Wild, Andreas et al. published their research in Journal of Polymer Science, Part A: Polymer Chemistry in 2009 |CAS: 146370-51-6

The Article related to thiophene anthracene polyphenylenevinylene polyphenyleneethynylene conjugated polymer photophys electrochem property, Chemistry of Synthetic High Polymers: Organic Condensation and Step Polymerization and other aspects.Computed Properties of 146370-51-6

On May 1, 2009, Wild, Andreas; Egbe, Daniel A. M.; Birckner, Eckhard; Cimrova, Vera; Baumann, Reinhard; Grummt, Ulrich-Walter; Schubert, Ulrich S. published an article.Computed Properties of 146370-51-6 The title of the article was Anthracene- and thiophene-containing MEH-PPE-PPVs: Synthesis and study of the effect of the aromatic ring position on the photophysical and electrochemical properties. And the article contained the following:

This contribution reports on the synthesis and characterization of thiophene- (P1, P2, and P3) and anthracene- (P4 and P5) containing PPE-PPV [poly(phenylene-ethynylene)-poly(phenylenevinylene)] copolymers. The thermostable, soluble and film-forming polymers were fully characterized by NMR, IR and elemental anal.; they exhibit high molar masses with polydispersity indexes below 2.5. The position of the thiophene in the polymeric backbone has insignificant influence on the spectroscopic properties of the polymers. In contrast, the anthracene-containing polymers reveal position dependent optical properties. A constant bathochromic shift of 50 nm was observed going from P4, where anthracene is surrounded by two double bonds, to P5, where anthracene is at the bridge between a triple bond and a double bond, as well as from P5 to P6 where anthracene is surrounded by two triple bonds. This correlates to the decrease of the observed anthracene band around 255 nm going from P4 through P5 to P6, amounting to the degree of contribution of the anthracene unit to the main chain conjugation. The phenomenon known as CN-PPV effect was observed in the case of P4 [Φf (solution) = 3%, Φf (solid) = 13%]. Electrochem. studies carried out under absolute inert conditions revealed lower electrochem. band gap energies, Egec, than Egopt. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2243-2261, 2009. The experimental process involved the reaction of 1-((2-Ethylhexyl)oxy)-4-methoxybenzene(cas: 146370-51-6).Computed Properties of 146370-51-6

The Article related to thiophene anthracene polyphenylenevinylene polyphenyleneethynylene conjugated polymer photophys electrochem property, Chemistry of Synthetic High Polymers: Organic Condensation and Step Polymerization and other aspects.Computed Properties of 146370-51-6

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem