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Cyclotrimerization of Acetylene in Gas Phase V+(C2H2)n Complexes: Detection of Intermediates and Products with Infrared Spectroscopy
Author(s) -
Joshua H. Marks,
Timothy B. Ward,
Antonio D. Brathwaite,
Sojourna Ferguson,
Michael A. Duncan
Publication year - 2019
Publication title -
the journal of physical chemistry a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.756
H-Index - 235
eISSN - 1520-5215
pISSN - 1089-5639
DOI - 10.1021/acs.jpca.9b04962
Subject(s) - acetylene , chemistry , mass spectrometry , infrared spectroscopy , benzene , spectroscopy , photodissociation , infrared , analytical chemistry (journal) , photochemistry , reaction intermediate , catalysis , organic chemistry , physics , chromatography , quantum mechanics , optics
Infrared laser spectroscopy and mass spectrometry were used to determine the structures of intermediates and products in the single-atom-catalyzed trimerization of acetylene to form benzene. Complexes of the form V + (C 2 H 2 ) n were produced in the gas phase via laser ablation in a pulsed-nozzle source, size-selected with a mass spectrometer, and studied with infrared laser photodissociation spectroscopy. Density functional theory calculations were performed in support of the experiments. Single- and double-acetylene complexes form V + (C 2 H 2 ) n metallacycle structures. Three-acetylene complexes exhibit a surprising dependence on the acetylene concentration, forming V + (C 2 H 2 ) 3 and (C 2 H 2 )V + (C 4 H 4 ) tri- and dimetallacycle ion structures at low concentrations and eventually V + (benzene) at higher concentrations. These observations reveal intermediates along the reaction path of acetylene cyclotrimerization to benzene.

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