4,4’’-Diiodo-5’-(4-Iodophenyl)-1,1’:3’,1’’-Terphenyl

1,3,5-Tris(4-iodophenyl)benzene is utilized in various applications:

• Supramolecular Chemistry: It serves as a building block for creating self-assembled structures due to its halogen bonding capabilities.
• Surface Science: The compound can form two-dimensional porous networks on surfaces like graphite.
• Material Science: It is involved in the development of covalent organic frameworks through Ullmann coupling reactions.

While specific biological activities of 1,3,5-Tris(4-iodophenyl)benzene are not extensively documented, it has been noted for its role in synthesizing water-soluble fluorophores. These fluorophores exhibit selective fluorescent quenching by copper ions through a static quenching mechanism. The compound's interaction with its environment can influence its efficacy and stability.

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