1357307-97-1

Basic information

• Product Name: 1,7-dithienyl-3,5-di(4-bromophenyl)borondifluoride-azadipyrromethene
• Synonyms: 1,7-dithienyl-3,5-di(4-bromophenyl)borondifluoride-azadipyrromethene
• CAS NO: 1357307-97-1
• Molecular Weight: 667.203
• Mol File: 1357307-97-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,7-dithienyl-3,5-di(4-bromophenyl)borondifluoride-azadipyrromethene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,7-dithienyl-3,5-di(4-bromophenyl)borondifluoride-azadipyrromethene(1357307-97-1)
• EPA Substance Registry System: 1,7-dithienyl-3,5-di(4-bromophenyl)borondifluoride-azadipyrromethene(1357307-97-1)

Safety Data

• Hazardous Substances Data: 1357307-97-1(Hazardous Substances Data)

Upstream product

• 1357307-23-3 C₁₄H₁₂BrNO₃S 
• 99-90-1 para-bromoacetophenone 
• 69837-05-4 1-(4-bromophenyl)-3-(thiophene-2-yl)prop-2-en-1-one 
• 1359981-12-6 (BrC₆H₄C₄HNC₄H₃S)2HN 
• 98-03-3 thiophene-2-carbaldehyde 
• 109-63-7 boron trifluoride diethyl etherate 

Downstream Products

• 1596799-30-2 C₄₀H₂₆BF₂N₃S₂ 
• 1596799-31-3 C₄₆H₃₈BF₂N₃S₂ 
• 1596799-32-4 C₄₂H₃₀BF₂N₃O₂S₂ 
• 1596799-33-5 C₄₄H₃₀BF₂N₃O₂S₂ 
• 1596799-34-6 C₄₂H₂₄BF₈N₃S₂ 
• 1596799-35-7 C₄₄H₃₆BF₂N₅S₂ 

Relevant articles and documents

Synthesis of covalently bonded boron-dipyrromethene-diarylethene for building a stable photosensitizer with photo-controlled reversibility

We report the synthesis and characterization of a photosensitizer containing boron-dipyrromethene and diarylethene. The photosensitizer has photo-controlled reversible photosensitivity and offers potential applications in photochemical catalysis and the d

Synthesis and Studies of Aza-BODIPY-Based π-Conjugates for Organic Electronic Applications

Aza-boron-dipyromethene (aza-BODIPY) derivatives 1-6 were synthesized for the first time by employing the palladium catalyzed Suzuki-Miyaura coupling on dibromo-aza-BODIPY. Photophysical and electrochemical properties of these compounds were studied in solution. Absorption and emission maxima were observed in the near-infrared (NIR) region and were found to extend up to 754 and 751 nm, respectively. NIR fluorescence quantum yields in chloroform were as high as 0.45. Optical band gaps were measured from the onset of absorption spectra in thin films and were found to be low (ca. 1.2-1.4 eV). Electrochemical studies provided insight into the reduction potentials of these compounds and consequently the electron affinity (EA). High electron affinity (ca. 4.5) was observed for these dyes. NIR absorption and emission, good quantum yield, and high electron affinity of these compounds promise their applications in microscope imaging and optoelectronic devices, mainly in solar cells and field-effect transistors.