Department of Science and Environment, Roskilde University, Universitetsvej 1, DK-4000 Roskilde, Denmark.
Molecules. 2021 Apr 21;26(9):2409. doi: 10.3390/molecules26092409.
Intramolecular NH…O,S,N interactions in non-tautomeric systems are reviewed in a broad range of compounds covering a variety of NH donors and hydrogen bond acceptors. H chemical shifts of NH donors are good tools to study intramolecular hydrogen bonding. However in some cases they have to be corrected for ring current effects. Deuterium isotope effects on C and N chemical shifts and primary isotope effects are usually used to judge the strength of hydrogen bonds. Primary isotope effects are investigated in a new range of magnitudes. Isotope ratios of NH stretching frequencies, νNH/ND, are revisited. Hydrogen bond energies are reviewed and two-bond deuterium isotope effects on C chemical shifts are investigated as a possible means of estimating hydrogen bond energies.
在非互变异构体系中,分子内 NH…O、S、N 相互作用在广泛的化合物范围内进行了综述,涵盖了各种 NH 供体和氢键受体。NH 供体的 H 化学位移是研究分子内氢键的良好工具。然而,在某些情况下,它们必须校正环电流效应。C 和 N 化学位移的氘同位素效应和一级同位素效应通常用于判断氢键的强度。对新的一系列幅度进行了一级同位素效应的研究。重新考察了 NH 伸缩振动频率 νNH/ND 的同位素比。氢键能进行了综述,并研究了 C 化学位移的两键氘同位素效应作为估算氢键能的可能方法。