-
2
-
-
10444236264
-
-
CAS nomenclature: phosphinothiocarbamides
-
CAS nomenclature: phosphinothiocarbamides.
-
-
-
-
3
-
-
10444273821
-
-
CAS nomenclature: phosphinecarbodithioates
-
CAS nomenclature: phosphinecarbodithioates.
-
-
-
-
4
-
-
10444252377
-
-
CAS nomenclature: (phosphinoalkyl)phosphine sulfides
-
CAS nomenclature: (phosphinoalkyl)phosphine sulfides.
-
-
-
-
5
-
-
10444231776
-
-
CAS nomenclature: (alkylthioalkyl)phosphines
-
CAS nomenclature: (alkylthioalkyl)phosphines.
-
-
-
-
8
-
-
68249083200
-
-
(a) E. Grishkevich-Trokhimovskii, Zh. Russ. Fiz.-Khim. O-va. 48 (1916) 880; Chem. Abstr. 11 (1917) 784.
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4243639745
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Fr. Patent No. 1,401,930, 26 April 1965
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27
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85087226180
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note
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2SH had degraded after being left for one month under normal laboratory lighting [35].
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64
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85087227910
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note
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+) = + 0.54 V vs. SCE.
-
-
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65
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10444226320
-
-
note
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The original paper [46] did not quote the reference used in determining this potential, so it has been assumed that it was reported vs. SCE.
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66
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37049107241
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see also: (a) T.A. George, D.D. Watkins, Inorg. Chem. 12 (1973) 398. (b) C.P. Sloan, J.H. Krueger, Inorg. Chem. 14 (1975) 1481. (c) B.A. Lange, K Libson, E. Deutsch, R.C. Elder, Inorg. Chem. 15 (1976) 2985. (d) D.L. Herting, C.P. Sloan, A.W. Cabral, J.M. Krueger, Inorg. Chem. 17 (1978) 1649. (e) I.K. Adzamli, K Libson, J.R. Lydon, R.C. Elder, E. Deutsch, Inorg. Chem. 18 (1979) 303. (f) J. McB. Harrowfield, J.M. Patrick, B.W. Skelton, A.M. White, Aust. J. Chem. 41 (1988) 159. (g) W. Weigand, G. Bosl, Z. Naturforsch. B: Chem. Sci. 47 (1992) 1165. (h) W. Weigand, G. Bosl, C. Robl, W. Amrein, Chem. Ber. 125 (1992) 1047.
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see also: (a) T.A. George, D.D. Watkins, Inorg. Chem. 12 (1973) 398. (b) C.P. Sloan, J.H. Krueger, Inorg. Chem. 14 (1975) 1481. (c) B.A. Lange, K Libson, E. Deutsch, R.C. Elder, Inorg. Chem. 15 (1976) 2985. (d) D.L. Herting, C.P. Sloan, A.W. Cabral, J.M. Krueger, Inorg. Chem. 17 (1978) 1649. (e) I.K. Adzamli, K Libson, J.R. Lydon, R.C. Elder, E. Deutsch, Inorg. Chem. 18 (1979) 303. (f) J. McB. Harrowfield, J.M. Patrick, B.W. Skelton, A.M. White, Aust. J. Chem. 41 (1988) 159. (g) W. Weigand, G. Bosl, Z. Naturforsch. B: Chem. Sci. 47 (1992) 1165. (h) W. Weigand, G. Bosl, C. Robl, W. Amrein, Chem. Ber. 125 (1992) 1047.
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see also: (a) T.A. George, D.D. Watkins, Inorg. Chem. 12 (1973) 398. (b) C.P. Sloan, J.H. Krueger, Inorg. Chem. 14 (1975) 1481. (c) B.A. Lange, K Libson, E. Deutsch, R.C. Elder, Inorg. Chem. 15 (1976) 2985. (d) D.L. Herting, C.P. Sloan, A.W. Cabral, J.M. Krueger, Inorg. Chem. 17 (1978) 1649. (e) I.K. Adzamli, K Libson, J.R. Lydon, R.C. Elder, E. Deutsch, Inorg. Chem. 18 (1979) 303. (f) J. McB. Harrowfield, J.M. Patrick, B.W. Skelton, A.M. White, Aust. J. Chem. 41 (1988) 159. (g) W. Weigand, G. Bosl, Z. Naturforsch. B: Chem. Sci. 47 (1992) 1165. (h) W. Weigand, G. Bosl, C. Robl, W. Amrein, Chem. Ber. 125 (1992) 1047.
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see also: (a) T.A. George, D.D. Watkins, Inorg. Chem. 12 (1973) 398. (b) C.P. Sloan, J.H. Krueger, Inorg. Chem. 14 (1975) 1481. (c) B.A. Lange, K Libson, E. Deutsch, R.C. Elder, Inorg. Chem. 15 (1976) 2985. (d) D.L. Herting, C.P. Sloan, A.W. Cabral, J.M. Krueger, Inorg. Chem. 17 (1978) 1649. (e) I.K. Adzamli, K Libson, J.R. Lydon, R.C. Elder, E. Deutsch, Inorg. Chem. 18 (1979) 303. (f) J. McB. Harrowfield, J.M. Patrick, B.W. Skelton, A.M. White, Aust. J. Chem. 41 (1988) 159. (g) W. Weigand, G. Bosl, Z. Naturforsch. B: Chem. Sci. 47 (1992) 1165. (h) W. Weigand, G. Bosl, C. Robl, W. Amrein, Chem. Ber. 125 (1992) 1047.
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85
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10444286480
-
-
note
-
The structure of these complexes may be considerably more complex than these formulae imply: in most cases, the formulae are based on microanalytical results. Coordinated primary and secondary phosphines are known to readily deprotonate, forming bridged phosphide species.
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86
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