The ability to rationally design and predictably construct crystalline solids has been the hallmark of crystal
engineering research over the past two decades. When building higher-order multicomponent cocrystals (i.e. crystals
containing more than two constituents), the differential and hierarchical way molecules interact and assemble in the solidstate is of pinnacle importance. To date, numerous examples of multicomponent crystals comprising organic molecules
leading to salts, cocrystals or ionic cocrystals have been reported. However, the crystal engineering of hybrid organicinorganic cocrystals with sophisticated inorganic building blocks is still poorly understood and mostly unexplored. Here,
we reveal the first efficient mechanochemical synthesis of higher-order hybrid organic-inorganic cocrystals based on the
structurally versatile – yet largely unexplored – cyclodiphos(V/V)azane heterosynthon building block. The novel hybrid
ternary and quaternary multicomponent cocrystals herein reported are held together by synergistic intermolecular
interactions (e.g., hydrogen- and halogen-bonding, Se-π and ion-dipole interactions). Notably, higher-order ternary and
quaternary cocrystals can be readily obtained either via direct synthetic routes from its individual components, or via
unprecedented telescopic approaches from lower-order cocrystal sets. In addition, computational modelling has also
revealed that the formation of higher-order cocrystals is thermodynamically driven, and that bulk moduli and
compressibilities are strongly dependent on the chemical composition and intermolecular forces present in the crystals,
which offer untapped potential for optimizing material properties.