Related Experiment Video
Updated: May 10, 2026

Electroactive Polymer Nanoparticles Exhibiting Photothermal Properties
Published on: January 8, 2016
2,4-Dimeth-oxy-6-[(E)-2-(4-meth-oxy-phenyl)ethen-yl]benzaldehyde.
Xiao-Lin Ge1, Qiu-Xiang Guan, Sheng-Song Deng
1School of Medical Engineering, Hefei University of Technology, Hefei 230009, People's Repulic of China.
Two similar C18H18O4 molecules were identified in the crystal structure. These molecules form a layered arrangement through C-H⋯π interactions, influencing their overall conformation.
Area of Science:
- Crystallography
- Organic Chemistry
- Supramolecular Chemistry
Background:
- Understanding molecular conformation and crystal packing is crucial in solid-state chemistry.
- C-H⋯π interactions are increasingly recognized as important non-covalent forces in molecular self-assembly.
Purpose of the Study:
- To characterize the crystal structure of the title compound, C18H18O4.
- To investigate the conformational properties and intermolecular interactions within the crystal lattice.
Main Methods:
- Single-crystal X-ray diffraction was employed to determine the molecular and crystal structure.
- Analysis of intermolecular contacts, including C-H⋯π interactions, was performed.
Main Results:
- Two conformationally similar molecules of C18H18O4 were found in the asymmetric unit.
- The dihedral angles between benzene rings were measured as 23.54(12)° and 31.11(12)°.
- C-H⋯π interactions with a minimum distance of 2.66 Å linked molecules into a layered structure.
Conclusions:
- The crystal structure reveals specific conformational preferences influenced by benzene ring orientations.
- C-H⋯π interactions play a significant role in directing the self-assembly of C18H18O4 into a layered architecture.
Related Concept Videos
Carboxylic Acids to Methylesters: Alkylation using Diazomethane
Hydrolysis of Chlorobenzene to Phenol: Dow Process
Structure and Nomenclature of Alcohols and Phenols
Alcohols are one of the most important functional groups in organic chemistry. The name of alcohol comes from the hydrocarbon from which it is derived. Alcohols are organic molecules containing the functional hydroxyl or –OH group directly bonded to carbon. Phenols have an OH group directly attached to a benzene ring. While alcohols are colorless, phenol is a white crystalline compound with a characteristic "hospital smell" odor.
As with other organic compounds, alcohols and phenols...
Structure and Nomenclature of Ethers
Ethers are organic compounds with an ether functional group which is characterized by an oxygen atom connected to two — identical or different — alkyl, aryl, or vinyl groups. The C–O–C linkage in dimethyl ether — the simplest ether — has an approximately tetrahedral bond angle of 110.3 degrees. The oxygen atom is sp3- hybridized, with the C–O distance being about 140 pm.
Classification of Ethers
Based on their attached substituent groups, ethers can be classified into two...
Preparation of Epoxides
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Reactions at the Benzylic Position: Oxidation and Reduction

