Metal complexes of functionalized sulfur containing ligands, X [1] synthesis of ruthenium(II) and platinum(II) 1-alkyne-1-thiolato complexes. X-ray structure analysis of trans-(Ph3P)2Pt[S-C≡C-C(CH3) 3]2;Metallkomplexe mit funktionalisierten schwefelliganden, X [1] ruthenium(II)- und platin(II)-1-alkin-1-thiolato-komplexe. Kristallstrukturanalyse von trans-(Ph3P)2Pt[S-C≡C-C(CH3)3] 2

Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences

Volumn 51, Issue 4, 1996, Pages 501-505

  Weigand, Wolfgang ^a   Weishäupl, Michael ^a   Robl, Christian ^b  

^a UNIVERSITY OF MUNICH   (Germany)

^b FRIEDRICH SCHILLER UNIVERSITY JENA   (Germany)

Author keywords

1 Alkyne 1 thiolato ligands; 31P CP MAS NMR spectra; Platinum complexes; Ruthenium complexes

Indexed keywords

CHELATION; CRYSTAL STRUCTURE; LIGANDS; METAL COMPLEXES; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PLATINUM COMPOUNDS; SULFUR; SYNTHESIS (CHEMICAL);

31P CP/MAS; FUNCTIONALIZED; PLATINUM COMPLEXES; RUTHENIUM COMPLEXES; X RAY STRUCTURE ANALYSIS;

RUTHENIUM COMPOUNDS;

EID: 0039566883     PISSN: 09320776     EISSN: None     Source Type: Journal    
DOI: 10.1515/znb-1996-0412     Document Type: Article

References (20)

1. X. Mitteilung der Reihe "Metallkomplexe mit funktionalisierten Schwefelliganden". IX. Mitteilung: G. Bosl, R. Wünsch, C. Robl, W. Weigand, in H. Werner, J. Sundermeyer (ed.): Stereoselective Reactions of Metal-Activated Molecules, S. 201, Vieweg Verlag, Braunschweig/Wiesbaden (1995).
2. L. Brandsma, H. D. Verkruijsse, in Synthesis of Acetylenes, Allenes and Cumulenes, A Laboratory Manual, Elsevier, Amsterdam (1981) und dort zit. Lit.
3. E. Schaumann, Tetrahedron 44, 1827 (1988).
4. a) W. Weigand, Z. Naturforsch. 46b, 1333 (1991);
5. b) W. Weigand, C. Robl, Chem. Ber. 126, 1807 (1993);
6. c) W. Weigand, C. Robl, Chimia 47, 273 (1993).
7. T.-Y. Lee, A. Mayr, J. Am. Chem. Soc. 116, 10300 (1994).
8. R. S. Sukhai, J. Meijer, L. Brandsma, Rec. Trav. Chim. Pays-Bas 96, 179 (1977).
9. W. A. Schenk, T. Stur, Z. Naturforsch. 45b, 1495 (1990).
10. S. J. Harris, D. R. M. Walton, J. Organomet. Chem. 127, Cl (1977); S. J. Harris, D. R. M. Walton, J. Chem. Soc. Chem. Commun. 1976, 1008.
11. S. J. Harris, D. R. M. Walton, J. Organomet. Chem. 127, Cl (1977); S. J. Harris, D. R. M. Walton, J. Chem. Soc. Chem. Commun. 1976, 1008.
12. A. Pines, M. G. Gibby, J. S. Waugh, J. Chem. Phys. 59, 569 (1973).
13. M. M. Maricq, J. S. Waugh, J. Chem. Phys. 70, 3300 (1979); E. Klaus, A. Sebald, Angew. Chem. 107, 713 (1995), Angew. Chem., Int. Ed. Engl. 34, 667 (1995).
14. M. M. Maricq, J. S. Waugh, J. Chem. Phys. 70, 3300 (1979); E. Klaus, A. Sebald, Angew. Chem. 107, 713 (1995), Angew. Chem., Int. Ed. Engl. 34, 667 (1995).
15. M. M. Maricq, J. S. Waugh, J. Chem. Phys. 70, 3300 (1979); E. Klaus, A. Sebald, Angew. Chem. 107, 713 (1995), Angew. Chem., Int. Ed. Engl. 34, 667 (1995).
16. M. T. Ashby, Comments Inorg. Chem. 10, 297 (1990).
17. M. Capdevila, W. Clegg, P. González-Duarte, B. Harris, I. Mira, J. Sola, I. C. Taylor, J. Chem. Soc., Dalton Trans. 1992, 2817 und dort zit. Lit.
18. U Nagel, Chem. Ber. 115, 1998 (1982).
19. T. G. Appleton, M. A. Bennett und I. B. Tomkins, J. Chem. Soc. Dalton Trans. 1976, 439.
20. M. I. Bruce, C. Hameister, A. G. Swincer, R. C. Wallis, Inorg. Synth. 21, 79 (1982).