Stare Jernej, Grdadolnik Jože, Mason Sax, Albinati Alberto, Eckert Juergen
Theory Department, National Institute of Chemistry, Hajdrihova 19, SI-1000 Ljubljana, Slovenia.
Institut Laue-Langevin, 6 rue Jules Horowitz, BP 156, 38042 Grenoble Cedex 9, France.
ACS Omega. 2024 Aug 29;9(36):38116-38125. doi: 10.1021/acsomega.4c05344. eCollection 2024 Sep 10.
The present work focuses on the case of an extremely short intramolecular O-H···O hydrogen bond (H-bond) found in 4-methoxypicolinic acid -oxide (MPANO). The donor···acceptor separation of 2.403 Å makes the H-bond in MPANO one of the shortest H-bonds known. We elucidated the structure and dynamics of the H-bond by two neutron-based techniques, namely, single-crystal diffraction and inelastic scattering (INS) vibrational spectroscopy. We also utilized conventional infrared (IR) spectroscopy as well as quantum chemical computations on isolated and periodic models. Both the protiated and deuterated variants of MPANO were investigated by INS and IR. All the methods used unequivocally confirm the existence of an extremely short, asymmetric H-bond, with the proton located near yet off the midpoint. The main relevant feature of the IR spectrum is an extremely broad, complex, and red-shifted OH (OD) stretching band spanning between 1800 and 500 cm and centered at about 1360 cm, which indicates the presence of extensive anharmonicity and coupling with other H-bond modes. Of the modes characteristic of H-bond dynamics, only the out-of-plane OH (OD) bending can clearly be detected in the INS spectra; it has a relatively high frequency indicative of the strength of the H-bond. The computed structure is in excellent agreement with the diffraction measurement when periodicity is taken into account. The calculated harmonic frequencies show a reasonable match with the observed spectral features, whereby the assignment of the IR and INS spectra is facilitated. The hydrogen stretching frequency, however, appears to be significantly overestimated, on account of the limitations of the harmonic approximation and the complex nature of the short H-bond.
本研究聚焦于在4-甲氧基吡啶酸 -氧化物(MPANO)中发现的极短分子内O-H···O氢键(H键)的情况。2.403 Å的供体···受体间距使MPANO中的H键成为已知最短的H键之一。我们通过两种基于中子的技术,即单晶衍射和非弹性散射(INS)振动光谱,阐明了该H键的结构和动力学。我们还利用了传统红外(IR)光谱以及对孤立和周期性模型的量子化学计算。通过INS和IR研究了MPANO的质子化和氘代变体。所有使用的方法都明确证实了存在一个极短的不对称H键,质子位于中点附近但偏离中点。IR光谱的主要相关特征是一个极其宽泛、复杂且红移的OH(OD)伸缩带,范围在1800至500 cm之间,中心约在1360 cm,这表明存在广泛的非谐性以及与其他H键模式的耦合。在H键动力学的特征模式中,只有面外OH(OD)弯曲在INS光谱中能清晰检测到;它具有相对较高的频率,表明H键的强度。考虑周期性时,计算得到的结构与衍射测量结果非常吻合。计算得到的谐波频率与观察到的光谱特征有合理的匹配度,从而便于对IR和INS光谱进行归属。然而,由于谐波近似的局限性和短H键的复杂性质,氢伸缩频率似乎被显著高估了。