[1]
|
Heeres, A., van Doren, H., Gotlieb, K. and Bleeker, I. (1997) Synthesis of α-and β-d-Glucopyranuronate 1-Phosphate and α-d-Glucopyranuronate 1-Fluoride: Intermediates in the Synthesis of d-Glucuronic Acid from Starch. Carbohydrate Research, 299, 221-227. https://doi.org/10.1016/S0008-6215(97)00030-X
|
[2]
|
Ziegler, M. and Zelewsky, A.V. (1998) Charge-Transfer Excited State Properties of Chiral Transition Metal Coordination Compounds Studied by Chiroptical Spectroscopy. Coordination Chemistry Reviews, 177, 257-300.
https://doi.org/10.1016/S0010-8545(98)00186-6
|
[3]
|
Dougan, S.J., Melchart, M., Habtemariam, A., Parsons, S. and Sadler, P.J. (2006) Phenylazo-Pyridine and Phenylazo-Pyrazole Chlorido Ruthenium (II) Arene Complexes: Arene Loss, Aquation and Cancer Cell Cytotoxicity. Inorganic Chemistry, 45, 10882-10894. https://doi.org/10.1021/ic061460h
|
[4]
|
Basuli, F., Das, A., Mostafa, G., Peng, S.M. and Bhattacharya, S. (2000) Chemistry of Ruthenium with Some Phenolic. Polyhedron, 19, 1663-1672.
https://doi.org/10.1016/S0277-5387(00)00404-6
|
[5]
|
Boelrijk, A.E.M., Anja, M., Jorna, J. and Reedijk, J. (1995) Containing a 2-(Phenyl) Azopyridine or a 2-(Nitrophenyl)Azopyridine Ligand. Journal of Molecular Catalysis A: Chemical, 103, 73-85. https://doi.org/10.1016/1381-1169(95)00112-3
|
[6]
|
Barf, G.A. and Sheldon, R.A. (1995) Ruthenium (II) 2-(Phenylazo) Pyridine Complexes as Epoxidation Catalysts. Journal of Molecular Catalyst A: Chemiccoll, 98, 143-146. https://doi.org/10.1016/1381-1169(95)00026-7
|
[7]
|
Bamba, K. (2004) Oxydation électrocatalytique de monosaccharides sur des complexes de ruthénium et sur le platine modifié par des adatomes métalliques. PhD Thesis, University of Poitiers, Poitiers, 70.
|
[8]
|
Bamba, K., Leger, J.M., Garnier, E., Bachmann, C., Servat, K. and Kokoh, K.B. (2005) Selective Electro-Oxidation of D-Glucose by RuCl2(azpy)2 Complexes as Electrochemical Mediators. Electrochimica Acta, 50, 3341-3346.
https://doi.org/10.1016/j.electacta.2004.12.007
|
[9]
|
Velders, A.H., Kooijman, H., Spek, A.L., Haasnoot, J.G., De Vos, D. and Reedijk, J. (2000) Strong Differences in the in Vitro Cytotoxicity of Three Isomeric Dichlorobis(2-Phenylazopyridine)Ruthenium(II) Complexes. Inorganic Chemistry, 39, 2966-2967. https://doi.org/10.1021/ic000167t
|
[10]
|
Hotze, A.C.G., Caspers, S.E., de Vos, D., Kooijman, H.S.A.L., Flamigni, A., Marina, B., Sava, G., Haasnoot, J.G. and Reedijk, J. (2004) Structure-Dependent in Vitro Cytotoxicity of the Isomeric Complexes [RuL2Cl2] (L = o-Tolylazopyridine and 4-Methyl-2-Phenylazopyridine) in Comparaison to [Ru(azpy)2Cl2]. Journal of Biological Inorganic Chemistry, 9, 354-364.
https://doi.org/10.1007/s00775-004-0531-6
|
[11]
|
Changsaluk, U. and Hansongnern, K. (2005) Dichlorobi(5methyl-2-(phenylazo) pyridine) Ruthénium (II) Complex: Charaterisation and NMR Sepectroscopy. Songklanakarin Journal of Science and Technology, 27, 739-749.
