Neue wege zum elassovalensystem

Askani, R.; Pelech, B.

doi:10.1016/s0040-4039(00)92794-1

Cited by 7 publications

(2 citation statements)

References 12 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…We have previously published experimental details for the conversion of dibromide 21 to the monobromides 4a ⇋ 4a ‘ 10c first reported by Askani 9a. Askani also prepared solutions of the mononitriles 4b ⇋ 4b ‘ from these monobromides 9c. However, the mononitriles were not purified or isolated and were only characterized by 60 MHz proton NMR spectra.…”

Section: Resultsmentioning

confidence: 99%

“…Many substituted semibullvalenes undergo degenerate Cope rearrangements via transition structures, which may exhibit C 2 , C S , or C 2v symmetry. , There are also semibullvalenes that are completely locked in one of the two possible valence tautomeric structures, e.g., benzosemibullvalenes. , Between these limiting cases, a considerable number of semibullvalenes exist whose Cope equilibria are more or less skewed by virtue of appropriately placed substituents (including monoannelation), ,− deuterium atoms, or heteroatoms 14 . These nondegenerate semibullvalenes merit renewed interest for several reasons.…”

Section: Introductionmentioning

confidence: 99%

See 1 more Smart Citation

Lifting of the Degeneracy in Semibullvalenes by Remote and Direct Substituents: A Quantitative Study Using Variable-Temperature Carbon-13 NMR Spectroscopy

Heubes¹,

Dietz²,

Quast³

et al. 2001

J. Org. Chem.

View full text Add to dashboard Cite

A series of six 1,5-(ethylmethyl)semibullvalenes (1a <==> 1a', 2 <==> 2', 3 <==>3') and two 4(2)-substituted semibullvalenes (4 <==> 4'), each undergoing Cope equilibria between nondegenerate valence tautomers, was investigated by carbon-13 NMR spectroscopy at a range of temperatures in several different solvents. Gompper's treatment of substituent perturbation was extended, specifically accounting for the effects of the substituents on chemical shifts, to allow the determination of the thermodynamic parameters for these skewed equilibria. These new treatments were used to determine the population difference (f - f ') between the valence tautomers and the perturbation thermodynamic quantities DeltaH(P), DeltaS(P), and DeltaG(P). The slow-exchange limit was reached for the parent 1,5-(ethylmethyl)semibullvalenes 3a<==> 3a' from which it was established that the preferred valence tautomer is 3a with the ethyl group on the cyclopropane ring. Despite considerable effort, the slow-exchange limit could not be reached in any of our other remotely substituted semibullvalenes. Provided that the ethyl group always prefers the cyclopropyl position as in 3a, the 1-ethyl-5-methylsemibullvalenes 1a, 2, and 3 are more stable by DeltaH(P) = 0.7-1.7 kJ mol(-1) than their valence tautomers 1a', 2', and 3'. In the directly substituted semibullvalenes (4 left harpoon ovet right harpoon 4'), the preferred valence tautomers 4a and 4b have the bromine atom or the nitrile group on the vinyl position (C(4)) rather than on the cyclopropane ring (C(2)) and are more stable than 4a' and 4b' by DeltaH(P) = 4.8 and 7.0 kJ mol(-1), respectively.

show abstract

Section: Resultsmentioning

confidence: 99%