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Phenylarsines

The Bart reaction can be carried a stage further. For example, dichloro-phenylarsine, CjHjAsCl, when added to an excess of sodium carbonate solution, gives CjHjAsfONa) this solution, if similarly treated with benzenedia-zonium chloride, affords diphenylarsinic acid, (CjHjjjAsf. OjOH. [Pg.312]

Good yields of phenylarsine [822-65-17, C H As, have been obtained by the reaction of phenylarsenic tetrachloride [29181-03-17, C H AsCl, or phenyldichloroarsine [696-28-6], C3H3ASCI25 with lithium aluminum hydride or lithium borohydride (41). Electrolytic reduction has also been used to convert arsonic acids to primary arsines (42). Another method for preparing primary arsines involves the reaction of arsine with calcium and subsequent addition of an alkyl haUde. Thus methylarsine [593-52-2], CH As, is obtained in 80% yield (43) ... [Pg.335]

Use of a pH buffer of 8—9 has been suggested as a substitute for the pH 7 buffer for more accurate analysis. Sodium thiosulfate [10102-17-7] Na2S202, or phenylarsine oxide [637-03-6] C H AsO, are the typical titrants. [Pg.485]

Phenylarsine with symmetric disubstituted diacetylenes ( -LiBu, benzene) forms arsoles 79 in 33-83% yield (68TL3257). [Pg.178]

Chlor-. of or combined with chlorine, chloro (as Chlorbenzoeadure, chlorobenzoic acid), chloride of (as Chlorzink, zinc chloride), chlorahnlich, a. like chlorine, chlorinous. Chlor-alaun, m. chloralum, -alkalien, n.pl. alkali-metal chlorides, -allyl, n, allyl chloride, -aluminium, n. aluminum chloride, -ammon, m., -ammonium, n. ammonium chloride, -amyl, n, amyl chloride, -antimon, n, antimony chloride, -arsenlk, n. chloride of arsenic, -arsenikldsung, /, (Pkarm.) solution of arsenious add, hydrochloric solution of arsenic, -arsinkampfstoff, m. chlorodi-phenylarsine, adamsite, chlorartig, a. like chlorine, chlorinous,... [Pg.90]

Table 4. Contribution from processes at various stages in the tri-phenylarsine benzene system ... Table 4. Contribution from processes at various stages in the tri-phenylarsine benzene system ...
The atmosphere surrounding the samples is also occasionally important. Grossmann has claimed that the smalt but significant difference he found between vacuum and air irradiations must be proportional to the rate of diffusion of dissolved oxygen through his phenylarsine lattices. Collins has found a similar dependence on CO atmosphere in the irradiation and annealing of (Cr,Mo,W)(CO)e. [Pg.91]

Finally, the bis(trimethylsilyl) phenylarsine 1720 reacts with DMF in the presence of catalytic amounts of NaOH to give 1721, with a related As=C bond, and HMDSO 7 [25] (Scheme 11.6). [Pg.256]

Abbreviations DEPC, diethylpyrocarbonate DCCD, Af.iV -dicyclohexylcarbodiimide EEDQ, N-ethyoxycarbonyl-2-ethoxy-1,2-dihydroquinoline NEM, A-ethylmaleimide PAO, phenylarsine oxide NPM, IV-phenylmaleimide PLP, pyridoxal phosphate DIDS, diisothiocyanostilbene disulfonate PITC, phenylisothiocyanate. [Pg.250]

Kulanthaivel et al. [28] found that the apical Na /H exchanger in human placenta (sensitive-type) was sensitive to phenylarsine oxide, a reagent specific for dithiols that are situated in close proximity (vicinal dithiols). Moreover, the effect of phenylarsine oxide was to decrease without affecting apparent affinity for... [Pg.253]

Balch, A.L., Fung, E.Y. and Olmstead, M.M. (1990) Polynuclear ((diphenylphosphmo)methyl) phenylarsine bridged complexes of gold(I). Bent chains of gold(I) and a role for Au(I)—Au(I) interactions in guiding a reaction. Journal of the American Chemical Society, 112, 5181-5186. [Pg.280]

Thus the synthesis of diheteroferrocenes depends on the availability of the corresponding heteroles, which have been prepared by just a few routes. l-Phenyl-2,5-disubstituted arsoles are prepared generally from the corresponding 1,3-diynes by the base-catalyzed addition of phenylarsine. In this manner, Markl and Hauptmann have prepared 1-phenyl-2,5-dimeth-ylarsole (25) in 30% yield.4 Subsequently, Mathey et al. used this arsole to prepare the first diarsaferrocene 26.5 (see Scheme 2.)... [Pg.327]

