The Antibonding Effect
Derek W. Smith
Abstract
Derek W. Smith
Abstract
It is shown that the consequence of filling both a bonding molecular orbital (MO) and its antibonding counterpart leads to a total orbital energy greater than that of the separated atoms. The resulting antibonding effect can be buffered if the antibonding MO mixes with higher empty MOs of the same symmetry. These considerations explain why Be 2 has a weak covalent bond, much stronger than in He 2 . The antibonding effect also helps to explain the weakness of the F-F, O-O, and N-N single bonds. It is also useful in dealing with the stereochemistry of d n transition metal ions ( n > 7); the favored coordination geometries are those that minimize the antibonding effect, or which allow its effective buffering.
OpenAlex reports 20 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
It is shown that the consequence of filling both a bonding molecular orbital (MO) and its antibonding counterpart leads to a total orbital energy greater than that of the separated atoms. The resulting antibonding effect can be buffered if the antibonding MO mixes with higher empty MOs of the same symmetry. These considerations explain why Be 2 has a weak covalent bond, much stronger than in He 2 . The antibonding effect also helps to explain the weakness of the F-F, O-O, and N-N single bonds. It is also useful in dealing with the stereochemistry of d n transition metal ions ( n > 7); the favored coordination geometries are those that minimize the antibonding effect, or which allow its effective buffering.
Key concepts: Antibonding molecular orbital, Covalent bond, Molecular orbital, Crystallography, Chemical bond, Chemical physics, Chemistry, Computational chemistry