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(a) Explain briefly what is meant by the chelate effect (b) How many 5 -membered chelate rings are present in \(\left[\mathrm{Co}(\mathrm{en})_{3}\right]^{2+},\left[\mathrm{Co}(\mathrm{bpy})_{3}\right]^{3+},[\mathrm{Co}(\mathrm{edta})]^{-}\) and \(\left[\mathrm{Co}(\text { dien })_{2}\right]^{3+} ?\)

Short Answer

Expert verified
(a) The chelate effect is the increased stability observed in metal complexes with polydentate ligands forming rings. (b) - \([\text{Co}( ext{en})_3]^{2+}\): 6 rings - \([\text{Co}( ext{bpy})_3]^{3+}\): 6 rings - \([\text{Co}( ext{edta})]^-\): 5 rings - \([\text{Co}( ext{dien})_2]^{3+}\): 4 rings.

Step by step solution

01

Understand the Chelate Effect

The chelate effect refers to the enhanced stability of a coordination compound containing one or more chelate rings. Chelation involves the binding of a polydentate ligand to a central metal ion wherein the ligand forms two or more bonds, creating a ring structure. This generally leads to increased stability compared to complexes with monodentate ligands.
02

Identify Ligands and Their Denticity

Identify the ligands in each complex:- In \([\text{Co}( ext{en})_3]^{2+}\), the ligand is ethylenediamine (\(\text{en}\)), which is bidentate.- In \([\text{Co}( ext{bpy})_3]^{3+}\), the ligand is bipyridine (\(\text{bpy}\)), also bidentate.- In \([\text{Co}( ext{edta})]^-\), the ligand is ethylenediaminetetraacetate (\(\text{edta}\)), which is hexadentate.- In \([\text{Co}( ext{dien})_2]^{3+}\), the ligand is diethylenetriamine (\(\text{dien}\)), which is tridentate.
03

Count Chelate Rings in Each Complex

For each complex, count the number of 5-membered chelate rings:- \([\text{Co}( ext{en})_3]^{2+}\): Each \(\text{en}\) forms two 5-membered rings; with 3 \(\text{en}\) ligands, there are 6 rings.- \([\text{Co}( ext{bpy})_3]^{3+}\): Similar to \(\text{en}\), each \(\text{bpy}\) forms two 5-membered rings; with 3 \(\text{bpy}\), there are 6 rings.- \([\text{Co}( ext{edta})]^-\): \(\text{edta}\) forms 5 rings, each being a 5-membered ring.- \([\text{Co}( ext{dien})_2]^{3+}\): Each \(\text{dien}\) forms 2 rings, resulting in 4 rings in total.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Coordination Compound
A coordination compound is composed of a central metal atom or ion that is surrounded by molecules or ions, known as ligands. These ligands can donate electrons to the metal to form coordinate covalent bonds. The unique ability of metal ions to form such bonds with ligands leads to the creation of diverse structures with various physical and chemical properties.

Each coordination compound is characterized by the number and type of ligands surrounding the central metal. The metal-ligand interaction is crucial, as it determines the compound's geometry, reactivity, and color. For example, in \([\text{Co}( ext{en})_3]^{2+}\), the central cobalt ion is surrounded by multiple ethylenediamine ligands, creating a symmetrical and stable complex.

  • The central metal ion can exhibit different oxidation states, affecting the coordination compound's overall charge and reactivity.
  • The coordination number, which is the number of ligand donor atoms attached to the metal, influences the complex's geometry.
Understanding coordination compounds is fundamental in fields like bioinorganic chemistry and catalysis, where they play a critical role.
Polydentate Ligand
Polydentate ligands, also known as chelating agents, can attach themselves to a metal ion at multiple points. This ability to form several bonds with the metal ion makes them highly effective in stabilizing metal complexes. They "wrap around" the metal like a claw, forming ring structures called chelate rings.

For instance, ethylenediamine (en) and bipyridine (bpy) are examples of bidentate ligands, meaning they can form two bonds with the central metal. Diethylenetriamine (dien) is a tridentate ligand, capable of forming three bonds, while ethylenediaminetetraacetate (edta) can attach to a metal ion with six bonds, classifying it as hexadentate.

