Abstract In the energy landscape of coordination‐driven self‐assembly processes, the isolation of kinetically formed supramolecular cages has long been identified as a challenging task. This study reports a reliable strategy for the selective isolation of kinetically or thermodynamically preferred stable coordination cages, whose formation depends on the degree of steric protection offered by the exterior…
ChemistryEurope Template
Write in a clean editor, then format for ChemistryEurope in one click — DocuGuru applies the official Wiley template with author–year references and exports a submission-ready PDF plus the editable LaTeX source. Free to start.
About the ChemistryEurope format
ChemistryEurope is a peer-reviewed journal published by Wiley, covering Catalytic C–H Functionalization Methods, Organoboron and organosilicon chemistry, Radical Photochemical Reactions.
| Publisher | Wiley |
|---|---|
| Reference style | Author–year (Chicago) Author–year — (Smith, 2023) in the text Smith, Ada, Ben Jones, and Cara Lee. 2023. "A Representative Article Title." ChemistryEurope 12 (3): 45–58.
Formats any DOI in ChemistryEurope style. No sign-up. |
| Publishes research in | Catalytic C–H Functionalization Methods Organoboron and organosilicon chemistry Radical Photochemical Reactions Synthesis and Properties of Aromatic Compounds Synthesis and characterization of novel inorganic/organometallic compounds |
| ISSN | 2751-4765 |
| Citation impact (2-yr) | 1.09 |
| h-index | 12 |
| i10-index | 18 |
| Total citations | 677 |
| Open access | Yes |
| Top institutions publishing here | Centre National de la Recherche Scientifique |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Papers published in ChemistryEurope per year
Citation impact of ChemistryEurope by publication year
Citations each year’s papers have accumulated so far — the most recent years are still building up.
Most-cited papers in ChemistryEurope
The enantioselective α-functionalisation of glycine Schiff base aryl esters through isothiourea catalysis is successfully demonstrated for 1,6-additions to para-quinone methides (21 examples, up to 95:5 dr and 96:4 er) and 1,4-additions to methylene substituted dicarbonyl or disulfonyl Michael acceptors (17 examples, up to 98:2 er). This nucleophilic organocatalysis approach gives access to a range of…
Abstract The optical and chiroptical properties of an aza‐HBC‐ oct ‐[5]helicene have been studied and also modulated by means of protonation or oxidation. In both cases, the generated species shows a new absorption band in the NIR region that is not present in the neutral species. This result enables this N‐doped nanographene to act both…
Abstract The emergence of thiol‐mediated uptake (TMU) as a powerful strategy to penetrate cells calls for the development of practical small‐molecule TMU tools for traceless delivery. Toward this goal, esters are explored here as bioreversible linkers between dynamic covalent cascade exchangers accounting for TMU and the protein of interest (POI). The method relies on α…
Enantioselective catalysis is one of the most prominent strategies in organic synthesis to access chiral bioactive compounds and advanced organic materials. Particularly, the development of chiral ligands has significantly advanced the efficiency and selectivity of transition metal‐catalyzed enantioselective transformations. Over recent decades, numerous chiral ligand classes with distinct geometrical and electronic properties have been established.…