SECONDARY-ION MASS-SPECTROMETRY OF GLYCOSYLATED PORPHYRINS

被引:8
作者
SPIRO, M
BLAIS, JC
BOLBACH, G
FOURNIER, F
TABET, JC
DRIAF, K
GAUD, O
GRANET, R
KRAUSZ, P
机构
[1] INST CURIE,PHYS & CHIM BIOMOLEC LAB,CNRS,URA 198,11 RUE PIERRE & MARIE CURIE,F-75231 PARIS 05,FRANCE
[2] UNIV PARIS 06,F-75231 PARIS 05,FRANCE
[3] UNIV PARIS 06,CHIM ORGAN STRUCT LAB,CNRS,ERS 73,F-75252 PARIS 05,FRANCE
[4] UNIV LIMOGES,CHIM SUBST NAT LAB,F-87060 PARIS,FRANCE
来源
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES | 1994年 / 134卷 / 2-3期
关键词
PORPHYRINS; GLYCOSYLATED; SECONDARY ION MASS SPECTROMETRY;
D O I
10.1016/0168-1176(94)03991-7
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
Solid secondary ion mass spectrometry (SIMS) has been used to study a series of acetylated precursors of glycosylated porphyrins in the course of their synthesis. Characteristic positive and negative spectra have been readily obtained for all the compounds up to more than 2000 Da. In addition to the protonated or deprotonated molecules, fragment ions arising from cleavages between the oxygen atom of the ether bond and the acetylated sugar units were observed; these fragments were more abundant in the negative spectra. The solid SIMS spectra are not complicated by chemical noise or chemical reactions occuring in the presence of a matrix which makes the method well suited for rapid screening during synthesis.
引用
收藏
页码:229 / 238
页数:10
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