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Example · Example 8

Q.[Sc(H2O)6]3+[\text{Sc}(\text{H}_2\text{O})_6]^{3+} is colourless, while [Ti(H2O)6]3+[\text{Ti}(\text{H}_2\text{O})_6]^{3+} is purple. Account for this difference in terms of the dd-electron configurations of Sc3+\text{Sc}^{3+} and Ti3+\text{Ti}^{3+} and the origin of colour in coordination compounds.

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Colour in a transition-metal complex arises from a dd-dd transition: an electron in the lower-energy t2gt_{2g} orbital set absorbing a photon of visible light and being promoted to the higher-energy e_g} set, across the crystal field gap Δo\Delta_o. For this to happen at all, the metal ion must have at least one d-electron available to promote. Sc3+\text{Sc}^{3+} has the electron configuration [Ar]3d0[\text{Ar}]3d^0 — it has lost all three of its valence electrons (two 4s, one 3d) to reach the +3+3 state, leaving it with zero d-electrons. With no electron to promote, no dd-dd transition is possible, no visible light is absorbed, and [Sc(H2O)6]3+[\text{Sc}(\text{H}_2\text{O})_6]^{3+} is colourless. Ti3+\text{Ti}^{3+}, immediately next to scandium, has the configuration [Ar]3d1[\text{Ar}]3d^1 — it retains one d-electron after losing its three valence electrons (two 4s, one 3d, leaving one 3d behind is incorrect phrasing; more precisely, Ti has configuration [Ar]3d24s2[\text{Ar}]3d^24s^2, and losing 3 electrons to form Ti3+\text{Ti}^{3+} leaves [Ar]3d1[\text{Ar}]3d^1). This single d-electron sits in the lower t2gt_{2g} set and readily absorbs a photon matching Δo\Delta_o (in the yellow-green region of the visible spectrum) to jump into the empty ege_g set. Because yellow-green light …

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