Journal of Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 115900 - 115900
Published: Dec. 1, 2024
Language: Английский
Journal of Catalysis, Journal Year: 2024, Volume and Issue: unknown, P. 115900 - 115900
Published: Dec. 1, 2024
Language: Английский
ACS Catalysis, Journal Year: 2025, Volume and Issue: unknown, P. 4665 - 4680
Published: March 5, 2025
Transition metal catalysis is an indispensable tool for organic synthesis that has been harnessed, modulated, and perfected many decades by careful selection of centers ligands, giving rise to synthetic methods with unparalleled efficiency chemoselectivity. Recent developments have demonstrated how light irradiation can also be recruited as a powerful dramatically alter the outcome catalytic reactions, providing access innovative pathways remarkable potential. In this context, adoption photochemical conditions mainstream strategy drive reactions unveiled exciting opportunities exploit rich excited-state framework transition metals applications. This Perspective examines advances in application complexes standalone photocatalysts, exploiting innate reactivity their excited states beyond common use photoredox catalysts. An account relevant examples dissected provide discussion on electronic reorganization, orbitals involved, associated different types states. analysis aims practitioners fundamental principles guiding strategies understand, design, apply light-activation homogeneous synthesis.
Language: Английский
Citations
2Accounts of Chemical Research, Journal Year: 2024, Volume and Issue: 57(15), P. 2194 - 2206
Published: July 23, 2024
ConspectusLewis π acids, particularly high-valent transition metals with vacant orbitals, can coordinate unsaturated compounds such as alkynes and alkenes by means of π-bonding. The coordination enhances the electrophilicity bound compounds, thereby facilitating reactions─such nucleophilic addition─that take place at ligated carbon-carbon multiple bonds. This activation phenomenon occurs ligand rather than metal atom, it has been extensively utilized in development catalytic methods. In addition to alkenes, aromatic featuring a phenyl ring be activated an electrophilic transition-metal unit (e.g., Cr(CO)
Language: Английский
Citations
9Chem Catalysis, Journal Year: 2024, Volume and Issue: 4(7), P. 101027 - 101027
Published: June 12, 2024
Language: Английский
Citations
6Environmental Science & Technology, Journal Year: 2025, Volume and Issue: unknown
Published: Jan. 13, 2025
Liquid crystal monomers (LCMs) of different chemical structures were widely detected in various environmental matrices. However, their health risk evaluation is lacking. Herein, three representative LCMs selected from 74 LCM candidates upon literature review and acute cytotoxicity evaluation, then Mus musculus exposed to the for 42 days at doses 0.5 50 μg/kg/d investigate hepatotoxicity mechanisms. Phenotypic histopathological results showed that (DTMDPB, MeO3bcH, 5OCB) induced hepatomegaly, only 5OCB fatty liver. DTMDPB MeO3bcH decreased total cholesterol (TCHO) triglyceride (TG) content, whereas increased TCHO, TG, alanine aminotransferase levels. Transcriptome molecular docking analysis revealed by agonizing farnesoid X receptor, resulting disruption unsaturated acid biosynthesis, ascorbic antioxidant pathways, circadian clock homeostasis. promoted inflammation altered acid, primary bile rhythm antagonizing aryl hydrocarbon receptor. antagonized peroxisome proliferator-activated receptors, leading liver caused steroid, cholesterol, terpenoid backbone biosynthesis pathways. This study provides references understanding with selection priority control LCMs.
Language: Английский
Citations
0Journal of the American Chemical Society, Journal Year: 2025, Volume and Issue: unknown
Published: March 6, 2025
Nucleophilic aromatic substitution (SNAr) reactions are widely employed in organic synthesis yet typically require the use of electron-deficient arenes for efficient reactivity. Herein, we report a photocatalytic protocol formal SNAr electron-rich 4-halophenols with azole nucleophiles under mild, redox-neutral conditions. The transformation proceeds via two-stage mechanism consisting initial halophenol oligomerization to produce key oligo(phenylene oxide) intermediate and its subsequent breakdown through enabled by photoredox-catalyzed arene umpolung. Reaction monitoring, stoichiometric control experiments, luminescence quenching data implicate phenoxyl radicals Brønsted acid-activated as reactive species stages, respectively. synthetic utility this method is demonstrated across 17 (pseudo)halophenols bearing variety leaving groups (F, Cl, Br, OMs, OTs) 22 examples.
Language: Английский
Citations
0Industrial & Engineering Chemistry Research, Journal Year: 2025, Volume and Issue: unknown
Published: April 3, 2025
Language: Английский
Citations
0Chemical Engineering Journal, Journal Year: 2025, Volume and Issue: unknown, P. 162338 - 162338
Published: April 1, 2025
Language: Английский
Citations
0Organic Letters, Journal Year: 2024, Volume and Issue: unknown
Published: Oct. 30, 2024
A visible-light induced intermolecular hydroamination of alkenes with azoles is reported, delivering pharmaceutically valuable N-benzyl in high yields excellent Markovnikov selectivity. Mechanistic studies suggest that the process initiated by energy transfer excited photocatalyst alkenes, followed single electron reduction, protonation, and subsequent oxidation to afford key alkyl carbocation intermediate. This protocol exhibits advantages broad functional group tolerance, atom economy, efficiency, mild reaction conditions.
Language: Английский
Citations
1Chem Catalysis, Journal Year: 2024, Volume and Issue: 4(7), P. 101062 - 101062
Published: July 1, 2024
Language: Английский
Citations
0Molecules, Journal Year: 2024, Volume and Issue: 29(17), P. 4077 - 4077
Published: Aug. 28, 2024
Recent years have seen increasing interest in uranyl(VI) photocatalysis. In this study, uranyl complexes were successfully synthesized from ligands
Language: Английский
Citations
0