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Alkanes mercury salts

Catalytic forms of copper, mercury and silver acetylides, supported on alumina, carbon or silica and used for polymerisation of alkanes, are relatively stable [3], In contact with acetylene, silver and mercury salts will also give explosive acetylides, the mercury derivatives being complex [4], Many of the metal acetylides react violently with oxidants. Impact sensitivities of the dry copper derivatives of acetylene, buten-3-yne and l,3-hexadien-5-yne were determined as 2.4, 2.4 and 4.0 kg m, respectively. The copper derivative of a polyacetylene mixture generated by low-temperature polymerisation of acetylene detonated under 1.2 kg m impact. Sensitivities were much lower for the moist compounds [5], Explosive copper and silver derivatives give non-explosive complexes with trimethyl-, tributyl- or triphenyl-phosphine [6], Formation of silver acetylide on silver-containing solders needs higher acetylene and ammonia concentrations than for formation of copper acetylide. Acetylides are always formed on brass and copper or on silver-containing solders in an atmosphere of acetylene derived from calcium carbide (and which contains traces of phosphine). Silver acetylide is a more efficient explosion initiator than copper acetylide [7],... [Pg.222]

Chlorine Chemistry in ODEs and Br-Cl Interactions MARINE BOUNDARY LAYER. 4.1 Sea Salt Aerosols Reactive Chlorine Reactive Bromine Reactive Iodine Surface Segregation Effects IMPACT OF HALOGEN CHEMISTRY ON SPECIES OTHER THAN OZONE. 5.1 Alkanes. 5.2 Mercury. 5.3 Sulfur SALT LAKES... [Pg.1935]

Oxidation of a-amino-acids with silver(ii) picolinate gives almost quantitative yields of nor-aldehydes silver oxide causes further oxidation to the nor-acid. The possibility is suggested of the simultaneous operation of a radical mechanism in solution and a two-electron shift process at the solid silver salt surface. Aryl alkanes and aryl alkanols are oxidized by silver(ii) picolinate to aldehydes and ketones, a-Aminoketones are dehydrogenated by mercury(ii) salts to ketones iminium ions, such as (139), are postulated as intermediates (Scheme 58). [Pg.123]


See other pages where Alkanes mercury salts is mentioned: [Pg.697]    [Pg.203]    [Pg.697]    [Pg.3]    [Pg.3]    [Pg.697]    [Pg.2326]    [Pg.272]    [Pg.3]    [Pg.375]    [Pg.343]    [Pg.360]    [Pg.387]    [Pg.432]    [Pg.472]    [Pg.802]    [Pg.806]    [Pg.806]    [Pg.49]    [Pg.119]    [Pg.428]    [Pg.450]    [Pg.500]    [Pg.500]    [Pg.531]    [Pg.532]    [Pg.549]    [Pg.552]    [Pg.902]    [Pg.904]    [Pg.906]    [Pg.906]    [Pg.907]    [Pg.908]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.5 , Pg.7 ]

See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.5 , Pg.7 , Pg.11 ]




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Mercury salts

Mercury salts reactions with alkanes

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