179803-79-3

Basic information

• Product Name: 9,10-bis-(4-hydroxyphenyl)anthracene
• Synonyms: 9,10-bis-(4-hydroxyphenyl)anthracene
• CAS NO: 179803-79-3
• Molecular Weight: 362.428
• Mol File: 179803-79-3.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 9,10-bis-(4-hydroxyphenyl)anthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9,10-bis-(4-hydroxyphenyl)anthracene(179803-79-3)
• EPA Substance Registry System: 9,10-bis-(4-hydroxyphenyl)anthracene(179803-79-3)

Safety Data

• Hazardous Substances Data: 179803-79-3(Hazardous Substances Data)

Upstream product

• 104-92-7 1-bromo-4-methoxy-benzene 
• 84-65-1 9,10-phenanthrenequinone 
• 523-27-3 9,10-Dibromoanthracene 
• 269409-70-3 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol 
• 5720-07-0 4-methoxyphenylboronic acid 
• 71597-85-8 (p-hydroxyphenyl)boronic acid 
• 6793-92-6 p-benzyloxyphenylbromide 
• 146631-00-7 [4-(benzyloxy)phenyl]boronic acid 
• 179803-77-1 9,10-bis(4-benzyloxyphenyl)anthracene 
• 24672-76-2 9,10-bis-(4-methoxy-phenyl)-anthracene 

Downstream Products

• 179803-81-7 9-[4-(4-ferrocenylbutoxy)phenyl]-10-(4-hydroxyphenyl)anthracene 
• 179803-92-0 9,10-bis[4-(4-ferrocenoylbutoxy)phenyl]anthracene 
• 1400693-53-9 9,10-bis(4-bromopropoxyphenyl)anthracene 
• 1384205-44-0 9,10-bis(4-(6-hydroxyhexyl)oxyphenyl)anthracene 
• 359820-37-4 9-(4-[(3-benzyloxy-4-nitro)phenoxy]phenyl)-10-(4-hydroxyphenyl)anthracene 
• 359820-33-0 9,10-bis(4-[(3-benzyloxy-4-nitro)phenoxy]phenyl)anthracene 

Relevant articles and documents

Novel methoxy spirobifluorene and alkyl substituted diphenylacene based organic blue light emitting polymers for application in organic electronics

We report on the synthesis and characterisation of a series of blue light emitting alkoxy substituted poly(spirobifluorenes) based on acene moiety. The obtained polymers had been fully characterised by FTIR, NMR, TGA, GPC techniques. The obtained polymers showed good photoluminescence and electroluminescence properties with blue fluorescence, obtained by supressing the excimer formation as a result of intermolecular interactions. The optical band gaps of all polymers were estimated to be in the range of 2.64–2.71 eV with good fluorescent quantum yield. The introduction of a spiro-structure in polymer backbone leads to its high thermal stability and good solubility in common organic solvents such as CH2Cl2, CH3Cl, toluene, tetrahydrofuran etc.

Artificial light-harvesting supramolecular polymeric nanoparticles formed by pillar[5]arene-based host-guest interaction

Artificial light-harvesting nanoparticles were prepared from supramolecular polymers comprised of pillar[5]arene with anthracene-derived donors and acceptors through host-guest interactions. The resulting water-dispersible nanoparticles displayed efficient energy transfer and excellent light harvesting ability in part because the steric bulk of pillar[5]arene suppressed the self-quenching of the chromophores.

Synthesis and properties of thermotropic liquid-crystalline polyesters containing 9,10-diphenylanthracene moiety in the main chain

We synthesized thermotropic liquid-crystalline polyesters in which 9,10-diphenylanthracene moieties are incorporated into the main chain type of polyester forming the chiral smectic C (Sm C*). The polymers were prepared by the isopropyltitanate-catalyzed reaction of biphenyldicarboxylic acid and the corresponding diols, with different ratios of diol of 9,10- diphenylanthracene moiety to the alkane diols (1, 5, and 10 mol %) under nitrogen atmosphere. The polymers exhibited thermotropic liquid crystals despite the presence of a bulky diphenylanthracene moiety in the main chain. The circular dichroism spectra revealed that a Sm C*phase was formed in the polymer with 1 mol % of anthracene moiety, although only an Sm A phase was formed in the other polymers. This is the first example of a Sm C*polyester containing a diphenylanthracene moiety in the main chain. Furthermore, we measured the optical properties of the polymers and found that they exhibited very high fluorescent efficiency. The fluorescence spectra of the thin film differed from that of a CH2Cl2 solution.