排序方式: 共有63条查询结果,搜索用时 15 毫秒
1.
Xavier Verdaguer Iolanda Marchueta Jordi Tormo Albert Moyano Miquel A. Perics Antoni Riera 《Helvetica chimica acta》1998,81(1):78-84
A convenient preparation of (1R,2S,3R,4S)-3-(neopentyloxy)isoborneol (= (1R,2S,3R,4S)-3-(2,2-dimethyl-propoxy)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol; 1a ), a valuable chiral auxiliary, is described. The synthesis involves six steps starting from the readily available camphorquinone ( 5 ) and gives 1a in 48% overall yield. The key step is the chemoselective hydrolysis of the less hindered 1,3-dioxolane moiety in the camphorquinone di-acetal 4 . 相似文献
2.
Conventional methods generally used to synthesize heterogeneous photocatalysts have some drawbacks, mainly the difficult control/preservation of catalysts’ morphology, size or structure, which strongly affect the photocatalytic activity. Supercritical carbon dioxide (scCO2)-assisted techniques have recently been shown to be a promising approach to overcome these limitations, which are still a challenge. In addition, compared to traditional methods, these innovative techniques permit the synthesis of high-performance photocatalysts by reducing the use of toxic and polluting solvents and, consequently, the environmental impact of long-term catalyst preparation. Specifically, the versatility of scCO2 allows to prepare catalysts with different structures (e.g., nanoparticles or metal-loaded supports) by several supercritical processes for the photocatalytic degradation of various compounds. This is the first updated review on the use of scCO2-assisted techniques for photocatalytic applications. We hope this review provides useful information on different approaches and future perspectives. 相似文献
3.
Tânia Regina Silva Eduard Westphal Hugo Gallardo Iolanda Cruz Vieira 《Electroanalysis》2014,26(8):1801-1809
This paper describes the development of a new sensor based on an ionic organic film. The amphiphilic molecule, 4‐[(4‐decyloxyphenyl)‐ethynyl]‐1‐methylpyridinium iodide (10PyI), which has liquid‐crystalline properties, was synthesized and applied in the construction of a GCE/10PyI sensor. Analytical parameters for caffeic acid, repeatability (4.8 %), reproducibility (2.8 %), linearity (two ranges: 9.9×10?7 to 3.8×10?5 mol L?1 and 4.7×10?5 to 9.9×10?5 mol L?1) and detection limits (9.0×10?7 mol L?1 and 8.7×10?6 mol L?1), were determined. The method was successfully applied in the determination of total phenolic compounds (TPC) in mate herb extracts. 相似文献
4.
Siqueira Iolanda Scheibe de Dweck Jo Toledo Filho Romildo Dias 《Journal of Thermal Analysis and Calorimetry》2020,142(4):1413-1428
Journal of Thermal Analysis and Calorimetry - The interest in the use of cellulose fibers of increasingly smaller sizes in cementitious materials has increased in recent years. This paper brings... 相似文献
5.
Determination of thiodicarb using a biosensor based on alfalfa sprout peroxidase immobilized in self-assembled monolayers 总被引:2,自引:0,他引:2
Sally K. Moccelini Iolanda C. Vieira Bruno G. Lucca Valdir S. Ferreira 《Talanta》2010,82(1):164-19760
A biosensor based on alfalfa sprout (Medicago sativa) homogenate as a source of peroxidase is proposed for the determination of thiodicarb by square-wave voltammetry. This enzyme was immobilized in self-assembled monolayers of l-cysteine on a gold electrode. Several parameters were investigated to evaluate the optimum conditions for operation of the biosensor. The analytical curve was linear for thiodicarb concentrations of 2.27 × 10−6 to 4.40 × 10−5 mol L−1 with a detection limit of 5.75 × 10−7 mol L−1. The lifetime of the Au-alfalfa sprout-SAMs was 20 days (at least 220 determinations). The average recovery of thiodicarb from samples of vegetable extracts ranged from 99.02 to 101.04%. The results obtained for thiodicarb in vegetable extracts using the proposed method are in close agreement with those using a high performance liquid chromatography procedure at the 95% confidence level. 相似文献
6.
Cationic surfactant vesicles accelerate the rate of thiolysis of p-nitrophenyl octanoate by n- heptylmercaptan by several million fold in the pH range from 4 to 6, providing an efficient system for ester thiolysis in aqueous solution that is functional even at pH4, i.e. more than 6 pH units below the pKa of the SH group. Analysis of the data in terms of an ion exchange formalism implies that this rate acceleration is due primarily to concentration of the reagents in the dimensionally-restrited environment provided by the vesicle, coupled with small contributions from enhanced dissociation and reactivity of the nucleophile at the vesicle surface(s). 相似文献
7.
