Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, USA.
J Am Chem Soc. 2012 Feb 1;134(4):2094-9. doi: 10.1021/ja2081907. Epub 2012 Jan 19.
Hydrogen bond interactions in small covalent model compounds (i.e., deprotonated polyhydroxy alcohols) were measured by negative ion photoelectron spectroscopy. The experimentally determined vertical and adiabatic electron detachment energies for (HOCH(2)CH(2))(2)CHO(-)(2a), (HOCH(2)CH(2))(3)CO(-) (3a), and (HOCH(2)CH(2)CH(OH)CH(2))(3)CO(-) (4a)reveal that hydrogen-bonded networks can provide enormous stabilizations and that a single charge center not only can be stabilized by up to three hydrogen bonds but also can increase the interaction energy between noncharged OH groups by 5.8 kcal mol(-1) or more per hydrogen bond. This can lead to pK(a) values that are very different from those in water and can provide some of the impetus for catalytic processes.
通过负离子光电子能谱法测量了小分子共价模型化合物(即去质子化多羟基醇)中的氢键相互作用。实验测定的(HOCH(2)CH(2))(2)CHO(-)(2a)、(HOCH(2)CH(2))(3)CO(-)(3a)和(HOCH(2)CH(2)CH(OH)CH(2))(3)CO(-)(4a)的垂直和绝热电子离解能表明,氢键网络可以提供巨大的稳定作用,并且单个电荷中心不仅可以通过多达三个氢键稳定,还可以使不带电荷的 OH 基团之间的相互作用能增加 5.8 kcal mol(-1)或更多/每一个氢键。这可能导致 pK(a)值与在水中非常不同,并为催化过程提供一些动力。