Structural characterization of triorganotin(IV) complexes with sodium fusidate and DFT calculations (377 views)
J Organomet Chem (ISSN: 0022-328x), 2010 May 1; 695(9): 1405-1413.
Export to BibTeX Export to EndNote
Paper type: Journal Article,
Impact factor: 2.205, 5-year impact factor: 2.073
Url: http://www.scopus.com/inward/record.url?eid=2-s2.0-77950187656&partnerID=40&md5=b2ac33bc796bd357b0d5c3b94cc6920a
Keywords: Ftir, Mössbauer Spectroscopy, Nmr, Steroid Carboxylate, Triorganotin(iv), Carboxylate Groups, Conventional Techniques, Coordinated Solvents, Dft Calculation, Dft Study, Isolated Compounds, Ligand Coordination, Monodentates, Monomeric Complexes, Nmr Spectroscopy, Nuclear Quadrupole Splitting, Oxygen Atom, Solid-State Complexes, Spectroscopic Measurements, Structural Characterization, Tetrahedral Arrangement, Tetrahedral Structures, Tetramethyl, Tin Center, Carboxylation, Esters, Fourier Transform Infrared Spectroscopy, Molybdenum, Molybdenum Compounds, Nuclear Magnetic Resonance, Organometallics, Probability Density Function, Sodium, Stoichiometry, Sulfur Compounds, Titanium Compounds, Nuclear Magnetic Resonance Spectroscopy, M Ssbauer Spectroscopy, Triorganotin (iv),
Affiliations:
*** IBB - CNR ***
Dipartimento di Chimica Inorganica e Analitica Stanislao Cannizzaro, Università degli Studi di Palermo, Viale delle Scienze, Ed. 17, 90128 Palermo, Italy
Istituto di Biostrutture e Bioimmagini, CNR, Dipartimento di Scienze Chimiche, Viale Andrea Doria 6, 95125 Catania, Italy
Centro grandi apparecchiature (CGA)-UniNetLab, Università degli Studi di Palermo, Via F. Marini 14, 90128 Palermo, Italy
References:
Blunden, S.J., Cusack, P.A., Hill, R., (1985) Industrial Uses of Tin Chemicals, , Royal Society of Chemistry, Burlington House, London, Londo
Crowe, A.J., (1987) Appl. Organomet. Chem., 1, pp. 143-155
Crowe, A.J., Antitumor activity of organotin compounds (1994) Metal Compounds in Cancer Therapy, pp. 147-179. , Fricker S. (Ed), Chapman and Hall, London
Gielen, M., Davies, A.G., Pannell, K., Tiekink, E., (2008) Tin Chemistry: Fundamentals Frontiers and Applications, , John Wiley & Sons, New York
Arkis, E., Balköse, D., (2005) Polym. Degrad. Stab., 88, pp. 46-51
Saxena, A.K., Huber, F., (1989) Coord. Chem. Rev., 95, pp. 109-123
Pellerito, L., Nagy, L., (2002) Coord. Chem. Rev., 224, pp. 111-150
Davies, A.G., (2004) Organotin Chemistry, , Wiley-VCH, Weinheim
Hadjikakou, S.K., Hadjiliadis, N., (2009) Coord. Chem. Rev., 253, pp. 235-249
Gielen, M., Tiekink, E.R.T., Tin compounds and their therapeutic potential (2005) Metallotherapeutic Drugs and Metal-Based Diagnostic Agents: The Use of Metals in Medicine, pp. 421-439. , Gielen M., and Tiekink E.R.T. (Eds), John Wiley & Sons, Chichester
Tabassum, S., Pettinari, C., (2006) J. Organomet. Chem., 691, pp. 1761-1766
Yin, H.D., Li, F.H., Li, L.W., Li, G., (2007) J. Organomet. Chem., 692, pp. 1010-1019
Gielen, M., Biesemans, M., de Vos, D., Willem, R., (2000) Inorg. Biochem., 79, pp. 139-145
Nath, M., Pokharia, S., Yadav, R., (2001) Coord. Chem. Rev., 99, pp. 215-220
