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2014 | 2 | 1 |
Tytuł artykułu

Spectral properties and photophysics of arylacetylenes in thin films

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
We report the photobehaviour of a series of eight structurally related arylacetylene derivatives, in solution as well as in pristine and PC61BM blended thin-_lms. The formation of both H- and J-aggregates in the solid state have been demonstrated, and, interestingly, an energy transfer from H-aggregates or/and from residual "unstacked" molecules to J-aggregates has been found, the latter being the only emitting species. The fuorescence quenching by PC61BM at di_erent loadings has been studied in blend films, and it has been found particularly effcient in the case of a symmetrical peripheral substitution of the acetylene derivative core. Preliminary time-resolved measurements in emission (ns resolution) and in absorption (fs resolution) con_rmed the H⟶J energy transfer and underlined the presence of delayed fuorescence from Jaggregates, formed by energy transfer from the long-lived first excited singlet state of H-aggregates. In all cases, a homogeneous surface morphology of thin films.
Wydawca
Rocznik
Tom
2
Numer
1
Opis fizyczny
Daty
otrzymano
2013-10-21
zaakceptowano
2013-10-26
online
2014-02-19
Twórcy
  • Department of Chemistry, and Centro di Eccellenza sui Materiali
    Innovativi Nanostrutturati (CEMIN), University of Perugia, via
    Elce di Sotto 8, 06123 Perugia, Italy
  • Department of Chemistry, and Centro di Eccellenza sui Materiali
    Innovativi Nanostrutturati (CEMIN), University of Perugia, via
    Elce di Sotto 8, 06123 Perugia, Italy
  • Department of Chemistry, and Centro di Eccellenza sui Materiali
    Innovativi Nanostrutturati (CEMIN), University of Perugia, via
    Elce di Sotto 8, 06123 Perugia, Italy
  • Department of Chemistry, and Centro di Eccellenza sui Materiali
    Innovativi Nanostrutturati (CEMIN), University of Perugia, via
    Elce di Sotto 8, 06123 Perugia, Italy
Bibliografia
  • [1] H. Xin, X. Guo, G.. Ren, M.D. Watson, S. A. Jenekhe, Adv. En.Mater. 2, 575(2012)
  • [2] A. Marrocchi, D. Lanari, A. Facchetti, A., L. Vaccaro, En. Eviron.Sci. 5, 8457 (2012)
  • [3] P.-Y. Huang, L.-H. Chen, C. Kim, C. Hsiu-Chieh, Y.-J. Liang, C.-Y. Feng, C.-M. Yeh, J.-C. Ho, C.-C. Lee, M.-C. Chen, ACS Appl.Mater. Interfaces 4, 6992 (2012)
  • [4] T. S. van der Poll, J. A. Love, T.-Q. Nguyen, G. C. Bazan, Adv.Mater. 24, 3646 (2012)
  • [5] A. Facchetti, Chem. Mater. 23, 733 (2011)
  • [6] A. Facchetti, L. Vaccaro, A. Marrocchi, Angew. Chem. Int. Ed.51, 3520 (2012)
  • [7] P. Berrouard, A. Najari, A. Pron, D. Gendron, P.-O. Morin, J.-R.Pouliot, J. Veilleux, M. Leclerc, Angew. Chem. Int. Ed. 51, 2068(2012)
  • [8] A. Marrocchi, Curr. Org. Synth. 9, 149 (2012)
  • [9] M. Hasegawa, M. Iyoda, Chem. Soc. Rev. 39, 2429 (2010)
  • [10] M. Leclerc, J.-F. Morin (eds.), Design and Synthesis of ConjugatedPolymers (Wiley-VCH, Weinheim, 2010)
  • [11] A.C. Grimsdale, K. L. Chan, R. E. Martin, P. G. Jokisz, A. B.Holmes, Chem. Rev. 109, 897 (2009).
