230623-63-9

Upstream product

• 108-86-1 bromobenzene 
• 104-13-2 4-Butylaniline 
• 106-37-6 1.4-dibromobenzene 
• 41492-05-1 p-bromobutylbenzene 
• 122-39-4 diphenylamine 
• 152270-84-3 N-(4-n-butylphenyl)-N-phenylbenzenamine 

Downstream Products

• 230623-64-0 (4-butyl-phenyl)-(4-hex-5-enyl-phenyl)-phenyl-amine 
• 230623-65-1 {4-[6-(tert-butyl-dimethyl-silanyloxy)-hexyl]-phenyl}-(4-butyl-phenyl)-phenyl-amine 
• 230623-66-2 (4-bromo-phenyl)-{4-[6-(tert-butyl-dimethyl-silanyloxy)-hexyl]-phenyl}-(4-butyl-phenyl)-amine 
• 230623-57-1 4-[{4-[6-(tert-butyl-dimethyl-silanyloxy)-hexyl]-phenyl}-(4-butyl-phenyl)-amino]-benzaldehyde 
• 230623-75-3 {4-[6-(tert-butyl-dimethyl-silanyloxy)-hexyl]-phenyl}-(4-butyl-phenyl)-{4-[2-(4-hexyl-thiophen-2-yl)-vinyl]-phenyl}-amine 
• 1383601-98-6 N-(4-n-butylphenyl)-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)benzenamine 
• 1383601-95-3 3,7-bis(4-(N-bromophenyl-N-(4-n-butylphenyl)amine)phenyl)dibenzothiophene-S,S-dioxide 

Relevant academic research and scientific papers

Novel green light-emitting polyfluorenes containing dibenzothiophene-S,S- dioxide-arylamine derivatives

Green light-emitting polyfluorenes were synthesized by Suzuki polycondensation via introducing dibenzothiophene-S,S-dioxide-(di-)tri- phenylamine (G1 and G2) moieties and dibenzothiophene-S,S- dioxide (SO) unit into the polyfluorene

Synthesis of functionalized organic second-order nonlinear optical chromophores for electrooptic applications

The design and syntheses of functionalized second-order nonlinear optical chromophores, suitable for covalent incorporation into functionalized high-performance polymers, are described. The chromophores with hydroxy alkyl functionality have diarylamino groups as the donor moiety and a styryl thiophene moiety as the conjugated bridge. The triarylamine parts of the molecules were synthesized using palladium-catalyzed C-N bond forming reactions. The conjugated bridge was assembled using the Wittig reaction. The acceptor groups were installed in the last steps of the syntheses.