Chandrasekhar, V., Nagendran, S., Baskar, V., (2002) Coord. Chem. Rev., 1, pp. 235-240
Hussain, M., Ahmad, M.S., Siddique, A., Hanif, M., Ali, S., Mirza, B., (2009) Chem. Biol. Drug. Des., 74, pp. 183-189
Shahzadi, S., Shahid, K., Ali, S., Bakhtiar, M., (2008) Turk. J. Chem., 32, pp. 333-353
Pellerito, C., Nagy, L., Pellerito, L., Szorcsik, A., (2006) J. Organomet. Chem., 691, pp. 1733-1747
Bertazzi, N., Bruschetta, G., Casella, G., Pellerito, L., Rotondo, E., Scopelliti, M., (2003) Appl. Organomet. Chem., 17, pp. 932-939
Szorcsik, A., Nagy, L., Sletten, J., Szalontanai, G., Kamu, E., Fiore, T., Pellerito, L., Kalman, E., (2004) J. Organomet. Chem., 689, pp. 1145-1154
Pellerito, C., D'Agati, P., Fiore, T., Mansueto, C., Mansueto, V., Stocco, G.C., Nagy, L., Pellerito, L., (2005) J. Inorg. Biochem., 92, pp. 347-350
Bertazzi, N., Casella, G., D'Agati, P., Fiore, T., Mansueto, C., Mansueto, V., Pellerito, C., Scopelliti, M., (2008) Appl. Organomet. Chem., 22, pp. 389-396
Basu Baul, T.S., Paul, A., Pellerito, L., Scopelliti, M., Singh, P., Verma, P., de Vos, D., Invest. New Drugs, , doi:10.1007/s10637-009-9293-x
Barber, J., Lian, L., Morris, G.A., Tehrani, M.H., (1989) Magn. Res. Chem., 27, pp. 740-747
Neumann, W.P., (1970) The Organic Chemistry of Tin, , Interscience, London
Stephens, P.J., Devlin, F.J., Chabalowski, C.F., Frisch, M.J., (1994) J. Phys. Chem., 98, pp. 11623-11627
Hertwig, R.H., Koch, W., (1997) Chem. Phys. Lett., 268, pp. 345-351
Godbout, N., Salahub, D.R., (1992) Can. J. Chem., 70, pp. 560-571
Cancès, M.T., Mennucci, B., Tomasi, J., (1997) J. Chem. Phys., 107, pp. 3032-3041
Cossi, M., Barone, V., Mennucci, B., Tomasi, J., (1998) Chem. Phys. Lett., 286, pp. 253-260
Kutzelnigg, W., Fleischer, U., Schindler, M., (1990) NMR-Basic Principles and Progress, 23, pp. 165-262. , Diehl P., Fluck E., Günther H., and Kosfeld R. (Eds), Springer, Heidelberg
Avalle, P., Harris, R.K., Fischer, R.D., (2002) Phys. Chem. Chem. Phys., 4, pp. 3558-3561
Vivas-Reyes, R., De Proft, F., Biesemans, M., Willem, R., Geerlings, P., (2002) J. Phys. Chem. A, 106, pp. 2753-2759
Casella, G., Ferrante, F., Saielli, G., (2008) Inorg. Chem., 47, pp. 4796-4807
Zhao, Y., Truhlar, D.G., (2004) J. Phys. Chem. A, 108, pp. 6908-6918
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, V. Bakken, 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. Johnson, W. Chen, M.WDeacon, G.B., Huber, F., Phillips, R.J., (1985) Inorg. Chim. Acta, 104, pp. 41-45
Whiffen, D.H., (1956) J. Chem. Soc., pp. 1350-1356
Smith, P.J., Tupčiauskas, A.P., (1978) Ann. Rep. NMR Spectrosc., 8, pp. 291-370
Wrackmeyer, B., (1985) Annu. Rep. NMR Spectrosc., 16, pp. 73-186
Sebald, A., (1996) Advanced Applications of NMR to Organometallic Chemistry, pp. 123-156. , Chapter 5. Gielen M., Willem R., and Wrackmeyer B. (Eds), John Wiley & Sons, Chichester
Bancroft, G.M., Platt, R.H., (1972) Adv. Inorg. Chem. Rad., 15, pp. 59-68
Collins, R.L., Travis, J.C., The electric field gradient tensor (1967) Mössbauer Effect Methodology, 3, pp. 123-161. , Gruverman I.J. (Ed), Plenum Press, New York
