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Walker studies

In 1948 Maxted and Walker studied the detoxification of catalyst poisons in the hydrogenation of aromatic hydrocarbons and found that the isomeric thienothiophenes 1 and 2 could be converted into the sul-fones of fully hydrogenated thienothiophenes 1 and 2, which do not poison the catalysts. This conversion is performed by brief preliminary hydrogenation and subsequent oxidation by hydrogen peroxide or per-molybdic acid. However, no data on the isolation or foe properties of these disulfones are available. It has been reported that direct oxidation of thienothiophenes 1 and 2 does not produce sulfones. [Pg.198]

Some ortho substitution usually occurs as well. For preparative purposes the sulphate is hydrolysed by acid to give a para-diphenol. Behrman and Walker studied the kinetics of oxidation of 2-hydroxy-pyridine and o-nitrophenol. For both these compounds the kinetics are second order, viz. [Pg.477]

Shaede and Walker studied the reaction of sodium amalgam with water in the presence of dinitrogen monoxide and methanol at various pH values. Radiolysis experiments had already established that dinitrogen monoxide is a very efficient, specific electron scavenger... [Pg.434]

Oyne and Walker studied reaction (26) at elevated temperatures (300—686 K)... [Pg.278]

Walker studied the protons emitted with energies of 70 Mev and above at a number of angles from a carbon target bombarded by a 195 Mev beam. [Pg.515]

Adsorption of phenol and its derivatives from aqueous solutions on active carbons and carbon blacks has been the subject matter of a large number of investigations. Jaroniec and coworkers,Enrique et al. Worch and Zakke, and Magne and Walker studied the adsorption of several phenols from aqueous solutions and found that the adsorption was partly physical and partly chemical in character. Aytekin, ChapUn, and Kiselev and Krasilinkov observed that the adsorption isotherms of phenol from aqueous solutions were step-wise, suggesting the possibility of rearrangement of phenol molecules in the adsorbed phase and their interaction with active sites on the carbon surface. Morris and Weber, however, found that the adsorption isotherms of phenols on active carbons show two plateaus, even... [Pg.150]

Jackson and Walker studied the applicability of pyrolysis combined with capillary column gas chromatography mass spectrometry to the examination of phenyl polymers (eg. styrene-isoprene copolymer) and polymer like phenyl ethers (eg. bis(m-(m-phenoxy phenoxy)phenyl)ether). They examined the effect of varying parameters affecting the nature of products formed and relative product distribution in routine pyrolysis. These parameters include the effects of pyrolysis temperature rise times, pyrolysis temperatures up to 985 C and pyrolysis duration. Temperature rise time (0.1 to 1.5 s) is not a critical factor in the Curie point pyrolysis of a styrene-isoprene copolymer, either with regard to the nature of the products formed or their relative distributions. Additionally, the variation of pyrolysis duration or hold time (2.0 to 12.5 s) at a fixed Curie temperature reflected no change in the nature of components formed however changes in product distributions were observed. Variations in Curie temperature at a fixed pyrolysis duration produced drastic changes in product distributions such as a three-... [Pg.147]

So far we have exclusively discussed time-resolved absorption spectroscopy with visible femtosecond pulses. It has become recently feasible to perfomi time-resolved spectroscopy with femtosecond IR pulses. Flochstrasser and co-workers [M, 150. 151. 152. 153. 154. 155. 156 and 157] have worked out methods to employ IR pulses to monitor chemical reactions following electronic excitation by visible pump pulses these methods were applied in work on the light-initiated charge-transfer reactions that occur in the photosynthetic reaction centre [156. 157] and on the excited-state isomerization of tlie retinal pigment in bacteriorhodopsin [155]. Walker and co-workers [158] have recently used femtosecond IR spectroscopy to study vibrational dynamics associated with intramolecular charge transfer these studies are complementary to those perfomied by Barbara and co-workers [159. 160], in which ground-state RISRS wavepackets were monitored using a dynamic-absorption technique with visible pulses. [Pg.1982]

Diller R, Malt S, Walker G 0, Cowen B R, Pippenger R, Bogomoini R A and Hochstrasser R M 1995 Femtosecond time-resolved infrared laser study of the J-K transition of bacteriorhodopsin Chem. Rhys. Lett. 241 109-15... [Pg.1999]

