Macropolyhedral boron-containing cluster chemistry. A synthetic approach via the auto-fusion of [6,9-(SMe2)2-arachno-B10H12

In an attempt to build up borane-based multicluster assemblies, thermolysis of [6,9-(SMe2)2-arachno-B10H12] 1 in inert hydrocarbon solution, followed by chromatographic separation, has resulted in the isolation not only of the previously established single-cluster product from this reaction, [5-(SMe2)-nido-B10H12] 2 (30%), but also the two two-cluster species [6,9-(SMe2)2-arachno-B10H11-1-(6-nido-B10H13)] 3 (20%) and [1,6-(nido-B10H13)2] 6 (ca. 0.5%) and the two three-cluster species [6,9-(SMe2)2-arachno-B10H10-1,5-(6-nido-B10H13)2] 4 (5%), characterized crystallographically, and [6,9-(SMe2)2-arachno-B10H10-1,3-(6-nido-B10H13)2] 5 (<1%), identified by NMR spectroscopy. An improved crystallographic investigation of [5-(SMe2)-nido-B10H12] 2 is also presented. The feasibility of the stability of species resulting from multiple adjacent substitution of nido-decaboranyl units on the [6,9-(SMe2)2-arachno-B10H12] skeleton is tested by DFT calculations. In an extension, to attempt the use of pre--linked two-cluster compounds as starting substrates, two-cluster [5-(SMe2)-4-(2-nido-B10H13)-nido-B10H11] 7 (0.6%) has been isolated from the reaction of SMe2 with [1,5-(nido-B10H13)2], other identified products being compound 1 (39%) and compound 3 (10.5%).     

Generation of excess minority carriers in mos devices due to gamma irradiation

The effect of gamma irradiation on MOS devices prepared under different oxidation conditions Is investigated. The C-V characteristics of the devices are studied before and after exposing the latter with gamma radiations of CO⁶⁰ (1.17 and 1.33 MeV gamma rays). For MOS transistor (n-channel depletion type devices) the C-V characteristics change slightly towards the negative voltage axis and the C_min also decreases after Irradiation. For MOS capacitor (wet oxide) there is a change from high frequency C-V characteristics to low frequency C-V characteristics. In the case of a MOS capacitor (HCl grown) breakdown occurs relatively at lower voltage.     

Innovative solution of a 2D elastic transmission problem¶

This article is concerned with a boundary-field equation approach to a class of boundary value problems exterior to a thin domain. A prototype of this kind of problems is the interaction problem with a thin elastic structure. We are interested in the asymptotic behavior of the solution when the thickness of the elastic structure approaches to zero. In particular, formal asymptotic expansions will be developed, and their rigorous justification will be considered. As will be seen, the construction of these formal expansions hinges on the solutions of a sequence of exterior Dirichlet problems, which can be treated by employing boundary element methods. On the other hand, the justification of the corresponding formal procedure requires an independence on the thickness of the thin domain for the constant in the Korn inequality. It is shown that in spite of the reduction of the dimensionality of the domain under consideration, this class of problems are, in general, not singular perturbation problems, because of appropriate interface conditions.     

Relativistic symmetries in the Rosen-Morse potential and tensor interaction using the Nikiforov-Uvarov method

Approximate analytical bound-state solutions of the Dirac particle in the fields of attractive and repulsive Rosen- Morse (RM) potentials including the Coulomb-like tensor (CLT) potential are obtained for arbitrary spin-orbit quantum number κ. The Pekeris approximation is used to deal with the spin-orbit coupling terms κ(κ± 1)r 2 . In the presence of exact spin and pseudospin (p-spin) symmetries, the energy eigenvalues and the corresponding normalized two-component wave functions are found by using the parametric generalization of the Nikiforov-Uvarov (NU) method. The numerical results show that the CLT interaction removes degeneracies between the spin and p-spin state doublets.     

