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AMMINECHROMIUM PEROXOCOMPLEXES

See related AMMINECHROMIUM PEROXOCOMPLEXES See other REDOX COMPOUNDS... [Pg.593]

This complex, formerly called pyridine perchromate and now finding application as a powerful and selective oxidant, is violently explosive when dry [1], Use while moist on the day of preparation and destroy any surplus with dilute alkali [2], Preparation and use of the reagent have been detailed further [3], The analogous complexes with aniline, piperidine and quinoline may be similarly hazardous [4], The damage caused by a 1 g sample of the pyridine complex exploding during desiccation on a warm day was extensive. Desiccation of the aniline complex had to be at ice temperature to avoid violent explosion [4]. Pyridinium chlorochromate is commercially available as a safer alternative oxidant of alcohols to aldehydes [5], See Chromium trioxide Pyridine Dipyridinium dichromate See Other AMMINECHROMIUM PEROXOCOMPLEXES... [Pg.1076]

METAL OXOHALOGENATES AMMINECHROMIUM PEROXOCOMPLEXES OXOSALTS OF NITROGENOUS BASES METALOXONON-METALLATES Organic group entries are fairly conventional, such as HALOALKENES NITROARL COMPOUNDS DIAZONIUM SALTS... [Pg.2120]


See other pages where AMMINECHROMIUM PEROXOCOMPLEXES is mentioned: [Pg.338]    [Pg.360]    [Pg.361]    [Pg.469]    [Pg.577]    [Pg.584]    [Pg.585]    [Pg.605]    [Pg.1078]    [Pg.1080]    [Pg.1108]    [Pg.1163]    [Pg.1186]    [Pg.1245]    [Pg.1246]    [Pg.1256]    [Pg.1478]    [Pg.1773]    [Pg.55]    [Pg.61]    [Pg.149]    [Pg.252]    [Pg.333]    [Pg.36]    [Pg.42]    [Pg.130]    [Pg.233]    [Pg.314]    [Pg.375]    [Pg.400]    [Pg.401]    [Pg.528]    [Pg.662]    [Pg.670]    [Pg.672]    [Pg.681]    [Pg.693]    [Pg.1134]    [Pg.1136]    [Pg.1137]    [Pg.1162]    [Pg.1214]    [Pg.1235]    [Pg.1291]    [Pg.1293]    [Pg.1302]   
See also in sourсe #XX -- [ Pg.37 ]




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AMMINECHROMIUM

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