Vl L, J R Walker and C R A Catlow 1984. A Molecular Dynamics Simulation Study of the iperionic Conductor Lithium Nitride I. Journal of Physical Chemistry 17 6623-34. [Pg.366]

Oxidative dimerization of various 2-benzyloxy-2-thiazoline-5-ones (222) catalyzed by iodine and triethylamine is another example of the nucleophilic reactivity of the C-4 atom (469) (Scheme 112). Treatment of 212 with pyrrolidinocyclohexene yields the amide (223) (Scheme 113). The mechanism given for the formation of 223 is proposed by analogy with the reactivitx of oxazolones with enamines (4701. 4-Substituted 2-phenylthiazol-5(4Hi-ones react with A -morphoiino-l-cyclohexene in a similar manner (562j. Recently. Barret and Walker have studied the Michael addition products... [Pg.432]

Johnson, D. J., Structural studies of PAN-based carbon fibers. In Chemistry and Physics of Carbon, Vol. 20, ed. P. L. Walker. Marcel Dekker, New York, 1987, pp. I 58. [Pg.138]

Quantitative studies of the effect of pyridine on the rate of hydrogenation of imns-crotonic acid in the presence of a platinum catalyst have been carried out by Maxted and Walker who concluded that... [Pg.191]

Jump, D. A. Walker, I. S. Modera, M. P. (1996). Field Measurements of Efficiency and Duct Retrofit Effectiveness in Residential Forced Air Distribution Systems. In Proceedings of the ACEEE 1996 Summer Study on Energy Efficiency in Buildings, Vol. 1, pp. 147-155. Washington, DC American Council for an Energy Efficient Economy. [Pg.211]

Faraday, in 1834, was the first to encounter Kolbe-electrolysis, when he studied the electrolysis of an aqueous acetate solution [1], However, it was Kolbe, in 1849, who recognized the reaction and applied it to the synthesis of a number of hydrocarbons [2]. Thereby the name of the reaction originated. Later on Wurtz demonstrated that unsymmetrical coupling products could be prepared by coelectrolysis of two different alkanoates [3]. Difficulties in the coupling of dicarboxylic acids were overcome by Crum-Brown and Walker, when they electrolysed the half esters of the diacids instead [4]. This way a simple route to useful long chain l,n-dicarboxylic acids was developed. In some cases the Kolbe dimerization failed and alkenes, alcohols or esters became the main products. The formation of alcohols by anodic oxidation of carboxylates in water was called the Hofer-Moest reaction [5]. Further applications and limitations were afterwards foimd by Fichter [6]. Weedon extensively applied the Kolbe reaction to the synthesis of rare fatty acids and similar natural products [7]. Later on key features of the mechanism were worked out by Eberson [8] and Utley [9] from the point of view of organic chemists and by Conway [10] from the point of view of a physical chemist. In Germany [11], Russia [12], and Japan [13] Kolbe electrolysis of adipic halfesters has been scaled up to a technical process. [Pg.92]

Pharmacokinetic studies demonstrated good oral bioavailability of maraviroc and a terminal half-life of 16-23 h following multiple dosing (Abel et al. 2003 Walker et al. 2005). Single doses of up to 900 mg and multiple doses of up to 300 mg BID for 28 days were well tolerated (Abel et al. 2003 Russell et al. 2003 Walker et al. 2005). In Phase 2a studies, treatment-naive HIV-1 patients with R5 virus who received maraviroc monotherapy at doses ranging from 25 mg QD to 300 mg BID for 10 days experienced a median viral load reduction of 1.64 log jg copies/mL and... [Pg.188]

Thus, as with studies on the double-crested cormorant in the Great Lakes (see Chapter 16 in Walker et al. 2006), there is evidence of a continuing (although reduced) effect of p,p -DDE on reproductive success even after environmental levels had fallen and eggshell thinning was much less. This raises the possibility that p,p -DDE may have had toxic effects other than eggshell thinning on these species (Nisbet 1989). There is the further complication that other OCs such as PCBs, dieldrin, and hep-tachlor epoxide were present in the same samples and may have had toxic effects. [Pg.114]


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See also in sourсe #XX -- [ Pg.213 , Pg.218 ]




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