G. Barlin, b) Mangalagiu II, Recent achievements in the chemistry, Chemistry of Heterocyclic Compounds, pp.2-730, 1982.

F. See-for-example-buron, N. Plé, A. Turck, G. Queguiner, G. Pettit et al., Synthesis of pyrazine alcaloids from Botryllus leachi. Diazines 43 The cephalostatins. 21. Synthesis of bis-steroidal pyrazine rhamnosides Review of cytotoxic cephalostatins and ritterazines: isolation and synthesis, J Org Chem J Nat Prod J Nat Prod, vol.707471, pp.2616-211922, 2005.

J. Kobayashi, Hyrtioseragamines A and B, new alkaloids from the sponge Hyrtios species, Org Lett, vol.13, pp.628-659, 2011.

H. Maier, Volatile Flavoring Substances in Foodstuffs, Angewandte Chemie International Edition in English, vol.9, issue.12, pp.917-943, 1970.
DOI : 10.1002/anie.197009171

D. Sloot and H. Hofman, Alkylpyrazines in Emmental cheese, Journal of Agricultural and Food Chemistry, vol.23, issue.2, p.358, 1975.
DOI : 10.1021/jf60198a027

I. Flament, M. Kohler, and R. Aschiero, ]pyrazines, identification et mode de formation, Helvetica Chimica Acta, vol.59, issue.7, pp.2308-2321, 1976.
DOI : 10.1002/hlca.19760590703

R. Weissleder and M. Pittet, Imaging in the era of molecular oncology. b) Vance E, Profile: What is that smell?, Nature Nature, vol.452455, pp.580-9726, 2008.

S. For, B. Ellsworth, Y. Wang, Y. Zhu, A. Pendri et al., Discovery of pyrazine carboxamide CB1 antagonists: the introduction of a hydroxyl group improves the pharmaceutical properties and in vivo efficacy of the series Heteroatom-linked indanylpyrazines are corticotropin releasing factor type-1 receptor antagonists, Bioorg Med Chem Lett Bioorg Med Chem Lett, vol.1717, pp.3978-826250, 2007.

V. Buchta, J. Jampilek, and K. Kralova, Synthesis and antimycobacterial evaluation of substituted pyrazinecarboxamides, Eur J Med Chem, vol.43, pp.1105-1118, 2008.

G. Vitale and G. Paglietti, Synthesis and in vitro antitumor activity of new quinoxaline derivatives

M. Heravi, K. Bakhtiari, M. Tehrani, N. Javadi, and H. Oskooie, Facile synthesis of quinoxaline derivatives using o-iodoxybenzoic acid (IBX) at room temperature

?. Gosh, P. Mandal, A. Cheeseman, G. Werstiuk, and E. , Greener approach toward one pot route to pyrazine synthesis, Green Chemistry Letters and Reviews, vol.14, issue.2, pp.127-161, 1972.
DOI : 10.1021/jf60228a058

A. Turck, N. Plé, F. Mongin, and G. Quéguiner, Advances in the directed metallation of azines and diazines (pyridines, pyrimidines, pyrazines, pyridazines, quinolines, benzodiazines and carbolines). Part 2: Metallation of pyrimidines, pyrazines, pyridazines and benzodiazines, b) Chevallier F, Mongin F, Functionalization of diazines and benzo derivatives through deprotonated intermediates, pp.4489-505595, 2001.
DOI : 10.1016/S0040-4020(01)00225-3

F. Toudic, A. Heynderickx, N. Plé, A. Turck, G. Quéguiner et al., Regioselective synthesis and metallation of tributylstannylfluoropyrazines. Application to the synthesis of some new fluorinated liquid crystals diazines. Part 34, Tetrahedron, vol.59, issue.33, pp.6375-841985, 2003.
DOI : 10.1016/S0040-4020(03)00849-4

A. Littke and G. Fu, Palladium-Catalyzed Coupling Reactions of Aryl Chlorides, Angewandte Chemie International Edition, vol.41, issue.22, pp.41-4176, 2002.
DOI : 10.1002/1521-3773(20021115)41:22<4176::AID-ANIE4176>3.0.CO;2-U

O. Willerval, A. Efficient-three-makarasen, M. Kuse, T. Nishikawa, and M. Isobe, 5-substituted pyrazine library Substituent effect of imino-O-arenesulfonates, a coupling partner in Suzuki-Miyaura reaction for substitution of the pyrazine ring: a study for the synthesis of coelenterazine analogs, ACS Combin Sci, vol.23, pp.13-449, 2011.

