Neutral Diboron Analogues of Archetypal Aromatic Species by Spontaneous Cycloaddition
Please always quote using this URN: urn:nbn:de:bvb:20-opus-142500
- Among the numerous routes organic chemists have developed to synthesize benzene derivatives and heteroaro- matic compounds, transition-metal-catalyzed cycloaddition reactions are the most elegant. In contrast, cycloaddition reactions of heavier alkene and alkyne analogues, though limited in scope, proceed uncatalyzed. In this work we present the first spontaneous cycloaddition reactions of lighter alkene and alkyne analogues. Selective addition of unactivated alkynes to boron–boron multiple bonds under ambient con- ditions yielded diborocarbonAmong the numerous routes organic chemists have developed to synthesize benzene derivatives and heteroaro- matic compounds, transition-metal-catalyzed cycloaddition reactions are the most elegant. In contrast, cycloaddition reactions of heavier alkene and alkyne analogues, though limited in scope, proceed uncatalyzed. In this work we present the first spontaneous cycloaddition reactions of lighter alkene and alkyne analogues. Selective addition of unactivated alkynes to boron–boron multiple bonds under ambient con- ditions yielded diborocarbon equivalents of simple aromatic hydrocarbons, including the first neutral 6p-aromatic dibora- benzene compound, a 2 p-aromatic triplet biradical 1,3-dibor- ete, and a phosphine-stabilized 2 p-homoaromatic 1,3-dihydro- 1,3-diborete. DFT calculations suggest that all three com- pounds are aromatic and show frontier molecular orbitals matching those of the related aromatic hydrocarbons, C6H6 and C4H42+, and homoaromatic C4H5+.…
Author: | Merle Arrowsmith, Julian Böhnke, Holger BraunschweigORCiD, Mehmet Celik, Christina Claes, William Ewing, Ivo Krummenacher, Katharina Lubitz, Christoph Schneider |
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URN: | urn:nbn:de:bvb:20-opus-142500 |
Document Type: | Preprint |
Faculties: | Fakultät für Chemie und Pharmazie / Institut für Anorganische Chemie |
Language: | English |
Year of Completion: | 2016 |
Pagenumber: | 4 |
Source: | Angewandte Chemie, International Edition, Volume 55, Issue 37, 11271–11275, doi:10.1002/anie.201602384 |
DOI: | https://doi.org/10.1002/anie.201602384 |
Dewey Decimal Classification: | 5 Naturwissenschaften und Mathematik / 54 Chemie / 546 Anorganische Chemie |
GND Keyword: | Diborane; Cycloaddition |
Tag: | Aromaticity; Biradicals; Boron; Cycloaddition; Multiple bonds |
Release Date: | 2017/01/13 |
EU-Project number / Contract (GA) number: | 669054 |
OpenAIRE: | OpenAIRE |
Licence (German): | Deutsches Urheberrecht |