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Mercury aryls

On the basis of results obtained with other mercury aryls the flow system decomposition of this compound in the presence of toluene was assumed to be first-order and homogeneous. The extent of decomposition for the 9 runs carried out was determined by isolation of the undecomposed aryl. Detailed analysis of other products was not attempted. [Pg.234]

Other metals capable of electrophilic substitution of C-H bonds are salts of palladium and, environmentally unattractive, mercury. Methane conversion to methanol esters have been reported for both of them [29], Electrophilic attack at arenes followed by C-H activation is more facile, for all three metals. The method for making mercury-aryl involves reaction of mercury diacetate and arenes at high temperatures and long reaction times to give aryl-mercury(II) acetate as the product it was described as an electrophilic aromatic substitution rather than a C-H activation [30],... [Pg.399]

Nitrogen dioxide plays an important role in the reaction. It is this compound that is responsible for the conversion of mercury aryl nitrates into nitroso derivatives. [Pg.113]

DFG MAK Confirmed Animal Carcinogen with Unknown Relevance to Humans NIOSH REL (Mercury, Aryl and Inorganic) CL 0.1 mg/m3 (skin)... [Pg.5]

ACGIH TLV TWA 0.01 mg/m Confirmed Human Carcinogen BEI 35 n (As)/L inorganic arsenic and methylated metabolites in urine BEI 35 ng/g creatinine total inorganic mercury in urine preshift 15 Hg/g creatinine total inorganic mercury in blood at end of shift at end of workweek. NIOSH REL (Arsenic, Inorganic) CL 0.002 mg(As) /m3/15M (Mercury, Aryl and Inorganic) CL 0.1 mg/m (skin)... [Pg.880]

The monoaryl boric acids, RB(OH)2, arc usually isolated, as stated al >o x, l)y the action of water on the type RBXg, aitliough in certain cases this leads to the formation of the oxide RBO. The phenyl eom >ound has l)ecn obtained b " boiling with water the product of reaction from magnesium phenyl bromide and boron trifluoride. The most remarkable feature of the type RE(OH)2 is that the action of iiiercuric chloride upon them leads to the production of mercury aryl halides (RHgX). The anisyl and phenetyl compounds do not yield oxides when heated, or form salts, and tlie jS-naphthyl acid exists in two modifications. Dehydration of the acids in maw gives the oxides, RBO. [Pg.220]


See other pages where Mercury aryls is mentioned: [Pg.233]    [Pg.10]    [Pg.15]    [Pg.274]    [Pg.871]    [Pg.872]    [Pg.872]    [Pg.874]    [Pg.875]    [Pg.877]    [Pg.878]    [Pg.879]    [Pg.879]    [Pg.881]    [Pg.881]    [Pg.881]    [Pg.983]    [Pg.1450]    [Pg.2401]    [Pg.714]    [Pg.1013]    [Pg.1033]    [Pg.2557]    [Pg.82]    [Pg.2176]   


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Aryl mercury

Aryl mercury

Aryl mercury compounds

Aryl-mercury bond dissociation

Mercury aryl derivatives

Mercury aryl halides

Mercury cathodes, arylation

With Aryl Mercury Chlorides

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