摘要

The in situ solvothermal reaction of 3,4-dicyano-1,2,5-thiadiazole with MCl2 (M = Co, Ni) and NaOH afforded two isomorphous complexes, [M-2(L)(2)(H2O)(2)](n) (L = 2,1,3-thiadiazole-4,5-dicarboxylate), which exhibit a rare non-interpenetrated (10,3)-d (utp) network topology and interesting magnetic behaviors: spin-canted antiferromagnetism for the Co-II complex, but simple antiferromagnetic coupling for the Ni-II.