1′-(diphenylphosphino)ferrocenecarboxylic acid and its P-oxide and methyl ester: Synthesis, characterization, crystal structure, and electrochemistry

Organometallics

Volumn 15, Issue 2, 1996, Pages 543-550

  Podlaha, Jaroslav ^a   Štěpnička, Petr ^a   Ludvík, Jiří ^a,b   Císařová, Ivana ^a  

^a CHARLES UNIVERSITY   (Czech Republic)

^b J HEYROVSKÝ INSTITUTE OF PHYSICAL CHEMISTRY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0000992198     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om950528q     Document Type: Article

References (21)

1. Butler, I. R.; Kalaji, M.; Nehrlich, L.; Hursthouse, M.; Karaulov, A. I.; Abdul Malik, K. M. J. Chem. Soc., Chem. Commun. 1995, 459.
2. Houlton, A.; Jasim, N.; Roberts, R. M. G.; Silver, J.; Cunningham, D.; McArdle, P.; Higgins, T. J. Chem. Soc., Dalton Trans. 1992, 2235.
3. Beer, P. D.; Nation, J. E.; McWhinnie, S. L. W.; Harman, M. E.; Hursthouse, M. B.; Ogden, M. I.; White, A. H. J. Chem. Soc., Dalton Trans. 1991, 2485.
4. Grossel, M. C.; Goldspink, M. R.; Knychala, J. P.; Cheetham, A. K.; Hriljac, J. A. J. Organomet. Chem. 1988, 352, C13.
5. (a) Podlahová, J.; Kratochvíl, B.; Podlaha, J.; Hašek, J. J. Chem. Soc., Dalton Trans. 1985, 2393 and references therein.
6. (b) Podlaha, J.; Jegorov, A.; Buděšínský, M.; Hanuš, V. Phosphorus Sulfur 1988, 37, 87 and references therein.
7. (c) Podlahová, J.; Hartl, F.; Podlaha, J.; Knoch, F. Polyhedron 1987, 6, 1987 and references therein.
8. Jegorov, A.; Podlaha, J. Catal. Lett. 1991, 8, 9.
9. (a) Seyferth, D.; Withers, H. P., Jr. J. Organomet. Chem. 1980, 185, C1.
10. (b) Seyferth, D.; Withers, H. P. Organometallics 1982, 1, 1275.
11. Osborne, A. G.; Whiteley, R. H.; Meads, R. E. J. Organomet. Chem. 1980, 193, 345.
12. (a) Little, W. F.; Reilley, C. N.; Johnson, J. D.; Sanders, A. P. J. Am. Chem. Soc. 1964, 86, 1382.
13. (b) Scholl, H.; Sochaj, K. Electrochim. Acta 1991, 36, 689.
14. Pilloni, G.; Longato, B.; Corain, B. J. Organomet. Chem. 1991, 420, 57.
15. Acetonitrile is known to be notoriously difficult to dry below 10 ppm level (see, e.g.: Burfield, D. R.; Lee, K. H.; Smithers, R. H. J. Org. Chem. 1977, 42, 3060); this amount corresponds, however, to the same order of molar concentration as that of the compounds studied.
16. Rosenblum, M.; Santer, J. O.; Glenn, H. W. J. Am. Chem. Soc. 1963, 85, 1450.
17. Exner, O. Correlations in Organic Chemistry (in Czech); SNTL Alfa Publishers: Prague, 1981.
18. Texeira, M. G.; Roffia, S.; Bignozzi, C. A.; Paradisi, C.; Paolucci, P. J. Electroanal. Chem. 1993, 345, 243.
19. Medina, J. C.; Goodnow, T. T.; Rojas, M. T.; Atwood, J. T.; Lynn, B. C.; Kaifer, A. E.; Gokel, G. W. J. Am. Chem. Soc. 1992, 114, 10583.
20. Sheldrick, G. M. Acta Crystallogr. 1990, A46, 467.
21. Sheldrick, G. M. SHELXL93: A computer program for crystal structure refinement; University of Göttingen, Germany, 1993.