Geng Y Romsted LS Froehner S Zanette D Magid LJ Cuccovia IM Chaimovich H 《Langmuir : the ACS journal of surfaces and colloids》2005,21(2):562-568
Sphere-to-rod transitions of cetyltrimethylammonium (CTA+) micelles with dichlorobenzoate counterions are remarkably substituent dependent. Simultaneous estimates of the interfacial molarities of H2O, MeOH, and Cl- and 2,6- and 3,5-dichlorobenzoate (2,6OBz and 3,5OBz) counterions were obtained by the chemical trapping method in mixed micelles of CTACl/CTA3,5OBz and CTACl/CTA2,6OBz without added salt. Increasing the CTA3,5OBz mole fraction produces a marked concurrent increase in interfacial 3,5OBz- and a decrease in interfacial H2O concentrations through the sphere-to-rod transition. No abrupt concentration changes are observed with increasing CTA2,6OBz mole fraction. Counterion-specific changes in the interfacial water concentration may be a major contributor to the delicate balance of forces governing micellar morphology. 相似文献
8.
Iolanda Porcar Rosa García Vicente Soria Concepcin Abad Agustín Campos 《Macromolecular Symposia》1997,119(1):241-252
The intrinsic fluorescence emission of poly (2-vinyl pyridine) has been exploited in order to gain insight into the nature of the interaction with artificial membranes. In this contribution, the study has been focused on the effect of the phospholipid bilayer composition on the association to the polymer. Fluorescence data have been converted into association isotherms and then analyzed in terms of both binding and partition models. Results show that the association is enhanced by the presence of negative charged phospholipid as a constituent of the liposomal membrane. The strong surface density dependence of the polymer-liposome association indicates the predominantly electrostatic nature of that interaction. 相似文献
9.
Craig Aalseth Erica Andreotti Dirk Arnold Joan-Albert Sanchez Cabeza Detlev Degering Andrea Giuliani Raquel Gonzales de Orduña Rodolfo Gurriaran Mikael Hult Martin Keillor Matthias Laubenstein Gilbert le Petit Romul Mircea Margineanu Murray Matthews Harry Miley Iolanda Osvath Monica Pellicciari Wolfango Plastino Hardy Simgen Marc Weber Robert Werzi 《Journal of Radioanalytical and Nuclear Chemistry》2009,282(3):731-735
Aerosol samples collected on filter media were analyzed using HPGe detectors employing varying background-reduction techniques in order to experimentally evaluate the opportunity to apply ultra-low background measurement methods to samples collected, for instance, by the Comprehensive Test Ban Treaty International Monitoring System (IMS). In this way, realistic estimates of the impact of low-background methodology on the sensitivity obtained in systems such as the IMS were assessed. The current detectability requirement of stations in the IMS is 30 μBq/m3 of air for 140Ba, which would imply ~106 fissions per daily sample. Importantly, this is for a fresh aerosol filter. One week of decay reduces the intrinsic background from radon daughters in the sample allowing much higher sensitivity measurement of relevant isotopes, including 131I. An experiment was conducted in which decayed filter samples were measured at a variety of underground locations using Ultra-Low Background (ULB) gamma spectroscopy technology. The impacts of the decay and ULB are discussed. 相似文献
10.
Quienly Godoi Dario Santos Jr. Lidiane C. Nunes Flávio O. Leme Iolanda A. Rufini José A.M. Agnelli Lilian C. Trevizan Francisco J. Krug 《Spectrochimica Acta Part B: Atomic Spectroscopy》2009
The performance of laser-induced breakdown spectrometry (LIBS) for the determination of Ba, Cd, Cr and Pb in toys has been evaluated by using a Nd:YAG laser operating at 1064 nm and an Echelle spectrometer with intensified charge-coupled device detector. Samples were purchased in different cities of São Paulo State market and analyzed directly without sample preparation. Laser-induced breakdown spectrometry experimental conditions (number of pulses, delay time, integration time gate and pulse energy) were optimized by using a Doehlert design. Laser-induced breakdown spectrometry signals correlated reasonably well with inductively coupled plasma optical emission spectrometry (ICP OES) concentrations after microwave-assisted acid digestion of selected samples. Thermal analysis was used for polymer identification and scanning electron microscopy to visualize differences in crater geometry of different polymers employed for toy fabrication. Results indicate that laser-induced breakdown spectrometry can be proposed as a rapid screening method for investigation of potentially toxic elements in toys. The unique application of laser-induced breakdown spectrometry for identification of contaminants in successive layers of ink and polymer is also demonstrated. 相似文献