Rhenium(I) carbonyl complexes of bis(N,N-diethylamino)carbeniumdithiocarboxylate, a novel inner-salt type sulfur donor ligand. Spectroscopic and structural studies

Inorganica Chimica Acta

Volumn 340, Issue , 2002, Pages 155-162

  Banerjee, Sangeeta Ray ^a   Nagasawa, Akira ^b   Zubieta, Jon ^a  

^a SYRACUSE UNIVERSITY   (United States)

^b SAITAMA UNIVERSITY   (Japan)

Author keywords

Binuclear complexes; Inner salt sulfur donor; Low valent rhenium carbonyl complexes

Indexed keywords

CHLORINE COMPOUNDS; LIGANDS; SULFUR;

BINUCLEAR COMPLEXES; CARBONYL COMPLEXES; ELECTROCHEMICAL CONDITIONS; MONONUCLEAR COMPLEXES; REVERSIBLE OXIDATION; RHENIUM CARBONYL COMPLEXES; STRUCTURAL STUDIES; SULFUR DONORS;

RHENIUM COMPOUNDS;

BRIDGED COMPOUND; CARBON 13; CARBONYL DERIVATIVE; CARBOXYLIC ACID DERIVATIVE; CHLORIDE; HYDROGEN; LIGAND; RHENIUM; SULFUR DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHELATION; CHEMICAL ANALYSIS; CHEMICAL BOND; CHEMICAL PARAMETERS; CHEMICAL REACTION; ELECTROCHEMISTRY; INFRARED RADIATION; OXIDATION; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION; SPECTROSCOPY; STRUCTURE ANALYSIS; X RAY ANALYSIS;

EID: 0037175571     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0020-1693(02)01056-3     Document Type: Article

References (33)

1. Cabeza J.A., Liamazares A., Riera V., Trivedi R. Organometallics. 17:1998;5580.
2. Azam K.A., Houssain Md.A., Hursthouse M.B., Kabir S.E., Malik K.M.A., Vahrenkamp H. J. Organomet. Chem. 555:1998;285. and references therein.
3. Yam V.W.-W., Wong K.M.-C., Cheung K.-K. Organometallics. 16:1997;1729. and references therein.
4. Udo K., Reinhard M., Werner W. Angew. Chem. 94:1982;300.
5. Abram U., Abram S., Schibli R., Alberto R., Dilworth J.R. Polyhedron. 17:1998;1303.
6. J. Chatt, R.H. Crabtree, J.R. Dilworth, R.L. Richards, J. Chem. Soc., Dalton Trans. (1974) 2358.
7. S.R. Fletcher, A.C. Skapski, J. Chem. Soc., Dalton Trans. (1974) 486.
8. J.F. Rowbottom, G. Wilkinson, J. Chem. Soc., Dalton Trans. (1974) 684.
9. J.F. Rowbottom, G. Wilkinson, J. Chem. Soc., Dalton Trans. (1974) 684.
10. J.F. Rowbottom, G. Wilkinson, J. Chem. Soc., Dalton Trans. (1972) 826.
11. J. Nakayama, I. Akiyama, J. Chem. Soc., Chem. Commun. (1992) 1552.
12. Nakayama J. Sulfur Lett. 15:1993;239.
13. Nagasawa A., Akiyama I., Mashima S., Nakayama J. Heteroatom Chem. 6:1995;45.
14. Miyashita I., Matsumoto K., Kobayashi M., Nagasawa A., Nakayama J. Inorg. Chim. Acta. 283:1998;256.
15. M. Abe, K. Isobe, M. Hirose, A. Nagasawa, private communication.
16. McConnachie C.A., Stiefel E.I. Inorg. Chem. 38:1999;964.
17. McConnachie C.A., Stiefel E.I. Inorg. Chem. 36:1997;6144.
18. Murray H.H., Wei L., Sherman S.E., Greaney M.A., Eriksen K.A., Cartensen B., Halbert T.R., Stiefel E.I. Inorg. Chem. 34:1995;841.
19. Wei L., Halbert T.R., Murray H.H., Stiefel E.I. J. Am.Chem. Soc. 112:1990;6431.
20. Stiefel E.I., Halbert T.R., Coyle C.L., Wei L., Pan W.H., Ho T.C., Chianelli R.R., Daage M. Polyhedron. 8:1989;1625. and reference therein.
21. Griffiths D.V., Parrott S.J., Togrou M., Dilworth J.R., Zheng Y., Ritter S., Abram U. Z. Anorg. Allg. Chem. 9:1998;624.
22. J.R. Dilworth, D.V. Griffiths, D. Vaughan, S.J. Parrott, Y. Zheng, J. Chem. Soc., Dalton Trans. (1997) 2931.
23. Dilworth J.R., Jabanputra P., Parrott S.J., Thompson R.M., Povey D.C., Zubieta J. Polyhedron. 11:1992;147.
24. J.R. Dilworth, R.A. Henderson, P. Dahlstrom, T. Nicholson, J. Zubieta, J. Chem. Soc., Dalton Trans. (1987) 529.
25. Bishop M.W., Chatt J., Dilworth J.R., Neaves B.D., Dahlstrom P., Hyde J., Zubieta J. J. Organomet. Chem. 213:1981;109.
26. Riddick J.A., Bunger W.B. Organic solvents. Weissberger A., Techniques of Chemistry. II:1970;Wiley, New York.
27. Cromer D.T., Waber J.T. International Tables for X-ray Crystallography. IV:1974;Kynoch Press, Birmingham, UK.
28. Creagh D.C., McAuley J.W.J. International Tables for X-ray Crystallography. C:1992;Kluwer Academic, Boston, MA. table 2.
29. SHELXTL PC™ Siemens Analytical X-ray Instruments, Inc., Madison, WI, 1990.
30. Wrighton M.S., Morse D.L., Gray H.B., Ottesen D.K. J. Am. Chem. Soc. 98:1976;1111.
31. Shaver R.J., Rillema D.P. Inorg. Chem. 31:1992;4101.
32. Koike K., Tanabe J., Toyama S., Tsubaki H., Sakamoto K., Westwell J.R., Johnson F.P.A., Hori H., Saitoh H., Ishitani O. Inorg. Chem. 39:2000;2777.
33. L.E. Sutton, ed., `Tables of Interatomic Distances and Configuration in Molecules and Ions', The Chemical Society Special Publication, No. 11, 18, The Chemical Society (London) (1958, 1965). Usual usage of the bond distances are: C-N, 1.33-1.47 Å; C=N, 1.30-1.34 Å; C≡N, 1.15-1.17 Å.