Bancroft, G.M., Kumar Das, V.G., Sham, T.K., Clark, M.G., (1976) J. Chem. Soc., Dalton Trans., pp. 643-654. , and references therein
Sham, T.K., Bancroft, G.M., (1975) Inorg. Chem., 14, pp. 2281-2284
Clark, M.G., Maddock, A.G., Platt, R.H., (1972) J. Chem. Soc., Dalton Trans., pp. 281-290
Parish, R.V., Structure and Bonding in Tin Compound (1984) Mössbauer Spectroscopy Applied to Inorganic Chemistry, 1, pp. 544-548. , Long G.J. (Ed), Plenum Press, New York
Ganis, P., Valle, G., Furlani, D., Tagliavini, G., (1986) J. Organomet. Chem., 302, pp. 165-170
Basu Baul, T.S., Singh, K.S., Holcapek, M., Jirasko, R., Rivarola, E., Linden, A., (2005) J. Organomet. Chem., 690, pp. 4232-4242
Basu Baul, T.S., Masharing, C., Ruisi, G., Jirasko, R., Holcapek, M., de Vos, D., Wolstenholme, D., Linden, A., (2007) J. Organomet. Chem., 692, pp. 4849-4862
Holeček, J., Nádvorník, M., Handlíř, K., Lyčka, A., (1983) J. Organomet. Chem., 241, pp. 177-184
Lockhart, T.P., Manders, W.F., (1986) Inorg. Chem., 25, pp. 892-895
Holeček, J., Lyčka, A., (1986) Inorg. Chim. Acta, 118, pp. L15-L16
Zubieta, J.A., Zuckerman, J.J., (1978) Prog. Inorg. Chem., 24, pp. 251-475
Blunden, S. J., Cusack, P. A., Hill, R., (1985) Industrial Uses of Tin Chemicals, , Royal Society of Chemistry, Burlington House, London, Londo
Crowe, A. J., (1987) Appl. Organomet. Chem., 1, pp. 143-155
Crowe, A. J., Antitumor activity of organotin compounds (1994) Metal Compounds in Cancer Therapy, pp. 147-179. , Fricker S. (Ed), Chapman and Hall, London
Arkis, E., Balk se, D., (2005) Polym. Degrad. Stab., 88, pp. 46-51
Saxena, A. K., Huber, F., (1989) Coord. Chem. Rev., 95, pp. 109-123
Davies, A. G., (2004) Organotin Chemistry, , Wiley-VCH, Weinheim
Hadjikakou, S. K., Hadjiliadis, N., (2009) Coord. Chem. Rev., 253, pp. 235-249
Yin, H. D., Li, F. H., Li, L. W., Li, G., (2007) J. Organomet. Chem., 692, pp. 1010-1019
Basu Baul, T. S., Paul, A., Pellerito, L., Scopelliti, M., Singh, P., Verma, P., de Vos, D., Invest. New Drugs, , doi: 10. 1007/s10637-009-9293-x
Neumann, W. P., (1970) The Organic Chemistry of Tin, , Interscience, London
Stephens, P. J., Devlin, F. J., Chabalowski, C. F., Frisch, M. J., (1994) J. Phys. Chem., 98, pp. 11623-11627
Hertwig, R. H., Koch, W., (1997) Chem. Phys. Lett., 268, pp. 345-351
Canc s, M. T., Mennucci, B., Tomasi, J., (1997) J. Chem. Phys., 107, pp. 3032-3041
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, V. Bakken, 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. Johnson, W. Chen, M. WDeacon, G. B., Huber, F., Phillips, R. J., (1985) Inorg. Chim. Acta, 104, pp. 41-45
Whiffen, D. H., (1956) J. Chem. Soc., pp. 1350-1356
Smith, P. J., Tup iauskas, A. P., (1978) Ann. Rep. NMR Spectrosc., 8, pp. 291-370
Bancroft, G. M., Platt, R. H., (1972) Adv. Inorg. Chem. Rad., 15, pp. 59-68
Collins, R. L., Travis, J. C., The electric field gradient tensor (1967) M ssbauer Effect Methodology, 3, pp. 123-161. , Gruverman I. J. (Ed), Plenum Press, New York
Bancroft, G. M., Kumar Das, V. G., Sham, T. K., Clark, M. G., (1976) J. Chem. Soc., Dalton Trans., pp. 643-654. , and references therein
