Abstract:(2) and 1.268 (2) A respectively. The boat conformation adopted by most 1,2-diazepine rings is unperturbed by the oxide ligand which serves to weaken the N=N double bond and lowers the activation energy for ring inversion.
“…The central seven-membered diazepinthione ring (atoms C4/C5/C7-C9/N1/N2) adopts a boat conformation. The boat conformation is predominantly observed for the seven-membered ring of benzodiazepine and its derivatives, even with different double-bond positions and widely differing substituents (Walkinshaw, 1985;Torres et al, 2005). The internal torsion angles of the ring are shown in Fig.…”
Key indicatorsSingle-crystal X-ray study T = 293 K Mean (C-C) = 0.008 Å R factor = 0.062 wR factor = 0.142 Data-to-parameter ratio = 17.3For details of how these key indicators were automatically derived from the article, see
“…The central seven-membered diazepinthione ring (atoms C4/C5/C7-C9/N1/N2) adopts a boat conformation. The boat conformation is predominantly observed for the seven-membered ring of benzodiazepine and its derivatives, even with different double-bond positions and widely differing substituents (Walkinshaw, 1985;Torres et al, 2005). The internal torsion angles of the ring are shown in Fig.…”
Key indicatorsSingle-crystal X-ray study T = 293 K Mean (C-C) = 0.008 Å R factor = 0.062 wR factor = 0.142 Data-to-parameter ratio = 17.3For details of how these key indicators were automatically derived from the article, see
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