J. Goossens, C. Bailly, S. Routier, and J. Mérour, Synthesis of 2,6-diphenylpyrazine derivatives and their DNA binding and cytotoxic properties, Eur J Med Chem, pp.40-1206, 2005.

M. Darabantu, L. Boully, A. Turck, N. Plé, D. Gündisch et al., Synthesis of new polyaza heterocycles, Synthesis and evaluation of diazine containing bioisosteres of, pp.61-2897, 2005.

J. Milne and S. Buchwald, An extremely active catalyst for the Negishi cross-coupling reaction, J Am Chem Soc, pp.126-13028, 2004.

B. Shook, D. Chakravarty, and P. Jackson, Microwave-assisted Sonogashira-type cross couplings of various heterocyclic methylthioethers, Tetrahedron Letters, vol.50, issue.9, pp.50-1013, 2009.
DOI : 10.1016/j.tetlet.2008.12.055

B. Tang, F. Wang, J. Li, Y. Xie, and M. Zhang, Reusable Cu 2 O/PPh 3 /TBAB system for the cross-couplings of aryl halides and heteroaryl halides with terminal alkynes, J Org Chem, pp.72-6294, 2007.

I. Malik, M. Hussain, A. Ali, T. Toguem, S. Basha et al., Synthesis of 2,3-disubstituted pyrazines and quinoxalines by Heck cross-coupling reactions of 2,3-dichloropyrazine and 2,3-dichloroquinoxaline. Influence of the temperature on the product distribution, Tetrahedron, pp.66-1637, 2010.

A. Fürstner, A. Leitner, M. Méndez, H. Krause, L. Boully et al., Iron-catalyzed cross-coupling reactions Plé N, Aryl-aryl bonds formation in pyridine and pyazine series. Diazines part 41, J Am Chem Soc J Heterocycl Chem, pp.124-13856, 2002.

J. Vanden-eynde, L. Pascal, Y. Van-haverbeke, P. Dubois, G. Lipunova et al., Quaternary ammonium saltassisted synthesis of extended pi-systems from methyldiazines and aromatic aldehydes Azinylarylethenes: synthesis and photophysical and photochemical properties, Synth Commun Russ Chem Rev, pp.32-3167, 2001.

S. Achelle and N. Plé, Pyrimidine as building block for the synthesis of functionalized piconjugated materials, Curr Org Synth, vol.2012, pp.9-163
URL : https://hal.archives-ouvertes.fr/hal-00862261

K. Shirai, A. Yanagisawa, H. Takahashi, K. Fukunishi, and M. Matsuoka, Syntheses and fluorescent properties of 2,5-diamino-3,6-dicyanopyrazine dyes, Dyes and Pigments, vol.39, issue.1, pp.39-49, 1998.
DOI : 10.1016/S0143-7208(98)00008-4

J. Kim, S. Shin, M. Matsuoka, and K. Fukunishi, Self-Assembling of Aminopyrazine Fluorescent Dyes and Their Solid State Spectra, Dyes and Pigments, vol.39, issue.4, pp.39-341, 1998.
DOI : 10.1016/S0143-7208(98)00017-5

K. Shirai, M. Matsuoka, and K. Fukunishi, New syntheses and solid state fluorescence of azomethine dyes derived from diaminomaleonitrile and 2,5-diamino-3,6-dicyanopyrazine, Dyes and Pigments, vol.47, issue.1-2, pp.47-107, 2000.
DOI : 10.1016/S0143-7208(00)00068-1

G. Angulo, J. Dobkowski, and A. Kapturkiewicz, Luminescence properties of diamino-dicyano substituted benzene and 1,4-pyrazine, Journal of Photochemistry and Photobiology A: Chemistry, vol.225, issue.1, pp.225-52, 2011.
DOI : 10.1016/j.jphotochem.2011.09.025

