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π-Conjugated Materials Derived From Boron-Chalcogenophene Combination. A Brief Description of Synthetic Routes and
Ankita Dhiman1, Lingamallu Giribabu2,3, Rajiv Trivedi1,3
1Catalysis and Fine Chemicals Department, CSIR-Indian Institute of Chemical Technology, Hyderabad, Uppal Road, Tarnaka, Hyderabad,, 500007, Telangana, India.
Abstract:
Functional materials composed of Boron-chalcogenophene conjugates have emerged as promising ensemble featuring commendable optoelectronic properties. This review describes the categories, synthetic routes and optoelectronic applications of a range of boron-chalcogenophene conjugates. Conjugation and linking of different types of tri- and tetra-coordinated boron moieties with chalcogenophenes have remained an important strategy for constructing a range of functional materials. Synthetic protocols have been devised to efficiently prepare such chemically robust conjugates, often exhibiting a myriad of photophysical properties, redox capabilities and also solid-state behaviors. Tin-boron and silicon-boron exchange protocols have been efficiently adapted to access these boron-chalcogenophenes. Few other commonly used methods namely, hydroboration of alkynes as well as electrophilic borylations are also mentioned. The chemical and electronic properties of such boron-chalcogenophene conjugates are directly influenced by the strong Lewis acid character of trivalent boranes which can further alter the intra- and inter- molecular Lewis acid-base interactions. Apart from the synthetic protocols, recent advances in the application of these boron-chalcogenophene conjugates towards analyte sensing, organic electronics, molecular switches and several other aspects will be discussed in this review.

