Poly[[1,2,3,6,7,8-hexahydro-2,7-bis(2-octyldodecyl)-1,3,6,8-dioxobenzo[lMn][3,8]phenanthroline-4,9-diyl][2,2'-bithiophene]-5,5'-diyl]
Classification Applications- Product Name
- Poly[[1,2,3,6,7,8-hexahydro-2,7-bis(2-octyldodecyl)-1,3,6,8-dioxobenzo[lMn][3,8]phenanthroline-4,9-diyl][2,2'-bithiophene]-5,5'-diyl]
- CAS No.
- 1100243-40-0
- Chemical Name
- Poly[[1,2,3,6,7,8-hexahydro-2,7-bis(2-octyldodecyl)-1,3,6,8-dioxobenzo[lMn][3,8]phenanthroline-4,9-diyl][2,2'-bithiophene]-5,5'-diyl]
- Synonyms
- N2200;PNDI(2OD)2T;P(NDI2OD-T2);PNDI-2T N2200;N2200/PNDI-2T;N2200/P(NDIOD-T2);P(NDI2OD-T2); N2200;4-methyl-9-(5'-methyl-[2,2'-bithiophen]-5-yl)-2,7-bis(2-octyldodecyl)benzo[lmn][3,8]phenanthroline-1,3,6,8(2H,7H)-tetraone;Poly[[1,2,3,6,7,8-hexahydro-2,7-bis(2-octyldodecyl)-1,3,6,8-dioxobenzo[lmn][3,8]phenanthroline-4,9-diyl][2,2'-bithiophene]-5,5'-diyl;Poly[[1,2,3,6,7,8-hexahydro-2,7-bis(2-octyldodecyl)-1,3,6,8-dioxobenzo[lMn][3,8]phenanthroline-4,9-diyl][2,2'-bithiophene]-5,5'-diyl]
- CBNumber
- CB72734786
- Molecular Formula
- (C62H88N2O4S2)n
- Formula Weight
- 0
- MOL File
- 1100243-40-0.mol
Poly[[1,2,3,6,7,8-hexahydro-2,7-bis(2-octyldodecyl)-1,3,6,8-dioxobenzo[lMn][3,8]phenanthroline-4,9-diyl][2,2'-bithiophene]-5,5'-diyl] Property
- Melting point:
- 308 °C (DSC transition temperature)
- solubility
- Soluble in chloroform, chlorobenzene, dichlorobenzene
N-Bromosuccinimide Price
- Product number
- 900961
- Product name
- P(NDI2OD-T2)
- Packaging
- 100MG
- Price
- $602
- Updated
- 2024/03/01
- Product number
- 900961
- Product name
- P(NDI2OD-T2)
- Packaging
- 500MG
- Price
- $2140
- Updated
- 2024/03/01
Poly[[1,2,3,6,7,8-hexahydro-2,7-bis(2-octyldodecyl)-1,3,6,8-dioxobenzo[lMn][3,8]phenanthroline-4,9-diyl][2,2'-bithiophene]-5,5'-diyl] Chemical Properties,Usage,Production
Classification
Organic n-type semiconducting materials, Organic photovoltaics, Polymer solar cells, Electron-acceptor polymers, OFETs, Perovskite solar cells.
Applications
PNDI(2OD)2T, a copolymer of naphthalene diimide (NDI) and bithiophene unit, has been intensively studied for use as an electron acceptor in polymer solar cells. This is due to its high electron mobility, high electron affinity, and broad light absorption. All polymer solar cells with PNDI(2OD)2T as an acceptor and J51 as a donor (fullerene-free) have demonstrated a power conversion efficiency over 8%.
PNDI(2OD)2T is also known as a high-mobility n-type polymer semiconductor. PNDI(2OD)2T-based OFET devices have electron mobilities up to 0.45–0.85 cm2V-1 s-1.
Description
PNDI(2OD)2T, a copolymer of naphthalene diimide (NDI) and bithiophene unit, has been intensively studied for use as an electron acceptor in polymer solar cells. This is due toits high electron mobility, high electron affinity, and broad light absorption. All polymer solar cells withPNDI(2OD)2T as an acceptor and J51 as a donor (fullerene-free) have demonstrated a power conversion efficiency over 8% .
Poly[[1,2,3,6,7,8-hexahydro-2,7-bis(2-octyldodecyl)-1,3,6,8-dioxobenzo[lMn][3,8]phenanthroline-4,9-diyl][2,2'-bithiophene]-5,5'-diyl] Preparation Products And Raw materials
Raw materials
Preparation Products
Poly[[1,2,3,6,7,8-hexahydro-2,7-bis(2-octyldodecyl)-1,3,6,8-dioxobenzo[lMn][3,8]phenanthroline-4,9-diyl][2,2'-bithiophene]-5,5'-diyl] Suppliers
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