Why is the Electron Configuration of Platinum Not [Xe]4f ^{14} 5d ^{10} 6s ^{0}?

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The electron configuration of platinum is [Xe]4f ^{14} 5d ^{9} 6s ^{1} due to the balance of electron-electron interactions and energy levels between the 5d and 6s orbitals. Although moving two electrons from the 6s to the 5d would create a fully paired d subshell, the repulsion from adding an electron to the d subshell outweighs the stability gained from completing it. The close energy levels of the 6s and 5d orbitals, along with the differences in electron repulsion between s and d orbitals, influence this configuration. Additionally, spin-orbit interactions play a role, as they are significant in d orbitals but negligible in s orbitals. Ultimately, these factors lead to the observed electron configuration for platinum.
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Homework Statement


Why is the electron configuration of neutral Platinum:

Pt = [Xe]4f ^{14} 5d ^{9} 6s ^{1}

and not?:

Pt = [Xe]4f ^{14} 5d ^{10} 6s ^{0}

I thought that if the two electrons from the 6s sub-shell were to move to the 5d sub-shell, then 5d sub-shell would be fully paired, hence stability? However, this is not the case as the actual configuration calls for only one electron to be moved from the 6s sub-shell, rather than two. Can someone explain to me why this is the case?
 
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This is a pretty good resource on advanced concepts regarding electron configurations in atoms:
http://pubs.acs.org/doi/full/10.1021/ed8001286?src=recsys
In case it's paywalled, the main point is that electron-electron interactions matter. In the case of platinum specifically, there is quite a lot going on. First, the 6s and 5d orbitals are very close in energy in the platinum system. In addition, there is a (generic) difference between electron repulsion in the d orbitals and in the s orbitals. S orbitals tend to be more diffuse and d orbitals tend to be more compact. Therefore, electron repulsion tends to drive d-orbital filling to higher energies than s-orbital filling. There are also spin-orbit interactions to consider (spin-orbit terms are zero in the s-orbital case but nonzero in the d-orbital case). These all combine and balance out in a certain way to give you the experimentally observed electron configuration. In the case of platinum, this means roughly that the repulsion felt by adding the final electron to the d-subshell is larger than the energy gained by completing that subshell, so the electron ends up in the s-orbital.
 
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