IR-UV double resonance spectroscopy of xanthine

被引:39
作者
Callahan, Michael P.
Crews, Bridgit
Abo-Riziq, Ali
Grace, Louis
de Vries, Mattanjah S. [1 ]
Gengeliczki, Zsolt
Holmes, Tiffani M.
Hill, Glake A.
机构
[1] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[2] Eotvos Lorand Univ, Inst Chem, H-1117 Budapest, Hungary
[3] Jackson State Univ, Computat Ctr Mol Struct & Interact, Jackson, MS 39217 USA
关键词
D O I
10.1039/b705042a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We present resonant two-photon ionization (R2PI), UV-UV, and IR-UV double resonance spectra of xanthine seeded in a supersonic jet by laser desorption. We show that there is only one tautomer of xanthine which absorbs in the wavelength range of 36 700 to 37 700 cm(-1). The IR-UV double resonance spectrum shows three strong bands at 3444, 3485, and 3501 cm-1, all of which we assign as N-H stretching vibrations. Comparison of the IR-UV double resonance spectrum with frequencies and intensities obtained from density functional theory (DFT) and second order Moller Plesset (MP2) calculations suggests that the observed xanthine is the diketo N(7)H tautomer.
引用
收藏
页码:4587 / 4591
页数:5
相关论文
共 39 条
[1]   Photochemical selectivity in guanine-cytosine base-pair structures [J].
Abo-Riziq, A ;
Grace, L ;
Nir, E ;
Kabelac, M ;
Hobza, P ;
de Vries, MS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (01) :20-23
[2]   New scale factors for harmonic vibrational frequencies using the B3LYP density functional method with the triple-ξ basis set 6-311+G(d,p) [J].
Andersson, MP ;
Uvdal, P .
JOURNAL OF PHYSICAL CHEMISTRY A, 2005, 109 (12) :2937-2941
[3]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[4]  
Berdys-Kochanska J, 2005, J PHYS CHEM A, V109, P11407, DOI [10.1021/jp053012l, 10.1021/jp0530121]
[5]   A theoretical investigation of the physical reason for the very different luminescence properties of the two isomers adenine and 2-aminopurine [J].
Broo, A .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (03) :526-531
[6]   ON THE NATURE OF XANTHINE AND SUBSTITUTED XANTHINES IN SOLUTION [J].
CAVALIERI, LF ;
FOX, JJ ;
STONE, A ;
CHANG, N .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1954, 76 (04) :1119-1122
[7]   AM1 and PM3 study of tautomerism of xanthine in the gas and aqueous phases [J].
Civcir, PÜ .
JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM, 2001, 545 :7-15
[8]   Ultrafast excited-state dynamics in nucleic acids [J].
Crespo-Hernández, CE ;
Cohen, B ;
Hare, PM ;
Kohler, B .
CHEMICAL REVIEWS, 2004, 104 (04) :1977-2019
[9]   Gaussian-3 (G3) theory for molecules containing first and second-row atoms [J].
Curtiss, LA ;
Raghavachari, K ;
Redfern, PC ;
Rassolov, V ;
Pople, JA .
JOURNAL OF CHEMICAL PHYSICS, 1998, 109 (18) :7764-7776
[10]  
FORESMAN JB, 1996, EPLORING CHEM ELECT