94211-97-9

Usage

Chemical class

Phenanthroline derivative

Common use

Chelating agent in analytical chemistry

Function

Selectively bind and separate metal ions

Structure

Phenanthroline core with a 4-(4-methylphenyl) group attached to one nitrogen atom

Chemical and physical properties

Influenced by the presence of the methylphenyl group

Applications

Coordination chemistry, catalysis, and material science

Utilization

Development of sensors, fluorescent probes, and synthesis of complex organic molecules

Upstream product

• 578-66-5 8-amino quinoline 
• 22422-21-5 4'-methyl-3-chloropropiophenone 

Relevant academic research and scientific papers

Synthesis, characterization, and a proton NMR study of topologically chiral copper(I) [2]-catenates and achiral analogues

Cu(I) catenates and the corresponding metal-free catenands in which one or both constitutive rings are oriented have been synthesized and characterized. Ring orientation is achieved by an appropriate substitution on the phenanthroline core of the macrocyc

Luminescent Metal Complexes. Part 5. Luminescence Properties of Ring-substituted 1,10-Phenanthroline Tris-complexes of Ruthenium(II)

The absorption characteristics, emission spectra, luminescent quantum yields, and lifetimes are reported for 24 ruthenium(II) tris-1,10-phenanthroline complexes in EtOH-MeOH solution.Quantum yields fall between 0.019 and 0.403, the highest values being re