When Alfred Werner was developing the field of coordination chemistry, it was argued by some that the optical activity he observed in the chiral complexes he had prepared was due to the presence of carbon atoms in the molecule. To disprove this argument, Werner synthesized a chiral complex of cobalt that had no carbon atoms in it, and he was able to resolve it into its enantiomers. Design a cobalt(III) complex that would be chiral if it could be synthesized and that contains no carbon atoms. (It may not be possible to synthesize the complex you design, but we will not worry about that for now.)

Short Answer

Expert verified
A possible chiral cobalt(III) complex that contains no carbon atoms is [Co(NH3)3Cl3]. This complex exhibits chirality due to different spatial arrangements of NH3 and Cl- ligands around the central cobalt ion. The complex has an octahedral geometry with a coordination number of 6, and its enantiomers are non-superimposable mirror images, emphasizing the presence of chirality.

Step by step solution

01

Understanding chirality

Chirality is a property of molecules where a molecule and its mirror image are non-superimposable, similar to left and right hands. Chiral molecules have one or more centers of chirality, usually a stereogenic carbon atom is involved with four different substituents (i.e., groups attached to the atom). However, metal complexes can also exhibit chirality, even though they may not contain stereogenic carbon atoms. A chiral metal complex typically involves a coordination number of four or higher.
02

Understanding cobalt(III) complex

A cobalt(III) complex refers to a metal complex containing a central cobalt ion in the oxidation state of +3, Co(III), bonded to other atoms or groups, which are known as ligands. The coordination number is the number of bonds between the central ion and its ligands.
03

Designing a chiral cobalt(III) complex

Since the desired complex must have no carbon atoms, we will focus on creating a chiral cobalt(III) complex with halide ligands or other inorganic ligands. Remember, the coordination number must be four or higher for the complex to exhibit chirality. In this context, the octahedral geometry (coordination number 6) seems to be the most suitable geometry. A possible chiral cobalt(III) complex to be synthesized would be [Co(NH3)3Cl3]. In this complex, the central cobalt(III) ion is bonded to three ammonia ligands (NH3) and three chloride ligands (Cl-). Overall, the complex is a neutral octahedral species and is chiral due to the different arrangement of NH3 and Cl- ligands around the cobalt center. Please note that the complex is hypothetical and may not be synthesized in reality.
04

Visualization of the chiral cobalt(III) complex

It could be helpful to draw the structure of the chiral [Co(NH3)3Cl3] complex, emphasizing the octahedral arrangement of the ligands. To visualize the chirality, you can draw both enantiomers, non-superimposable mirror images. In conclusion, a possible chiral cobalt(III) complex that contains no carbon atoms is [Co(NH3)3Cl3]. This complex exhibits chirality due to different spatial arrangements of NH3 and Cl- ligands around the central cobalt ion.

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Most popular questions from this chapter

Metallic elements are essential components of many important enzymes operating within our bodies. Carbonic anhydrase, which contains \(\mathrm{Zn}^{2+}\) in its active site, is responsible for rapidly interconverting dissolved \(\mathrm{CO}_{2}\) and bicarbonate ion, \(\mathrm{HCO}_{3}^{-}\). The zinc in carbonic anhydrase is tetrahedrally coordinated by three neutral nitrogencontaining groups and a water molecule. The coordinated water molecule has a \(\mathrm{p} K_{a}\) of \(7.5,\) which is crucial for the enzyme's activity. (a) Draw the active site geometry for the \(\mathrm{Zn}(\mathrm{II})\) center in carbonic anhydrase, just writing "N" for the three neutral nitrogen ligands from the protein. (b) Compare the \(\mathrm{p} K_{a}\) of carbonic anhydrase's active site with that of pure water; which species is more acidic? (c) When the coordinated water to the \(\mathrm{Zn}(\mathrm{II})\) center in carbonic anhydrase is deprotonated, what ligands are bound to the \(\mathrm{Zn}(\mathrm{II})\) center? Assume the three nitrogen ligands are unaffected. \((\mathbf{d})\) The \(\mathrm{p} K_{a}\) of \(\left[\mathrm{Zn}\left(\mathrm{H}_{2} \mathrm{O}\right)_{6}\right]^{2+}\) is \(10 .\) Suggest an explanation for the difference between this $\mathrm{p} K_{a}$ and that of carbonic anhydrase. (e) Would you expect carbonic anhydrase to have a deep color, like hemoglobin and other metal-ion-containing proteins do? Explain.

(a) If a complex absorbs light at \(610 \mathrm{nm},\) what color would you expect the complex to be? (b) What is the energy in joules of a photon with a wavelength of \(610 \mathrm{nm}\) ? (c) What is the energy of this absorption in \(\mathrm{kJ} / \mathrm{mol} ?\)

Sketch the structure of the complex in each of the following compounds and give the full compound name: (a) $c i s-\left[\operatorname{PtBr} \mathrm{Cl}\left(\mathrm{NO}_{2}\right)_{2}\right]^{2-}$ (b) $\left[\mathrm{Mn}(\mathrm{CO})_{3}\left(\mathrm{C}_{6} \mathrm{H}_{6}\right)\right]^{+}$ (c) $\left.c i s-\left[\mathrm{Cr} \mathrm{Cl}_{4}\right)\left(\mathrm{OH}_{2}\right)_{2}\right]^{-}$ (d) trans-[Co(OH)(en) \(\left._{2} \mathrm{Cl}\right]^{+}\)

For each of the following pairs, identify the molecule or ion that is more likely to act as a ligand in a metal complex: (a) carbonic acid \(\left(\mathrm{H}_{2} \mathrm{CO}_{3}\right)\) or carbonate \(\left(\mathrm{CO}_{3}^{2-}\right),(\mathbf{b})\) water $\left(\mathrm{H}_{2} \mathrm{O}\right)\( or hydronium ion \)\left(\mathrm{H}_{3} \mathrm{O}^{+}\right),(\mathbf{c})\( phosphine \)\left(\mathrm{PH}_{3}\right)$ or phosphoric acid \(\left(\mathrm{H}_{3} \mathrm{PO}_{4}\right)\).

Write out the ground-state electron configurations of (a) \(\mathrm{Sc}^{2+}\) (b) \(\mathrm{Mo}^{2+}\) (c) \(\mathrm{Rh}^{3+}\), (d) \(\mathrm{Fe}^{3+}\).

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