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Boron antimony—hydrogen bonds

Of the solvents, aromatic and olefinic hydrocarbons are r-donors ( r-EPD) alcohols, ethers, amines, carboxamides, nitriles, ketones, sulfoxides and N- and P-oxides are n-donors (n-EPD), and haloalkanes are cr-donors (cr-EPD). Boron and antimony triha-lides are acceptor solvents (r-EPA), as are halogens and mixed halogens (c-EPA), and liquid sulfur dioxide (ti-EPA). In principle, all solvents are amphoteric in this respect, i.e. they may act as a donor (nucleophile) and an acceptor (electrophile) simultaneously. For example, water can act as a donor (by means of the oxygen atom) as well as as an acceptor (by forming hydrogen bonds). This is one of the reasons for the exceptional importance of water as a solvent. [Pg.21]

What type of compounds will be covered in this overview. Strictly, only compounds which have at least one metal-carbon bond (with the exception of metal carbides) are called organometaiiic. However, this definition was not adopted in this chapter because many families of compounds that are relevant in organometaiiic chemistry would not be included (e.g., alkoxides). By metal we mean any element from groups 1 (except hydrogen), 2, 3 (including lanthanides and actinides), 4, 5, 6, 7, 8, 9, 10, 11, 12, 13 (except boron), 14 (except carbon and silicon), and 15 (antimony and bismuth only). Most of the available thermochemical data for all these species are freely available in a single on-line database the NIST Chemistry WebBook Unless stated otherwise, all the data included in this chapter were quoted from that reference. [Pg.606]


See other pages where Boron antimony—hydrogen bonds is mentioned: [Pg.4113]    [Pg.4112]    [Pg.56]    [Pg.162]    [Pg.160]    [Pg.156]   
See also in sourсe #XX -- [ Pg.2 , Pg.2 , Pg.3 , Pg.3 , Pg.4 , Pg.4 ]




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