Ethanamine, N-triphenylphosphoranylidene-

• Formula: C₂₀H₂₀NP
• Molecular weight: 305.3533
• IUPAC Standard InChI: InChI=1S/C20H20NP/c1-2-21-22(18-12-6-3-7-13-18,19-14-8-4-9-15-19)20-16-10-5-11-17-20/h3-17H,2H2,1H3 Copy

  
• IUPAC Standard InChIKey: HDISZNSQGZXVLN-UHFFFAOYSA-N Copy
• CAS Registry Number: 47182-04-7
• Chemical structure:
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• Information on this page:
  • Phase change data
  • Gas phase ion energetics data
  • References
  • Notes
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Phase change 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: William E. Acree, Jr., James S. Chickos

Gas phase ion energetics 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 as indicated in comments:
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

Ionization energy determinations

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.

Pilcher and Skinner, 1983
Pilcher, G.; Skinner, H.A., Thermochemistry of organometallic compounds, 1983, 43-90, https://doi.org/10.1002/9780470771686.ch2 . [all data]

Claydon, Fowell, et al., 1960
Claydon, Ann P.; Fowell, P.A.; Mortimer, C.T., 658. Heats of formation and bond energies. Part III. Trimethylphosphine oxide, N-ethyltrimethylphosphine imine, and N-ethyltri-phenylphosphine imine, J. Chem. Soc., 1960, 3284, https://doi.org/10.1039/jr9600003284 . [all data]

Starzewski and Dieck, 1979
Starzewski, K.A.O.; Dieck, H.t., Electronic structure and reactivity. 8. Iminophosphoranes- simple ylide analogues? An investigation of quantitative and sphenomenological differences, Inorg. Chem., 1979, 18, 3307. [all data]

Notes

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• Symbols used in this document:
  

  ΔsubH°

  Enthalpy of sublimation at standard conditions

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