Thiacalixarenes, a subclass of "third generation" calixarenes, exhibit many interesting features such as enlarged ring size, facile chemical modification, and metal complexation due to the presence of bridging sulfur atoms. The thiacalixarene scaffold is a unique host with vast possibilities for functionalization not only at the upper and lower rim but also at the bridging sulfide groups. Modified thiacalixarenes have been used for many applications such as the detection and separation of biologically important cations, anions, and bio-analytes, mimicking molecular logic gates and devices, and synthesis of self-assembled coordination cages, multinuclear complexes, magnetic materials and luminescent materials. This review article summarizes recent developments in the derivatization methods of thiacalixarenes and their utilization in various applications.

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A hexaphenylbenzene-based receptor 3 has been synthesized that forms a fluorescent spherical aggregate in mixed aqueous media due to its aggregation-induced emission enhancement attributes. These fluorescent spherical aggregates show ratiometric response toward cyanide ions via nucleophilic addition and undergo deaggregation to form smaller nanoaggregates. In addition, the solution-coated paper strips of 3 can detect cyanide ions in the range of ∼2.6 ng/cm(2), thus, providing a simple, portable, and low-cost method for detection of cyanide ions in aqueous media. Receptor 3 also behaves as a set-reset memorized sequential logic circuit with chemical inputs of CN(-) ions and trifluoroacetic acid or H(+) (pH ≤ 3).

A highly selective fluorescent chemodosimeter based on rhodamine is synthesized which undergoes Cu(2+) driven hydrolysis in aqueous media to produce fluorescence turn-on changes with a detection limit up to the nanomolar range.