Welcome to LookChem.com Sign In|Join Free
  • or
Pyren-N,N-Dimethylanilin-Komplex, also known as Pyren-N,N-dimethylaniline complex, is a chemical compound formed by the interaction between pyrene and N,N-dimethylaniline. Pyrene is a polycyclic aromatic hydrocarbon consisting of four fused benzene rings, while N,N-dimethylaniline is an organic compound with a primary amine group and two methyl groups attached to the nitrogen atom. The complex formation occurs due to the interaction between the electron-rich nitrogen atom of N,N-dimethylaniline and the electron-deficient pyrene molecule, resulting in a charge-transfer complex. This complex has potential applications in the field of supramolecular chemistry, as it can be used to study the interactions between different molecules and to develop new materials with unique properties.

7381-80-8

Post Buying Request

7381-80-8 Suppliers

Recommended suppliers

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

7381-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7381-80-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,8 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7381-80:
(6*7)+(5*3)+(4*8)+(3*1)+(2*8)+(1*0)=108
108 % 10 = 8
So 7381-80-8 is a valid CAS Registry Number.

7381-80-8Relevant academic research and scientific papers

Exciplex Photophysics. 7. Steric Effects in Exciplex Photophysics

Cheung, Seung Tong,Ware, William R.

, p. 466 - 473 (1983)

The influence of steric interference with sandwich-type exciplex formation has been investigated by using mono- and di-tert-butylsubstitution of N,N'-dimethylaniline (DMA).Pyrene was the electron acceptor and studies were carried out with both steady-state and fluorescence lifetime techniques in hexane and tetrahydrofuran (THF).All the rate constants of the classical exciplex mechanism were determined along with temperature coefficients.It was found that the most significant effect of tert-butyl substitution was a substantial decrease in the process (AQ)* -> A* + Q.Solvent effects, exciplex thermodynamics, and activation parameters are discussed for the unsubstituted and tert-butyl-substituted systems.

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 7381-80-8