[1] Basosi, R., Lunga, G. D., & Pogni, R. (1996). Resolution enhancement of nitrogen hyperfine patterns in the EPR spectra of Cu(II) complexes: FT analysis of Cu(II)(His-Gly)2. Applied Magnetic Resonance, 11, 437–442. DOI: 10.1007/bf03162239. http://dx.doi.org/10.1007/BF03162239CrossrefGoogle Scholar
[2] Bräuer, B., Rüffer, T., Kirmse, R., Griebel, J., Weigend, F., & Salvan, G. (2007). Spin density distribution in oxamato-type transition metal complexes. Polyhedron, 26, 1773–1775. DOI: 10.1016/j.poly.2006.09.075. http://dx.doi.org/10.1016/j.poly.2006.09.075CrossrefGoogle Scholar
[3] Carbone, V., Chung, R., Endo, S., Hara, A., & El-Kabbani, O. (2008). Structure of aldehyde reductase in ternary complex with coenzyme and the potent 20α-hydroxysteroid dehydrogenase inhibitor 3,5-dichlorosalicylic acid: Implications for inhibitor binding and selectivity. Archives of Biochemistry and Biophysics, 479, 82–87. DOI: 10.1016/j.abb.2008.08.014. http://dx.doi.org/10.1016/j.abb.2008.08.014Web of ScienceCrossrefGoogle Scholar
[4] Della Lunga, G., Pogni, R., & Basosi, R. (1994). Computer simulation of EPR spectra in the slow-motion region for copper complexes with nitrogen ligands. The Journal of Physical Chemistry, 98, 3937–3942. DOI: 10.1021/j100066a006. http://dx.doi.org/10.1021/j100066a006CrossrefGoogle Scholar
[5] Della Lunga, G., Pogni, R., & Basosi, R. (1995). Discrimination of copper-nitrogen ligand coordination by Fourier analysis of EPR spectra in mobile phase. Journal of Magnetic Resonance, Series A, 114, 174–178. DOI: 10.1006/jmra.1995.1124. http://dx.doi.org/10.1006/jmra.1995.1124CrossrefGoogle Scholar
[6] Della Lunga, G., Pezzato, M., Baratto, M. C., Pogni, R., & Basosi, R. (2003). A new program based on stochastic Liouville equation for the analysis of superhyperfine interaction in CW-EPR spectroscopy. Journal of Magnetic Resonance, 164, 71–77. DOI: 10.1016/s1090-7807(03)00183-6. http://dx.doi.org/10.1016/S1090-7807(03)00183-6CrossrefGoogle Scholar
[7] Dhagat, U., Endo, S., Sumii, R., Hara, A., & El-Kabbani, O. (2008). Selectivity determinants of inhibitor binding to human 20α-hydroxysteroid dehydrogenase: Crystal structure of the enzyme in ternary complex with coenzyme and the potent inhibitor 3,5-dichlorosalicylic acid. Journal of Medicinal Chemistry, 51, 4844–4848. DOI: 10.1021/jm8003575. http://dx.doi.org/10.1021/jm8003575CrossrefGoogle Scholar
[8] Diaz, A., Pogni, R., Cao, R., & Basosi, R. (1998). EPR characterization of a series of mono- and bis-thiosemicarbazone copper(II) complexes. Inorganica Chimica Acta, 275–276, 552–556. DOI: 10.1016/s0020-1693(97)06067-2. http://dx.doi.org/10.1016/S0020-1693(97)06067-2CrossrefGoogle Scholar
[9] El-Kabbani, O., Scammells, P. J., Day, T., Dhagat, U., Endo, S., Matsunaga, T., Soda, M., & Hara, A. (2010). Structurebased optimization and biological evaluation of human 20α-hydroxysteroid dehydrogenase (AKR1C1) salicylic acidbased inhibitors. European Journal of Medicinal Chemistry, 45, 5309–5317. DOI: 10.1016/j.ejmech.2010.08.052. http://dx.doi.org/10.1016/j.ejmech.2010.08.052CrossrefGoogle Scholar
