New analysis of the Comet-Tail (AΠi − XΣ) system in the CO isotopic molecule

The emission spectra of the 0-2, 4-2, and 6-1 bands of the Comet-Tail (A²Π_i − X²Σ⁺) system in the ¹⁴C¹⁶O⁺ isotopic molecule, comprising nearly 600 lines, have been recorded and analyzed for the first time. The spectra have been photographed under high resolution by using conventional spectroscopy, and it was possible to separate and observe most of the lines of all the 12 branches of this transition. The reduction of the individual bands’ spectra has been performed by nonlinear least-squares procedure and by means of effective Hamiltonians of Brown et al. the rovibronic structure parameters have been obtained. The currently investigated bands of the Comet-Tail system and the earlier analyzed bands of the A − X and B − A systems in the ¹⁴C¹⁶O⁺ molecule have been merged together. The results of this global fit made it possible to derive a new set of the equilibrium molecular constants for the A and X states. Then the RKR potential curve parameters for both A and X states and Franck-Condon factors as well as r-centroids for the A − X transition have been calculated for the ¹⁴C¹⁶O⁺ molecule.     

Rotational Analysis of the 1–4 Band of the B 2Σ+–X 2Σ+ System of 14C16O+

ABSTRACT

High-resolution emission spectrum of the 1–4 band of the B ²Σ⁺–X ²Σ⁺ transition of ¹⁴C¹⁶O⁺ was observed for the first time by conventional emission spectroscopy. The band spectrum was excited in a water-cooled Geissler lamp filled with commercial gaseous carbon monoxide enriched in about 80% of the radiocarbon ¹⁴C. A rotational analysis has been carried out and obtained molecular constants have been merged with previously published data for the B ²Σ⁺–A ²Π_i and A ²Π_i–X ²Σ⁺ transitions. The principal equilibrium constants for the ground X ²Σ⁺ state obtained from this work are ω_e = 2121.7726(98), ω_e x _e = 13.9055(27), B _e = 1.815290(30), α_e = 1.6594(33) × 10^?2, and γ_e = ? 0.377(73) × 10^?4 cm^?1. Also, presently known experimental equilibrium molecular constants of the X ²Σ⁺ states of the CO⁺ isotopic molecules are summarized and isotopic dependence of the B _e and ω _e constants is discussed.     

Global fittings of NNO and NNO vibrational-rotational line positions using the effective Hamiltonian approach

An effective Hamiltonian built up to sixth order in the Amat-Nielsen ordering scheme describing all rovibrational energy levels in the ground electronic state and containing in explicit form all resonance interaction terms due to the approximate relations between harmonic frequencies ω₁≈2ω₂ and ω₃≈4ω₂ was applied to model the observed rovibrational line positions (collected from the literature) of ¹⁴N¹⁵N¹⁶O and ¹⁵N¹⁴N¹⁶O isotopologues of nitrous oxide. For ¹⁴N¹⁵N¹⁶O, 124 effective Hamiltonian parameters were fitted to near 28 000 observed line positions covering the 0.8-8860 cm⁻¹ spectral range. The RMS of the weighted fit is 0.00126 cm⁻¹ and dimensionless standard deviation is 1.48. For ¹⁵N¹⁴N¹⁶O, 121 effective Hamiltonian parameters were fitted to more than 31 000 observed line positions covering the same spectral interval. The RMS of the weighted fit is 0.00185 cm⁻¹ and dimensionless standard deviation is 1.85. In both cases the models describe all available line positions with precision compatible to the measurement uncertainties. A number of local resonance perturbations was found and discussed. Among these perturbations there are interpolyad resonance Coriolis interactions. A comparison of HITRAN-2008 data with the calculations based on the fitted models is presented.     

Structural and 14N EFG Information on Solid Imidazole by 13C CP/MAS NMR Data

Residual dipolar coupling between carbons and ¹⁴N nuclei in the ¹³C CPMAS NMR spectrum of solid imidazole is studied. Calculations of expected splittings with a previously reported equation leads to the complete assignment of the solid state carbon chemical shifts. Additionally, information is provided on the location of ¹⁴N electric field gradient axes at the N-H site.     

The He scattering and reactions on C and cluster states of C

The ⁶He+¹²C elastic and inelastic scattering and the ⁶He+¹²C→α+¹⁴C reaction have been measured using a 18.0 MeV ⁶He beam. Experimental results for the elastic scattering are in fair agreement with optical model predictions, using the potentials found in the analysis of ⁶Li scattering on ¹²C at similar energies. In triple coincidences, the ⁶He+¹²C→¹⁰Be+2α reactions were clearly seen, with the ¹⁰Be nucleus left in ground and several excited states. The dominant mechanism of this reaction is sequential decay through cluster states of ¹⁴C.     

