New Re(I) tricarbonyl-diimine complexes with N,N′-bis(substituted benzaldehyde)-1,2-diiminoethane Schiff base ligands: Synthesis, spectroscopic and electrochemical studies and crystal structures

Polyhedron

Volumn 29, Issue 6, 2010, Pages 1600-1606

  Mirkhani, Valiollah ^a   Kia, Reza ^b   Vartooni, Akbar Rostami ^a   Fun, Hoong Kun ^c  

^a UNIVERSITY OF ISFAHAN   (Iran)

^b ISLAMIC AZAD UNIVERSITY   (Iran)

^c SCHOOL OF PHYSICS   (Malaysia)

Author keywords

Diimine ligands; Tricarbonylrhenium(I) complexes; X ray crystallography

Indexed keywords

COMPLEX NETWORKS; CYCLIC VOLTAMMETRY; FOURIER TRANSFORM INFRARED SPECTROSCOPY; HYDROGEN BONDS; INDIUM COMPOUNDS; LIGANDS; MOLECULES; RHENIUM COMPOUNDS; SELF ASSEMBLY; SYNTHESIS (CHEMICAL); ULTRAVIOLET VISIBLE SPECTROSCOPY;

CRYSTALS STRUCTURES; DIIMINE COMPLEXES; DIIMINE LIGAND; ELECTROCHEMICAL STUDIES; NEIGHBORING MOLECULES; SCHIFF-BASE LIGANDS; SPECTROSCOPIC STUDIES; STRUCTURE PROPERTY; SUBSTITUTED BENZALDEHYDES; TRICARBONYLRHENIA(I) COMPLEX;

X RAY CRYSTALLOGRAPHY;

EID: 77950300904     PISSN: 02775387     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.poly.2010.01.035     Document Type: Article

References (27)

1. Doleck T., Attard J., Fronczek F.R., Moskun A., and Isovitsch R. Inorg. Chim. Acta 362 (2009) 3872
2. Potgieter K., Mayer P., Gerber T.I.A., and Booysen I.N. Polyhedron 28 (2009) 2808
3. Blower P.J. Transition. Met. Chem. 23 (1998) 109
4. Hoshino N. Coord. Chem. Rev. 174 (1998) 77
5. Uhlenbrock S., Wegner R., and Krebs B. J. Chem. Soc., Dalton Trans. (1996) 3731
6. In: Grätzel M. (Ed). Energy Resources through Photochemistry and Catalysis (1983), Academic Press, New York
7. Chen Y., Liu W., Jin J.-S., Liu B., Zou Z.-G., Zuo J.-L., and You X.-Z. Organomet. Chem. 694 (2009) 763
8. Hawecker J., Lehn J.M., and Ziessel R. J. Chem. Soc., Chem. Commun. (1983) 536
9. Sullivan B.P., and Meyer T.J. J. Chem. Soc., Chem. Commun. (1984) 1244
10. Calzaferri G., Hadener K., and Li J. J. Photochem. Photobiol., A 64 (1992) 259
11. Kutal C., Corbin A.J., and Ferraudi G. Organometallics 6 (1987) 553
12. Vogler A., and Kunkely H. Coord. Chem. Rev. 200-202 (2000) 991
13. Jurisson S.S., and Lydon J.D. Chem. Rev. 99 (1999) 2205
14. smart, Bruker Molecular Analysis Research Tool, Bruker AXS Inc., Madison, Wisconsin, USA, 2005.
15. saint (Version V7.12A), Data Reduction and Correction Program, Bruker AXS Inc., Madison, Wisconsin, USA, 2005.
16. sadabs (Version 2004/1), An Empirical Absorption Correction Program. Bruker AXS Inc., Madison, Wisconsin, USA.
17. Sheldrick G.M. Acta Crystallogr., Sect. A 64 (2008) 112
18. tom Dieck H., and Renk I.W. Chem. Ber. 104 (1971) 92
19. Itokazu M.K., Polo A.S., and Murakami Iha N.Y. J. Photochem. Photobiol., A 160 (2003) 27
20. Busby M., Matousek P., Towrie M., and Vlček Jr. A. Inorg. Chim. Acta 360 (2007) 885
21. Veroni I., Mitsopoulou C.A., and Lahoz F.J. J. Organomet. Chem. 693 (2008) 2451
22. Reger D.L., Watson R.P., and Smith M.D. J. Organomet. Chem. 692 (2007) 3094
23. Machura B., Kruszynski R., Jaworska M., Lodowski P., Penczek R., and Kusz J. Polyhedron 27 (2008) 1767
24. Kia R., Mirkhani V., Kálmán A., and Deák A. Polyhedron 26 (2007) 1711
25. Kia R., Mirkhani V., Kálmán A., and Deák A. Polyhedron 26 (2007) 2906
26. Lommerse J.P.M., Stone A.J., Taylor R., and Allen F.H. J. Am. Chem. Soc. 118 (1996) 3108
27. Reddy D.S., Craig D.C., and Desiraju G.R. J. Chem. Soc., Chem. Commun. (1994) 1457