946612-29-9

Upstream product

• 103-67-3 benzyl-methyl-amine 
• 156028-26-1 1,6,7,12-tetrachloro-perylene-3,4,9,10-tetracarboxylic acid dianhydride 
• 618-36-0 rac-methylbenzylamine 

Downstream Products

• 949464-61-3 N,N'-bis(α-methylbenzyl)-1,6,7,12-tetrakis(4-methoxyphenoxy)perylene-3,4:9,10-tetracarboxylic acid bisimide 
• 1391904-02-1 C₅₂H₃₀Cl₂N₂O₆ 
• 946612-28-8 N,N'-bis(α-methylbenzyl)-1,6,7,12-tetrafluoroperylene-3,4:9,10-tetracarboxylic acid bisimide 

Relevant academic research and scientific papers

Fluorinated rylenetetracarboxylic acid derivatives and use thereof

The present invention relates to fluorinated rylenetetracarboxylic acid derivatives, to a process for their preparation and to their use, especially as n-type semiconductors.

Fluorescent J-aggregates of core-substituted perylene bisimides: Studieson structure-property relationship, nucleation-elongation mechanism, an d sergeants-and-soldiers principle

A series of highly soluble and fluorescent, at core tetraaryloxy- substituted and in imide positions hydrogen atom containing perylene bisimide (PBI) dyes 1a-e with varying peripheral side chains have been synthesized and thoroughly characterized. The sel

Synthetic routes to core-fluorinated perylene bisimide dyes and their properties

Numerous core-fluorinated perylene bisimide (PBI) dyes with various substituents at the imide positions have been synthesized by different methods. Core-difluorinated PBIs 4a-f are obtained by imidization of difluoro-substituted perylene bisanhydride 1 wi

Supramolecular construction of fluorescent J-aggregates based on hydrogen-bonded perylene dyes

(Figure Presented) Luminous nanorods: The self-assembly of core-twisted perylene bisimide fluorophores (see structures) in nonpolar organic solvents is directed by hydrogen-bonding interactions. This supermolecular concept resulted in one-dimensional J-ag