving group, which also facilitates earlier steps by serving as a protecting group at nitrogen. Further functionalisation of the metathesis products is possible both prior to and after aromatisation. The net result is a powerful strategy for the de novo synthesis of highly substituted heteroaromatic scaffolds. 相似文献
94.
Hugon C Aubert G Sakellariou D 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2012,214(1):124-134
Mapping (or plotting) the magnetic field has a critical importance for the achievement of the homogeneous magnetic field necessary to standard MR experiments. A powerful tool for this purpose is the Spherical Harmonic Expansion (SHE), which provides a simple way to describe the spatial variations of a field in free space. Well-controlled non-zero spatial variations of the field are critical to MRI. The resolution of the image is directly related to the strength of the gradient used to encode space. As a result, it is desirable to have strong variations of the field. In that case, the SHE cannot be used as is, because the field modulus variations are affected by the variations of all components of the field. In this paper, we propose a method based on the SHE to characterize such variations, theoretically and experimentally, in the limit of an axisymmetric magnetic field. Practical applications of this method are proposed through the examples of single-sided magnet design and characterization, along with Stray-Field Imaging (STRAFI). 相似文献
95.
96.
Skogvold SM Mikkelsen O Billon G Garnier C Lesven L Barthe JF 《Analytical and bioanalytical chemistry》2006,384(7-8):1567-1577
Microelectrodes of silver–copper alloys have been evaluated for use in voltammetric analyses. Increased overpotential towards the hydrogen overvoltage reaction (HER) was found as a function of increased copper content in the silver. A study of oxidizing products by cyclic voltammetry (CV) in NaOH solution showed ten anodic and eight cathodic peaks which are described in the present paper. The behaviour of these alloy electrodes is somewhere between pure silver and pure copper electrodes. Differential pulse anodic stripping voltammetry (DPASV) was used to measure zinc, cadmium and lead in ultrapure water only (18 MΩcm), and good linearity was found for all metals (r
2=0.998) in the range of 0.5 to 5 ppb with a 600- to 1,200-s plating time. It was additionally found that cadmium and lead were better separated on the alloy electrodes compared to pure silver electrodes. Measurements of nickel were carried out on alloy electrodes by use of adsorptive differential pulse cathodic stripping voltammetry (Ad-DPCSV), and good linearity (r
2=1.000) was found in the range from 0.5 to 5 ppb with an adsorption time of 120 s. The alloy electrodes were also found to be sensitive to nitrate, and good linearity (r
2=0.997) was found in the range from 1 mg L−1 to 100 mg L−1 using differential pulse voltammetry (DPV) scanning from −450 mV to −1,500 mV. Addition of nitrate in ultrapure water afforded two different peaks related to the successive reductions of nitrate and nitrite. In ammonium buffer solution (pH 8.6) only one peak resulting from reduction of nitrate was observed. Furthermore, the use of alloy electrodes containing 17% Cu was tested in real samples, by installing it in a voltammetric system for monitoring of zinc and lead in a polluted river, the river Deûle, near the town of Douai in northern France. Results were found to be in agreement with parallel measurements carried out by ICP-MS. 相似文献
97.
Cedric Lecouvey 《Journal of Algebraic Combinatorics》2003,18(2):99-133
We use Kashiwara's theory of crystal bases to study plactic monoids for U
q(so
2n+1) and U
q(so
2n
). Simultaneously we describe a Schensted type correspondence in the crystal graphs of tensor powers of vector and spin representations and we derive a Jeu de Taquin for type B from the Sheats sliding algorithm. 相似文献
98.
An efficient laboratory synthesis for melatonin and other related indoles utilising enamides and enecarbamates is described. 相似文献
99.
Stphanie Norsikian Cedric Tresse Marc Franois‐Eude Louis Jeanne‐Julien Guillaume Masson Vincent Servajean Grgory Genta‐Jouve Jean‐Marie Beau Emmanuel Roulland 《Angewandte Chemie (International ed. in English)》2020,59(16):6612-6616
A total synthesis of tiacumicin B, a natural macrolide whose remarkable antibiotic properties are used to treat severe intestinal infections, is reported. The strategy is in part based on the prior synthesis of the tiacumicin B aglycone, and on the decisive use of sulfoxides as anomeric leaving groups in hydrogen‐bond‐mediated aglycone delivery (HAD). This new HAD variant permitted highly β‐selective rhamnosylation and noviosylation. To increase convergence, the rhamnosylated C1–C3 fragment thus obtained was anchored to the C4–C19 aglycone fragment by adapting the Suzuki–Miyaura cross‐coupling used for the aglycone synthesis. Ring‐size‐selective macrolactonization provided a compound engaged directly in the noviolysation step with virtually total β selectivity. The final efficient removal of all the protecting groups provided synthetic tiacumicin B. 相似文献
100.
Hoffmann C Faure AC Vancaeyzeele C Roux S Tillement O Pauthe E Goubard F 《Analytical and bioanalytical chemistry》2011,399(4):1653-1663
In this study, fibronectin-nanoparticles bioconjugates are developed and characterized. Multilabeled nanoparticles are composed of a core of the rare-earth oxide Gd(2)O(3):Tb(3+), capped with a set of Rhodamine B isothiocyanate encapsulated in a silica matrix and functionalized by a carboxylated polyethylene glycol shell. These nanoparticles are stabilized in aqueous solution and are found to contain about 400 carboxyl groups on their surface. Nanoparticle bioconjugation with highly purified human plasma fibronectin (Fn) is mediated by 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and N-hydroxysuccinimide, resulting in an amide linkage between the carboxylic acid-terminated surface of the nanoparticle and the primary amine of Fn. The bioconjugation temperature and pH are optimized. The Local structure and global conformation of fibronectin-nanoparticle bioconjugates (FnNP*) are studied by fluorescence spectroscopy and enzymatic sites accessibility. Protein biochemical functionalities are globally conserved, and the protein is actually labeled. Elaboration of such complexes provides a promising bimodal contrasting agent for in vivo imaging. 相似文献