Metal phthalocyanines,
a highly versatile class of aromatic,
planar,
macrocyclic molecules with a chelated central metal ion, are topical
objects of ongoing research and particularly interesting due to their
magnetic properties. However, while the current focus lies almost
exclusively on spin-Zeeman-related effects, the high symmetry of the
molecule and its circular shape suggests the exploitation of light-induced
excitation of 2-fold degenerate vibrational states in order to generate,
switch, and manipulate magnetic fields at the nanoscale. The underlying
mechanism is a molecular pseudorotation that can be triggered by infrared
pulses and gives rise to a quantized, small, but controllable magnetic
dipole moment. We investigate the optical stimulation of vibrationally
induced molecular magnetism and estimate changes in the magnetic shielding
constants for confirmation by future experiments.