Halogens boron-halogen compounds

Gmelin Handbook Volumes on Boron and its Compounds (a) Main Volume (1926) (b) Supplement vol. 1 (1954) (c) Compounds 8 (NSSV 33), The tetrahydroborate ion and its derivatives (1976) (d) Compounds 9 (NSSV 34), Boron-halogen compounds , Part 1 (1976) (e) Compounds 10 (NSSV 37), Boron compounds with coordination number 4 (1976) (f) Compounds 15 (NSSV 46), Amine-boranes (1977) (g) Compounds 19 (NSSV 53), Boron-halogen compounds , Part 2 (1978) (h) Supplement Volumes (1980-82), Springer-Verlag, Berlin. 

Borverbindungen 9 Boron-Halogen Compounds, Part 1. Literature coverage from 1950 to the end of 1974. 

Amine—borane adducts have the general formula R3N BX where R = H, alkyl, etc, and X = alkyl, H, halogen, etc. These compounds, characterized by a coordinate covalent bond between boron and nitrogen, form a class of reducing agents having a broad spectmm of reduction potentials (5). 

Interactions between non-halogen-containing IIIB compounds and transition-metal complexes are found in 6.5.3. Most of these IIIB compounds are boron-containing heterocycles. A series of interesting sandwich compounds, including triple- and tetradecked complexes, are synthesized by methods in 6.5.2.1-6.5.3. 

Flame resistance A1203, antimony oxides, boron compounds, halogen compounds, phosphate esters, metal hydrates, magnesium compounds, tin compounds, molybdenum compounds, silicones Al, B, Br, Cl, Mo, P, Sb, Si, Sn, Zn... 

Fluorine also reacts with other halogens, forming interhalogen compounds. While with bromine and iodine it reacts vigorously at ordinary temperatures, with chlorine the reaction occurs at 200°C. Such interhalogen products with these halogens include iodine heptafluoride, bromine trifluoride, bromine pentafluoride, and chlorine trifluoride. Metalloid elements, such as arsenic, silicon, selenium, and boron also inflame in a stream of fluorine, forming fluorides. 

Lewis acids such as boron trihalides will also form stronger bonds with fluoride than with the other halogens, and can be used to abstract fluoride selectively from halogenated compounds. Some examples of Friedel-Crafts alkylations with fluoro-haloalkanes in which only fluoride is displaced are sketched in Scheme 4.14. As shown by the last example, however, hydride migrations can readily occur under such strongly acidic reaction conditions. 

Pohland, E. Concerning Non-metal Halogen Compounds. II. Information on Boron Tribromide. Z. anorg. Chem. 201. 282 (1931). 

In principle, oxidation could occur simultaneously during a HDH (reduction) reaction. For example any de-halogenated compounds could be oxidised to C02 in the anode compartment. Thus in the case of pentachlorophenol the phenol produced by the HDH could be oxidised at a suitable anode (e.g. boron-doped diamond) to C02 ... 

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