Geometric isotope effect of deuteration in a hydrogen-bonded host–guest crystal

• Published in: Nature communications Vol. 9; no. 1; pp. 481 - 9
• Main Authors: Shi, Chao, Zhang, Xi, Yu, Chun-Hua, Yao, Ye-Feng, Zhang, Wen
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 02.02.2018; Nature Publishing Group; Nature Portfolio
• Subjects: 140/131; 639/301/119/2795; 639/638/541/961; 639/766/119/996; Deuteration; Deuterium; Dielectric properties; Humanities and Social Sciences; Hydrogen; Hydrogen bonding; Hydrogen bonds; Internal pressure; Isotope effect; multidisciplinary; Polymorphism; Science; Science (multidisciplinary); Terephthalate
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-018-02931-8

Deuteration of a hydrogen bond by replacing protium (H) with deuterium (D) can cause geometric changes in the hydrogen bond, known as the geometric H/D isotope effect (GIE). Understanding the GIEs on global structures and bulk properties is of great importance to study structure–property relationships of hydrogen-bonded systems. Here, we report a hydrogen-bonded host–guest crystal, imidazolium hydrogen terephthalate, that exemplifies striking GIEs on its hydrogen bonds, phases, and bulk dielectric transition property. Upon deuteration, the donor–acceptor distance in the O–H···O hydrogen bonds in the host structure is found to increase, which results in a change in the global hydrogen-bonded supramolecular structure and the emergence of a new phase (i.e., isotopic polymorphism). Consequently, the dynamics of the confined guest, which depend on the internal pressure exerted by the host framework, are substantially altered, showing a downward shift of the dielectric switching temperature. Deuterating a hydrogen bond can change the bond’s geometry, a phenomenon known as the geometric isotope effect (GIE). Here, the authors find that a hydrogen-bonded host–guest crystal, imidazolium hydrogen terephthalate, exhibits significant GIE on its hydrogen bonds, changing its crystal phases and bulk dielectric properties.