Pople diagram
A Pople diagram or Pople's Diagram is a diagram which describes the relationship between various calculation methods in computational chemistry. It was initially introduced in January 1965 by Sir John Pople, KBE FRS, during the Symposium of Atomic and Molecular Quantum Theory in Florida.[1] The Pople Diagram can be either 2-dimensional or 3-dimensional, with the axes representing ab initio methods, basis sets and treatment of relativity.[2] The diagram attempts to balance calculations by giving all aspects of a computation equal weight.
History
[edit]
John Pople first introduced the Pople Diagram during the Symposium on Atomic and Molecular Quantum Theory held on Sanibel Island, Florida, in January 1965. He called it a "hyperbola of quantum chemistry", which illustrates the inverse relationship between the sophistication of a calculational method and the number of electrons in a molecule that can be studied by that method.[1] Alternative (reverse) arrangement of the vertical axis or interchange of the two axes are also possible.[3][4]
Three-Dimensional Pople Diagrams
[edit]The 2-dimensional Pople diagram describes the convergence of the quantum-mechanical nonrelativistic electronic energy with the size of the basis set and the level of electron correlation included in the wavefunction.[5] In order to reproduce accurate experimental thermochemical properties, secondary energetic contributions have to be considered. The third dimension of the Pople diagram consists of such energetic contributions. These contributions may include: spin–orbit interaction, scalar relativistic, zero-point vibrational energy, and deviations from the Born–Oppenheimer approximation. The three-dimensional Pople diagram (also known as the Csaszar cube.[6]) describes the energy contributions involved in quantum chemistry composite methods.[7]
See also
[edit]References
[edit]- ^ a b Karplus, Martin (July 1990). "Three-dimensional "Pople diagram"". J. Phys. Chem. 14 (94): 5435–5436. doi:10.1021/j100377a002.
- ^ Dolg, Michael (17 February 2015). Computational Methods in Lanthanide and Actinide Chemistry. John Wiley & Sons, 2015. p. 480. ISBN 9781118688281.
- ^ Vereecken, Luc; Franciscob, Joseph (2012). "Theoretical studies of atmospheric reaction mechanisms in the troposphere". Chem. Soc. Rev. 41 (19): 6259–6293. doi:10.1039/C2CS35070J. PMID 22660412.
- ^ Auer, Alexander A. (September 4, 2014). "Electron Correlation - Methods beyond Hartree-Fock, how to approach chemical accuracy" (PDF). Max-Planck-Institute for Chemical Energy Conversion, Mülheim. Archived from the original (PDF) on March 4, 2016. Retrieved October 21, 2015.
- ^ J. A. Pople (1965). "Two‐Dimensional Chart of Quantum Chemistry". Journal of Chemical Physics. 43 (10): S229–S230. Bibcode:1965JChPh..43S.229P. doi:10.1063/1.1701495.
- ^ G. Tarczay; A. G. Csaszar; W. klopper; H. M. quiney (2001). "Anatomy of relativistic energy corrections in light molecular systems". Molecular Physics. 99 (21): 1769. Bibcode:2001MolPh..99.1769T. doi:10.1080/00268970110073907. S2CID 56163821.
- ^ A. Karton (2016). "A computational chemist's guide to accurate thermochemistry for organic molecules" (PDF). Wiley Interdisciplinary Reviews: Computational Molecular Science. 6 (3): 292–310. doi:10.1002/wcms.1249. S2CID 102248364.