937041-72-0

Upstream product

• 586-78-7 para-nitrophenyl bromide 
• 15721-78-5 di[p-(2,4,4-trimethyl-2-pentyl)phenyl]amine 
• 350-46-9 4-Fluoronitrobenzene 

Downstream Products

• 937041-74-2 N,N-bis[4-(1,1,3,3-tetramethylbutyl)phenyl]-p-phenylenediamine 
• 1213714-81-8 N,N-bis(4-bromophenyl)-N',N'-bis(4-(2,4,4-trimethylpentan-2-yl)phenyl)-1,4-phenylenediamine 

Relevant academic research and scientific papers

N,N,N′,N′- tetraphenyl-1,4-phenylenediamine-fluorene alternating conjugated polymer: Synthesis, characterization, and electrochromic application

A novel N,N,N′N′-tetraphenyl-l,4-phenylenediamine (TPPA)-containing aromatic dibromide (3), N,N,-bis(4-bromophenyl)-N′, N′-bis(4-(2,4,4-trimethylpentan-2-yl)phenyl)-1,4-phe.n.ylenediamine, was successfully synthesized. The novel, conjugated polymer (4) ha

Use of Rylene Derivatives as Photosensitizers in Solar Cells

Use of rylene derivatives I with the following definition of the variables: X together both —COOM; Y a radical -L-NR1R2 ??(y1) -L-Z-R3 ??(y2) the other radical hydrogen; together both hydrogen; R is optionally substituted (het)aryloxy, (het)arylthio; P is —NR1R2; B is alkylene; optionally substituted phenylene; combinations thereof; A is —COOM; —SO3M; —PO3M2; D is optionally substituted phenylene, naphthylene, pyridylene; M is hydrogen; alkali metal cation; [NR5]4+; L is a chemical bond; optionally indirectly bonded, optionally substituted (het)arylene radical; R1, R2 are optionally substituted (cyclo)alkyl, (het)aryl; together optionally substituted ring comprising the nitrogen atom; Z is —O—; —S—; R3 is optionally substituted alkyl, (het)aryl; R′ is hydrogen; optionally substituted (cyclo)alkyl, (het)aryl; R5 is hydrogen; optionally substituted alkyl (het)aryl; m is 0, 1, 2; n, p m=0: 0, 2, 4 where: n+p=2, 4, if appropriate 0; m=1: 0, 2, 4 where: n+p=0, 2, 4; m=2: 0, 4, 6 where: n+p=0, 4, 6, or of mixtures thereof as photosensitizers in solar cells.