Published TCIMAIL newest issue No.197
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Boronic Acid Derivative for the Synthesis of Diarylacetylenes
Acetylene-1,2-diyl bis(boronic acid pinacol ester) (1) is utilized as a building block for symmetric diaryl acetylenes.1) Some compounds with unique properties have been synthesized from 1. For instance, Therien et al. have reported the synthesis of a polymer 3 through Suzuki-Miyaura cross-coupling with 1 and a diiodonaphthalene derivative 2.2) 3 has an interesting property in that it can wrap and disperse single-walled carbon nanotubes in polar organic solvents. Additionally, He and Rivard et al. have synthesized diarylacetylenes from 1 and then obtained tetraarylbutadienes.3) The tetraarylbutadienes show blue or green emission by adjusting functional groups on the aryl moieties.
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References
- 1) Synthesis of Water-Soluble Poly(p-phenyleneethynylene) in Neat Water under Aerobic Conditions via Suzuki-Miyaura Polycondensation Using a Diborylethyne Synthon
- 2) Phase Transfer Catalysts Drive Diverse Organic Solvent Solubility of Single-Walled Carbon Nanotubes Helically Wrapped by Ionic, Semiconducting Polymers
- 3) Modular Synthesis of Diarylalkynes and Their Efficient Conversion into Luminescent Tetraarylbutadienes