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the valence electronic environments of actinides, and transition element
groups which have been studied more thoroughly.

Chemical bonding is related

we shialdina of boncing (d or f) orbital electrons by s and p orbitals.
Arong the groups of transition elements, the degree of shielding follows the
order:

Lanthanides

(4f mites

Actinides

(Sf orbitals) »

main group
transition elements

(3,4 or 5d orbitals)

This spatial difference in electronic structure results in chemical properties
of the actinide elements which are expected to be intermediate between the
characteristic behavior of the lanthanides and main group transition elements

(Cotton and Wilkinson, 1966).
The main aroup transition elements, by nature of having their valence
electrons at the periphery of atom, interact strongly with ligands.

These

interactions result in large variations in the chemical properties of succeeding main qroup transition elements which are well known.

In contrast to

the variations exhibited in succeeding "d” group transition elements, the
cherical behavior of the trivalent lanthanide elements in the marine environrent is quite similar.

This behavior is well illustrated by the relatively

tow concentration differences (when each element concentration is normalized
te its natural abundance in shale) observed for the trivalent lanthanides in
sea water and mineralogical phases of marine sediments (Goldberg et al.,1963;
Piner, 1975).

Unlike the main group transition elements, the lanthanides form

restly fonic compounds and exhibit chemical properties which are largely deterwined by the size of the nrs jon.

The size of each of the 14 succeeding

Varthanides steadily decreases with increasing atomic number (the lanthanide
Cemtrection) and these elements thus form increasingly stronger metal-ligand

coetleres with decreasing size; which may partly explain the small

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