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The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory | Vol.109, Issue.18 | 1970-01-01 | Pages -

The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory

Theoretical Studies on the Intramolecular Hydrogen Bond and Tautomerism of 8-Mercaptoquinoline in the Gaseous Phase and in Solution Using Modern DFT Methods

Andrew E.Shchavlev;Alexei N.Pankratov;Alexei V.Shalabay  
Abstract

A theoretical quantum chemical study of the intramolecular hydrogen bonding interactions in 8-mercapto-quinoline has been carried out.Special attention has been paid to the rotation of S-H bond and intramolecular proton-transfer reactions.Therewith,the B3LYP/6-311++G(d,p),B3LYP/6-31+G(2d,2p),MPW1K/6-311++G(d,p),MPWlK/6-31+G(2d,2p),BH&HLYP/6-311++G(d,p),and G96LYP/6-311++G(d,p) methods have been used.By means of the Onsager and PCM reaction field methods,the effects of solvent on hydrogen-bond energies,conformational equilibria,rotational barriers,and tautomerism in aqueous solution have been studied.These simulations were done at the MPW1K/6-31 l++G(d,p) and B3LYP/6-311++G(d,p) levels.Natural-bond orbital analysis has been performed to study the intramolecular hydrogen bond (IHB) in the gaseous phase and in aqueous medium.The stability of forms under consideration in solution does not coincide with that in the gaseous phase,underlining a great importance of the electrostatic influence of solvent.Double-proton transfer in the prototropic tautomerization of 8-mercaptoquinoline,one water molecule complex in the gaseous phase and in solution,has been systematically studied.The double-proton transfer occurs conceitedly and synchronously.The water-assisted tautomerization is kinetically less,but thermodynamically more favorable,compared to that of the single-proton transfer.As in the case with single-proton transfer,for water-assisted reaction,the tautomerization energies and barrier heights decrease with the increase in dielectric constant,which implies faster and more complete tautomerization of 8-mercaptoquinoline in a polar solvent.

Original Text (This is the original text for your reference.)

Theoretical Studies on the Intramolecular Hydrogen Bond and Tautomerism of 8-Mercaptoquinoline in the Gaseous Phase and in Solution Using Modern DFT Methods

A theoretical quantum chemical study of the intramolecular hydrogen bonding interactions in 8-mercapto-quinoline has been carried out.Special attention has been paid to the rotation of S-H bond and intramolecular proton-transfer reactions.Therewith,the B3LYP/6-311++G(d,p),B3LYP/6-31+G(2d,2p),MPW1K/6-311++G(d,p),MPWlK/6-31+G(2d,2p),BH&HLYP/6-311++G(d,p),and G96LYP/6-311++G(d,p) methods have been used.By means of the Onsager and PCM reaction field methods,the effects of solvent on hydrogen-bond energies,conformational equilibria,rotational barriers,and tautomerism in aqueous solution have been studied.These simulations were done at the MPW1K/6-31 l++G(d,p) and B3LYP/6-311++G(d,p) levels.Natural-bond orbital analysis has been performed to study the intramolecular hydrogen bond (IHB) in the gaseous phase and in aqueous medium.The stability of forms under consideration in solution does not coincide with that in the gaseous phase,underlining a great importance of the electrostatic influence of solvent.Double-proton transfer in the prototropic tautomerization of 8-mercaptoquinoline,one water molecule complex in the gaseous phase and in solution,has been systematically studied.The double-proton transfer occurs conceitedly and synchronously.The water-assisted tautomerization is kinetically less,but thermodynamically more favorable,compared to that of the single-proton transfer.As in the case with single-proton transfer,for water-assisted reaction,the tautomerization energies and barrier heights decrease with the increase in dielectric constant,which implies faster and more complete tautomerization of 8-mercaptoquinoline in a polar solvent.

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Andrew E.Shchavlev;Alexei N.Pankratov;Alexei V.Shalabay,.Theoretical Studies on the Intramolecular Hydrogen Bond and Tautomerism of 8-Mercaptoquinoline in the Gaseous Phase and in Solution Using Modern DFT Methods. 109 (18), - .

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