Lecture #34 | ||
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Lecture Outline | Transition Metal Complexes
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Crystal field theory addresses all the "puzzles" from the previous lecture. | ||
Developing the idea of crystal field theory.. | ||
Following what happens to the outer d-orbitals when a transition metal ion is placed in a spherically distributed negative charge, and then one that has octahedrally deployed negative charges. | ||
The weak field splitting and strong field splitting of the d-orbitals illustrated. | ||
You need to know the relative crystal field strengths of a restricted number of ligands indicated here. | ||
The electron configuration in the weak field complex CoF63- and the strong field complex Co(NH3)63+. | ||
Co3+ complex ions, their crystal field splitting energies, the color of light absorbed, and the color that the complex appears. | ||
Leaving the discussion of coordination number = 6 (octahedral geometries) and proceeding to coordination number four. | ||
Returning to an octahedral geometry, we look at the effect of having a weak ligand plus five stronger ligands. The weak ligand is assumed to be on the z-axis which stabilizes transition metal ion valence orbitals directed that way | ||
Co3+ transition metal complex ions with one of the ligands varying shifts the wavelength of light absorbed to longer wavelengths as that one ligand becomes "weaker" in the field it produces. | ||
Measured optical properties (colors) of Co3+ transition metal complex ions. What do you estimate the color of the last complex to be? This last complex is meant to be just the trans geometric isomer. | ||
The tetrahedral crystal field geometry (without demonstrating how to generate the result) turns out to be the exact inverse orbital order of that seen in the octahedral geometry. |