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A classmate says, "A strong-field ligand means that the ligand binds strongly to the metal ion." Is your classmate correct? Explain.

Short Answer

Expert verified
Your classmate's statement is not entirely correct. A strong-field ligand refers to its effect on the ligand-field splitting energy in transition metal complexes, but it does not necessarily mean that the ligand binds strongly to the metal ion. The strength of binding depends on various factors, such as the nature of the bond, electronegativity of the ions, and their sizes.

Step by step solution

01

Understanding Strong-Field Ligands

Strong-field ligands are those that have a relatively large ligand-field splitting energy, which causes a greater energetic split between d-orbitals involved in metal-ligand bonding in transition metal complexes. The ligand-field splitting energy is a measure of the energy required to promote an electron from the lower-energy d-orbitals (t2g) to the higher-energy d-orbitals (eg). The greater the ligand-field splitting energy, the greater the energy difference between the two sets of d-orbitals.
02

Strength of Binding

The strength of binding between a ligand and a metal ion is primarily determined by the nature of the bond they form, which could be ionic, covalent, or coordinate covalent (dative). Stronger bonds are generally associated with higher bond dissociation energy, which means more energy is required to break the bond between them.
03

Relation between Strong-Field Ligands and Binding Strength

The term "strong-field ligand" refers to the ligand's effect on the ligand-field splitting energy, but it does not necessarily imply that the ligand binds strongly to the metal ion. A strong-field ligand can affect the energy difference between the d-orbitals, but it is not directly related to the bond strength between the ligand and the metal ion. The binding strength of a ligand to a metal ion often depends on other factors, such as electronegativity, the size of the ion, and the type of bonding involved.
04

Conclusion

Your classmate's statement is not entirely correct. A strong-field ligand means that it causes a greater ligand-field splitting energy in the transition metal complex, but it does not necessarily mean that the ligand binds strongly to the metal ion. The strength of binding depends on various factors, such as the nature of the bond, electronegativity of the ions, and their sizes.

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Most popular questions from this chapter

One of the more famous species in coordination chemistry is the Creutz-Taube complex: It is named for the two scientists who discovered it and initially studied its properties. The central ligand is pyrazine, a planar six-membered ring with nitrogens at opposite sides. (a) How can you account for the fact that the complex, which has only neutral ligands, has an odd overall charge? (b) The metal is in a low-spin configuration in both cases. Assuming octahedral coordination, draw the d-orbital energy-level diagram for each metal. (c) In many experiments the two metal ions appear to be in exactly equivalent states. Can you think of a reason that this might appear to be so, recognizing that electrons move very rapidly compared to nuclei?

A classmate says, "A weak-field ligand usually means the complex is high spin." Is your clasmmate correct? Explain.

The most important oxides of iron are magnetite, \(\mathrm{Fe}_{3} \mathrm{O}_{4}\), and hematite, \(\mathrm{Fe}_{2} \mathrm{O}_{3}\). (a) What are the oxidation states of iron in these compounds? (b) One of these iron oxides is ferrimagnetic, and the other is antiferromagnetic. Which iron oxide is likely to show which type of magnetism? Explain. Transition-Metal Complexes (Section 23.2)

Two Fe(II) complexes are both low spin but have different ligands. A solution of one is green and a solution of the other is red. Which solution is likely to contain the complex that has the stronger-field ligand? [Section 23.6]

A complex is written as \(\mathrm{NiBr}_{2} \cdot 6 \mathrm{NH}_{2}\), (a) What is the oxidation state of the Ni atom in this complex? (b) What is the likely coordination number for the complex? (c) If the complex is treated with excess \(\mathrm{AgNO}_{3}\left(\mathrm{aq}_{2}\right)\), how many moles of AgBr will precipitate per mole of complex?

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