Synthesis of the NH 2 -MIL-101(Al) Metal-Organic Framework (MOF) with bis(hydrotris(pyrazolyl)borato)iron(II), [Fe(HB(pz) 3 ) 2 ], added to the reaction medium yielded [Fe(HB(pz) 3 ) 2 ]@NH 2 -MIL101(Al) encapsulation products, further denoted as S@Ms, in a course of a 'bottle-around-the-ship' assembly. [Fe(HB(pz) 3 ) 2 ] is a spin-crossover (SCO) compound with a gradual spin transition at 290-440K for the bulk material (repeated cycles), associated with a pronounced colour change from the red low spin (LS) state to the white high-spin 10 (HS) state. The identity of S@Ms, with a maximum loading of iron complex at ~11 wt% (0.16 molecules per Al 3 OL 3 moiety), was confirmed by PXRD and spectroscopic evidences. The entrapped complex, which is stable in air, and cannot be removed by vacuum drying is confined in the cages of the framework. N 2 and CO 2 gas adsorption measurements on the dry S@M composite with different iron complex loadings confirm the absence of most of the initial NH 2 -MIL-101(Al) porosity. The S@M composite material demonstrate a gradual thermally induced transition from red low-spin (LS) state to light yellow HS state, associated with the colour of the matrix, 15 chiefly over the range 300-450 K, which is close to the 290-440 K temperature range for [Fe(HB(pz) 3 ) 2 ]. The thermally induced HS form of S@M does not return to LS upon cooling to room temperature, and the metastable HS form relaxes only very slowly, which becomes noticeable only after weeks of storage. Rapid, almost complete relaxation and decrease of magnetic moment for up to ~97% of the whole sweep could be triggered by addition of n-hexane, as evidenced by change of colour and magnetic measurements. Via mechanic stress akin to action of capillary forces, the adsorbed liquid effectively amplifies the otherwise very weak 'matrix effect' by increasing the 20 effective local pressure imposed on the transiting molecules, thus favouring even further the LS state. The immersion of the dried composites into practically any typical solvents, incl. MeOH, DMSO, DMF, i PrOH, BuOH, t-BuOH, THF, ethylacetate, CH 2 Cl 2 , CHCl 3 CCl 4 , toluene, mesitylene, cyclohexane also induces a spin state change, which is evidenced by change of colour. The effect is fully reversible: the metastable HS state could be reinstated upon drying the sample at elevated temperature and subsequent cooling. The materials were thoroughly characterized by AAS, PXRD, gas sorption analysis, IR spectroscopy, magnetic measurements, and optical 25 reflectivity measurements. Thereby a novel MOF-based material with isolated SCO units is proposed, which demonstrate a salient relaxative 'solvent assisted matrix-effect' on metastable entrapped sites, potentially suitable for light-driven single-unit addressability.