With an aim to combine the catalytic properties of Pd nanoparticles (NPs) with the excellent characteristics of porous layered double hydroxides (LDH), in the present study, four different catalysts (Pd/Fe 3 O 4 -CoTiMgAlLDH, Pd/Fe 3 O 4 -CoTiMgLDH, Pd/Fe 3 O 4 -CoTiAlLDH and Pd/Fe 3 O 4 -CoTiLDH) were synthesized by supporting Pd NPs onto four different Fe 3 O 4 -LDH supports, which were synthesized by varying the metals in LDH. The catalytic activity of these catalysts was studied for Suzuki coupling and reductive degradation of dyes. Pd/Fe 3 O 4 -CoTiMgLDH outperformed the other catalysts in both reactions. The synthesized catalysts were examined via different characterization techniques like X-ray diffraction (XRD), Brunauer-Emmett-Teller analysis (BET), X-ray photoelectron spectroscopy (XPS), thermogravimetric analysis (TGA), high resolution transmission electron microscopy (HR-TEM), field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray (EDX), energy dispersive X-ray mapping (SEM-EDX mapping), inductively coupled plasma atomic emission spectroscopy (ICP-AES) and vibrating sample magnetometry (VSM).On the basis of results obtained from XPS and the experimental data, Fe 3 O 4 -CoTiMgLDH was found to be the support of choice as it not only stabilized the Pd 0 NPs but also increased the electron density on the anchored Pd 0 species, which enhanced the catalytic activity of Pd/Fe 3 O 4 -CoTiMgLDH for studied organic transformations.