An azobenzene-containing, zirconium based metal organic framework ((MOF)-M-Azo), upon irradiation with ultraviolet (UV) light at 365 +/- 10 nm, underwent trans-to-cis isomerization of its azobenzene pendants to furnish the cis-isomer content of 21% ((MOF21%)-M-Azo) in 30 min at the photostationary state and underwent backward isomerization into (MOF1%)-M-Azo upon either irradiation with visible light (420-480 nm) or heating. When the cis-isomer content increased, the diffusion rate and amount of CO2 adsorbed into the nanochannels of (MOF)-M-Azo decreased considerably. When erythrosine B, a polarity-probing guest, was used, it showed a red shift upon exposure of (MOF20%)-M-Azo superset of EB to visible light, indicating that the interior environment of (MOF)-M-Azo turns less polar as the trans-isomer content becomes higher. In sharp contrast, the adsorption profiles of (MOF15%)-M-Azo and (MOF1%)-M-Azo for Ar having an analogous kinetic diameter to CO2 but no quadrupole moment and a smaller polarizability were virtually identical to one another. Therefore, it is likely that CO2 experiences a dominant effect of a polar effect rather than a steric effect in the crystalline nanochannels.