Grid-corner analogues: Synthesis, characterisation and spectroscopic properties of meridional complexes of tridentate NNO Schiff-base ligands

Polyhedron

Volumn 29, Issue 1, 2010, Pages 178-187

  Stefankiewicz, Artur R ^a,b   Wałesa Chorab, Monika ^b   Szcześniak, Hanna B ^b   Patroniak, Violetta ^b   Kubicki, Maciej ^b   Hnatejko, Zbigniew ^b   Harrowfield, Jack ^a  

^a UNIVERSITÉ LOUIS PASTEUR   (France)

^b ADAM MICKIEWICZ UNIVERSITY   (Poland)

Author keywords

N,N,O donor ligands; Schiff bases; Self assembly; Transition metal ions

Indexed keywords

CHELATION; COBALT COMPOUNDS; COPPER COMPOUNDS; LIGANDS; METAL IONS; SILVER COMPOUNDS; SPECTROSCOPIC ANALYSIS; TRANSITION METALS; X RAY CRYSTALLOGRAPHY; ZINC COMPOUNDS;

ANALOG SYNTHESIS; DONOR LIGANDS; N,N,O-DONOR LIGAND; O-DONOR; PYRIDINE-2; SCHIFF-BASE; SCHIFF-BASE LIGANDS; SPECTROSCOPIC PROPERTY; TRANSITION METAL IONS; TRIDENTATE SCHIFF-BASE;

SELF ASSEMBLY;

EID: 77957832891     PISSN: 02775387     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.poly.2009.06.069     Document Type: Article

References (36)

1. Rojo J., Lehn J.-M., Baum G., Fenske D., Waldmann O., and Mueller P. Chemistry (1999) 517
2. Ziessel R. Coord. Chem. Rev. 216 (2001) 195
3. Glasson C.R.K., Lindoy L.F., and Meehan G.V. Coord. Chem. Rev. 252 (2008) 940
4. Meyer C.D., Joiner C.S., and Stoddart J.F. Chem. Soc. Rev. 36 (2007) 1705
5. Nitschke J.R., and Lehn J.-M. Proc. Natl. Acad. Sci. USA 100 (2003) 11970
6. Stefankiewicz A.R., and Lehn J.-M. Chem. Eur. J. 15 (2009) 2500
7. Nitschke J.R. Acc. Chem. Res. 40 (2007) 103
8. Opstal T., and Verpoort F. Angew. Chem., Int. Ed. 42 (2003) 2876
9. Adhikary C., Bera R., Dutta B., Jana S., Bocelli G., Cantoni A., Chaudhuri S., and Koner S. Polyhedron 27 (2008) 1556
10. Kumar P.R., Upreti S., and Singh A.K. Polyhedron 27 (2008) 1610
11. Patroniak V., Stefankiewicz A.R., Lehn J.-M., and Kubicki M. Eur. J. Inorg. Chem 10 (2005) 4168
12. Balamurugan A., Balossier G., Laurent-Maquin D., Pina S., Rebelo A.H.S., Faure J., and Ferreira J.M.F. Dent. Mater. 24 (2008) 1343
13. Chohan Z.H., and Kausar S. Chem. Pharm. Bull. 41 (1993) 951
14. Kurtoglu M., Purtas F., and Toroglu S. Trans. Met. Chem. 33 (2008) 705
15. Anzellotti A.I., and Farrell N.P. Chem. Soc. Rev. 37 (2008) 1629
16. Ruben M., Lehn J.-M., and Muller P. Chem. Soc. Rev. 35 (2006) 1056
17. Stupp S.I. Chem. Rev. 105 (2005) 1023
18. Ruben M., Rojo J., Romero-Salguero F.J., Uppadine L.H., and Lehn J.-M. Angew. Chem., Int. Ed. 43 (2004) 3644
19. Majumder A., Rosair G.M., Mallick A., Chattopadhyay N., and Mitra S. Polyhedron 25 (2006) 1753
20. Juhasz G., Hayami S., Sato O., and Maeda Y. Chem. Phys. Lett. 364 (2002) 164
21. Hayami S., and Maeda Y. Inorg. Chim. Acta 255 (1997) 181
22. J.R. Dilworth, S.D. Howe, D.J. Hutson, J.R. Miller, J. Silver, R.M. Thompson, M. Harman, M.B. Hursthouse, J. Chem. Soc., Dalton Trans. (1994) 3553-3562.
23. Mukhopadhyay A., and Pal S. J. Chem., Crystallogr. 35 (2005) 737
24. Reedig N., Triller M.U., Purshe D., Rompel A., and Krebs B. Z. Anorg. Allg. Chem. 628 (2002) 2458
25. Epstein D.M., Choudhary S., Churchill M.R., Keil K.M., Eliseev A.V., and Morrow J.R. Inorg. Chem. 40 (2001) 1591
26. Patroniak V., Stefankiewicz A.R., Lehn J.-M., Kubicki M., and Hoffmann M. Chemistry (2006) 144
27. L. Rigamonti, A. Cinti, A. Forni, A. Pasini, O. Piovesana, Eur. J. Inorg. Chem. (2008) 3633-3647.
28. Pachon L.D., Golobic A., Kozlevcar B., Gamez P., Kooijman H., Spek A.L., and Reedijk J. Inorg. Chim. Acta 357 (2004) 3697
29. Shi Q., Xu L., Ji J., Li Y., Wang R., Zhou Z., Cao R., Hong M., and Chan A.S.C. Inorg. Chem. Commun. 7 (2004) 1254
30. Kalsani V., Ammon H., Jackel F., Rabe J.P., and Schmittel M. Chem. Eur. J. 10 (2004) 5481
31. Rojo J., Romero-Salguero F.J., Lehn J.-M., Baum G., and Fenske D. Chemistry (1999) 1421
32. Scaltrito D.V., Thompson D.W., O'Callaghan J.A., and Meyer G.J. Coord. Chem. Rev. 208 (2000) 243
33. Fatin-Rouge N., Blanc S., Pfeil A., Rigault A., Albrecht-Gary A.M., and Lehn J.M. Helv. Chim. Acta 84 (2001) 1694
34. Pitt C.G., Bao Y., Thompson J., Wani M.C., Rosenkrantz H., and Metterville J. J. Med. Chem. 29 (1986) 1231
35. CrysAlis CCD (Version 1.171.32.5) and CrysAlis RED (Version 1.171.32.5). Oxford Diffraction Ltd. 2007.
36. Sheldrick G.M. Acta Crystallogr., Sect. A 64 (2008) 112