H. Kim, J. , R. Shin, S. Matsuoka, M. Fukunishi et al., Self-Assembling of Aminopyrazine Fluorescent Dyes and Their Solid State Spectra, Dyes and Pigments, vol.39, issue.4, pp.41-183, 1999.
DOI : 10.1016/S0143-7208(98)00017-5

A. Poreddy, B. Asmelash, W. Neumann, and R. Dorshow, A Highly Efficient Method for the N-Alkylation of Aminopyrazines: Synthesis of Hydrophilic Red Fluorescent Dyes, Synthesis, vol.2010, issue.14, pp.2383-92, 2010.
DOI : 10.1055/s-0029-1220009

R. Rajagopalan, W. Neumann, A. Poreddy, R. Fitch, J. Freskos et al., Hydrophilic Pyrazine Dyes as Exogenous Fluorescent Tracer Agents for Real-Time Point-of-Care Measurement of Glomerular Filtration Rate, Journal of Medicinal Chemistry, vol.54, issue.14, pp.54-5048, 2011.
DOI : 10.1021/jm200257k

G. , C. H. Lin, L. Lee, N. Yang, C. Neumann et al., Multicompartment polymer nanostructures with ratiomeric dualemission pH-sensitivity, J Am Chem Soc, pp.133-8534, 2011.

C. Zhao, Q. Dai, T. Seino, Y. Cui, S. Nishizawa et al., Strong and selective binding of amiloride to thymine base opposite AP sites in DNA duplexes : simultaneous binding to DNA phophate backbone Strong and selective binding of amiloride to an abasic site in RNA duplexes: thermodynamic characterization and microRNA detection, Chem Commun Angew Chem Int Ed, pp.1185-7516369, 2006.

J. Jaung, M. Matsuoka, and K. Fukunishi, Syntheses and properties of new styryl dyes derived from 2,3-dicyano-5-methylpyrazines, Dyes and Pigments, vol.31, issue.2, pp.31-141, 1996.
DOI : 10.1016/0143-7208(95)00096-8

M. Matsuoka and K. Fukunishi, Dicyanopyrazine studies. Part V: Syntheses and characteristics of chalcone analogues of dicyanopyrazine, Dyes Pigm, pp.40-51, 1998.

J. Jaung, M. Matsuoka, and K. Fukunishi, Syntheses and characterization of new styryl fluorescent dyes from DAMN. Part II, Dyes and Pigments, vol.34, issue.4, pp.34-255, 1997.
DOI : 10.1016/S0143-7208(96)00086-1

M. and D. Studies, Syntheses and characterization of new bis-styryl fluorescent dyes from DAMN, Part III Dyes Pigm, pp.36395-405, 1998.

J. Kim, Y. Choi, B. Kim, D. Choi, and S. Kim, Crystal morphology and their lattice contraction control for the topochemical reaction of bis(phenyl-ethenyl)-dicyanopyrazines

J. Kim, M. Matsuoka, K. Fukunishi, K. Ahn, D. Lee et al., Selective Topochemical Photodimerization of Styryldicyanopyrazines in the Solid State, Journal of Chemical Research, vol.762589, issue.2, pp.422-8132, 1999.
DOI : 10.1039/a808684b

R. Cristiano, E. Westphal, I. Bechtold, A. Bortoluzzi, and H. Gallardo, Synthesis and optical/thermal properties of low molecular mass V-shaped materials based on 2,3-dicyanopyrazine, Tetrahedron, vol.63, issue.13, pp.2851-2859, 2007.
DOI : 10.1016/j.tet.2007.01.045

C. Jang, C. Song, S. Jung, J. Jaung, C. Jang et al., Topochemically photoreacted fluorescent dimers of 2,3-dicyanopyrazines, Dicyanopyrazine Dimers Linked with Cyclobutane Ring by [2+2]Photocycloaddition, pp.49-542165, 2011.
DOI : 10.1016/j.dyepig.2011.10.015

B. Lee, J. Jaung, B. Lee, J. Jaung, and S. Jeong, Synthesis and characteristics of dicyanopyrazine dyes containing spiropyran group, Synthesis of spiropyran substituted, pp.135-177, 2002.