  • Polydentate ligands can improve the stability of a complex through the chelate effect, where the formation of multiple bonds provides more attachment points, reducing the likelihood of the ligand detaching.
  • They enable the formation of more complex and large structures with specialized functions, such as ion transport and catalysis.
Polydentate ligands are key in metal extraction processes and in medicine, particularly for detoxifying heavy metal ions.
Denticity
Denticity refers to the number of donor atoms a ligand uses to bind to a central metal ion. It is an important concept for understanding the coordination and stability of metal complexes. Different ligands exhibit different denticities, categorized as monodentate, bidentate, tridentate, etc., based on the number of binding sites they have.

For example:

  • A monodentate ligand like water (Hâ‚‚O) uses just one donor atom to bind to the metal.
  • A bidentate ligand such as ethylenediamine (en) uses two donor atoms to form a ring structure with the metal.
  • A hexadentate ligand like ethylenediaminetetraacetate (edta) can use six donor atoms.
Higher denticity generally means better complex stability as it allows the formation of several chelate rings, which significantly strengthens the attachment to the central metal ion. Understanding denticity helps in predicting and rationalizing the structural and chemical properties of a coordination complex.
Stability of Metal Complexes
The stability of metal complexes is influenced by several factors, including the nature of the ligands, the metal's oxidation state, and the overall geometry of the complex. A key contributor to complex stability is the chelate effect, where polydentate ligands form ring structures with the metal ion.

The creation of these rings increases stability for a few reasons:

  • Entropy Consideration: The formation of a chelate complex releases more atoms into the solution than the simpler ligand binding. This increase in entropy (disorder) favors complex formation.
  • Multiple Attachment Points: Polydentate ligands, by offering several places of attachment, reduce the likelihood of the complex breaking apart, as all bonds would need to break simultaneously for the ligand to detach.
It's important to know that other factors such as solvent interactions and ligand size also play a role. Metal complexes with high stability are crucial in numerous applications, including drug design and industrial catalysis.

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Most popular questions from this chapter

(a) Draw the structure of the complex ion represented by \(\mathrm{Co}^{2+}(\mathrm{aq}) .\) (b) The ion \(\left[\mathrm{Cr}\left(\mathrm{H}_{2} \mathrm{O}\right)_{5}(\mathrm{OH})\right]^{2+}\) forms a dinuclear complex in solution. Write an equation for this reaction and draw the structure of the dichromium product. Is there a change in oxidation state during the reaction? (c) Yellow solutions of ammonium vanadate \(\left[\mathrm{NH}_{4}\right]\left[\mathrm{VO}_{3}\right]\) in dilute sulfuric acid contain \(\left[\mathrm{VO}_{2}\right]^{+} .\) Draw a possible structure for the solution species represented by \(\left[\mathrm{VO}_{2}\right]^{+}\) given that the oxo ligands are cis to each other.

Calculate the spin-only magnetic moment for each of the following octahedral complexes: (a) \(\left[\operatorname{Mn}(\mathrm{en})_{3}\right]^{3+}\) (high-spin) (b) \(\left[\mathrm{Fe}(\mathrm{en})_{3}\right]^{2+}\) (high-spin) (c) \(\left[\mathrm{Ni}\left(\mathrm{HOCH}_{2} \mathrm{CH}_{2} \mathrm{NH}_{2}\right)_{2}\left(\mathrm{OCH}_{2} \mathrm{CH}_{2} \mathrm{NH}_{2}\right)\right]^{+}\)

Explain why there is only one spin arrangement for an octahedral \(d^{8}\) or \(d^{9}\) metal ion.

Stability constant data for the formation of \(\left[\mathrm{MnF}_{6}\right]^{4-}\) from \(\left[\mathrm{Mn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+}\) include the following: \(\log K_{1}=5.52, \log \beta_{2}=9.02 .\) Determine \(K_{1}\) and \(K_{2},\) and comment on the relative positions of the equilibria describing the first two ligand displacements.

Estimate the charge distribution over the metal and donor atoms in the complex ions (a) \(\left[\mathrm{Fe}(\mathrm{bpy})_{3}\right]^{2+}\) and (b) \(\left[\mathrm{CrF}_{6}\right]^{3-}\).

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