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1.
Phys Rev Lett ; 107(23): 233401, 2011 Dec 02.
Artículo en Inglés | MEDLINE | ID: mdl-22182086

RESUMEN

The determination of spin and orbital magnetic moments from the free atom to the bulk phase is an intriguing challenge for nanoscience, in particular, since most magnetic recording materials are based on nanostructures. We present temperature-dependent x-ray magnetic circular dichroism measurements of free Co clusters (N=8-22) from which the intrinsic spin and orbital magnetic moments of noninteracting magnetic nanoparticles have been deduced. An exceptionally strong enhancement of the orbital moment is verified for free magnetic clusters which is 4-6 times larger than the bulk value. Our temperature-dependent measurements reveal that the spin orientation along the external magnetic field is nearly saturated at ~20 K and 7 T, while the orbital orientation is clearly not.

2.
Chem Commun (Camb) ; 56(3): 368-371, 2020 Jan 02.
Artículo en Inglés | MEDLINE | ID: mdl-31808780

RESUMEN

Two pentadentate N3,P2 ligands coordinate zinc(ii) by their N3 pocket. Four free phosphine donors allow the coordination of four AuCl moieties leading to a pentanuclear ZnAu4 complex. In contrast, the attempt to use the phosphines for chelating coordination of two Rh(CO)Cl units results in a well-organized rearrangement that ends up with the formation of a metallomacrocycle in high yields.

3.
J Chem Phys ; 131(12): 124306, 2009 Sep 28.
Artículo en Inglés | MEDLINE | ID: mdl-19791880

RESUMEN

In this letter, we report the first infrared spectrum of C(76)(2-). This multiply charged anion has been studied in an electrodynamic ion trap held at room temperature using tunable infrared radiation from a free-electron laser. Resonant vibrational excitation is found to cause electron detachment and the resulting singly negatively charged as well as the remaining doubly charged parent ion are monitored as a function of IR wavelength in an experimental scheme that we term infrared multiphoton electron detachment spectroscopy. The obtained IR spectra are contrasted to computed vibrational spectra using density functional theory. The dianionic molecule retains its overall symmetry (i.e., D(2) point group) with a (1)A(1) ground state with respect to the neutral fullerene. Spectral shifts of characteristic tangential modes relative to the neutral cage are shown to originate from the excess charge density.

4.
Chem Commun (Camb) ; 53(88): 12016-12019, 2017 Nov 02.
Artículo en Inglés | MEDLINE | ID: mdl-29057406

RESUMEN

Complexes of the type [Cp*Ir(N,N')Cl]+ (N,N' = 2-(2-dialkylaminopyrimidin-4-yl)pyrimidine) can undergo roll-over cyclometallation leading to a novel N,N'-donor site. Following this strategy heterobimetallic complexes including iridium(iii) and a Group X metal centre in the oxidation state +II were achieved.

5.
Chem Rev ; 100(11): 4059-86, 2000 Nov 08.
Artículo en Inglés | MEDLINE | ID: mdl-11749340
6.
J Neural Transm (Vienna) ; 113(8): 995-1013, 2006 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-16835696

RESUMEN

Subcellular fractionation represents an essential technique for functional proteome analysis. Recently, we provided a subcellular fractionation protocol for minute amounts of tissue that yielded a nuclear fraction, a membrane and organelle fraction, and a cytosolic fraction. In the current study, we attempted to improve the protocol for the isolation of integral membrane proteins, as these are particularly important for brain function. In the membrane and organelle fraction, we increased the yield of membranes and organelles by about 50% by introducing a single re-extraction step. We then tested two protocols towards their capacity to enrich membrane proteins present in the membrane and organelle fraction. One protocol is based on sequential solubilization using subsequent increases of chaotropic conditions such as urea, thereby partitioning hydrophobic proteins from hydrophilic ones. The alternative protocol applies high-salt and high-pH washes to remove non-membrane proteins. The enrichment of membrane proteins by these procedures, as compared to the original membrane and organelle fraction, was evaluated by 16-BAC-SDS-PAGE followed by mass spectrometry of randomly selected spots. In the original membrane and organelle fraction, 7 of 50 (14%) identified proteins represented integral membrane proteins, and 15 (30%) were peripheral membrane proteins. In the urea-soluble fraction, 4 of 33 (12%) identified proteins represented integral membrane proteins, and 10 (30%) were peripheral membrane proteins. In the high-salt/high-pH resistant sediment, 12 of 45 (27%) identified proteins were integral membrane proteins and 13 (29%) represented peripheral membrane proteins. During the analysis, several proteins involved in neuroexocytosis were detected, including syntaxin, NSF, and Rab3-interaction protein 2. Taken together, differential centrifugation in combination with high-salt and high-pH washes resulted in the highest enrichment of integral membrane proteins and, therefore, represents an adequate technique for region-specific profiling of membrane proteins in the brain.


Asunto(s)
Química Encefálica , Fraccionamiento Celular/métodos , Proteínas de la Membrana/aislamiento & purificación , Proteoma/aislamiento & purificación , Fracciones Subcelulares , Animales , Centrifugación , Electroforesis en Gel de Poliacrilamida , Alcoholes Grasos , Femenino , Concentración de Iones de Hidrógeno , Masculino , Proteínas de la Membrana/análisis , Proteoma/análisis , Compuestos de Amonio Cuaternario , Ratas , Ratas Sprague-Dawley , Sales (Química) , Solubilidad , Espectrometría de Masa por Láser de Matriz Asistida de Ionización Desorción
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