2.2]Paracyclophane bis(pyridine)-based metallosupramolecular rhombs in the gas phase: Competitive cleavage of non-covalent and weak covalent bonds.

Abstract

The gas-phase fragmentation behavior of self-assembled metallo-supramolecular rhombs based on an unusual chiral [2.2]paracyclophane bis(pyridine) ligand is studied by collision-induced dissociation mass spectrometry. The fragmentation patterns strongly depend on the charge state of the respective mass-selected aggregate. For the doubly charged ions, simple symmetric fragmentation is observed in full accordance with previous results reported for related metallo-supramolecular species. The triply charged species cleaves unsymmetrically which can be rationalized by a preferred formation of ions with low charge density. CID of the quadruply charged rhomb reveals a complex fragmentation. Besides ligand oxidation to the radical cation, facile cleavage of the central covalently bound part of the [2.2]paracyclophane ligand takes place which is even preferred over rupture of the weak dative pyridine-Pd bond.