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Extreme oxatriquinanes and a record C-O bond length.

Nature chemistry (2012-11-24)
Gorkem Gunbas, Nema Hafezi, William L Sheppard, Marilyn M Olmstead, Irini V Stoyanova, Fook S Tham, Matthew P Meyer, Mark Mascal
RESUMEN

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 ∼1.43 Å in length, but oxatriquinane has been found to have C-O bond lengths of 1.54 Å. 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 Å. Chemical synthesis and an X-ray crystallographic study of these compounds validated the results of the modelling work and, finally, an extraordinary 1.622 Å C-O bond was observed in 1,4,7-tri-tert-butyloxatriquinane.

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Dietiléter, anhydrous, ACS reagent, ≥99.0%, contains BHT as inhibitor
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Dietiléter, suitable for HPLC, ≥99.9%, inhibitor-free
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Dietiléter, ACS reagent, anhydrous, ≥99.0%, contains BHT as inhibitor
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Dietiléter
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Dietiléter, reagent grade, ≥98%, contains ≤2% ethanol and ≤10ppm BHT as inhibitor
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Dietiléter, ACS reagent, ≥98.0%, contains ≤2% ethanol and ≤10ppm BHT as inhibitor
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Dietiléter, analytical standard