Suitability of ion pump for evacuation of a closed He cycled Mössbauer cryostat

For Mössbauer studies at very low temperatures, the target holder kept at 11°K with the help of a closed He cycle Mössbauer shroud, has to be insulated by evacuating the outside enclosure surrounding the shroud. The target is kept in thermal contact with the cryostat cold finger through He gas at atmospheric pressure. This provides a vibrationless thermal contact between the two. The evacuation of the outside chamber has to be vibration free which can be accomplished by means of a suitable ion pump which is totally vibration free. However, use of Vac-ion pump here could not be made successful because the pump did not work at all after little pumping. To find out the cause of pump's failure, RGA was employed which showed the presence of He gas in the outside chamber at the time of purging of He gas in the internal chamber. The pump, however, worked efficiently again when the dry N₂ gas purged in place of Helium. This points out that totally vibration free Vac-ion pumps cannot be used for evacuation of such cryostats. Here, diffusion pump was used subsequantly taking extra precautions to minimise the vibrations.     

Decay of126m Sb and the energy levels of126Te

The decay characteristics of 19 min^126m Sb have been studied using Ge(Li) and scintillation spectrometers. The sources of^126m Sb were obtained by the (n, p) reaction on enriched¹²⁶Te. The gamma rays of energies 414.4±0.3, 666.7±0.5 and 696.1±0.5 keV were found decaying with a half-life of 19 min. The study of beta spectra employing an anthracene crystal yielded two beta groups with end-point energies of 1.9±0.15 and 2.5±0.15 MeV. The results of singles and coincidence measurements have been incorporated into a decay scheme with excited states of¹²⁶Te at 666.7, 1,362.8 and 1,777.2 keV.     

Studies in fluorinated 1,3-diketones and related compounds Part X. Synthesis of some new polyfluorinated 1,3-diketones,their copper 1,3-diketonates and spectral studies

The reaction of tetrafluoro-1,2-diiodobenzene with tellurium yields an oil which, on treatment with bromine yields perfluorotelluranthrene- 9,9,10,10-tetrabromide. The latter is reduced by sodium sulfide to perfluorotelluranthrene. The crystal structure of perfluorotelluranthrene is reported.     

On some nonself mappings

Let X be a Banach space, let K be a non–empty closed subset of X and let T : K → X be a non–self mapping. The main result of this paper is that if T satisfies the contractive–type condition (1.1) below and maps ?K (?K the boundary of K) into K then T has a unique fixed point in K.     

The decay of Ho and Ho

The disintegration characteristics of ^164mHo and ^164gHo have been studied using a high-resolution Ge(Li) spectrometer. Radioactive samples of ^164mHo and ^164gHo were obtained through the (n, 2n) reaction on spectroscopically pure holmium oxide with 14 MeV neutrons. The isomeric cross-section ratio for the yields of the ground and metastable states has been estimated to be 1.0±0.25. Gamma rays of 37.7 and 56.1 keV energy have been assigned to the decay of ^164mHo and 73.4 and 91.5 keV γ-rays are attributed to the decay of ^164gHo by electron capture and negaton emission, respectively. The branching ratio for the electron capture decay of ^164gHo to the levels in ¹⁶⁴Dy has been estimated accurately from the analysis of X-ray intensities. The results have been incorporated into a decay scheme.     

Poisson-Jacobi transforms

The solutions of the Jacobi difference heat equation ▽ _n v(n, t)=(δ/δt)v (n, t) are considered. The theory of Poisson-Jacobi transform is developed to solve the equation. Convergence and inversion theorems are established.

     

Non-linear As(P) incorporation in GaAs1−yPy on GaAs and InAs1−yPy on InP

We find anion incorporation into both GaAs_1−yP_y on GaAs and InAs_1−yP_y on InP during gas source molecular beam epitaxy (GSMBE) is not linearly related to the hydride gas fluxes within our reactor. The deviation from an ideal model, i.e., y = ƒ_P/(ƒ_P+ƒ_As), where As(P) is the flux of AsH₃ (PH₃), can be as large as a factor of two. GaAsP exhibits the largest degree of nonlinearity and incorporation is found to depend quadratically on the fluxes over a wide range of flux ratio. Significant deviations are also found for InAsP; however, anion incorporation can be modeled with y = ƒ_P/(ƒ_P+βƒ_As).     

New insights into the visible-light-induced DNA cleavage activity of dipyridoquinoxaline complexes of bivalent 3d-metal ions

Dipyridoquinoxaline (dpq) complexes of bivalent 3d-metal ions, viz., [FeII(dpq)3](PF6)2 (1), [CoII(dpq)3](ClO4)2 (2), [NiII(dpq)3](ClO4)2 (3), [CuII(dpq)2(H2O)](ClO4)2 (4), [ZnII(dpq)3](ClO4)2 (5), and [ZnII(dpq)2(DMF)2](ClO4)2 (5a) (DMF = N,N-dimethylformamide), are prepared and their photoinduced DNA cleavage activity studied. Structural characterization for the complexes 1 and 5a is done by single-crystal X-ray crystallography. All the complexes show efficient binding propensity to calf thymus DNA with a binding constant (K) value of approximately 10(5) M(-1). Complexes 1, 2, and 4 show metal-based cyclic voltammetric responses at 1.2, 0.4, and 0.09 V (vs SCE) in DMF 0.1 M [Bun4N](ClO4) assignable to the respective FeIII/FeII, CoIII/CoII, and CuII/CuI couples. The NiII and ZnII complexes do not show any metal-based redox process. The dpq-based reductions are observed in the potential range of -1.0 to -1.7 V vs SCE. DNA melting and viscosity data indicate the groove-binding nature of the complexes. Control experiments using distamycin-A suggest a minor groove-binding propensity of the complexes. The complexes exhibit photoinduced cleavage of supercoiled pUC19 DNA in UV light of 365 nm. The diamagnetic d6-FeII and d10-ZnII complexes are cleavage-inactive on irradiation with visible light. The paramagnetic d7-CoII and d9-CuII complexes exhibit efficient DNA cleavage activity on photoirradiation at their respective d-d band. The paramagnetic d8-NiII complex displays only minor DNA cleavage activity on irradiation at its d-d band. The DNA cleavage reactions at visible light under aerobic conditions involve the formation of hydroxyl radical. The CoII complex shows photocleavage of DNA under an argon atmosphere. Theoretical calculations on the complexes suggest a photoredox pathway in preference to a type-2 process forming singlet oxygen for the visible-light-induced DNA cleavage activity of the 3d-metal complexes. The theoretical data also predict that the photoredox pathway is favorable for the 3d7-CoII and 3d9-CuII complexes to exhibit DNA cleavage activity, while the analogous 3d6-FeII and 3d8-NiII complexes are energetically unfavorable for the exhibition of such activity under visible light. The CoII and CuII complexes are better suited for designing and developing new metal-based PDT agents than their cleavage-inactive FeII, NiII, and ZnII analogues.