Copper(II)-assisted hydrolysis of 2,4,6-tris(2-pyridyl)-1,3,5-triazine. Part 2. Crystal structures of [bis(2-pyridylcarbonyl)amido](pyridine-2-carboxamide)copper(II) trifluoromethanesulphonate and [bis(2-pyridylcarbonyl)amido][2,4,6-tris(2-pyridyl)-1,3,5-triazine]copper(II) trifluoromethanesuiphonate
Two compounds of formula [Cu{(NC5H4Co)2N}(NC5H4CONH2)][CF3SO3](1) and [Cu{(NC5H4CO)2N}(tptz)][CF3SO3], (2), where (NC5H4CO)2N– and NC5H4CONH2 are bis(2-pyridylcarbonyl)amide and pyridine-2-carboxamide and tptz = 2,4,6-tris(2-pyridyl)-1,3,5-triazine respectively, have been obtained from aqueous solutions of tptz and copper(II) trifluoromethanesulphonate. Crystals of complex (1) are monoclinic with a= 9.927(4), b= 26.727(5), c= 8.594(4)Åβ= 98.72(2)°, space group P21/n, and Z= 4. Crystals of complex (2) are triclinic with a= 9.177(3), b= 10.735(3), c= 18.231(4)Å, α= 102.65(2), β= 106.60(2), γ= 93.89(3)°, space group P, and Z= 2. The structure of (1) consists of [Cu{NC5H4CO)2N}(NC5H4CONH2)]+ mononuclear cations plus semi-co-ordinated CF3SO3– anions. The copper(II) ion is in a distorted octahedral environment: the three nitrogen atoms of the bis(2-pyridylcarbonyl)amido ligand and the pyridine one of the carboxamide form a distorted square plane around the copper whereas the axial positions are occupied by the oxygen atom of the carboxamide and by an oxygen atom of the CF3SO3– group with Cu–O bonds different from each other and significantly longer than the equatorial ones. The structure of (2) is made up of [Cu{(NC5H4CO)2N}(tptz)]+ mononuclear cations and non-co-ordinated CF3SO3– groups. The copper(II) ion is six-co-ordinated: the three nitrogen atoms of the bis(2 pyridylcarbonyl)amido ligand and one nitrogen atom of the triazine ring of tptz form a distorted square plane around the copper, while two nitrogen atoms from two pyridyl rings of tptz occupy the axial sites. The two Cu–N axial bonds are very close but significantly longer than the equatorial ones. The structure of (1) contains as ligands the two main products of the copper(II)-assisted tptz hydrolysis, whereas in the structure of (2) the co-ordination polyhedron around copper(II) is achieved by one of these products and tptz. The possibility of synthesizing copper(II) complexes containing unhydrolysed tptz is discussed in the light of the structure of complex (2).