Welcome to LookChem.com Sign In|Join Free
  • or
9,9'-Spirobi[9H-fluorene]-2,2',7,7'-tetramine is a complex organic compound with the molecular formula C24H20N4. It is characterized by a unique spirobifluorene structure, which consists of two fluorene units bridged by an amine group. 9,9'-Spirobi[9H-fluorene]-2,2',7,7'-tetramine is known for its potential applications in the field of materials science, particularly in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices due to its electronic and photophysical properties. The tetramine functional groups in the molecule contribute to its ability to form strong intermolecular interactions, which can influence its performance in these applications. Research into compounds like this one is ongoing to explore their full potential in advanced technologies.

376356-61-5

Post Buying Request

376356-61-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

376356-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 376356-61-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,6,3,5 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 376356-61:
(8*3)+(7*7)+(6*6)+(5*3)+(4*5)+(3*6)+(2*6)+(1*1)=175
175 % 10 = 5
So 376356-61-5 is a valid CAS Registry Number.

376356-61-5Downstream Products

376356-61-5Relevant academic research and scientific papers

Organic sol-gel synthesis of microporous molecular networks containing spirobifluorene and tetraphenylmethane nodes

Moon, Su-Young,Mo, Hye-Rim,Ahn, Min-Kyoon,Bae, Jae-Sung,Jeon, Eunkyung,Park, Ji-Woong

, p. 1758 - 1766 (2013)

The microporous molecular networks based on rigid tetrafunctional units are synthesized via organic sol-gel polymerization of 2,2′,7,7′- tetraamino-9,9′-spirobifluorene (TASBF) and/or tetrakis(4-aminophenyl) methane (TAPM) with a diisocyanate, hexamethylene diisocyanate (HDI), or p-phenylene diisocyanate. This study is performed as an extension of our previous report on the first organic sol-gel method, which enabled the synthesis of microporous molecular networks via a two-stage mechanism involving the formation of colloidal dispersions of the nanoparticulate molecular networks and their subsequent growth to monolithic networks on solvent evaporation. The sol-gel-synthesized molecular networks obtained by incorporating TASBF as a network former show improved porosity, processability, and thermal stability than the TAPM-based system. The improved porosity of TASBF-based networks is attributed to higher rigidity of the spirobifluorene compared with the tetraphenylmethane units. We also demonstrate the synthesis of mixed organic molecular networks by sol-gel copolymerization of the two network formers, TASBF and TAPM, and a diisocyanate monomer. The sol-gel transformation of TASBF/TAPM/HDI occurred at longer reaction times with increasing the amount of TASBF in the TASBF/TAPM/HDI mixture. The results indicate that the organic sol-gel method can be further optimized by adjusting various synthesis parameters to create new functional organic molecular network materials.

Molecular Tectonics. Porous Hydrogen-Bonded Networks Built from Derivatives of 9,9'-Spirobifluorene

Fournier, Jean-Hugues,Maris, Thierry,Wuest, James D.

, p. 1761 - 1775 (2007/10/03)

Molecules with multiple sites that induce strong directional association tend to form open networks with significant volumes available for the inclusion of guests. Such molecules can be conveniently synthesized by grafting diverse sticky sites onto geomet

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 376356-61-5