Nonclassicality generated by propagation of atoms through a cavity field

We successively pass two V-type three-level atoms through a single-mode cavity field. Considering the field to be initially in a classical state, we evaluate various statistical properties such as the quasiprobability Q function, Wigner distribution, Mandel?s Q parameter and normal squeezing of the resulted field. We notice that the sequential crossing of atoms induces nonclassicality into the character of a pure classical state (coherent field). The initial thermal field shows sub-Poissonian as well as squeezing property after interacting with the V atoms.     

Supramolecular helix and β-sheet through self-assembly of two isomeric tetrapeptides in crystals and formation of filaments and ribbons in the solid state

Single crystal X-ray diffraction studies show that the β-turn structure of tetrapeptide I, Boc-Gly-Phe-Aib-Leu-OMe (Aib: α-amino isobutyric acid) self-assembles to a supramolecular helix through intermolecular hydrogen bonding along the crystallographic a axis. By contrast the β-turn structure of an isomeric tetrapeptide II, Boc-Gly-Leu-Aib-Phe-OMe self-assembles to a supramolecular β-sheet-like structure via a two-dimensional (a, b axis) intermolecular hydrogen bonding network and π-π interactions. FT-IR studies of the peptides revealed that both of them form intermolecularly hydrogen bonded supramolecular structures in the solid state. Field emission scanning electron micrographs (FE-SEM) of the dried fibrous materials of the peptides show different morphologies, non-twisted filaments in case of peptide I and non-twisted filaments and ribbon-like structures in case of peptide II.     

Family of double-cubane Mn4Ln2 (Ln = Gd, Tb, Dy, Ho) and Mn4Y2 complexes: a new Mn4Tb2 single-molecule magnet

The synthesis and characterization of a family of Mn(2)(III)Mn(2)(II)Ln(III)(2) complexes (Ln = Gd (1), Tb (2), Dy (3), and Ho (4)) of formula [Mn(4)Ln(2)O(2)(O(2)CBu(t))(6)(edteH(2))(2)(NO(3))(2)] are reported, where edteH(4) is N,N,N',N'-tetrakis(2-hydroxyethyl)ethylenediamine. The analogous Mn(4)Y(2) (5) complex has also been prepared. They were obtained from reaction of Ln(NO(3))(3) or Y(NO(3))(3) with Mn(O(2)CBu(t))(2), edteH(4), and NEt(3) in a 2:3:1:2 molar ratio. The crystal structures of representative 1 and 2 were obtained, and their core consists of a face-fused double-cubane [Mn(4)Ln(2)(μ(4)-O(2-))(2)(μ(3)-OR)(4)] unit. Such double-cubane units are extremely rare in 3d metal chemistry and unprecedented in 3d-4f chemistry. Variable-temperature, solid-state dc and ac magnetic susceptibility studies on 1-5 were carried out. Fitting of dc χ(M)T vs T data for 5 gave J(bb) (Mn(III)···Mn(III)) = -32.6(9) cm(-1), J(wb) (Mn(II)···Mn(III)) = +0.5(2) cm(-1), and g = 1.96(1), indicating a |n, 0, n> (n = 0-5) 6-fold-degenerate ground state. The data for 1 indicate an S = 12 ground state, confirmed by fitting of magnetization data, which gave S = 12, D = 0.00(1) cm(-1), and g = 1.93(1) (D is the axial zero-field splitting parameter). This ground state identifies the Mn(II)···Gd(III) interactions to be ferromagnetic. The ac susceptibility data independently confirmed the conclusions about 1 and 5 and revealed that 2 displays slow relaxation of the magnetization vector for the Mn(4)Tb(2) analogue 2. The latter was confirmed as a single-molecule magnet by observation of hysteresis below 0.9 K in magnetization vs dc field scans on a single crystal of 2·MeCN on a micro-SQUID apparatus. The hysteresis loops also displayed well-resolved quantum tunneling of magnetization steps, only the second 3d-4f SMM to do so.     

Coupled tapered/uptapered optical beams

For the first time we propose the phenomenon of coupled tapering and uptapering in two mutually incoherent beams coaxially co-propagating in a nonlinear medium with small gain or loss. During tapering or uptapering, the widths and powers of the beams evolve in such a manner that they always satisfy the condition of soliton pairing. It is shown that under certain condition one beam can taper/uptaper, while, other uptaper/taper during coupled tapering/uptapering which is quite counterintuitive.     

Synthesis, characterization and catecholase-like activity of [Mn2L2(μ1,5-dca)2(dca)2]·H2O [L?=?N,N′-ethylenebis(2-benzoylpyridineimine), dca?=?dicyanamide]

A dinuclear Mn^II complex, namely [Mn₂L₂(μ_1,5-dca)₂(dca)₂]·H₂O [L = N,N′-ethylenebis(2-benzoylpyridineimine), dca = dicyanamide], has been synthesized and structurally characterized in order to study its catecholase-like activity. Single-crystal X-ray analysis revealed that the molecule possesses a center of inversion at the midpoint of the line bisecting the adjacent metal centers of the dimers. The coordination number of each Mn^II center is seven, and the coordination geometry is approximately distorted pentagonal bipyramid. The complex is an efficient catalyst for the oxidation of 3,5-di-tert-butylcatechol to 3,5-di-tert-butylbenzoquinone under air in methanol solution but is inactive in acetonitrile solution. A kinetic study of the catalysis was treated on the basis of the Michaelis–Menten model and reveals high turnover numbers (k _cat = 4.5 × 10² h⁻¹) in methanol.     

Designing of peptide aptamer targeting the receptor-binding domain of spike protein of SARS-CoV-2: an in silico study

Molecular Diversity - Short synthetic peptide molecules which bind to a specific target protein with a high affinity to exert its function are known as peptide aptamers. The high specificity of...     

A generalized central sets theorem in partial semigroups

Semigroup Forum - The most powerful formulation of the Central Sets Theorem in an arbitrary semigroup was proved in the work of De, Hindman, and Strauss. The sets which satisfy the conclusion of...