Intramolecular Halogen Bonds Assist in Activating Carbonyl Groups for the Catalytic Synthesis of Bis(indolyl)methanes
Ortho-carboxyl substitution increases the acidity of hypervalent diaryliodonium salts and makes them useful catalysts in the synthesis of bis(indolyl)methanes under mild conditions, with yields up to 98%. The halogen bond-assisted hydrogen bonding was demonstrated by crystal structure analysis. The interaction distance of 2.619 Å between I<sup>(III)</sup> and the carboxyl O atom indicates either a long covalent or a very short halogen bond; analysis of the electron density shows the latter description is appropriate.
Authors
- Ulli Englert (ORCID: https://orcid.org/0000-0002-2623-0061)
- Yingying Hou (ORCID: https://orcid.org/0009-0001-0561-5835)
- Ruimin Wang (ORCID: https://orcid.org/0000-0002-0697-2893)
- Limin Wang (ORCID: https://orcid.org/0000-0002-4025-5361)
- Lin Zhu (ORCID: https://orcid.org/0000-0002-9217-159X)
- Taiyou Liu
Institutions
- East China University of Science and Technology (CN)
- Shanxi University (CN)
- RWTH Aachen University (DE)
Publication Details
- Journal
- Chemistry - An Asian Journal
- Published
- 2025-03-14
- DOI
- https://doi.org/10.1002/asia.202401545
- Citations
- 4
- Primary Topic
- Synthesis of Indole Derivatives
- Type
- article
- Field-Weighted Citation Impact
- 3.74