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Copolymers based on 3-alkylthiophene and Thiophene Functionalized with Pyrene Chromophore

Published online by Cambridge University Press:  06 February 2014

Edgar González-Juárez
Affiliation:
Centro de Investigación en Ingeniería y Ciencias Aplicadas (CIICAp), Universidad Autónoma del Estado de Morelos (UAEM). Av. Universidad No. 1001, Col. Chamilpa, C.P. 62209, Cuernavaca, Morelos, México.
Marisol Güizado-Rodríguez
Affiliation:
Centro de Investigación en Ingeniería y Ciencias Aplicadas (CIICAp), Universidad Autónoma del Estado de Morelos (UAEM). Av. Universidad No. 1001, Col. Chamilpa, C.P. 62209, Cuernavaca, Morelos, México.
Víctor Barba-López
Affiliation:
Centro de Investigaciones Químicas (CIQ), Universidad Autónoma del Estado de Morelos (UAEM). Av. Universidad No. 1001, Col. Chamilpa, C.P. 62209, Cuernavaca, Morelos, México.
Mario Rodríguez
Affiliation:
Centro de Investigaciones en Óptica A.C., Loma del Bosque No. 115, Col. Lomas del Campestre, C.P. 37150, León, Guanajuato, México.
Gabriel Ramos-Ortíz
Affiliation:
Centro de Investigaciones en Óptica A.C., Loma del Bosque No. 115, Col. Lomas del Campestre, C.P. 37150, León, Guanajuato, México.
José Luis Maldonado
Affiliation:
Centro de Investigaciones en Óptica A.C., Loma del Bosque No. 115, Col. Lomas del Campestre, C.P. 37150, León, Guanajuato, México.
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Abstract

As a preliminary study aiming to possible applications, novel polythiophenes (PTs) derivatives of 3-hexylthiophene and a thiophene functionalized with pyrene chromophore were synthesized. Homopolymer and copolymers of these monomers were obtained in different stoichiometric ratios which allow obtaining structure-property relation of each of the polymers. PTs were characterized by FT-IR, 1H NMR, UV-vis, DSC-TGA, GPC and fluorescence experiments. Polymers have λmax between 345 to 450 nm and an emission band at 485 and 542 nm. Low molecular weights distribution (Mn = 875 to 1600 g/mol) and thermostable products (Td = 336 to 474°C) were obtained. These PTs functionalized with aromatic molecules and π-conjugated systems could offer interesting applications such as optical sensors, nonlinear optics and photovoltaic cells.

Type
Articles
Copyright
Copyright © Materials Research Society 2014 

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References

REFERENCES

Yamamoto, T., Macromol. Rapid Commun. 23, 583 (2002).3.0.CO;2-I>CrossRefGoogle Scholar
Casa, D.C., Morguera, F.A., Bizarri, C.P., Lanzi, M., Synth. Met. 124, 467 (2001).CrossRefGoogle Scholar
Wang, B., Watt, S., Hong, M., Domercq, B., Sun, R., Kippelen, B., Collard, D.M., Macromolecules 41, 5156 (2008)Google Scholar
Gonçalves, V.C., Costa, L.M.M., Cardoso, M.R., Mendonca, C.R., Balogh, D.T., J. Appl. a. Polym. Sci. 114, 680 (2009).CrossRefGoogle Scholar
Fraleoni-Morgera, A., Della-Casa, C., Lanzi, M., Costa-Bizzarri, P., Macromolecules a. 36, 8617 (2003).CrossRefGoogle Scholar
Barbarella, G., Bongini, A., Zambianchi, M., Macromolecules 27, 3039 (1994).CrossRefGoogle Scholar
Abd-El-Aziz, A.S., Dalgakiran, S., Kucukkaya, I., Wagner, B.D., Electrochim. Acta 89, 445 (2013).CrossRefGoogle Scholar
Winnik, F.M., Chem. Rev. 93, 587 (1993).CrossRefGoogle Scholar
Xu, L., Zhao, J., Liu, R., Liu, H., Liu, J., Wang, H., Electrochim. Acta 55, 8855 (2010).CrossRefGoogle Scholar