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- Mays, H, et al.
(författare)
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Spontaneous formation of reverse vesicles with soybean phosphatidyl ethanolamine in mixture with triglyceride and some water
- 1999
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Ingår i: Langmuir. - 0743-7463 .- 1520-5827. ; 15, s. 8072-8079
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Tidskriftsartikel (refereegranskat)abstract
- Mixing the phospholipid soybean phosphatidyl ethanolamine (PE) with the triglyceride triolein and a trace amount of water leads to a spontaneous formation of isotropic aggregates. Evidence for the existence of such aggregates in pseudo-three-component systems is presented here for the first time. Dynamic light scattering and cryogenic temperature transmission electron microscopy reveal polydisperse spherical particles with radii in the range of 250-840 nm and a mean radius of the order 600 nm. From the results of both depolarized light scattering and time-resolved electro-optical birefringence (Kerr effect) the presence of aggregates with an optical anisotropy (rodlike or wormlike reverse micelles as well as particles with lamellar structure) can be excluded. The remaining possibilities are reverse vesicles and a dispersed cubic bicontinuous phase, where our results favor reverse vesicles. A necessary condition for the formation of reverse vesicles is a saturation of the PE-triolein mixture with water; at lower water content the particles are significantly smaller.
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- Sun, L C, et al.
(författare)
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Binuclear ruthenium-manganese complexes as simple artificial models for photosystem II in green plants
- 1997
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Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 1520-5126 .- 0002-7863. ; 119:30, s. 6996-7004
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Tidskriftsartikel (refereegranskat)abstract
- As part of a project aimed at developing models for photosystem II (PSII) in green plants, we have prepared a series of model compounds (7, 8, and 13). In these compounds, a photosensitizer, ruthenium(II) tris(bipyridyl) complex (to mimic the function of P-680 in PSII), was covalently linked to a manganese(II) ion through different bridging ligands. The structures of the compounds were characterized by electron paramagnetic resonance measurements and electrospray ionization mass spectrometry. The interaction between the ruthenium and manganese moieties within the complex was probed by steady-state and time-resolved emission measurements. When the binuclear complexes are exposed to flash photolysis in the presence of an electron acceptor such as methylviologen (MV2+), it could be shown that after the initial electron transfer from the excited state of Ru(II) in compound 7, forming Ru(III) and MV+., an intramolecular electron transfer from coordinated Mn(II) to the photogenerated Ru(III) occurred with a first-order rate constant of 1.8 x 10(5) s(-1), regenerating Ru(II). This is believed to be the first supramolecular system where a manganese complex has been used as an electron donor to a photo-oxidized photosensitizer, Possible extensions to develop the manganese donor, and thus to approach the function of reaction center in PSII, are indicated.
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