Affiliation:
1. Wilhelm-Ostwald-Institut für Physikalische und Theoretische Chemie Universität Leipzig Linnéstr. 2 04103 Leipzig Germany
2. Institut für Organische Chemie Universität Leipzig Linnéstr. 3 04103 Leipzig Germany
3. Leibniz Institut für Oberflächenmodifizierung (IOM) Permoserstraße 15 04318 Leipzig Germany
Abstract
AbstractMass spectrometry frequently reveals the existence of transient gas phase ions that have not been synthesized in solution or in bulk. These elusive ions are, therefore, often considered to be primarily of analytical value in fundamental gas phase studies. Here, we provide proof‐of‐concept that the products of ion‐molecule reactions in mass spectrometers may be collected on surfaces to generate condensed matter and thus serve as building blocks to synthesize new compounds. The highly reactive fragment anion [B12Br11]− was generated in a mass spectrometer and converted to [B12Br11N2]− in the presence of molecular nitrogen followed by its mass‐selection and soft‐landing on surfaces. The molecular structure of [B12Br11N2]−, which has not been synthetically obtained before, was confirmed by conventional methods of molecular analysis, including nuclear magnetic resonance and infrared spectroscopy. The [B12Br11N2]− ion is stable on surfaces and in solution at room temperature, but thermal annealing induces elimination of N2 and provides access to the highly reactive intermediate [B12Br11]− in the condensed phase, which can be further used as a reagent, for example, for electrophilic aromatic substitutions. Thus, isolation of [B12Br11N2]− expands the repertoire of the available diazo ions that can be employed as versatile intermediates in various chemical transformations.
Funder
Volkswagen Foundation
Deutsche Forschungsgemeinschaft
Subject
General Chemistry,Catalysis
Cited by
9 articles.
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