1262-52-8

Usage

Uses

Used in Biological Research and Imaging:
2,2'-Bis[4-(dimethylamino)phenyl]-2,2'-bi[indan]-1,1',3,3'-tetrone is used as a fluorescent dye for labeling biomolecules and monitoring cellular processes in fluorescence microscopy, flow cytometry, and live-cell imaging. Its high photostability and unique properties make it suitable for these applications.
Used in Organic Electronic Devices:
2,2'-Bis[4-(dimethylamino)phenyl]-2,2'-bi[indan]-1,1',3,3'-tetrone is studied for its potential in the development of organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic solar cells, due to its unique optical and electronic properties.
Used in Solar Cell Applications:
2,2'-Bis[4-(dimethylamino)phenyl]-2,2'-bi[indan]-1,1',3,3'-tetrone is also being investigated as a sensitizing dye in solar cell applications, where it can potentially enhance the efficiency and performance of these devices by improving light absorption and charge transport.

Upstream product

• 1225-30-5 2-<4-(N,N-dimethylamino)phenyl>indane-1,3-dione 
• 56479-60-8 2-(p-(dimethylamino)phenyl)indane-1,3-dion-2-yl radical 
• 158139-98-1 2-(4-Dimethylamino-phenyl)-2λ³-indan-1,3-dione 

Downstream Products

• 56479-60-8 2-(p-(dimethylamino)phenyl)indane-1,3-dion-2-yl radical 
• 158139-98-1 2-(4-Dimethylamino-phenyl)-2λ³-indan-1,3-dione 

Relevant academic research and scientific papers

Regularities of reversible radical dissociation in liquid crystals

The effect of liquid-crystalline ordering of alkylcyanobiphenyls on the thermodynamic parameters of reversible dissociation of the dimeric 2,2′-bis[2-(p-dimethylaminophenyl)indane-1,3-dione] to the 2-(p-dimethylaminophenyl)indane-1,3-diyl radicals was found. The angular dependence of the ESR spectra of the radicals in the smectic mesophase is related to their orientation along the liquid crystal director.

The influence of liquid crystal ordering on reversible radical dissociation

The influence of liquid crystal ordering in nematic, smectic and Isotropic phases on thermodynamic parameters of a reversible thermal dissociation of dimeric 2,2-bis[2-(p-dimethylaminophenyl)indan-1,3-dione] into two stables 2-(p-dimethylaminophenyl)indan-l,3-dione-2-yl radicals was investigated.

Sterically Hindered Free Radicals. Part 22. Dimerization and EPR Spectroscopy of Indanedionyl and 9-Acylfluorenyl Radicals

2-Phenylindanedionyl radicals 5a, their p- and o-monosubstituted derivatives and related compounds 5b-h recombine by C-C bond formation giving 6a-h.In contrast, o-substituted derivatives 5i-k and the 2-tert-butylindanedionyl radicals 5l react to give the

INFLUENCE OF ONIUM SUBSTITUENT IN PHTHALOYL RING ON THERMODYNAMIC PARAMETERS OF EQUILIBRIUM BETWEEN DIMER AND FREE RADICALS OF 2-(4-DIMETHYLAMINOPHENYL)-1,3-INDANDIONES

2,2'-Bis diperchlorate and 2,2'-bis diperchlorate have very definite thermochromic and mechanochromic properties, owing to reversible dissociation into free radicals.The rupture energy of the central bond C2-C2' in 5-substituted 2,2'-bis in acetonitrile is 63-75 kJ/mole; in the dimer with the bulky 5-(2,4,6-triphenylpyridinium) substituent, the rupture energy is 51 kJ/mole.The equilibrium constants follow the Hammett equation (? = 1.53, acetonitrile, 293 K).Radicals with onium substituents are thermodynamically the most stable of the arylindandionyl radicals that are thus far known, owing to the significant contribution of electrostatic interactions.