Abstract: Organocatalyzed atom transfer radical polymerization (O-ATRP) was performed under air using core modified N-aryl phenoxazines as photoredox catalysts (PCs) to synthesize poly(methyl methacrylate) in a controlled fashion with initiator efficiency (I* = Mn,theo/Mn × 100) ranging from 84 to 99% and dispersity being ∼1.2–1.3. Reduction of the reaction vial headspace was key for enabling…
Abstract: Atom transfer radical polymerization (ATRP) is one of the most powerful methodologies for polymerization. Well‐controlled ATRP of N‐isopropylacrylamide (NIPAAm) could be obtained in organic‐water mixture solvent with conventional metal catalyst/ligand catalyst system. However, the mixture solvent is not suitable for copolymerization of NIPAAm with hydrophobic monomers. Moreover, further purification of metal was required for…
Abstract: We report a photocatalytic version of the Barbier type reaction using readily available allyl or benzyl bromides and aromatic aldehydes or ketones as starting materials to generate allylic or benzylic alcohols. The reaction proceeds at room temperature under visible light irradiation with the organic dye 3,7-di(4-biphenyl)1-naphthalene-10-phenoxazine as a photocatalyst and DIPEA as sacrificial electron…
Abstract: Photoinduced controlled radical polymerizations (CRPs) have provided a variety of approaches for the synthesis of polymers possessing targeted structures, compositions, and functionalities with the added capability for spatial and temporal control, presenting the potential for new materials development. However, the scalability and reliability of these systems can be limited as a consequence of dependence…
Abstract: N,N-Diaryl dihydrophenazines are employed as organic photoredox catalysts (PCs) for photoinduced electron/energy transfer–reversible addition–fragmentation chain transfer (PET-RAFT) polymerization. The ability of these PCs to mediate PET-RAFT is heavily dependent on the ability of the PC to access a photoexcited intramolecular charge transfer state. The use of PCs displaying intramolecular charge transfer in the excited…
Abstract: C–N cross-coupling is an important class of reactions with far-reaching impacts across chemistry, materials science, biology, and medicine. Transition metal complexes can elegantly orchestrate diverse aminations but typically require demanding reaction conditions, precious metal catalysts, or oxygen-sensitive procedures. Here, we introduce a mild nickel-catalyzed C–N cross-coupling methodology that operates at room temperature using an…
Abstract: The development and application of a novel endo furan-protected maleimide building block is reported. The endo isomer undergoes deprotection at temperatures ∼50 °C below the exo derivative. This enables a simple and powerful approach to quantitatively and selectively introduce functional maleimide groups via temperature modulation. Reference: Discekici, E. H.; St. Amant, A. H.; Nguyen,…
Abstract: A key feature of prominent transition-metal-containing photoredox catalysts (PCs) is high quantum yield access to long-lived excited states characterized by a change in spin multiplicity. For organic PCs, challenges emerge for promoting excited-state intersystem crossing (ISC), particularly when potent excited-state reductants are desired. Herein, we report a design exploiting orthogonal π-systems and an intermediate-energy…
Abstract: Through the study of structure–property relationships using a combination of experimental and computational analyses, a number of phenoxazine derivatives have been developed as visible light absorbing, organic photoredox catalysts (PCs) with excited state reduction potentials rivaling those of highly reducing transition metal PCs. Time-dependent density functional theory (TD-DFT) computational modeling of the photoexcitation of…
Herein, we demonstrate a dual organophotoredox/copper catalytic strategy toward challenging decarboxylative olefination processes proceeding in high yields and selectivities. This operationally simple method uses photoactive organic molecules and Cu(II)-complexes as catalysts to provide rapid access to a wide variety of olefins from inexpensive synthetic and biomass-derived carboxylic acids under mild light-mediated conditions. Mechanistic investigations suggest…