Comparison of IRMPD, Ar-tagging and IRLAPS for vibrational spectroscopy of Ag+(CH3OH)

被引:21
作者
Altinay, Gokhan [1 ]
Metz, Ricardo B. [1 ]
机构
[1] Univ Massachusetts, Dept Chem, Amherst, MA 01003 USA
基金
美国国家科学基金会;
关键词
Non-covalent complex; Photofragment; Infrared laser-assisted photodissociation; IRLAPS; IRMPD; Argon-tagging; INFRARED PHOTODISSOCIATION SPECTROSCOPY; MULTIPLE-PHOTON DISSOCIATION; CLUSTER IONS; PHOTOFRAGMENT SPECTROSCOPY; GAS-PHASE; MEDIATED PHOTODISSOCIATION; TRANSITION-METAL; BOND ACTIVATION; MOLECULAR-IONS; C-H;
D O I
10.1016/j.ijms.2010.05.016
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
Gas-phase Ag+(CH3OH) molecules are produced in a laser ablation source, cooled in a supersonic expansion and their vibrational spectrum is measured by photofragment spectroscopy in a reflectron time-of-flight mass spectrometer. Three techniques - infrared multiple photon dissociation (IRMPD), argon-tagging, and infrared laser-assisted photodissociation spectroscopy (IRLAPS) - are used to measure the vibrational spectra of ions produced under identical conditions. The sharpest spectrum is obtained using IRLAPS, a two-color scheme in which a tunable OPO/OPA infrared laser excites the O-H stretch and a TEA-CO2 laser dissociates the vibrationally excited ions via absorbing multiple C-O stretch photons. The O-H stretch is observed at 3660 cm(-1). Monitoring loss of argon from Ag+(CH3OH)(Ar) gives a slightly broader peak, with no significant shift. The vibrational spectrum obtained using IRMPD is shifted to 3635 cm(-1) is substantially broader, and is asymmetrical, tailing to the red. Analysis of the experimental results is aided by comparison with hybrid density functional theory computed harmonic and anharmonic frequencies. (C) 2010 Elsevier B.A All rights reserved.
引用
收藏
页码:41 / 45
页数:5
相关论文
共 39 条
[1]   The low-lying electronic states of FeO+:: Rotational analysis of the resonance enhanced photodissociation spectra of the 6Π7/2←X 6Σ+ system [J].
Aguirre, F ;
Husband, J ;
Thompson, CJ ;
Stringer, KL ;
Metz, RB .
JOURNAL OF CHEMICAL PHYSICS, 2003, 119 (19) :10194-10201
[2]   Vibrational Spectroscopy of Intermediates in Benzene-to-Pheno Conversion by FeO+ [J].
Altinay, Gokhan ;
Metz, Ricardo B. .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2010, 21 (05) :750-757
[3]   Vibrational Spectroscopy of Intermediates in Methane-to-Methanol Conversion by FeO+ [J].
Altinay, Gokhan ;
Citir, Murat ;
Metz, Ricardo B. .
JOURNAL OF PHYSICAL CHEMISTRY A, 2010, 114 (15) :5104-5112
[4]   Mass-selective vibrational spectroscopy of vanadium oxide cluster ions [J].
Asmis, Knut R. ;
Sauer, Joachim .
MASS SPECTROMETRY REVIEWS, 2007, 26 (04) :542-562
[5]   High-resolution spectroscopy of cluster ions [J].
Bieske, EJ ;
Dopfer, O .
CHEMICAL REVIEWS, 2000, 100 (11) :3963-3998
[6]   Intramolecular energy transfer in highly vibrationally excited methanol .1. Ultrafast dynamics [J].
Boyarkin, OV ;
Lubich, L ;
Settle, RDF ;
Perry, DS ;
Rizzo, TR .
JOURNAL OF CHEMICAL PHYSICS, 1997, 107 (20) :8409-8422
[7]   Collisionally enhanced isotopic selectivity in multiphoton dissociation of vibrationally excited CF3H [J].
Boyarkin, OV ;
Kowalczyk, M ;
Rizzo, TR .
JOURNAL OF CHEMICAL PHYSICS, 2003, 118 (01) :93-103
[8]   Nonlinear intensity dependence in the infrared multiphoton excitation and dissociation of methanol pre-excited to different energies [J].
Boyarkin, OV ;
Rizzo, TR ;
Rueda, D ;
Quack, M ;
Seyfang, G .
JOURNAL OF CHEMICAL PHYSICS, 2002, 117 (21) :9793-9805
[9]  
BOYARKIN OV, 1995, BER BUNSEN PHYS CHEM, V99, P504
[10]   Electronic and vibrational spectroscopy and vibrationally mediated photodissociation of V+(OCO) [J].
Citir, M ;
Altinay, G ;
Metz, RB .
JOURNAL OF PHYSICAL CHEMISTRY A, 2006, 110 (15) :5051-5057