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(2Z,2'Z)-3,3'-(((1E,1'E)-(2-cyclohexyl-1,3-dioxoisoindoline-4,7-diyl)bis(ethene-2,1-diyl))bis(4,1-phenylene))bis(2-(4-nitrophenyl)acrylonitrile) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1387566-54-2

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1387566-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1387566-54-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,7,5,6 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1387566-54:
(9*1)+(8*3)+(7*8)+(6*7)+(5*5)+(4*6)+(3*6)+(2*5)+(1*4)=212
212 % 10 = 2
So 1387566-54-2 is a valid CAS Registry Number.

1387566-54-2Downstream Products

1387566-54-2Relevant academic research and scientific papers

Organic bulk heterojunction solar cells based on solution processable small molecules (A-π-A) featuring 2-(4-nitrophenyl) acrylonitrile acceptors and phthalimide-based π-linkers

Sharma,Mikroyannidis,Kurchania, Rajnish,Thomas, K. R. Justin

, p. 13986 - 13995 (2012/08/08)

A novel small molecule-based organic donor SM [(2Z,2′Z)-3,3′- (((1E,1′E)-(2-cyclohexyl-1,3-dioxoisoindoline-4,7-diyl)bis(ethene-2, 1-diyl))bis(4,1-phenylene))bis(2-(4-nitrophenyl)-acrylonitrile)] featuring 2-(4-nitrophenyl)acrylonitrile as the acceptor and a π-conjugation bridge composed of phthalimide and styryl units, with an A-π-A type structure, has been synthesized. It showed a long wavelength absorption band having an absorption maximum around 635 nm and the optical bandgap was 1.63 eV, which is lower than most reported conjugated polymers, including poly(3-hexylthiophene) (P3HT). The photovoltaic properties were investigated by constructing bulk heterojunction organic solar cell devices using SM as the electron donor and fullerene derivatives, i.e. PC60BM and PC70BM as the electron acceptors with the device architecture ITO/PEDOT:PSS/SM:PC 60BM or PC70BM/Al. The effect of the SM/fullerene derivative weight ratio and the processing solvent were carefully investigated to improve the performance of the organic solar cells. The optimized organic solar cell with SM:PC60BM and SM:PC70BM cast from THF solvent, at a weight ratio of 1:3 showed power conversion efficiencies (PCEs) of about 1.70% and 2.56%, respectively. The enhanced value of PCE for the BHJ photovoltaic device based on PC70BM is related to the better absorption of PC70BM in the visible region compared to that of PC60BM. The SM:PC70BM blends cast from a DIO-THF mixture and subsequent thermal annealing exhibited improved PCEs of 3.68% and 4.14%, respectively.

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