J. Jaung, Synthesis of new porphyrins with dicyanopyrazine moiety and their optical properties, Dyes and Pigments, vol.72, issue.3, pp.315-336, 2007.
DOI : 10.1016/j.dyepig.2005.09.006

T. Mori and K. Ariga, Antioxaydant-substituted tetrapyrazinoporphyrazine as a fluorescent sensor for basic anions, Chem Commun, pp.3951-3954, 2012.

F. Bure?, H. ?ermáková, J. Kulhánek, M. Ludwig, W. Kuznik et al., Structure-Property Relationships and Nonlinear Optical Effects in Donor-Substituted Dicyanopyrazine-Derived Push-Pull Chromophores with Enlarged and Varied ??-Linkers, European Journal of Organic Chemistry, vol.443, issue.3, pp.529-567
DOI : 10.1002/ejoc.201101226

S. Haroutounian and J. Katzenellenbogen, 4???-Hydroxystyryldiazines: Synthesis and fluorescence properties, Tetrahedron, vol.51, issue.6, pp.1585-98, 1995.
DOI : 10.1016/0040-4020(94)01050-A

S. Achelle, A. Barsella, C. Baudequin, and C. B. , Synthesis and Photophysical Investigation of a Series of Push???Pull Arylvinyldiazine Chromophores, The Journal of Organic Chemistry, vol.77, issue.8, pp.4087-96, 2012.
DOI : 10.1021/jo3004919
URL : https://hal.archives-ouvertes.fr/hal-00862264

A. Aranda, S. Achelle, F. Hammerer, F. Mahuteau-betzer, and M. Teulade-fichou, Vinyl-diazine triphenylamines and their N-methylated derivatives: Synthesis, photophysical properties and application for staining DNA, Dyes and Pigments, vol.95, issue.2, pp.400-407, 2012.
DOI : 10.1016/j.dyepig.2012.04.009
URL : https://hal.archives-ouvertes.fr/hal-00863086

V. Schmitt, J. Fischer, and H. Detert, Linear and Angular Distyrylpyrazines with Terminal Donor Groups: Synthesis, Solvatochromism, and Acidochromism of the Electronic Spectra, ISRN Organic Chemistry, vol.13, issue.1???3, pp.589012-589022, 2011.
DOI : 10.1039/b006764o

N. Nemkovich, H. Detert, and V. Schmitt, Localized excitation effect on dipole moments of oligophenylenevinylenes in their excited Franck???Condon state, Chemical Physics, vol.378, issue.1-3, pp.37-41, 2010.
DOI : 10.1016/j.chemphys.2010.09.011

S. Al-hazmy, A. Babaqi, E. Daltrozzo, M. Klink, J. Sauter et al., A new diolefinic laser dye: 2, 5-bis-2-(2-naphthyl) vinyl pyrazine (B2NVP), J Photochem Photobiol A: Chem 1999:122;17?22. b) The spectra, Proc Indian Acad Sci, vol.2105, issue.22, pp.5-25, 1993.

C. Wink and H. Detert, Donor-substituted distyrylpyrazines: influence of steric congestion on UV-Vis absorption and fluorescence, Journal of Physical Organic Chemistry, vol.54, issue.2, pp.144-50, 2013.
DOI : 10.1002/poc.2978

B. Schmidt, Bis(arylvinyl)pyrazines, -pyrimidines, and ?pyridazines As Imaging Agents for

J. Collette and A. Harper, Chemically responsive fluorophores exhibiting large color changes, Nanoscale Optics and Applications, pp.122-157, 2002.
DOI : 10.1117/12.453778

S. Yan, R. Huang, Y. Zhou, M. Zhang, M. Deng et al., Aptamer-based turn-on fluorescent four-branched quaternary ammonium pyrazine probe for selective thrombin detection, Chem. Commun., vol.126, issue.4, pp.1273-1278, 2011.
DOI : 10.1039/C0CC02792H

F. Wu, S. Bae, and J. Hong, A selective fluorescent sensor for Pb(II) in water, Tetrahedron Letters, vol.47, issue.50, pp.8851-8855, 2006.
DOI : 10.1016/j.tetlet.2006.10.060

