Infrared action spectroscopy of fundamental nitrilium ions: Protonated vinyl- and ethyl cyanide

被引:1
作者
Thorwirth, Sven [1 ]
Asvany, Oskar [1 ]
Harding, Michael E. [2 ]
Jusko, Pavol [1 ,5 ]
McCarthy, Michael C. [3 ]
Bruenken, Sandra [4 ]
Schlemmer, Stephan [1 ]
机构
[1] Univ Cologne, Phys Inst 1, Zulpicher Str 77, D-50937 Cologne, Germany
[2] Karlsruher Inst Technol KIT, Inst Nanotechnol, Campus Nord,Postfach 3640, D-76021 Karlsruhe, Germany
[3] Harvard & Smithsonian, Ctr Astrophys, 60 Garden St, Cambridge, MA 02138 USA
[4] Radboud Univ Nijmegen, Inst Mol & Mat, FELIX Lab, Toernooiveld 7, NL-6525 ED Nijmegen, Netherlands
[5] Max Planck Inst Extraterr Phys, Giessenbachstr 1, D-85748 Garching, Germany
关键词
Protonated vinyl cyanide; Protonated ethyl cyanide; Infrared action spectroscopy; Ion traps; CCSD(T) calculations; GAUSSIAN-BASIS SETS; VIBRATIONAL PREDISSOCIATION; DISSOCIATIVE RECOMBINATION; MANY-BODY; CHEMISTRY; CCSD(T); HCNH+; ACRYLONITRILE; PERTURBATION; DERIVATIVES;
D O I
10.1016/j.jms.2022.111615
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Infrared action spectra of the protonated forms of two fundamental organic nitriles, vinyl cyanide, C2H3CN, and ethyl cyanide, C2H5CN, have been observed using the FELion 22-pole ion trap apparatus and the Free Electron Laser for Infrared eXperiments (FELIX) at Radboud University, Nijmegen (The Netherlands). Vibrational bands of both ions were observed in the wavenumber regime between 300 and 2500 cm(-1) and spectroscopically assigned based on results from anharmonic force field calculations performed here at the coupled cluster level of theory. As the action spectroscopy scheme used in the present study probes the Ne-tagged weakly bound complexes, C2H3CNH+-Ne and C2H5CNH+-Ne, corresponding quantum-chemical calculations of these systems were also performed. Significant blueshifts observed for the strong-CNH+ bending modes indicate that the neon atom is attached to the proton bound to the nitrile group in both molecular ions.
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页数:9
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