112078-00-9

Upstream product

• 24544-04-5 2,6-diisopropylbenzenamine 
• 156028-26-1 1,6,7,12-tetrachloro-perylene-3,4,9,10-tetracarboxylic acid dianhydride 
• 128-69-8 perylene-3,4,9,10-tetracarboxylic acid 3,4:9,10-dianhydride 
• 4048-33-3 6-amino-1-hexanol 

Downstream Products

• 112078-03-2 N,N'-bis(2,6-diisopropylphenyl)-1,6,7,12-tetra(4-bromophenoxy)perylene-3,4:9,10-tetracarboxylic acid diimide 
• 1172630-55-5 2Cl-diPBI 
• 1172630-54-4 N,N'-2,6-diisopropylphenyl-1,12-dichloroperylene diimide 
• 1173169-94-2 C₆₀H₅₀N₄O₄ 
• 1243652-12-1 C₉₆H₇₆Cl₄N₄O₈ 
• 1243652-13-2 C₁₄₄H₁₁₄Cl₄N₆O₁₂ 
• 112078-08-7 5,6,12,13-tetrakis(4-(tert-butyl)phenoxy)-2,9-bis(2,6-diisopropylphenyl)anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone 
• 951208-58-5 2,9-bis(2,6-diisopropylphenyl)-5,6,12,13-tetrakis(3-methoxyphenoxy)anthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone 

Relevant academic research and scientific papers

Facile synthesis of pure 1,6,7,12-tetrachloroperylene-3,4,9,10-tetracarboxy bisanhydride and bisimide

A robust and scalable procedure to obtain pure 1,6,7,12-tetrachloroperylene-3,4,9,10-tetracarboxy bisanhydride, a highly valuable synthon, has been developed via synthesis of a novel intermediate compound 1,6,7,12-perylene-3,4,9,10-tetracarboxy tetrabutylester.

Fluorofluorescent Perylene Bisimides

Perfluorinated liquids can exhibit immiscibility with organic solvents and water, and provide orthogonal opportunities in chemistry. Examples of emissive dyes that display only fluorous phase solubility are limited, despite the many potential applications. Perylene bisimides are among the most versatile dyes and are known for their outstanding stability and high quantum yields. Herein, we report the synthesis of two new fluorofluorescent perylene bisimide dyes, designed to be soluble in the fluorous phases. These two dyes possess unique photophysical properties, including dramatic increases in fluorescence quantum yields when treated with Bronsted acids as well as aggregation in the fluorous phase.

Synthesis and characterization of fluorescent dyes and their applications for the enhancement of growth rate of Chlorella vulgaris

Spectral conversion of solar radiation from green to red light can enhance the photosynthesis efficiency of microalgae. This can lead to significant increase in microalgal growth. Four perylene-based fluorescent dyes were synthesized to convert wavelengths of light from green (500–570 nm) to orange-red (580–650 nm). These dyes were applied in microalgal cultivation system using two methodologies: (1) light-converting layer, and (2) light-converting medium. The dyes were dissolved in either ethanol or water to form light-converting layers between microalgae culture and the light source. Under converted light in both set-ups, Chlorella vulgaris cultures showed maximum increase in lipid productivity by 13.00% and 17.15%, and biomass productivity by 31.65% and 37.66% compared to the control. Overall, the cultivation results confirmed beneficial effects of modified light on microalgae cultures both on their lipid and biomass productivities. Note that both growth parameters achieved higher performance in the light-converting medium thereby the effectiveness of the cultivation method was validated.

