Sattler Dominik, Schlesinger Maik, Mehring Michael, Schalley Christoph A
Institut für Chemie und Biochemie, Freie Universität Berlin, Takustrasse 3, 14195 Berlin (Germany).
Fakultät für Naturwissenschaften, Institut für Chemie, Professur Koordinationschemie, Technische Universität Chemnitz, Strasse der Nationen 62, 09111 Chemnitz (Germany).
Chempluschem. 2013 Sep;78(9):1005-1014. doi: 10.1002/cplu.201300122. Epub 2013 Jun 17.
The mass spectrometric characterisation of bismuth-oxido clusters is described together with tandem mass spectrometric experiments aimed at investigating their gas-phase chemistry. Clusters with different ligand shells (nitrate, salicylates, and methacrylate) and different sizes ({Bi O }, {Bi O }, and {Bi O }) were selected for this study. The following aspects were addressed by (tandem) electrospray ionisation Fourier-transform ion-cyclotron-resonance (ESI-FTICR) mass spectrometry: 1) Electrospray ionisation was used successfully for the generation of intact cluster ions, but led to rather complicated distributions of charge states and solvent adducts. The cluster core remained intact. 2) Mass spectrometry was used to follow the cluster growth from {Bi O } to {Bi O } and finally {Bi O } clusters. These experiments revealed that careful tuning of the conditions is required to avoid precipitates forming that hamper ESI ionisation. The stages of growth strongly depend on the experimental conditions. 3) Fragmentation experiments in the gas phase performed with the {Bi O } clusters obtained in the growth experiments resulted in the preferential formation of {Bi O } fragments and point to the particular stability of this cluster and its role in cluster growth. 4) Solution-phase ligand-exchange reactions on {Bi O } salicylate clusters were qualitatively monitored by mass spectrometry, but were limited by the complicated ion series formed that led to overlapping isotope patterns. 5) A number of fragmentation reactions occurred within the ligand shell when the clusters surrounded by an organic ligand shell were subjected to infrared multiphoton dissociation experiments. 6) For the nitrate clusters, fragmentation within the core was observed yielding {Bi O } fragments together with the corresponding clusters of reduced size.
本文描述了铋氧化簇的质谱表征以及旨在研究其气相化学的串联质谱实验。本研究选择了具有不同配体壳层(硝酸盐、水杨酸盐和甲基丙烯酸酯)和不同尺寸({Bi O }、{Bi O }和{Bi O })的簇。通过(串联)电喷雾电离傅里叶变换离子回旋共振(ESI-FTICR)质谱法研究了以下几个方面:1)电喷雾电离成功用于生成完整的簇离子,但导致电荷态和溶剂加合物的分布相当复杂。簇核心保持完整。2)质谱法用于跟踪从{Bi O }到{Bi O }以及最终到{Bi O }簇的簇生长过程。这些实验表明,需要仔细调整条件以避免形成妨碍ESI电离的沉淀。生长阶段强烈依赖于实验条件。3)对生长实验中获得的{Bi O }簇进行的气相裂解实验导致优先形成{Bi O }碎片,并表明该簇的特殊稳定性及其在簇生长中的作用。4)通过质谱对{Bi O }水杨酸盐簇上的溶液相配体交换反应进行了定性监测,但受到形成的复杂离子系列导致同位素模式重叠的限制。5)当被有机配体壳包围的簇进行红外多光子解离实验时,在配体壳内发生了许多裂解反应。6)对于硝酸盐簇,观察到核心内的裂解,产生{Bi O }碎片以及相应尺寸减小的簇。