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1025922-86-4

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1025922-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1025922-86-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,5,9,2 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1025922-86:
(9*1)+(8*0)+(7*2)+(6*5)+(5*9)+(4*2)+(3*2)+(2*8)+(1*6)=134
134 % 10 = 4
So 1025922-86-4 is a valid CAS Registry Number.

1025922-86-4Downstream Products

1025922-86-4Relevant academic research and scientific papers

Solid-supported Zn(ii) porphyrin tweezers as optical sensors for diamines

Elisa, Lubian,Baldini, Francesco,Giannetti, Ambra,Trono, Cosimo,Carofiglio, Tommaso

, p. 3678 - 3680 (2010)

A melamine-bridged bis-Zn(ii) porphyrin dyad covalently attached onto amino-functionalized TentaGel polymer beads or controlled pore glass (CPG) undergoes a reversible and marked colour change from purple to green upon exposure to a biogenic diamine such as cadaverine both in organic and aqueous media.

Efficient sensitization of dye-sensitized solar cells by novel triazine-bridged porphyrin-porphyrin dyads

Zervaki, Galateia E.,Roy, Mahesh S.,Panda, Manas K.,Angaridis, Panagiotis A.,Chrissos, Emmanouel,Sharma, Ganesh D.,Coutsolelos, Athanassios G.

, p. 9813 - 9825 (2013/09/23)

Two novel porphyrin-porphyrin dyads, the symmetrical Zn[Porph]-Zn[Porph] (2) and unsymmetrical Zn[Porph]-H2[Porph] (4), where Zn[Porph] and H2[Porph] are the metalated and free-base forms of 5-(4-aminophenyl)-10,15,20-triphenylporphyrin, respectively, in which two porphyrin units are covalently bridged by 1,3,5-triazine, have been synthesized via the stepwise amination of cyanuric chloride. The dyads are also functionalized by a terminal carboxylic acid group of a glycine moiety attached to the triazine group. Photophysical measurements of 2 and 4 showed broaden and strengthened absorptions in their visible spectra, while electrochemistry experiments and density functional theory calculations revealed negligible interaction between the two porphyrin units in their ground states but appropriate frontier orbital energy levels for use in dye-sensitized solar cells (DSSCs). The 2- and 4-based solar cells have been fabricated and found to exhibit power conversion efficiencies (PCEs) of 3.61% and 4.46%, respectively (under an illumination intensity of 100 mW/cm2 with TiO2 films of 10 μm thickness). The higher PCE value of the 4-based DSSC, as revealed by photovoltaic measurements (J-V curves) and incident photon-to-current conversion efficiency (IPCE) spectra of the two cells, is attributed to its enhanced short-circuit current (Jsc) under illumination, high open-circuit voltage (Voc), and fill factor (FF) values. Electrochemical impedance spectra demonstrated shorter electron-transport time (τd), longer electron lifetime (τe), and high charge recombination resistance for the 4-based cell, as well as larger dye loading onto TiO2.

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