Molecular pyramids - from tetrahedranes to [6]pyramidanes.

Autor: Sun Q; Organisch-Chemisches Institut, Universität Münster, Münster, Germany., Mück-Lichtenfeld C; Organisch-Chemisches Institut, Universität Münster, Münster, Germany., Kehr G; Organisch-Chemisches Institut, Universität Münster, Münster, Germany., Erker G; Organisch-Chemisches Institut, Universität Münster, Münster, Germany. erker@uni-muenster.de.
Jazyk: angličtina
Zdroj: Nature reviews. Chemistry [Nat Rev Chem] 2023 Oct; Vol. 7 (10), pp. 732-746. Date of Electronic Publication: 2023 Aug 23.
DOI: 10.1038/s41570-023-00525-7
Abstrakt: The study of 3D architectures at a molecular scale has fascinated chemists for generations. This includes molecular pyramids with all-carbon frameworks, such as trigonal, tetragonal and pentagonal pyramidal geometries. A small number of substituted tetrahedranes and all-carbon [4]-[5]pyramidanes have been experimentally generated and studied. Although the hypothetical unsubstituted parent [3]-[6]pyramidanes have only been explored computationally, the formal replacement of carbon vertices with isolobal main group element fragments has provided a number of examples of stable hetero[m]pyramidanes, which have been isolated and amply characterized. In this Review, we highlight the synthesis and chemical properties of [3]-[6]pyramidanes and summarize the progress in the development of chemistry of pyramid-shaped molecules.
(© 2023. Springer Nature Limited.)
Databáze: MEDLINE