95942-95-3

Usage

Uses

Used in Analytical Chemistry:
1,10-Phenanthroline, 3,8-diphenylis used as a chelating agent for forming stable complexes with metal ions. These complexes are valuable in analytical chemistry for detecting and quantifying metal ions in various samples.
Used in Catalysis:
In the field of catalysis, 1,10-Phenanthroline, 3,8-diphenylis employed to form complexes with metal ions that can act as catalysts, enhancing the rate of chemical reactions and improving the efficiency of industrial processes.
Used in Material Science:
1,10-Phenanthroline, 3,8-diphenylis also utilized in material science, where its metal complexes can be integrated into the development of new materials with specific properties, such as conductivity, magnetism, or optical characteristics.
Used in Organic Synthesis:
1,10-Phenanthroline, 3,8-diphenylserves as a key intermediate in the synthesis of various organic compounds, contributing to the advancement of organic chemistry and the creation of novel molecules with potential applications.
Used as a Fluorescent Probe:
1,10-Phenanthroline, 3,8-diphenylis used as a fluorescent probe for studying interactions between DNA and proteins. Its fluorescence properties allow researchers to monitor and analyze these interactions, providing valuable insights into biological processes.
Used in Antimicrobial Applications:
1,10-Phenanthroline, 3,8-diphenylhas been investigated for its potential antimicrobial properties, which could be harnessed in the development of new antimicrobial agents to combat resistant bacteria and other pathogens.
Used in Anticancer Applications:
1,10-Phenanthroline, 3,8-diphenylis also being explored for its potential anticancer properties, with the aim of developing new therapeutic strategies to treat various types of cancer.
Overall, 1,10-Phenanthroline, 3,8-diphenylis a versatile compound with a wide range of applications across different scientific and technological fields, from analytical chemistry and catalysis to material science, organic synthesis, and biological research.

Upstream product

• 39588-59-5 3,6,7,9-tetrahydro-5H-<1,4>diazepino<1,2,3,4-lmn><1,10>phenanthroline-3,9-dione 
• 1422669-86-0 2,9-dichloro-3,8-diphenyl-1,10-phenanthroline 
• 71-43-2 benzene 
• 1422669-63-3 2,10-diphenyl-6,7-dihydro-3H-[1,4]diazepino[1,2,3,4-lmn][1,10]phenanthroline-3,9(5H)-dione 
• 15302-99-5 6,7-dihydro-5H-[1,4]diazepino[1,2,3,4-l,m,n][1,10]phenanthroline-4,8-diium dibromide 
• 66-71-7 1,10-Phenanthroline 
• 208054-16-4 4,7-dibromo-3,8-diphenyl-[1,10]phenanthroline 
• 100125-12-0 3,8-dibromo-1,10-phenathroline 
• 98-80-6 phenylboronic acid 
• 17838-69-6 ethyl 3-oxo-2-phenylpropanoate 

Relevant academic research and scientific papers

Europium(III) complex fluorescent sensor for dual channel recognition of Sn2+ and Cu2+ ions in water

A new europium(III) complex Eu(tta)3L1 (1a) (L1 = (2-(3,5-dimethoxyphenyl)-1H-imidazo[4,5-f][1,10]phenanthroline), tta = 2-thenoyltrifluoroacetone) has been prepared and synthesized. The structure of complex was completely

The Heteroleptic Cu(I) Photosensitizer-Containing 3,8-Disubstituted Phenanthroline: Synthesis, Photophysical Properties and Photocatalytic Hydrogen Evolution from Water

Four novel heteroleptic Cu(I) photosensitizers with 3,8-diaryl-2,9-diisopropyl-1,10-phenanthroline derivatives as electron-donating bidentate N-ligands have been designed and synthesized. The metal copper complexes are studied in light-driven water reduct

Linear o-phenanthroline compound and preparation method and application thereof

The invention belongs to the field of catalytic chemistry, and particularly relates to a linear o-phenanthroline compound and a preparation method and application thereof. The preparation method of alinear o-phenanthroline bidentate nitrogen ligand as sho

Direct arylation of phenanthroline derivatives via oxidative C-H/C-H cross-coupling: Synthesis and discovery of excellent ligands

A concise synthetic protocol for aryl functionalized phenanthrolines has been developed. It was demonstrated that 3,8-diphenyl-1,10-phenanthroline (7a) is competent in promoting transition-metal-free direct arylation and 2,3,8,9-tetraphenyl-1,10-phenanthroline (8a) is a highly efficient ligand in the in situ Pd-catalysed Heck reaction.

Synthesis and characterization of novel rhenium (I) complexes with large Stokes shift for applications in organic electroluminescent devices

Two novel tricarbonyl rhenium(I) (Re(I)) complexes with versatile building block (1,10-phenanthroline), i.e., Re-PPhen and Re-FPPhen (PPhen, 3,8-diphenyl-1,10-phenanthroline; FPPhen, 3,8-bis(4-fluorophenyl)-1,10- phenanthroline), were designed, synthesize

Iron-catalyzed asymmetric epoxidation of β,β-disubstituted enones

The combination of Fe(OTf)2 and novel phenanthroline ligands enables the catalytic asymmetric epoxidation of acyclic β,β- disubstituted enones, which have been a heretofore inaccessible substrate class. The reaction provides highly enantioenriched α,β-epoxyketones (up to 92% ee) that can be further converted to functionalized β-ketoaldehydes with an all-carbon quaternary center.