13815-90-2

Upstream product

• 13731-82-3 2,5-dibromoterephtalic acid 
• 1074-24-4 2,5-dibromo-p-xylene 
• 106-42-3 para-xylene 
• 20871-01-6 2,5-dibromo-4-methylbenzoic acid 
• 63525-48-4 2,5-dibromoterephthalaldehyde 

Downstream Products

• 50880-39-2 2,5-dibromobenzene-1,4-carboxamide 
• 148079-53-2 1-(2,5-Dibromo-4-pentanoyl-phenyl)-pentan-1-one 
• 197370-00-6 (2,5-dibromo-1,4-phenylene)bis((4-butylphenyl)methanone) 
• 421554-39-4 2.5-bis(p-bromobenzoyl)-1,4-dibromobenzene 
• 136296-63-4 2',5'-dibromo-4-decyl-4'-(4-decylbenzoyl)benzophenone 
• 18013-97-3 2,5-dibromo-terephthalic acid diethyl ester 
• 896445-16-2 2-(4-tert-butylphenyl)-5-(2,5-dibromo-4-(5-(4-tertbutylphenyl)-1,3,4-oxadiazol-2-yl)phenyl)-1,3,4-oxadiazole 
• 896445-18-4 C₃₀H₃₂Br₂N₄O₄ 
• 791717-65-2 2,5-dibromoterephthalyldihydrazide 
• 421554-40-7 2,5-bis(p-iodobenzyl)-1,4-diiodobenzene 
• 717883-04-0 1-(4-acetyl-2,5-dibromophenyl)ethanone 
• 1198153-35-3 2,5-dibromo-4-(2,3-dihydro-pyrido[4,3-b][1,4]oxazin-4-carbonyl)-benzoic acid 
• 136296-62-3 2,5-dibromo-1,4-bis(4-tert-butylphenylcarbonyl)benzene 
• 1314743-37-7 2,5-dibromo-1,4-bis[4-(trifluoromethyl)phenylcarbonyl]benzene 

Relevant academic research and scientific papers

Dipolar Quinoidal Acene Analogues as Stable Isoelectronic Structures of Pentacene and Nonacene

Quinoidal thia-acene analogues, as the respective isoelectronic structures of pentacene and nonacene, were synthesized and an unusual 1,2-sulfur migration was observed during the Friedel-Crafts alkylation reaction. The analogues display a closed-shell qui

Preparation and Properties of a Polycyclic p-Quinodimethane with Two Oxygen Bridges and its Radical Cation in Comparison with the Isomeric o-Quinodimethane

We prepared an electron-rich p-quinodimethane compound, 2,9-dibromo-7,14-dimesityl-5,12-dioxapentacene (1). The quinoidal character was clarified by bond-length alternation in the central ring. Clear vibrational structures in both absorption and emission

Synthesis of 5,12-Diazapentacenes and Their Properties

An efficient synthesis via a precursor route to a new class of linear dialkyldiaminoazapentacenes is reported. The synthetic route involves the coupling of 4-substituted aniline derivatives to 2,5-dibromoterephthalonitrile via Buchwald-Hartwig amination f

Rational design of thermally activated delayed fluorescence emitters with aggregation-induced emission employing combined charge transfer pathways for fabricating efficient non-doped OLEDs

The development of luminescent materials simultaneously possessing thermally activated delayed fluorescence (TADF), aggregation-induced emission (AIE), and high luminescence efficiency in the solid state is urgent for fabricating efficient non-doped organ

Stereoisomerism of ladder-type acceptor molecules and its effect on photovoltaic properties

Asymmetrical side chains were widely used in conjugated molecules, but related stereoisomeric phenomenan is rarely investigated. Herein, two stereoisomers based on ladder-type acceptor IDT-BT-R with asymmetrical side chains were synthesized and their prop

Tuning J-aggregate Formation and Emission Efficiency in Cationic Diazapentacenium Dyes

Enhancement of the luminescence efficiency of two new diazapentacenium salts (D1 and D2) of more than 55 for D1 and 22 times for D2) in poor solvents, acetonitrile and/or dichloromethane, was observed and rationalized as formation of emissive J-aggregates. Both compounds displaying 4-n-decylphenyl substituents at the 7,14-carbons and phenyl (D1) or 2,6-difluorophenyl (D2) substituents at the quaternary nitrogen atoms in 5,12-positions have been synthetized in a two-step procedure involving a two-fold Buchwald-Hartwig-type CN cross-coupling and an electrophilic Friedel-Crafts-type cyclization. The optical properties of the dicationic diazapentacenium salts in various solvents and in thin films have been investigated by steady-state and time-resolved absorption and photoluminescence spectroscopies. In thin films and in good solvents, isolated molecules coexist with aggregates. Nonetheless, D1 is seven times more emissive than D2, reflecting a higher J-aggregate contribution in the former.

Thiophenylbenzene derivative as well as preparation method and application thereof Donor material and preparation method thereof

The invention provides a thiophene benzene derivative and a preparation method and application thereof, and a donor material and a preparation method thereof, and belongs to the technical field of organic polymer solar cells. The invention provides 1, 4 -

PREPARING METHOD OF SYNTHESIZING INDACENO DITHIENOTHIOPHENE COMPOUND

Provided is a manufacturing method of synthesizing an indaseno-dithienothiophene compound using, as a novel starting material, a bis(thieno[3,2-b] thiophen-2-yl)-bismethanone derivative. The manufacturing method of synthesizing the indaseno-dithienothiophene compound has an excellent synthetic yield and improves production efficiency.COPYRIGHT KIPO 2020

Fluorescent molecule with changing color induced by ratio of two display static pressures, and preparation method thereof

The invention discloses a fluorescent molecule with a changing color induced by a ratio of two display static pressures, and a preparation method thereof. The chemical structure of the above pressureinduced ratio color-changing material is shown in the de

A carbazole derivative and its preparation and use

The invention discloses a carbazole derivative and its preparation and use, the carbazole derivatives in order to toluene, 2, 5 - two bromine to benzene dicarboxylic acyl chloride and carbazole as raw material successively through the Friedel-crafts acyla