X‐ray diffraction measurements were carried out on nine members of the isothiocyanatobiphenyl homologous series (nBT) in their smectic E (SmE) phase, with the aim of estimating the layer thickness and deriving orthorhombic unit cell parameters for the SmE phase. The data obtained are discussed in relation to molecular reorientation motion around the short axis in that phase.

Methanol adsorption into the porous 2D bimetallic coordination network {[Ni(cyclam)]₃[W(CN)₈]₂}_n (cyclam = 1,4,8,11-tetraazacyclotetradecane) causes significant modification of its structure and magnetic properties. Fully reversible transformations between the three states of the network: anhydrous, hydrated and methanol-modified are observed with the transition to the magnetic ordered state at T_c equal to 4.9 K, 8.3 K and 11.4 K respectively. All three phases have a metamagnetic character but the methanol-modified one most easily turns to ferromagnetic and shows a hysteresis loop with coercivity field of 250 Oe. The differences in magnetic behaviour of the anhydrous and guest-induced forms of the compound are discussed in terms of changes in the structure: CN-bridge geometry and distance between the layers.