F. Wu, Y. Xiang, Y. Wu, and F. Xie, Study of interaction of a fluorescent probe with DNA, Journal of Luminescence, vol.129, issue.11, pp.1286-91, 2009.
DOI : 10.1016/j.jlumin.2009.06.010

N. Hebbar, Y. Ramondenc, G. Plé, G. Dupas, and N. Plé, Push???pull structures with a pyrazine core and hexatriene chain: synthesis and light-emitting properties, Tetrahedron, vol.65, issue.21, pp.4190-200, 2009.
DOI : 10.1016/j.tet.2009.03.042

N. Hebbar, C. Fiol-petit, Y. Ramondenc, G. Plé, and N. Plé, A new series of rod-like conjugated molecules with a pyrazine or a bipyrazine core. Synthesis and light emitting properties, Tetrahedron, vol.67, issue.12, pp.2287-98, 2011.
DOI : 10.1016/j.tet.2011.01.068
URL : https://hal.archives-ouvertes.fr/hal-01018101

. Di, (aryleneethynyl)pyrazine derivatives: synthesis, structural and optoelectronic properties, and light-emitting devices¨,devices¨, New J Chem, vol.28, pp.912-920, 2004.

F. Türksoy, G. Hughes, A. Batsanov, and M. Bryce, Phenylene???2,5-dimethylpyrazine co-oligomers: synthesis by Suzuki couplings, X-ray structures of neutral and diprotonated teraryl species and efficient blue emission, J. Mater. Chem., vol.12, issue.7, pp.1554-1561, 2003.
DOI : 10.1039/B303472K

F. Fugisawa, A. Ramos, P. Filho, O. Serra, and M. Zaniquelli, Formation of thin luminescent Eu3+-LB films by in situ coordination with 2,3,5,6-tetra(2???-pyridyl)pyrazine and 1-octadecanol in pure and mixed Langmuir monolayers, Journal of Luminescence, vol.132, issue.5, pp.1116-1137, 2012.
DOI : 10.1016/j.jlumin.2011.12.081

R. Saito, S. Machita, S. Suzuki, and A. Katoh, Synthesis and Spectroscopic Properties of 2,5-Bis(benzoazol-2-yl)pyrazines, HETEROCYCLES, vol.75, issue.3, pp.531-537, 2008.
DOI : 10.3987/COM-07-11226

R. Saito, Y. Matsumura, S. Suzuki, and N. Okazaki, Intensely blue-fluorescent 2,5-bis(benzoimidazol-2-yl)pyrazine dyes with improved solubility: their synthesis, fluorescent properties, and application as microenvironment polarity probes, Tetrahedron, vol.66, issue.42, pp.8273-8282, 2010.
DOI : 10.1016/j.tet.2010.08.036

P. Thirumurugan and P. Perumal, The synthesis and photophysical studies of pyridinyl-1,2,4-triazine derivatives and use as a fluorescent sensor for ferric salts, Dyes and Pigments, vol.88, issue.3, pp.403-415, 2011.
DOI : 10.1016/j.dyepig.2010.07.013

R. Tsien and S. Lippard, Fluorescent sensors for Zn 2+ based on a fluorescein platform: synthesis, properties and intracellular distribution, J Am Chem Soc, vol.123, pp.7831-7872, 2001.

X. Zhang, D. Hayes, S. Smith, S. Friedle, and S. Lippard, New Strategy for Quantifying Biological Zinc by a Modified Zinpyr Fluorescence Sensor, Journal of the American Chemical Society, vol.130, issue.47, p.15788, 2008.
DOI : 10.1021/ja807156b

D. Buccella, J. Horowitz, and S. Lippard, Understanding Zinc Quantification with Existing and Advanced Ditopic Fluorescent Zinpyr Sensors, Journal of the American Chemical Society, vol.133, issue.11, pp.4101-4115, 2011.
DOI : 10.1021/ja110907m
URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3077067

