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2,5-bis(2-thienyl)terephthaloyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1209012-29-2

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1209012-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1209012-29-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,9,0,1 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1209012-29:
(9*1)+(8*2)+(7*0)+(6*9)+(5*0)+(4*1)+(3*2)+(2*2)+(1*9)=102
102 % 10 = 2
So 1209012-29-2 is a valid CAS Registry Number.

1209012-29-2Relevant academic research and scientific papers

Narrow band gap D-A copolymer of indacenodithiophene and diketopyrrolopyrrole with deep HOMO level: Synthesis and application in field-effect transistors and polymer solar cells

Wang, Xiaochen,Luo, Hao,Sun, Yeping,Zhang, Maojie,Li, Xiaoyu,Yu, Gui,Liu, Yunqi,Li, Yongfang,Wang, Haiqiao

, p. 371 - 377 (2012)

A novel fused ladder alternating D-A copolymer, PIDT-DPP, with alkyl substituted indacenodithiophene (IDT) as donor unit and diketopyrrolopyrrole (DPP) as acceptor unit, was designed and synthesized by Pd-catalyzed Stille-coupling method. The copolymer sh

4,9-dihydro-4,4,9,9-tetrahexyl- s -indaceno[1,2- b:5,6- b ′]dithiophene as a π-spacer of donor-π-acceptor dye and its photovoltaic performance with liquid and solid-state dye-sensitized solar cells

Cai, Liping,Moehl, Thomas,Moon, Soo-Jin,Decoppet, Jean-David,Humphry-Baker, Robin,Xue, Zhaosheng,Bin, Liu,Zakeeruddin, Shaik M,Graetzel, Michael

supporting information, p. 106 - 109 (2014/01/23)

A new D-π-A organic dye, LC-5, containing 4,9-dihydro-4,4,9,9- tetrahexyl-s-indaceno[1,2-b:5,6-b′]-dithiophene as a novel π-conjugated spacer has been synthesized and tested as a sensitizer in dye-sensitized solar cells (DSC). Volatile and ionic liquid electrolytes have been used in conjunction with the synthesized dye, and the electrolyte influence on the photovoltaic performance of DSCs was investigated. A detailed investigation, including transient photocurrent/photovoltage decay measurements and electrochemical impedance spectroscopy data, provide important conclusions about the influence of electrolytes on the photovoltaic parameters.

Synthesis and characterization of planar five-ring-fused dithiophene-dione

Wang, Jing,Zeng, Weijing,Xu, Huan,Li, Bin,Cao, Xiaoping,Zhang, Haoli

experimental part, p. 681 - 688 (2012/06/04)

A series of new organic semiconductors based on s-indaceno[1,2-b:5,6- b′]dithiophene-4,9-dione was successfully synthesized and characterized. The electron withdrawing carbonyl group lowers the LUMO energy levels, leading to increased electronegativities, which is beneficial for high photo-stability in air. The n-alkyl substituted compounds, 1c and 1d, crystallize with the rigid coplanar systems packed into slipped face-to-face π-stacks. Interestingly, 1c and 1d also show liquid crystalline behaviors, which give highly ordered molecular packing over large area.

Indacenodithiophene and Indacenodiselenophene Polymers and their Use as Organic Semiconductors

-

, (2011/10/10)

The invention relates to conjugated polymers comprising indacenodithiophene or indacenoselenophene units or derivatives thereof, to methods of their preparation, to novel monomer units used therein, to the use of the polymers in organic electronic (OE) de

Indacenodithiophene semiconducting polymers for high-performance, air-stable transistors

Zhang, Weimin,Smith, Jeremy,Watkins, Scott E.,Gysel, Roman,McGehee, Michael,Salleo, Alberto,Kirkpatrick, James,Ashraf, Shahid,Anthopoulos, Thomas,Heeney, Martin,McCulloch, Iain

supporting information; experimental part, p. 11437 - 11439 (2010/10/03)

High-performance, solution-processed transistors fabricated from semiconducting polymers containing indacenodithiohene repeat units are described. The bridging functions on the backbone contribute to suppressing large-scale crystallization in thin films. However, charge carrier mobilities of up to 1 cm2/(V s) for a benzothiadiazole copolymer were reported and, coupled with both ambient stability and long-wavelength absorption, make this family of polymers particularly attractive for application in next-generation organic optoelectronics.

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