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

A compound. Colorant and colored resin composition

The present invention addresses the problem of providing a colored resin composition capable of forming a color filter excellent in light resistance, a colorant contained in the colored resin composition, and a benzoperylene compound useful as a dye. A co

A SELF EMISSION TYPE COMPOSITION, A COLOR CONVERSION LAYER MANUFACTURED BY USING THEREOF AND A COLOR FILTER COMPRISING THE COLOR CONVERSION LAYER AND DISPLAY DEVICE

In Chemical Formula, and each independently have an integer of, trimethylphenyl, and independently of hydrogen, substituted or unsubstituted linear alkyl 1, substituted or non 1-substituted R1 2 alkyl, 6 - substituted or unsubstituted 2 4 alkyl, 6 - subst

PERYLENE BISIMIDE BASED COMPOUNDS AND DYES COMPRISING THE SAME

The present invention relates to a perylene bisimide-based compound represented by the following chemical formula 1 capable of providing dye having less fluorescence reduction at a high temperature while having excellent solubility in an organic solvent,

COLORED COMPOSITION, COLOR CONVERSION OPTICAL FILTER COMPRISING THE COLORED COMPOSITION, AND DISPLAY DEVICE

Embodiments of the present invention are described below. Provided is a coloring composition for a color conversion optical filter used in a display including white light as a light source, capable of efficiently converting a specific wavelength into a specific wavelength to which a specific backlight light is absorbed, and improving color reproducibility of the display. To solve this problem, the present invention provides the following. Coloring composition for color conversion optical filters used in liquid crystal displays or organic EL displays, wherein the following formula (1) is used. (In the formula (1), A represents the following formulae (1-A) and B: (1-B). In the formula (1-A), R represents a hydrogen atom. 1 To R5 Each independently represents a hydrogen atom or an alkyl group 1 having 10 carbon atoms. In formula (1-B), R represents a hydrogen atom. 6 To R10 Each independently represents a hydrogen atom, a halogen atom, an alkyl group having 1 or 10 carbon atoms, or a methoxy group. However, this is not limited thereto. R6 To R10 A coloring composition, comprising: a perylene compound represented by a substituent represented by a substituent represented by the following general formula; and a binder resin.

Perylenetetracarboxy-3,4:9,10-diimide derivatives with large two-photon absorption activity

Three new perylenetetracarboxy-3,4:9,10-diimides, bearing 2,6-diisopropylphenyl groups at the imide positions and 4-(R-ethynyl)phenoxy moieties (R = 4,7-di(2-thienyl)benzo[c][1,2,5]thiadiazole (P2), pyrene (P3) or pyrene-CH2OCH2 (P4)) at the four bay positions, were prepared, along with the known related derivative (R = phenyl (P1)), and well characterized. They have large two-photon absorption (TPA) cross-sections (σ2), as determined by the Z-scan technique, the highest values being reached with P2 which bears a planar π-delocalized donor moiety. P3 is characterized by higher σ2 values than both P1, as expected for the higher π-conjugation of the donor pyrene moiety with respect to phenyl, and P4, due to the presence of the flexible and non-conjugated CH2OCH2 bridge between the pyrene and the ethynyl fragment in the latter compound. The molecular geometry of P1-P4 has been optimized by DFT modeling, showing that in P2 and P3 the bay substituents are stacked due to the π-π interactions of both pyrene and thiophene groups. The LUMO of P1-P4 lies at the same energy and is essentially delocalized on the perylene core whereas the HOMO and HOMO?1 of both P2 and P3 are degenerate and do not show contribution from the perylene core contrarily to that of P1 and P4. The HOMO-LUMO gap is therefore essentially influenced by the HOMO which reflects the electronic charge delocalization on the bay substituents, the lower gaps being observed for P2 and P3, which are characterized by the best TPA properties.

A DYE DISPERSION COMPOSITION, A SELF EMISSION TYPE PHOTOSENSITIVE RESIN COMPOSITION, A COLOR CONVERSION LAYER, A COLOR FILTER COMPRISING, AND A DISPLAY DEVICE

The invention provides a dye dispersion liquid composition, a self-luminous photosensitive resin composition, a color conversion layer, a color filter and a display device. The dye dispersion composition includes (A) a fluorescent dye having a solubility