Abstract
Since d-orbitals are central to the problem of valence shell expansion, we should first discuss the nature of d-orbitals. In the free atom, there are five d-orbitals, each of equal energy and having the electron distributions shown in Fig. 1. Although the degenerate energy level will be split by the field of the ligands, the angular parts of the orbital wave functions will remain unchanged. On the basis of angularity (geometry alone), d-orbitals should have considerable overlap with suitably oriented 2s or 2p orbitals on the ligand.
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© 1977 Springer-Verlag Berlin Heidelberg
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Kwart, H., King, K. (1977). Theoretical Basis for d-Orbitals. In: d-Orbitals in the Chemistry of Silicon, Phosphorus and Sulfur. Reactivity and Structure Concepts in Organic Chemistry, vol 3. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-46342-6_2
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DOI: https://doi.org/10.1007/978-3-642-46342-6_2
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-642-46344-0
Online ISBN: 978-3-642-46342-6
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