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Conventional hydrogen bond donors

Similar to conventional QSAR, a speciLc LSER equation is limited for a speciLc set of compounds. In subsequent studies, Kamlet et al. (1987) found that dependency of solubility in water on polarity/polarizability is different for aromatic liquids than for aliphatic liquids. For liquid aromatic compounds with a hydrogen-bond acceptor and without hydrogen-bond donors, the LSER is... [Pg.53]

The conventional hydrogen bond X-H- Y is formed by the proton donor X-H with a proton acceptor Y, which is an atom with a lone pair (X and Y are all highly electronegative atoms such as F, O, N, and Cl). Some non-conventional hydrogen bonds that do not conform to this condition are discussed below ... [Pg.411]

Conventional hydrogen bonds are formed between a proton donor, such as an O-H or N-H group and a proton acceptor, such as oxygen or nitrogen lone pair. In all such cases a nonbonding electron pair acts as the weak base component. [Pg.413]

Hydrogen bond donor (only) pyrrole (may accept an H-bond, but not of the conventional variety)... [Pg.302]

See other pages where Conventional hydrogen bond donors is mentioned: [Pg.17]    [Pg.433]    [Pg.434]    [Pg.437]    [Pg.437]    [Pg.1504]    [Pg.222]    [Pg.222]    [Pg.246]    [Pg.294]    [Pg.299]    [Pg.1118]    [Pg.17]    [Pg.433]    [Pg.434]    [Pg.437]    [Pg.437]    [Pg.1504]    [Pg.222]    [Pg.222]    [Pg.246]    [Pg.294]    [Pg.299]    [Pg.1118]    [Pg.350]    [Pg.298]    [Pg.142]    [Pg.11]    [Pg.13]    [Pg.25]    [Pg.43]    [Pg.562]    [Pg.156]    [Pg.143]    [Pg.77]    [Pg.265]    [Pg.82]    [Pg.175]    [Pg.617]    [Pg.254]    [Pg.735]    [Pg.223]    [Pg.230]    [Pg.306]    [Pg.225]    [Pg.55]    [Pg.213]    [Pg.294]    [Pg.314]    [Pg.315]    [Pg.53]    [Pg.528]    [Pg.831]    [Pg.219]    [Pg.219]    [Pg.250]    [Pg.45]   
See also in sourсe #XX -- [ Pg.436 ]

See also in sourсe #XX -- [ Pg.295 ]



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Conventional bonding

Donor bonds

Donor hydrogenation

Hydrogen bonding donors

Hydrogenation hydrogen donors

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