Sham, T. K., Bancroft, G. M., (1975) Inorg. Chem., 14, pp. 2281-2284
Clark, M. G., Maddock, A. G., Platt, R. H., (1972) J. Chem. Soc., Dalton Trans., pp. 281-290
Parish, R. V., Structure and Bonding in Tin Compound (1984) M ssbauer Spectroscopy Applied to Inorganic Chemistry, 1, pp. 544-548. , Long G. J. (Ed), Plenum Press, New York
Basu Baul, T. S., Singh, K. S., Holcapek, M., Jirasko, R., Rivarola, E., Linden, A., (2005) J. Organomet. Chem., 690, pp. 4232-4242
Basu Baul, T. S., Masharing, C., Ruisi, G., Jirasko, R., Holcapek, M., de Vos, D., Wolstenholme, D., Linden, A., (2007) J. Organomet. Chem., 692, pp. 4849-4862
Hole ek, J., N dvorn k, M., Handl, K., Ly ka, A., (1983) J. Organomet. Chem., 241, pp. 177-184
Lockhart, T. P., Manders, W. F., (1986) Inorg. Chem., 25, pp. 892-895
Hole ek, J., Ly ka, A., (1986) Inorg. Chim. Acta, 118, pp. L15-L16
Zubieta, J. A., Zuckerman, J. J., (1978) Prog. Inorg. Chem., 24, pp. 251-475
J Organomet Chem (ISSN: 0022-328x), 2010 May 1; 695(9): 1405-1413.
Export to BibTeX Export to EndNote
Paper type: Journal Article,
Impact factor: 2.205, 5-year impact factor: 2.073
Url: http://www.scopus.com/inward/record.url?eid=2-s2.0-77950187656&partnerID=40&md5=b2ac33bc796bd357b0d5c3b94cc6920a
Keywords: Ftir, Mössbauer Spectroscopy, Nmr, Steroid Carboxylate, Triorganotin(iv), Carboxylate Groups, Conventional Techniques, Coordinated Solvents, Dft Calculation, Dft Study, Isolated Compounds, Ligand Coordination, Monodentates, Monomeric Complexes, Nmr Spectroscopy, Nuclear Quadrupole Splitting, Oxygen Atom, Solid-State Complexes, Spectroscopic Measurements, Structural Characterization, Tetrahedral Arrangement, Tetrahedral Structures, Tetramethyl, Tin Center, Carboxylation, Esters, Fourier Transform Infrared Spectroscopy, Molybdenum, Molybdenum Compounds, Nuclear Magnetic Resonance, Organometallics, Probability Density Function, Sodium, Stoichiometry, Sulfur Compounds, Titanium Compounds, Nuclear Magnetic Resonance Spectroscopy, M Ssbauer Spectroscopy, Triorganotin (iv),
Affiliations:
*** IBB - CNR ***
Dipartimento di Chimica Inorganica e Analitica Stanislao Cannizzaro, Università degli Studi di Palermo, Viale delle Scienze, Ed. 17, 90128 Palermo, Italy
Istituto di Biostrutture e Bioimmagini, CNR, Dipartimento di Scienze Chimiche, Viale Andrea Doria 6, 95125 Catania, Italy
Centro grandi apparecchiature (CGA)-UniNetLab, Università degli Studi di Palermo, Via F. Marini 14, 90128 Palermo, Italy
References:
Blunden, S.J., Cusack, P.A., Hill, R., (1985) Industrial Uses of Tin Chemicals, , Royal Society of Chemistry, Burlington House, London, Londo
Crowe, A.J., (1987) Appl. Organomet. Chem., 1, pp. 143-155
Crowe, A.J., Antitumor activity of organotin compounds (1994) Metal Compounds in Cancer Therapy, pp. 147-179. , Fricker S. (Ed), Chapman and Hall, London
Gielen, M., Davies, A.G., Pannell, K., Tiekink, E., (2008) Tin Chemistry: Fundamentals Frontiers and Applications, , John Wiley & Sons, New York
Arkis, E., Balköse, D., (2005) Polym. Degrad. Stab., 88, pp. 46-51
Saxena, A.K., Huber, F., (1989) Coord. Chem. Rev., 95, pp. 109-123
