IRMPD spectroscopic and computational study of gas phase IM(Ura-H)(Ura)]+ and [M(Ura-H)(H2O)n]+ (M = Sr, Ba; n=1,2) complexes

被引:13
作者
Power, Ashley A. [1 ]
Ali, Osama Y. [1 ]
Burt, Michael B. [1 ]
Fridgen, Travis D. [1 ]
机构
[1] Mem Univ Newfoundland, Dept Chem, St John, NF A1N 4T8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
IRMPD spectroscopy; Metal cation; Uracil; DNA base; Ion-molecule complex; PHOTON DISSOCIATION SPECTROSCOPY; METAL-ION BINDING; TANDEM MASS-SPECTROMETRY; CYTOSINE WATSON-CRICK; UNIMOLECULAR REACTIVITY; NUCLEIC-ACIDS; CATIONS; DNA; URACIL; CU;
D O I
10.1016/j.ijms.2012.08.020
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 multiple photon dissociation (IRMPD) spectroscopy in a Fourier transform ion cyclotron resonance mass spectrometer is used to investigate the structures of Sr2+ or Ba2+ complexes with uracil in the gas phase. [ Sr(Ura-H)(Ura)]., [Ba(Ura-H)(Ura)(+), [Sr(Ura-H)(H2O)](+), [Ba(Ura-H)(H2O), and [Sr(Ura-H)(H2O)(2)](+) were examined in the N-H/O-H stretching region from 3200 to 3900 cm(-1). Calculations for the corresponding structures and infrared spectra were carried out using the B3LYP density functional theory in conjunction with the 6-31+G(d,p) basis set for the non-metal atoms and with the LANL2DZ basis set with relativistic core potential on Ba and Sr. The results were in good agreement with similar studies involving Pb2+ which showed that all lowest energy monomer structures involved an N3 deprotonated uracil molecule with the metal cation bound between the N3 and O4 positions. The [Sr(Ura-H)(Ura)](+) and [Ba(Ura-H)(Ura)]. complexes were found to have a tetracoordinate metal ion, and both singly and doubly solvated complexes proved to have the water molecules coordinated to the metal ion. For all the complexes studied, the computed spectra for the lowest energy structures agreed very well with the experimental IRMPD spectra obtained. The structures of the Sr2+ and Ba2+ complexes are compared with those of the Pb2+-centred complexes. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:233 / 240
页数:8
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