Results 171 to 180 of about 52,437 (280)

The Chemistry of Subphthalocyanines: Synthetic Strategies for their Axial, Peripheral, and Remote Postfunctionalization

open access: yesChemistryEurope, EarlyView.
From axial and peripheral reactivity to remote derivatization, the chemical versatility of subphthalocyanines (SubPcs) renders them ideal scaffolds for the design of advanced functional materials. This review assembles the synthetic toolbox, key reaction conditions, and future challenges in SubPc functionalization, guiding the development of next ...
Marta Gómez‐Gómez   +4 more
wiley   +1 more source

Scedosporium-induced keratitis: insights from a case study. [PDF]

open access: yesJ Ophthalmic Inflamm Infect
Fathima L   +3 more
europepmc   +1 more source

Bis(phenolate) N‐Heterocyclic Carbene [OCO] Pincer Ligands: A Unique Family for the Stabilization of Transition Metal Centers and Main Group Elements

open access: yesChemistryEurope, EarlyView.
This review highlights the coordination chemistry of NHC bis‐phenolate ligands with metal centers, emphasizing structural features, redox and optical properties, and catalytic applications. Key roles in polymerization, nitrogen reduction catalysis, and small molecule activation are discussed, showcasing the versatility and potential of [OCO]M complexes
Johanna Frey   +3 more
wiley   +1 more source

Unlocking Biomolecule Modification with Light‐Promoted Photocatalyst‐Free Approaches: Current Tools, Challenges, and Perspectives

open access: yesChemistryEurope, EarlyView.
This Perspective focuses on photocatalyst‐free, photoinduced modifications of biomolecules, emphasizing transformations mediated by electron donor–acceptor complexes. Mechanistic aspects, current limitations, and future opportunities are discussed, providing insight into the field of bioconjugation.
Milene Hornink   +3 more
wiley   +1 more source

Shedding Light on Synthetic Autocatalysis: From Conventional Closed‐Shell Chemistries to Overlooked Open‐Shell Occurrences

open access: yesChemistry – A European Journal, EarlyView.
Why add another catalyst when the product itself holds the power to catalyze its own formation? Autocatalysis in synthetic chemistry enhances reaction efficiency and uncovers novel catalytic behavior across both closed‐shell and open‐shell systems, expanding reactivity and enabling innovative design strategies.
Jaspreet Kaur, Joshua P. Barham
wiley   +1 more source

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