Scalar Charged Particle in Presence of Magnetic and Aharonov–Bohm Fields Plus Scalar–Vector Killingbeck Potentials

The generalized form of Killingbeck potential is an attractive Coulomb term plus a linear term and a harmonic oscillator term, i.e. ?a/r + br + λr ², which has a useful application in quarkonium spectroscopy. The ground state energy with the corresponding wave function are obtained for any arbitrary m-state in two-dimensional Klein–Gordon equation with equal mixture of scalar–vector Killingbeck potentials in the presence of constant magnetic and singular Ahoronov–Bohm flux fields perpendicular to the plane where the interacting charged particle is confined. The analytical exact iteration method is used in our solution. We obtain the energy eigensolutions for particle and antiparticle corresponding to S(r) = V(r) and S(r) = ?V(r) cases, respectively. Some special cases like the Coulomb, harmonic oscillator potentials and the nonrelativistic limits are found in presence and absence of external fields.     

Characterization of the 46.9-nm soft X-ray laser beam from a capillary discharge

Intense lasing had been obtained from argon plasma in the soft X-ray region from a capillary discharge plasma system. Different diagnostics have been used to characterize the lasing properties by recording the temporal, spatial, and spectral profiles of the emission. The divergence measurement indicates that the soft X-ray laser beam has good directionality with a divergence of 3.5 mrad. The spectrum of the laser beam measured using a transmission grating showed intense lasing line at 46.9 nm. Diffraction orders as high as 10th orders were observed. The temporal profile recorded with a vacuum diode showed a distinct laser peak with a pulse width ~1.2 ns (FWHM). In addition, the coherence of the X-ray laser beam was also confirmed from the high-contrast interference fringes (visibility ~85 %) recorded using double slits.     

Cationic ruthenium complex of the formula [RuCl(2,6-diacetylpyridine)(PPh3)2]BArF and its catalytic activity in the formation of enol esters

A new ruthenium 2,6-diacetylpyridine complex was synthesized and applied in the atom-economic synthesis of enol esters through Markovnikov-directed addition of carboxylic acids to terminal alkynes. The ruthenium complex [RuCl(dap)(PPh₃)₂]⁺BArF^? was synthesized from [RuCl₂(PPh₃)₂] and the corresponding ligand 2,6-diacetylpyridine (dap). The complex was characterized structurally. The new ruthenium complex was utilized under ambient conditions as a catalyst in the Markovnikov addition of carboxylic acids to terminal alkynes to afford the corresponding enol esters in 93% to 52% isolated yields (85?°C, 16?h reaction time, 1?mol% catalyst loading).     

Application of differential reactivity towards synthesis of lamellarin and 8-oxoprotoberberine derivatives: Study of photochemical properties of aryl-substituted benzofuran-8-oxoprotoberberines

A unique differential reactivity between dihydroisoquinolines and 3-nitrocoumarins was observed and was exploited for the efficient construction of lamellarins and their isomeric benzofuran-8-oxoprotoberberine derivatives under acid-catalyzed or base-promoted conditions. Further, these prepared aryl-substituted benzofuran-8-oxoprotoberberine derivatives bearing electron-donating substituents on benzofuran moiety are found to be benchtop stable but light-sensitive, and can undergo oxidative ring-opening reaction to give the corresponding keto products when exposed to visible light under aerobic conditions.     

Stream-lined synthesis of 3-hydroxy-β-lactams: Norrish-Yang type II photocyclizations of β-ketoformamides

A photochemical approach to 3-phenyl-3-hydroxy-β-lactams (3-HβLs) is reported. Irradiation of aryl-β-ketoformamides with a UV light band centered at 300?nm provides the corresponding 3-aryl-3-HβLs with good conversion. The scope of the photocyclization is explored with an electronically diverse panel of substrates that provides mechanistic insight supporting a Norrish-Yang type II cyclization. A flexible synthetic route to phenyl-β-ketoformamides, followed by photoirradiation, allows for efficient incorporation of the β-lactam pharmacophore into aromatic organic scaffolds. Taken collectively, the improved and optimized synthetic route to provide both β-ketoformamides and 3-HβLs—in combination with the expanded analysis of substrate scope and limitations—reported herein will serve as a necessary reference for the direct, atom-economical, radical-mediated installation of 3-HβL scaffolds en route to the generation of other biologically active small molecules.