Characterization of various analytes using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry and 2-[(2E)-3-(4-tert-butylphenyl).2-methylprop-2-enylidene]malononitrile matrix

被引:59
作者
Wyatt, MF [1 ]
Stein, BK [1 ]
Brenton, AG [1 ]
机构
[1] Univ Coll Swansea, Dept Chem, EPSRC Natl Mass Spectrometry Serv Ctr, Swansea SA2 8PP, W Glam, Wales
关键词
D O I
10.1021/ac050732f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
2-[(2E)-3-(4-tert-Butylphenyl)-2-mediylprop-2-enyfidenelmalononittile (DCTB) is a nonpolar, aprotic matrix and was used in the analysis of a variety of compounds by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS). The classes of compounds include coordination compounds, organometallics, conjugated organic compounds (including porphyrins and phthalocyanines), carbohydrates, calixarenes, and macrocycles. For some samples, comparisons are made with spectra acquired with the use of 1,8,9-trihydroxyanthracene (dithranol), 2,5-dihydroxybenzoic acid, and 2,4,6-trihydroxyacetophenone matrixes. Traditionally, the majority of these compounds would have been analyzed by fast-atom bombardment (FAB), liquid secondary ion mass spectrometry (LSIMS), or electrospray techniques, but this work shows that MALDI-TOFMS using DCTB has advantages over these techniques, particularly FAB and LSIMS. Certain limitations of DCTB are noted, for example, in the analysis of water-soluble compounds such as peptides, proteins, and oligonucleotides, and good working practices for the use of the matrix are also outlined.
引用
收藏
页码:199 / 206
页数:8
相关论文
共 36 条
[1]   The coordination chemistry and reactivity of group 13 metal(I) heterocycles [J].
Baker, RJ ;
Jones, C .
COORDINATION CHEMISTRY REVIEWS, 2005, 249 (17-18) :1857-1869
[2]   First-generation chiral metallodendrimers: Stereoselective synthesis of rigid D-3-symmetric tetranuclear ruthenium complexes [J].
Bodige, S ;
Torres, AS ;
Maloney, DJ ;
Tate, D ;
Kinsel, GR ;
Walker, AK ;
MacDonnell, FM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (43) :10364-10369
[3]   Matrix-assisted laser desorption/ionization of amphiphilic fullerene derivatives [J].
Brown, T ;
Clipston, NL ;
Simjee, N ;
Luftmann, H ;
Hungerbühler, H ;
Drewello, T .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2001, 210 (1-3) :249-263
[4]   Cofacial porphyrin-ferrocene dyads and a new class of conjugated porphyrin [J].
Cammidge, AN ;
Scaife, PJ ;
Berber, G ;
Hughes, DL .
ORGANIC LETTERS, 2005, 7 (16) :3413-3416
[5]  
CHALLINOR L, UNPUB
[6]  
Chan Y.-H., UNPUB
[7]  
COOK MK, UNPUB
[8]   Lanthanide halide and nitrate complexes with potentially tridentate bisphosphine dioxide-ether donors [J].
Fawcett, J ;
Platt, AWG ;
Vickers, S ;
Ward, MD .
POLYHEDRON, 2004, 23 (16) :2561-2567
[9]   Analysis of ruthenium carbonyl-porphyrin complexes: a comparison of matrix-assisted laser desorption/ionisation time-of-flight, fast-atom bombardment and field desorption mass spectrometry [J].
Frauenkron, M ;
Berkessel, A ;
Gross, JH .
EUROPEAN MASS SPECTROMETRY, 1997, 3 (06) :427-438
[10]   Organic synthesis via transition metal complexes.: 112.: Reactivity enhancement of group VI Fischer carbene complexes by copper and rhodium catalysts:: Experimental proof of a carbene rhodium complex as an intermediate [J].
Göttker-Schnetmann, I ;
Aumann, R ;
Bergander, K .
ORGANOMETALLICS, 2001, 20 (16) :3574-3581