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Preparation, characterization, and catalytic properties of bimetallic coordination polymer constructed from 2‐aminoterephthalic acid as linker, zinc cations as node, and cis‐dioxo molybdenum units as catalytic active sites are reported via two pathways. Molybdenum centers were placed in N,O positions created by condensation reaction of 2‐aminoterephthalic acid with salicylaldehyde while zinc cations coordinated via carboxylic acid groups of linker to achieve infinite chains of metalo‐ligand. The obtained coordination polymer was fully characterized and its catalytic properties in the epoxidation of olefins with tert‐butyl hydroperoxide (TBHP) described. In comparison with previously reported heterogenized molybdenum catalysts, this new coordination polymer exhibited good conversion as well as high selectivity in the epoxidation of olefins. The catalyst is stable under ambient conditions and could be reused as active catalyst for at least five times.

Nitroarene reduction has played a crucial role in the environment remediation and public health. However, few research studies have been undertaken regarding the use of infinite coordination polymer-based catalysts in this process. Herein, we are looking for a way to catalyze the reduction of nitroarenes using a new and well-designed coordination polymer-based palladium catalyst. The Co-BDC-NH 2 coordination polymer was prepared through a co-precipitation reaction between 2-amino-1,4-benzenedicarboxylic acid as a linker and the cobalt cation as a node. Functionalization of the prepared Co-BDC-NH 2 with 2-pyridinecarboxaldehyde and subsequent metallation with a Pd cation led to the formation of the final catalyst, i.e., Co-BDC-NH 2 -py-Pd. It has been specified that palladium species substantially contribute to the reduction of nitroarenes in the presence of hydrazine hydrate (N 2 H 4 •H 2 O). The highest conversion (100%) of nitroarenes to the corresponding amines was achieved under relatively mild conditions. This heterogeneous catalyst was able to catalyze the reduction of nitroarenes to desired products without changing other substituents. The reusability and stability of the catalyst were confirmed through four consecutive reduction tests without a major decrease in catalytic activity.