Gas-phase reactions of Sc+, Y+, and Lu+ with alcohols. Effects of the class and chain length of alcohols on the nature of primary products

被引:28
作者
Geribaldi, S
Breton, S
Decouzon, M
Azzaro, M
机构
[1] Lab. de Chimie Physique Organique, UFR Faculté des Sciences, Univ. de Nice-Sophia Antipolis, Nice
[2] Lab. de Chimie Physique Organique, UFR Faculté des Sciences, Univ. de Nice-Sophia Antipolis, 06108 Nice Cedex 2, Parc Valrose
关键词
D O I
10.1016/S1044-0305(96)00052-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The primary gas-phase reactions between methanol, ethanol, propan-1-ol, propan-2-ol, and 2-methylpropan-2-ol and the isovalent rare earth metal ions Sc+, Y+, and Lu+ generated by laser desorption-ionization of metal targets have been investigated by using a Fourier transform ion cyclotron resonance mass spectrometer. The three metal ions react exothermically with all the alcohols. The overall reactivity is controlled by the high oxophilicity of these metals, and the primary metallated ions obtained are principally oxygenated species. However, the number and the nature of these primary products depends on the electronic configuration of the metal ions as well as on the class and the principal chain length of alcohols. The order of reactivity is Y+ > Sc+ > Lu+. The Y+ and Sc+ ions principally react via C-O and O-H insertions, whereas Lu+ reacts by direct abstraction or via various five-center electrocyclic mechanisms as a function of the class and the alcohol chain length. (C) 1996 American society for Mass Spectrometry
引用
收藏
页码:1151 / 1160
页数:10
相关论文
共 73 条
[1]   REACTIONS OF TRANSITION-METAL IONS WITH ALKYL-HALIDES AND ALCOHOLS IN GAS-PHASE - EVIDENCE FOR METAL INSERTION AND BETA-HYDROGEN ATOM SHIFT [J].
ALLISON, J ;
RIDGE, DP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1976, 98 (23) :7445-7447
[2]   REACTIONS OF ATOMIC METAL-IONS WITH ALKYL-HALIDES AND ALCOHOLS IN THE GAS-PHASE [J].
ALLISON, J ;
RIDGE, DP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1979, 101 (17) :4998-5009
[3]   ION-CYCLOTRON DOUBLE RESONANCE [J].
ANDERS, LR ;
BEAUCHAM.JL ;
DUNBAR, RC ;
BALDESCH.JD .
JOURNAL OF CHEMICAL PHYSICS, 1966, 45 (03) :1062-&
[4]   THE CHEMISTRY OF ATOMIC TRANSITION-METAL IONS - INSIGHT INTO FUNDAMENTAL-ASPECTS OF ORGANOMETALLIC CHEMISTRY [J].
ARMENTROUT, PB ;
BEAUCHAMP, JL .
ACCOUNTS OF CHEMICAL RESEARCH, 1989, 22 (09) :315-321
[5]   PERIODIC TRENDS IN TRANSITION METAL-HYDROGEN, METAL-CARBON, AND METAL-OXYGEN BOND-DISSOCIATION ENERGIES - CORRELATION WITH REACTIVITY AND ELECTRONIC-STRUCTURE [J].
ARMENTROUT, PB ;
HALLE, LF ;
BEAUCHAMP, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (21) :6501-6502
[6]   FOURIER-TRANSFORM MASS-SPECTROMETRIC STUDIES OF ISOVALENT RARE-EARTH IONS SC+, Y+ AND LU+ WITH METHANOL - FORMATION OF DIMETHOXIDE METAL SPECIES M(OCH3)2+ [J].
AZZARO, M ;
BRETON, S ;
DECOUZON, M ;
GERIBALDI, S .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1993, 128 (1-2) :1-20
[7]  
BEAUCHAMP JL, 1992, NATO ADV SCI I C-MAT, V367, P287
[8]   GAS-PHASE ION CHEMISTRY OF FLUOROMETHANES BY ION-CYCLOTRON RESONANCE SPECTROSCOPY - NEW TECHNIQUES FOR DETERMINATION OF CARBONIUM-ION STABILITIES [J].
BLINT, RJ ;
MCMAHON, TB ;
BEAUCHAM.JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1974, 96 (05) :1269-1278
[9]  
BOHME DK, 1974, INTERACTION IONS MOL
[10]   THE PREPARATION AND CHARACTERIZATION OF VOLATILE DERIVATIVES OF TRIVALENT METALS USING FLUORINATED ALKOXIDE LIGANDS - X-RAY STRUCTURES OF [SC(OCH(CF3)2)3(NH3)2]2, [PR(OCME(CF3)2)3(NH3)2]2, [Y(OCME(CF3)2)3(THF)3] AND [PR(OCME2(CF3))3]3 [J].
BRADLEY, DC ;
CHUDZYNSKA, H ;
HAMMOND, ME ;
HURSTHOUSE, MB ;
MOTEVALLI, M ;
RUOWEN, W .
POLYHEDRON, 1992, 11 (03) :375-379