408359-97-7

Upstream product

• 589-87-7 1,4-bromoiodobenzene 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 201802-67-7 4-(diphenylamino)phenyl boronic acid 
• 122-39-4 diphenylamine 
• 36809-26-4 4-N,N-diphenylamino-1-bromobenzene 
• 201733-56-4 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-5,5-dimethyl-1,3,2-dioxaborinane 

Downstream Products

• 408359-98-8 4′-(4-(N,N-diphenylamino)-phenyl)-2,2′:6′,2″-terpyridine 
• 830325-93-4 (4-(7-bromobenzo[c][1,2,5]thiadiazol-4-yl)-N,N-diphenyl-aniline) 
• 1196890-66-0 3,6-bis-[(4'-diphenylamino)biphenyl-4-yl]-2,5-dioctylpyrrolo[3,4-c]pyrrole-1,4-dione 
• 1415100-76-3 2,9-bis[4-(diphenylamino)phenyl]-1,10-phenanthroline-5,6-dione 
• 1415100-79-6 3,6-bis[4-(diphenylamino)phenyl]-9,10-phenanthrenequinone 
• 1564262-24-3 N-octyl-3,6-bis[4-(4-(diphenylamino)phenyl)phenyl]-1,4-diketo-pyrrolo[3,4-c]pyrrole 

Relevant academic research and scientific papers

Diphenylamine end-capped 1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole (DPP) derivatives with large two-photon absorption cross-sections and strong two-photon excitation red fluorescence

Novel donor-π-bridge-acceptor-π-bridge-donor (D-π-A-π-D)-type 1,4-diketo-3,6-diphenylpyrrolo[3,4-c]pyrrole (DPP) derivatives with end-capping diphenylamine groups have been synthesized and shown to exhibit large two-photon absorption cross-sections over a wide range of wavelengths with strong two-photon excitation red fluorescence.

A new, highly fluorescent terpyridine which responds to zinc ions with a large red-shift in emission

A sequence of three metal-catalysed aryl coupling reactions leads to the new ligand 4′-(4-N,N-diphenylaminophenyl)2,2′:6′,2″-terpyridine, the intense ICT emission of which undergoes a large red-shift upon binding of zinc ions, providing a unique response over other common metal ions.