## Abstract The conformational properties of ferric complexes of poly(__N__^ε^‐acetoacetyl‐L‐lysine), poly(__N__^δ^‐acetoacetyl‐L‐ornithine), and poly(__N__^γ^‐acetoacetyl‐L‐diaminobutyric acid) were investigated in 1:1 water/dioxane by CD techniques. Optical activity was found in the visible and i
Ferric complexes of acetoacetyl derivatives of poly(L-lysine), poly(L-ornithine), and poly(L-diaminobutyric acid). I. Preparation and absorption properties in solution
✍ Scribed by M. Palumbo; A. Cosani; M. Terbojevich; G. Bacchion; E. Peggion
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1976
- Tongue
- English
- Weight
- 639 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
Poly(N^ε^‐acetoacetyl‐L‐lysine), poly(N^δ^‐acetoacetyl‐L‐ornithine) and poly(N^γ^‐acetoacetyl‐L‐diaminobutyric acid) form colored complexes with ferric ions in water/dioxane solutions. These complexes are soluble at pH values lower than 2.8 and show their maximum absorption at 257 nm in the uv and at 478 nm in the visible region; whereas the ferric complex of the model compound n‐hexylacetoacetamide exhibits absorptions centered at 258 and 536 nm, respectively. It is shown that in the complex of the model compound one metal ion is bound per acetoacetamide group, while in the complexes of the three polymers two β‐ketoamides side chains are bound per ferric ion under the same solvent, pH, concentration, and ionic strength conditions. The binding constants of ferric ions to the three polymers, and the formation constant of the ferric complex of the model compound are also evaluated.
📜 SIMILAR VOLUMES
## Abstract The cupric complexes of poly(__N__^ε^‐acetoacetyl‐L‐lysine), [Lys(Acac)]~n′~ poly(__N__^δ^‐acetoacetyl‐L‐ornithine), [Orn(Acac)]~n′~ and poly(__N__^γ^‐acetoacetyl‐L‐diaminobutyric acid), [A~2~bu‐(Acac)]~n~, as well as of the model compound __n__‐hexyl acetoacetamide, have been investiga
## Abstract The binding isotherms of sodium decyl sulfate to poly(L‐ornithine), poly(D,L‐ornithine), and poly(L‐lysine) at neutral pH were determined potentiometrically. The nature of a highly cooperative binding in all three cases suggests a micelle‐like clustering of the surfactant ions onto the