Results 181 to 190 of about 11,273 (240)
This minireview highlights recent advances in catalyst development and mechanistic strategies that enable photochemical and photocatalytic reactivity under 700–1000 nm NIR light, emphasizing how long‐wavelength excitation expands opportunities in both synthetic chemistry and biology.
Santosh K. Pagire +3 more
wiley +1 more source
Multi-Halogenated Indoles as Antimicrobial and Antivirulence Agents Against Drug-Resistant Staphylococcus aureus. [PDF]
Sim M, Boya BR, Kim YG, Lee JH, Lee J.
europepmc +1 more source
A terminology for electrophile‐nucleophile interactions based on names that refer to the electrophile group/atom may offer the advantage to be descriptive, consistent, complete, systematic, clear, and, most important, invariant. Likely, a terminology that employs only the terms σ‐hole bond, π‐hole bond, and p‐hole bond may not.
Andrea Pizzi +5 more
wiley +1 more source
Surgical Approach for Sciatic Nerve Entrapment Secondary to Biopolymer Injection. [PDF]
Lancheros-Ramirez P +2 more
europepmc +1 more source
Photocatalytic cross‐coupling: A redox‐neutral photochemical method enables direct C(sp2)─C(sp2) bond formation between phenols and heteroaryl halides using an organic dye and base. Complementary radical generation allows efficient cross‐coupling in up to 91% yield. Mechanistic studies, DFT, HTE, and machine learning rationalize and predict reactivity,
Matthew C. Carson +4 more
wiley +1 more source
Synthesis and Characterization of the μ<sub>6</sub>‑F Compounds [NEt<sub>4</sub>][F(Cl<sub>2</sub>)<sub>3</sub>] and [NEt<sub>4</sub>][F(Br<sub>2</sub>)<sub>3</sub>]. [PDF]
Schmid JR +5 more
europepmc +1 more source
A novel carbon dots material (BUL‐CDs) with an initial afterglow brightness (406 cd m−2) far exceeding that of other afterglow luminescent materials was developed. Furthermore, the BUL‐CDs exhibited time‐dependent afterglow colors, excitation‐dependent afterglow colors, and thermochromic afterglow in response to triplet variables.
Yupeng Liu +13 more
wiley +1 more source
Mechanism of a Halogen Exchange Reaction in Water: Catalysis by Aqueous Media. [PDF]
Mandal I +4 more
europepmc +1 more source
Expanding the application of chlorinated anilines as molecular templates to achieve a series of solid-state [2 + 2] cycloaddition reactions. [PDF]
White GK, Unruh DK, Groeneman RH.
europepmc +1 more source

