954097-62-2

Upstream product

• 143-15-7 1-dodecylbromide 
• 611-99-4 4,4'-Dihydroxybenzophenone 
• 322762-23-2 bis-(4-dodecyloxy-phenyl)-methanone 

Downstream Products

• 1154754-92-3 2',3'-dibromo-9',10'-bis(dodecyloxy)-3,3,3'',3''-tetrakis[4-(dodecyloxy)phenyl]dispiro[thiirane-2,6'-pentacene-13',2''-thiirane] 
• 1154754-95-6 2'-bromo-3,3,3'',3''-tetrakis[4-(dodecyloxy)phenyl]dispiro[thiirane-2,6'-pentacene-13',2''-thiirane] 
• 954097-68-8 6-benzhydrylidene-13-[bis-(4-dodecyloxy-phenyl)-methylene]-6,13-dihydro-pentacene 
• 911239-34-4 13-[bis-(4-dodecyloxy-phenyl)-methylene]-13H-pentacene-6-thione 
• 954097-66-6 13-[bis-(4-dodecyloxy-phenyl)-methylene]-13H-pentacen-6-one 
• 954097-64-4 6-[bis-(4-dodecyloxy-phenyl)-methylene]-6,13-dihydro-pentacene 

Relevant academic research and scientific papers

Expeditious synthesis of contorted hexabenzocoronenes

Contorted hexabenzocoronenes (HBCs) have been synthesized in an expedited manner utilizing a double Barton-Kellogg olefination reaction and a subsequent Scholl cyclization. The scope of both transformations was investigated using a series of pentacene qui

Molecular wires from contorted aromatic compounds

(Figure Presented) In a twist: A design strategy for molecule-based electronic materials using aromatic compounds with a nonplanar core is presented. A new class of hexabenzocoronene is put forth that has its core severely distorted out of planarity into a corrugated structure. When substituted with four alkoxy side chains, this material self-assembles into infinitely long columns through stacking (see picture) and acts as an active layer in field-effect transistors.