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The ionic radii of the lanthanides decrease from 103 pm (La 3+) to 86 pm (Lu 3+) in the lanthanide series, electrons are added to the 4f shell.This first f shell is inside the full 5s and 5p shells (as well as the 6s shell in the neutral atom); the 4f shell is well-localized near the atomic nucleus and has little effect on chemical bonding.
[1] Relatively more stable entities with unpaired electrons do exist, e.g. the nitric oxide molecule has one. According to Hund's rule, the spins of unpaired electrons are aligned parallel and this gives these molecules paramagnetic properties. The most stable examples of unpaired electrons are found on the atoms and ions of lanthanides and ...
This phenomenon is often referred to as the orbital penetration effect. The shielding theory also contributes to the explanation of why valence-shell electrons are more easily removed from the atom. Additionally, there is also a shielding effect that occurs between sublevels within the same principal energy level. An electron in the s-sublevel ...
In chemistry and atomic physics, an electron shell may be thought of as an orbit that electrons follow around an atom's nucleus.The closest shell to the nucleus is called the "1 shell" (also called the "K shell"), followed by the "2 shell" (or "L shell"), then the "3 shell" (or "M shell"), and so on further and further from the nucleus.
The lanthanide contraction, i.e. the reduction in size of the Ln 3+ ion from La 3+ (103 pm) to Lu 3+ (86.1 pm), is often explained by the poor shielding of the 5s and 5p electrons by the 4f electrons.
The p z orbital is the same as the p 0 orbital, but the p x and p y are formed by taking linear combinations of the p +1 and p −1 orbitals (which is why they are listed under the m = ±1 label). Also, the p +1 and p −1 are not the same shape as the p 0 , since they are pure spherical harmonics .
Valence bond theory complements molecular orbital theory, which does not adhere to the valence bond idea that electron pairs are localized between two specific atoms in a molecule but that they are distributed in sets of molecular orbitals which can extend over the entire molecule. Although both theories describe chemical bonding, molecular ...
For transition metals the orbitals of the incomplete (n−1)d subshell are included, and for lanthanides and actinides incomplete (n−2)f and (n−1)d subshells. The orbitals involved can be in an inner electron shell and do not all correspond to the same electron shell or principal quantum number n in a given element, but they are all at ...