Cotte-Rodríguez Ismael, Hernandez-Soto Heriberto, Chen Hao, Cooks R Graham
Department of Chemistry, Purdue University, West Lafayette, Indiana 47907, USA.
Anal Chem. 2008 Mar 1;80(5):1512-9. doi: 10.1021/ac7020085. Epub 2008 Feb 5.
Desorption electrospray ionization (DESI) mass spectrometry is used for the rapid (<5 s), selective, and sensitive detection of trace amounts of the peroxide-based explosives, hexamethylene triperoxide diamine (HMTD), tetracetone tetraperoxide (TrATrP), and triacetone triperoxide (TATP), directly from ambient surfaces without any sample preparation. The analytes are observed as the alkali metal ion complexes. Remarkably, collision-induced dissociation (CID) of the HMTD, TATP, and TrATrP complexes with Na(+), K(+), and Li(+) occurs with retention of the metal, a process triggered by an unusual homolytic cleavage of the peroxide bond, forming a distonic ion. This is followed by elimination of a fragment of 30 mass units, shown to be the expected neutral molecule, formaldehyde, in the case of HMTD, but shown by isotopic labeling experiments to be ethane in the cases of TATP and TrATrP. Density functional theory (DFT) calculations support the suggested fragmentation mechanisms for the complexes. Binding energies of Na+ of 40.2 and 33.1 kcal/mol were calculated for TATP-Na(+) and HMTD-Na(+) complexes, suggesting a strong interaction between the peroxide groups and the sodium ion. Increased selectivity is obtained either by MS/MS or by doping the spray solvent with additives that produce the lithium and potassium complexes of TATP, HMTD, and TrATrP. Addition of dopants into the solvent spray increased the signal intensity by an order of magnitude. When pure alcohol or aqueous hydrogen peroxide was used as the spray solvent, the (HMTD + Na)+ complex was able to bind a molecule of alcohol (methanol or ethanol) or hydrogen peroxide, providing additional characteristic ions to increase the selectivity of analysis. DESI also allowed the rapid detection of peroxide explosives in complex matrixes such as diesel fuel and lubricants using single or multiple cation additives (Na(+), K(+), and Li(+), and NH4(+)) in the spray solvent. Low-nanogram detection limits were achieved for HMTD, TrATrP, and TATP in these complex matrixes. The DESI response was linear over 3 orders of magnitude for HMTD and TATP on paper surfaces (1-5000 ng), and quantification of both peroxide explosives from paper gave precisions (RSD) of less than 3%. The use of pure water and compressed air as the DESI spray solution and nebulizing gas, respectively, showed similar ionization efficiencies to those obtained using methanol/water mixtures and nitrogen gas (the typical choices). An alternative ambient method, desorption atmospheric pressure chemical ionization (DAPCI), was also used to detect trace amounts of HMTD and TATP in air by complexation with gas-phase ammonium ions (NH4(+)) generated by atmospheric pressure ammonia ionization.
解吸电喷雾电离(DESI)质谱用于直接从环境表面快速(<5秒)、选择性且灵敏地检测痕量的过氧化物基炸药,如六亚甲基三过氧化二胺(HMTD)、四丙酮四过氧化合物(TrATrP)和三丙酮三过氧化合物(TATP),无需任何样品制备。分析物以碱金属离子络合物的形式被观测到。值得注意的是,HMTD、TATP和TrATrP与Na(+)、K(+)和Li(+)形成的络合物在碰撞诱导解离(CID)过程中金属得以保留,这一过程由过氧化物键不寻常的均裂引发,形成一个双电荷离子。随后消除一个30质量单位的碎片,在HMTD的情况下该碎片被证明是预期的中性分子甲醛,但在TATP和TrATrP的情况下经同位素标记实验表明是乙烷。密度泛函理论(DFT)计算支持了所提出的络合物碎片化机制。计算得出TATP - Na(+)和HMTD - Na(+)络合物的Na+结合能分别为40.2和33.1千卡/摩尔[13],表明过氧化物基团与钠离子之间存在强相互作用。通过串联质谱(MS/MS)或在喷雾溶剂中添加能生成TATP、HMTD和TrATrP的锂和钾络合物的添加剂可提高选择性。向溶剂喷雾中添加掺杂剂使信号强度提高了一个数量级。当使用纯酒精或过氧化氢水溶液作为喷雾溶剂时,(HMTD + Na)+络合物能够结合一分子酒精(甲醇或乙醇)或过氧化氢,提供额外的特征离子以提高分析的选择性。DESI还能使用喷雾溶剂中的单种或多种阳离子添加剂(Na(+)、K(+)、Li(+)和NH4(+))快速检测复杂基质(如柴油燃料和润滑剂)中的过氧化物炸药。在这些复杂基质中,HMTD、TrATrP和TATP的检测限低至纳克级别。在纸表面,HMTD和TATP的DESI响应在3个数量级(1 - 5000纳克)内呈线性,从纸张上定量两种过氧化物炸药的精密度(相对标准偏差,RSD)小于3%。分别使用纯水和压缩空气作为DESI喷雾溶液和雾化气体,其电离效率与使用甲醇/水混合物和氮气(典型选择)时相似。另一种常压方法,解吸大气压化学电离(DAPCI),也被用于通过与大气压氨电离产生的气相铵离子(NH4(+))络合来检测空气中痕量的HMTD和TATP。