dicyclohexyl N,N-diisobutylcarbamoylmethylphosphine oxide

D(CH)D(iB)CMPO structure
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General infos Separation factors Distribution coefficients References
Abbreviation(s)

D(CH)D(iB)CMPO

Chemical group

carbamylalkylphosphine oxide

Formula

C22H42NO2P not CHON

Molecular mass

383.557 g/mol

Separation factors
Factor Value Conc. Add. ligand Aq. acid Organic diluent Temp. Contact time Additional Ref.
Am/Fe 4.7 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Y 1.2 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Zr 0.04 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Mo 0.35 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Tc 14 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Ru 83 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Rh 500 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Pd 17 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/La 3.3 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Ce 1.6 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Pr 1.1 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Nd 1.1 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Sm 0.89 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am/Eu 0.86 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Distribution coefficients
Element Value Conc. Add. ligand Aq. acid Organic diluent Temp. Contact time Additional Ref.
Fe 0.53 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Y 2.1 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Zr 62 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Mo 7.1 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Tc 0.18 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Ru 0.03 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Rh 0.005 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Pd 0.15 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
La 0.76 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Ce 1.6 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Pr 2.3 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Nd 2.3 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Sm 2.8 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Eu 2.9 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am 2.5 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am ≈80 0.25 M   HNO3 0.25 M Tetrachloroethylene 25°C 1 min [1]
Am ≈90 0.25 M   HNO3 0.5 M Tetrachloroethylene 25°C 1 min [1]
Am ≈50 0.25 M   HNO3 1 M Tetrachloroethylene 25°C 1 min [1]
Am ≈2.5 0.25 M   HNO3 3 M Tetrachloroethylene 25°C 1 min [1]
Am ≈2 0.25 M   HNO3 6 M Tetrachloroethylene 25°C 1 min [1]
References

  1. doi:10.1080/07366298608917877