Measurement of uranium and its isotopes at trace levels in environmental samples using mass spectrometry

Actinides have widely entered the environment as a result of nuclear accidents and atmospheric weapon testing. These radionuclides, especially uranium, are outstanding radioactive pollutants, due to their high radiotoxicity and long half-lives. In addition to this, since depleted uranium (DU) has been used in the Balkan conflict in 1999, there has been a concern about the possible consequences of its use for the people and environment. Therefore, accurate, precise and simple determination methods are necessary in order to evaluate the human dose and the concentration and effects of these nuclides in the environment. The principal isotopes of uranium e.g. ²³⁵U and ²³⁸U are of primordial origin and ²³⁴U present in radioactive equilibrium with ²³⁸U. ²³⁶U occurs in nature at ultra trace concentrations with a ²³⁶U: ²³⁸U atom ratio of 10⁻¹⁴. Concentrations of uranium in soil samples were determined using inductively coupled plasma mass spectrometry (ICP-MS) and isotope ratios of uranium were measured using a thermal ionisation mass spectrometer. Radioactive dis-equilibrium of ²³⁴/²³⁸U, depletion of ²³⁵/²³⁸U and significant evidence of ²³⁶U/²³⁸U were noticed in soil samples.      

14N Study of Aromatic Nitroso Compounds

The ¹⁴N NQR frequencies of selected aromatic C-nitroso compounds were measured using cross relaxation double resonance. The monomers have high ¹⁴N NQR frequencies with Χ and η values of 5700 to 6100 kHz and 0.5 ± 0.1, respectively. The dimers and polymer show lower frequencies with values of 2300 to 2600 kHz and 0.8 ± 0.05. Benzofuroxan has values typical of both the monomer and dimer.     

Solution Structures of Pyrophthalones,III: Complementary Application of 14N/16N-NMR Spectroscopy to Study Solution Structures of Pyrophthalones

The solution structures of nine pyrophthalone-type substances are determined by ¹⁴N / ¹⁵N-NMR-spectroscopy. Mostly depending on the conditions (solvent, solubility, chemical nature of the compound), both isotopes can be used complementary to obtain reliable data. Additionally, for some compounds ¹⁵N solid state NMR data are available and demonstrate the structural identity in solution and the solid state.     

Energy transfers between Sm and Eu in YPO4, LaP5O14 and LaP3O9 phosphates. Potential quantum cutters for red emitting phosphors

This work concerns the studies of energy transfers between Sm³⁺ and Eu³⁺ ions in some phosphates as new luminescent materials emitting in the orange-red color. The choose of ions is based on the possibility of quantum cutting process and the matrices are selected according to the 5d bands position of Sm³⁺ ion. The Sm³⁺ and Eu³⁺ doped YPO₄, LaP₅O₁₄ and LaP₃O₉ are synthesized and spectroscopic studies in ultraviolet and vacuum ultraviolet ranges have been achieved.     

Zur Herstellung von 14C- und 3H-markiertem Guajakolglycerinäther und dessen Metabolismus im Tierkörper

Für die Herstellung von Guajakol-[1,3-¹⁴C]glycerinäther, [7-¹⁴C]Guajakolgylycerinäther und ³H-Guajakolglycerinäther werden Synthesevorschriften angegeben. Der Metbolismus wird mit Hilfe der ¹³C- oder ³H-markierten Verbindung im Tierexperiment verfolgt. Dabei kann nachgewiesen werden, daβ Guajakolglycerinä;ther hauptsächlich in nicht veränderter Form durch Urin und Galle wieder ausgeschieden wird. Nur in Spuren werden als Metaboliten Brenzkatechin und Guajakol gefunden.     

Cr3+,Yb3+,Er3+共掺磷酸盐铒玻璃转镜调Q激光性质研究

研究了Cr³⁺,Yb³⁺,Er³⁺共掺磷酸盐铒玻 璃转镜调Q激光性质.三种Er₂O₃掺杂浓度的激光实验结果表明，在Er₂O₃名义掺杂浓 度为0.5wt％时，玻璃的综合激 光性质最好，重复频率为0.1Hz时，它的激光阈值功率为14.5mJ，最大输出能量为9.6mJ ，斜率效率为0.55％.在同种实验条件下，比较了Cr14和Kigre公司生产的QE-7S激光性质参数，实验表明，前者激光阈值功率稍低，而后者的斜率效率和最大输出功率略高. 关键词： 3+-Yb³⁺-Er³⁺共掺')" href="#">Cr³⁺-Yb³⁺-Er³⁺共掺 磷酸 盐玻璃 光谱性质 激光性质     

First observation of F

We measured the excitation function for ¹³O + p elastic scattering to obtain data on the unknown ¹⁴F nucleus. The ground state and several low-lying excited states in ¹⁴F were observed and spin/parity assignments were made. ¹⁴F appears to be much less unstable than was predicted. We compare theoretical predictions for the ¹⁴F level scheme with the experimental results.     

