Palladium-Catalyzed Dehydrohalogenative Polycondensation of 2-Bromo-3-hexylthiophene: An Efficient Approach to Head-to-Tail Poly(3-hexylthiophene)
Journal of the American Chemical Society2010Vol. 132(33), pp. 11420–11421
Citations Over TimeTop 1% of 2010 papers
Abstract
Dehydrohalogenative polycondensation of 2-bromo-3-hexylthiophene was successful with Herrmann's catalyst and tris(2-dimethylaminophenyl)phosphine as catalyst precursors, giving head-to-tail poly(3-hexylthiophene) (HT-P3HT) with high molecular weight (M(n) = 30,600, M(w)/M(n) = 1.60) and high regioregularity (98%) in almost quantitative yield (99%).
Related Papers
- → High basicity of phosphorus–proton affinity of tris-(tetramethylguanidinyl)phosphine and tris-(hexamethyltriaminophosphazenyl)phosphine by DFT calculations(2006)61 cited
- → Synthesis of the tertiaryphosphine derivatives of iron carbonyl phosphines: preparation of tetracarbonyl[tris(2-furyl)phosphine]iron(0), pentacarbonylbis[μ-bis(2-furyl)phosphido]-[tris(2-furyl)phosphine]diiron(0), tetracarbonyl[tris(2-benzofuryl) phosphine]iron(0) and pentacarbonylbis[μ-bis(2-benzofuryl) phosphido]-[tris(2-benzofuryl) phosphine]diiron-(0)(1995)16 cited
- → Tris(n-butyl)phosphine, Tris(tert-butyl)phosphine and Tris(trimethylsilyl)phosphine(1995)22 cited
- → Structural and electronic properties of tris(4-trifluoromethyltetrafluorophenyl)phosphine(2015)1 cited