Synthesis and DPPH radical scavenging activity of prenylated phenol derivatives

The synthesis of twenty six prenylated phenols derivatives is reported. These compounds were obtained under mild conditions via Electrophilic Aromatic Substitution (EAS) coupling reactions between phenol derivatives containing electron-donor subtituents and 3-methyl-2-buten-1-ol using BF(3)×OEt(2). Dialkylations were also produced with this method. The formation of a chroman ring by intramolecular cyclization between a sp2 carbon from the prenyl group with the hydroxyl substituent in the ortho position occurred with some phenols. All the synthesized compounds were evaluated as antioxidants according to a DPPH radical scavenging activity assay. IC(50) values of five synthesized compounds indicated they were as good antioxidants as Trolox?.     

Structural and electronic effects on the exchange interactions in dinuclear bis(phenoxo)-bridged copper(II) complexes

Computational methods based on density functional theory have been employed to analyze the magnetic properties of dinuclear bis(phenoxo)-bridged Cu^II complexes. While the largest part of complexes in that family show antiferromagnetic coupling, we focus our study on those cases with distorted geometries that present ferromagnetic behaviour. The calculations reproduce such a magnetic behaviour, and a structural analysis reveals the main role played by several structural parameters, such as the Cu–O–Cu bridging angle. The out-of-plane shift of the phenoxo ring and the hinge distortion of the Cu₂O₂ central framework that are also important for similar hydroxo and alkoxo complexes. In this case the conformation of the phenoxo groups and the rotation of the phenyl rings can also play an important role. The last part of this work is dedicated to analyze the influence of the substituents of the phenoxo ring on the magnetic properties, which is especially important for structures with large out-of-plane shifted phenoxo rings. The presence of π electron releasing groups favours a ferromagnetic coupling.     

CVT法生长GaP多晶

阐述了CVT(化学气相输运)法生长GaP的基本反应和输运速度,采用CVT法生长出了GaP多晶.设计了石英管的结构以制造出一个局部的低温区域,防止了GaP在管壁的生长.生长出的GaP多晶相对密度为98;,红外透过率达到30;,努普硬度为611kg/mm2.散射颗粒测试表明主要的光散射颗粒为多晶中存在的孔隙.     

Chemical and carbon isotopic composition of dissolved organic carbon in a regional confined methanogenic aquifer

This study demonstrates the advantage of a combined use of chemical and isotopic tools to understand the dissolved organic carbon (DOC) cycle in a regional confined methanogenic aquifer. DOC concentration and carbon isotopic data demonstrate that the soil zone is a primary carbon source of groundwater DOC in areas close to recharge zones. An in-situ DOC source linked to organic rich sediments present in the aquifer matrix is controlling the DOC pool in the central part of the groundwater flow system. DOC fractions, 13C-NMR on fulvic acids and 14C data on DOC and CH4 support the hypothesis that the in-situ DOC source is a terrestrial organic matter and discard the Ordovician bedrock as a source of DOC.     

An adeno-associated viral vector transduces the rat hypothalamus and amygdala more efficient than a lentiviral vector

Background  

This study compared the transduction efficiencies of an adeno-associated viral (AAV) vector, which was pseudotyped with an AAV1 capsid and encoded the green fluorescent protein (GFP), with a lentiviral (LV) vector, which was pseudotyped with a VSV-G envelop and encoded the discosoma red fluorescent protein (dsRed), to investigate which viral vector transduced the lateral hypothalamus or the amygdala more efficiently. The LV-dsRed and AAV1-GFP vector were mixed and injected into the lateral hypothalamus or into the amygdala of adult rats. The titers that were injected were 1 × 10⁸ or 1 × 10⁹ genomic copies of AAV1-GFP and 1 × 10⁵ transducing units of LV-dsRed.     

Isolation of NO(3)(-)-N as 1-phenylazo-2-naphthol (Sudan-1) for measurement of delta(15)N

The conversion of nitrate (NO(3)(-)) to 1-phenylazo-2-naphthol (Sudan-1) has been examined as a method for natural abundance measurement of delta(15)N of NO(3)(-). The reaction results in dilution of NO(3)(-)-N with only one reagent-derived N and the product is readily concentrated from dilute samples by reverse phase chromatography. There is systematic isotopic fractionation during the reaction, but this can be allowed for by analysing known NO(3)(-) standards along with each sample set. Sudan-1 prepared from surface water samples containing approximately 50 &mgr;g NO(3)(-)-N can be analysed by automated continuous flow isotope ratio mass spectrometry with a precision of 0.2 per thousand (one standard deviation) and the accuracy is not affected by interference from other nitrogenous species in the sample or reagents. Copyright 1999 John Wiley & Sons, Ltd.