Diffusion Methods (diffusion + methods)

Distribution by Scientific Domains


Selected Abstracts


Metal-Directed Self-Assembly: Two New Metal-Binicotinate Grid Polymeric Networks and Their Fluorescence Emission Tuned by Ligand Configuration

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 13 2004
Benlai Wu
Abstract Two new 2-D metal-binicotinate coordination polymers, namely, [CdII(bpdc)]n (1) and {[ZnII8(bpdc)8(H2O)8](H2O)8}n (2) (H2bpdc = binicotinic acid) have been synthesized using hydrothermal and three-layer diffusion methods, respectively. Single-crystal X-ray analyses revealed that both are extended grid networks of the (4,4) topology. Their structures alter with the configuration and function of bpdc. The achiral, free H2bpdc has axial chirality induced by metal coordination in 1, and bpdc connects to four metal centers forming a 2-D (4,4) net with three kinds of apertures generated through self-assembly. In 2, however, bpdc connects to three metal centers, fabricating a microporous framework containing hydrophilic channels. Studies on the solid emission spectra of the free ligand, 1, and 2 confirmed, that the configuration of bpdc resulting from metal-directed coordination has a profound effect on the fluorescence emissions of 1 and 2. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) [source]


CHEMICAL CHARACTERIZATION AND ANTIFUNGAL ACTIVITY OF ORIGANUM ONITES L. ESSENTIAL OILS AND EXTRACTS

JOURNAL OF FOOD SAFETY, Issue 1 2009
MIHRIBAN KORUKLUOGLU
ABSTRACT Essential oils (EOs) and extracts (methanol, acetone and diethyl ether) of fresh and dried oregano (Origanum onites L.) were used to determine the antifungal effect on Alternaria alternata, Aspergillus flavus (two strains), Aspergillus niger (two strains), Aspergillus parasiticus, Fusarium semitectum, Fusarium oxysporum, Mucor racemosus and Penicillium roqueforti by disk diffusion methods. Minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) of all samples were determined. The antifungal activity of the fresh herb was greater than that of the dried herb. MIC values for fresh and dried methanol extracts were 150,950 µg/mL and 750,950 µg/mL, respectively. MFC values for methanol extracts were determined between 300 and 1200 µg/mL for fresh oregano and between 750 and 1100 µg/mL for dried oregano. The EOs of fresh and dried oregano totally inhibited test fungi. EOs produced the lowest MIC and MFC values: 8.5 µg/mL and 9.0 µg/mL, respectively (P < 0.005). The highest extract activity was exhibited by fresh oregano against A. alternata (24 mm) followed by P. roqueforti (20 mm). The greatest total antifungal effect was observed from methanol extracts. The chemical composition of fresh oregano EO and extracts was examined using gas chromatography-mass spectrometry (GC-MS). Over 80 volatiles were detected, of which 42 were positively identified by matching both MS fragmentation patterns with standardized retention characteristics. p-Cymene, thymol and carvacrol were the most prominent, followed by ,-pinene, camphor and borneol. PRACTICAL APPLICATIONS In the past decade interest in natural antimicrobial plant extracts has been growing. Various plants have historically been used for the purposes of food preservation and flavor enhancement as well as medicinal purposes. An example is oregano, the leafy part of the plant belonging to the Labiatae family. It has been used to improve the flavor and the organoleptic properties of many foods from numerous cultures. It has also been used to prolong the storage life of foods probably because of antifungal properties. The preservative nature of fresh oregano has been employed in many food applications, including meat and fish products, as well as in pharmaceuticals, alternative medicines and natural therapies. [source]


Diffusion technique for 15N and inorganic N analysis of low-N aqueous solutions and Kjeldahl digests,

RAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 11 2008
Rui Rui Chen
Diffusion of ammonia is a common sample preparation method for the stable isotope analysis of inorganic nitrogen in aqueous solution. Classical diffusion methods usually require 6,12 days of diffusion and often focus on 15N/14N analysis only. More recent studies have discussed whether complete N recovery was necessary for the precise analysis of stable N isotope ratios. In this paper we present a newly revised diffusion technique that allows correct and simultaneous determination of total N and 15N at% from aqueous solutions and Kjeldahl digests, with N concentrations down to sub-0.5-mg,N,L,1 levels, and it is tested under different conditions of 15N isotope labelling. With the modification described, the diffusion time was reduced to 72,h, while the ratios of measured and expected 15N at% were greater than 99% and the simultaneous recovery of total N was >95%. Analysis of soil microbial biomass N and its 15N/14N ratio is one of the most important applications of this diffusion technique. An experiment with soil extracts spiked with 15N-labelled yeast showed that predigestion was necessary to prevent serious N loss during Kjeldahl digestion of aqueous samples (i.e. soil extracts). The whole method of soil microbial biomass N preparation for 15N/14N analysis included chloroform fumigation, predigestion, Kjeldahl digestion and diffusion. An experiment with soil spiked with 15N-labelled yeast was carried out to evaluate the method. Results showed a highly significant correlation of recovered and added N, with the same recovery rate (0.21) of both total N and 15N. A kN value of 0.25 was obtained based on the data. In conclusion, the diffusion method works for soil extracts and microbial biomass N determination and hence could be useful in many types of soil/water studies. Copyright © 2008 John Wiley & Sons, Ltd. [source]


7Li, 31P, and 1H Pulsed Gradient Spin-Echo (PGSE) Diffusion NMR Spectroscopy and Ion Pairing: On the Temperature Dependence of the Ion Pairing in Li(CPh3), Fluorenyllithium, and Li[N(SiMe3)2] amongst Other Salts

CHEMISTRY - A EUROPEAN JOURNAL, Issue 5 2005
Ignacio Fernández
Abstract 7Li, 31P, and 1H variable-temperature pulsed gradient spin-echo (PGSE) diffusion methods have been used to study ion pairing and aggregation states for a range of lithium salts such as lithium halides, lithium carbanions, and a lithium amide in THF solutions. For trityllithium (2) and fluorenyllithium (9), it is shown that ion pairing is favored at 299 K but the ions are well separated at 155 K. For 2-lithio-1,3-dithiane (13) and lithium hexamethyldisilazane (LiHMDS 16), low-temperature data show that the ions remain together. For the dithio anion 13, a mononuclear species has been established, whereas for the lithium amide 16, the PGSE results allow two different aggregation states to be readily recognized. For the lithium halides LiX (X = Br, Cl, I) in THF, the 7Li PGSE data show that all three salts can be described as well-separated ions at ambient temperature. The solid state structure of trityllithium (2) is described and reveals a solvent-separated ion pair formed by a [Li(thf)4]+ ion and a bare triphenylmethide anion. [source]