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Giant micelles of organoplatinum(II) gemini amphiphiles.

ABSTRACT: Organoplatinum(II) gemini amphiphiles with two different chain lengths are synthesized and characterized. Self-assembly at the air-water interface is investigated as a function of chain length and reduction in surface area by using Langmuir-trough techniques. The Langmuir-trough experiments lead to a conjecture that surface aggregates may be the adsorbing units. Atomic force microscopy on the transferred Langmuir-Schaefer films reveals spontaneous formation of wormlike micellar aggregates. A shear-induced transition and alignment are proposed for the observed effects.

SUBMITTER: Maran U

PROVIDER: S-EPMC3974412 | biostudies-literature | 2008 May

REPOSITORIES: biostudies-literature

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Giant micelles of organoplatinum(II) gemini amphiphiles.

Maran Umamageswaran U Conley Hiram H Frank Markus M Arif Atta M AM Orendt Anita M AM Britt David D Hlady Vladimir V Davis Robert R Stang Peter J PJ

Langmuir : the ACS journal of surfaces and colloids 20080426 10

Organoplatinum(II) gemini amphiphiles with two different chain lengths are synthesized and characterized. Self-assembly at the air-water interface is investigated as a function of chain length and reduction in surface area by using Langmuir-trough techniques. The Langmuir-trough experiments lead to a conjecture that surface aggregates may be the adsorbing units. Atomic force microscopy on the transferred Langmuir-Schaefer films reveals spontaneous formation of wormlike micellar aggregates. A she ...[more]

PMID: 18439034

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Project description:A detailed mechanistic investigation of the thermal reactions of a series of bisphosphine alkylplatinum(II) enolate complexes is reported. The reactions of methylplatinum enolate complexes in the presence of added phosphine form methane and either free or coordinated enone, depending on the steric properties of the enone. Kinetic studies were conducted to determine the relationship between the rates and mechanism of beta-hydrogen elimination from enolate complexes and the rates and mechanism of beta-hydrogen elimination from alkyl complexes. The rates of reactions of the enolate complexes were inversely dependent on the concentration of added phosphine, indicating that beta-hydrogen elimination from the enolate complexes occurs after reversible dissociation of a phosphine. A normal, primary kinetic isotope effect was measured, and this effect was consistent with rate-limiting beta-hydrogen elimination or C-H bond-forming reductive elimination to form methane. Reactions of substituted enolate complexes were also studied to determine the effect of the steric and electronic properties of the enolate complexes on the rates of beta-hydrogen elimination. These studies showed that reactions of the alkylplatinum enolate complexes were retarded by electron-withdrawing substituents on the enolate and that reactions of enolate complexes possessing alkyl substituents at the beta-position occurred at rates that were similar to those of complexes lacking alkyl substituents at this position. Despite the trend in electronic effects on the rates of reactions of enolate complexes and the substantial electronic differences between an enolate and an alkyl ligand, the rates of decomposition of the enolate complexes were similar to those of the analogous alkyl complexes. To the extent that the rates of reaction of the two types of complexes are different, those involving beta-hydrogen elimination from the enolate ligand were faster. A difference between the rate-determining steps for decomposition of the two classes of complexes and an effect of stereochemistry on the selectivity for beta-hydrogen elimination are possible origins of the observed phenomena.

Dataset Information

Giant micelles of organoplatinum(II) gemini amphiphiles.

Publications

Giant micelles of organoplatinum(II) gemini amphiphiles.

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