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Synthesis and Characterization of New Polyaryleneethynylenes based on 3-Hexyl Multisubstituted Oligothiophene Blocks

Published online by Cambridge University Press:  21 March 2011

Silvia Destri
Affiliation:
Consiglio Nazionale delle Ricerche, Istituto di Chimica delle Macromolecole, Via Bassini, 15, 20133 Milano, Italy
William Porzio
Affiliation:
Consiglio Nazionale delle Ricerche, Istituto di Chimica delle Macromolecole, Via Bassini, 15, 20133 Milano, Italy
Irina A. Khotina
Affiliation:
Russian Academy of Sciences, A.N.Nesmeyanov Inst. of Organoelement Compounds, Vavilov 28, 117813 Moscow, Russia
Chiara Botta
Affiliation:
Consiglio Nazionale delle Ricerche, Istituto di Chimica delle Macromolecole, Via Bassini, 15, 20133 Milano, Italy
Roberto Consonni
Affiliation:
Consiglio Nazionale delle Ricerche, Istituto di Chimica delle Macromolecole, Via Bassini, 15, 20133 Milano, Italy
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Abstract

A series of new regioregular polyaryleneethynylene obtained by condensation of 3-hexyl multisubstituted oligothiophene derivatives with benzene and anthracene compounds were prepared. A complete NMR characterization of the starting monomers and model compounds lead to a deep investigation of the corresponding macromolecules. Both small and large molecules were optically characterized, the former, particularly when containing anthracene, moieties display noticeable photoluminescence quantum yield. In the polymers the photoluminescence quantum yield is lower than that of the starting molecules when anthracene is present, while the polymers containing benzene are more luminescent.

Type
Research Article
Copyright
Copyright © Materials Research Society 1999

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References

1. Braun, D. and Hegeer, A.J., Appl.Phys.Lett 58, 1982 (1991).Google Scholar
2. Wang, C., Xie, X, LeGoff, E., Albritton-Thomas, J., Kannewurf, C.R. and Kanatzidis, G., Synth. Met., 74, 71 (1995).Google Scholar
3. Destri, S., Khotina, I.A., Porzio, W. and Botta, C., Optical Materials, 9, 411 (1998).Google Scholar
4. Palmans, A.R.A., Smith, P. Weder, C. Macromolecules 32, 4677 (1999).Google Scholar
5. Yamamoto, T., Yamada, W., Takagi, M., Kuzu, K., Maruyama, T., Ooba, N., Tomaru, S., Kurihara, T., Kaino, T., Kubota, K., Macromolecules 27, 6620 (1994).Google Scholar
6. Yamamoto, T., Honda, K., Ooba, N. and Tomaru, S., Macromolecules 31, 7 (1998).Google Scholar
7. Li, J. and Pang, Y., Macromolecules 30, 7487 (1997).Google Scholar
8. Destri, S., Porzio, W., Khotina, I.A., Botta, C., Consonni, R., Macromolecules subm.Google Scholar
9. a) Stephens, R.D. and Castro, C.E., J.Org. Chem. 28, 3313 (1963); b) W.B.Austin, N.Below, W.J.Kelleghan, K.S.Y.J.Lau, Org.Chem. 46, 2280 (1981).Google Scholar
10. Harris, S.J. and Walton, D.R.M., Tetrahedron 34, 1037 (1978).Google Scholar
11. Benincori, T., Bongiovanni, G., Botta, C., Cerullo, G., Lanzani, G., Mura, A., Rossi, L., Sannicolò, F., Tubino, R., Phys. Rev B 58, 9082 (1998).Google Scholar
12. Oelkrug, D., Egelhaaf, H.-J., Gierschner, J., Tompert, A., Synth. Met. 76, 249 (1996).Google Scholar