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Protonation of typical unstrained amides and lactams is heavily favored at oxygen. In contrast, protonation of the highly distorted lactam 1-azabicyclo[2.2.2]octan-2-one is heavily favored at nitrogen. What structures occupy "crossover boundaries" where N- and O-protonation are nearly equienergetic? Density function theory calculations at the B3LYP/6-31G* level, as well as QCISD(T)/6-31G* calculations, predict that 1-azabicyclo[3.3.1]nonan-2-one favors N-protonation at nitrogen only very slightly (

2,8-Dioxabicyclo[5.1.0]octa-3,5-diene ("2,3-epoxyoxepin") has been postulated as an intermediate in ring-opening metabolism of benzene. Density functional theory (B3LYP/6-31G*) is employed to study the activation and reaction energies for ring-opening isomerization of 2,3-epoxyoxepin, its 4,5-benzo derivative, and its 3,6-hexamethylene derivative. The results are compared with published experimental data. The markedly different fates of these three molecules suggest a means for testing the postulated metabolic pathway.

Three lactams having, respectively, ~20, ~10, and 0 kcal/mol of resonance energy have been subjected to electrospray ionization mass spectrometry (ESI/MS) as well as to attempted reaction with dimethyldioxirane (DMDO). The ESI/MS for all three lactams are consistent with fragmentation from the N-protonated, rather than the O-protonated tautomer. Each exhibits a unique fragmentation pathway. DFT calculations are employed to provide insights concerning these pathways. N-Ethyl-2-pyrrolidinone and 1-azabicyclo[3.3.1]nonan-2-one, the full- and half-resonance lactams, are unreactive with DMDO. The "Kirby lactam" (3,5,7-trimethyl-1-azaadamantan-2-one) has zero resonance energy and reacts rapidly with DMDO to generate a mixture of reaction products. The structure assigned to one of these is the 2,2-dihydroxy-N-oxide, thought to be stabilized by intramolecular hydrogen bonding and buttressing by the methyl substituents. A reasonable pathway to this derivative might involve formation of an extremely labile N-oxide, in a purely formal sense, an example of the hitherto-unknown amide N-oxides, followed by hydration with traces of moisture.

The core ionization energies of three strained lactams have been measured and compared with those of model lactams, amides, amines, and ketones. In general, the high values for N1s and the low values for O1s in planar amide (lactam) linkages compared to those in model amines and ketones are consistent with traditional resonance arguments. The N1s and O1s data for the distorted lactams 1,3-di-tert-butylaziridinone and 1-azabicyclo-[3.3.1]nonan-2-one are consistent with a reduced positive charge on nitrogen and a reduced negative charge on oxygen in accord with the classical resonance viewpoint

La base de Troger est une amine dont la dissymetrie est due uniquement a la geometrie pyramidale de l'azote. Elle est etudiee d'apres les spectres UV et RMN du proton

Ab initio molecular orbital calculations, employing the STO-3G basis set, have been used to calculate proton affinities of substituted benzaldehydes and 2-phenylpropenes (..cap alpha..-methylstyrenes). The results are correlated with (an updated compendium of) Brown-Okamoto sigma/sup +/ values as well as with the Taft dual-substituent-parameters (DSP) equation. Comparisons are made with correlations of experimental gas-phase data. Comparisons of correlations of calculational and experimental data are made for benzenium and benzyl cations.