New combination bands in CCH2 around 0.83 μm recorded using FT-ICLAS

Fourier-transform intracavity laser absorption spectroscopy allowed five ¹²C¹³CH₂ Σ⁺-Σ⁺ bands, all from the ground state, to be identified in the 0.83 μm range. Their rotational analysis was performed and rotational constants are provided. Three of these bands, with origins at 11616.9684(18), 11737.2356(14), and 11761.0322(23) cm⁻¹, have never been reported before. Their upper states are assigned to , respectively.     

3D 1H-13C-14N correlation solid-state NMR spectrum

Nitrogen-14 (spin I = 1) has always been a nucleus difficult to observe in solid-state NMR and until recently its observation was restricted to one-dimensional (1D) spectra. We present here the first 3D ¹H–¹³C–¹⁴N NMR correlation spectrum. This spectrum was acquired on a test sample l-histidine·HCl·H₂O using a recently developed technique, which consists in indirectly observing ¹⁴N nuclei via dipolar recoupling with an HMQC-type experiment.     

Proton Dynamics in Letovicite, (NH4)3H(SO4)2: A H and N NMR Spectroscopic Study

The improper ferroelastic phase letovicite (NH₄)₃H(SO₄)₂ has been studied by ¹H MAS NMR as well as by static ¹⁴N NMR experiments in the temperature range of 296–425 K. The ¹H MAS NMR resonance from ammonium protons can be well distinguished from that of acidic protons. A third resonance appears just below the phase transition temperature which is due to the acidic protons in the paraelastic phase. The lowering of the second moment M₂ for the ammonium protons takes place in the same temperature range as the formation of domain boundaries, while the signals of the acidic protons suffer a line narrowing in the area of T_c. The static ¹⁴N NMR spectra confirm the temperature of the motional changes of the ammonium tetrahedra. Two-dimensional ¹H NOESY spectra indicate a chemical exchange between ammonium protons and the acidic protons of the paraphase.     

Investigation of two- and three-nucleon transfer reactions in12C +56Fe

Multi-nucleon transfer reactions⁵⁶Fe(¹²C, X) have been studied at an incident¹²C energy of 60 MeV. Angular distributions of¹⁰Be and⁹Be corresponding to 2p and 2p 1n transfer reactions in transition to low-lying states in the residual nuclei have been measured. The angular distribution data for 2p transfer have been analysed in terms of finite range DWBA calculations assuming a one-step transfer of two protons. The spectroscopic factors for three low-lying transitions observed in⁵⁶Fe(¹²C,¹⁰Be)⁵⁸Ni have been extracted. Transfer probabilities for the ground state transition in two- and three-nucleon stripping channels have been obtained and compared with the corresponding sequential transfer probabilities in order to emphasise the role of direct transfer of nucleons vis-a-vis sequential transfer.     

Emission analysis of Pr and Tm: Ca2Gd2W3O14 phosphors

5 mol% of Pr³⁺ and Tm³⁺ ions activated calcium gadolinium tungstate (Ca₂Gd₂W₃O₁₄₎ phosphors were synthesized by traditional solid state reaction method. Crystalline phase structure was identified from the X-ray diffraction (XRD) profiles. From the scanning electron microscopy (SEM) images, we have observed the agglomeration of the particles, and average grain size is around 40-300 nm. Using the energy dispersive X-ray analysis (EDAX) and Fourier transform infrared (FTIR) spectra, identified the elements and functional groups present in the prepared phosphors. The emission spectrum of Pr³⁺: Ca₂Gd₂W₃O₁₄ powder phosphors have shown an intense red emission at 615 nm with the excitation wavelength λ_exci=450 nm and thus these red color emitting powder phosphors are used as one of the components in the preparation of WLEDs. The excitation spectrum of Tm³⁺: Ca₂Gd₂W₃O₁₄ powder phosphor has shown a ligand to metal charge transfer (W-O) band (LMCT) within the WO₄²⁻ group. Emission spectrum of Tm³⁺: Ca₂Gd₂W₃O₁₄ phosphors have shown blue emissions at 453 nm (¹D₂→³F₄).     

Ground state rotational spectrum of nitrogen trifluoride: The K = 3 splittings of NF3 and NF3

The ground state rotational spectrum of the ¹⁴NF₃ and ¹⁵NF₃ isotopic species of nitrogen fluoride has been observed in the ∼450-810 GHz frequency range. This investigation allowed us to improve the rotational parameters for both isotopologues. In particular, for the first time the K = 3 line splitting parameter and the sextic centrifugal distortion constants have been determined for ¹⁵NF₃.     

Thermonuclear reaction rates from (p,n) reactions

Thermonuclear reaction rates for the temperature range 1≤T ₉≤5 have been extracted from experimentally measured (p, n) cross sections for⁴⁵Sc⁵⁰Ti,⁵¹V,⁵⁴Cr,⁵⁵Mn and⁵⁹Co nuclides below 5 MeV bombarding energy. These reaction rates are important in the build-up of medium and heavy nuclides in the stellar evolution process and nucleosynthesis. To enhance the usefulness of these reaction rates in astrophysical calculations, they have been fitted to an analytic function of temperature, valid throughout the temperature range considered here.