Chapter 22: Problem 29
Draw two linkage isomers of [Mn(NH3)5(NO2)]2+.
Short Answer
Expert verified
The two linkage isomers of [Mn(NH3)5(NO2)]2+ are one where NO2 is bound through the nitrogen atom (nitro isomer) and another where NO2 is bound through an oxygen atom (nitrito isomer).
Step by step solution
01
Understanding Linkage Isomerism
Linkage isomerism occurs when a ligand can bind to a metal ion through two different atoms. In the complex ion [Mn(NH3)5(NO2)]2+, the ligand that can show linkage isomerism is the nitrito group, NO2. It can bond through the nitrogen atom (as 'nitro' NO2-) or through an oxygen atom (as 'nitrito' ONO-).
02
Drawing the First Linkage Isomer
For the first isomer, attach the nitro group (NO2-) to the manganese (Mn) center via the nitrogen atom. The five ammonia (NH3) molecules are attached to the Mn in the remaining coordination sites.
03
Drawing the Second Linkage Isomer
For the second isomer, attach the nitrito group (ONO-) to the manganese (Mn) center via one of the oxygen atoms. Again, the five ammonia (NH3) molecules are attached to the Mn in the remaining coordination sites.
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Coordination Chemistry
Coordination chemistry is a branch of inorganic chemistry that deals with the structure and properties of coordination compounds. These compounds consist of a central metal atom or ion (often called a coordination center) surrounded by molecules or anions, termed ligands. Coordination compounds are notable for their vibrant colors, role in biological systems, and industrial applications such as catalysis.
Ligands are ions or neutral molecules that can have one or more points of attachment to the metal, called donor atoms. They bond to the metal at the coordination sites, creating a coordination sphere. The number of ligand attachments to the central atom is known as the coordination number, which can vary from two to as many as six or even higher in some complexes.
In the exercise provided, we focus on the coordination complex [Mn(NH3)5(NO2)]2+ where the central metal ion is manganese (Mn) with a coordination number of six.
Ligands are ions or neutral molecules that can have one or more points of attachment to the metal, called donor atoms. They bond to the metal at the coordination sites, creating a coordination sphere. The number of ligand attachments to the central atom is known as the coordination number, which can vary from two to as many as six or even higher in some complexes.
Ligands and Coordination Number
The ligands are not just placeholders; they profoundly influence the chemical reactivity and properties of the metal center. For instance, some ligands are strong field, causing a large splitting in the d-orbitals of the metal, while others are weak field, causing less splitting. This affects the magnetic and optical properties of the compound.In the exercise provided, we focus on the coordination complex [Mn(NH3)5(NO2)]2+ where the central metal ion is manganese (Mn) with a coordination number of six.
Metal-Ligand Bonding
Metal-ligand bonding is intrinsic to coordination chemistry. The nature of the bond between the metal and its ligands can significantly impact the stability, color, and reactivity of a coordination compound. Bonds in these complexes are typically categorized as coordinate covalent or dative, where both electrons come from the ligand as it donates them to the empty orbitals of the metal ion.
The strength and character of metal-ligand bonds are influenced by several factors, including:
In our example of [Mn(NH3)5(NO2)]2+, the point of attachment, or the donor atom, changes how the ligand bonds to the metal center. Understanding this metal-ligand interaction is critical when we delve into concepts like linkage isomerism, as changing the bonding site on a ligand can result in different isomers of a complex.
The strength and character of metal-ligand bonds are influenced by several factors, including:
- The charge on the metal ion
- The electronegativity and size of the ligand
- The arrangement and character of the metal's atomic orbitals
In our example of [Mn(NH3)5(NO2)]2+, the point of attachment, or the donor atom, changes how the ligand bonds to the metal center. Understanding this metal-ligand interaction is critical when we delve into concepts like linkage isomerism, as changing the bonding site on a ligand can result in different isomers of a complex.
Isomerism in Coordination Compounds
Isomerism in coordination compounds refers to the occurrence of two or more compounds that have the same formula but a different arrangement of atoms. These different arrangements can lead to varied physical and chemical properties. Linkage isomerism, as showcased in the exercise, is a type of coordination isomerism and occurs when a ligand that can coordinate through more than one atom is bonded in its different binding modes.
Understanding linkage isomerism is essential for the students as it illustrates how different forms of the same molecular formula can exhibit distinctly different chemical behaviors. Discussing the structures visually with accurate diagrams is an effective way to highlight the differences. When students can visualize these concepts, they can better understand the underlying principles of coordination chemistry and isomerism.
Linkage Isomerism
Linkage isomers have the same connectivity between the central metal and the ligands, but the specific donor atom varies. In the exercise [Mn(NH3)5(NO2)]2+, the NO2 can attach via the nitrogen to form a 'nitro' isomer, or via an oxygen to form a 'nitrito' isomer. This subtle change can impact properties like solubility, reactivity, and color.Understanding linkage isomerism is essential for the students as it illustrates how different forms of the same molecular formula can exhibit distinctly different chemical behaviors. Discussing the structures visually with accurate diagrams is an effective way to highlight the differences. When students can visualize these concepts, they can better understand the underlying principles of coordination chemistry and isomerism.