Spin Glass and ferromagnetism in disordered Kondo lattice

The competition among spin glass (SG), ferromagnetism and Kondo effect has been analysed in a Kondo lattice model where the inter-site coupling $J_{ij}$ between the localized magnetic moments is given by a generalized Mattis model \cite{Mattis} which represents an interpolation between ferromagnetism and a highly disordered spin glass. Functional integral techniques with of Grassmann fields has been used to obtain the partition function. The static approximation and the replica symmetric ansatz has also been used. The solution of the problem is presented as a phase diagram temperature $T$ {\it versus} $J_K$ (the strength of the intra-site interaction). If $J_K$ is small, for decreasing temperature there is a second order transition from a paramagnetic to a spin glass phase For lower temperatures, a first order transition appears where solutions for the spin glass order parameter and the local magnetizations are simultaneously non zero. For very low temperatures, the local magnetizations becomes thermodinamically stables. For high $J_K$, the Kondo state is dominating. These results could be helpful to clarify the experimental situation of $CeNi_{1-x}Cu_{x}$.Comment: 4 pages, 1 figure, accept to be published in Physica

Approaching ultra-strong coupling in Transmon circuit-QED using a high-impedance resonator

In this experiment, we couple a superconducting Transmon qubit to a high-impedance $645\ \Omega$ microwave resonator. Doing so leads to a large qubit-resonator coupling rate $g$, measured through a large vacuum Rabi splitting of $2g\simeq 910$ MHz. The coupling is a significant fraction of the qubit and resonator oscillation frequencies $\omega$, placing our system close to the ultra-strong coupling regime ($\bar{g}=g/\omega=0.071$ on resonance). Combining this setup with a vacuum-gap Transmon architecture shows the potential of reaching deep into the ultra-strong coupling $\bar{g} \sim 0.45$ with Transmon qubits

Correction: π-Facial selectivity in the Diels–Alder reaction of glucosamine-based chiral furans and maleimides

Correction for 'π-Facial selectivity in the Diels-Alder reaction of glucosamine-based chiral furans and maleimides' by Cornelis H. M. van der Loo et al., Org. Biomol. Chem., 2023, 21, 1888-1894, https://doi.org/10.1039/D2OB02221D. </p

Correction: π-Facial selectivity in the Diels–Alder reaction of glucosamine-based chiral furans and maleimides

Correction for 'π-Facial selectivity in the Diels-Alder reaction of glucosamine-based chiral furans and maleimides' by Cornelis H. M. van der Loo et al., Org. Biomol. Chem., 2023, 21, 1888-1894, https://doi.org/10.1039/D2OB02221D. </p

Ginzburg-Landau functional for nearly antiferromagnetic perfect and disordered Kondo lattices

Interplay between Kondo effect and trends to antiferromagnetic and spin glass ordering in perfect and disordered bipartite Kondo lattices is considered. Ginzburg-Landau equation is derived from the microscopic effective action written in three mode representation (Kondo screening, antiferromagnetic correlations and spin liquid correlations). The problem of local constraint is resolved by means of Popov-Fedotov representation for localized spin operators. It is shown that the Kondo screening enhances the trend to a spin liquid crossover and suppresses antiferromagnetic ordering in perfect Kondo lattices and spin glass ordering in doped Kondo lattices. The modified Doniach's diagram is constructed, and possibilities of going beyond the mean field approximation are discussed.Comment: 18 pages, RevTeX, 7 EPS figures include

Synthesis, Structure and Reactivity of Sulfur-Rich Cyclopentadienyl-Transition Metal Complexes: Sulfur Chemistry from an Organometallic Point of View

Metal-sulfur centers play an important role in the activity of metalloproteins in enzymatic catalysis and the activity of metal sulfides as heterogeneous catalysts. The systematic search for M[BOND]S model compounds led to the discovery of an interesting and novel structural chemistry, which stems from the numerous coordination possibilities of sulfur ligands. The intention of this review article is to present and outline new approaches to sulfur chemistry from the organometallic point of view. Reactive cyclopentadienyl-transition metal fragments incorporate elemental sulfur to give polynuclear sulfur-rich complexes, which can contain either mono-, di- or polysulfido ligands or several such ligands in combined form. The versatile structural chemistry of the complexes formed and their reactivity towards organic, inorganic and organometallic compounds are discussed, and examples of some simple and rational procedures for their synthesis starting from cyclopentadienylcarbonyl- and cyclopentadienylhydrido-complexes are outlined. Their reactivity is manifested in numerous metal- and ligandcentered reactions. Finally the, albeit far less extensive, complex chemistry of the other chalcogens (O, Se, Te) is also considered for comparison, thus providing a more detailed survey of particular aspects of this area of chemistry