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Click reactions with a "catch-and-release" functionality featuring both cross-linking and bond cleavage may have unique biomedical applications. However, despite the high demand, such reactions are rarely known in the toolbox of biochemists. Herein we introduce a robust click reaction of selenoalkynes that not only facilitates mild cross-linking with azides but also permits exceptionally facile cleavage of the C─Se bond in the adducts. This highly efficient ruthenium-catalyzed protocol features high chemoselectivity and regioselectivity, mild conditions, broad substrate scope, and good tolerance of functional groups and solvents. The compatibility with air and water as well as biomolecules has been demonstrated in parallel with the "catch-and-release" functionality.
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http://dx.doi.org/10.1002/anie.202513792 | DOI Listing |
J Am Chem Soc
August 2025
Department of Chemistry, The University of Texas at Austin, 105 East 24th Street, Stop A5300, Austin, Texas 78712-1224, United States.
Described here is the effect of anionic metalates─chlorocobaltate and nitratocobaltate─on the heat-driven separation of the critical element cobalt from potentially competing transition metal salts. Resins bearing the hexadentate glycolamide receptor (PS-) exhibit sorption capacities, = 1.33 mmol/g for CoCl and = 0.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Department of Chemistry and the Hong Kong Branch of Chinese National Engineering Research Centre for Tissue Restoration & Reconstruction, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong SAR, China.
Click reactions with a "catch-and-release" functionality featuring both cross-linking and bond cleavage may have unique biomedical applications. However, despite the high demand, such reactions are rarely known in the toolbox of biochemists. Herein we introduce a robust click reaction of selenoalkynes that not only facilitates mild cross-linking with azides but also permits exceptionally facile cleavage of the C─Se bond in the adducts.
View Article and Find Full Text PDFJ Am Chem Soc
July 2025
Department of Chemistry, Bogazici University, Bebek, Istanbul 34342, Türkiye.
Polymer brushes engineered to "specifically capture" and "release on demand" analytes such as dyes, proteins, and cells find biomedical applications ranging from protein immobilization to cell death. Utilizing a disulfide-linker-containing monomer as a building block enables the fabrication of a redox-responsive polymer brush platform with the "catch and release" attribute. Herein, thiol-reactive redox-responsive polymer brushes are fabricated using a pyridyl disulfide-based monomer, and their postpolymerization functionalization is demonstrated via thiol-disulfide exchange reaction with thiol-containing dyes, (bio)molecules, and cell adhesive ligands.
View Article and Find Full Text PDFPLoS One
June 2025
Department of Life and Environmental Sciences, Bournemouth University, Poole, United Kingdom.
The manipulation of species' attributes through selective breeding can produce domesticated traits including decreased stress responses (i.e., selecting for high stress resilience).
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Department of Chemistry, University of Illinois, Urbana, IL, 61820, USA.
Small molecule solutions to many contemporary societal challenges await discovery, but the artisanal and manual process via which this class of chemical matter is typically accessed limits the discovery of new functions. Automated assembly of (N-methyl iminodiacetic acid) MIDA or (tetramethyl N-methyl iminodiacetic acid) TIDA boronate building blocks via iterative C─C bond formation, an approach we call "block chemistry", alternatively enables generalized and automated preparation of many different types of small molecules in a modular fashion. But in its current form, this engine cannot also leverage nitrogen atoms as iteration handles.
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