DOI: 10.1002/anie.199503031. Oligothiophenes—Yet Longer? Synthesis, Characterization, and Scanning Tunneling Microscopy Images of Homologous, Isomerically Pure Oligo(alkylthiophene)s

Oligothiophenes—Yet Longer? Synthesis, Characterization, and Scanning Tunneling Microscopy Images of Homologous, Isomerically Pure Oligo(alkylthiophene)s

10.1002/anie.199503031

Crossref journal-article

Wiley

Angewandte Chemie International Edition in English (311)

Bibliography

BÃ¤uerle, P., Fischer, T., Bidlingmeier, B., Rabe, J. P., & Stabel, A. (1995). OligothiophenesâYet Longer? Synthesis, Characterization, and Scanning Tunneling Microscopy Images of Homologous, Isomerically Pure Oligo(alkylthiophene)s. Angewandte Chemie International Edition in English, 34(3), 303â307. Portico.

Authors 5

Peter Bäuerle (first)
Thomas Fischer (additional)
Bernd Bidlingmeier (additional)
Jürgen P. Rabe (additional)
Andreas Stabel (additional)

References 36 Referenced 221

10.1002/ange.19941060717
10.1002/anie.199407631
{'key': 'e_1_2_1_2_2', 'first-page': '202', 'volume': '35', 'author': 'Pearson D. L.', 'year': '1994', 'journal-title': 'Polym. Prepr.'} / Polym. Prepr. by Pearson D. L. (1994)
10.1002/ange.19941061322
10.1002/anie.199413601
Lithographic structural dimensions of <10 nm have been reported recently: C. Joachim 2nd European Conference on Molecular Electronics Banz September 4–9 1994.
10.1016/0379-6779(91)91110-V
10.1016/0379-6779(93)90483-D
10.1016/0379-6779(91)91108-M
10.1002/adma.19920040209
10.1021/ja00058a035
10.1021/ja00072a026
10.1002/adma.19910030307
10.1016/0379-6779(93)91090-O
10.1002/polb.1993.090310115
10.1021/la00054a021
10.1088/0031-8949/44/1/018
10.1002/adma.19940060714
10.1021/ja00015a067
10.1002/adma.19920040707
M.Sato M.Hiroi Chem. Lett.1994 985–988. (10.1246/cl.1994.985)
P.Bäuerle F.Pfau H.Schlupp F.Würthner K.‐U.Gaudl M. BalpardaCaro P.Fischer J. Chem. Soc. Perkin Trans. 2 1993 489–494. (10.1039/P29930000489)
10.1002/ange.19740860902
10.1002/anie.197402911
10.3987/R-1983-10-1937
10.1021/jo01254a019
10.1002/cber.19811141120
10.3987/R-1987-07-1793
10.1002/ange.19931050136
10.1002/anie.199300761
10.1021/ja00033a063
10.1021/ja00075a042
Polymerization of 3‐dodecyl‐2 2′‐bithiophene [16] which corresponds to half of quaterthiophene1 leads to a polymer that also has one solubilizing group per two thiophene units. The polymer has an oxidation potential ofEpa= 0.35 V vs Fc/Fc+.
10.1088/0031-8949/1993/T49A/045
10.1016/0379-6779(94)90010-8
10.1111/j.1365-2818.1988.tb01423.x

Dates

Type	When
Created	21 years, 7 months ago (Jan. 16, 2004, 9:21 a.m.)
Deposited	1 year, 10 months ago (Oct. 10, 2023, 3:08 p.m.)
Indexed	4 months, 1 week ago (April 26, 2025, 1:04 a.m.)
Issued	30 years, 6 months ago (Feb. 21, 1995)
Published	30 years, 6 months ago (Feb. 21, 1995)
Published Online	21 years, 8 months ago (Dec. 22, 2003)
Published Print	30 years, 6 months ago (Feb. 21, 1995)

Funders 0

None

BibTeX

@article{B_uerle_1995, title={Oligothiophenes—Yet Longer? Synthesis, Characterization, and Scanning Tunneling Microscopy Images of Homologous, Isomerically Pure Oligo(alkylthiophene)s}, volume={34}, ISSN={0570-0833}, url={http://dx.doi.org/10.1002/anie.199503031}, DOI={10.1002/anie.199503031}, number={3}, journal={Angewandte Chemie International Edition in English}, publisher={Wiley}, author={Bäuerle, Peter and Fischer, Thomas and Bidlingmeier, Bernd and Rabe, Jürgen P. and Stabel, Andreas}, year={1995}, month=feb, pages={303–307} }

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