Related Experiment Video
Updated: May 26, 2026

A Two-Step Protocol for Umpolung Functionalization of Ketones Via Enolonium Species
Published on: August 16, 2018
2-[(Pyridin-3-yl-amino)-meth-yl]phenol
This study details the crystal structure of a novel organic compound, C(12)H(12)N(2)O. The molecule exhibits significant twisting between aromatic rings and forms a layered structure through specific hydrogen bonding interactions.
Area of Science:
- Crystallography
- Organic Chemistry
- Supramolecular Chemistry
Background:
- Understanding molecular conformation and intermolecular interactions is crucial in crystal engineering.
- Organic compounds with amino and hydroxyl groups can participate in diverse hydrogen bonding networks.
Purpose of the Study:
- To elucidate the crystal structure and hydrogen bonding patterns of the title compound, C(12)H(12)N(2)O.
- To investigate the role of substituents in directing crystal packing and supramolecular assembly.
Main Methods:
- Single-crystal X-ray diffraction analysis was employed to determine the three-dimensional molecular structure.
- Analysis of hydrogen bonding interactions and their influence on crystal architecture.
Main Results:
- The crystal structure reveals a significant twist (68.79°) between the aromatic rings linked by a -CH(2)-NH- group.
- The hydroxyl group acts as both a hydrogen bond donor and acceptor, forming chains along the b axis and contributing to a layered structure.
Conclusions:
- The specific arrangement of functional groups dictates the observed supramolecular architecture.
- The hydrogen bonding network in C(12)H(12)N(2)O leads to the formation of a distinct layer structure in the solid state.
More Related Videos
06:46Facile Preparation of (2Z,4E)-Dienamides by the Olefination of Electron-deficient Alkenes with Allyl Acetate
Published on: June 21, 2017
10:42Preparation of N-(2-alkoxyvinyl)sulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines
Published on: January 3, 2018
Related Concept Videos
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...
Acidity and Basicity of Alcohols and Phenols
Benzene to Phenol via Cumene: Hock Process
Physical Properties of Alcohols and Phenols
Alcohols possess a higher boiling point than aliphatic hydrocarbons of similar...
Hydrolysis of Chlorobenzene to Phenol: Dow Process
Oxidation of Phenols to Quinones
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox property is crucial in...