Pellerito, L., Nagy, L., (2002) Coord. Chem. Rev., 224, pp. 111-150
Davies, A.G., (2004) Organotin Chemistry, , Wiley-VCH, Weinheim
Hadjikakou, S.K., Hadjiliadis, N., (2009) Coord. Chem. Rev., 253, pp. 235-249
Gielen, M., Tiekink, E.R.T., Tin compounds and their therapeutic potential (2005) Metallotherapeutic Drugs and Metal-Based Diagnostic Agents: The Use of Metals in Medicine, pp. 421-439. , Gielen M., and Tiekink E.R.T. (Eds), John Wiley & Sons, Chichester
Tabassum, S., Pettinari, C., (2006) J. Organomet. Chem., 691, pp. 1761-1766
Yin, H.D., Li, F.H., Li, L.W., Li, G., (2007) J. Organomet. Chem., 692, pp. 1010-1019
Gielen, M., Biesemans, M., de Vos, D., Willem, R., (2000) Inorg. Biochem., 79, pp. 139-145
Nath, M., Pokharia, S., Yadav, R., (2001) Coord. Chem. Rev., 99, pp. 215-220
Chandrasekhar, V., Nagendran, S., Baskar, V., (2002) Coord. Chem. Rev., 1, pp. 235-240
Hussain, M., Ahmad, M.S., Siddique, A., Hanif, M., Ali, S., Mirza, B., (2009) Chem. Biol. Drug. Des., 74, pp. 183-189
Shahzadi, S., Shahid, K., Ali, S., Bakhtiar, M., (2008) Turk. J. Chem., 32, pp. 333-353
Pellerito, C., Nagy, L., Pellerito, L., Szorcsik, A., (2006) J. Organomet. Chem., 691, pp. 1733-1747
Bertazzi, N., Bruschetta, G., Casella, G., Pellerito, L., Rotondo, E., Scopelliti, M., (2003) Appl. Organomet. Chem., 17, pp. 932-939
Szorcsik, A., Nagy, L., Sletten, J., Szalontanai, G., Kamu, E., Fiore, T., Pellerito, L., Kalman, E., (2004) J. Organomet. Chem., 689, pp. 1145-1154
Pellerito, C., D'Agati, P., Fiore, T., Mansueto, C., Mansueto, V., Stocco, G.C., Nagy, L., Pellerito, L., (2005) J. Inorg. Biochem., 92, pp. 347-350
Bertazzi, N., Casella, G., D'Agati, P., Fiore, T., Mansueto, C., Mansueto, V., Pellerito, C., Scopelliti, M., (2008) Appl. Organomet. Chem., 22, pp. 389-396
Basu Baul, T.S., Paul, A., Pellerito, L., Scopelliti, M., Singh, P., Verma, P., de Vos, D., Invest. New Drugs, , doi:10.1007/s10637-009-9293-x
Barber, J., Lian, L., Morris, G.A., Tehrani, M.H., (1989) Magn. Res. Chem., 27, pp. 740-747
Neumann, W.P., (1970) The Organic Chemistry of Tin, , Interscience, London
Stephens, P.J., Devlin, F.J., Chabalowski, C.F., Frisch, M.J., (1994) J. Phys. Chem., 98, pp. 11623-11627
Hertwig, R.H., Koch, W., (1997) Chem. Phys. Lett., 268, pp. 345-351
Godbout, N., Salahub, D.R., (1992) Can. J. Chem., 70, pp. 560-571
Cancès, M.T., Mennucci, B., Tomasi, J., (1997) J. Chem. Phys., 107, pp. 3032-3041
Cossi, M., Barone, V., Mennucci, B., Tomasi, J., (1998) Chem. Phys. Lett., 286, pp. 253-260
Kutzelnigg, W., Fleischer, U., Schindler, M., (1990) NMR-Basic Principles and Progress, 23, pp. 165-262. , Diehl P., Fluck E., Günther H., and Kosfeld R. (Eds), Springer, Heidelberg
Avalle, P., Harris, R.K., Fischer, R.D., (2002) Phys. Chem. Chem. Phys., 4, pp. 3558-3561
Vivas-Reyes, R., De Proft, F., Biesemans, M., Willem, R., Geerlings, P., (2002) J. Phys. Chem. A, 106, pp. 2753-2759
Casella, G., Ferrante, F., Saielli, G., (2008) Inorg. Chem., 47, pp. 4796-4807
Zhao, Y., Truhlar, D.G., (2004) J. Phys. Chem. A, 108, pp. 6908-6918
