Dynamic formation of coordination polymers versus tetragonal prisms and unexpected magnetic superexchange coupling mediated by encapsulated anions in the cobalt(II) 1,3-bis(pyrid-4-ylthio)propan-2-one series |
| |
Authors: | Wu Benlai Yuan Daqiang Lou Benyong Han Lei Liu Caiping Zhang Chunxi Hong Maochun |
| |
Institution: | State Key Laboratory of Structural Chemistry, Fujian Institute of the Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China. |
| |
Abstract: | The reactions of cobalt(II) halides and flexible ligand L L=1,3-bis(pyrid-4-ylthio)propan-2-one] under different conditions generated a series of complexes with various structural motifs ranging from tetragonal-prismatic cages to 1-3D coordination polymers. The layer diffusion of cobalt(II) chloride and L in methanol/acetone at 25 degrees C gave rise to a 3D polymer, Co(L)2Cl2].Me2CO. At 30 degrees C, the slow diffusion of diethyl ether into the blue dimethylformamide (DMF) solution of complex 1 afforded a 1D polymer, Co(L)Cl2(DMF)2. However, at 10 degrees C, the diffusion of diethyl ether into the DMF solution of complex 1 produced a tetragonal-prismatic cage, Co2(L)4Cl2]Cl2.Et2O.DMF.2MeOH.4H2O. The reaction of cobalt(II) bromide and L in DMF at 10 degrees C yielded a dimer, Co2(L)4Br2]Br2.6DMF.2H2O, with a cage structure similar to. The preparation of the series of compounds indicates the subtle relationship between structures and tunable reaction conditions. It is also found that the structural motifs vary according to the ligand conformations and that the formation of tetragonal-prismatic cages and may be templated by anionic guests. Magnetic studies on complexes in a temperature range 4-300 K disclose that L is unfavorable for a long-range magnetic interaction; however, intramolecular spin-coupling constants of -19.6 and -21.5 cm-1 for and indicate rather strong magnetic superexchanges arising from the overlap of the dz2 orbitals of the cobalt(II) and pz orbitals of the encapsulated halide anions. Electron paramagnetic resonance (EPR) spectra of complexes 3 and 4 in solution and solid give information that both complexes are high-spin cobalt(II) compounds with a rhombic distortion of the axial zero-field splitting. Interestingly, the intramolecular magnetic-exchange coupling in 3 and 4 mediated by the encapsulated anion Cl- or Br- is also reflected by the EPR spectra. |
| |
Keywords: | |
本文献已被 PubMed 等数据库收录! |
|