937040-91-0

Upstream product

• 112100-07-9 bis(2,6-diisopropylphenyl)-5,6,12,13-tetraphenoxyanthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H, 9H)-tetraone 
• 24544-04-5 2,6-diisopropylbenzenamine 
• 937041-68-4 N-(2,6-diisopropylphenyl)-1,6,7,12-tetraphenoxyperylene-3,4:9,10-tetracarboxy-9,10-monoanhydride-3,4-monoimide 

Downstream Products

• 1039429-97-4 N-(2,6-diisopropylphenyl)-N'-(2-aminoethyl)-1,6,7,12-tetraphenoxyperylene-3,4:9,10-tetracarboxydiimide 
• 1039429-98-5 N-(2,6-diisopropylphenyl)-N'-(2-carboxyethyl)-1,6,7,12-tetraphenoxyperylene-3,4:9,10-tetracarboxydiimide 
• 1093664-54-0 N-(2,6-diisopropylphenyl)-N'-(2-(1,3-dicarboxypropyl))-1,6,7,12-tetraphenoxyperylene-3,4:9,10-tetracarboxdiimide 

Relevant academic research and scientific papers

Kinetically Trapped Supramolecular Assembly of Perylene Dianhydride Derivative in Methanol: Optical Spectra, Morphology, and Mechanisms

Supramolecular self-assembly has attracted increasing attention as a breakthrough methodology in the fields of nanoscience and nanotechnology. Herein, a perylene dianhydride derivative (TP-PDA) self-assembles into well-defined nanospheres through a nuclea

Synthesis and use of clickable bay-region tetrasubstituted perylene tetracarboxylic tetraesters and a perylene monoimide diester as energy acceptors

Two novel bay-region chlorine- or phenoxy-substituted perylene tetracarboxylic tetrapropargylesters (PTTEs) and a phenoxy-substituted perylene monoimide dipropargylester (PMIDE) were synthesized, photophysically characterized, and decorated with energy donating coumarin chromophores by means of microwave-assisted Cu(I)-catalyzed 1,3-dipolar cycloaddition reactions.

Water-soluble rylene dyes, methods for preparing the same and uses thereof as fluorescent labels for biomolecules

The present invention relates to novel rylene diimide compounds, a method for preparing said compounds, the use of said compounds as fluorescent label for biomolecules as well as a method for purifying bioconjugates.

Water-soluble monofunctional perylene and terrylene dyes: Powerful labels for single-enzyme tracking

All in one: Exceptionally photostable, highly fluorescent, water-soluble, and monofunctional perylene and terrylene dyes bearing reactive groups for covalent attachment to biomolecules have been synthesized (see picture). Single-molecule enzyme tracking r

Use of Rylene Derivatives as Photosensitizers in Solar Cells

Use of rylene derivatives I with the following definition of the variables: X together both —COOM; Y a radical -L-NR1R2 ??(y1) -L-Z-R3 ??(y2) the other radical hydrogen; together both hydrogen; R is optionally substituted (het)aryloxy, (het)arylthio; P is —NR1R2; B is alkylene; optionally substituted phenylene; combinations thereof; A is —COOM; —SO3M; —PO3M2; D is optionally substituted phenylene, naphthylene, pyridylene; M is hydrogen; alkali metal cation; [NR5]4+; L is a chemical bond; optionally indirectly bonded, optionally substituted (het)arylene radical; R1, R2 are optionally substituted (cyclo)alkyl, (het)aryl; together optionally substituted ring comprising the nitrogen atom; Z is —O—; —S—; R3 is optionally substituted alkyl, (het)aryl; R′ is hydrogen; optionally substituted (cyclo)alkyl, (het)aryl; R5 is hydrogen; optionally substituted alkyl (het)aryl; m is 0, 1, 2; n, p m=0: 0, 2, 4 where: n+p=2, 4, if appropriate 0; m=1: 0, 2, 4 where: n+p=0, 2, 4; m=2: 0, 4, 6 where: n+p=0, 4, 6, or of mixtures thereof as photosensitizers in solar cells.