Tuning the polarization along linear polyaromatic strands for rationally inducing mesomorphism in lanthanide nitrate complexes

Article abstract of DOI:10.1002/chem.200601389

The opposite orientation of the ester spacers in the rodlike ligands L4^C12 (benzimidazole-OOC-phenyl) and L5^C12 (benzimidazole-COO-phenyl) drastically changes the electronic structure of the aromatic systems, without affecting their meridional Incoordination to trivalent lanthanides, Ln¹¹¹, and their thermotropic liquid crystalline (i.e., mesomorphic) behaviors. However, the rich mesomorphism exhibited by the complexes [Ln(L4^C12)-(NO₃)₃] (Ln = La-Lu) vanishes in [Ln-(L5^C12)(NO₃)₃], despite superimposable molecular structures and comparable photophysical properties. Density functional theory (DFT) and time-dependant DFT calculations performed in the gas phase show that the inversion of the ester spacers has considerable effects on the electronic structure and polarization of the aromatic groups along the strands, which control residual intermolecular interactions responsible for the formation of thermotropic liquid-crystalline phases. As a rule of thumb, an alternation of electron-poor and electron-rich aromatic rings favors intermolecular interactions between the rigid cores and consequently mesomorphism, a situation encountered for L4^C12, L5^C12, [Ln(L4^C12)(NO₃)₃], but not for [Ln(L5 ^C12)(NO₃)₃]. The intercalation of an additional electron-rich diphenol ring on going from [Ln(L5^C12)-(NO ₃)₃] to [Ln(L6^C12)(NO₃)₃] restores mesomorphism despite an unfavorable orientation of the ester spacers, in agreement with our simple predictive model.