Evidence for an i13/2 neutron band in133Sm

A rotational band of nine γ-rays has been observed in¹³³Sm. The moment of inertia of the band indicates that it has a higher deformation than expected for states in nuclei in this region. The properties are such that it can be interpreted as being due to the odd neutron occupying the ν i2/13 nn intruder orbital. This is the first evidence for the occupation of this orbital in nuclei with neutron number N<73.     

N-Amination of pyrrole and indole heterocycles with monochloramine (NH2Cl)

A survey of several electrophilic ammonia reagents for the N-amination of indole- and pyrrole-containing heterocycles revealed that monochloramine (NH(2)Cl) is an excellent reagent for this transformation. Pyrroles and indoles containing a variety of substitution were aminated on nitrogen with isolated yields ranging from 45% to 97%.     

A comparison of the solid-state structures of a series of phenylseleno-halogen and pseudohalogen compounds,PhSeX (X = Cl,CN, SCN)

Structural and spectroscopic data on the series of compounds “PhSeX”, where X = Cl, CN or SCN, are reported and compared with previously reported data on “PhSeX” systems (X = Br and I). The chloro-compound displays a “square” motif, Ph₄Se₄Cl₄, in the solid state, linked by long Se–Se bonds [2.993(3)–3.035(3) Å], and forms a loosely held network of Se₄ and Cl₄ squares in its extended structure. In contrast, the pseudohalogen derivatives, PhSeCN and PhSeSCN, consist of essentially monomeric units, which form chains held together by weak Se?N interactions in the solid state. These Se?N interactions are much shorter in PhSeCN, 3.023(3)–3.065(4) Å, than in PhSeSCN, 3.348(4) Å. Weaker Se?N contacts are also present between the chains. The structure of PhSeSCN described here is the first reported crystallographic study of a selenium thiocyanate compound. Spectroscopic studies suggest that all three compounds exist as monomers in solution. The results reported herein illustrate the subtle differences in the solid-state structures of PhSeX compounds.     

Tunable band structure effects on ballistic transport in graphene nanoribbons

Graphene nanoribbons (GNR) in mutually perpendicular electric and magnetic fields are shown to exhibit dramatic changes in their band structure and electron transport properties. A strong electric field across the ribbon induces multiple chiral Dirac points, closing the semiconducting gap in armchair GNRs. A perpendicular magnetic field induces partially formed Landau levels as well as dispersive surface-bound states. Each of the applied fields on its own preserves the even symmetry Ek=E−k of the subband dispersion. When applied together, they reverse the dispersion parity to be odd and gives Ee,k=−Eh,−k and mix the electron and hole subbands within the energy range corresponding to the change in potential across the ribbon. This leads to oscillations of the ballistic conductance within this energy range.     

Growth and dc conductivity studies of tripotassium sodium dichromate single crystal

DC electrical conductivity studies were carried out along the three crystallographic axes for tripotassium sodium dichromate (K₃Na(CrO₄)₂ or KNCr). Earlier studies of phase transition in this crystal show successive phase transitions at 239 K and 853 K. In this paper we report the dc electrical conductivity measurements in the temperature region 303–430 K along the crystallographic axes. An anomaly in conductivity was obtained around 326 K along both the axes. This may be attributed as due to a newly observed phase transition in the crystal. DSC taken for the sample also shows exothermic peak supporting the occurrence of newly observed phase transition.