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115208-28-1

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115208-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115208-28-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,2,0 and 8 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 115208-28:
(8*1)+(7*1)+(6*5)+(5*2)+(4*0)+(3*8)+(2*2)+(1*8)=91
91 % 10 = 1
So 115208-28-1 is a valid CAS Registry Number.

115208-28-1Relevant articles and documents

Excited-state lifetime modulation in triphenylene-based conjugated polymers [5]

Rose,Lugmair,Swager

, p. 11298 - 11299 (2001)

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Naphthodithiophene-2,1,3-benzothiadiazole copolymers for bulk heterojunction solar cells

Wang, Bao,Tsang, Sai-Wing,Zhang, Weifeng,Tao, Ye,Wong, Man Shing

supporting information; experimental part, p. 9471 - 9473 (2011/10/12)

Two newly synthesized naphthodithiophene-based copolymers, PNB, exhibit a low optical bandgap of ~1.64 eV with which the solar cells fabricated from the blend of PNB and PC71BM afforded a power conversion efficiency of 5.3% with external quantum efficiency over 60% in a broad spectral range.

New phenyl-substituted PPV derivatives for polymer light-emitting diodes-synthesis, characterization and structure-property relationship study

Chen, Zhi-Kuan,Lee, Nancy Hoi Sim,Huang, Wei,Xu, Yi-She,Cao, Yong

, p. 1009 - 1020 (2007/10/03)

Three new PPV derivatives with dialkoxyphenyl substituents, BEH2P-PPV, BEH3P-PPV, and BEH4P-PPV have been synthesized. The polymers were characterized by FT-IR, 1H NMR, and elemental analysis. The polymers possess excellent solubility, high molecular weights, high photoluminescence efficiencies and good thermal stability. The influence of substitution pattern on the formation of structural defects has been investigated by measuring the signal due to tolane-bisbenzyl moieties (TBB) in the proton NMR spectra. BEH2P-PPV with a steric phenyl group at the ortho-position on the side phenyl ring shows the lowest amount of TBB, which indicates suitable steric hindrance can be applied to suppress the formation of irregular head-to-head and tail-to-tail linkage in the polymer chains. In addition, the polarity of solvents used for the Gilch polymerization will also affect the amount of irregular structure in the polymers. Polar solvents such as THF will result in polymers with low TBB content. Energy level measurement from cyclic voltammetry revealed that the influences of the substitution pattern on the HOMOs and LUMOs are different. The three polymers possess similar HOMO energy levels while the LUMO of BEH4P-PPV is much higher than that of the other two polymers. Polymer light-emitting diodes fabricated from BEH2P-PPV, BEH3P-PPV, and BEH4P-PPV with the configuration of ITO/PEDOT/polymer/Ba/Al, emitted bright blue-green to green light with the maximum peaks at 496, 488, and 525 nm, respectively. The turn-on electric field and maximum external quantum efficiencies of the diodes are 0.30, 0.50, and 0.42 MV/cm and 0.37%, 0.66%, and 0.25% respectively. The quantum efficiency is mainly determined by the electron injection from the cathode. With the highest luminance, lowest turn-on electric field, and good quantum efficiency as well as negligible structural defects, BEH2P-PPV is the most promising material among the three polymers for polymer light-emitting diodes.

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