Chapter 24: Problem 26
Write names for the following coordination compounds: (a) \(\left[\mathrm{Cd}(\mathrm{en}) \mathrm{Cl}_{2}\right]\) (b) \(\mathrm{K}_{4}\left[\mathrm{Mn}(\mathrm{CN})_{6}\right]\) (c) \(\left[\mathrm{Cr}\left(\mathrm{NH}_{3}\right)_{5} \mathrm{CO}_{3}\right] \mathrm{Cl}\) (d) \(\left[\mathrm{Ir}\left(\mathrm{NH}_{3}\right)_{4}\left(\mathrm{H}_{2} \mathrm{O}\right)_{2}\right]\left(\mathrm{NO}_{3}\right)_{3}\)
Short Answer
Step by step solution
(a) Identify the central atom and ligands for the first coordination compound
(a) Name the first coordination compound
(b) Identify the central atom and ligands for the second coordination compound
(b) Name the second coordination compound
(c) Identify the central atom and ligands for the third coordination compound
(c) Name the third coordination compound
(d) Identify the central atom and ligands for the fourth coordination compound
(d) Name the fourth coordination compound
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
IUPAC Nomenclature
When naming a coordination compound, we identify and name the ligands first, followed by the central metal atom. Ligands are named in alphabetical order regardless of their charge, with prefixes like 'di-', 'tri-', 'tetra-', etc., to indicate the number of each type. Neutral ligands are typically given their common names (e.g., water is 'aqua'), whereas anionic ligands end in 'o' (e.g., chloride becomes 'chlorido').
The central metal's name is then stated, with a Roman numeral in parentheses indicating the metal's oxidation state. If there's a counter-ion present (outside the coordination sphere), it is named last, just like in the naming of salts. For example, the name 'dichloridoethylenediaminecadmium(II)' reveals that the compound includes a cadmium ion with an oxidation state of +2, coordinated with two chloride ions and one ethylenediamine molecule.
Transition Metal Complexes
The coordination of ligands to a central metal ion is facilitated through coordinate covalent bonds, which are formed when both electrons in a bonding pair come from the same atom. Transition metals are particularly suited to forming such bonds owing to their d orbitals, which can accommodate the shared electron pairs.
Several examples highlighted in the exercise, such as \(\mathrm{K}_{4}[\mathrm{Mn}(\mathrm{CN})_{6}]\) or \(\left[\mathrm{Ir}\left(\mathrm{NH}_{3}\right)_{4}\left(\mathrm{H}_{2}\mathrm{O}\right)_{2}\right]\left(\mathrm{NO}_{3}\right)_{3}\), illustrate diverse coordination numbers and ligand types. These factors, among others, ultimately influence the properties such as geometry, stereochemistry, and reactivity, of the transition metal complexes.
Ligands in Coordination Chemistry
In the examples given in the exercise, we encounter a variety of ligands, such as ethylenediamine (en), chloride (Cl), cyanide (CN), ammonia (NH3), carbonate (CO3), and water (H2O). Ligands can be classified based on the number of attachment points or bonding locations they provide to the metal center:
- Monodentate ligands: Bind through a single atom, like chloride or water.
- Bidentate ligands: Have two binding sites, such as ethylenediamine, which can wrap around the metal ion and bind it at two points.
- Polydentate (or chelating) ligands: Possess multiple binding sites, allowing them to form stable rings with the central atom, greatly enhancing the stability of the complex.
These ligands can also bring about different colors in coordination compounds due to variations in metal-ligand bonding, which affects the d-electron configuration of the metal ion. As a result, understanding ligands is crucial for predicting and explaining the behavior of transition metal complexes in chemical reactions.