A cobalt(II) hydrogen-bonded organic framework exhibiting uniaxial negative thermal expansion and field-induced slow magnetic relaxation

Abstract

The magnetic and thermal expansion properties of a cobalt(II) hydrogen-bonded organic framework (CoHOF), [Co(H2O)6](NPS)2 (1, HNPS = naphthalene-2-sulphonic acid), constructed by hexaaquacobalt(II) and organsulfonate were reported. Single-crystal X-ray diffraction reveals a porous 2D hydrogen-bonded framework of 1 sustained by multiple and charge-assisted intermolecular hydrogen bonding interactions. Variable-temperature single-crystal combined with powder X-ray diffraction and thermal gravimetric analyses confirms the high thermal stability of the CoHOF. The dynamic changes of the crystal lattice indicate uniaxial negative thermal expansion (NTE) behavior along the c-axis direction through a possible slippage motion. Magnetic measurements indicate the Co2+ ions show uniaxial magnetic anisotropy with D = −92.5 cm−1. A.C. susceptibility measurements reveal field-driven slow magnetic relaxation of 1. These results provide a rare cobalt(II) hydrogen-bonded organic framework showing single-ion magnetism and negative thermal expansion properties.