Materiais moleculares funcionais contendo n-heterociclos - capes
Materiais moleculares funcionais contendo n-heterociclos - capes Materiais moleculares funcionais contendo n-heterociclos - capes
1,4-Diaryl and Schiff’s base LC compounds 10031477 (2002); S. Torgova, A. Strigazzi. Mol. Cryst. liq.Cryst., 375, 61 (2002); R. Giménez, M. Pinol, J.L. Serrano.Chem. Mater., 16, 1377 (2004); M. Grell, D.D.C. Bradley.Adv. Mater., 11, 895 (1999).[4] S. Velazquez, R. Alvarez, C. Perez, F. Gago, C. De J.Balzarini, M. Camaraza. J. antivir. Chem. Chemother. 9,481 (1998); S. Palhagen, R. Canger, O. Heriksen, J.A. vanParys, M.E. Riviere, M.A. Karolchyk. Epilepsy Res., 43,115 (2001); V. Calderone. Curr. Med. Chem., 9, 1385(2002).[5] J.T. Sharp. In Synthetic applications of 1,3-dipolarcycloaddition chemistry toward heterocycles and naturalproducts, A. Padwa, W.H. Pearson (Eds), pp. 473–538,Wiley-Interscience, New York (2002).[6] S. Içli, A.S. Astley, C. Timur, O. Anaç, O. Sezer, K.Dabak. J. Lumin., 82, 41 (1999).[7] K. Sivakumar, F. Xie, B.M. Cash, S. Long, H.N.Barnhill, Q. Wang. Org. Lett., 6, 4603 (2004).[8] H.C. Kolb, M.G. Finn, K.B. Sharpless. Angew. Chem.113, 1998 (2001); H.C. Kolb, M.G. Finn, K.B. Sharpless.Angew. Chem. int. Ed., 40, 2004 (2001).[9] V.V. Rostovtsev, L.G. Green, V.V. Fokin, K.B.Sharpless. Angew. Chem. int. Ed. 41, 2596 (2002); Q.Wang, T.R. Chan, R. Hilgraf, V.V. Fokin, K.B.Sharpless. J. Am. chem. Soc., 125, 3192 (2003); Y.-M.Wu, J. Deng, X. Fang, O.-Y. Chen. J. fluorine Chem.,125, 1415 (2004).[10] H. Gallardo, F. Ely, A.J. Bortoluzzi, G. Conte. Liq.Cryst., 32, 667 (2005).[11] H. Fahmi, T. Lovell, R. Hilgraf, V.V. Rostovtsev, L.Noodleman, K.B. Sharpless, V.V. Fokin. J. Am. chem.Soc., 127, 210 (2005).[12] G. Conte, F. Ely, H. Gallardo. Liq. Cryst., 32, 1213(2005).[13] G. Conte, R. Cristiano, F. Ely, H. Gallardo. Synth.Commun., 36, 951 (2006).
Tetrahedron 63 (2007) 2851–2858Synthesis and optical/thermal properties of low molecular massV-shaped materials based on 2,3-dicyanopyrazineRodrigo Cristiano, a Eduard Westphal, a Ivan H. Bechtold, b Adailton J. Bortoluzzi aand Hugo Gallardo a, *a Departamento de Quımica, Universidade Federal de Santa Catarina, 88040-900 Florianopolis, SC, Brazilb Departamento de Fısica, Universidade Federal de Santa Catarina, 88040-900 Florianopolis, SC, BrazilReceived 1 November 2006; revised 8 January 2007; accepted 22 January 2007Available online 25 January 2007Abstract—A novel series of luminescent low molecular mass materials containing a 2,3-dicyanopyrazine central core were synthesizedthrough an esterification reaction between diphenol 10 and different aromatic carboxylic acids 1–6, containing terminal long alkyl chains.They have a similar V-shaped geometry with lack of planarity between the two arms, confirmed by the X-ray structure of the central core.The optical and thermal properties of these compounds were evaluated. They show blue fluorescence in solution (l maxem 440–480 nm) withquantum fluorescence yields (F F ) from 0.003 to 0.1 and Stokes shifts of around 90 nm. In solid state, optical band gaps (E g ) were from3.14 to 3.32 eV. Thin films of 11, 13, and 14 exhibited blue fluorescence (l maxem 430–456 nm), and 12, 15, and 16 (more bulky) displayed greenfluorescence (l maxem 488–512 nm). Most of the materials exhibited good thermal stability, exhibiting an amorphous glassy state after melting.Transparent amorphous films were easily obtained through spin coating and characterized by AFM analysis.Ó 2007 Elsevier Ltd. All rights reserved.1. IntroductionOrganic compounds that exhibit a variety of interestingoptical, electrical, photoelectrical, and magnetic propertiesin the solid state have found widespread use in a growingnumber of practical applications, including their utility asemitters in light-emitting diodes, 1 laser dyes, 2 photoconductors,3 optical switches, 4 and optical data storage devices. 