Y. Kubota, H. Hara, S. Tanaka, K. Funabiki, and M. Matsui, Synthesis and Fluorescence Properties of Novel Pyrazine???Boron Complexes Bearing a ??-Iminoketone Ligand, Organic Letters, vol.13, issue.24, pp.6544-6551, 2011.
DOI : 10.1021/ol202819w

G. Ge, J. He, H. Guo, F. Wang, and D. Zou, Highly efficient phosphorescent iridium (III) diazine complexes for OLEDs: Different photophysical property between iridium (III) pyrazine complex and iridium (III) pyrimidine complex, Journal of Organometallic Chemistry, vol.694, issue.19, pp.3050-3057, 2009.
DOI : 10.1016/j.jorganchem.2009.05.037

B. Coe, J. Fielden, S. Foxon, I. Asselberghs, K. Clays et al., Two-Dimensional, Pyrazine-Based Nonlinear Optical Chromophores with Ruthenium(II) Ammine Electron Donors, Inorganic Chemistry, vol.49, issue.22, pp.10718-10744, 2010.
DOI : 10.1021/ic1019197

M. Pizzotti, R. Ugo, D. Roberto, and S. Bruni, -1,2-Bis(4-pyridyl)ethylene as Linkers, Organometallics, vol.21, issue.26, pp.5830-5870, 2002.
DOI : 10.1021/om020633h
URL : https://hal.archives-ouvertes.fr/hal-00479516

K. Kudo, A. Momotake, Y. Kanna, Y. Nishimura, and T. Arai, Development of a quinoxalinebased fluorescent probe for quantitative estimation of protein binding site polarity, Chem Commun, pp.3867-3876, 2011.

B. Bachowska, G. Matusiak, and G. , 1, 4-phenylenedivinylene) bis-quinoxaline and a series of styryl derivatives of quinoxaline and quinoline as promising electro-and photoluminescent materials, Chem Heterocycl Compd, vol.245, pp.2-80, 2009.

P. Thirumurugan, D. Muralidharan, and P. Perumal, The synthesis and photophysical studies of quinoxaline and pyridopyrazine derivatives, Dyes and Pigments, vol.81, issue.3, pp.245-53, 2009.
DOI : 10.1016/j.dyepig.2008.10.018

J. Jaung, Synthesis and halochromism of new quinoxaline fluorescent dyes, Dyes and Pigments, vol.71, issue.3, pp.245-50, 2006.
DOI : 10.1016/j.dyepig.2005.07.008

C. Jang, Y. Lee, S. Han, and J. Jaung, The synthesis and optical characterization of quinoxalines bearing 2,2???:6???,2???-terpyridine, 2?:6?,2?-terpyridine, pp.101-105, 2008.
DOI : 10.1016/j.dyepig.2007.10.012

V. Arun, P. Robinson, S. Manju, P. Leeju, G. Varsha et al., A novel fluorescent bisazomethine dye derived from 3-hydroxyquinoxaline-2-carboxaldehyde and, Dyes Pigm, vol.282, pp.3-268, 2009.

V. Arun, S. Mathew, P. Robinson, M. Jose, V. Nampoori et al., The tautomerism, solvatochromism and non-linear optical properties of fluorescent 3-hydroxyquinoxaline-2-carboxalidine-4-aminoantipyrine, Dyes and Pigments, vol.87, issue.2, pp.149-57, 2010.
DOI : 10.1016/j.dyepig.2010.03.012

H. Wang, G. Chen, Y. Liu, L. Hu, X. Xu et al., The synthesis and characterization of novel dipolar fluorescent materials based on a quinoxaline core, Dyes and Pigments, vol.83, issue.3, pp.269-75, 2009.
DOI : 10.1016/j.dyepig.2009.03.007

X. Cao, J. F. Li, Y. Chen, W. Duan, X. Yang et al., Triphenylamine-modified quinoxaline derivatives as two-photon photoinitiators, New Journal of Chemistry, vol.17, issue.7, pp.1578-82, 2009.
DOI : 10.1039/b900464e

K. Thomas, J. Lin, and Y. Tao, Quinoxalines Incorporating Triarylamines:?? Potential Electroluminescent Materials with Tunable Emission Characteristics, Chemistry of Materials, vol.14, issue.6, pp.2796-802, 2002.
DOI : 10.1021/cm0201100

