Search results for "Bromide"
showing 10 items of 591 documents
Kinetic evidence for the solubilization of pyridine-2-azo-p-dimethylaniline in alkanediyl-α,ω-bis(dimethylcetylammonium nitrate) surfactants. Role of…
2004
The incorporation of the bidentate ligand pyridine-2-azo-p-dimethylaniline (PADA) into micellar aggregates of the dimeric cationic surfactants propanediyl-, hexanediyl- and dodecanediyl-alpha,omega-bis(dimethylcetylammonium nitrate) (16-3-16,2NO(3)(-), 16-6-16,2NO(3)(-) and 16-12-16,2NO(3)(-), respectively) has been studied at 25 degreesC by examining the kinetics of the complexation reaction of the Ni(II) ion with this ligand. For comparison, cetyltrimethylammonium nitrate ( CTAN), which can be considered as the "monomeric'' surfactant of 16-3-16,2NO(3)(-), has also been used. The kinetic data have shown that, for 16-3-16,2NO(3)(-) and CTAN, at a surfactant concentration below the critical…
Kinetik der Bromierung von Phenolen und phenolischen Mehrkernverbindungen, 1. Mechanismus und meßmethode
1975
Die Bromierung von 2-(2-Hydroxy-5-methylbenzyl)-4,6-dimethylphenol (1) und 2-[2-Hydroxy-3-(2-hydroxy-5-methylbenzyl)-5-methylbenzyl]-4,6-dimethylphenol (2a) wurde in Eisessig bei 22°C untersucht. Die Reaktion last sich fur [Br2]0 = 1,4·10−3 bis 6,0·10−3 mol dm + und Konzentrationen der phenolischen Verbindungen [P]0 zwischen 1,1·10−3 und 5,5·10−3mol dm−3 durch das folgende Geschwindigkeitsgesetz beschreiben: Wahrend die gebildete Bromverbindung keinen Einflus auf die Reaktionsgeschwindigkeit hat, verlangsamt der entstehende Bromwasserstoff die Reaktion. Die Bromierung ist trotzdem zur Bestimmung der Reaktionsfahigkeit von Phenolen und phenolischen Mehrkernverbindungen gut geeignet, da die R…
Process Intensification through Coupled Photocatalysis-Ozonation of Contaminated Bromide Containing Waters
2013
Strategy assessment to mediate between purification targets and bromate production during purification of bromide containing water by means of photoc…
2013
Process Intensification by Using Ozonation Coupled with TiO2 Photocatalysis for Treating Bromide and/or Bromate Ions Containing Water: The Role of Co…
2014
Ag2 and Ag3 clusters: synthesis, characterization, and interaction with DNA.
2015
Subnanometric samples, containing exclusively Ag2 and Ag3 clusters, were synthesized for the first time by kinetic control using an electrochemical technique without the use of surfactants or capping agents. By combination of thermodynamic and kinetic measurements and theoretical calculations, we show herein that Ag3 clusters interact with DNA through intercalation, inducing significant structural distortion to the DNA. The lifetime of Ag3 clusters in the intercalated position is two to three orders of magnitude longer than for classical organic intercalators, such as ethidium bromide or proflavine. Fil: Buceta, David. Universidad de Santiago de Compostela; España Fil: Busto, Natalia. Unive…
A microscopic monomeric mechanism for interpreting intrinsic optical bistability observed in Yb3+-doped bromide materials
2004
We present a mechanism able to show intrinsic bistable behaviour involving single Yb3+ ions embedded into bromide lattices, in which intrinsic optical bistability (IOB) has been observed. The mechanism is based on the experimentally found coupling between the Yb3+ ion and the totally symmetric local mode of vibration of the [YbBr6]3- coordination unit. The model reproduces the IOB observed in CsCdBr3:1% Yb3+ and allows to understand the experimentally found presence of the phenomenon in the other bromides, but its absence in Cs3Lu2Cl9:Yb3+.
CCDC 854063: Experimental Crystal Structure Determination
2012
Related Article: A.Molina-Ontoria, R.Garcia, A.Gouloumis, F.Giacalone, M.R.Torres, N.Martin|2012|Eur.J.Org.Chem.|2012|3581|doi:10.1002/ejoc.201200115
CCDC 1425265: Experimental Crystal Structure Determination
2016
Related Article: T. Mäkelä, K. Rissanen|2016|Dalton Trans.|45|6481|doi:10.1039/C6DT00414H
CCDC 977381: Experimental Crystal Structure Determination
2016
Related Article: Christoph Deckert, Denis Bittner, Luca M. Carrella, Dieter Schollmeyer and Eva Rentschler|2016|Eur.J.Inorg.Chem.||1738|doi:10.1002/ejic.201501400