Conjugated Polymers 1991
DOI: 10.1007/978-94-011-3476-7_12
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Cited by 21 publications
(9 citation statements)
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“…The intermediate 1 was prepared according to literature. [21] The dibromide 1 was first converted to the corresponding diboronate ester 2 (64 %), and then Suzuki coupling with commercially available methyl 2-bromobenzoate gave the tetraphenylene diester 3 in 77 % yield. Addition of four equivalents of 4-octylphenyllithium generated the corresponding diol which was ring closed by BF 3 .…”
Section: Polymer Synthesismentioning
confidence: 99%
“…The intermediate 1 was prepared according to literature. [21] The dibromide 1 was first converted to the corresponding diboronate ester 2 (64 %), and then Suzuki coupling with commercially available methyl 2-bromobenzoate gave the tetraphenylene diester 3 in 77 % yield. Addition of four equivalents of 4-octylphenyllithium generated the corresponding diol which was ring closed by BF 3 .…”
Section: Polymer Synthesismentioning
confidence: 99%
“…For G. Horowitz,24 the first field effects were clearly demonstrated in the 1970s (although at this date, organic photovoltaic components with yields less that 0.1 % had already been published) 25–27. Finally, it is above all the groups of R. H. Friend28, 29 and F. Garnier30, 31 who did much to contribute to the emergence of this domain to which one of the authors made a modest contribution 32. Its development has only really come about though since 2000 24, 33, 34…”
Section: The Birth Of Organic Electronics and The Coupled Developmentmentioning
confidence: 96%
“…15 Nevertheless, high quantum yields for luminescence were revealed for other conjugated polymers such as poly(p-phenylenevinylene), which exhibits a larger band gap (Egap ≈ 2.5 eV, within the range of visible light) 2 in contrast to poly(acetylene) (Egap ≈ 1.4 eV). 16 . This emission is induced by the radiative recombination of a singlet polaron exciton, more figuratively spoken, of an electron-hole pair formed by excitation.…”
Section: Polyfluorenementioning
confidence: 99%
“…[ppm] = 8 16. 8.12 (m, 1H, H-4), 7.56-7.47 (m, 2H, H-1, H-3), 7.25-7.17 (m, 10H, H-15, H-16, H-17), 7.16-7.07 (m, 1H, H-8), 7.00-6.94 (m, 1H, H-6), 4.19-4.15 (m, 2H, H-18), 1.99-1.94 (m, 2H, H-19), 1.63-1.57 (m, 2H, H-20), 1.46-1.29 (m, 8H, H-21, H-22, H-23, H-24), 0.89 (t, 3 JHH = 6.5 Hz, 1H, H-25).…”
mentioning
confidence: 99%