152269-98-2

Usage

Uses

1. Used in the Electronics Industry:
1,4-Dibromo-2,5-bis(decyloxy)benzene is used as an intermediate in the production of new, efficient blue light-emitting polymers for light-emitting diodes (LEDs). Its unique molecular structure contributes to the development of advanced materials with improved light-emitting properties, enhancing the performance and efficiency of LED devices.
2. Used in the Chemical Synthesis Industry:
As an intermediate compound, 1,4-dibromo-2,5-bis(decyloxy)benzene can be utilized in the synthesis of various other organic compounds and materials. Its bromine and decyloxy functional groups make it a versatile building block for creating a wide range of products with different applications in the chemical industry.
3. Used in the Research and Development Sector:
Due to its unique structure and potential applications, 1,4-dibromo-2,5-bis(decyloxy)benzene is also used in research and development for exploring new chemical reactions, material properties, and potential uses in various fields. This includes the development of new polymers, pharmaceuticals, and other advanced materials.

Upstream product

• 112-29-8 1-bromo dodecane 
• 14753-51-6 2,5-dibromohydroquinone 
• 123-31-9 hydroquinone 
• 129236-97-1 1,4-bis(decyloxy)benzene 

Downstream Products

• 850446-24-1 2,5-didecyloxy-1,4-bis(4-formylphenyl)benzene 
• 1334177-77-3 (4-bromo-2,5-bis(decyloxy)phenyl)boronic acid 
• 1600515-41-0 1,4-bis(2',2-dithienyl)-2,5-bis(decyloxy)benzene 

Relevant academic research and scientific papers

New efficient blue light emitting polymer for light emitting diodes

The synthesis, by the Suzuki coupling reaction, of a novel soluble blue light emitting polymer, poly{(9,9-dihexyl-2,7-fluorene-alt-co-[2,5-bis(decyloxy)-1,4-phenylene]} (PDHFDDOP) is reported. PDHFDDOP exhibits photoluminescence (PL quantum efficiency of

Bipyridyl ligand and preparation method thereof, ruthenium supramolecular self-assembly body containing bipyridyl ligand and preparation method and application of ruthenium supramolecular self-assembly

The invention provides a novel bipyridyl bidentate ligand and a preparation method thereof. The structural formula of the novel bipyridyl bidentate ligand is shown in the specification. The inventionfurther provides a ruthenium supramolecular self-assembly body of the ligand and a preparation method of the ruthenium supramolecular self-assembly body. The preparation method comprises the followingsteps: putting a prepared ruthenium receptor and a bipyridyl ligand into a container, adding a mixed solvent of methanol and dichloromethane in equal proportion, stirring for a period of time at roomtemperature, spin-drying the solution to a certain volume after the reaction is finished, slowly adding diethyl ether, and separating out solid powder, namely the ruthenium supramolecular self-assembly body containing the bipyridyl ligand. The self-assembly body is a novel ruthenium-containing self-assembly compound, and has a good inhibition effect on cancer tumor cell lines A549 and HepG-2.

Benzothiadiazole, hexylthiophen and alkoxy benzene based solution processable copolymer: Effect of the electron withdrawing substituents (fluorine atoms) on electrochemical, optical and electrochromic properties

4,7-Bis(4-hexyl-5-(trimethylstannane) -2-thienyl) ?2,1,3-benzothiadiazole (HTBT) coupled with 2,5-bis (decyloxy)-1,4-dibromobenzene to afford the donor-π-bridge-donor-acceptor conjugated poly (4,7-bis (4-hexyl-2-thienyl) ?2,1,3-benzothiadiazole-co-p-didec

Poly[(arylene ethynylene)-alt-(arylene vinylene)]s Based on Anthanthrone and Its Derivatives: Synthesis and Photophysical, Electrochemical, Electroluminescent, and Photovoltaic Properties

Anthanthrone and its derivatives are large polycyclic aromatic compounds (PACs) that pose a number of challenges for incorporation into the structure of soluble conjugated polymers. For the first time, this group of PACs was employed as the building blocks for the synthesis of copolymers (P1-P5) based on poly[(arylene ethynylene)-alt-(arylene vinylene)]s backbone (-Ph-C=C-Anth-C=C-Ph-CH - CH-Ph-CH - CH-)n. During the synthesis of P1-P5, different alkyloxy side chains were incorporated in order to tune the properties of the polymers. Of the copolymer series only P1 (containing anthanthrone and branched 2-ethylhexyloxy side chains on phenylenes), P2 and P3 (for which the anthanthrones containing carbonyl groups were converted to anthanthrene containing alkyloxy substituents) were soluble. The photophysical, electrochemical, electroluminescent and photovoltaic properties of P1-P3 are reported, compared and discussed with respect to the effects of side chains.

Aryl trihydroxyborate salts: Thermally unstable species with unusual gelation abilities

A series of aryl trihydroxyborate salts were synthesized and found to form gels in benzene. The compounds were thermally unstable and readily underwent protodeboronation in solution and the solid state. Gelation could be induced without decomposition via sonication. Subsequent characterization studies revealed an unusual dependence of gel properties on alkyl chain length.

Phenylene-functionalized polythiophene derivatives for light-emitting diodes: Their synthesis, characterization and properties

The design, synthesis and characterization of a new series of conjugated polymers, poly[(3-(4′-n-butylphenyl)thiophene-2,5-diyl)(2,5-dialkoxy-1,4- phenylene)(4-(4′-n-butylphenyl)thiophene-2,5-diyl)] are described in this contribution. Three polymers modif

Excimer formation in oligo[2,5-bis(hexadecyloxy)-1,4-phenylene]s followed by fluorescence spectroscopy

Using the steady-state and time-resolved fluorescence spectroscopy, the behavior of "hairy-rod" oligo- and poly[2,5-bis(hexadecyloxy)-1,4-phenylene]s in tetrahydrofuran solutions was investigated. The materials were prepared by the Yamamoto coupling reaction using zinc as a reducing metal, the nickel(II)/triphenylphosphine complex as a catalyst, and 2,2′-bipyridine as a coligand. The appropriate oligomer fractions were separated by fractional precipitation and characterized by GPC and end group analysis. The fluorescence quantum yield of oligomers and polymers increased with their increasing conjugation length. The fluorescence emission spectra of polymers and longer oligomers exhibited one emission maximum at 390 nm with a single-exponential decay and fluorescence lifetimes (τ) around 1 ns. The substitution in positions 2 and 5 forces the adjacent backbone benzene units out of the plane, which results in twist angles 60-80°, and the bulky substituents exclude the cofacial sandwich-type configuration necessary for excimer formation. However, with shorter oligomers, another emission band at 460 nm appeared. Fluorescence decays at 460 nm were found to be double-exponential with longer excited-state lifetimes [e.g. τ1 = 6.9 ns (76%), τ2 = 2.4 ns (24%)]. With shorter oligomers (dimer, trimer), we assume a sandwich-type configuration with sufficiently close interchain distance and hence the excimer can form. Hydrophobic interactions of long aliphatic side chains in a polar medium play an important role in the excimer formation.