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Visible light-driven photocatalytic thiol-ene/yne reactions using anisotropic 1D BiS nanorods: a green synthetic approach

Nanoscale, ISSN: 2040-3372, Vol: 15, Issue: 35, Page: 14551-14563
2023
  • 4
    Citations
  • 0
    Usage
  • 3
    Captures
  • 1
    Mentions
  • 217
    Social Media
Metric Options:   Counts1 Year3 Year

Metrics Details

  • Citations
    4
  • Captures
    3
  • Mentions
    1
    • News Mentions
      1
      • News
        1
  • Social Media
    217
    • Shares, Likes & Comments
      217
      • Facebook
        217

Most Recent News

Indian Institute of Technology (IIT) Patna Reports Findings in Nanorods (Visible light-driven photocatalytic thiol-ene/yne reactions using anisotropic 1D Bi2S3 nanorods: a green synthetic approach)

2023 SEP 06 (NewsRx) -- By a News Reporter-Staff News Editor at Daily India Report -- New research on Nanotechnology - Nanorods is the subject

Article Description

Thiol-ene/yne click reactions play a significant role in creating carbon-sulfur (C-S) bonds, and there has been a growing interest in using visible-light photoredox catalysis for their formation. In this study, anisotropic 1D BiS nanorods were prepared using a simple polyol-assisted reflux method, and they were used as catalysts for the thiol-ene/yne click reactions under visible light irradiation. The developed protocol is highly compatible and tolerant to various substrates with excellent product yields. Also, thiol-ene and -yne reactions achieved maximum TONs of 93 and 95, respectively. Detailed mechanistic studies were conducted and supported by NMR studies, radical trapping utilizing TEMPO, and ESI-MS product analysis. The ability of BiS nanorods to catalyze thiol-ene/yne reactions is primarily due to the creation of photoexcited holes, which aid in the formation of thiyl radicals. This method can be scaled up to the gram-scale synthesis of benzyl styryl sulfide with an excellent chemical yield of 90%. The 1D BiS nanorods also demonstrated structural and morphological stability throughout five reaction cycles while maintaining a favorable photocatalytic activity. The developed methodology had the advantages of broad substrate scope, mild reaction conditions, scaled-up synthesis, and nonrequirement of free radical initiators.

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