  • [12] A. Heeger, F. Hide, B. Schwartz, M. A. Diaz-Garcia, Chem Phys.Lett. 256, 424 (1996).
  • [13] C. Li, Y. Li, Macromol. Chem. Phys. 209, 1541 (2008)
  • [14] F. Diederich, P. J. Stang, R. R. Tykwinski (eds), Acetylene Chemistry:Chemistry, Biology, and Materials Science (Wiley-VCH:Weinheim, Germany, 2005)
  • [15] Bunz, U. H.F. Chem. Rev. 100, 1605 (2000).[PubMed]
  • [16] W. Zhang, S.M. Kraft, J. S. Moore, J. Am. Chem. Soc. 126, 329(2004)
  • [17] P. Siemsen, R. C. Livingston, F. Diederich, Angew. Chem. Int.Ed. 39, 2632 (2000)
  • [18] K. Sonogashira, Metal Catalyzed cross-coupling reactions(Wiley-VCH, Weinheim, Germany, 1998)
  • [19] K. Weiss, A. Michel, E.-M. Auth, E.H.F. Bunz, T. Mangel, K.Mullen, Angew. Chem. Int. Ed. 25, 506 (1997)
  • [20] R.R. Schrock, Polyhedron 14, 3177 (1995).
  • [21] W. A, Braunecker, S. D. Oosterhout, Z. R. Owczarczyk, R.E. Larsen, B. W. Larson, D. S. Ginley, O. V. Boltalina, S. H.Strauss, N. Kopidakis, D. C. Olson, Macromolecules 46, 3367(2013)
  • [22] C. Kästner, S. Rathgeber, D.A.M. Egbe, H. Hoppe, J. Mater.Chem. A 1, 3961 (2013)
  • [23] S. Rochat, T. M. Swager, ACS Appl. Mater. Interface 5, 4488(2013)
  • [24] C. Kästner, B. Muhsin, A. Wild, D. A. M Egbe, S. Rathgeber, H.Hoppe, J. Polym. Sci. B 51, 868 (2013)
  • [25] A. Operamolla, R. Ragni, O. H. Omar, G. Iacobellis, A. Cardone,F. Babudri, G. Farinola, Curr. Org. Synth. 9, 764 (2012)
  • [26] A. Marrocchi, I. Tomasi, L. Vaccaro, Isr. J. Org. Chem. 52, 42(2012)
  • [27] F. Silvestri, A. Marrocchi, Int. J. Mol. Sci. 11, 1471 (2010)
  • [28] A.C Grimsdale, K. L. Chan, R.E Martin, P.G Jokisz, A.B Holmes,Chem. Soc. Rev. 109, 897 (2009).
  • [29] Q. Niu, Y. Lu, H. Sun, X. Li, X. Tao, Dyes and Pigments 97, 184(2013)
  • [30] F. Feng, J. Yang, D. Xie, T. D. McCarley, K. S. Schanze, J. Phys.Chem. Lett. 4, 1410 (2013)
  • [31] B. A. Coombs, S. R. Rutter, A. E. Goeta, H. A. Sparkes, A. S.Batsanov, A. Beeby, RSC Adv. 2, 1870 (2012)
  • [32] S. Cook, H. Ohkita, Y. Kim, J. J. Benson-Smith, D. D. C. Bradley,J. R. Durrant, Chem. Phys. Lett. 445, 276 (2007)
  • [33] K.-Y. Pu, B. Zhang, Z. Ma, P. Wang, X.-Y. Qi, R.-F. Chen, L.-H.Wang, Q.-L. Fan, W. Huang, Polymer 47, 1970 (2006)
  • [34] P. V. James, P. K. Sudeep, C. H. Suresh, K. G. Thomas, J. Phys.Chem. A 110, 4329 (2006)
  • [35] U. H. F. Bunz, J. M. Imhof, R. K. Bly, C. G. Bangcuyo, L. Rozanski,D. A. Vanden Bout, Macromolecules 38, 5892 (2005)
  • [36] M. Levitus, G. Zepeda, H. Dang, C. Godinez, T.-A. V. Khuong,K. Schmieder, M. A. Garcia-Garibay, J. Org. Chem. 66, 3188(2001).
