| Literature DB >> 28560843 |
Markus Rohdenburg1, Martin Mayer2, Max Grellmann2, Carsten Jenne3, Tobias Borrmann1, Florian Kleemiss4, Vladimir A Azov1,5, Knut R Asmis2, Simon Grabowsky4, Jonas Warneke6.
Abstract
It is common and chemically intuitive to assign cations electrophilic and anions nucleophilic reactivity, respectively. Herein, we demonstrate a striking violation of this concept: The anion [B12 Cl11 ]- spontaneously binds to the noble gases (Ngs) xenon and krypton at room temperature in a reaction that is typical of "superelectrophilic" dications. [B12 Cl11 Ng]- adducts, with Ng binding energies of 80 to 100 kJ mol-1 , contain B-Ng bonds with a substantial degree of covalent interaction. The electrophilic nature of the [B12 Cl11 ]- anion is confirmed spectroscopically by the observation of a blue shift of the CO stretching mode in the IR spectrum of [B12 Cl11 CO]- and theoretically by investigation of its electronic structure. The orientation of the electric field at the reactive site of [B12 Cl11 ]- results in an energy barrier for the approach of polar molecules and facilitates the formation of Ng adducts that are not detected with reactive cations such as [C6 H5 ]+ . This introduces the new chemical concept of "dipole-discriminating electrophilic anions."Entities:
Keywords: bond theory; borates; ion-molecule reactions; noble gases
Year: 2017 PMID: 28560843 DOI: 10.1002/anie.201702237
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336