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Halogen donor

Halogen donors are chemicals that release active chlorine or bromine when dissolved in water. After release, the halogen reaction is similar to that of chlorine or bromide from other sources. SoHd halogen donors commonly used in cooling water systems include l-bromo-3-chloro-5,5-dimethyIhydantoin, l,3-dichloro-5,5-dimethyIhydantoin, and sodium dichloroisocyanurate. [Pg.272]

Halogens add to the double bond of the alcohol to afford the corresponding dihalo derivatives, eg, CgH CHXCHXCH20H, where X = Cl or Br. The allyHc chloride C H Cl [2687-12-9] can be obtained by treatment of the alcohol with hydrochloric acid, thionyl chloride, or carbon tetrachloride—triphenylphosphine as the halogen donor. [Pg.175]

More general procedures for additions of halogen fluorides to highly fluori-nated olefins involve reactions with a source of nucleophilic fluoride ion, such as an alkali metal fluoride, in the presence of aposttive halogen donor [62 107, lOff, 109, 110, 111] (equations 11 and 12) These processes are likely to occur by the generation and capture of perfluorocarbamonic intermediates Tertiary fluormated carbanions can be isolated as cesium [112], silver [113], or tns(dimethylamino)sul-... [Pg.65]

X-ray Structures and Electronic Spectra of the Jt-Halogen Complexes between Halogen Donors and Acceptors with jr-Receptors... [Pg.10]

Roewer G, Herzog U, Trommer K, Muller E, Friihauf S (2002) Silicon Carbide - A Survey of Synthetic Approaches, Properties and Applications 101 59-136 Rosa A, Ricciardi G, Gritsenko O, Baerends EJ (2004) Excitation Energies of Metal Complexes with Time-dependent Density Functional Theory 112 49-116 Rosokha SV, Kochi JK (2007) X-ray Structures and Electronic Spectra of the n-Halogen Complexes between Halogen Donors and Acceptors with jc-Receptors. 126 137-160 Rudolf P, see Golden MS (2004) 109 201-229... [Pg.225]

Resin cures utilise the same resins that are used for butyl rubber, but more resin (ca. 10-12 phr) and a halogen donor (10 phr), typically bromobutyl, or polychloroprene, are required. Although heat stability is slightly improved by resin curing when compared to sulphur cures, the effect is not as marked as in the resin curing of butyl. [Pg.98]


See other pages where Halogen donor is mentioned: [Pg.272]    [Pg.287]    [Pg.295]    [Pg.365]    [Pg.365]    [Pg.370]    [Pg.370]    [Pg.371]    [Pg.375]    [Pg.376]    [Pg.376]    [Pg.376]    [Pg.380]    [Pg.380]    [Pg.381]    [Pg.385]    [Pg.387]    [Pg.393]    [Pg.394]    [Pg.394]    [Pg.399]    [Pg.401]    [Pg.402]    [Pg.402]    [Pg.258]    [Pg.80]    [Pg.147]    [Pg.149]    [Pg.306]    [Pg.314]   
See also in sourсe #XX -- [ Pg.287 , Pg.291 ]




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Complexes of Halogen-Donors

Donor halogen derivatives

Donor/acceptor complexes, halogen

Donor/acceptor complexes, halogen correlations

Gold complexes halogen-donors

Halogen donor solvents

Halogen-donor Ligands

Halogen/hydrogen donors

Osmium complexes halogen donors

Palladium complexes halogen donors

Platinum complexes halogen donors

Reaction conditions for reductive replacement of halogen and tosylate by hydride donors

Rhodium complexes halogen donors

Ruthenium complexes halogen donors

Silver complexes halogen-donors

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