Light scattering from aqueous solutions of poly(acrylamide‐<i>co</i>‐maleic anhydride)

Ionescu, L; Petrea, Ion; Bujor, Ingrid Ionescu; Demetrescu, Ioana

doi:10.1002/macp.1983.021840512

Cited by 7 publications

(1 citation statement)

References 6 publications

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“…The reaction with alkylamines, however, led to the desired products. In water, the hexadecylamide soaps showed phase separation below 25 "C, independent of the degree of hexadecyl load from 25 up to 50% based on the anhydride. The dodecylamide polymers did not.…”

Section: Synthesis Of Polysoapsmentioning

confidence: 99%

Polymeric surfactant systems in the asymmetric hydrogenation of amino acid precursors with a rhodium complex

Flach

Grassert

Oehme

1994

Macro Chemistry & Physics

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The synthesis of new types of soluble and insoluble amphiphilic systems is described, being polysoaps, crosslinked polysoaps, an amphiphilised ion exchanger, and ion exchangers loaded with ionic surfactants. It was possible to synthesise insoluble polymeric systems which nevertheless showed micellar properties. The polymers were tested as aids in the stereospecific hydrogenation of (2)-methyl a-acetamidocinnamate to the methyl ester of N-acetylphenylalanine ( R ) by means of an optically active rhodium complex in water. With linear polysoaps the effect on the reaction was dependent on the structure of the soap molecules. The enantioselectivity of the reaction with monomeric surfactants in water was almost attained. Crosslinked polysoaps showed the same effects on the hydrogenation as linear polysoaps with an analogous structure. Macromolecular ion exchangers loaded with amphiphilic counterions gave in hydrogenation almost the same effect as these counterions give when they are not bound to an insoluble carrier. Enantioselectivities and reaction rates were usually slightly lower than with monomeric surfactants. However, there is an advantage in the separation of catalyst and product after reaction. It was shown that the rhodium-containing amphiphilic ion exchangers could be reused for up to 9 times. GeneralMicellar catalysis has been developed into an important field in organic chemistry'-3). Occurring in a colloid medium, some reactions are influenced in rate and stereoselectivity 4* j). Common disadvantages of micellar catalysis, however, are the low capacity of micellar systems and the difficulties in the separation of products and surfactants after the reaction.We are interested in the asymmetric hydrogenation of amino acid precursors such as (2)-methyl-a-acetamidocinnamate by means of optically active rhodium(1) complexes. From previous experiments it was concluded that this hydrogenation may be carried out in organic solvents, e. g. methanol, and in aqueous surfactant dispersions as well6") (Scheme 1).The excellent results with monomeric surfactants led us to the idea to synthesise a polymeric, insoluble surfactant system to be used in hydrogenation in water which could serve as a carrier for the catalyst, filtered off after reaction and reused after separation from the product.Several workers already used insoluble polymers as supports for metal complex catalysts *s9), but the binding of a metal complex in a micelle-analogous insoluble Macromol.

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Section: Synthesis Of Polysoapsmentioning

confidence: 99%