55373-68-7

Upstream product

• 886-65-7 trans,trans-1,4-Diphenyl-1,3-butadiene 
• 536-74-3 phenylacetylene 

Downstream Products

• 55373-72-3 C₁₇H₁₅BrS 
• 16212-85-4 3,6-diphenyl-1,2-dithiin 
• 936577-05-8 C₃₂H₂₆O₂ 
• 1447761-32-1 dimethyl 4,4'-((1Z,3Z)-1,4-diphenylbuta-1,3-diene-1,4-diyl)dibenzoate 
• 1450-63-1 1,1,4,4-tetraphenyl-1,3-butadiene 
• 23460-46-0 (Z,Z)-1,4-di(ethylthio)-1,4-diphenyl-1,3-butadiene 
• 17589-28-5 (Z,Z)-1,4-diphenyl-1,3-butadiene-1,4-dithiol 
• 1142-22-9 (E)-1,4-diphenylbut-2-ene 
• 891-22-5 3,6-diphenylpyridazine 
• 1445-78-9 2,5-Diphenyl-thiophene 
• 52516-76-4 (Z)(Z)-1-Brom-4-chlor-1,4-diphenylbuta-1,3-dien 
• 55373-69-8 (Z,Z)-1,4-dichloro-1,4-diphenyl-1,3-butadiene 
• 55373-71-2 ((1Z,3E)-1-bromobuta-1,3-diene-1,4-diyl)dibenzene 
• 13343-79-8 (E)-1,4-Diphenylbut-1-en-3-yne 

Relevant academic research and scientific papers

New linear π-conjugated polymers via Suzuki coupling of (1Z, 3Z)-1,4-dibromo-1,4-diaryl-buta-1,3-diene with aromatic diborates: Synthesis and photophysical properties

A series of new linear π-conjugated polymers have been synthesized via Suzuki coupling of (1. Z, 3. Z)-1,4-dibromo-1,4-diaryl-buta-1,3-diene with aromatic diborates. The structures were characterized by NMR spectroscopy, IR spectroscopy and GPC. All of th

Regio- and Stereoselective Polymerization of Diynes with Inorganic Comonomer: A Facile Strategy to Conjugated Poly(p-arylene dihalodiene)s with Processability and Postfunctionalizability

Development of new methodologies for synthesizing polymers with novel structures and unique properties is a fundamentally important area in polymer science. Herein, a novel synthetic strategy to conjugated poly(p-arylene dihalodiene)s (PADs) with high reg

Reversible and hydrogen bonding-assisted piezochromic luminescence for solid-state tetraaryl-buta-1,3-diene

Reversible piezochromic luminescence and aggregation induced emission properties of 4,4′-((Z,Z)-1,4-diphenylbuta-1,3-diene-1,4-diyl)dibenzoic acid are reported. The photoluminescent color of it changes from blue to yellow-green upon grinding, which can be

Mild and selective palladium-catalyzed dimerization of terminal alkynes to form symmetrical (Z,Z)-1,4-dihalo-1,3-dienes

A regioselective and stereoselective palladium-catalyzed dimerization of terminal alkynes method for the synthesis of symmetrical (Z,Z)-1,4-dihalo-1,3- dienes is presented. In the presence of a catalytic amount of PdX2 and 3 equiv of CuX2