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The d electron count or number of d electrons is a chemistry formalism used to describe the electron configuration of the valence electrons of a transition metal center in a coordination complex. [ 1 ] [ 2 ] The d electron count is an effective way to understand the geometry and reactivity of transition metal complexes.
neutral counting: Fe contributes 8 electrons, each CO contributes 2 each: 8 + 2 × 5 = 18 valence electrons ionic counting: Fe(0) contributes 8 electrons, each CO contributes 2 each: 8 + 2 × 5 = 18 valence electrons conclusions: this is a special case, where ionic counting is the same as neutral counting, all fragments being neutral.
So as opposed to main-group elements, a valence electron for a transition metal is defined as an electron that resides outside a noble-gas core. [3] Thus, generally, the d electrons in transition metals behave as valence electrons although they are not in the outermost shell.
The current consensus in the general chemistry community is that unlike the singular octet rule for main group elements, transition metals do not strictly obey either the 12-electron or 18-electron rule, but that the rules describe the lower bound and upper bound of valence electron count respectively.
When counting electrons for each cluster, the number of valence electrons is enumerated. For each transition metal present, 10 electrons are subtracted from the total electron count. For example, in Rh 6 (CO) 16 the total number of electrons would be 6 × 9 + 16 × 2 − 6 × 10 = 86 – 60 = 26.
Other rules exist for other elements, such as the duplet rule for hydrogen and helium, and the 18-electron rule for transition metals. The valence electrons can be counted using a Lewis electron dot diagram as shown at the right for carbon dioxide. The electrons shared by the two atoms in a covalent bond are counted twice, once for each atom ...
The maximum oxidation state in the first row transition metals is equal to the number of valence electrons from titanium (+4) up to manganese (+7), but decreases in the later elements. In the second row, the maximum occurs with ruthenium (+8), and in the third row, the maximum occurs with iridium (+9).
The greater stabilization that results from metal-to-ligand bonding is caused by the donation of negative charge away from the metal ion, towards the ligands. This allows the metal to accept the σ bonds more easily. The combination of ligand-to-metal σ-bonding and metal-to-ligand π-bonding is a synergic effect, as each enhances the other.