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5,10-bis(p-tolyl)-16-oxa-15,17-dihydrotripyrrane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

313944-52-4

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313944-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 313944-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,9,4 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 313944-52:
(8*3)+(7*1)+(6*3)+(5*9)+(4*4)+(3*4)+(2*5)+(1*2)=134
134 % 10 = 4
So 313944-52-4 is a valid CAS Registry Number.

313944-52-4Downstream Products

313944-52-4Relevant academic research and scientific papers

Expedient synthesis of corroles by oxidant-mediated, direct α-α' coupling of tetrapyrromethanes

Ka,Cho,Lee

, p. 8121 - 8125 (2000)

Oxidant mediated coupling of tetrapyrromethanes resulted in the exclusive formation of meso-substituted corroles in more than 60% yields. The similar coupling reaction of 1,14-unsubstituted 16-oxatripyrromethane with 5-tolyldipyrromethane carried out in acetonitrile also gave expanded corroles as a single product. In both cases acid catalysts are not necessary for the direct α-α' coupling reaction. (C) 2000 Elsevier Science Ltd.

Molecular engineering of boryl oxasmaragdyrins through peripheral modification: Structure-efficiency relationship

Mane, Sandeep B.,Hung, Chen-Hsiung

, p. 4825 - 4841 (2015/03/18)

Expanded porphyrins with the absorption profile down to the infrared region through increased p-conjugation are suitable candidates for a low energy sensitizer. Oxasmaragdyrin boron complexes, a class of aromatic-coremodified expanded porphyrin with 22 π -electrons, have been recently utilized as an efficient low energy sensitizer in dye-sensitized solar cells. In this paper, we have prepared a series of eight novel boryl oxasmaragdyrins through molecular engineering on the periphery and their overall photovoltaic performances in dye-sensitized solar cells are evaluated. With the help of photophysical, electrochemical, and photovoltaic studies, it is revealed that molecular structure, especially the number and position of the donor-acceptor groups play a pivotal role in their photovoltaic performance. Presence of the two well-separated split Soret bands in the 400-500 nm region of UV/Vis spectrum ensures broader coverage of absorption wavelengths. Even though the two-an-choring-group dyes (SM5-SM8 ) bind strongly to TiO2 compared to one-anchoring-group dyes (SM1-SM4), the latter have superior photovoltaic performance than the former. Dye SM1 , with two hexyloxyphenyl donors and one carboxylic acid anchor showed the best overall conversion efficiency of 4.36% (JSC = 10.91 mAcm-2 ; VOC = 0.59 V; FF = 0.68). This effective modulation of photovoltaic performance through structural engineering of the dyes will serve as a guideline for the future design of efficient low energy light-harvesting sensitizers.

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