Pressure-Induced Structural Effects in the Square Lattice ( sql ) Topology Coordination Network Sql-1-Co-NCS·4OX.

A high-pressure study of a switching coordination network of square lattice topology ( sql ) loaded with o -xylene (OX), [Co(4,4'-bipyridine) 2 (NCS) 2 ] n ·4nC 8 H 10 (sql-1-Co-NCS·4OX), was conducted up to approximately 1 GPa to investigate pressure-induced structural changes. Previous reports revealed that sql-1-Co-NCS exhibits multiple phases thanks to its ability to switch between closed (nonporous) and several open (porous) phases in the presence of various gases, vapors, and liquids. Networks of such properties are of topical interest because they can offer high working capacity and improved recyclability for gas adsorption. The monoclinic crystal structure of sql-1-Co-NCS·4OX at 100 K was previously reported to show an increase in interlayer separation of more than 100% compared to the corresponding closed phase, sql-1-Co-NCS, when exposed to gases or vapors under ambient conditions. Herein, a tetragonal crystal form of sql-1-Co-NCS·4OX (space group I 4/ mmm , Phase I) that exists at 0.1 MPa/303 K is reported. Exposure of Phase I to high pressure using penetrable pressure transmitting media (OX and 1:1 vol MeOH/EtOH) did not result in further separation of the sql networks. Rather, compression of the crystals and release of adsorbed OX molecules occurred. These pressure-induced changes are discussed in terms of structural voids, framework conformation, and molecular packing of the sql layers. Although Phase I retained tetragonal symmetry throughout the investigated pressure range, the interlayer voids occupied by OX molecules were significantly reduced between 0.3 and 0.5 GPa; further compression above 0.5 GPa induced structural disorder. Additionally, analysis of the electron count present in the pores of sql-1-Co-NCS confirmed the multistep evacuation of OX molecules from the crystal, and two intermediate phases, I a and I b , differing in the OX loading level, are postulated.