In recent times, selective hydrogenation of biomass-derived 5-hydroxymethylfurfural(5-HMF) to produce novel difuranic polyol scaffold 2,5-dihydroxymethylfuran (DHMF) has attracted the interests of the many researchers due to its peculiar symmetrical structure as well as its wide application as a monomer for the preparation of cross-linked polyesters and polyurethane. Copper-based catalysts have been explored accountable for the selective catalytic hydrogenation however the hurdles are still associated with the strongly reducing H2 atmosphere and oxidizing C-O bond that makes the Cu 0 and Cu x+ surface active species unstable, limiting the rational design of highly efficient integrated catalyst systems. To address this, herein, we built catalytic systems for 5-HMF hydrogenation with stable and balanced Cu 0 and Cu x+ active surface species inside the nanocage of catechol based Porous-Organic-Polymer (POP) endowed with large surface areas, impressive stabilities, and spatial restriction inhibiting NPs aggregation.Batch reactor screening indentified that superior catalytic performance (DHMF selectivity of 98%) has been achieved with our newly designed Cu@C-POP at 150ºC temperature and 20 bar H2 pressure, which was also higher than that of other reported copper catalysts. Comprehensive characterizations understanding with H2-TPR and XPS study revealed that substantially boosted activity is induced by the presence of bulk CuOx phase and atomically dispersed Cu species incorporating isolated Cu ions, which are further confirmed through the positive binding energy shift of Cu-2p3/2 XPS spectra (~0.4eV). The Cu environment in our catalytic systems comprises predominantly square planar (well probably Jahn-Teller distorted Oh) which we gleaned from the EXAFS analysis featuring two adjacent copper atoms with the valence state in between of 0 and +2 as validated by XANES absorption edge positions. EXAFS studies further revealed a