116287-98-0

Usage

General Description

1,10-Phenanthroline, 2,9-bis(4-methylphenyl)- is a chemical compound with two 4-methylphenyl groups attached to the 2 and 9 positions of the phenanthroline molecule. 1,10-Phenanthroline, 2,9-bis(4-methylphenyl)- is often used as a chelating ligand in coordination chemistry, where it can form stable complexes with metal ions. Its ability to form complexes with metals makes it a valuable compound for use in various chemical and biological applications, such as in the fields of catalysis, bioinorganic chemistry, and materials science. Additionally, 1,10-Phenanthroline, 2,9-bis(4-methylphenyl)- has been studied for its potential applications in the development of new materials and as a precursor for the synthesis of other organic compounds.

Upstream product

• 624-31-7 4-tolyl iodide 
• 5144-89-8 1,10-phenanthroline hydrate 
• 2417-95-0 p-tolyllithium 
• 66-71-7 1,10-Phenanthroline 

Downstream Products

• 116288-00-7 Propionic acid 4-[9-(4-formyl-phenyl)-[1,10]phenanthrolin-2-yl]-benzyl ester 
• 120085-99-6 2,9‐bis(4-formylphenyl)‐1,10‐phenanthroline 
• 259251-55-3 (2-p-anisyl-9-(4-methyl-2-pyridyl)-1,10-phenanthroline)(2,9-bis(p-tolyl)-1,10-phenanthroline)ruthenium(II) hexafluorophosphate 
• 259251-57-5 (2,6-bis(3-isoquinolyl)-(4-tolyl)pyridine)(2,9-bis(p-tolyl)-1,10-phenanthroline)ruthenium(II) hexafluorophosphate 
• 190973-64-9 (4'-tolyl-2,2',6',2''-terpyridine)(2,9-bis(p-tolyl)-1,10-phenanthroline)ruthenium(II) hexafluorophosphate 
• 190973-71-8 (C₁₅N₃H₁₀C₆H₄CH₃)Ru(CH₃C₆H₄C₁₂N₂H₆C₆H₃CH₃)⁽¹⁺⁾*PF₆^(1-)*CH₃CN=C₁₅N₃H₁₀C₆H₄CH₃RuCH₃C₆H₄C₁₂N₂H₆C₆H₃CH₃PF₆*CH₃CN 
• 1065070-91-8 C₃₂H₂₈N₂O₄ 
• 157523-11-0 2,9-bis(p-hydroxymethylphenyl)-1,10-phenanthroline 
• 116287-99-1 2-(4-Bromomethyl-phenyl)-9-(4-dibromomethyl-phenyl)-[1,10]phenanthroline 
• 136003-83-3 2,9-bis-4-(bromomethylphenyl)-1,10-phenanthroline 
• 120085-98-5 2,9-bis(4-(dibromomethyl)phenyl)-1,10-phenanthroline 
• 136059-96-6 {(2,9-bis(4-methylphenyl)-1,10-phenanthroline)2copper}tetrafluoroborate 
• 136088-30-7 3Cu⁽¹⁺⁾*C₆H₃(CH₂)3O₃(C₆H₄C₁₂N₂H₆C₆H₄)3O₃(CH₂)3C₆H₃*3C₁₂H₆N₂(C₆H₄CH₃)2*3BF₄^(1-)*3H₂O 

Relevant academic research and scientific papers

Self-assembling, chromogenic receptors for the recognition of medically important substrates and their method of use

A chromogenic receptor comprises a self-assembled chromogenic compound having at least one intrinsic binding site. The chromogenic compound is characterized by the property of producing a reversible color change responsive to binding a target substrate to

Synthesis of bis-porphyrins containing a 2,9-diphenyl-1,10-phenanthroline spacer

The synthesis of bis-porphyrins disposed in an oblique fashion is described. The tetrapyrrole rings are linked via a 2,9-diphenyl-1,10-phenanthroline spacer. Two routes have been investigated: a step wise procedure and a direct strategy involving a double cyclisation step. From the bis-free base porphyrin, synthesized with an overall yield of 1% from 2,9-di(p-tolyl)-1,10-phenanthroline, an unsymmetrical zinc (II) porphyrin free base system was prepared and isolated in view of excited state energy and electron transfer.

SYNTHESIS OF AN OBLIQUE BIS-PORPHYRIN SYSTEM CONTAINING A 1,10-PHENANTHROLINE SPACER

A molecule consisting of two porphyrin rings (free base or Zn complex) rigidly held by a 1,10-phenanthroline nucleus has been made ; the centre-to-centre separation is about 13 angstroem.