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排序方式: 共有130条查询结果,搜索用时 15 毫秒
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Craviso GL Chatterjee I Publicover NG 《Bioelectrochemistry (Amsterdam, Netherlands)》2003,60(1-2):57-64
Effects of powerline frequency (50/60 Hz) electric and magnetic fields on the central nervous system may involve altered neurotransmitter release. This possibility was addressed by determining whether 60-Hz linearly polarized sinusoidal magnetic fields (MFs) alter the release of catecholamines from cultured bovine adrenal chromaffin cells, a well-characterized model of neural-type cells. Dishes of cells were placed in the center of each of two four-coil Merritt exposure systems that were enclosed within mu-metal chambers in matched incubators for simultaneous sham and MF exposure. Following 15-min MF exposure of the cells to flux densities of 0.01, 0.1, 1.0 or 2 mT, norepinephrine and epinephrine release were quantified by high-performance liquid chromatography (HPLC) coupled with electrochemical detection. No significant differences in the release of either norepinephrine or epinephrine were detected between sham-exposed cells and cells exposed to MFs in either the absence or presence of Bay K-8644 (2 microM) or dimethylphenylpiperazinium (DMPP, 10 microM). Consistent with these null findings is the lack of effect of MF exposure on calcium influx. We conclude that catecholamine release from chromaffin cells is not sensitive to 60-Hz MFs at magnetic flux densities in the 0.01-2 mT range. 相似文献
3.
S. Dattagupta R. Vaidyanathan R. Indira 《Zeitschrift für Physik B Condensed Matter》1984,57(4):319-328
The relaxation behaviour of a model disordered system is studied. The model considered is a nearest neighbour Ising chain in which the bond strengths are distributed at random between the discrete values +J and -J with equal probability. The system is prepared in a given state and is allowed to relax to a new state of equilibrium. This approach to equilibrium is probed by means of an applied, weak, time-dependent magnetic field. The relevant physical quantity is a nonequilibrium susceptibility which is calculated exactly. A comparison between this, and the corresponding quantity for the pure chain, reveals certain distinctive features of the time-dependent properties of disordered systems.Deceased 相似文献
4.
Gustavo Santiso‐Quinones Rafael E. Rodriguez‐Lugo 《Acta Crystallographica. Section C, Structural Chemistry》2013,69(8):859-861
The compound [2‐(aminomethyl)pyridine‐κ2N,N′][chlorido/trifluoromethanesulfonato(0.91/0.09)][(10,11‐η)‐5H‐dibenzo[a,d]cyclohepten‐5‐amine‐κN](triphenylphosphane‐κP)ruthenium(II) trifluoromethanesulfonate dichloromethane 0.91‐solvate, [Ru(CF3SO3)0.09Cl0.91(C6H8N2)(C15H13N)(C18H15P)]CF3SO3·0.91CH2Cl2, belongs to a series of RuII complexes that had been tested for transfer hydrogenation, hydrogenation of polar bonds and catalytic transfer hydrogenation. The crystal structure determination of this complex revealed disorder in the form of two different anionic ligands sharing the same coordination site, which other spectroscopic methods failed to characterize. The reduced catalytic activity of the title compound was not fully understood until the crystallographic data provided evidence for the mixed ligand species. The crystal structure clearly shows that the majority of the synthesized material has a chloride ligand present. Only a small portion of the material is the expected complex [RuII(OTf)(ampy)(η2‐tropNH2)(PPh3)]OTf, where OTf is triflate or trifluoromethanesulfonate, ampy is 2‐(aminomethyl)pyridine and tropNH2 is 5H‐dibenzo[a,d]cyclohepten‐5‐amine. 相似文献
5.
Sanjeev Kumar Aavula Anil ChikkulapalliN. Hanumanthappa Indira JyothiC.H. Vinod Kumar Sulur G. Manjunatha 《Tetrahedron letters》2013
A series of carboxylic acids were converted into their corresponding esters using the Pd/C catalyzed hydrogenation conditions in the presence of catalytic bromobenzene in alcohols and the method could also be applicable for the transesterification of esters. Good to excellent yields were obtained for different aliphatic or aromatic starting materials. The success of this esterification relies on the in situ generation of hydrobromic acid (HBr) from bromobenzene which provides a mild and acidic reaction environment. The palladium catalyst exhibits a remarkable activity and is reusable for up-to three consecutive cycles. 相似文献
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Back Cover: Experimental and Theoretical Study of the Reactivity of Gold Nanoparticles Towards Benzimidazole‐2‐ylidene Ligands (Chem. Eur. J. 30/2016) 下载免费PDF全文
Dr. María Rodríguez‐Castillo Gustavo Lugo‐Preciado Dr. Danielle Laurencin Dr. Frederik Tielens Dr. Arie van der Lee Dr. Sébastien Clément Dr. Yannick Guari Dr. José M. López‐de‐Luzuriaga Dr. Miguel Monge Dr. Françoise Remacle Dr. Sébastien Richeter 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(30):10680-10680
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C. Aguilar‐Lugo R. Le Lagadec Alexander D. Ryabov G. Cedillo Valverde S. Lopez Morales L. Alexandrova 《Journal of polymer science. Part A, Polymer chemistry》2009,47(15):3814-3828
Cationic substitutionally inert cyclometalated ruthenium (II) and osmium (II) complexes, ([Mt(o‐C6H4‐2‐py)(LL)2]PF6), where LL‐1,10‐phenanthroline (phen) or 2,2′‐bipyridine (bipy), were used for radical polymerization of styrene. Gradual modification of the complexes within the series allowed comparison of the catalytic activity and the redox properties. There was no correlation between the reducing powers of the complexes and their catalytic activities. The osmium compound of the lowest reduction potential was not active. All the ruthenium complexes catalyzed the polymerization of styrene in a controlled manner; but the level of control and the catalytic activity were different under the same polymerization conditions. [Ru(o‐C6H4‐2‐py)(phen)2]PF6 demonstrated the best catalytic performance though its redox potential was the highest. It catalyzed the “living” polymerization with a reasonable rate at a catalyst‐to‐initiator ratio of 0.1. 1 equiv. of Al(OiPr)3 accelerated the polymerization and improved the control, but higher amount of Al(OiPr)3 did not speed up the polymerization and moved the process into the uncontrollable regime. Under the most optimal conditions, the controlled polymerization occurs fast without any additive and the catalyst degradation. Added free ligands inhibited the polymerization suggesting that the catalytically active ruthenium intermediates are generated via the reversible dechelation of bidentate phen or bipy ligands. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3814–3828, 2009 相似文献
10.
D. B. Parihar Om Prakash Indira Bajaj R. P. Tripathi K. K. Verma 《Mikrochimica acta》1971,59(3):393-398
Summary High explosives having the sameR
f
values on a thin-layer chromatogram and difficult to separate are readily resolved as their coloured -complexes with aromatic amines. After liberation from their complexes on the plate, up to 1.5 g of the explosives can be conveniently estimated at their characteristic absorption maxima.
Zusammenfassung Hochexplosive Substanzen mit gleichenR f -Werten auf Dünnschichtchromatogrammen, die sich schlecht trennen lassen, werden als gefärbte -Komplexe mit aromatischen Aminen gut voneinander getrennt. Nach Freisetzung aus den Komplexen auf der Platte können bis zu 1,5 g der Explosivstoffe bei ihrem charakteristischen Absorptionsmaximum auf übliche Weise bestimmt werden.相似文献