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1252993-34-2

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1252993-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1252993-34-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,2,9,9 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1252993-34:
(9*1)+(8*2)+(7*5)+(6*2)+(5*9)+(4*9)+(3*3)+(2*3)+(1*4)=172
172 % 10 = 2
So 1252993-34-2 is a valid CAS Registry Number.

1252993-34-2Downstream Products

1252993-34-2Relevant academic research and scientific papers

Jacketed polymers with dendritic carbazole side groups and their applications in blue light-emitting diodes

Jin, Hao,Xu, Yiding,Shen, Zhihao,Zou, Dechun,Wang, Dan,Zhang, Wei,Fan, Xinghe,Zhou, Qifeng

, p. 8468 - 8478 (2010)

Styrene-based monomers with the first- and second-generation dendronized carbazoles were synthesized by a convergent strategy. Conventional free radical polymerizations were carried out to synthesize the dendronized jacketed polymers using these two monomers. The apparent molecular weights of the two polymers determined by gel permeation chromatography were 57 000 and 34 000 g/mol, respectively. The polymers had excellent thermal stability with their 5% weight loss temperatures all above 360 °C. Their photophysical properties in solutions and films were investigated. Different solvents had negligible effects on their UV-vis or photoluminescent (PL) spectra. A 10 nm blue shift of the emission peak was observed in the PL spectra of films compared with those of solutions. After the films were annealed, the emission peaks became narrower. X-ray diffraction techniques were utilized to examine the phase structures of the dendronized jacketed polymers. The first-generation polymer formed a hexatic columnar nematic phase, while the second-generation one exhibited a columnar nematic phase. This stiff main-chain conformation and the dendritic side-group structure could reduce the intramolecular interactions and aggregations of the carbazole side groups and prevent the formation of excimers, which would be beneficial to the optoelectronic properties. The two polymers showed similar electrochemical properties. Their HOMO levels were about -5.3 eV, which was quite close to that of PEDOT:PSS. Electroluminescent (EL) devices were fabricated in two configurations. A new emission peak was found in the EL spectra compared with the PL spectra. All the devices emitted blue lights and possessed low driving voltages. An introduction of an electron-transporting layer could greatly improve the device properties. The best device could reach a luminescence of 2195 cd/m2, a current efficiency of 0.240 cd/A, and an external quantum efficiency of 0.353%.

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