Coordination entities of a pyrene-based iminopyridine ligand: Structural and photophysical properties

A pyrene-based iminopyridine ligand L has been prepared and displays the absorption and emission properties expected for pyrene-based derivatives in solution. Ligand L, as well as two neutral and, one monocationic coordination entities, respectively formulated as [ZnLCl2] 1, [ReLCl(CO)(3)] 3 and [CuL2] (BF4) 2, have been crystallized and analyzed by single crystal X-ray diffraction analysis. The corresponding crystal structures indicate the formation of supramolecular architectures generated by offset pi...pi stacking between pyrene fragments and strong C-H center dot center dot center dot pi is interactions in coordination entity 1. For the cationic coordination entity 2, the crystal packing reveals the presence of C-H center dot center dot center dot F and C-H center dot center dot center dot pi interactions and numerous C-H center dot center dot center dot pi contacts interconnecting the molecules into a 3D network. As for coordination entity 3, hydrogen bonding and pi center dot center dot center dot pi stacking link the molecules in a three dimensional manner. Zinc(II) and copper(I) coordination entities have also been studied through isothermal titration calorimetry, which indicate a strong binding and a different stoichiometry for both coordination entities. Photophysical studies of the ligand and corresponding coordination entities show a monomer type pyrene emission and a higher fluorescence quantum yield for the zinc coordination entity 1 as compared with copper 2 and rhenium 3 coordination entities. (C) 2017 Elsevier Ltd. All rights reserved.