|
[12]
|
N’Guessan, K.N., Kafoumba, B., Ouattara, W.P. and Nahossé, Z. (2017) Theoretical Investigation of the Structure Activity Relationships (SARs) of a Series of Five Isomeric α, β, γ, δ, ε Ruthenium Complexes RuCl2L2 with Azopyridine Ligands [L = azpy, tazpy, 4mazpy, 5mazpy]. International Journal of Engineering Research and Application, 7, 58-70. https://doi.org/10.9790/9622-0706015870
|
[13]
|
Kouakou, N.N., Mamadou, R.K., Kafoumba, B., Ouattara, W.P. and Nahossé, Z. (2017) Quantitative Structure Anti-Cancer Activity Relationship (QSAR) of a Series of Ruthenium Complex Azopyridine by the Density Functional Theory (DFT) Method. Computational Molecular Bioscience, 7, 19-31.
https://doi.org/10.4236/cmb.2017.72002
|
[14]
|
Ackermann, M.N., Moore, K.B., Colligan, A.S., Thomas-Wohlever, J.A. and Warren, K.J. (2003) Inorganic Chemistry in Nuclear Imaging and Radiotherapy: Current and Future Directions. Journal of Organometallic Chemistry, 667, 81-89.
https://doi.org/10.1016/S0022-328X(02)02140-X
|
[15]
|
Ackermann, M.N., Fairbrother, W.G., Amin, N.S., Deodene, C.J., Lamborg, C.M. and Martin, P.T. (1996) Tetracarbonylmolybdenum Complexes of 2-(phenylazo)pyridine Ligands. Correlations of Molybdenum-95 Chemical Shifts with Electronic, Infrared, and Electrochemical Properties. Journal of Organometallic Chemistry, 523, 145-151.
|
[16]
|
Kooijman, H., Hotze, C.G., Capers, S.E., Haasnoot, J.G., Reedijk, J. and Spek, A.L. (2004) α-Dichlorobis(2-phenylazo-4,6-dimathylpyridine)ruthénium (II) Chloroform. Acta Crystallographica E, 60, m247-m249.
https://doi.org/10.1107/S1600536804001618
|
[17]
|
Affi, S.T., Bamba, K. and Ziao, N. (2015) Computational Characterization of Organometallic Ligands Coordinating Metal: Case of Azopyridine Ligands. Journal of Theoretical and Computational Chemistry, 14, Article ID: 1550006.
https://doi.org/10.1142/S0219633615500066
|
[18]
|
Goswami, S., Chakravarty, A.R. and Chakravorty, A. (1981) Chemistry of Ruthenium. 2. Synthesis, Structure, and Redox Properties of 2-(arylazo)pyridine Complexes. Inorganic Chemistry, 20, 2246-2250.
https://doi.org/10.1021/ic50221a061
|
[19]
|
Bao, T., Krause, K. and Krause, R.A. (1988) Hydroxide-Assisted Stereospecific Isomerization of a Trans-Dichlorobischelate of Ruthenium (II). Inorganic Chemistry, 27, 759-761. https://doi.org/10.1021/ic00277a037
|
[20]
|
Velders, A.H., van der Schilden, K., Hotze, A.A., Reedijk, J., Kooijman, H. and Spek, A.L. (2004) Dichlorobis(2-phenylazopyri dine)ruthenium(II) Complexes: Characterisation, Spectroscopic and Structural Properties of Four Isomers. Dalton Transactions, 448-455. https://doi.org/10.1039/B313182C
|
[21]
|
Jager, M., Freitag, L. and González, L. (2015) Using Computational Chemistry to Design Ru Photosensitizers with Directional Charge Transfer. Coordination Chemistry Reviews, 304-305, 146-165. https://doi.org/10.1016/j.ccr.2015.03.019
|
[22]
|
Petersson, G.A., Malick, D.K., Wilson, W.G., Ochterski, J.W., Montgomery, J.A. and Frisch, J.M.J. (1998) Calibration and Comparison of the Gaussian-2, Complete Basis Set, and Density Functional Methods for Computational Thermochemistry. The Journal of Chemical Physics, 109, Article ID: 10570.
https://doi.org/10.1063/1.477794
|
[23]
|
Zheng, K.C., Kuang, D.B., Wang, J.P. and Shen, Y. (2000) Electronic Structure and Related Chemical Properties of Complexes M(bpy)2+3(M=Fe,Ru,Os). Acta Physico-Chimica Sinica, 16, 608. https://doi.org/10.3866/PKU.WHXB20000707
|
[24]
|
Becke, A.D. (1993) A New Mixing of Hartree-Fock and Local Density-Functional Theories. The Journal of Chemical Physics, 98, 1372-1377.
