Castellanos A, Benigni P, Hernandez D R, DeBord J D, Ridgeway M E, Park M A, Fernandez-Lima F
Department of Chemistry and Biochemistry, Florida International University, Miami, FL 33199, USA.
Bruker Daltonics, Inc., Billerica, Massachusetts 01821, USA.
Anal Methods. 2014 Dec 7;6(23):9328-9332. doi: 10.1039/C4AY01655F.
In the present paper, we showed the advantages of trapped ion mobility spectrometry coupled too mass spectrometry (TIMS-MS) combined with theoretical calculations for fast identification (millisecond timescale) of polycyclic aromatic hydrocarbons (PAH) compounds from complex mixtures. Accurate PAH collision cross sections (CCS, in nitrogen as a bath gas) are reported for the most commonly encountered PAH compounds and the ability to separate PAH geometric isomers is shown for three isobaric pairs with mobility resolution exceeding 150 (3-5 times higher than conventional IMS devices). Theoretical candidate structures (optimized at the DFT/B3LYP level) are proposed for the most commonly encountered PAH compounds showing good agreement with the experimental CCS values (<5%). The potential of TIMS-MS for the separation and identification of PAH compounds from complex mixtures without the need of lengthy pre-separation steps is illustrated for the case of a complex soil mixture.
在本论文中,我们展示了阱式离子迁移谱与质谱联用(TIMS-MS)结合理论计算在从复杂混合物中快速鉴定(毫秒级时间尺度)多环芳烃(PAH)化合物方面的优势。报告了最常见PAH化合物的准确碰撞截面(CCS,以氮气作为缓冲气体),并展示了对于三对同量异位体,迁移率分辨率超过150(比传统离子迁移谱设备高3 - 5倍)时分离PAH几何异构体的能力。针对最常见的PAH化合物提出了理论候选结构(在DFT/B3LYP水平上进行优化),其与实验CCS值显示出良好的一致性(<5%)。对于复杂土壤混合物的情况,说明了TIMS-MS无需冗长的预分离步骤即可从复杂混合物中分离和鉴定PAH化合物的潜力。