Wyatt Mark F, Stein Bridget K, Brenton A Gareth
EPSRC National Mass Spectrometry Service Center, Department of Chemistry, University of Wales Swansea, Swansea, United Kingdom.
J Am Soc Mass Spectrom. 2006 May;17(5):672-5. doi: 10.1016/j.jasms.2006.01.009. Epub 2006 Mar 15.
Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) has been shown to be an effective technique for the characterization of organometallic, coordination, and highly conjugated compounds. The preferred matrix is 2-[(2E)-3-(4-tert-butylphenyl)-2-methylprop-2-enylidene]malononitrile (DCTB), with radical ions observed. However, MALDI-TOFMS is generally not favored for accurate mass measurement. A specific method had to be developed for such compounds to assure the quality of our accurate mass results. Therefore, in this preliminary study, two methods of data acquisition, and both even-electron (EE+) ion and odd-electron (OE+.) radical ion mass calibration standards, have been investigated to establish the basic measurement technique. The benefit of this technique is demonstrated for a copper compound for which ions were observed by MALDI, but not by electrospray (ESI) or liquid secondary ion mass spectrometry (LSIMS); a mean mass accuracy error of -1.2 ppm was obtained.
基质辅助激光解吸/电离飞行时间质谱(MALDI-TOFMS)已被证明是一种用于表征有机金属化合物、配位化合物和高度共轭化合物的有效技术。首选的基质是2-[(2E)-3-(4-叔丁基苯基)-2-甲基丙-2-烯叉基]丙二腈(DCTB),观察到了自由基离子。然而,MALDI-TOFMS一般不太适合进行精确质量测量。必须为这类化合物开发一种特定方法,以确保我们精确质量结果的质量。因此,在这项初步研究中,研究了两种数据采集方法以及偶电子(EE+)离子和奇电子(OE+·)自由基离子质量校准标准,以建立基本测量技术。该技术的优势在一种铜化合物上得到了证明,通过MALDI观察到了该化合物的离子,但电喷雾(ESI)或液体二次离子质谱(LSIMS)未观察到;获得的平均质量准确度误差为-1.2 ppm。