[1] A. M. Magill and B. F. Yates, An assessment of theoretical protocols for calculation of the pKa values of the prototype imidazolium cation, Aust. J. Chem. 57 (2004), 1205-1210.
[2] K. J. Cavell, A. M. Magill, and B. F. Yates, Basicity of nucleophilic carbenes in aqueous and nonaqueous solvents-theoretical predictions, J. Am. Chem. Soc. 126 (2004), 8717-8274.
[3] Y. Fu, L. Liu, H.-Z. Yu, Y. Wang, and Q.-X. Guo, Quantum-chemical predictions of absolute standard redox potentials of diverse organic molecules and free radicals in acetonitrile, J. Am.
Chem. Soc. 127 (2005), 7227-7234.
[4] A. M. Toth, M. D. Liptak, D. L. Philips, and G. C. Shields, Accurate relative pKa calculations for carboxylic acids using complete basis set and Gaussian-n models combined with continuum solvation methods, J. Chem. Phys. 114 (2001), 4595-4606.
[5] C. O. Silva, E. C. da Silva, and M. A. C. Nascimento, Ab initio calculations of absolute pKa values in aqueous solution II. Aliphatic alcohols, thiols, and halogenated carboxylic acids, J.
Phys. Chem. A 104 (2000), 2402-2409.
[6] E. Budzisz, Synthesis, reactions and biological activity of phosphorus-containing derivatives
of chromone and coumarin, Phosphor Sulfur Silicon 179 (2004), 2131-2147. [7] E. Budzisz, Wlasciwosci biologiczne fosfonianowych pochodnych chromonu i kumaryny,
Farmacja Polska 59 (2003), 677-683.
[8] E. Budzisz, J. Graczyk-Wojciechowska, R. Zieba, and B. Nawrot, A new series of 2-substituted 3-phosphonic derivatives of chromone. Part II. Synthesis, in vitro alkylating and in vivo anti-
tumor activity, New J. Chem 26 (2002), 1799-1804.
[9] R. Deng, J. Wu, and L. Long, Lanthanide complexes of bis(4-hydroxy-3-coumarinyl) acetic acid and their anticoagulant action, Bul. Soc. Chim. Belg. 101 (1992), 439-443. [10] I. Kostova, I. Manolov, S. Konstantinov, and M. Karaivanova, Synthesis, physicochemi-cal characterisation and cytotoxic screening of new complexes of cerium, lanthanum and neodymium with warfarin and coumachlor sodium salts, Eur. J. Med. Chem. 34 (1999), 63-68.
ÇUJSE
7
(2010), No. 1
15
[11] I. Manolov, I. Kostova, T. Netzeva, S. Konstantinov, and M. Karaivanova, Cytotoxic activity
of cerium complexes with coumarin derivatives. Molecular modeling of the ligands, Arch.
Pharm. Pharm. Med. Chem. 333 (2000), 93-98. [12] I. Kostova, I. Manolov, and M. Karaivanova, Synthesis, physicochemical characterization, and
cytotoxic screening of new zirconium complexes with coumarin derivatives, Archiv. Pharm.
Pharm. Med. Chem. 334 (2001), 157-162. [13] V. D. Karaivanova, I. Manolov, M. L. Minassyan, N. D. Danchev, and S. M. Samurova, Metal
complexes of warfarin sodium, Pharmazie. 49 (1994), 856-857. [14] E. Budzisz, B. K. Keppler, G. Giester, M. Wozniczka, A. Kufelnicki, and B. Nawrot, Synthesis,
crystal structure and cytotoxicity of novel palladium (II) complex with coumarin derived
ligand, Eur. J. Inorg. Chem. 2004 (2004), 4412-4419. [15] E. Budzisz, U. Krajewska, and M. Rozalska, Cytotoxic and proapoptotic effects of new Pd(II)
and Pt(II)-complexes with 3-ethanimidoyl-2-methoxy-2H-1,2-benzoxaphosphinin-4-ol-2-oxide,
Pol. J. Pharmacol. 56 (2004), 473-478. [16] E. Budzisz and S. Pastuszko, Reaction of dimethyl 2-methyl- and dimethyl 2 phenyl-4-oxo-
4H-chromen-3-yl-phosphonate with amines, Tetrahedron 55 (1999), 4815-4824. [17] H. Kolancılar, C. Karapire, U. Oyman, and S. Idi, Fluorescence emission and photooxida-
tion studies with 5,6- and 6,7-benzocoumarins and a 5,6-benzochromone under direct and
concentrated sun light, J. Photochem. Photobiol A: Chem. 153 (2002), 173-184. [18] E. Budzisz, M. Malecka, M. Wozniczka, and A. Kufelnicki, Crystal Structure, protolytic
properties and alkylating activity of 5-A3-(1-amino-ethylidene)-2-methoxy-2-oxo-2,3-dihydro-2
benzo[e][1,2]oxaphosphinin-4-one, J. Mol. Struct. 753 (2005), 113-118. [19] C. (Öğretir, C. Yenikaya, and H. Berber, A quantum chemical study on structure of 1,2-
bis(diphenylphosphinoyl)ethane and phenol cocrystal, J. Mol. Struct.: THEOCHEM 686
(2004), 153-157.
[20] C. Oüğgretir, C. Yenikaya, and H. Berber, A quantum chemical study on structure of 1,2-Bis(diphenylphosphinoyl)ethane and hydroquinone cocrystal, J. Mol. Struct.: THEOCHEM
725 (2005), 207-214.
[21] CAChe WorkSystem Pro, Version 6.1.12, FCS Inc., 15244 NW Greenbrier Parkway, Beaverton,
Oregon, 2004.
[22] M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, M. A. Robb, J. R. Cheeseman, J. A. Montgomery Jr., T. Vreven, K. N. Kudin, J. C. Burant, J. M. Millam, S. S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G. A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J. E. Knox, H. P. Hratchian, J. B. Cross, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, P. Y. Ayala, K. Morokuma, G. A. Voth, P. Salvador, J. J. Dannenberg, V. G. Zakrzewski, S. Dapprich, A. D. Daniels, M. C. Strain, O. Farkas, D. K. Malick, A. D. Rabuck, K. Raghavachari, J. B. Foresman, J. V. Ortiz, Q. Cui, A. G. Baboul, S. Clifford, J. Cioslowski, B. B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R. L. Martin, D. J. Fox, T.
Keith, M. A. Al-Laham, C. Y. Peng, A. Nanayakkara, M. Challacombe, P. M. W. Gill, B.
16
Sıdır et al.
Johnson,
W
. Chen, M. W. Wong, C. Gonzalez, and J. A. Pople, Gaussian 03, Gaussian, Inc.,
Pittsburgh, PA, 2003.
[23] J. B. Foreseman and 7E. Frisch, Exploring chemistry with electronic structure methods, 2. ed.,
Gaussian Inc., Pitssburgh 1996. [24] I. Georgieva, T. Mihaylov, G. Bauer, and N. Trendafilova, Effect of the nature of mendiaxon
- — X+ interactions (X+ = Na+, Cu+, H+) and the hydrogen bonding on the v(C = O)
behavior: theoretical and spectroscopic study, Chemical Physics 300 (2004), 119-131. [25] D. D. Perrin, Dissociation constants of organic bases in aqueous solution, first supplement,
Pergamon, Oxford, 1972.
Thank you for copying data from http://www.arastirmax.com