5Low molecular mass materials that are able to form stablefilms are particularly interesting in such functional systemsdue to their well-defined molecular structures and molecularweights, and also because they can be easily purified.Among these materials and their organization states, twoclasses in particular have been extensively exploited: fluorescentliquid crystals, 6 as the self organizing properties ofthese materials can lead to defect-free layers with high carriermobility for electroluminescence devices, and varioustypes of amorphous molecular glass, because of their goodprocessability, transparency, and homogeneity. 7Dicyanopyrazine derivatives have been synthesized and arevaluable in a broad range of chemistry fields due to theirapplications as functional dyes, nonlinear optical materials,etc. 8 They have strong electron withdrawing ability and,Keywords: 2,3-Dicyanopyrazine; Luminescent materials; X-ray structure;Functional dyes.* Corresponding author. Fax: +55 48 3721 6850; e-mail: hugo@qmc.ufsc.brdespite possessing a small chromophoric system, they presentstrong fluorescence even in solid state. 9 In this context,our research is focused on fluorescent molecular materialscontaining electron deficient N-heterocycles that can exhibiteither liquid crystalline phases 10 or a stable glassy state foropto-electronic applications.In this paper, we report on the synthesis of a series of fluorescent2,3-dicyanopyrazine derivatives (11–16) possessinga similar V-shaped geometry 11 with some lack of planarity,in order to achieve a mesomorphic or film forming behavior.The photophysical properties in solution and in thin film,along with the thermal behavior of these compounds, werealso evaluated.2.1. Synthesis2. Results and discussionScheme 1 outlines the synthesis of the series of 2,3-dicyanopyrazinederivatives. Anisil 7 was prepared from 4-methoxybenzaldehydethrough benzoin condensation followed byhydroxyl group oxidation using CuSO 4 /pyridine. A condensationreaction of anisil 7 with diaminomaleonitrile(DAMN) in the presence of a catalytic amount of p-toluenesulfonicacid (p-TsOH) gave the 2,3-dicyanopyrazine derivative8 in good yield (90%). An attempt to achieve methyl0040–4020/$ - see front matter Ó 2007 Elsevier Ltd. All rights reserved.doi:10.1016/j.tet.2007.01.045
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1,4-Diaryl and Schiff’s base LC compounds 10031477 (2002); S. Torgova, A. Strigazzi. Mol. Cryst. liq.Cryst., 375, 61 (2002); R. Giménez, M. Pinol, J.L. Serrano.Chem. Mater., 16, 1377 (2004); M. Grell, D.D.C. Bradley.Adv. Mater., 11, 895 (1999).[4] S. Velazquez, R. Alvarez, C. Perez, F. Gago, C. De J.Balzarini, M. Camaraza. J. antivir. Chem. Chemother. 9,481 (1998); S. Palhagen, R. Canger, O. Heriksen, J.A. vanParys, M.E. Riviere, M.A. Karolchyk. Epilepsy Res., 43,115 (2001); V. Calderone. Curr. Med. Chem., 9, 1385(2002).[5] J.T. Sharp. In Synthetic applications of 1,3-dipolarcycloaddition chemistry toward heterocycles and naturalproducts, A. Padwa, W.H. Pearson (Eds), pp. 473–538,Wiley-Interscience, New York (2002).[6] S. Içli, A.S. Astley, C. Timur, O. Anaç, O. Sezer, K.Dabak. J. Lumin., 82, 41 (1999).[7] K. Sivakumar, F. Xie, B.M. Cash, S. Long, H.N.Barnhill, Q. Wang. Org. Lett., 6, 4603 (2004).[8] H.C. Kolb, M.G. Finn, K.B. Sharpless. Angew. Chem.113, 1998 (2001); H.C. Kolb, M.G. Finn, K.B. Sharpless.Angew. Chem. int. Ed., 40, 2004 (2001).[9] V.V. Rostovtsev, L.G. Green, V.V. Fokin, K.B.Sharpless. Angew. Chem. int. Ed. 41, 2596 (2002); Q.Wang, T.R. Chan, R. Hilgraf, V.V. Fokin, K.B.Sharpless. J. Am. chem. Soc., 125, 3192 (2003); Y.-M.Wu, J. Deng, X. Fang, O.-Y. Chen. J. fluorine Chem.,125, 1415 (2004).[10] H. Gallardo, F. Ely, A.J. Bortoluzzi, G. Conte. Liq.Cryst., 32, 667 (2005).[11] H. Fahmi, T. Lovell, R. Hilgraf, V.V. Rostovtsev, L.Noodleman, K.B. Sharpless, V.V. Fokin. J. Am. chem.Soc., 127, 210 (2005).[12] G. Conte, F. Ely, H. Gallardo. Liq. Cryst., 32, 1213(2005).[13] G. Conte, R. Cristiano, F. Ely, H. Gallardo. Synth.Commun., 36, 951 (2006).