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Tetrahaloborate

See other diazonium tetrahaloborates, high-nitrogen compounds, n-... [Pg.1219]

ALKYLBORANES, ALKYLHALOBORANES AZOCARBABORANES, BORANES, CARBABORANES DIAZONIUM TETRAHALOBORATES, HALOBORANES... [Pg.79]

ARENEDIAZONIUM OXIDES, DIAZONIUM CARBOXYLATES DIAZONIUM PERCHLORATES, DIAZONIUM SULFATES DIAZONIUM SULFIDES AND DERIVATIVES DIAZONIUM TETRAHALOBORATES, DIAZONIUM TRIIODIDES... [Pg.116]

DEVARDA S ALLOY DIAZONIUM TETRAHALOBORATES ISOXAZOLES NITROBENZALDEHYDES NITROBENZYL COMPOUNDS... [Pg.169]

The diazonium salt decomposes violently above 25°C or when dry. See other DIAZONIUM TETRAHALOBORATES... [Pg.684]

See Other DIAZONIUM TETRAHALOBORATES, HIGH-NITROGEN COMPOUNDS, N-OXIDES... [Pg.1267]

See diazonium tetrahaloborates (reference 5), induction period incidents... [Pg.2269]

DIAZONIUM CARBOXYLATES DIAZONIUM PERCHLORATES DIAZONIUM SUEFATES DIAZONIUM SUEFIDES AND DERIVATIVES DIAZONIUM TETRAHALOBORATES DIAZONIUM TRIIODIDES See also TETRAZOLES... [Pg.2303]

Diaza-2-boracycloalkanes, 93 Diazirines, 93 Diazoazoles, 94 Diazo compounds, 94 Diazoethers, 96 Diazomethane salts, 96 Diazonium carboxylates, 96 Diazonium perchlorates, 96 Diazonium salts, 97 Diazonium sulfates, 98 Diazonium sulfides and derivatives, 99 Diazonium tetrahaloborates, 100 Diazonium triiodides, 101 a-Diazo-/J-oxosulfones, 102 Diazotisation, 102... [Pg.2637]

N-Trialkyl-B-trihaloborazines can be prepared without difficulty from alkylammonium halide or alkylamine and trihaloborane 4> when the resulting alkylammonium tetrahaloborate or alkylamine-trihalo-borane is refluxed in chlorobenzene. Yields are nearly quantitative in most cases. This same observation holds true for N-triaryl-B-trihalo-borazines. Extensive studies using thermogravimetric methods in addition to preparative methods did not provide for the isolation or identification of any intermediates between the amine-trihaloborane and the borazine stage of the reaction 45 4fl>. [Pg.66]

Halide ion Y" in the form of soluble tetraalkylammonium salts can in some cases displace halide ion X forming a mixed-halogen adduct. However, the method has met with variable success. It is successful with tetrahaloborate ions (80) and with Me3N BI3 (9). A similar reaction with insoluble silver halides or pseudohalides has also given mixed adducts (43). [Pg.150]

See other pages where Tetrahaloborate is mentioned: [Pg.595]    [Pg.598]    [Pg.690]    [Pg.724]    [Pg.886]    [Pg.1025]    [Pg.504]    [Pg.82]    [Pg.118]    [Pg.63]    [Pg.99]    [Pg.32]    [Pg.2065]    [Pg.687]    [Pg.775]    [Pg.956]    [Pg.1085]    [Pg.2265]    [Pg.2305]    [Pg.2358]    [Pg.595]    [Pg.598]    [Pg.690]    [Pg.724]    [Pg.886]    [Pg.1025]    [Pg.33]    [Pg.147]    [Pg.149]    [Pg.149]   


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Aryldiazonium tetrahaloborates

DIAZONIUM TETRAHALOBORATES

Tetrahaloborate adducts

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