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171.
Silvia Sternativo Francesca Del Verme Antonella Calandriello Lorenzo Testaferri Marcello Tiecco 《Tetrahedron》2010,66(34):6851-9385
Variously substituted aziridines were conveniently prepared by an aza-Michael Initiated Ring Closure (aza-MIRC) reaction starting from vinyl selenones and primary amines, aminoalcohols or diamines. The reactions proceed in very high yields at room temperature in toluene or water. A significant rate acceleration was observed under aqueous conditions. 相似文献
172.
Diogo P. Rivelli Carlos A. H. Filho Rebeca L. Almeida Cristina D. Ropke Tânia C. H. Sawada Silvia B. M. Barros 《Photochemistry and photobiology》2010,86(5):1005-1007
Chlorogenic acid is a natural potent antioxidant. It can be used in cosmetics formulations, but for this purpose its photochemical stability should be determined to ensure that the compound will not be degraded after UV radiation exposure. To evaluate this possibility, the concentration of a chlorogenic acid solution was determined by HPLC before and after UVA and UVB irradiation. The results indicate that chlorogenic acid is not degraded under UVA or UVB irradiation. 相似文献
173.
Silvia Tavazzi Dr. Leonardo Silvestri Dr. Luciano Miozzo Dr. Antonio Papagni Prof. Peter Spearman Dr. Sandra Ianelli Dr. Alberto Girlando Prof. Andrea Camposeo Dr. Marco Polo Dr. Dario Pisignano Dr. 《Chemphyschem》2010,11(2):429-434
Blue amplified spontaneous emission at room temperature is demonstrated from the exposed face of the strongly emitting organic semiconductor 1,1,4,4‐tetraphenyl‐1,3‐butadiene in single crystal form. The symmetry of the crystal and calculation of lattice sums indicate the J‐type organization of the molecular transition moments. The minimum in the lowest exciton dispersion branch, from which emission takes place, is found at the edge of the Brillouin zone leading to a dominant vibronic emission since the zero‐phonon line is forbidden. The observed gain narrowed line is attributed to the vibronic replica which becomes amplified with increased pumping. The reported emission is along the normal to the exposed crystal face, important for the development of vertical cavity geometry lasers based on organic single crystals. The threshold excitation fluence of 400 μJ cm?2 is comparable to other organic crystalline systems, even if the amplification path is much reduced as a consequence of the vertical geometry. Considering these relevant aspects, the optical characterization of this material is provided. The polarized absorption spectra are reported and the properties of the lowest‐energy excitonic state investigated. Calculation of the electronic transitions for the isolated molecule, lattice sums for the transition at lowest energy, and the symmetry of the crystal allow attributing the largest face of the samples and the observed optical bands in the spectra. Polarized time‐resolved spectra are also reported allowing to identify the intrinsic excitonic emission. 相似文献
174.
Alesso G Cinellu MA Stoccoro S Zucca A Minghetti G Manassero C Rizzato S Swang O Ghosh MK 《Dalton transactions (Cambridge, England : 2003)》2010,39(42):10293-10304
The first six-membered gold(III) N^C^N pincer complex was obtained in good yield, under very mild conditions, by transmetalation of [Hg(κC-N^C^N)Cl] (N^CH^N = 1,3-bis(pyridin-2-ylmethyl)benzene, HL(1)) with Na[AuCl(4)]. The X-ray crystal structure of [Au(N^C^N)Cl][PF(6)] showed that the fused six-membered metallacycles each exist in a strongly puckered boat conformation. As shown by the (1)H NMR spectra in various solvents, the same structure is also retained in solution: no inversion of the six-membered metallacycles is observed in DMSO up to 95 °C. This correlates well with a reaction barrier of 17.5 kcal/mole, as determined by quantum chemical calculations. The reactivity of the present pincer complex is compared to that of the analogous 1,3-bis(2-pyridyl)benzene, HL(2), derivative, which has five-membered fused metallacycles. Sharp differences are found in the reactions with phosphines, such as PPh(3) and dppe (1,2-bis-diphenylphosphino-ethane), and with silver salts. Theoretical calculations were carried out on the two pincer complexes in order to try to understand these differences, and we found that the gold-chlorine bond is significantly stronger in the case of the complex containing five-membered metallacyclic rings. 相似文献
175.
Based on continuous methodical advances and developments, solid-state NMR spectroscopy has become a powerful tool for the
investigation of various materials, including polymers, glasses, zeolites, fullerenes, and many others. During the past decade,
solid-state NMR spectroscopy also found increasing interest for the study of biomolecules. For example, membrane proteins
reconstituted into lipid environments such as bilayers or vesicles, protein aggregates such as amyloid fibrils, as well as
carbohydrates can now be studied by solid-state NMR spectroscopy. This review briefly introduces the principles of solid-state
NMR spectroscopy and highlights novel methodical trends. Selected applications demonstrate the possibilities of solid-state
NMR spectroscopy as a valuable bioanalytical tool. 相似文献
176.
