Premium
Ground‐State Structure of the Proton‐Bound Formate Dimer by Cold‐Ion Infrared Action Spectroscopy
Author(s) -
Thomas Daniel A.,
Marianski Mateusz,
Mucha Eike,
Meijer Gerard,
Johnson Mark A.,
von Helden Gert
Publication year - 2018
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201805436
Subject(s) - dimer , chemistry , protonation , formate , infrared spectroscopy , ion , photodissociation , spectroscopy , proton , infrared , crystallography , ground state , photochemistry , atomic physics , physics , biochemistry , organic chemistry , quantum mechanics , optics , catalysis
The proton‐bound dicarboxylate motif, RCOO − ⋅H + ⋅ − OOCR, is a prevalent chemical configuration found in many condensed‐phase systems. The proton‐bound formate dimer HCOO − ⋅H + ⋅ − OOCH was studied utilizing cold‐ion IR action spectroscopy in the range 400–1800 cm −1 . The spectrum obtained at ca. 0.4 K of ions captured in He nanodroplets was compared to that measured at ca. 10 K by photodissociation of Ar‐ion complexes. Similar band patterns are obtained by the two techniques that are consistent with calculations for a C 2 symmetry structure with a proton shared equally between the two formate moieties. Isotopic substitution experiments point to the nominal parallel stretch of the bridging proton appearing as a sharp, dominant feature near 600 cm −1 . Multidimensional anharmonic calculations reveal that the bridging proton motion is strongly coupled to the flanking −COO − framework, an effect that is in line with the expected change in −C=O bond rehybridization upon protonation.