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Boron Compounds Borane-Sodium borohydride

Electroless nickel—boron baths use sodium borohydride or dimethylamine borane [74-94-2] in place of sodium hypophosphite (see Boron compounds). The nickel—boron aHoy is brittle, highly stressed, and much more expensive than nickel—phosphoms aHoys. Nickel—boron is mainly used to replace gold in printed circuit board plating. [Pg.108]

Any of these BH3 compounds adds readily to most alkenes at room temperature or lower temperatures. The reactions usually are carried out in ether solvents, although hydrocarbon solvents can be used with the borane-dimethyl sulfide complex. When diborane is the reagent, it can be generated either in situ or externally through the reaction of boron trifluoride with sodium borohydride ... [Pg.421]

Hydrazine—borane compounds are made by the reaction of sodium borohydride and a hydrazine salt in THF (23,24). The mono-(N2H4 BH ) and di-(N2H4 2BH2) adducts are obtained, depending on the reaction conditions. These compounds have been suggested as rocket fuels (25) and for chemical deposition of nickel—boron alloys on nonmetallic surfaces (see Metallic COATINGS) (26). [Pg.277]

Boron forms a remarkable series of binary compounds with hydrogen—the boranes. These compounds include diborane, B2H6, and more complex compounds such as decaborane, B10H14. Anionic versions of these compounds, the borohydrides, are known the most important is BH4 as sodium borohydride, NaBH4. [Pg.722]

The boranes are an extensive series of binary compounds of boron and hydrogen, somewhat analogous to the hydrocarbons. The starting point for borane production is the reaction (in an organic solvent) of sodium borohydride with boron trifluoride ... [Pg.722]

Volatile boron compounds, especially boranes, are usually more toxic than boric acid or soluble borates (Table 29.9) (NAS 1980). However, there is little commercial production of synthetic boranes, except for sodium borohydride — one of the least toxic boranes (Sprague 1972). Boron trifluoride is a gas used as a catalyst in several industrial systems, but on exposure to moisture in air, it reacts to form a stable dihydride (Rusch etal. 1986). Eor boric oxide dusts, occupational exposures to 4.1 mg/m (range 1.2 to 8.5) are associated with eye irritation dryness of mouth, nose and throat sore throat and cough (Garabrant et al. 1984). [Pg.1572]

Triethylaluminum, 204 Triisobutylaluminum, 205 Trimethylaluminum, 22, 205 Vilsmeier reagent-Lithium tri-r-butoxy-aluminum hydride, 342 Boron Compounds Alkyldimesitylboranes, 8 Allenylboronic acid, 36 9-Borabicyclo[3.3.1]nonane, 92 Borane-Dimethylamine, 42 Borane-Dimethyl sulfide-Sodium borohydride, 25... [Pg.406]

Boron Hydrides The boron hydrides, or boranes, are volatile, molecular compounds with formulas B Hm. The simplest is diborane (B2H6), the dimer of the unstable BH3. Diborane can be prepared by the reaction of sodium borohydride (NaBH4) and iodine in an appropriate organic solvent ... [Pg.822]


See other pages where Boron Compounds Borane-Sodium borohydride is mentioned: [Pg.309]    [Pg.31]    [Pg.638]    [Pg.110]    [Pg.638]    [Pg.290]    [Pg.307]    [Pg.910]    [Pg.185]    [Pg.38]   
See also in sourсe #XX -- [ Pg.42 ]




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Boron Compounds borohydride

Boron boranes

Boron borohydride

Boron compounds

Sodium borohydride borane

Sodium borohydride compounds

Sodium compounds

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