503475-44-3

Upstream product

• 313050-71-4 N-(4-bromophenyl)-N-(9,9-dimethyl-9H-fluoren-2-yl)-9,9-dimethyl-9H-fluoren-2-amine 
• 132898-95-4 2,2'-bithiophene-5-boronic acid 
• 28320-31-2 2-bromo-9,9-dimethyl-9H-fluorene 
• 62-53-3 aniline 
• 479719-88-5 2-([2,2'-bithiophen]-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 144981-85-1 2-iodo-9,9-dimethyl-9H-fluorene 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 922737-38-0 5'-(4-(bis(9,9-dimethyl-9H-fluoren-2-yl)amino)phenyl)-2,2'-bithiophene-5-carbaldehyde 
• 1383782-66-8 2-[N,N-bis-(9,9-dimethylfluoren-2-yl)aminophenyl]-2'-bromo-5,5'-bisthiophene 
• 1389321-71-4 2-[N,N-bis-(9,9-dimethylfluoren-2-yl)aminophenyl]-5,5'-bithiophene-2' boronic acid pinacol ester 
• 1389321-72-5 4-[2-(N,N-bis-(9,9-dimethylfluoren-2-yl)-4-aminophenyl)-5,5'-bisthiophene-2']phthalonitrile 
• 1229021-75-3 C₅₀H₄₉NO₃S₂Si 
• 1229021-74-2 C₄₄H₃₄INS₂ 
• 950923-79-2 C₄₆H₃₇NS₂ 

Relevant academic research and scientific papers

The role of borole in a fully conjugated electron-rich system

The reaction of the 3,3′-dilithiobithieno complex with Tip-B(OMe)2 affords a borole with an extended conjugated electron-rich π-electron system; the electronic perturbation by the introduction of push-pull substituents is described.

Convergent synthesis of near-infrared absorbing, "push-pull", bisthiophene-substituted, zinc(II) phthalocyanines and their application in dye-sensitized solar cells

Zinc(II) phthalocyanine dyes that contain triarylamine-terminated bisthiophene and hexylbisthiophene groups have been synthesized by a convergent approach by using carboxytriiodo-ZnPc as a precursor. Further transformation of the iodo groups by a Pd-catal

NAPHTHALENE MONOIMIDE DERIVATIVES AND USE THEREOF AS PHOTOSENSITIZERS IN SOLAR CELLS AND PHOTODETECTORS

The present invention relates to compounds of the formulae Ia and Ib in which the variables R, n, A, B, R1 and R2 are each as defined in the description. The present invention further relates to the use of compounds of the formula Ia