[10] El-Kabbani, O., Dhagat, U., & Hara, A. (2011). Inhibitors of human 20α-hydroxysteroid dehydrogenase (AKR1C1). The Journal of Steroid Biochemistry and Molecular Biology, 125, 105–111. DOI: 10.1016/j.jsbmb.2010.10.006. http://dx.doi.org/10.1016/j.jsbmb.2010.10.006CrossrefGoogle Scholar
[11] Goodman, B. A., & Raynor, J. B. (1970). Electron spin resonance of transition metal complexes. Advances in Inorganic Chemistry and Radiochemistry, 13, 135–362. DOI: 10.1016/s0065-2792(08)60336-2. http://dx.doi.org/10.1016/S0065-2792(08)60336-2CrossrefGoogle Scholar
[12] Goodman, B. A., Palivan, C. G., & Cristescu, C. (1995). Characterization by electron paramagnetic resonance of the coordination environment of copper in some copper(II) complexes of asymmetric triazines having high superoxide dismutase activity. Polyhedron, 14, 2523–2535. DOI: 10.1016/0277-5387(95)00049-x. http://dx.doi.org/10.1016/0277-5387(95)00049-XCrossrefGoogle Scholar
[13] Goodman, B. A., Palivan, C. G., Palivan, H., & Tomas, S. (2003). Local structure is critical for superoxide dismutase activity in copper complexes: Relationship between EPR parameters, structure and activity in some sterically hindered copper(II) bis(hydrazono-triazine) complexes. Applied Magnetic Resonance, 25, 13–28. DOI: 10.1007/bf03166963. http://dx.doi.org/10.1007/BF03166963CrossrefGoogle Scholar
[14] Grimes, P. E. (1999). The safety and efficacy of salicylic acid chemical peels in darker racial-ethnic groups. Dermatologic Surgery, 25, 18–22. DOI: 10.1046/j.1524-4725.1999.08145.x. http://dx.doi.org/10.1046/j.1524-4725.1999.08145.xCrossrefGoogle Scholar
[15] Hathaway, B. J., & Tomlinson, A. A. G. (1970). Copper amonia complexes. Coordination Chemistry Reviews, 5, 1–43. DOI: 10.1016/s0010-8545(00)80073-9. http://dx.doi.org/10.1016/S0010-8545(00)80073-9CrossrefGoogle Scholar
[16] Hathaway, B. J., & Billing, D. E. (1970). The electronic properties and stereochemistry of mono-nuclear complexes of copper(II) ion. Coordination Chemistry Reviews, 5, 143–207. DOI: 10.1016/s0010-8545(00)80135-6. http://dx.doi.org/10.1016/S0010-8545(00)80135-6CrossrefGoogle Scholar
[17] Korabik, M., Repická, Z., Martiška, L., Moncol, J., Švorec, J., Padělková, Z., Lis, T., Mazúr, M., & Valigura, D. (2011). Hydrogen-bond-based magnetic exchange between μ-diethylicotinamide(aqua)bis(X-salicylato)coper(II) polymeric chains. Zeitschrift für anorganische und allgemeine Chemie, 637, 224–231. DOI: 10.1002/zaac.201000301. CrossrefGoogle Scholar
[18] Krishnakumar, V., & Mathammal, R. (2009). Density functional and experimental studies on the FT-IR and FT-Raman spectra and structure of benzoic acid and 3,5-dichlorosalicylic acid. Journal of Raman Spectroscopy, 40, 264–271. DOI: 10.1002/jrs.2118. http://dx.doi.org/10.1002/jrs.2118CrossrefWeb of ScienceGoogle Scholar
[19] Mathur, R., & Mathur, P. (1998). Monomeric Cu(II) complexes with tetradenate bis(benzimidazole) ligand; synthesis, EPR, spectral and electrochemical studies. Polyhedron, 17, 2607–2615. DOI: 10.1016/s0277-5387(97)00431-2. http://dx.doi.org/10.1016/S0277-5387(97)00431-2CrossrefGoogle Scholar
[20] Maroszová, J., Martiška, L., Valigura, D., Koman, M., & Glowiak, T. (2006). Poly[[bis(4-chlorosalicylato-κO)copper (II)]-di-μ-3-pyridylmethanol-κ
2N:O;κ
