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The problem is reminiscent of the changes in the pressure-area isotherms of fatty acids in the presence of large cationic complexes in the aqueous airface. (a) Murakata, T.; Miyashita, T.; Matsuda, M. J. Phys. Chem. 1988, 92, 6040. (b) Palacin, S.; Barraud, R. A. J. Chem. Soc., Chem. Commun. 1989, 45. (c) DeArmond, M. K.; Samha, H.; Dvorak, O. Langmuir 1994, 10, 343. (d) Samha, H.; DeArmond, M. K. Langmuir 1994, 10, 4157.
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The problem is reminiscent of the changes in the pressure-area isotherms of fatty acids in the presence of large cationic complexes in the aqueous airface. (a) Murakata, T.; Miyashita, T.; Matsuda, M. J. Phys. Chem. 1988, 92, 6040. (b) Palacin, S.; Barraud, R. A. J. Chem. Soc., Chem. Commun. 1989, 45. (c) DeArmond, M. K.; Samha, H.; Dvorak, O. Langmuir 1994, 10, 343. (d) Samha, H.; DeArmond, M. K. Langmuir 1994, 10, 4157.
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The problem is reminiscent of the changes in the pressure-area isotherms of fatty acids in the presence of large cationic complexes in the aqueous airface. (a) Murakata, T.; Miyashita, T.; Matsuda, M. J. Phys. Chem. 1988, 92, 6040. (b) Palacin, S.; Barraud, R. A. J. Chem. Soc., Chem. Commun. 1989, 45. (c) DeArmond, M. K.; Samha, H.; Dvorak, O. Langmuir 1994, 10, 343. (d) Samha, H.; DeArmond, M. K. Langmuir 1994, 10, 4157.
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note
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Such nomenclature is similar to but distinct from the subphase and surface nomenclature adopted by Simha and DeArmond (see ref 14d). They used the term subphase for complexes that dissolve in the subphase and surface for complexes formed at the air-water interface.
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