Detailed investigation of the tautomerism of oxadiazoles, thiadiazoles, and selenadiazoles containing hydroxy, mercapto, or
selenyl groups in position 2 and 5 of the five-membered ring was carried out at MP2, MP4, and CCSD(T) levels of theory. The
relative stabilities of the tautomers of the heterocycles were investigated in gas phase. It is found that the dioxo form
is the preferred tautomer if the exocyclic group is hydroxy. If the exocyclic group is mercapto or selenyl group the most
stable tautomer is the mixed mercapto/thione or selenyl/selone form. The barriers of intramolecular proton transfer are too
large and tautomerization should not occur. 相似文献
177.
Duquesnoy E Marongiu B Castola V Piras A Porcedda S Casanova J 《Natural product communications》2010,5(12):1995-1998
Two samples (leaves and twigs) of Abies alba Miller from Corsica were extracted using supercritical CO2 and their chemical compositions were compared with those of the essential oils obtained from the same batch of plant material. In total 45 components were identified using combined analysis by GC (RI), GC-MS and 13C NMR. It was observed that the contents of monoterpenes (mainly represented by limonene, alpha-pinene and camphene) were significantly lower in the supercritical fluid extract (SFE) than in the essential oil (EO). Conversely, the proportions of sesquiterpenes were much higher in CO2 extracts than in essential oils (around 30% vs 4%). Cis-abienol, a diterpene alcohol, was identified only in SFE, and the proportions of this constituent (7.5% and 17.3%) were determined using quantitative 13C NMR since it was under estimated using the standard conditions of GC. 相似文献
178.
San Martin A Rovirosa J Carrasco A Orejarena S Soto-Delgado J Contreras R Chamy MC 《Natural product communications》2010,5(12):1859-1864
The sesquiterpene pacifenol is one of the main constituents of the red alga Laurencia claviformis. Earlier work on the semisynthetic derivatives of pacifenol afforded a series of halogenated sesquiterpenes. The aim of the present work was to obtain new hydroxylated derivatives of halogenated sesquiterpenes by means of microbial transformation using Aspergillus niger, Gibberella fujikuroi and Mucor plumbeus. The best results were obtained with M. plumbeus. The microbiological transformation by M. plumbeus of pacifenol, and two semisynthetic derivatives, is described. The structures of the new compounds obtained were determined by spectroscopic means. 相似文献
179.
A mixed‐polymeric electrokinetic chromatography system has been developed for the simultaneous determination of a contaminant like oversulfated condroitin sulfate (OSCS) and impurities expressed as dermatan (Der) in heparin (Hep) samples. The EKC system consisted of 0.5% w/v polymeric β‐CD, 0.4% w/v tetronic® 1107 and 400 mM tris‐phosphate buffer at pH 3.5. The optimized electrophoretic conditions included the use of an uncoated‐silica capillary of 50 cm of total length and 75 μm id, an applied voltage of ?7 kV, a temperature of 30°C and 200 nm UV‐detection. The highly sensitive method developed showed low values of LOD, 0.07% w/w (0.07 μg/mL) (OSCS) and 0.1% w/w (0.1 μg/mL) (Der), and values of LOQ 0.2% w/w (0.2 μg/mL) (OSCS) and 0.3% w/w (0.3 μg/mL) (Der) with a concentration level of Hep sample as low as 0.1 mg/mL. Additional parameters of validation such as specificity, linearity, accuracy, and robustness were evaluated according to international guidelines. Owing to its simplicity, high sensitivity, and reliability, the proposed method can be an advantageous alternative to the traditional methodologies for the analysis of Hep in raw material and specially in finished products because of the low amounts of Hep sample required. 相似文献
180.
Given a square matrix A, the inverse subspace problem is concerned with determining a closest matrix to A with a prescribed invariant subspace. When A is Hermitian, the closest matrix may be required to be Hermitian. We measure distance in the Frobenius norm and discuss applications to Krylov subspace methods for the solution of large‐scale linear systems of equations and eigenvalue problems as well as to the construction of blurring matrices. Extensions that allow the matrix A to be rectangular and applications to Lanczos bidiagonalization, as well as to the recently proposed subspace‐restricted SVD method for the solution of linear discrete ill‐posed problems, also are considered.Copyright © 2013 John Wiley & Sons, Ltd. 相似文献