Observation of poly(ethylene glycol) clusters with the chlorine anion in the gas phase under electrospray conditions

Abstract

It is demonstrated herein that poly(ethylene glycol) (PEG) oligomers can form stable complexes with the chlorine anion in the gas phase as evidenced by results from electrospray ionization mass spectrometry (ESI-MS) and molecular dynamics simulation. While the formation of crown-ether-like structures by acyclic polyethers in their complexes with alkali metal cations coordinated by the ether oxygen atoms has been extensively studied, the possibility of forming 'inversed' quasi-cyclic structures able to bind a monoatomic anion has not been proved till now. We have observed the formation of stable gas-phase complexes of oligomers of PEG-400 with the Cl(-) anion experimentally by ESI-MS for the first time. It is suggested that a necessary precondition for obtaining the polyether-chlorine anion clusters is the prevention of the formation of neutral ion pairs. Molecular dynamics simulation has demonstrated the wrapping of the Cl(-) anion by the PEG chain, to stabilize the PEG(n)•Cl(-) clusters in the gas phase. The conformation of the polyether chain in such quasi-cyclic or quasi-helical complexes is 'inversed' compared with that in the complexes with cations: that is its hydrogen atoms are turned towards the central anion. Awareness of the possibility of the Cl(-) anion being trapped in quasi-cyclic PEG structures may be of practical importance when considering the intermolecular interactions of PEGs.