In this contribution we propose an alternative catalytic system based on MOF derivatives and small pore zeolites for the selective conversion of CO 2 into light olefins, using the lowest metal loadings and highest GHSV reported in literature. The catalyst synthesis involves deriving InÀ Zr oxides from MOFs containing these metals in their structure, i. e. (Zr)UiO-67-bipy-In, via direct calcination in the presence of the zeolite, avoiding co-precipitation, washing and mixing steps. This effectively creates a truly bifunctional InÀ Zr zeolite catalyst, opposed to physical mixtures of two catalysts using different precursors. The good dispersion and low loadings of the MOF-derived InÀ Zr oxide supplemented with the strong acidity of chabazitetype zeolites allows to couple the activation of CO 2 with CÀ C coupling, obtaining space time yields of 0.1 mol of CO 2 converted to light olefins per gram of In per hour at 375°C, under the GHSV conditions employed.