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Photochemistry mediated by visible light is attractive as it avoids the limitations of higher energy UV light. Photo-induced copper-mediated reversible deactivation radical polymerisation (photo Cu-RDRP) typically requires both a copper catalyst and a separate photocatalyst (PC) to exploit lower energy irradiation. However, by covalently anchoring a PC to another reagent, dual functionality can be established. Herein, a simiplified approach is demonstrated using a modified commerically available dye as an initiator and PC simultaneously. A visibly fluorescent and highly absorbing dye, Hostasol Yellow, is chemically incorporated into a polymer following irradiation under six different UV and visible light wavelengths, resulting in high monomer conversion (>90%) and polymers with low dispersity (≤1.13). The wavelength-dependent behaviour of the dye was probed, reaffirming a mismatch between reactivity and absorptivity. Kinetic studies show high monomer conversions within just a few minutes, with good end-group fidelity confirmed by chain extension and matrix-assisted laser desorption/ionization time-of-flight (MALDI-ToF). The versatility of this PC initiator was extended to give a wide variety of molecular weights (2700-420 000 g mol) and different hydrophobic, hydrophilic and semi-fluorinated polyacrylates.
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http://dx.doi.org/10.1039/d5sc05171a | DOI Listing |
Chem Sci
August 2025
University of Warwick, Department of Chemistry Library Road Coventry CV4 7AL UK
Photochemistry mediated by visible light is attractive as it avoids the limitations of higher energy UV light. Photo-induced copper-mediated reversible deactivation radical polymerisation (photo Cu-RDRP) typically requires both a copper catalyst and a separate photocatalyst (PC) to exploit lower energy irradiation. However, by covalently anchoring a PC to another reagent, dual functionality can be established.
View Article and Find Full Text PDFPharmaceuticals (Basel)
December 2024
N. P. Bechtereva Institute of the Human Brain, Russian Academy of Sciences, 197022 St. Petersburg, Russia.
-succinimidyl-[F]fluorobenzoate ([F]SFB) is commonly prepared through a three-step procedure starting from [F]fluoride ion. A number of methods for the single-step radiosynthesis of [F]SFB have been introduced recently, including the radiofluorination of diaryliodonium salts and the Cu-mediated F-fluorination of pinacol aryl boronates and aryl tributyl stannanes, but they still have the drawbacks of lengthy product purification procedures. In the present work, two approaches for the direct labeling of [F]SFB from diaryliodonium (DAI) salt () and pinacol aryl boronate () are evaluated, with a major focus on developing a fast and simple SPE-based purification procedure.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Universität Göttingen, Institut für Anorganische Chemie, Tammannstrasse 4, D-37077, Göttingen, Germany.
Hydrogen bonds involving the oxygen atoms of intermediates that result from copper-mediated O activation play a key role for controlling the reactivity of Cu/O active sites in metalloenzymes and synthetic model complexes. However, structural insight into H-bonding in such transient species as well as thermodynamic information about proton transfer to or from the O-derived ligands is scarce. Here we present a detailed study of the reversible interconversion of a μ-peroxodicopper(II) complex ([1]) and its μ-hydroperoxo congener ([2]) via (de)protonation, including the isolation and structural characterization of several H-bond donor (HBD) adducts of [1] and the determination of binding constants.
View Article and Find Full Text PDFChem Sci
August 2024
Institute of Macromolecular Chemistry, Czech Academy of Sciences Heyrovského nám. 2 162 06 Prague 6 Czech Republic
Synthesis of complex polymeric architectures (CPAs) reversible-deactivation radical polymerization (RDRP) currently relies on the rather inefficient attachment of monofunctional initiation/transfer sites onto CPA precursors. This drawback seriously limits the overall functionality of the resulting (macro)initiators and, consequently, also the total number of installable polymeric chains, which represents a significant bottleneck in the design of new polymeric materials. Here, we show that the (macro)initiator functionality can be substantially amplified by using trichloroacetyl isocyanate as a highly efficient vehicle for the rapid and clean introduction of trichloroacetyl groups (TAGs) into diverse precursors.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2024
Department of Urology, Second Hospital of Dalian Medical University, Dalian, 116023, China.
Despite the initial efficacy of enzalutamide in castration-resistant prostate cancer (CRPC), inevitable resistance remains a significant challenge. Here, the synergistic induction of copper-dependent cell death (cuproptosis) in CRPC cells is reported by enzalutamide and copper ionophores (elesclomol/disulfiram). Mechanistically, enzalutamide treatment increases mitochondrial dependence in CRPC cells, rendering them susceptible to cuproptosis, as evidenced by specific reversal with the copper chelator tetrathiomolybdate.
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