Vanadium oxide anion cluster reactions with methyl isobutyrate and methyl methacrylate monomer and dimer: a study by FT/ICR mass spectrometry

被引:37
作者
Dinca, A [1 ]
Davis, TP
Fisher, KJ
Smith, DR
Willett, GD
机构
[1] Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Sch Chem Engn & Ind Chem, Sydney, NSW 2052, Australia
关键词
Fourier transform ion cyclotron resonance mass spectrometry; laser ablation; vanadium oxide cluster anions; methyl isobutyrate; methyl methacrylate; ion-molecule reactions;
D O I
10.1016/S1387-3806(98)14243-4
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Laser ablation of vanadium pentoxide (V2O5) powder produces VO3-, V2O5-, V3O7-, V3O8-, and V4O10- cluster ions which have subsequently been reacted with methyl isobutyrate, methyl methacrylate monomer and its dimer in the ion cell region of a Fourier transform ion cyclotron resonance mass spectrometer. Gas phase ion/molecule chemistry has revealed that reactivity decreases with increased mass of the vanadium oxide cluster anions. VO3-, V2O5-, and V3O7- ions react with the three reagents, methyl isobutyrate, methyl methacrylate and its dimer, respectively, either by addition of a whole reagent molecule or an associated fragment. All products formed are a result of parallel processes. V4O10- undergoes no reaction for reaction times of up to 500 s, while V3O8- adds a water molecule. Although the ions possess a net negative charge, the reactive site toward electron rich reagents such as methyl isobutyrate, methyl methacrylate and its dimer is the under-coordinated vanadium atom. This observation is supported by the lack of reactivity toward the studied reagents by those anions (V3O8- and V4O10-) whose most likely stable structures contain fully coordinated vanadium atoms. (C) 1999 Elsevier Science B.V.
引用
收藏
页码:73 / 84
页数:12
相关论文
共 55 条
[51]   A photoelectron spectroscopic study of monovanadium oxide anions (VOx-, x=1-4) [J].
Wu, HB ;
Wang, LS .
JOURNAL OF CHEMICAL PHYSICS, 1998, 108 (13) :5310-5318
[52]  
XU YC, 1996, INT J MASS SPECTROM, V158, P249
[53]   Living polymerizations of polar and nonpolar monomers by the catalysis of organo rare earth metal complexes [J].
Yasuda, H ;
Ihara, E .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1997, 70 (08) :1745-1767
[54]   SYNTHESIS OF HIGH-MOLECULAR-WEIGHT POLY(METHYL METHACRYLATE) WITH EXTREMELY LOW POLYDISPERSITY BY THE UNIQUE FUNCTION OF ORGANOLANTHANIDE(III) COMPLEXES [J].
YASUDA, H ;
YAMAMOTO, H ;
YAMASHITA, M ;
YOKOTA, K ;
NAKAMURA, A ;
MIYAKE, S ;
KAI, Y ;
KANEHISA, N .
MACROMOLECULES, 1993, 26 (26) :7134-7143
[55]   A tandem mass spectrometry and Fourier transform ion cyclotron resonance (FT-ICR) study of RMn(+)(crown-ether) complexes in the gas phase [J].
Zagorevskii, DV ;
Holmes, JL ;
Watson, CH ;
Eyler, JR .
EUROPEAN MASS SPECTROMETRY, 1997, 3 (01) :27-36