Photoluminous copper(II)-2,2′-dipyridylamine coordination frameworks: Two-dimensional superstructures based on hydrogen bonds and π…π/C–H…π interaction

Abstract

Treatment of Cu 2(OAc) 4·2H 2O with 2,2′-dipyridylamine (dpa) in 1:2 molar ratio in MeCN–H 2O results neutral [Cu(OAc) 2(dpa)]·2H 2O ( 1) which on subsequent treatment with 1 equiv of NaBF 4 affords [Cu(OAc)(dpa) 2]BF 4 ( 2). The complexes are characterized using microanalytical, spectroscopic, magnetic, thermal, electrochemical, and other physicochemical results. Electrochemical electron transfer study of 1 and 2 in MeCN solutions show a reductive response presumably due to copper(II)–copper(I) couple. Thermal study (TG-DTA) of 1 reveals a weight loss of 9.21% at 70–85 K corresponding to two crystalline water molecules. Structures of 1 and 2 are solved by X-ray diffraction study. Compound 1 adopts a distorted octahedral CuN 2O 4 environment coordinated through two N atoms of dpa and four O atoms of two chelating acetates with elongated axial bonds. In 2, copper(II) is ligated by four N atoms of two dpa units and two O atoms of an acetate in chelating fashion resulting a cationic core of [Cu(OAc)(dpa) 2] +. Crystal packings show that mononuclear units of 1 self-assemble through cooperative hydrogen bonds and π…π interaction and of 2, through hydrogen bonds along with C–H…π interaction leading to 2D sheets. Both the complexes show high-energy intraligand 1(π…π ∗) fluorescence and intraligand 3(π…π ∗) phosphorescence in glassy solutions (DMF at 77 K).