K. Thomas, M. Velusamy, J. Lin, C. Chuen, and Y. Tao, Chromophore-Labeled Quinoxaline Derivatives as Efficient Electroluminescent Materials, Chemistry of Materials, vol.17, issue.7, pp.1860-1866, 2005.
DOI : 10.1021/cm047705a

T. Lin, Y. Huang, B. Huang, and Y. Lee, Synthesis and two-photon properties of a multi-polar chromophore based on tetra-quinoxalinylethylene scaffold, Tetrahedron Letters, vol.52, issue.50, pp.6748-53, 2011.
DOI : 10.1016/j.tetlet.2011.10.019

H. Burrows, S. Fonseca, B. Gigante, M. Esteves, and A. Guerreiro, Fluorescence Study of Dehydroabietic Acid-Based Bipolar Arylamine-Quinoxalines, Journal of Fluorescence, vol.103, issue.2, pp.227-258, 2006.
DOI : 10.1007/s10895-005-0048-6

G. Bernardo, M. Esteves, A. Guerreiro, B. Gigante, and J. Morgado, Luminescence properties of bipolar stylbeneamine???quinoxalines, Optical Materials, vol.31, issue.2, pp.320-327, 2008.
DOI : 10.1016/j.optmat.2008.05.001

X. Xu, S. Chen, L. Li, G. Yu, C. Di et al., Photophysical properties of polyphenylphenyl compounds in aqueous solutions and application of their nanoparticles for nucleobase sensing, Journal of Materials Chemistry, vol.100, issue.22, pp.2555-61, 2008.
DOI : 10.1039/b801984c

L. Gooßen, M. Gerhards, and W. Thiel, Simple Access to Sol-Gel Precursors Bearing Fluorescent Aromatic Core Units, Eur J Org Chem, vol.2012, pp.2142-51

C. , A. B. Try, A. Ruiperez, C. Sessler, and J. , Dipyrrolylquinoxalines : Efficient Sensors for Fluoride Anion in Organic Solution, J Am Chem Soc, vol.121, p.10438, 1999.

P. Anzenbacher, A. Try, H. Miyaji, K. Jurs?, V. Lynch et al., Fluorinated Calix[4]pyrrole and Dipyrrolylquinoxaline:?? Neutral Anion Receptors with Augmented Affinities and Enhanced Selectivities, Dipyrrolylquinoxaline : Neutral Anion Receptors with Augmented Affinities and Enhanced Selectivities, pp.10268-72, 2000.
DOI : 10.1021/ja002112w

J. Sessler, H. Maeda, T. Mizuno, V. Lynch, and H. Furuta, Quinoxaline-oligopyrroles: Improved pyrrole-based anion receptors, Chem Commun, pp.862-865, 2002.
DOI : 10.1002/chin.200227198

D. Aldakov and P. Anzenbacher, Dipyrrolyl Quinoxalines with Extended Chromophores are Efficient Fluorimetric Sensors for Pyrophosphate., ChemInform, vol.34, issue.40, pp.1394-1399, 2003.
DOI : 10.1002/chin.200340162

J. Sessler, H. Maeda, T. Mizuno, V. Lynch, H. Furuta et al., Quinoxaline-Bridged Porphyrinoids, Journal of the American Chemical Society, vol.124, issue.45, pp.13474-13483, 2002.
DOI : 10.1021/ja0273750

L. Wang, X. Zhu, W. Wong, J. Guo, W. Wong et al., Dipyrrolylquinoxaline-bridged Schiff bases: a new class of fluorescent sensors for mercury(ii), Dalton Transactions, vol.66, issue.19, pp.3235-3275, 2005.
DOI : 10.1039/b505676d

Y. Hu, Q. Li, H. Li, Q. Guo, Y. Lu et al., Hg(II) turn-on and, A novel class of Cd(II)

K. Yusuff, Two new fluorescent heterocyclic perimidines: first syntheses, crystal structure, and spectral characterization, Tetrahedron Lett, vol.51, pp.2174-2181, 2010.

