Di-n-propyl ether, protonated

• Formula: C₆H₁₅O⁺
• Molecular weight: 103.1822
• Information on this page:
  • Ion clustering data
  • References
  • Notes
• Other data available:
  • Reaction thermochemistry data
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Ion clustering 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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Clustering reactions

C₆H₁₅O⁺ +  = (C₆H₁₅O⁺ • )

By formula: C₆H₁₅O⁺ + C₂H₃N = (C₆H₁₅O⁺ • C₂H₃N)

Free energy of reaction

C₆H₁₅O⁺ +  = (C₆H₁₅O⁺ • )

By formula: C₆H₁₅O⁺ + C₄H₁₀O = (C₆H₁₅O⁺ • C₄H₁₀O)

Bond type: Hydrogen bonds of the type OH-O between organics

C₆H₁₅O⁺ +  = (C₆H₁₅O⁺ • )

By formula: C₆H₁₅O⁺ + C₆H₁₄O = (C₆H₁₅O⁺ • C₆H₁₄O)

Bond type: Hydrogen bonds of the type OH-O between organics

Bond type: Hydrogen bonds between protonated and neutral organics

C₆H₁₅O⁺ +  = (C₆H₁₅O⁺ • )

By formula: C₆H₁₅O⁺ + H₂O = (C₆H₁₅O⁺ • H₂O)

Bond type: Hydrogen bond (positive ion to hydride)

(C₆H₁₅O⁺ • ) +  = (C₆H₁₅O⁺ • 2)

By formula: (C₆H₁₅O⁺ • H₂O) + H₂O = (C₆H₁₅O⁺ • 2H₂O)

Bond type: Hydrogen bond (positive ion to hydride)

(C₆H₁₅O⁺ • 2) +  = (C₆H₁₅O⁺ • 3)

By formula: (C₆H₁₅O⁺ • 2H₂O) + H₂O = (C₆H₁₅O⁺ • 3H₂O)

Bond type: Hydrogen bond (positive ion to hydride)

(C₆H₁₅O⁺ • 3) +  = (C₆H₁₅O⁺ • 4)

By formula: (C₆H₁₅O⁺ • 3H₂O) + H₂O = (C₆H₁₅O⁺ • 4H₂O)

Bond type: Hydrogen bond (positive ion to hydride)

(C₆H₁₅O⁺ • 4) +  = (C₆H₁₅O⁺ • 5)

By formula: (C₆H₁₅O⁺ • 4H₂O) + H₂O = (C₆H₁₅O⁺ • 5H₂O)

Bond type: Hydrogen bond (positive ion to hydride)

(C₆H₁₅O⁺ • 5) +  = (C₆H₁₅O⁺ • 6)

By formula: (C₆H₁₅O⁺ • 5H₂O) + H₂O = (C₆H₁₅O⁺ • 6H₂O)

Bond type: Hydrogen bond (positive ion to hydride)

Free energy of reaction

References

Go To: Top, Ion clustering data, Notes

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

Bromilow, Abboud, et al., 1980
Bromilow, J.; Abboud, J.L.M.; Lebrilla, C.B.; Taft, R.W.; Scorrano, G.; Lucchini, V., Oxonium Ions. Solvation by Single Acetonitrile Molecules in the Gas Phase and by Bulk Solvents, J. Am. Chem. Soc., 1980, 103, 18, 5448, https://doi.org/10.1021/ja00408a028 . [all data]

Grimsrud and Kebarle, 1973
Grimsrud, E.P.; Kebarle, P., Gas Phase Ion Equilibria Studies of the Solvation of the Hydrogen Ion by Methanol, Dimethyl Ether and Water. Effect of Hydrogen Bonding, J. Am. Chem. Soc., 1973, 95, 24, 7939, https://doi.org/10.1021/ja00805a002 . [all data]

Larson and McMahon, 1982
Larson, J.W.; McMahon, T.B., Formation, Thermochemistry, and Relative Stabilities of Proton - Bound dimers of Oxygen n - Donor Bases from Ion Cyclotron Resonance Solvent - Exchange Equilibria Measurements, J. Am. Chem. Soc., 1982, 104, 23, 6255, https://doi.org/10.1021/ja00387a016 . [all data]

Lias, Liebman, et al., 1984
Lias, S.G.; Liebman, J.F.; Levin, R.D., Evaluated gas phase basicities and proton affinities of molecules heats of formation of protonated molecules, J. Phys. Chem. Ref. Data, 1984, 13, 695. [all data]

Keesee and Castleman, 1986
Keesee, R.G.; Castleman, A.W., Jr., Thermochemical data on Ggs-phase ion-molecule association and clustering reactions, J. Phys. Chem. Ref. Data, 1986, 15, 1011. [all data]

Meot-Ner (Mautner), Sieck, et al., 1994
Meot-Ner (Mautner), M.; Sieck, L.W.; Liebman, J.F.; Scheiner, S.; Duan, X., The Ionic Hydrogen Bond. 5. Polydentate and Solvent-Bridged Structures. Complexing of the Proton and the Hydronium Ions by Polyethers, J. Am. Chem. Soc., 1994, 116, 17, 7848, https://doi.org/10.1021/ja00096a047 . [all data]

Notes

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• Symbols used in this document:
  

  T	Temperature
  ΔrG°	Free energy of reaction at standard conditions
  ΔrH°	Enthalpy of reaction at standard conditions
  ΔrS°	Entropy of reaction at standard conditions

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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