4973-47-1

Upstream product

• 3592-44-7 bis(chloromethyl)sulfide 
• 603-35-0 triphenylphosphine 

Downstream Products

• 74794-95-9 bis<2-(o-ethynylphenyl)vinyl> sulfide 
• 74794-94-8 bis<2-(o-ethynylphenyl)vinyl> sulfide 
• 74794-93-7 bis<2-(o-ethynylphenyl)vinyl> sulfide 
• 4973-48-2 trans,cis-bis<β-styryl> sulfide 
• 4973-49-3 trans,trans-bis<β-styryl> sulfide 
• 206-20-2 acenaphtho[1,2-c]thiophene 
• 38261-06-2 C₂₄H₂₆S 
• 73785-93-0 bis<4-(o-ethynylphenyl)-1,3-butadienyl> sulfide 
• 74794-98-2 2-(o-ethynylphenyl)vinyl 4-(o-ethynylphenyl)-1,3-butadienyl sulfide 
• 14458-51-6 syn-1,6:8,13-Bismethano<14>annulen 

Relevant academic research and scientific papers

Diferrocenyl molecular wires. the role of heteroatom linkers

Diferrocenyl molecular "wires", in which two ferrocenes are linked by a conjugated chain, allowing the communication of redox information between the ferrocenes, are a versatile platform on which to investigate notions of molecular conductivity. In this paper, we examine the role of heteroatoms=including O, P, S, and Se, as well as C atoms in various oxidation states=separated from the ferrocenes by intervening double bonds which minimize any steric effects. Surprisingly, oxygen is a better electronic mediator than sulfur, a phenomenon we attribute to superior molecular orbital overlap. These fundamental studies on redox coupling will help to guide the design of efficient organic conductors for organic electronics.