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, V. Bakken, 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. Johnson, W. Chen, M.WDeacon, G.B., Huber, F., Phillips, R.J., (1985) Inorg. Chim. Acta, 104, pp. 41-45
Whiffen, D.H., (1956) J. Chem. Soc., pp. 1350-1356
Smith, P.J., Tupčiauskas, A.P., (1978) Ann. Rep. NMR Spectrosc., 8, pp. 291-370
Wrackmeyer, B., (1985) Annu. Rep. NMR Spectrosc., 16, pp. 73-186
Sebald, A., (1996) Advanced Applications of NMR to Organometallic Chemistry, pp. 123-156. , Chapter 5. Gielen M., Willem R., and Wrackmeyer B. (Eds), John Wiley & Sons, Chichester
Bancroft, G.M., Platt, R.H., (1972) Adv. Inorg. Chem. Rad., 15, pp. 59-68
Collins, R.L., Travis, J.C., The electric field gradient tensor (1967) Mössbauer Effect Methodology, 3, pp. 123-161. , Gruverman I.J. (Ed), Plenum Press, New York
Bancroft, G.M., Kumar Das, V.G., Sham, T.K., Clark, M.G., (1976) J. Chem. Soc., Dalton Trans., pp. 643-654. , and references therein
Sham, T.K., Bancroft, G.M., (1975) Inorg. Chem., 14, pp. 2281-2284
Clark, M.G., Maddock, A.G., Platt, R.H., (1972) J. Chem. Soc., Dalton Trans., pp. 281-290
Parish, R.V., Structure and Bonding in Tin Compound (1984) Mössbauer Spectroscopy Applied to Inorganic Chemistry, 1, pp. 544-548. , Long G.J. (Ed), Plenum Press, New York
Ganis, P., Valle, G., Furlani, D., Tagliavini, G., (1986) J. Organomet. Chem., 302, pp. 165-170
Basu Baul, T.S., Singh, K.S., Holcapek, M., Jirasko, R., Rivarola, E., Linden, A., (2005) J. Organomet. Chem., 690, pp. 4232-4242
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Structural characterization of triorganotin(IV) complexes with sodium fusidate and DFT calculations
Three new complexes of the steroid sodium fusidate (sodium 2-[(1S,2S,5R,6S,7S,10S,11S,13S, 14Z,15R,17R)-13-(acetyloxy)-5,17-dihydroxy-2,6,10,11-tetramethyl tetracyclo[8.7.0.02,7.011,15] heptadecan-14-ylidene]-6-methylhept-5-enoate = (NaFusidate, NaFA)]), with triorganotin(IV) moieties have been prepared and investigated by conventional techniques as FTIR, Mössbauer, ESI-MS and NMR spectroscopy. The isolated compounds showed stoichiometries organotin(IV)/fusidate 1/1, R3Sn(IV)FA (R = Me, FA1; Bu, FA2; Ph, FA3). The ligand coordination sites were determined by FTIR spectroscopic measurements. In the complexes, the carboxylate group of the fusidate ligand behaves as monodentate monoanionic donor, binding the Sn(IV) through one oxygen atom. On the basis of C-Sn-OCOO angles, calculated through the rationalization of the 119Sn Mössbauer parameter nuclear quadrupole splitting, it has been confirmed that, in all the solid state complexes, the Sn(IV) was tetracoordinated in a distorted tetrahedral structure. Further data from 119Sn CP-MAS spectra confirmed the distorted tetrahedral arrangement. In MeOH solution, 1H, 13C and 119Sn NMR spectroscopy showed monomeric complexes, where the carboxylate group mainly acts as monodentate ester-type ligand, and the occurrence of a coordinated solvent molecule to the tin center, as validated by non-relativistic NMR DFT study. © 2010 Elsevier B.V. All rights reserved.