A. Katoh, M. Takahashi, and J. Ohkanda, Synthesis of 2,3-Disubstituted 6-Aminoquinoxalines and Their Application to New Fluorescence Derivatization Reagents for Carboxylic Acids, Chemistry Letters, vol.25, issue.5, pp.369-70, 1996.
DOI : 10.1246/cl.1996.369

Y. Matsumura and A. Katoh, Synthesis of 2,3-dimorpholino-6-aminoquinoxaline derivatives and application to a new intramolecular fluorescent probe, Journal of Luminescence, vol.128, issue.4, pp.625-655, 2008.
DOI : 10.1016/j.jlumin.2007.10.012

P. Dixneuf, Solution , solid state structure and fluorescence studies of 2 , 3-functionalized quinoxalines : evidence for a ?-delocalized keto-enamine form with N ? HO intramolecular hydrogen bonds, New J Chem, vol.25, pp.391-396, 2001.

R. Duke and T. Gunnlaugsson, Fluorescent sensing of anions using a bis-quinoxaline amidothiourea based supramolecular cleft; an example of an anion-induced deprotonation event, Tetrahedron Letters, vol.51, issue.41, pp.5402-5407, 2010.
DOI : 10.1016/j.tetlet.2010.07.168

H. Benzeid, E. Mothes, E. Essassi, P. Faller, and G. Pratviel, A thienoquinoxaline and a styryl-quinoxaline as new fluorescent probes for amyloid-?? fibrils, Comptes Rendus Chimie, vol.15, issue.1, pp.79-85, 2012.
DOI : 10.1016/j.crci.2011.10.009

K. Thomas and P. Tyagi, ]quinoxaline, The Journal of Organic Chemistry, vol.75, issue.23, pp.8100-8111, 2010.
DOI : 10.1021/jo1016663

S. Butini, Pyrroloquinoxaline hydrazones as fluorescent probes for amyloid fibrils, Org Biomol Chem, vol.9, pp.5137-5185, 2011.

S. Matsumoto, E. Batmunkh, M. Akazome, Y. Takata, and M. Tamano, Novel formation of diimidazo[1,2-a:2???,1???-c]quinoxaline derivatives and their optical properties, Organic & Biomolecular Chemistry, vol.17, issue.446, pp.5941-5945, 2011.
DOI : 10.1039/c1ob06002c

K. Wang, W. Shi, J. Jia, S. Chen, and H. Ma, Characterization of 2-phenylbenzo[g]quinoxaline derivatives as viscosity-sensitive fluorescent probes, Talanta, vol.77, issue.5, pp.1795-1804, 2009.
DOI : 10.1016/j.talanta.2008.10.021

P. Wang, Z. Xie, O. Wong, C. Lee, N. Wong et al., New 1H-pyrazolo[3,4- b]quinoxaline derivatives as sharp green-emitting dopants for highly efficient electroluminescent devices, Chem. Commun, pp.1404-1409, 2002.

J. Wong, O. Lee, and C. , Synthesis, photoluminescence and electroluminescence of new 1H-pyrazolo[3,4-b]quinoxaline derivatives, Journal of Materials Chemistry, vol.13, issue.8, pp.13-1894, 2003.
DOI : 10.1039/b302972g

R. Podsiad?y, A. Szymczak, and K. Podemska, The synthesis of novel, visible-wavelength, oxidizable polymerization sensitizers based on the 8-halogeno-5,12-dihydroquinoxalino, Dyes Pigm, vol.2, pp.82-365, 2009.

R. Bolligarla and S. Das, Synthesis of new intramolecular charge transfer A???D???A tetrathiafulvalene-fused triads exhibiting large solvent sensitive emission behavior, Tetrahedron Letters, vol.52, issue.19, pp.2496-500, 2011.
DOI : 10.1016/j.tetlet.2011.03.016

C. Jia, J. Zhang, J. Bai, L. Zhang, Z. Wan et al., Synthesis, physical properties and self-assembly of conjugated donor???acceptor system based on tetrathiafulvalene and functionalized with binding sites, Dyes and Pigments, vol.94, issue.3, pp.403-412, 2012.
DOI : 10.1016/j.dyepig.2012.02.008