Urine CVAA Solid phase microextraction headspace sampling, followed by GC/MS with El ionisation Deuterated CVAA Phenylarsine oxide LOD 500 ppt Short window for detection. Lack of validation in human samples. [Pg.131]

It is noteworthy that, unlike the previously described induces of PTPC opening, GD3 is able to exert its effect on mitochondria even in the presence of submicromolar calcium concentration (Kristal and Brown, 1999a), a property shared only by the most potent PT inducers, such as the thiol cross-linking agent phenylarsine oxide and by the peptide mastoparan. This low calcium requirement is important because intracellular calcium concentration during CD95-mediated apoptosis was not described to rise above 0.4 pM (Oshimi and Miyazaki, 1995). [Pg.299]

Phenylarsine oxide (20 [rM 30 minutes) is used as an inhibitor for receptor-mediated (clathrin-mediated) endocytosis (48). [Pg.353]

Water/waste water Measure initial temperature and pH and protect sample from light throughout the procedure. Phenylarsine oxide is used as Amperometric titration 0.5 mg/L No data APHA 1998 (Method 2350-C) (Method 4500-CL02-C) (Method 4500-CL02-E)... [Pg.115]

For APHA Methods 2350-C and 4500-CL02-E, amperometric analyzers are used to measure chlorine dioxide in water. Amperometric analyzers measure the current that is necessary to maintain a constant concentration of titrant as chlorine dioxide reduces the titrant (e.g., phenylarsine oxide). This method is limited by interference from compounds that might react with the titrant (e.g., chlorine and chloroamine) (APHA 1998). [Pg.117]

Chlorine gas may be identified readdy by its distinctive color and odor. Its odor is perceptible at 3 ppm concentration in air. Chlorine may be measured in water at low ppm by various titrimetry or colorimetric techniques (APHA, AWWA and WEF. 1999. Standard Methods for the Examination of Water and Wastewater, 20th ed. Washington DC American Pubhc Health Association). In iodometric titrations aqueous samples are acidified with acetic acid followed by addition of potassium iodide. Dissolved chlorine liberates iodine which is titrated with a standard solution of sodium thiosulfate using starch indicator. At the endpoint of titration, the blue color of the starch solution disappears. Alternatively, a standardized solution of a reducing agent, such as thiosulfate or phenylarsine oxide, is added in excess to chlorinated water and the unreacted reductant is then back titrated against a standard solution of iodine or potassium iodate. In amperometric titration, which has a lower detection limit, the free chlorine is titrated against phenyl arsine oxide at a pH between 6.5 and 7.5. [Pg.212]

The total free chlorine in wastewaters as measured by colorimetric techniques constitutes both the dissolved molecular chlorine, hypochlorite ion, OCl, and hypochlorous acid. An equilibrium exists between these species, the concentrations of which depend on the temperature and pH of the waste-water. Concentration of the hypochlorous acid may be estimated from the K value or from the ratio (33% of the measured concentration of free chlorine). The free chlorine may be measured by amperometric titration after the addition of a phosphate buffer solution to produce a pH between 6.5 and 7.5. The sample is titrated against a standard solution of phenylarsine oxide. Alternatively, the syringaldazine (3,5-dimethoxy-4-hydroxybenzaldazine) colorimetric test may be performed. This color-forming reagent in 2-propanol yields a colored product with free chlorine, the absorbance of which may be... [Pg.388]

Phenylarsine bis (diethyl dithiocarbamate), secondary bonding by, 15 30-31 Phenylazidosilanes, properties, 9 141 (Phenylazo)acetaldoxime complexes, osmium, 37 270... [Pg.233]

Ammonium perchlorate Ammonium perchlorate Arsenic hydride, Hydrogen arsenide Distilled arsine, Phenylarsine, Diphenylarsine... [Pg.42]


See other pages where Phenylarsines is mentioned: [Pg.229]    [Pg.748]    [Pg.748]    [Pg.503]    [Pg.286]    [Pg.714]    [Pg.90]    [Pg.96]    [Pg.261]    [Pg.945]    [Pg.1055]    [Pg.222]    [Pg.121]    [Pg.122]    [Pg.346]    [Pg.353]    [Pg.627]    [Pg.1482]    [Pg.14]    [Pg.68]    [Pg.96]    [Pg.124]    [Pg.172]    [Pg.277]    [Pg.285]    [Pg.402]    [Pg.139]   


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Bis phenylarsine

Inhibitors phenylarsine oxides

Phenylarsine

Phenylarsine oxide

Phenylarsine, reaction with diacetylenes Phenyl azide, dipolar additions

Phenylarsinic oxide

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