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From thiophene to Sulflower

Konstantin Yuryevich Chernichenko 1
Konstantin Yuryevich Chernichenko
Elizabeth Sergeevna Balenkova 1
Elizabeth Sergeevna Balenkova
Valentin Georgievich Nenajdenko
Published 2008-07-17
Focus articleVolume 18, Issue 4, 171-179
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Chernichenko K. Y., Balenkova E. S., Nenajdenko V. G. From thiophene to Sulflower // Mendeleev Communications. 2008. Vol. 18. No. 4. pp. 171-179.
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Chernichenko K. Y., Balenkova E. S., Nenajdenko V. G. From thiophene to Sulflower // Mendeleev Communications. 2008. Vol. 18. No. 4. pp. 171-179.
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TY - JOUR
DO - 10.1016/j.mencom.2008.07.001
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.07.001
TI - From thiophene to Sulflower
T2 - Mendeleev Communications
AU - Chernichenko, Konstantin Yuryevich
AU - Balenkova, Elizabeth Sergeevna
AU - Nenajdenko, Valentin Georgievich
PY - 2008
DA - 2008/07/17
PB - Mendeleev Communications
SP - 171-179
IS - 4
VL - 18
ER -
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@article{2008_Chernichenko,
author = {Konstantin Yuryevich Chernichenko and Elizabeth Sergeevna Balenkova and Valentin Georgievich Nenajdenko},
title = {From thiophene to Sulflower},
journal = {Mendeleev Communications},
year = {2008},
volume = {18},
publisher = {Mendeleev Communications},
month = {Jul},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.07.001},
number = {4},
pages = {171--179},
doi = {10.1016/j.mencom.2008.07.001}
}
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Chernichenko, Konstantin Yuryevich, et al. “From thiophene to Sulflower.” Mendeleev Communications, vol. 18, no. 4, Jul. 2008, pp. 171-179. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.07.001.
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Abstract

Several new approaches toward annulated oligothiophenes, including Sulflower, the first fully heterocyclic circulene, have been proposed.