https://doi.org/10.1063/1.464304
|
[25]
|
Foresman, J.B. and Frisch, E. (1996) Exploring Chemistry with Electronic Structure Methods. Second Edition, Gaussian Inc., Pittsburgh.
|
[26]
|
Frisch, M., Trucks, G., Schlegel, H., Scuseria, G., Robb, M., Cheeseman, J., Montgomery, J.J., Vreven, T., Kudin, K., Burant, J., Millam, J., Iyengar, S., Tomasi, J., Barone, V., Mennucci, B., Cossi, M., Scalmani, G., Rega, N., Petersson, H., Nakatsuji, M., Hada, M., Ehara, K., Hasegawa, J., Fukuda, R., Toyota, K., Ishida, M., Nakajima, T., Honda, Y., Kitao, O., Nakai, H., Klene, M., Li, X., Knox, J.E., Hratchian, H.P., Cross, J.B., Bakken, V., Adamo, C., Jaramillo, J., Gomperts, R., Stratmann, R.E., Yazyev, O., Austin, J.A., Cammi, R., Pomelli, C., Ochterski, J.W., Ayala, P.Y., Morokuma, K., Voth, G.A., Salvador, P., Dannenberg, J.J., Zakrzewski, V.G., Dapprich, S., Daniels, A.D., Strain, M.C., Farkas, O., Malick, K., Rabuck, D., Raghavachari, K., Foresman, J.B., Ortiz, J.V., Cui, Q., Baboul, A.G., Clifford, S., Cioslowski, J., Stefanov, B.B., Liu, G., Liashenko, A., Piskorz, P., Komaromi, I., Martin, R.L., Fox, D.J., Keith, T., Al-Laham, M.A., Peng, Y.C., Nanayakkara, A., Challacombe, M., Gill, P.W., Johnson, B., Chen, W., Wong, M.W., Gonzaler, C. and Pople, J.A. (2004) Gaussian 03, Revision E.01. Gaussian, Wallingford.
|
[27]
|
Reed, A.E., Curtiss, L.A. and Weinhold, F. (1988) Intermolecular Interactions from a Natural Bond Orbital, Donor-Acceptor Viewpoint. Chemical Review, 88, 899-926.
|
[28]
|
Glendening, E.D., Reed, A.E., Carpenter, J.E. and Weinhold, F. (1996-2001) The NBO3.0 Program. University of Wisconsin, Madison.
|
[29]
|
Barone, V. and Cossi, M. (1998) Quantum Calculation of Molecular Energies and Energy Gradients in Solution by a Conductor Solvent Model. The Journal of Physical Chemistry A, 102, 1995-2001. https://doi.org/10.1021/jp9716997
|
[30]
|
Cossi, M., Rega, N., Scalmani, G. and Barone, V. (2003) Energies, Structures, and Electronic Properties of Molecules in Solution with the C-PCM Solvation Model. Journal of Computational Chemistry, 24, 669-681. https://doi.org/10.1002/jcc.10189
|
[31]
|
Shriver, D.F. and Atkins, P. (1999) Inorganic Chemistry. 3rd Edition, Oxford University Press, New York, 235-236.
|
[32]
|
Chen, J.C.L.J., Qian, L. and Zheng, K.C. (2005) Electronic Structures and SARs of the Isomeric Complexes α-, β-, γ-[Ru(mazpy)2Cl2] with Different Antitumor Activities. Journal of Molecular Structure: THEOCHEM, 728, 93-101.
https://doi.org/10.1016/j.theochem.2005.05.005
|
[33]
|
Bamba, K., Patrice, O., Nobel, N. and Ziao, N. (2016) SARs Investigation of α-, β-, γ-, δ-, ε-RuCl2(Azpy)2 Complexes as Antitumor Drugs. Computational Chemistry, 4, 1-10. https://doi.org/10.4236/cc.2016.41001
|
[34]
|
Oziminski, W., Narbutt, J., Michalik, J. and Smulek, W. (2010) Theoretical Investigations on the Structure Bonding in Neutral Trinitrate Complexes of Americium (III) and Europium (III) with. Centre of Radiochemistry and Nuclear Chemistry.
