Iron-59 complexes of lipophilic hexadentate phenolate-derivatized cyclohexanetriamine ligands

Inorganica Chimica Acta

Volumn 242, Issue 1-2, 1996, Pages 201-204

  Bollinger, James E ^a   Banks, William A ^b   Kastin, Abba J ^b   Roundhill, D Max ^a  

^a Tulane University   (United States)

^b TULANE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Chelate complexes; Iron; Lipophilic complexes; Multidentate N,O ligand

Indexed keywords

IRON; LIGANDS; MASS SPECTROMETRY;

BLOOD-BRAIN BARRIER; CHELATE COMPLEX; DISTRIBUTION COEFFICIENT; ELECTRONIC ABSORPTION SPECTRA; LIPOPHILIC COMPLEXES; MASS SPECTROSCOPY; N ,O LIGANDS; SCHIFF BASE CONDENSATION;

IRON COMPOUNDS;

EID: 0011860916     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/0020-1693(95)04867-7     Document Type: Article

References (22)

1. R.C. Hider and A.D. Hall, Prog. Med. Chem., 28 (1991) 41.
2. (a) R.J. Motekaitis, A.E. Martell and M.J. Welch, Inorg. Chem., 33 (1994) 1241;
3. (b) A.J. Carty and D.G. Tuck, Prog. Inorg. Chem. 19 (1975) 245;
4. (c) I.A. Sheka, L.S. Chaus and T.T. Mityureva, in G. Wilkinson (ed.), The Chemistry of Gallium, Pergamon, 1987, Vol 3, Ch. 25.1;
5. (d) D.G. Tuck, Pure Appl. Chem., 55 (1983) 1477.
6. D.A. Moore, P.E. Fanwick and M.J. Welch, Inorg. Chem., 29 (1990) 672.
7. S. Liu, E. Wong, S.J. Rettig and C. Orvig, Inorg. Chem., 32 (1993) 4268.
8. M.A. Green, C.J. Mathias, W.L. Neumann, P.E. Fanwick, M. Janik and E.A. Deutsch, J. Nucl. Med., 34 (1993) 228.
9. C. Hershko (ed.), Baillière's Clinical Haematology, Vol. 2, Iron Chelating Therapy, Ballière Tindall, London, 1989.
10. A.E. Martell, R.J. Motekaitis, I. Murase, L.F. Sala, R. Stoldt, C.Y. Ng, H. Rosenkrantz and J.J. Metterville, Inorg. Chim. Acta, 138 (1987) 215.
11. T.M. Garrett, T.J. McMurry, M.W. Hosseini, Z.E. Reyes, F.E. Hahn and K.N. Raymond, J. Am. Chem. Soc., 113 (1991) 2965.
12. T.B. Karpishin, M.S. Gebhard, E.I. Solomon and K.N. Raymond, J. Am. Chem. Soc., 113 (1991) 2977.
13. J.E. Bollinger, J.T. Mague, C.J. O'Connor, W.A. Banks and D.M. Roundhill, J. Chem. Soc., Dalton Trans., (1995) 1677.
14. For an example of similar ligands with hydroxy functional groups, see K. Hegetschweiler, M. Ghisletta, T.F. Fässler, R. Nesper, H.W. Schmalle and G. Rihs, Inorg. Chem., 32 (1993) 2032.
15. S. Liu, L. Gelmini, S.J. Rettig, R.C. Thompson and C. Orvig, J. Am. Chem. Soc., 114 (1992) 6081.
16. J.E. Bollinger, W.A. Banks, A.J. Kastin, M.J. Welch and D.M. Roundhill, J. Nucl. Med. Biol., in press.
17. J.E. Bollinger, J.T. Mague, W.A. Banks, A.J. Kastin and D.M. Roundhill, Inorg. Chem., 34 (1995) 2143.
18. S.A. Koch and M. Millar, J. Am. Chem. Soc., 104 (1982) 5255.
19. R.H. Heistand, II, R.B. Lauffer, E. Fikrig and L. Que, Jr., J. Am. Chem Soc., 104 (1982) 2789.
20. K.N. Raymond, S.S. Isied, LD. Brown, F.R. Fronczek and J.H. Nibert, J. Am. Chem. Soc., 98 (1976) 1767.
21. B.P. Gaber, V. Miskowski and T.G. Spiro, J. Am. Chem. Soc., 96 (1974) 6868.
22. R.R. Eng, in S.E. Swenburg, J.J. Conklin (ed.), Imaging Techniques in Biology and Medicine, Academic Press, San Diego, CA, 1988, pp. 168-171.