2O:N]. Acta Crystallographica Section E, E62,62, m1164–m1166. DOI: 10.1107/s1600536806006817. http://dx.doi.org/10.1107/S1600536806006817CrossrefGoogle Scholar
[21] Martiška, L., Husáriková, L., Repická, Z., Valigura, D., Valko, M., & Mazúr, M. (2010). EPR study of 5-chlorosalicylate-Cu(II)-3-pyridylmethanol ternary complex systems in frozen water-methanol solutions. Applied Magnetic Resonance, 39, 423–435. DOI: 10.1007/s00723-010-0178-0. http://dx.doi.org/10.1007/s00723-010-0178-0CrossrefWeb of ScienceGoogle Scholar
[22] Martiška, L., Husáriková, L., Repická, Z., Valigura, D., Valko, M., & Mazúr, M. (2011). EPR study of 5-chlorosalicylate-Cu(II)-N,N-diethylnicotinamide ternary complex systems in frozen water-methanol solutions. Applied Magnetic Resonance, 40, 405–411. DOI: 10.1007/s00723-011-0223-7. http://dx.doi.org/10.1007/s00723-011-0223-7Web of ScienceCrossrefGoogle Scholar
[23] Martiška, L. (2011). Relations between composition, structure and properties of copper(II) complexes with potential bioactive ligands. Ph.D. thesis, Slovak University of Technology, Bratislava. Google Scholar
[24] McPhail, D. B., & Goodman, B. A. (1987). An electron spin resonance investigation of the nature of the complexes formed between copper(II) and glycylhistidine. Journal of the Chemical Society, Faraday Transactions 1,83, 3683–3692. DOI: 10.1039/f19878303683. CrossrefGoogle Scholar
[25] Mojumdar, S. C., Martiška, L., Valigura, D., & Melník, M. (2003). Thermal and spectral properties of halogenosalicylato-Cu(II) complexes. Journal of Thermal Analalysis and Calorimetry, 74, 905–914. DOI: 10.1023/b:jtan.0000011022.51234.19. http://dx.doi.org/10.1023/B:JTAN.0000011022.51234.19CrossrefGoogle Scholar
[26] Mojumdar, S. C., Martiška, L., Valigura, D., & Melník, M. (2005). Thermal and spectral properties of Cu(II)-5-halogenosalicylates with or without nicotinamide. Journal of Thermal Analalysis and Calorimetry, 81, 243–250. DOI: 10.1007/s10973-005-0773-8. http://dx.doi.org/10.1007/s10973-005-0773-8CrossrefGoogle Scholar
[27] Palivan, C. G., & Goodman, B. A. (2001). Determination of the copper coordination environment in superoxide dismutases and complexes with SOD activity using molecular mechanics force field calculations and electron paramagnetic resonance spectroscopy. In S. G. Pandalai (Ed.), Recent research developments in inorganic & organometallic chemistry (pp. 141–159). Trivandrum, Kerala, India: Research Signpost. Google Scholar
[28] Paul, B. K., Samanta, A., & Guchhait, N. (2010a). Influence of chlorine substitution on intramolecular hydrogen bond energy and ESIPT barrier: Experimental and theoretical measurements on the photophysics of 3,5-dichlorosalicylic acid. Journal of Molecular Structure, 977, 78–89. DOI: 10.1016/j.molstruc.2010.05.018. http://dx.doi.org/10.1016/j.molstruc.2010.05.018CrossrefGoogle Scholar
[29] Paul, B. K., Samanta, A., & Guchhait, N. (2010b). Deciphering the photophysics of 5-chlorosalicylic acid: Evidence for excited-state intramolecular proton transfer. Photochemistry & Photobiology Sciences, 9, 57–67. DOI: 10.1039/b9pp00094a. http://dx.doi.org/10.1039/b9pp00094aCrossrefGoogle Scholar