|
[35]
|
Singh, R.K., Verma, S.K. and Sharma, P.D. (2011) DFT Based Study of Interaction between Frontier Orbitals of Transition Metal Halides and Thioamides. International Journal of Chemtech Research, 3, 1571-1579.
|
[36]
|
Juris, A., Balzani, V., Barigelletti, F., Campagna, S., Belser, P. and von Zelewsky, A. (1988) Ru(II) Polypyridine Complexes: Photophysics, Photochemistry, Eletrochemistry, and Chemiluminescence. Coordination Chemistry Reviews, 84, 85-277.
https://doi.org/10.1016/0010-8545(88)80032-8
|
[37]
|
Vitnik, V.D., Vitnik, Z.J., Banjac, N.R., Valentic, N.V., Uscumlic, G.S. and Juranic, I.O. (2014) Quantum Mechanical and Spectroscopic (FT-IR, 13C, 1H NMR and UV) Investigations of Potent AntiepilepticDrug 1-(4-Chloro-Phenyl)-3-Phenyl Succinimide. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 117, 42-53. https://doi.org/10.1016/j.saa.2013.07.099
|
[38]
|
Prasad, M., Sri, N., Veeraiah, A., Veeraiah, V. and Chaitanya, K. (2013) Molecular Structure, Vibrational Spectroscopic (FT-IR, FT-Raman), UV-Vis Spectra, First Order Hyperpolarizability NBO Analysis, HOMO and LUMO Analysis, Thermodynamic Properties of 2,6-Dichloropyrazine by Ab Inito HF and Density Functional Method. Journal of Atomic and Molecular Sciences, 4, 1-17.
|
[39]
|
Fleming, I. (1976) Frontier Orbitals and Organic Chemical Reactions. John Wiley & Sons, New York.
|
[40]
|
Chen, L., Liu, L., Chen, J.C., Shi, S., Tan, C.T., Zheng, K.C. and Ji, L.N. (2008) Experimental and Theoretical Studies on the DNA-Binding and Spectral Properties of Water-Soluble Complex [Ru(MeIm)4(dpq)]2+. Journal of Molecular Structure, 881, 156-166. https://doi.org/10.1016/j.molstruc.2007.09.010
|
[41]
|
Chen, J.C., Li, J., Wu, W. and Zheng, K.C. (2006) Structures and Activities of a Series of the Isomeric Complexes RuCl2(azpy)2. Acta Physico-Chimica Sinica, 22, 391-396.
|
[42]
|
Fan, W.J., Cai, J.W., Yang, G.J., Chi, J.W., Zhou, D., Tan, D.Z. and Zhang, R.Q. (2016) Aggregation of Metal-Free Organic Sensitizers on TiO2(101) Surface for Use in Dye-Sensitized Solar Cells: A Computational Investment. Computational and Theoretical Chemistry, 1093, 1-8. https://doi.org/10.1016/j.comptc.2016.08.006
|
[43]
|
Umer, M., Ibnelwaleed, A.H., Muhammad, D., Shakeel, A. and Khalil, H. (2015) Theoretical Study of Benzene/Thiophene Based Photosensitizers for Dye Sensitized Solar Cells (DSSCs). Dyes and Pigments, 118, 152-158.
https://doi.org/10.1016/j.dyepig.2015.03.003
|
[44]
|
Shalabi, A., El Mahdy, A., Taha, H. and Soliman, K. (2005) The Effects of Macrocycle and Anchoring Group Replacements on the Performance of Porphyrin Based Sensitizer: DFT and TD-DFT Study. Journal of Physics and Chemistry of Solids, 76, 22-33. https://doi.org/10.1016/j.jpcs.2014.08.002
|
[45]
|
Li, M., Kou, L., Diao, L., Zhang, Q., Li, Z., Wu, Q., Lu, W., Pan, D. and Wei, Z. (2015) Theoretical Study of WS-9-Based Organic Sensitizers for Unusual vis/NIR Absorption and Highly Efficient Dye-Sensitized Solar Cells. Journal of Physics and Chemistry of Solids, 119, 9782-9790.
|
[46]
|
Sun, C., Li, Y., Song, P. and Ma, F. (2016) An Experimental and Theoretical Investigation of the Electronic Structures and Photoelectrical Properties of Ethyl Red and Carminic Acid for DSSC Application. Materials, 9, E813.
https://doi.org/10.3390/ma9100813
|