Infrared spectroscopic observation of the argon isomer distribution in evaporative ensembles of I-•ROH•Arm (R=methyl, ethyl, isopropyl) clusters

被引:37
作者
Nielsen, SB
Ayotte, P
Kelley, JA
Johnson, MA [1 ]
机构
[1] Yale Univ, Sterling Chem Lab, New Haven, CT 06520 USA
[2] Univ Copenhagen, Dept Chem, HC Orsted Inst, DK-2100 Copenhagen O, Denmark
关键词
D O I
10.1063/1.480292
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
Vibrational predissociation spectra of argon-solvated iodide-alcohol clusters (I-. ROH . Ar-m, ROH=MeOH, EtOH, i-PrOH) are reported in the OH stretching region (3200-3400 cm-1). The spectra display multiple peaks associated with the ionic H-bonded OH stretching fundamental, which vary according to the extent of argon solvation. At small m, the number of peaks reflects the total number of attached argon atoms, such that peaks associated with fewer argons persist (with a small blue shift) in the spectra of the larger clusters, while new peaks appear red shifted by about 12 cm(-1) with each additional argon. The effect saturates in a manner that depends on the particular alcohol (m(max)=6 for MeOH, 5 for EtOH, and 4 for i-PrOH). We interpret these observations to indicate the presence of multiple isomers in the evaporative ensemble, which are distinguishable according to the different arrangements of argon atoms among two effective binding sites. (C) 1999 American Institute of Physics. [S0021-9606(99)01045-4].
引用
收藏
页码:9593 / 9599
页数:7
相关论文
共 50 条
[1]   HYDRATION OF HALIDE NEGATIVE IONS IN GAS PHASE .2. COMPARISON OF HYDRATION ENERGIES FOR ALKALI POSITIVE AND HALIDE NEGATIVE IONS [J].
ARSHADI, M ;
YAMDAGNI, R ;
KEBARLE, P .
JOURNAL OF PHYSICAL CHEMISTRY, 1970, 74 (07) :1475-&
[2]   A cluster study of anionic hydration:: Spectroscopic characterization of the I-•Wn, 1≤n≤3, supramolecular complexes at the primary steps of solvation [J].
Ayotte, P ;
Weddle, GH ;
Kim, J ;
Kelley, J ;
Johnson, MA .
JOURNAL OF PHYSICAL CHEMISTRY A, 1999, 103 (04) :443-447
[3]   Vibrational predissociation spectroscopy of the (H2O)6-•Arn, n≥6, clusters [J].
Ayotte, P ;
Bailey, CG ;
Kim, J ;
Johnson, MA .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (02) :444-449
[4]   Vibrational spectroscopy of the ionic hydrogen bond:: Fermi resonances and ion-molecule stretching frequencies in the binary X-•H2O (X = Cl, Br, I) complexes via argon predissociation spectroscopy [J].
Ayotte, P ;
Weddle, GH ;
Kim, J ;
Johnson, MA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (47) :12361-12362
[5]   Mass-selected "matrix isolation'' infrared spectroscopy of the I-.(H2O)2 complex:: making and breaking the inter-water hydrogen-bond [J].
Ayotte, P ;
Weddle, GH ;
Kim, J ;
Johnson, MA .
CHEMICAL PHYSICS, 1998, 239 (1-3) :485-491
[6]   Vibrational spectroscopy of small Br-•(H2O)n and I-•(H2O)n clusters:: Infrared characterization of the ionic hydrogen bond [J].
Ayotte, P ;
Bailey, CG ;
Weddle, GH ;
Johnson, MA .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (18) :3067-3071
[7]   An infrared study of the competition between hydrogen-bond networking and ionic solvation:: Halide-dependent distortions of the water trimer in the X-•(H2O)3, (X = Cl, Br, I) systems [J].
Ayotte, P ;
Weddle, GH ;
Johnson, MA .
JOURNAL OF CHEMICAL PHYSICS, 1999, 110 (15) :7129-7132
[8]  
AYOTTE P, IN PRESS J PHYS CH A
[9]  
BADGER RM, 1940, J CHEM PHYS, V8, P288, DOI DOI 10.1063/1.1750645
[10]   Vibrational predissociation spectra of I-center dot(H2O): Isotopic labels and weakly bound complexes with Ar and N-2 [J].
Bailey, CG ;
Kim, J ;
Dessent, CEH ;
Johnson, MA .
CHEMICAL PHYSICS LETTERS, 1997, 269 (1-2) :122-127