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2,4,6-trimesityl-1,3,5-triphenylborazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1400973-77-4

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1400973-77-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1400973-77-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,0,9,7 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1400973-77:
(9*1)+(8*4)+(7*0)+(6*0)+(5*9)+(4*7)+(3*3)+(2*7)+(1*7)=144
144 % 10 = 4
So 1400973-77-4 is a valid CAS Registry Number.

1400973-77-4Downstream Products

1400973-77-4Relevant academic research and scientific papers

Polymorphism, fluorescence, and optoelectronic properties of a borazine derivative

Kervyn, Simon,Fenwick, Oliver,Di Stasio, Francesco,Shin, Yong Sig,Wouters, Johan,Accorsi, Gianluca,Osella, Silvio,Beljonne, David,Cacialli, Franco,Bonifazi, Davide

, p. 7771 - 7779 (2013)

We have prepared a new borazine derivative that bears mesityl substituents at the boron centers and displays exceptional chemical stability. Detailed crystallographic and solid-state fluorescence characterizations revealed the existence of several polymorphs, each of which showed different emission profiles. In particular, a bathochromic shift is observed when going from the lower- to the higher-density crystal. Computational investigations of the conformational dynamics of borazine 1 in both the gas phase and in the solid state using molecular dynamics (MD) simulations showed that the conformation of the peripheral aryl groups significantly varies when going from an isolated molecule (in which the rings are able to flip over the 90° barrier at RT) to the crystals (in which the rotation is locked by packing effects), thus generating specific nonsymmetric intermolecular interactions in the different polymorphs. To investigate the optoelectronic properties of these materials by fabrication and characterization of light-emitting diodes (LEDs) and light-emitting electrochemical cells (LECs), borazine 1 was incorporated as the active material in the emissive layer. The current and radiance versus voltage characteristics, as well as the electroluminescence spectra reported here for the first time are encouraging prospects for the engineering of future borazine-based devices. Copyright

BORAZINE DERIVATIVES

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Page/Page column 29-30, (2012/10/08)

The present invention is directed to new borazine derivatives and their use in the manufacture of electronic devices, in particular electroluminescent and semiconductor devices. More specifically, the present invention relates to new stable borazine derivatives comprising boron atoms substituted by aryl groups and to their use in one or more layers of an electroluminescent or a semiconductor device, in particular in the emissive layer of organic light-emitting devices (OLED).

BORAZENE DERIVATIVES

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Page/Page column 38-39, (2012/10/08)

The present invention is directed to new borazene derivatives and their use in the manufacture of electronic devices, in particular electroluminescent and semiconductor devices. More specifically, the present invention relates to new stable borazene derivatives comprising boron atoms substituted by aryl groups and to their use in one or more layers of an electroluminescent or a semiconductor device, in particular in the emissive layer of organic light-emitting devices (OLED).

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