Question

Tetracyanoethene in benzene forms an orange solution, but when this solution is mixed with a solution of anthracene in benzene, a brilliant blue-green color is produced, which fades rapidly; colorless crystals of a compound of composition \(\mathrm{C}_{14} \mathrm{H}_{10} \cdot \mathrm{C}_{2}(\mathrm{CN})_{4}\) then are depositied. Explain the color changes that occur and write a structure for the crystalline product.

Short answer

The color changes are due to a charge-transfer complex between anthracene and TCNE. The crystalline product is a 1:1 complex \\( \mathrm{C}_{14} \mathrm{H}_{10} \cdot \mathrm{C}_{2}(\mathrm{CN})_{4}\\).

Step-by-step solution

Identify Initial Solutions

Begin by examining the two solutions involved: Tetracyanoethene in benzene, which forms an orange solution, and anthracene in benzene, which is a colorless solution.

Formation of Charge-Transfer Complex

When these two solutions are mixed, a charge-transfer complex forms between tetracyanoethene (TCNE) and anthracene. The interaction between the electron-rich anthracene and the electron-poor TCNE results in a brilliant blue-green color.

Color Change Mechanism

The brilliant blue-green color is due to electronic transitions in the charge-transfer complex, and this color fades rapidly as the complex reacts chemically to form a more stable product.

Formation of the Crystalline Product

As the complex reacts further, it forms a stable, colorless crystalline product. The composition of the deposit is given by the molecular formula \( \mathrm{C}_{14} \mathrm{H}_{10} \cdot \mathrm{C}_{2}(\mathrm{CN})_{4} \), indicating a 1:1 complex between anthracene and tetracyanoethene.

Structure of the Crystalline Product

The crystalline product involves anthracene acting as a donor molecule and TCNE as an acceptor, forming a 1:1 complex. The structure likely features stacking interactions between the planar molecules of anthracene and TCNE, stabilizing the formation as colorless crystals.

Key concepts

Tetracyanoethene

Tetracyanoethene (TCNE) is a fascinating molecule that plays an important role in the formation of charge-transfer complexes. TCNE is known for its electron-deficient nature due to the presence of four electron-withdrawing cyano groups attached to its ethene backbone. This characteristic makes it an excellent electron acceptor.

When TCNE is dissolved in benzene, it forms an orange solution. This color arises from electronic transitions within the TCNE molecules as they interact with light. The orange color is a result of the presence of conjugated double bonds and cyano groups that absorb specific wavelengths of light.

• TCNE acts as an electron acceptor due to its structure.
• Its interaction with anthracene leads to new color changes.
• The interaction of TCNE with other species can significantly alter the solution's color.

Understanding the behavior of TCNE is essential for studying charge-transfer complexes and their subsequent reactions.

Anthracene

Anthracene is an important organic compound, famous for its three fused benzene rings, making it a part of the polycyclic aromatic hydrocarbons (PAHs). Its structure contributes to its electron-rich nature, making it an excellent electron donor in chemical reactions.

When anthracene is dissolved in benzene, it results in a colorless solution, unlike TCNE. However, the intriguing chemistry begins when anthracene encounters an electron-poor species such as TCNE.

• Anthracene's electron-rich property makes it readily form complexes with electron acceptors like TCNE.
• Its structure allows for efficient electronic transitions, leading to visible color changes in reactions.
• In charge-transfer reactions, anthracene acts as a donor, enabling the formation of colorful complexes.

Studying anthracene's role in reactions enriches our understanding of electron transfer dynamics in chemical complexes.

Color Changes in Chemical Reactions

Color changes during chemical reactions can provide valuable information about the processes occurring at the molecular level. In the reaction involving TCNE and anthracene, the initial mixing creates a brilliant blue-green color. This striking color is due to the formation of a charge-transfer complex between the two components.

These complexes result from the transfer of electrons from the electron-rich anthracene to the electron-deficient TCNE. The blue-green color arises from specific electronic transitions within this newly formed complex. However, this color is not stable and fades quickly.

• The fading of the color indicates further chemical changes, ultimately leading to a more stable product.
• Such color transitions are indicative of path and progress of chemical reactions.
• Understanding these transitions help in identifying the stages of the reaction and formation of products.

Observing these color changes can signal the completion of reactions and the formation of new bonds or complexes.

Crystalline Product Structure

The final stage in the reaction between TCNE and anthracene is the formation of a crystalline product. This occurs after the initial color changes have faded, leaving behind colorless crystals with a composition of \( \mathrm{C}_{14} \mathrm{H}_{10} \cdot \mathrm{C}_{2}(\mathrm{CN})_{4} \).

These crystals are the result of a stable 1:1 complex formed through stacking interactions between the planar structures of anthracene and TCNE. Here, anthracene typically acts as the electron donor and TCNE as the electron acceptor.

• The crystalline product is indicative of the stability achieved post-reaction.
• Stacking interactions between the molecules contribute to the stability and structure of the crystals.
• Understanding the structural properties of these crystalline complexes is key in material science and chemistry.

The orderly arrangement in the crystal lattice results in a stable and definitive structure, which can have applications in developing new materials with unique properties.