Résultats de recherche pour « Magnetic isotope effects »

We use a recently developed formalism (combining an adiabatic expansion and dynamical mean-field theory) to obtain expressions for isotope effects on electronic properties in correlated systems. As an example we calculate the isotope effect on electron effective mass for the Holstein model as a function of electron-phonon interaction strength and doping. Our systematic expansion generates diagrams neglected in previous studies, which turn out to give the dominant contributions. The isotope effect is small unless the system is near a lattice instability. We compare this to experiment.

Thermochemical sulfate reduction experiments with simple amino acid and dilute concentrations of sulfate reveal significant degrees of mass-independent sulfur isotope fractionation. Enrichments of up to 13‰ for (33)S are attributed to a magnetic isotope effect (MIE) associated with the formation of thiol-disulfide, ion-radical pairs. Observed (36)S depletions in products are explained here by classical (mass-dependent) isotope effects and mixing processes. The experimental data contrasts strongly with multiple sulfur isotope trends in Archean samples, which exhibit significant (36)S anomalies. These results support an origin other than thermochemical sulfate reduction for the mass-independent signals observed for early Earth samples.

In this paper the magnetic behaviour of undoped and 15% F doped SmFeAsO (Sm-1111) and LaFeAsO (La-1111) samples is presented and discussed. Magnetization measurements are not a simple tool to use for the characterisation of the new family of Fe-based superconductors because magnetic impurities can be easily formed during the preparation procedure and may affect the magnetic signal. In spite of this problem bulk magnetization measurements, properly treated, may give very useful information. In the undoped samples we gathered the main aspects of the physical behavior of the 1111 phase, i.e. the onset of the Spin Density Wave (SDW), the antiferromagnetic ordering at the Sm sublattice and the susceptibility increase with increasing temperature above the SDW temperature, and, in addition, we were able to estimate the Pauli contribution to susceptibility and therein the Wilson ratio both for LaFeAsO and SmFeAsO compounds, and the amplitude of the jump at the SDW temperature. In the doped samples, while the presence of magnetic signals due to impurities is dominating in the normal state, the superconducting behavior may be clearly observed and studied. In particular, in the Sm-1111 superconducting sample the coexistence-competition between superconductivity and antiferromagnetic ordering of the Sm ions was clearly observed.

One possible explanation for magnetosensing in biology, such as avian magnetoreception, is based on the spin dynamics of certain chemical reactions that involve radical pairs. Radical pairs have been suggested to also play a role in anesthesia, hyperactivity, neurogenesis, circadian clock rhythm, microtubule assembly, etc. It thus seems critical to probe the credibility of such models. One way to do so is through isotope effects with different nuclear spins. Here we briefly review the papers involving spin-related isotope effects in biology. We suggest studying isotope effects can be an interesting avenue for quantum biology.

We analyze the magnetization, magnetic torque and susceptibility data of La2-xSrxCu(16,18)O4 and YBa2(63,65)CuO7-x near Tc in terms of the universal 3D-XY scaling relations. It is shown that the isotope effect on Tc mirrors that on the anisotropy. Invoking the generic behavior of the anisotropy the doping dependence of the isotope effects on the critical properties, including Tc, correlation lengths and magnetic penetration depths are traced back to a change of the mobile carrier concentration.

Human retinoblastoma cells were proven to possess some very unusual DNApolβ species. Being 23.5 kDa monomers, which itself is not common for the DNApolβ superfamily members, these chromatin associated proteins manifests most of the DNApolβ-specifc functional peculiarities making them legitimate targets for DNA repair cytostatic inhibitors. Particularly, these tumor specific enzymes were found to be very sensitive to 25Mg2+-, 43Ca2+- and 67Zn2+-promoted magnetic isotope effects (MIE) caused a marked DNA sequence growth limitation as well as a formation of the size-invalid, i.e. too short in length, DNA fragments, totally inappropriate for the DNA repair purpose. This MIE-DNApolβ match may serve a starting point for further move towards the paramagnetic path in current developments of anti-cancer strategies.

When uranyl nitrate is photolysed in the water solution, light isotope ${}^{235}{\rm U}$ is separated from isotope ${}^{238}{\rm U}$ ; an enrichment factor $K = 1.04$ . The initial samples were depleted by a light isotope of uranium ${}^{235}{\rm U}$ (degree $β= 0.00455$). Regenerated uranyl nitrate was enriched by an isotope of uranium ${}^{235}{\rm U}$ (degree $α= 0.00464$). Uranium tetrafluoride was depleted by an isotope of uranium ${}^{235}{\rm U}$ (degree $β= 0.00446$). Uranium isotopes are separated by the magnetic isotope effect (MIE) in uranyl nitrate photoreduction.

Weak magnetic fields have been shown to influence biological processes; however, the underlying mechanisms remain unknown as the energies involved are far below thermal energies challenging classical explanations. Microtubule cytoskeletal fibers offer an ideal system to test weak magnetic field effects due to their self-assembling capabilities, sensitivity to magnetic fields, and their central role in cellular processes. In this study, we use a combination of experiments and simulations to explore how nuclear spin dynamics affect microtubule polymerization by examining interactions between magnesium isotope substitution and weak magnetic fields. Our experiments reveal an isotope-dependent effect explicitly arising from nuclear spin properties. This nuclear spin-driven effect is enhanced under an applied weak 3-millitesla magnetic field. Our theoretical radical pair model achieves quantitative agreement with our experimental observations. These results support a connection between quantum spin dynamics and microtubule assembly, providing further insights into how weak magnetic fields may influence biomolecular functions.

Underdoped cuprates exhibit a normal-state pseudogap, and their spins and doped carriers tend to spatially separate into 1- or 2-D stripes. Some view these as central to superconductivity, others as peripheral and merely competing. Using La$_{2-x}$Sr$_x$Cu$_{1-y}$Zn$_y$O$_4$ we show that an oxygen isotope effect in $T_c$ and in the superfluid density can be used to distinguish between the roles of stripes and pseudogap and also to detect the presence of impurity scattering. We conclude that stripes and pseudogap are distinct, and both compete and coexist with superconductivity.