Combined Experimental and Theoretical Study of the Benzocaine/Ar van der Waals System in Supersonic Expansions

被引:10
|
作者
Leon, Iker [1 ]
Aguado, Edurne [1 ]
Lesarri, Alberto [1 ]
Fernandez, Jose A. [1 ]
Castano, Fernando [1 ]
机构
[1] Univ Basque Country, Dept Quim Fis, Fac Ciencia & Tecnol, E-48080 Bilbao, Spain
来源
JOURNAL OF PHYSICAL CHEMISTRY A | 2009年 / 113卷 / 06期
关键词
INDUCED FLUORESCENCE SPECTROSCOPY; MICROSOLVATED MOLECULAR CLUSTERS; INTERMOLECULAR BINDING-ENERGIES; LOCAL-ANESTHETICS; NA+ CHANNELS; ETHYL; COMPLEXES; METHYL; BLOCK; MEMBRANES;
D O I
10.1021/jp808723r
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
The electronic spectra of Benzocaine center dot Ar-n, n = 0-4 were obtained using two-color resonance enhanced multiphoton ionization; the 1:1 and 1:2 clusters were investigated by ultraviolet/ultraviolet hole burning, stimulated emission pumping, and other laser spectroscopies. A single isomer was found for the 1: 1 cluster, while two isomers of the 1:2 cluster were found: one with the two Ar atoms on the same side of the chromophore, and the other with the two Ar atoms sitting on opposite sides of the chromophore. The observed shifts point to the existence of a single isomer for the 1:3 and 1:4 species. Dissociation energies for the neutral ground and first excited electronic state and the ion ground electronic state of the complexes have been determined by the fragmentation threshold method and by ab initio calculations conducted at the MP2 level with 6-31++g(2d, p), 6-311++g(2d, p) and AUG-cc-pVTZ basis sets. The results are compared with those obtained for other similar systems.
引用
收藏
页码:982 / 988
页数:7
相关论文
共 50 条
  • [21] Ab initio study of van der Waals interaction of CO2 with Ar
    Marshall, PJ
    Szczesniak, MM
    Sadlej, J
    Chalasinski, G
    terHorst, MA
    Jameson, CJ
    JOURNAL OF CHEMICAL PHYSICS, 1996, 104 (17): : 6569 - 6576
  • [22] Theoretical study on van der Waals and charge transfer interactions between molecules
    Maki, J
    Yoshimoto, T
    Nagao, H
    Nishikawa, K
    SYNTHETIC METALS, 2001, 120 (1-3) : 765 - 766
  • [23] A theoretical study of van der Waals neon trimer using Faddeev equations
    Korobitsin A.A.
    Kolganova E.A.
    Physics of Particles and Nuclei Letters, 2017, 14 (7) : 971 - 974
  • [24] A theoretical study of the rovibrational levels of the bosonic van der Waals neon trimer
    Salci, Moses
    Levin, Sergey B.
    Elander, Nils
    Yarevsky, Evgeny
    JOURNAL OF CHEMICAL PHYSICS, 2008, 129 (13):
  • [25] Theoretical and REMPI spectroscopic study on phenylhydrazine and phenylhydrazine-(Ar)n (n=1, 2) van der Waals complexes
    Xiao, Daoqing
    Yu, Dan
    Xu, Xiling
    Yu, Zijun
    Cheng, Min
    Du, Yikui
    Zheng, Weijun
    Zhu, Qihe
    Zhang, Cunhao
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2009, 11 (18) : 3532 - 3538
  • [26] A theoretical study of the prereaction process of the H•••HF van der Waals molecule
    Takayanagi, T
    Kurosaki, Y
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 1999, 1 (06) : 1099 - 1103
  • [27] GeSe: Optical Spectroscopy and Theoretical Study of a van der Waals Solar Absorber
    Murgatroyd, Philip A. E.
    Smiles, Matthew J.
    Savory, Christopher N.
    Shalvey, Thomas P.
    Swallow, Jack E. N.
    Fleck, Nicole
    Robertson, Craig M.
    Jackel, Frank
    Alaria, Jonathan
    Major, Jonathan D.
    Scanlon, David O.
    Veal, Tim D.
    CHEMISTRY OF MATERIALS, 2020, 32 (07) : 3245 - 3253
  • [28] Theoretical and Experimental Investigations on the Growth of SnS van der Waals Epitaxies on Graphene Buffer Layer
    Leung, Kelvin K.
    Wang, Wei
    Shu, Haibo
    Hui, Yeung Yu
    Wang, Shifeng
    Fong, Patrick W. K.
    Ding, Feng
    Lau, Shu Ping
    Lam, Chi-hang
    Surya, Charles
    CRYSTAL GROWTH & DESIGN, 2013, 13 (11) : 4755 - 4759
  • [29] VIBRATIONAL STRUCTURE OF THE AR-NO+ VAN-DER-WAALS CATION
    FOURRE, I
    RAOULT, M
    CHEMICAL PHYSICS, 1995, 199 (2-3) : 215 - 225
  • [30] Interplay between ion-π and Ar/π Van der Waals interactions
    Quinonero, David
    Frontera, Antonio
    Deya, Pere M.
    COMPUTATIONAL AND THEORETICAL CHEMISTRY, 2012, 998 : 51 - 56