How Can CN-, P(CH3)3, and SCN- Act as Both σ-Donors and π-Acceptors?

AI Thread Summary
CN-, P(CH3)3, and SCN- can act as both σ-donors and π-acceptors due to their possession of lone pair electrons and available π* orbitals. This dual behavior is explained by the concept of "pi-backbonding," where electron density is donated into antibonding orbitals. Such interactions are significant in catalysis, particularly in processes involving bond breaking. Understanding these ligand properties enhances insights into coordination chemistry. The discussion emphasizes the importance of these mechanisms in various chemical reactions.
ReidMerrill
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Homework Statement


Describe, using sketches, how the following ligands can act as both σ-donors and π-acceptors:
CN-
P(CH3)3
SCN-

Homework Equations

The Attempt at a Solution



I suspect it has something to do with these ligands having lone pair electrons AND open π* orbitals.
How correct is this and if it is wrong then what is the explanation?
 
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ReidMerrill said:
I suspect it has something to do with these ligands having lone pair electrons AND open π* orbitals.
How correct is this and if it is wrong then what is the explanation?
This is basically correct. Look up "pi-backbonding" for a good explanation. Bonus fact: Electron backdonation into antibonding orbitals turns out to be really important in catalysis where bond breaking is important.
 
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