期刊
NATURE CHEMISTRY
卷 4, 期 12, 页码 1018-1023出版社
NATURE RESEARCH
DOI: 10.1038/NCHEM.1502
关键词
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资金
- National Science Foundation [CHE-0957798, CHE-1058483]
- Turkish Higher Education Council
- Direct For Mathematical & Physical Scien [1058483] Funding Source: National Science Foundation
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [0957798] Funding Source: National Science Foundation
- Division Of Chemistry [1058483] Funding Source: National Science Foundation
Oxatriquinanes are fused, tricyclic oxonium ions that are known to have exceptional stability compared to simple alkyl oxonium salts. C-O bonds in ethers are generally similar to 1.43 angstrom in length, but oxatriquinane has been found to have C-O bond lengths of 1.54 angstrom. A search of the Cambridge Structural Database turned up no bona fide C-O bond length exceeding this value. Computational modelling of oxatriquinane alongside other alkyl oxonium ions indicated that the electronic consequences of molecular strain were primarily responsible for the observed bond elongation. We also show that substitution of the oxatriquinane ring system with alkyl groups of increasing steric demand pushes the C-O bond to unheard of distances, culminating in a tert-butyl derivative at a predicted 1.60 angstrom. Chemical synthesis and an X-ray crystallographic study of these compounds validated the results of the modelling work and, finally, an extraordinary 1.622 angstrom C-O bond was observed in 1,4,7-tri-tert-butyloxatriquinane.
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