References

1.
T. A. Skotheim, R. L. Elsenbaumer and J. R. Reynolds, Handbook of Conducting Polymers, 2nd edn., Marcel Dekker, New York, 1998.
2.
Handbook of Organic Conductive Molecules and Polymers, ed. H. S. Nalwa, Wiley, Chichester, 1997, vol. 1–4.
3.
Light-emitting diodes based on conjugated polymers
Burroughes J.H., Bradley D.D., Brown A.R., Marks R.N., Mackay K., Friend R.H., Burns P.L., Holmes A.B.
Nature, 1990
4.
Organic Electroluminescent Devices
Sheats J.R., Antoniadis H., Hueschen M., Leonard W., Miller J., Moon R., Roitman D., Stocking A.
Science, 1996
5.
Electroluminescence in conjugated polymers
Friend R.H., Gymer R.W., Holmes A.B., Burroughes J.H., Marks R.N., Taliani C., Bradley D.D., Santos D.A., Brédas J.L., Lögdlund M., Salaneck W.R.
Nature, 1999
7.
Substituted polythiophenes designed for optoelectronic devices and conductors
Andersson M.R., Thomas O., Mammo W., Svensson M., Theander M., Inganäs O.
Journal of Materials Chemistry A, 1999
8.
Advances in organic field-effect transistors
Sun Y., Liu Y., Zhu D.
Journal of Materials Chemistry A, 2005
9.
Light-Emitting Polythiophenes
Perepichka I.F., Perepichka D.F., Meng H., Wudl F.
Advanced Materials, 2005
12.
Linear Ladder-Type π-Conjugated Polymers Composed of Fused Thiophene Ring Systems
Oyaizu K., Iwasaki T., Tsukahara Y., Tsuchida E.
Macromolecules, 2004
14.
Annelated Heptathiophene: A Fragment of a Carbon–Sulfur Helix
Rajca A., Wang H., Pink M., Rajca S.
Angewandte Chemie - International Edition, 2000
17.
H. Hopf, Classics in Hydrocarbon Chemistry: Syntheses, Concepts, Perspectives, Wiley-VCH, Weinheim, 2000.
18.
“Sulflower”: A New Form of Carbon Sulfide
Chernichenko K.Y., Sumerin V.V., Shpanchenko R.V., Balenkova E.S., Nenajdenko V.G.
Angewandte Chemie - International Edition, 2006
19.
Synthesis and properties of some heterocirculenes
Dopper J.H., Wynberg H.
Journal of Organic Chemistry, 1975
20.
Synthesis and resolution of some heterohelicenes
Wynberg H., Groen M.B., Schadenberg H.
Journal of Organic Chemistry, 1971
21.
Photochemically induced cyclization of some furyl- and thienylethenes
Kellogg R.M., Groen M.B., Wynberg H.
Journal of Organic Chemistry, 1967
22.
Use of thieno[2,3-b]thiophene in the synthesis of heterohelicenes by double photocyclizations
Dopper J.H., Oudman D., Wynberg H.
Journal of the American Chemical Society, 1973
23.
Dehydrogenation of heterohelicenes by a Scholl type reaction. Dehydrohelicenes
Dopper J.H., Oudman D., Wynberg H.
Journal of Organic Chemistry, 1975
24.
10.1016/j.mencom.2008.07.001_bib24
Erdtman
J. Chem. Soc., Chem. Commun., 1968
25.
Dithienothiophenes
Ozturk T., Ertas E., Mert O.
Tetrahedron, 2005
26.
A Novel Synthesis of Dithieno[2,3-b:3′,2′-d]thiophene and its Bromo Derivatives
Nenajdenko V.G., Gribkov D.V., Sumerin V.V., Balenkova E.S.
Synthesis, 2003
27.
Synthesis, oxidation, and electronic spectra of four dithienothiophenes
Janssen M.J., De Jong F.
Journal of Organic Chemistry, 1971
28.
New Syntheses of Tricyclic Thiophenes and Cyclic Tetrathiophenes Using Transition-Metal-catalyzed Cyclization
Iyoda M., M. Humayun Kabir S., Miura M., Sasaki S., Harada G., Kuwatani Y., Yoshida M.
Heterocycles, 2000
29.
Bromination, deuteration, and lithiation of the dithienyls
Kellogg R.M., Schaap A.P., Wynberg H.
Journal of Organic Chemistry, 1969
31.
Organic Syntheses, Coll. Vol. 5, ed. H. E. Baumgarten, John Wiley & Sons, New York, 1973, p. 149.(Organic Syntheses, ed. W. E. Parham, John Wiley & Sons, New York, 1964, vol. 44, p. 9).
32.
A New Route to Annulated Oligothiophenes
Nenajdenko V.G., Sumerin V.V., Chernichenko K.Y., Balenkova E.S.
Organic Letters, 2004
33.
Fourier Transform Raman and DFT Study of Three Annulated Oligothiophenes with Different Molecular Shapes
Malavé Osuna R., Ponce Ortiz R., Ruiz Delgado M.C., Nenajdenko V.G., Sumerin V.V., Balenkova E.S., Hernández V., López Navarrete J.T.
ChemPhysChem, 2007
34.
Push−Pull Bithienyl Chromophore with an Unusual Transverse Path of Conjugation
Ponce Ortiz R., Osuna R.M., Hernández V., López Navarrete J.T., Vercelli B., Zotti G., Sumerin V.V., Balenkova E.S., Nenajdenko V.G.
Journal of Physical Chemistry A, 2007
35.
M. G. Voronkov and V. E. Udre, Khim. Geterotsikl. Soedin., 1968, 43.[Chem. Heterocycl. Compd. (Engl. Transl.), 1968, 4, 33].
36.
10.1016/j.mencom.2008.07.001_bib36
Miyasaka
Synlett, 2004
37.
Synthesis of Heterocyclic Cyclopolyaromatics Containing Similar Kinds of Nuclei
Kauffmann T., Greving B., König J., Mitschker A., Woltermann A.
Angewandte Chemie International Edition in English, 1975
39.
Planar [6]Radialenes: Structure, Synthesis, and Aromaticity of Benzotriselenophene and Benzotrithiophene
Patra A., Wijsboom Y., Shimon L. ., Bendikov M.
Angewandte Chemie - International Edition, 2007
41.
S. S. Bukalov, L. A. Leites, K. A. Lyssenko, R. R. Aysin, A. A. Korlyukov, J. V. Zubavichus, K.Yu. Chernichenko, E. S. Balenkova, V. G. Nenajdenko and M.Yu. Antipin, J. Phys. Chem., 2008, submitted.