Three new complexes of the steroid sodium fusidate (sodium 2-[(1S,2S,5R,6S,7S,10S,11S,13S, 14Z,15R,17R)-13-(acetyloxy)-5,17-dihydroxy-2,6,10,11-tetramethyl tetracyclo[8.7.0.02,7.011,15] heptadecan-14-ylidene]-6-methylhept-5-enoate = (NaFusidate, NaFA)]), with triorganotin(IV) moieties have been prepared and investigated by conventional techniques as FTIR, Mössbauer, ESI-MS and NMR spectroscopy. The isolated compounds showed stoichiometries organotin(IV)/fusidate 1/1, R3Sn(IV)FA (R = Me, FA1; Bu, FA2; Ph, FA3). The ligand coordination sites were determined by FTIR spectroscopic measurements. In the complexes, the carboxylate group of the fusidate ligand behaves as monodentate monoanionic donor, binding the Sn(IV) through one oxygen atom. On the basis of C-Sn-OCOO angles, calculated through the rationalization of the 119Sn Mössbauer parameter nuclear quadrupole splitting, it has been confirmed that, in all the solid state complexes, the Sn(IV) was tetracoordinated in a distorted tetrahedral structure. Further data from 119Sn CP-MAS spectra confirmed the distorted tetrahedral arrangement. In MeOH solution, 1H, 13C and 119Sn NMR spectroscopy showed monomeric complexes, where the carboxylate group mainly acts as monodentate ester-type ligand, and the occurrence of a coordinated solvent molecule to the tin center, as validated by non-relativistic NMR DFT study. © 2010 Elsevier B.V. All rights reserved.
Structural characterization of triorganotin(IV) complexes with sodium fusidate and DFT calculations
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Structural characterization of triorganotin(IV) complexes with sodium fusidate and DFT calculations
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Pellerito O, Prinzivalli C, Foresti E, Sabatino P, Abbate M, Casella G, Fiore T, Scopelliti M, Pellerito C, Giuliano M, Grasso G, Pellerito L
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* Synthesis, chemical characterization and biological activity of new histone acetylation/deacetylation specific inhibitors: A novel and potential approach to cancer therapy (440 views)
J Chem Res (ISSN: 0162-0134, 1873-3344, 0162-0134print), 2013 Sep; 125: 16-25.
Impact Factor: 3.274
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Travaglia A, La Mendola D, Magrì A, Nicoletti VG, Pietropaolo A, Rizzarelli E
* Copper, BDNF and Its N-terminal domain: inorganic features and biological perspectives (506 views)
Chemistry (ISSN: 1521-3765, 0947-6539, 1521-3765electronic), 2012 Dec 3; 18(49): 15618-15631.
Impact Factor: 5.831
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La Mendola D, Magrì A, Vagliasindi LI, Hansson Ö, Bonomo RP, Rizzarelli E
* Copper(II) complex formation with a linear peptide encompassing the putative cell binding site of angiogenin (448 views)
Dalton T (ISSN: 1477-9234, 1477-9226, 1477-9234electronic), 2010 Nov 28; 39(44): 10678-10684.
Impact Factor: 3.647
View Export to BibTeX Export to EndNote
La Mendola D, Magrì A, Campagna T, Campitiello MA, Raiola L, Isernia C, Hansson O, Bonomo RP, Rizzarelli E
* A doppel alpha-helix peptide fragment mimics the copper(II) interactions with the whole protein (1115 views)
Chemistry (ISSN: 0947-6539, 1521-3765, 1521-3765electronic), 2010 Jun 1; 16(21): 6212-6223.
Impact Factor: 5.476
View Export to BibTeX Export to EndNote
Cella L, Liuzzi R, Magliulo M, Conson M, Camera L, Salvatore M, Pacelli R
* Radiotherapy of large target volumes in Hodgkin's lymphoma: Normal tissue sparing capability of forward IMRT versus conventional techniques (451 views) (PDF 236 views)
Radiat Oncol Radiation Oncology (ISSN: 1748-717x), 2010 May 11; 5(1): 33-33.
Impact Factor: 2.409
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Total impact factor: 20.637 (20.637 excluding Abstracts).
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