519 research outputs found
A Novel Means of Favorably Tipping the Balance between Cytopathic and Regulatory T Cells
AbstractIn this issue of Immunity, Zheng and coworkers present a strategy to create transplantation tolerance with three critical elements, the combined administration of rapamycin, an agonist IL-2/Fc, and an antagonist mutant IL-15/Fc cytolytic-fusion protein to inhibit cytopathic effects but retain negative regulatory T cells, to permit allograft retention in animal models
Q-dependence of the inelastic neutron scattering cross section for molecular spin clusters with high molecular symmetry
For powder samples of polynuclear metal complexes the dependence of the
inelastic neutron scattering intensity on the momentum transfer Q is known to
be described by a combination of so called interference terms. They reflect the
interplay between the geometrical structure of the compound and the spatial
properties of the wave functions involved in the transition. In this work, it
is shown that the Q-dependence is strongly interrelated with the molecular
symmetry of molecular nanomagnets, and, if the molecular symmetry is high
enough, is actually completely determined by it. A general formalism connecting
spatial symmetry and interference terms is developed. The arguments are
detailed for cyclic spin clusters, as experimentally realized by e.g. the
octanuclear molecular wheel Cr8, and the star like tetranuclear cluster Fe4.Comment: 8 pages, 1 figures, REVTEX
Exchange-coupling constants, spin density map, and Q dependence of the inelastic neutron scattering intensity in single-molecule magnets
The Q dependence of the inelastic neutron scattering (INS) intensity of
transitions within the ground-state spin multiplet of single-molecule magnets
(SMMs) is considered. For these transitions, the Q dependence is related to the
spin density map in the ground state, which in turn is governed by the
Heisenberg exchange interactions in the cluster. This provides the possibility
to infer the exchange-coupling constants from the Q dependence of the INS
transitions within the spin ground state. The potential of this strategy is
explored for the M = +-10 -> +- 9 transition within the S = 10 multiplet of the
molecule Mn12 as an example. The Q dependence is calculated for powder as well
as single-crystal Mn12 samples for various exchange-coupling situations
discussed in the literature. The results are compared to literature data on a
powder sample of Mn12 and to measurements on an oriented array of about 500
single-crystals of Mn12. The calculated Q dependence exhibits significant
variation with the exchange-coupling constants, in particular for a
single-crystal sample, but the experimental findings did not permit an
unambiguous determination. However, although challenging, suitable experiments
are within the reach of today's instruments.Comment: 11 pages, 6 figures, REVTEX4, to appear in PR
Butterfly hysteresis loop at non-zero bias field in antiferromagnetic molecular rings: cooling by adiabatic magnetization
At low temperatures, the magnetization of the molecular ferric wheel NaFe
exhibits a step at a critical field due to a field-induced
level-crossing. By means of high-field torque magnetometry we observed a
hysteretic behavior at the level-crossing with a characteristic butterfly shape
which is analyzed in terms of a dissipative two-level model. Several unusual
features were found. The non-zero bias field of the level-crossing suggests the
possibility of cooling by adiabatic magnetization.Comment: 4 pages, 5 figures, REVTEX4, to appear in PR
Spin dynamics of molecular nanomagnets fully unraveled by four-dimensional inelastic neutron scattering
Molecular nanomagnets are among the first examples of spin systems of finite
size and have been test-beds for addressing a range of elusive but important
phenomena in quantum dynamics. In fact, for short-enough timescales the spin
wavefunctions evolve coherently according to the an appropriate cluster
spin-Hamiltonian, whose structure can be tailored at the synthetic level to
meet specific requirements. Unfortunately, to this point it has been impossible
to determine the spin dynamics directly. If the molecule is sufficiently
simple, the spin motion can be indirectly assessed by an approximate model
Hamiltonian fitted to experimental measurements of various types. Here we show
that recently-developed instrumentation yields the four-dimensional
inelastic-neutron scattering function S(Q,E) in vast portions of reciprocal
space and enables the spin dynamics to be determined with no need of any model
Hamiltonian. We exploit the Cr8 antiferromagnetic ring as a benchmark to
demonstrate the potential of this new approach. For the first time we extract a
model-free picture of the quantum dynamics of a molecular nanomagnet. This
allows us, for example, to examine how a quantum fluctuation propagates along
the ring and to directly test the degree of validity of the
N\'{e}el-vector-tunneling description of the spin dynamics
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