Organic aqua regia-Powerful liquids for dissolving noble metals

Angewandte Chemie - International Edition

Volumn 49, Issue 43, 2010, Pages 7929-7932

  Lin, Wei ^a   Zhang, Rong Wei ^a   Jang, Seung Soon ^a   Wong, Ching Ping ^a   Hong, Jung Il ^a  

^a Georgia Institute of Technology   (United States)

Author keywords

Dissolution; Noble metals; Selectivity; Solvolysis; Thionyl chloride

Indexed keywords

AQUA REGIA; HIGH DISSOLUTION RATE; N ,N-DIMETHYLFORMAMIDE; NOBLE METALS; ORGANIC SOLUTIONS; REACTION CONDITIONS; SELECTIVE DISSOLUTION; SELECTIVITY; SOLVOLYSIS; THIONYL CHLORIDES;

CHLORINE COMPOUNDS; DIMETHYLFORMAMIDE; METAL RECOVERY; METALS; PRECIOUS METALS; SOLVENTS;

DISSOLUTION;

EID: 78349283060     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201001244     Document Type: Article

References (32)

1. 2/py mixtures does not change the nonstoichiometric (as is discussed later) feature of the reactions.
2. B. C. H. Steele, A. Heinzel, Nature 2001, 414, 345.
3. J. Zhang, K. Sasaki, E. Sutter, R. R. Adzic, Science 2007, 315, 220.
4. B. Lim, et al., Science 2009, 324, 1302.
5. F. T. Awadalla, R. E. Molnar, G. M. Riteey, US Patent, 5,304,233, 1992.
6. R. I. Edwards, M. J. Nattrass, US Patent 4,105,742, 1978.
7. J. B. Lakewood, C. Arvada, US Patent 4,041,126, 1977.
8. M. T. Rnen, M. Kemell, M. Leskela, T. Repo, Inorg. Chem. 2007, 46, 3251.
9. T. Mortier, A. Persoons, T. Verbiest, Inorg. Chem. Commun. 2005, 8, 1075.
10. L. Cau, et al., Dalton Trans. 2003, 1969.
11. Y. Nakao, J. Chem. Soc. Chem. Commun. 1992, 426.
12. G. Senanayake, Hydrometallurgy 2008, 90, 46.
13. P. H. Qi, J. B. Hiskey, Hydrometallurgy 1991, 27, 47.
14. C. Bou, M. Cruells, M. T. Romero, J. Vinals, Hydrometallurgy 1998, 48, 343.
15. L. Pazderski, Magn. Reson. Chem. 2007, 45, 24.
16. H. Schmidbaur, P. Jandik, Inorg. Chim. Acta 1983, 74, 97.
17. B. Bovio, A. Burini, B. R. Pietroni, J. Organomet. Chem. 1993, 452, 287.
18. 2 at room temperature or even at 70 C (reflux) for 1 week.
19. G. Ricca, F. Severini, Polymer 1988, 29, 880.
20. P. W. Schenk, R. Steudel, Angew. Chem. 1963, 75, 792
21. Angew. Chem. Int. Ed. Engl. 1963, 2, 685.
22. R. Steudel, Y. Steudel, Eur. J. Inorg. Chem. 2007, 4385.
23. J. A. Cade, W. Gerrard, Nature 1953, 172, 29.
24. J. P. E. Human, J. A. Mills, Nature 1946, 158, 877.
25. F. Higashi, T. Mashimo, I. Takahashi, J. Polym. Sci. Polym. Chem. 1986, 24, 97.
26. E. E. Garcia, C. V. Greco, I. M. Hunsberger, J. Am. Chem. Soc. 1960, 82, 4430.
27. S. V. Vinogradova, V. A. Pankratov, V. V. Korshak, L. I. Komarova, Russ. Chem. Bull. 1971, 20, 450.
28. W. K. Istone, R. J. Brodd, J. Electrochem. Soc. 1982, 129, 1853.
29. J. Volke, J. Urban, V. Volkeova, Electrochim. Acta 1994, 39, 2049.
30. th ECS meeting, 2008, Abstract no. 1530.
31. A. A. Berlin, E. F. Razvodovskii, J. Polym. Sci. Part C 1967, 16, 369.
32. I. A. El-Sakka, N. A. Hassan, J. Sulfur Chem. 2005, 26, 33.