2004
DOI: 10.1021/ma0495947
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Synthesis and Characterization of Poly(triarylamine)s Containing Isothianaphthene Moieties

Abstract: We report the synthesis, characterization, and properties of a new class of hole−transport dyes, poly(dithienylisothianaphthene phenyldiamine)s (poly-DTITNPDs). These polymers are characterized by the presence of a low band gap isothianaphthene (ITN) and triarylamine units in the main chain. A modified Ullmann polycondensation reaction using a phase-transfer catalyst was utilized to prepare these polymers. The optical, thermal, and electrochemical properties were studied and compared to those of poly(triphenyl… Show more

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Cited by 40 publications
(17 citation statements)
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“…Figure 1b (30)(31)(32), and the band gap energy, E g , for PTAA was found to be 2.95 eV from previous PL spectroscopy (23). The barrier height for hole injection ( b φ ) at the PTAA/metal interface can be evaluated using the following equation (16):…”
Section: Resultsmentioning
confidence: 96%
“…Figure 1b (30)(31)(32), and the band gap energy, E g , for PTAA was found to be 2.95 eV from previous PL spectroscopy (23). The barrier height for hole injection ( b φ ) at the PTAA/metal interface can be evaluated using the following equation (16):…”
Section: Resultsmentioning
confidence: 96%
“…During the last decade, more active Pd‐, Cu‐, and Ni‐based catalysts have been developed, allowing for a decrease in catalyst loadings and reaction temperatures . These catalytic systems have afforded high molecular weight PTAAs in Ullmann‐type, Yamamoto, Buchwald‐Hartwig, and Suzuki‐Miyaura polymerizations using conventional and microwave heating …”
Section: Introductionmentioning
confidence: 99%
“…14 Kisselev and Thelakkat achieved the synthesis of polymer containing ITN and triaryl amine groups, a new class of lightharvesting dyes with band gap values below 1.8 eV. 15 Recently, Swager and co-workers reported the synthesis of push-pull-type near-IR fluorophores containing isobenzofuran and isothianaphthene subunits. 16 Cava and co-workers reported the synthesis and electropolymerization of 1,3-dithienylnaphtho[c]thiophene 3.…”
Section: Introductionmentioning
confidence: 99%