[1] Alston, J. R., Kobayashi, S., Younts, T. J., & Poler, J. C. (2010). Synthesis and characterization of rigid +2 and +3 heteroleptic dinuclear ruthenium(II) complexes. Polyhedron, 29, 2696–2702. DOI: 10.1016/j.poly.2010.06.012. http://dx.doi.org/10.1016/j.poly.2010.06.012CrossrefGoogle Scholar
[2] Balzani, V., Ceroni, P., Juris, A., Venturi, M., Campagna, S., Puntoriero, F., & Serroni, S. (2001). Dendrimers based on photoactive metal complexes. Recent advances. Coordination Chemistry Reviews, 219–221, 545–572. DOI: 10.1016/s0010-8545(01)00351-4. http://dx.doi.org/10.1016/S0010-8545(01)00351-4Web of ScienceCrossrefGoogle Scholar
[3] Bodige, S., Torres, A. S., Maloney, D. J., Tate, D., Kinsel, G. R., Walker, A. K., & MacDonnell, F. M. (1997). First-generation chiral metallodendrimers: Stereoselective synthesis of rigid D3-symmetric tetranuclear ruthenium complexes. Journal of the American Chemical Society, 119, 10364–10369. DOI: 10.1021/ja9720467. http://dx.doi.org/10.1021/ja9720467CrossrefGoogle Scholar
[4] Campagna, S., Di Pietro, C., Loiseau, F., Maubert, B., McClenaghan, N., Passalacqua, R., Puntoriero, F., Ricevuto, V., & Serroni, S. (2002). Recent advances in luminescent polymetallic dendrimers containing the 2,3-bis(2′-pyridyl)pyrazine bridging ligand. Coordination Chemistry Reviews, 229, 67–74. DOI: 10.1016/s0010-8545(02)00042-5. http://dx.doi.org/10.1016/S0010-8545(02)00042-5CrossrefGoogle Scholar
[5] Dutta, S., Baitalik, S., Ghosh, M., Flörke, U., & Nag, K. (2011). Structural, photophysical and electrochemical studies of [RuN6]2+ complexes having polypyridine and azole mixeddonor sites. Inorganica Chimica Acta, 372, 227–236. DOI: 10.1016/j.ica.2011.01.082. http://dx.doi.org/10.1016/j.ica.2011.01.082Web of ScienceCrossrefGoogle Scholar
[6] Funaki, T., Yanagida, M., Onozawa-Komatsuzaki, N., Kawanishi, Y., Kasuga, K., & Sugihara, H. (2009). Ruthenium (II) complexes with π expanded ligand having phenylene-ethynylene moiety as sensitizers for dye-sensitized solar cells. Solar Energy Materials and Solar Cells, 93, 729–732. DOI: 10.1016/j.solmat.2008.09.011. http://dx.doi.org/10.1016/j.solmat.2008.09.011Web of ScienceCrossrefGoogle Scholar
[7] Hagfeldt, A., Boschloo, G., Sun, L., Kloo, L., & Pettersson, H. (2010). Dye-sensitized solar cells. Chemical Reviews, 110, 6595–6663. DOI: 10.1021/cr900356p. http://dx.doi.org/10.1021/cr900356pCrossrefWeb of ScienceGoogle Scholar
[8] Hagfeldt, A., & Grätzel, M. (1995). Light-induced redox reactions in nanocrystalline systems. Chemical Reviews, 95, 49–68. DOI: 10.1021/cr00033a003. http://dx.doi.org/10.1021/cr00033a003CrossrefGoogle Scholar
[9] Hagfeldt, A., & Grätzel, M. (2000). Molecular photovoltaics. Accounts of Chemical Research, 33, 269–277. DOI: 10.1021/ar980112j. http://dx.doi.org/10.1021/ar980112jCrossrefGoogle Scholar
[10] Huang, W., & Han, C. D. (2006). Ruthenium(II) complexinduced dispersion of montmorillonite in a segmented mainchain liquid-crystalline polymer having side-chain terpyridine group. Macromolecules, 39, 8207–8209. DOI: 10.1021/ma0619637. http://dx.doi.org/10.1021/ma0619637CrossrefGoogle Scholar
[11] Günes, S., & Sariciftci, N. S. (2008). Hybrid solar cells. Inorganica Chimica Acta, 361, 581–588. DOI: 10.1016/j.ica.2007.06.042. http://dx.doi.org/10.1016/j.ica.2007.06.042CrossrefGoogle Scholar
