New polydentate and polynucleating N-donor ligands from amines and 2,4,6-trichloro-1,3,5-triazine

Tetrahedron Letters

Volumn 43, Issue 38, 2002, Pages 6783-6786

  De Hoog, Paul ^a   Gamez, Patrick ^a   Driessen, Willem L ^a   Reedijk, Jan ^a  

^a LEIDEN UNIVERSITY   (Netherlands)

Author keywords

1,3,5 triazine derivatives; First generation dendrimer; N containing ligands

Indexed keywords

2,4,6 TRICHLORO 1,3,5 TRIAZINE; AMINE; LIGAND; TRIAZINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL PROCEDURES; DRUG SYNTHESIS;

EID: 0037119669     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01498-3     Document Type: Article

References (18)

1. Saalfrank R.W., Löw N., Trummer S., Sheldrick G.M., Teichert M., Stalke D. Eur. J. Inorg. Chem. 1998;559-563.
2. Lehn J.-M., Kneisel B.O., Baum G., Fenske D. Angew. Chem., Int. Ed. Engl. 35:1996;1838-1840.
3. Saalfrank R.W., Löw N., Kareth S., Seitz F., Hampel D., Stalke D., Teichert M. Angew. Chem., Int. Ed. Engl. 37:1998;172-175.
4. Kahn O. Molecular Magnetism. 1993;VCH, New York.
5. Zanello P., Tamburini S., Vigato P.A., Mazzochin G.A. Coord. Chem. Rev. 77:1987;165-273.
6. Bencini I., Gatteschi D. EPR of Exchange Coupled Systems. 1990;Springer, Berlin.
7. Bertini I., Luchinat C. NMR of Paramagnetic Molecules in Biological Systems. 1986;Benjamin-Cummings, Boston.
8. Lehn J.-M. Supramolecular Chemistry. 1995;VCH, Weinheim.
9. Aromí G., Gamez P., Roubeau O., Kooijman H., Spek A.L., Driessen W.L., Reedijk J. Angew. Chem., Int. Ed. 41:2002;1168-1170.
10. Garmouna M., Blanchoud H., Teil M.-J., Blanchard M., Chevreuil M. Water Air Soil Poll. 132:2001;1-17.
11. Klenke B., Stewart M., Barrett M.P., Brun R., Gilbert I.H. J. Med. Chem. 44:2001;3440-3452.
12. Patel H.S., Patel V.C. Eur. Polym. J. 2001;2263-2271.
13. Timmerman P., Prins L.J. Eur. J. Org. Chem. 2001;3191-3205.
14. Bielejewska A.G., Marjo C.E., Prins L.J., Timmerman P., de Jong F., Reinhoudt D.N. J. Am. Chem. Soc. 123:2001;7518-7533.
15. Batten S.R., Hoskins B.F., Moubaraki B., Murray K.S., Robson R. Chem. Commun. 2000;1095-1096.
16. Gamez P., de Hoog P., Roubeau O., Lutz M., Driessen W.L., Spek A.L., Reedijk J. Chem. Commun. 2002;1488-1489
17. (b) de Hoog, P.; Gamez, P.; Roubeau, O.; Lutz, M.; Driessen, W. L.; Spek, A. L.; Reedijk, J. New J. Chem., in press.
18. Several elemental analyses on compound 4 have led to disparate and too low experimental percentages of carbone (up to 2%). This might be due to the violent decomposition of 4 above 250°C.