Collision-assisted stripping for determination of microsolvation-dependent protonation sites in hydrated clusters by cryogenic ion trap infrared spectroscopy: the case of benzocaineH+(H2O)n

被引:14
作者
Hirata, Keisuke [1 ,2 ,3 ]
Haddad, Fuad [4 ]
Dopfer, Otto [3 ,4 ]
Ishiuchi, Shun-ichi [1 ,2 ,3 ]
Fujii, Masaaki [1 ,3 ,5 ]
机构
[1] Tokyo Inst Technol, Inst Innovat Res, Lab Chem & Life Sci, Midori Ku, 4259 Nagatsuta Cho, Yokohama, Kanagawa 2268503, Japan
[2] Tokyo Inst Technol, Sch Sci, Dept Chem, Meguro Ku, 2-12-1 Ookayama, Tokyo 1528550, Japan
[3] Tokyo Inst Technol, Inst Innovat Res, Tokyo Tech World Res Hub Initiat WRHI, Midori Ku, Nagatsuta Cho 4259, Yokohama, Kanagawa 2268503, Japan
[4] Tech Univ Berlin, Inst Opt & Atomare Phys, Hardenbergstr 36, D-10623 Berlin, Germany
[5] Tokyo Inst Technol, Sch Life Sci & Technol, Midori Ku, 4259 Nagatsuta Cho, Yokohama, Kanagawa 2268503, Japan
基金
日本学术振兴会;
关键词
P-AMINOBENZOIC ACID; GAS-PHASE; PHOTODISSOCIATION SPECTROSCOPY; ENANTIOSELECTIVE PROTONATION; IR-SPECTRA; PROTOMERS; COLD; SPECTROMETRY; CARBENIUM; SOLVENT;
D O I
10.1039/d1cp05762f
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 protonation site of molecules can be varied by their surrounding environment. Gas-phase studies, including the popular techniques of infrared spectroscopy and ion mobility spectrometry, are a powerful tool for the determination of protonation sites in solvated clusters but often suffer from inherent limits for larger hydrated clusters. Here, we present collision-assisted stripping infrared (CAS-IR) spectroscopy as a new technique to overcome these problems and apply it in a proof-of-principle experiment to hydrated clusters of protonated benzocaine (H+BC), which shows protonation-site switching depending on the degree of hydration. The most stable protomer of H+BC in the gas phase (O-protonated) is interconverted into its most stable protomer in aqueous solution (N-protonated) upon hydration with three water molecules. CAS-IR spectroscopy enables us to unambiguously assign protonation sites and quantitatively determine the relative abundance of various protomers.
引用
收藏
页码:5774 / 5779
页数:6
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