The distance between 4-H and adjacent H on the substitutional benzene ring in benzo[c]carbazole was calculated in terms of molecular structure parameters. The result showed that the distance is shorter than the sum of...The distance between 4-H and adjacent H on the substitutional benzene ring in benzo[c]carbazole was calculated in terms of molecular structure parameters. The result showed that the distance is shorter than the sum of van der Vaals' radii of two hydrogen atoms. This means that there is a steric hinderance between them. This effect will make the bond angle stretch and the bond length extend, or cause the molecule to distort, thus making benzo[c]carbazoles become unstable in thermodynamics. On the contrary there is no such effect for benzo[a]carbazoles. This conclusion has been confirmed by the result of calculation of the distance between the same two atoms with software GaussView. So the skeleton of benzo[c]carbazoles in sediments may be breached or isomerized with increasing maturity. It is consistent with the decrease of the ratio of benzo[c]carbazole to benzo[a]carbazole in hydrocarbon migration, suggesting that [c]/[a] not only changes with the distance of migration, but also may be influenced by maturity.展开更多
文摘The distance between 4-H and adjacent H on the substitutional benzene ring in benzo[c]carbazole was calculated in terms of molecular structure parameters. The result showed that the distance is shorter than the sum of van der Vaals' radii of two hydrogen atoms. This means that there is a steric hinderance between them. This effect will make the bond angle stretch and the bond length extend, or cause the molecule to distort, thus making benzo[c]carbazoles become unstable in thermodynamics. On the contrary there is no such effect for benzo[a]carbazoles. This conclusion has been confirmed by the result of calculation of the distance between the same two atoms with software GaussView. So the skeleton of benzo[c]carbazoles in sediments may be breached or isomerized with increasing maturity. It is consistent with the decrease of the ratio of benzo[c]carbazole to benzo[a]carbazole in hydrocarbon migration, suggesting that [c]/[a] not only changes with the distance of migration, but also may be influenced by maturity.
