2,6-Diethylpyridine, protonated


Reaction thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Michael M. Meot-Ner (Mautner) and Sharon G. Lias

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Individual Reactions

C9H14N+ + Water = (C9H14N+ • Water)

By formula: C9H14N+ + H2O = (C9H14N+ • H2O)

Bond type: Hydrogen bond (positive ion to hydride)

Quantity Value Units Method Reference Comment
Δr54.4kJ/molPHPMSMeot-Ner M. and Sieck, 1983gas phase; (H), ΔrS should be 113.6 J/mol*K
Quantity Value Units Method Reference Comment
Δr120.J/mol*KPHPMSMeot-Ner M. and Sieck, 1983gas phase; (H), ΔrS should be 113.6 J/mol*K

Free energy of reaction

ΔrG° (kJ/mol) T (K) Method Reference Comment
9.6394.PHPMSMeot-Ner M. and Sieck, 1983gas phase; (H), ΔrS should be 113.6 J/mol*K

C9H14N+ + Pyridine, 2,6-diethyl- = (C9H14N+ • Pyridine, 2,6-diethyl-)

By formula: C9H14N+ + C9H13N = (C9H14N+ • C9H13N)

Quantity Value Units Method Reference Comment
Δr95.4kJ/molPHPMSMeot-Ner M. and Sieck, 1983gas phase
Quantity Value Units Method Reference Comment
Δr156.J/mol*KPHPMSMeot-Ner M. and Sieck, 1983gas phase

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Meot-Ner M. and Sieck, 1983
Meot-Ner M.; Sieck, L.W., The Ionic Hydrogen Bond. 1. Sterically Hindered Bonds. Solvation and Clustering of Sterically Hindered Amines and Pyridines, J. Am. Chem. Soc., 1983, 105, 10, 2956, https://doi.org/10.1021/ja00348a005 . [all data]


Notes

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