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Journal ArticleDOI

Hydrogen elimination from ethylene by laser-ablated Zr atoms: An infrared spectroscopic investigation of the reaction intermediates in a solid argon matrix

Han-Gook Cho, +1 more
- 07 Apr 2004 - 
- Vol. 108, Iss: 18, pp 3965-3972
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TLDR
In this article, the hydrogen elimination reaction of ethylene by laser-ablated Zr atoms has been investigated by means of infrared spectroscopy, and three different groups of product absorptions based on the behaviors upon broad-band photolysis and annealing are identified.
Abstract
Intermediates of the hydrogen elimination reaction of ethylene by laser-ablated Zr atoms have been isolated in an argon matrix and investigated by means of infrared spectroscopy. The strong absorptions in the region of 1500−1660 cm-1 are due to the Zr−H stretching modes of several intermediates. There are at least three different groups of product absorptions based on the behaviors upon broad-band photolysis and annealing. Among them, the insertion and dihydrido complexes, presumed in previous studies of the hydrogen elimination of ethylene by Zr atoms, are identified. In addition, the remaining Zr−H stretching absorptions, along with absorptions in the C⋮C stretching and other regions, suggest that ethynyl zirconium trihydride is also formed in the hydrogen elimination reaction. Formation of this compound is consistent with the fact that C2H2 and C2D2 as well as CHCD are produced in the reaction of Zr + CH2CD2. Density functional theory calculations for the reaction intermediates are also carried out, an...

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Citations
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Journal ArticleDOI

The C−H Activation of Methane by Laser-Ablated Zirconium Atoms: CH2ZrH2, the Simplest Carbene Hydride Complex, Agostic Bonding, and (CH3)2ZrH2

TL;DR: In this paper, the authors used a large basis set with polarization functions to predict a C1 symmetry structure with agostic C−H-ZrH-1 bonding and distance of 2.5 cm-1.300 A.
Journal ArticleDOI

Infrared spectrum and bonding in uranium methylidene dihydride, CH2=UH2.

TL;DR: Uranium atoms activate methane upon ultraviolet excitation to form the methyl uranium hydride CH3-UH, which undergoes alpha-H transfer to produce uranium methylidene dihydride, CH2=UH2, which is found to be less reactive in methane activation than thorium atoms.
Journal ArticleDOI

Photoreversible hydrogen migration system in a solid argon matrix formed by the reaction of methyl fluoride with laser-ablated titanium atoms

TL;DR: The photoreversible system of titanium methylidene and methyltitanium fluoride complexes has been formed by the reaction of methyl fluoride and laser-ablated Ti atoms and isolated in a solid argon matrix.
Journal ArticleDOI

Persistent photo-reversible transition-metal methylidene system generated from reaction of methyl fluoride with laser-ablated zirconium atoms and isolated in a solid argon matrix.

TL;DR: A photoreversible transition-metal methylidene system has been formed for the first time by reaction of methyl fluoride and laser-ablated Zr atoms, isolated in solid argon, and investigated by means of infrared spectroscopy.
Journal ArticleDOI

Infrared spectra of CH3-CrH, CH3-WH, CH2=WH2, and CH[triple bond]WH3 formed by activation of CH4 with Cr and W atoms.

TL;DR: Matrix infrared spectra and DFT/B3LYP calculations show that CH[triple bond]WH3 is a stable molecule with C3v symmetry, but other levels of theory were required to describe agostic distortion for CH2=WH2.
References
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Journal ArticleDOI

Reactions of boron atoms with molecular oxygen. Infrared spectra of BO, BO2, B2O2, B2O3, and BO−2 in solid argon

TL;DR: In this article, the product infrared spectrum was dominated by three strong 11B isotopic bands at 1299.3, 1282.8, and 1274.6 cm−1 with 10B counterparts at 1347.6, 1330.7, and 1322.2 cm− 1.
Journal ArticleDOI

Pulsed laser-assisted reactions of boron and nitrogen atoms in a condensing nitrogen stream

TL;DR: In this article, the major product NNBN and the minor products NBN and BNN were identified by mixed nitrogen and boron isotopic multiplets from the FTIR spectra in solid nitrogen.
Journal ArticleDOI

Theoretical study of the binding of ethylene to second-row transition-metal atoms

TL;DR: The binding energy curve as a function of atomic number of the metal shows the usual characterestic minimum in the middle of the row as mentioned in this paper, mainly due to the loss of exchange when the bonds are formed.
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