  • [37] E. Bartollini, M. Seri, S. Tortorella, A. Facchetti, T. J. Marks, A.Marrocchi, L. Vaccaro, RSC Adv. 3, 9288 (2013)
  • [38] M. Seri, A. Marrocchi, D. Bagnis, R. Ponce, A. Taticchi, T.J.Marks, A. Facchetti, Adv. Mater. 23, 3827 (2011)
  • [39] P. Wolfer, M. L. Santarelli, L. Vaccaro, L. Yu, T. D. Anthopulos,P. Smith, N. Stingelin, A. Marrocchi, Org. Electron. 12, 1886(2011)
  • [40] F. Silvestri, A. Marrocchi, M. Seri, C. Kim, A. Facchetti, A. Taticchi,T. J. Marks, J. Am. Chem. Soc. 132, 6109 (2010)
  • [41] A. Marrocchi, F. Silvestri, M. Seri, A. Facchetti, A. Taticchi, T. J.Marks. Chem. Commun., 1380 (2009)
  • [42] A. Marrocchi, M. Seri, C. Kim, A. Facchetti, A. Taticchi, T. J.Marks, Chem. Mater. 21, 2592 (2009)
  • [43] S. R. Saudari, Y. J. Lin, Y. Lai, C. R. Kagan, Adv. Mater. 22, 5063(2010)
  • [44] H. Yan, Y. Zheng, R. Blache, C. Newman, S. Lu, J. Woerle, A.Facchetti, Adv. Mater. 20, 3393 (2008).
  • [45] A. K. K. Kyaw, D. H. Wang, D. Wynands, J. Zhang, T.-Q. Nguyen,G. C. Bazan, A. J. Heeger, Nano Lett. 13, 3796 (2013).[PubMed]
  • [46] R. Flamini, I. Tomasi, A. Marrocchi, B. Carlotti, A. Spalletti, J.Photochem. Photobiol. A 223, 140 (2011)
  • [47] A. Marrocchi, A. Spalletti, S. Ciorba, M. Seri, F. Elisei, A. Taticchi,J. Photochem. Photobiol. A 211, 162 (2010)
  • [48] I. Votta, A. Marrocchi, L. Vaccaro, unpublished results.
  • [49] B. Carlotti, D. Fuoco, F. Elisei, Phys. Chem. Chem. Phys. 12,15580, (2010).
  • [50] T. Del Giacco, B. Carlotti, A. Barbafina, S. De Solis and F. Elisei,Phys. Chem. Chem. Phys. 13, 2188 (2011).[Crossref]
  • [51] A. Mishra, R. K. Behera, P. K. Behera, B. K. Mishra, G. B. Behera,Chem. Rev. 100, 1973 (2000) and references therein.
  • [52] M. Kasha, H.R. Rawls, M.A. El-Bayoumi, Pure Appl. Chem. 11,371 (1965).
  • [53] S.D. Spencer, C. Bougher, P.J. Heaphy, V.M. Murcia, C.P. Gallivan,A. Monfette, J.D. Andersen, J.A. Cody, Solar Energy Materials& Solar Cells 112, 202 (2013).
  • [54] G. de Miguel, M. Ziólek, M. Zitnan, J.A. Organero, S.S. Pandey,S. Hayase, A. Douhal, J. Phys. Chem. C 116, 9379 (2012).
  • [55] J.-H. Hsu, W. Fann, P.-H. Tsao, K.-R. Chuang, S.-A. Chen, J.Phys. Chem. A 103, 2375 (1999).
  • [56] N.C. Maiti, S. Mazumdar, N. Periasamy, J. Phys. Chem. B 102,1528 (1998).
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_oph-2014-0001
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