We present herein a host-guest supramolecular system by which we were able to obtain precise control of the stereospecificity of a new and unusual adiabatic photoisomerization reaction capable of restoring reversibly the original configuration. The host-guest system is composed of (a) a naphthalene ring linked centrosymmetrically-via sp(2) hybridized oxygen atoms-with methoxytriethyleneglycol chains (1) and (b) a nanotubular cage formed by four self-assembled face-to-face beta-cyclodextrins threaded onto the long "axle" of 1. The compound 1 can exist in distinct cis,cis, cis,trans, and trans,trans conformations that are spectrally distinguishable (see Scheme (1)). Spectroscopic and kinetic manifestations of the torsional isomerization of 1 in the lowest excited singlet state both in solution and within the tubular cage were investigated. The results provide clear evidence that the compact cavity completely blocks the photoisomerization pathway manifested in common solution (cis,cis* -> cis,trans*), allowing observation of stereospecific, volume-conserving turning of the naphthalene ring about the two "quasidouble" bonds C(Naph)-O by phi approximate to 180 degrees (cis,cis* -> trans,trans*). The photoisomerization is purely adiabatic, and the encaged molecule restores its original configuration by generating torque thermally, when relaxing to the ground state.