Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Arsenic acid esters

Arsenic acid esters and other oxaorganic compounds 245... [Pg.237]

Although most of the macrocycles that contain phosphorus or arsenic which have thus far been prepared, are primarily transition metals binders, two compounds have been prepared which are essentially crown ethers containing phosphorus. Kudrya, Shtepanek and Kirsanovhave prepared two compounds which are essentially polyoxygen macrocycles but which contain one or two methylphosphonic acid esters as part of the ring. These two macrocycles are shown below as 7d and 17 and are both prepared by the reaction of 2,2 [oxybis(ethyleneoxy)] bisphenolate with methylphosphonic dichloride in a mixture of acetonitrile and benzene. The crystalline monomer 16) and dimer 17) were isolated in 17% and 11% yields respectively as indicated in Eq. (6.13). [Pg.273]

Phosphoric acid esters having a low content of arsenic can be obtained by treating with 0.1-10% adsorbents such as activated clay, active carbon, alumina, and silica gel to decrease the arsenic content. Thus, 100 parts lauryl phosphate containing 10.3 ppm As and 2 parts activated clay were mixed at 60-70°C for 2 h and filtered to give lauryl phosphate only containing 0.6 ppm As [28]. [Pg.559]

The chemistry of sulphonic acids, esters and their derivatives The chemistry of alkanes and cycloalkanes Supplement S The chemistry of sulphur-containing functional groups The chemistry of organic arsenic, antimony and bismuth compounds The chemistry of enamines (2 parts)... [Pg.1058]

Formic and oxalic acids and their salts in the presence of mineral acid reduce arsenic acid and arsenates the reaction is accelerated by boiling.10 Tartaric acid does not appear to form complexes with arsenic acid 11 such as are formed with arsenious acid. Certain sugars, namely fructose and less rapidly sucrose, but not glucose, maltose or lactose, form labile esters of arsenic acid during fermentation in the presence of this acid the reaction is purely a chemical one and not biochemical.12... [Pg.189]

Fuel additives - [AMNES-CYCLOALIPHATIC AMINES] (Vol 2) - [SULFONIC ACIDS] (Vol 23) -arsenic compds as [ARSENIC COMPOUNDS] (Vol 3) -boron compds as [BORON COMPOUNDS - BORIC ACID ESTERS] (Vol 4) -coordination compounds as [COORDINATION COMPOUNDS] (Vol 7) -ethers m [ETHERS] (Vol 9) -magnesium alkyls as [MAGNESIUM COMPOUNDS] (Vol 15) -polyamines as [DIAMINES AND HIGHER AMINES ALIPHATIC] (Vol 8) -htanates as [TITANIUM COMPOUNDS - ORGANIC] (Vol 24) -use of copper compounds [COPPER COMPOUNDS] (Vol 7)... [Pg.425]

Inorganic arsenic complexes based on oxygen ligands is scarce. Simple esters of arsenic acid, As(0)(0R)3 (R = Me, Ft, n-Pr, n-Bu, CeHn) have tetragonal structures. Reaction of the diol ligand 2,4-dimethyl-2,4-pentanediol with AsCfr affords an arsenic chloride complex in which the As atom is part of a six-membered ring (37). ... [Pg.240]

These As-O bonded species are related by the fact that they contain arsenic in the +3 oxidation state and have one organo substituent bonded to the arsenic. The general formulas are as follows arsonous acids, RAs(OH)2 arsonous acid anhydrides, RAsO arsonous acid esters, RAs(OR )2-... [Pg.264]

Human Pharmacologic Characcericties of 14 Glycolic Acid Esters (Based on Edgewood Arsenal Studies, 1960-1971)... [Pg.84]

The esters of arsinic acid are more thermally labile, often resinifying on distillation. However, catalysed pyrolyses using alkyl halides, salts or mineral acids afford useful yields ca 50%) of arsenic(III) esters . The mechanism is considered to involve the pyrolysis of an alkoxyarsonium salt 7 is formed with the catalyst. [Pg.544]

The pyrolysis of organoarsenic compounds containing the arsenyl moiety has some limited preparative applications [arsenyl (As=0) by analogy with phosphoryl (P=0)]. The compounds are based on the arsonic acid RAs(0)(0H)2, the arsinic acid R2As(0)0H and the arsine oxide R3As=0 structures. The acids are in interesting contrast with the phosphorus series. The phosphonic and phosphinic esters are prepared from the phosphorus(III) precursors via the Arbuzov synthesis. This synthetic route fails with the arsenic analogues, and further, if an alkyl halide or a salt is added in the pyrolysis of arsonic or arsinic acid esters a retro-Arbuzov reaction takes place . ... [Pg.544]

The pyrolysis of arsonic acid esters results in low yields of arsenic(III) esters. [Pg.544]


See other pages where Arsenic acid esters is mentioned: [Pg.86]    [Pg.3288]    [Pg.86]    [Pg.3288]    [Pg.300]    [Pg.28]    [Pg.66]    [Pg.471]    [Pg.544]    [Pg.471]    [Pg.544]    [Pg.166]    [Pg.245]    [Pg.127]    [Pg.265]    [Pg.817]    [Pg.875]    [Pg.199]    [Pg.544]    [Pg.544]   
See also in sourсe #XX -- [ Pg.245 ]

See also in sourсe #XX -- [ Pg.3 , Pg.245 ]




SEARCH



Arsenic acid

Arsenous Acid

© 2024 chempedia.info