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177716-59-5

177716-59-5 Structure

177716-59-5 Structure
IdentificationBack Directory
[Name]

POLY[2-METHOXY-5-(3′,7′-DIMETHYLOCTYLOXY)-1,4-PHENYLENEVINYLENE]
[CAS]

177716-59-5
[Synonyms]

MODO-PPV
MDMO-PPV
Regular- MDMO-PPV
MDMO-PPV light-emitting polymer
Poly[2-methoxy-5-(3,7-dimethyoctyoxyl)-1,4-phenylenevinylene]
Poly[2-methoxy-5-(3,7-dimethyloctyloxy) phenylenevinylene-1,4-diyl]
Poly[[2-[(3,7-dimethyloctyl)oxy]-5-methoxy-1,4-phenylene]-1,2-ethenediyl]
Poly[2-methoxy-5-(3′,7′-dimethyloctyloxy)-1,4-phenylenevinylene],MDMO-PPV
[Molecular Formula]

(C19H28O2)n
[MDL Number]

MFCD03458070
[MOL File]

177716-59-5.mol
Chemical PropertiesBack Directory
[solubility ]

toluene, xylene, tetrahydrofuran, chloroform, chlorobenzene, cyclohexanone: soluble
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

MDMO-PPV can also be used in the fabrication of bulk heterojunction solar cells(BHJ).
[Definition]

ChEBI: Haloperidol is a compound composed of a central piperidine structure with hydroxy and p-chlorophenyl substituents at position 4 and an N-linked p-fluorobutyrophenone moiety. It has a role as a serotonergic antagonist, a first generation antipsychotic, a dopaminergic antagonist, an antidyskinesia agent and an antiemetic. It is a hydroxypiperidine, an organofluorine compound, an aromatic ketone, a tertiary alcohol and a member of monochlorobenzenes.
[General Description]

MDMO-PPV is a dialkoxy substituted poly(p-phenylenevinylene) (PPV) based conjugating polymer which has long side chains that form flexible films for organic electronics. It is a piezoresistant polymer with HOMO and LUMO orbital positions at 5.4 and 3.4 eV, respectively. MDMO-PPV forms an active layer that can be used in photoconductive and electroluminescent applications. Its processability and film-forming properties are superior to MEH-PPV.
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