608-93-5Relevant articles and documents
Electroreduction of hexachlorobenzene in micellar aqueous solutions of Triton-SP 175
Merica, Simona G.,Banceu, Claudia E.,Jedral, Wojciech,Lipkowski, Jacek,Bunce, Nigel J.
, p. 1509 - 1514 (1998)
The electrochemical reduction of hexachlorobenzene (HCB) has been studied in micellar aqueous solutions using Triton-SP 175 which, unlike conventional surfactants, is acid-labile. At pH 3, the hydrophobic residue cleaves from the hydrophilic chain, leaving a solution without surface- active properties and allowing recovery of the electrolysis products from the solution. A micellar solution containing 0.1% v/v Triton-SP 175 and 1% v/v heptane as cosolvent was indefinitely stable in the presence of 0.05 M sodium sulfate as an environmentally friendly supporting electrolyte. Electrolytic dehalogenation to less chlorinated benzenes was studied at a wide variety of cathodes; in all cases a quantitative material balance of phenyl residues was achieved. Lead was the preferred cathode in terms of both the degree of dechlorination achieved and the current efficiency. The electrochemical reduction of hexachlorobenzene (HCB) has been studied in micellar aqueous solutions using Triton-SP 175 which, unlike conventional surfactants, is acid-labile. At pH3, the hydrophobic residue cleaves from the hydrophilic chain, leaving a solution without surface-active properties and allowing recovery of the electrolysis products from the solution. A micellar solution containing 0.1% v/v Triton-SP 175 and 1% v/v heptane as cosolvent was indefinitely stable in the presence of 0.05 M sodium sulfate as an environmentally friendly supporting electrolyte. Electrolytic dehalogenation to less chlorinated benzenes was studied at a wide variety of cathodes; in all cases a quantitative material balance of phenyl residues was achieved. Lead was the preferred cathode in terms of both the degree of dechlorination achieved and the current efficiency.
Synthesis of Decorated Carbon Structures with Encapsulated Components by Low-Voltage Electric Discharge Treatment
Bodrikov, I. V.,Pryakhina, V. I.,Titov, D. Yu.,Titov, E. Yu.,Vorotyntsev, A. V.
, p. 60 - 69 (2022/03/17)
Abstract: Polycondensation of complexes of chloromethanes with triphenylphosphine by the action of low-voltage electric discharges in the liquid phase gives nanosized solid products. The elemental composition involving the generation of element distribution maps (scanning electron microscopy–energy dispersive X?ray spectroscopy mapping) and the component composition (by direct evolved gas analysis–mass spectrometry) of the solid products have been studied. The elemental and component compositions of the result-ing structures vary widely depending on the chlorine content in the substrate and on the amount of triphenylphosphine taken. Thermal desorption analysis revealed abnormal behavior of HCl and benzene present in the solid products. In thermal desorption spectra, these components appear at an uncharacteristically high temperature. The observed anomaly in the behavior of HCl is due to HCl binding into a complex of the solid anion HCI-2 with triphenyl(chloromethyl)phosphonium chloride, which requires a relatively high temperature (up to 800 K) to decompose. The abnormal behavior of benzene is associated with its encapsulated state in nanostructures. The appearance of benzene begins at 650 K and continues up to temperatures above 1300?K.
Frustrated Lewis pairs incorporating the bifunctional Lewis acid 1,1′-fc{B(C6F5)2}2: Reactivity towards small molecules
Tirfoin, Rémi,Gilbert, Jessica,Kelly, Michael J.,Aldridge, Simon
, p. 1588 - 1598 (2018/02/09)
Applications of the bifunctional ferrocenediyl Lewis acid 1,1′-fc{B(C6F5)2}2 in frustrated Lewis pair (FLP) chemistry are described. The coordination (or otherwise) of a range of sterically encumbered C-, N- and P-centred Lewis bases has been investigated, with lutidine, tetramethylpiperidine, PPh3, PtBu3 and the expanded ring carbene 6Dipp being found to be sterically incapable of coordinate bond formation. The chemistry of a range of these FLPs in the presence of H2O, NH3, CO2 and cyclohexylisocyanate (CyNCO) has been investigated, with the patterns of reactivity identified including simple coordination chemistry, E-H bond cleavage and C-B insertion.
Nickel-catalyzed hydrodehalogenation of aryl halides
Weidauer, Maik,Irran, Elisabeth,Someya, Chika I.,Haberberger, Michael,Enthaler, Stephan
supporting information, p. 53 - 59 (2013/08/25)
In the present study, the nickel-catalyzed dehalogenation of aryl and alkyl halides with iso-propyl zinc bromide or tert-butylmagnesium chloride has been examined in detail. With a straightforward nickel complex as pre-catalyst good to excellent yields and chemoselectivities were feasible for a variety of aryl and alkyl halides.