[12] Kalinowska-Lis, U., Żurowska, B., & Ochocki, J. (2011). Spectroscopic and magnetic evidence of coordination properties of bioactive diethyl (pyridin-4-ylmethyl)phosphate ligand with chloride transition-metal ions. Chemical Papers, 65, 660–666. DOI: 10.2478/s11696-011-0056-8. http://dx.doi.org/10.2478/s11696-011-0056-8CrossrefGoogle Scholar
[13] Klein, C., Baranoff, E., Grätzel, M., & Nazeeruddin, M. K. (2011). Convenient synthesis of tridentate 2,6-di(pyrazol-1-yl)-4-carboxypyridine and tetradentate 6,6′-di(pyrazol-1-yl)-4,4′-dicarboxy-2,2′-bipyridine ligands. Tetrahedron Letters, 52, 584–587. DOI: 10.1016/j.tetlet.2010.12.001. http://dx.doi.org/10.1016/j.tetlet.2010.12.001Web of ScienceCrossrefGoogle Scholar
[14] Li, B., Wang, L., Kang, B., Wang, P., & Qiu, Y. (2006). Review of recent progress in solid-state dye-sensitized solar cells. Solar Energy Materials and Solar Cells, 90, 549–573. DOI: 10.1016/j.solmat.2005.04.039. http://dx.doi.org/10.1016/j.solmat.2005.04.039Web of ScienceCrossrefGoogle Scholar
[15] Matsuda, K., Stone, M. T., & Moore, J. S. (2002). Helical pitch of m-phenylene ethynylene foldamers by double spin labeling. Journal of the American Chemical Society, 124, 11836–11837. DOI: 10.1021/ja027437m. http://dx.doi.org/10.1021/ja027437mCrossrefGoogle Scholar
[16] Muro, M. L., & Castellano, F. N. (2007). Room temperature photoluminescence from [Pt(4′-C≡CR-tpy)Cl]+ complexes. Dalton Transactions, 2007, 4659–4665. DOI: 10.1039/b7098 86c. http://dx.doi.org/10.1039/b709886cCrossrefWeb of ScienceGoogle Scholar
[17] O’Regan, B., & Grätzel, M. (1991). A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films. Nature, 353, 737–740. DOI: 10.1038/353737a0. http://dx.doi.org/10.1038/353737a0CrossrefGoogle Scholar
[18] Puntoriero, F., Campagna, S., Stadler, A. M., & Lehn, J. M. (2008). Luminescence properties and redox behavior of Ru(II) molecular racks. Coordination Chemistry Reviews, 252, 2480–2492. DOI: 10.1016/j.ccr.2007.12.009. http://dx.doi.org/10.1016/j.ccr.2007.12.009CrossrefGoogle Scholar
[19] Puntoriero, F., Sartorel, A., Orlandi, M., La Ganga, G., Serroni, S., Bonchio, M., Scandola, F., & Campagna, S. (2011). Photoinduced water oxidation using dendrimeric Ru(II) complexes as photosensitizers. Coordination Chemistry Reviews, 255, 2594–2601. DOI: 10.1016/j.ccr.2011.01.026. http://dx.doi.org/10.1016/j.ccr.2011.01.026CrossrefWeb of ScienceGoogle Scholar
[20] Spiccia, L., Deacon, G. B., & Kepert, C. M. (2004). Synthetic routes to homoleptic and heteroleptic ruthenium(II) complexes incorporating bidentate imine ligands. Coordination Chemistry Reviews, 248, 1329–1341. DOI: 10.1016/j.ccr.2004.04.008. http://dx.doi.org/10.1016/j.ccr.2004.04.008CrossrefGoogle Scholar
[21] Tan, L. F., Wang, F., Chao, H., Zhang, S., Fei, J. J., & Ji, L. N. (2008). DNA interactions of the functionalized (mixed polypyridine)ruthenium(II) complex bis(2,2′-bipyridine-κN
1,κN
1′)(methyldipyrido[3,2-a:2′,3′-c]phenazine-11-carboxylate-κN
4,κN
5)ruthenium(2+) ([Ru(bpy)2 (dppz-11-CO2Me)]2+). Helvetica Chimica Acta, 91, 1251–1260. DOI: 10.1002/hlca.200890136. http://dx.doi.org/10.1002/hlca.200890136CrossrefWeb of ScienceGoogle Scholar
[22] Vougioukalakis, G. C., Philippopoulos, A. I., Stergiopoulos, T., & Falaras, P. (2011). Contributions to the development of ruthenium-based sensitizers for dye-sensitized solar cells. Coordination Chemistry Reviews, 255, 2602–2621. DOI: 10.1016/j.ccr.2010.11.006. http://dx.doi.org/10.1016/j.ccr.2010.11.006CrossrefWeb of ScienceGoogle Scholar
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