Five new complexes M(Hmna)2 [M=Mn(II) (1), Co(II) (2), Ni(II) (3), Cu(II) (4) and Zn(II) (5), H2mna=2-mercaptonicotinic acid] have been synthesized and characterized by elemental analyses, IR spectra, thermogravimetric
analyses. In addition, molar specific heat capacities and enthalpy changes of reactions were determined by a microcalorimeter
at 298.15 K. All the complexes exhibited similar IR spectra, the sulfur and oxygen atoms from monoanionic Hmna− ligand coordinated to M2+ in a bidentate fashion.
The thermal stability of M(Hmna)2 complexes varied in the sequence 1>2>3>4>5. The complexes were stable up to about 300°C and decomposed to oxides at higher temperatures. The molar specific heat capacities
of the complexes were determined in the range between 106.452±0.399 and 145.920±0.423 J mol−1 K−1. The enthalpy changes of reactions, ΔrHmθ, were determined from 18.28±0.05 to 52.59±0.07 kJ mol−1 for complexes 1–5, indicating that the thermodynamic stability of M(Hmna)2 increased in the sequence from Mn2+ to Zn2+.
Fourteen new complexes with the general formula of Ln(Hmna)3·nH2O (n=2 for Ln=La-Ho and n=1 for Er-Lu, H2mna=2-mercaptonicotinic acid) were synthesized and characterized by elemental analyses, IR spectra and thermogravimetric analyses.
In addition, molar specific heat capacities were determined by a microcalorimeter at 298.15 K. The IR spectra of the prepared
complexes revealed that carboxyl groups of the ligands coordinated with Ln(III) ions in bidentate chelating mode. Hydrated
complexes lost water molecules during heating in one step and then the anhydrous complexes decomposed directly to oxides Ln2O3, CeO2, Pr6O11 and Tb4O7. The values of molar specific heat capacities for fourteen solid complexes were plotted against the atomic numbers of lanthanide,
which presented as ‘tripartite effect’. It suggested a certain amount of covalent character existed in the bond of Ln3+ and ligands, according with nephelauxetic effect of 4f electrons of rare earth ions.