Explaining weird trend of d- and f- block elements.

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The discussion centers on the trends in atomic radii among d-block and f-block elements, noting that these trends deviate from the expected decrease across periods. For d-block elements, atomic radii initially increase from vanadium to chromium, then stabilize before decreasing again, indicating horizontal similarities not seen in s- and p-block elements. The f-block elements exhibit little to no change in atomic radii across the period. The conversation highlights the importance of experimental data derived from bond lengths in covalent compounds, which complicates the understanding of these trends. Theoretical models, while useful, do not account for the observed horizontal similarities. The concept of Slater screening is introduced as a potential explanation for the behavior of d- and f-block elements, differentiating it from the shielding effect, which involves how inner electrons shield outer electrons from the nucleus's charge.
ash64449
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Hello friends,

I noticed from Wikipedia the following information:
Atomic radii:
4th period(only d-block elements):
Sc:160 pm
Ti : 140 pm
V : 135 pm
Cr : 140 pm
Mn: 140 pm
Fe : 140 pm
Co : 135 pm
Ni : 135 pm
Cu :135 pm
Zn : 135 pm

Normally across the period atomic radii should decrease. But d-block elements do not follow this trend. It increases From V to Cr and them remains constant and decreases and remains constant again.

So they show horizontal similarities too.. Can some one explain me this strange trend?

More stranger trend is of f-block elements.. They don't change their radii at all if we go across the period!
 
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As far as I remember the experimental radii are half the distance of the atoms in a crystal lattice.
However, the metals crystalize in different lattices, which influences the radii.
Better take the calculated values from the table below.
 
DrDu said:
As far as I remember the experimental radii are half the distance of the atoms in a crystal lattice.
However, the metals crystalize in different lattices, which influences the radii.
Better take the calculated values from the table below.

Which table? can you explain this trend?

Not only this one,ionization enthalpy too follow the same way as atomic radii. But a little difference.

So i thought understanding atomic radii would help to understand everything.
 
DrDu said:
I meant the table with the theoretical atomic radii by Clementi in
http://en.wikipedia.org/wiki/Atomic_radii

Why?

I mean that is theoretical. Shouldn't we go for experimental results?

Yes. the theoretical models follow the general trend. But i think we should stick to experimental results..

Do you think no satisfactory explanations can be given to the trend observed experimentally?
 
The experimental values are derived from bond lengths of covalent substances. Hence you have to discuss the average bond lengths of d-block elements in mainly covalent compounds. This is much more complicated than discussing the shrinking of d- or f-orbitals.
 
DrDu said:
The experimental values are derived from bond lengths of covalent substances. Hence you have to discuss the average bond lengths of d-block elements in mainly covalent compounds. This is much more complicated than discussing the shrinking of d- or f-orbitals.

So, Can We say that d-block elements follow the same periodicity of that of s- and p- blocks?

I mean by experimental results obtained by deriving bond lengths, it is observed that some elements have same atomic radii.. i.e,they show horizontal similarities. s- and p- block don't show like that.

but theoretical models show no horizontal similarities.
 
Last edited:
My best guess is Slater-screening. Electrons can screen other electrons from the positively charged nucleus, but it depends on how the electrons occupy the orbitals (which itself seems random for d- and f-block elements). This way, depending on the screening of other electrons, the distance of the outer electrons from the nucleus can be very similar.
 
  • #10
sveegaard said:
My best guess is Slater-screening. Electrons can screen other electrons from the positively charged nucleus, but it depends on how the electrons occupy the orbitals (which itself seems random for d- and f-block elements). This way, depending on the screening of other electrons, the distance of the outer electrons from the nucleus can be very similar.

How is Slater-screening different from Shielding Effect?
 

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