Abstract
Two series of 2,5-dihalopyridine-Cu(I)A (A = I, Br) complexes based on 2-X-5-iodopyridine and 2-X-5-bromopyridine (X = F, Cl, Br and I) are characterized by using single-crystal X-ray diffraction analysis to examine the nature of C2-X2···A-Cu and C5-X5···A-Cu halogen bonds. The reaction of the 2,5-dihalopyridines and Cu(I) salts allows the synthesis of eight 1-D coordination polymers and a discrete structure. The resulting Cu(I)-complexes are linked by C-X···A-Cu halogen bonds forming 3-D supramolecular networks. The C-X···A-Cu halogen bonds formed between halopyridine ligands and copper(I)-bound halide ions are stronger than C-X···X'-C interactions between two 2,5-dihalopyridine ligands. The C5-I5···I-Cu and C5-Br5···Br-Cu halogens bonds are shorter for C2-fluorine than C2-chlorine due to the greater electron-withdrawing power of fluorine. In 2,5-diiodopyridine-Cu(I)Br complex, the shorter C2-I2···Br-Cu [3.473(5) Å] distances are due to the combined polarization of C2-iodine by C2-I2···Cu interactions and para-electronic effects offered by the C5-iodine, whilst the long halogen bond contacts for C5-I5···Br-Cu [3.537(5) Å] are indicative that C2-iodine has a less para-electronic influence on the C5-iodine. In 2-fluoro-5-X-pyridine-Cu(I) complexes, the C2-fluorine is halogen bond passive, while the other C2-halogens in 2,5-dihalopyridine-Cu(I), including C2-chlorine, participate in halogen bonding interactions.