Aryl diazonium electrografting is a versatile methodology for the functionalization of electrode surfaces, yet its usage has been hampered by both the short lifespan of aryl diazonium cations in aqueous solution and the harsh conditions required to generate them . This can make accessing complicated aryl diazonium cations and derivatized surfaces thereof difficult. The usage of triazabutadienes has the potential to address many of these issues as triazabutadienes are stable enough to endure multiple-step chemical syntheses and can persist for several hours in aqueous solution, yet upon UV exposure rapidly release aryl diazonium cations under mild conditions (i.e., 0 °C, pH 7 aqueous solution). Herein is described the synthesis and utilization of a versatile, highly water-soluble triazabutadiene scaffold which can be used to access complicated aryl diazonium cations (via photochemical decaging with a commercially available 365 nm UV irradiation source), which themselves can be used to directly derivatize electrode surfaces with desired organic moieties.
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http://dx.doi.org/10.1021/acs.langmuir.4c04848 | DOI Listing |
Langmuir
March 2025
Department of Chemistry, University of York, Heslington, York YO10 5DD, U.K.
Aryl diazonium electrografting is a versatile methodology for the functionalization of electrode surfaces, yet its usage has been hampered by both the short lifespan of aryl diazonium cations in aqueous solution and the harsh conditions required to generate them . This can make accessing complicated aryl diazonium cations and derivatized surfaces thereof difficult. The usage of triazabutadienes has the potential to address many of these issues as triazabutadienes are stable enough to endure multiple-step chemical syntheses and can persist for several hours in aqueous solution, yet upon UV exposure rapidly release aryl diazonium cations under mild conditions (i.
View Article and Find Full Text PDFOrg Lett
November 2024
School of Chemistry, University of Hyderabad, Gachibowli 500046, Telangana, India.
Allyl amines are vital components in various biologically important molecules and play a significant role in their function. Presently, most methods are geared toward the preparation of di- and trisubstituted allyl amines, leaving a gap for the development of more versatile approaches. We herein describe an approach to yield tetrasubstituted allyl amines through palladium (Pd)-catalyzed regioselective dicarbofunctionalization of masked N-phthalimide-protected propargyl amines.
View Article and Find Full Text PDFACS Omega
September 2024
Analytical Chemistry and Electrochemistry Lab (LR99ES15), Department of Chemistry, Faculty of Sciences, University of Tunis El Manar, Tunis 2092, Tunisia.
Two-dimensional (2D) nanomaterials are useful for building gas sensors owing to their desirable electronic and optical properties. However, they usually suffer from selectivity, because they cannot discriminate between gas molecules. Functionalization with organic molecules can be used to tailor their surfaces to recognize a specific family of compounds.
View Article and Find Full Text PDFR Soc Open Sci
September 2024
Department of Chemistry and Biochemistry, University of Southern Indiana, Evansville, IN 47712, USA.
Sci Rep
August 2024
Chemistry Department, Faculty of Science, Mansoura University, Mansoura, 35516, Egypt.
In this research, we reported the synthesis of effective sulphonated sugarcane bagasse (SCB@SA) biosorbent based on agriculture waste materials via a simple diazotization strategy for the removal of methylene blue (MB) and Bismarck Brown R(BB) dyes from waste water samples. First, the sugarcane bagasse (SCB) waste was collected, grinded, and sieved to obtain the desired size. Secondly, the SCB powder is modified with sulfanilinic acid (SA) via the formation of its diazonium salt to introduce sulfonic groups on the SCB surface.
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