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Title
Data from: Electronic and mechanical anharmonicities in the vibrational spectra of the H-bonded, cryogenically cooled X‾∙HOCl (X=Cl, Br, I) complexes: Characterization of the strong anionic H-bond to an acidic OH group
Creator
Stropoli, Santino J
Johnson, Mark A
Date Created and/or Issued
Time period of project: 2021-01-01 to 2022-04-01
Contributing Institution
UC San Diego, Research Data Curation Program
Collection
Center for Aerosol Impacts on Chemistry of the Environment (CAICE)
Rights Information
Under copyright
Constraint(s) on Use: This work is protected by the U.S. Copyright Law (Title 17, U.S.C.). Use of this work beyond that allowed by "fair use" or any license applied to this work requires written permission of the copyright holder(s). Responsibility for obtaining permissions and any use and distribution of this work rests exclusively with the user and not the UC San Diego Library. Inquiries can be made to the UC San Diego Library program having custody of the work.
Use: This work is available from the UC San Diego Library. This digital copy of the work is intended to support research, teaching, and private study.
Rights Holder and Contact
UC Regents
Description
Publication Abstract: We report vibrational spectra of the H2-tagged, cryogenically cooled X‾∙HOCl (X = Cl, Br and I) ion-molecule complexes and analyze the resulting band patterns with electronic structure calculations and an anharmonic theoretical treatment of nuclear motions on extended potential energy surfaces. The complexes are formed by “ligand exchange” reactions of X‾∙(H2O)n clusters with HOCl molecules at low pressure (~10−2 mbar) in a radio-frequency ion guide. The spectra generally feature many bands in addition to the fundamentals expected at the double harmonic level. These “extra bands” appear in patterns that are similar to those displayed by the X‾∙HOD analogues, where they are assigned to excitations of nominally IR forbidden overtones and combination bands. The interactions driving these features include mechanical and electronic anharmonicities. Particularly intense bands are observed for the v = 0 → 2 transitions of the out-of-plane bending soft modes of the HOCl molecule relative to the ions. These involve displacements that act to break the strong H-bond to the ion, which give rise to large quadratic dependences of the electric dipoles (electronic anharmonicities) that drive the transition moments for the overtone bands. On the other hand, overtone bands arising from the intramolecular OH bending modes of HOCl are traced to mechanical anharmonic coupling with the v = 1 level of the OH stretch (Fermi resonances). These interactions are similar in strength to those reported earlier for the X‾∙HOD complexes.
Research Data Curation Program, UC San Diego, La Jolla, 92093-0175 (https://lib.ucsd.edu/rdcp)
Stropoli, Santino J.; Khuu, Thien; Boyer, Mark A.; Karimova, Natalia V.; Gavin-Hanner, Coire F.; Mitra, Sayoni; Lachowicz, Anton L.; Yang, Nan; Gerber, R. Benny; McCoy, Anne B.; and Johnson, Mark A. (2022). Data from: Electronic and mechanical anharmonicities in the vibrational spectra of the H-bonded, cryogenically cooled X−∙HOCl (X=Cl, Br, I) complexes: Characterization of the strong anionic H-bond to an acidic OH group. In Center for Aerosol Impacts on Chemistry of the Environment (CAICE). UC San Diego Library Digital Collections. https://doi.org/10.6075/J0ZS2WPJ
Type
dataset
Identifier
ark:/20775/bb36272408
Language
English
Subject
Anharmonicity
Hydrogen bond
Interface
Spectroscopy
Infrared

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