2,6-Pyridinedicarbonitrile: Synthesis, Properties, and Applications

A key intermediate for advanced materials in OLEDs, photocatalysis, and MOFs.

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Key Advantages

Versatile Chemical Reactivity

The two nitrile groups on the pyridine ring are highly reactive, enabling a wide range of transformations such as cyclizations, hydrolysis, and reductions, making it a valuable precursor for diverse chemical structures.

Organic Electronics Applications

Its derivatives are crucial for developing high-performance OLEDs, particularly as Thermally Activated Delayed Fluorescence (TADF) emitters due to the electronic properties conferred by the pyridine-dicarbonitrile core.

Photocatalytic Efficiency

Incorporating this structure into frameworks like CTFs or molecular aggregates enhances photocatalytic activity for key reactions such as hydrogen production and CO2 reduction.

Key Applications

Organic Light-Emitting Diodes (OLEDs)

Used in the design of efficient TADF emitters and electron-transporting materials, contributing to brighter and more energy-efficient displays and lighting.

Metal-Organic Frameworks (MOFs)

Pyridine-2,6-dicarboxylic acid derivatives serve as ligands for constructing porous MOFs with applications in gas storage, separation, and catalysis.

Photocatalysis

Incorporated into frameworks for sustainable chemical reactions, including hydrogen production, water splitting, and CO2 reduction under visible light.

Pharmaceutical Intermediates

Acts as a fundamental building block in the synthesis pathways of various pharmaceutical compounds, contributing to drug development.