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Ch.21 - Transition Elements and Coordination Chemistry
Chapter 21, Problem 21.140d

Cobalt(III) trifluoroacetylacetonate, Co1tfac23, is a sixcoordinate, octahedral metal chelate in which three planar, bidentate tfac ligands are attached to a central Co atom:
(d) Draw a crystal field energy-level diagram for Co1tfac23, and predict its magnetic properties. (In this complex, tfac is a strong-field ligand.)

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Key Concepts

Here are the essential concepts you must grasp in order to answer the question correctly.

Crystal Field Theory

Crystal Field Theory (CFT) explains how the arrangement of ligands around a central metal ion affects its electronic structure and energy levels. In octahedral complexes, the d-orbitals split into two energy levels: the lower-energy t2g and the higher-energy eg orbitals. The extent of this splitting depends on the nature of the ligands, with strong-field ligands causing a larger splitting, which influences the complex's magnetic properties.
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The study of ligand-metal interactions helped to form Ligand Field Theory which combines CFT with MO Theory.

Ligand Field Strength

Ligand field strength refers to the ability of a ligand to influence the energy levels of the d-orbitals in a metal complex. Strong-field ligands, like tfac in this case, cause significant splitting of the d-orbitals, leading to low-spin configurations where electrons pair up in the lower energy orbitals. This property is crucial for predicting the magnetic behavior of the complex, as low-spin complexes tend to be diamagnetic.
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Strong-Field Ligands result in a large Δ and Weak-Field Ligands result in a small Δ.

Magnetic Properties of Complexes

The magnetic properties of coordination complexes are determined by the presence of unpaired electrons in their d-orbitals. A complex with unpaired electrons is paramagnetic, while one with all paired electrons is diamagnetic. In the case of Co1tfac23, the strong-field tfac ligands lead to a low-spin state, resulting in no unpaired electrons and thus a diamagnetic property, which can be predicted from the crystal field energy-level diagram.
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For octahedral complexes, Weak-Field Ligands create High-spin complexes and Strong-Field Ligands create Low-spin complexes.
Related Practice
Textbook Question

In acidic aqueous solution, the complex trans-[Co(en)2Cl1]2+(aq) undergoes the following substitution reaction:

trans-[Co(en)2Cl1]+(aq) + H2O(l) → trans-[Co(en)2(H2O)Cl]2+(aq) + Cl(aq)

The reaction is first order in trans-[Co(en)2Cl2]+(aq), and the rate constant at 25°C is 3.2×10–5 s–1.

e. Draw a crystal field energy-level diagram for ​trans-[Co(en)2Cl2]+ that takes account of the fact that Cl is a weaker-field ligand than ethylenediamine.

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Textbook Question

Cobalt(III) trifluoroacetylacetonate, Co(tfac)3, is a sixc oordinate, octahedral metal chelate in which three planar, bidentate tfac ligands are attached to a central Co atom:

(a) Draw all possible diastereoisomers and enantiomers of Co(tfac)3.

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Textbook Question

Cobalt(III) trifluoroacetylacetonate, Co(tfac)3, is a sixcoordinate, octahedral metal chelate in which three planar, bidentate tfac ligands are attached to a central Co atom:

(b) Diastereoisomers A and B have dipole moments of 6.5 D and 3.8 D, respectively. Which of your diastereoisomers is A and which is B?

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Textbook Question

Based on effective nuclear charge (Zeff), which ion is the strongest oxidizing agent? 

(a) Cu2+

(b) Ni2+

(c) Fe2+

(d) Mn2+

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Textbook Question

Look at the location in the periodic table of elements A, B, C, and D. What is the electron configuration of the transition metal in each of the following ions?  

(a) A2+

(b) B+

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Textbook Question

The oxalate ion is a bidentate ligand as indicated in Figure 21.8. Would you expect the carbonate ion to be a monodentate or bidentate ligand? Explain your reasoning.

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