[30] Paul, B. K., Samanta, A., & Guchhait, N. (2011). On the photophysics of 3,5,6-trichlorosalicylic acid: Spectroscopic study combined with Hartree-Fock and density functional theory calculations. Journal of Fluorescence, 21, 1265–1279. DOI: 10.1007/s10895-010-0809-8. http://dx.doi.org/10.1007/s10895-010-0809-8CrossrefWeb of ScienceGoogle Scholar
[31] Pelikán, P., Liška, M., Valko, M., & Mazúr, M. (1996). Quantitative analysis of EPR spectra of powdered samples containing a mixture of various paramagnetic particles. Journal of Magnetic Resonance, Series A, 122, 9–15. DOI: 10.1006/jmra.1996.0169. http://dx.doi.org/10.1006/jmra.1996.0169CrossrefGoogle Scholar
[32] Pogni, R., Della Lunga, G., & Basosi, R. (1993). Multimicrowave frequency EPR in the structural characterization of copper(II) dipeptide complexes. Journal of the American Chemical Society, 115, 1546–1550. DOI: 10.1021/ja00057a047. http://dx.doi.org/10.1021/ja00057a047CrossrefGoogle Scholar
[33] Pogni, R., Baratto, M. C., Diaz, A., & Basosi, R. (2000). EPR characterization of mono(thiosemicarbazones) copper(II) complexes. Journal of Inorganic Biochemistry, 79, 333–337. DOI: 10.1016/s0162-0134(99)00166-x. http://dx.doi.org/10.1016/S0162-0134(99)00166-XCrossrefGoogle Scholar
[34] Roberts, W. E. (2004). Chemical peeling in ethnic/dark skin. Dermatologic Therapy, 17, 196–205. DOI: 10.1111/j.1396-0296.2004.04020.x. http://dx.doi.org/10.1111/j.1396-0296.2004.04020.xCrossrefGoogle Scholar
[35] Sakaguchi, U., & Addison, A. W. (1979). Spectroscopic and redox studies of some copper(II) complexes with biomimetic donor atoms: Implications for protein copper centres. Journal of the Chemical Society, Dalton Transactions, 1979, 600–608. DOI: 10.1039/dt9790000600. http://dx.doi.org/10.1039/dt9790000600CrossrefGoogle Scholar
[36] Šĭpoš, R., Szabó-Plánka, T., Rockenbauer, A., Nagy, N. V., Šima, J., Melník, M., & Nagypál, I. (2008). Equilibria of 3-pyridylmethanol with copper(II). A comparative electron spin resonance study by the decomposition of spectra in liquid and frozen solutions. The Journal of Physical Chemistry A, 112, 10280–10286. DOI: 10.1021/jp805210v. http://dx.doi.org/10.1021/jp805210vWeb of ScienceCrossrefGoogle Scholar
[37] Szabó-Plánka, T., Moncol, J., Tóth, E., Gyurcsik, B., Nagy, N. V., Vasková, Z., Rockenbauer, A., & Valigura, D. (2011). ESR and pH-potentiometric study of the mixed-ligand complex formation in the copper(II)-4-fluorosalicylic acid-N,N-diethylnicotinamide system: Structure and spectral properties of [Cu(4-fluorosalicylate)2(N,N-diethylnicotinamide)2 (H2O)2] complex. Polyhedron, 30, 2421–2429. DOI: 10.1016/ j.poly.2011.06.030. http://dx.doi.org/10.1016/j.poly.2011.06.030CrossrefWeb of ScienceGoogle Scholar
[38] Thiele, H., Erstling, J., Such, P., & Höfer, P. (1992). WINEPR. Bremen and Rheinstetten, Germany: Bruker-Franzen Analytik GmbH and Bruker Analytische Messtechnik GmbH. Google Scholar
[39] Weber, R. T. (1995). WIN-EPR SimFonia, Version 1.2 [computer software]. Billerica, MA, USA: EPR Division, Bruker Instruments, Inc. Google Scholar
[40] Weil, J. A., Bolton, J. R., & Wertz, J. E. (1994). Electron paramagnetic resonance spectroscopy: Elementary theory and practical applications. New York, NY, USA: Wiley. Google Scholar
Comments (0)