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Query: KEGG:D02259 (NaI)
 1,823 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The slightly yellow polymeric complexes [Au(2)Cl(2)(P(2)pz)(3)](n), 1 x 6CHCl(3), (P(2)pz is 3,6-bis(diphenylphosphino)pyridazine) and [[Au(2)(P(2)pz)(3)](PF(6))(2)](n), 2, are prepared by the stoichiometric reaction of AuCl(tht) (tht is tetrahydrothiophene) and P(2)pz in either dichloromethane or dichloromethane/methanol, respectively. Addition of 2 equiv of AuCl(tht) to a dichloromethane solution of 1 equiv of P(2)pz generates the simple (AuCl)(2)(P(2)pz) compound, 3. Compound 3 contains nearly linear P-Au-Cl units with intermolecular Au.Au separations of 3.570 A. Au(2)I(2)(P(2)pz)(3), 4, is prepared by reacting excess NaI with 2 in a dichloromethane/methanol mixture. Characterization of 1, 2, and 4 by X-ray crystallography confirms the 2:3 gold/ligand ratio of all three complexes. The coordination polymer 1 maintains a high degree of solvation in the solid-state with three chloroform adducts hydrogen-bonded to the chloride ligand on each gold atom. These chloroform molecules are sandwiched between the two-dimensional polymeric sheets of 1. The crystal structure of 4 reveals an empty, iodide-capped metallocryptand cage with the tetrahedrally distorted gold atoms and the nitrogen atoms on the pyridazine rings directed away from the center of the cavity. No metal ion encapsulation was observed for complex 4. Complex 2 forms one-dimensional arrays of [Au(2)(P(2)pz)(2)](2+) metallomacrocycles connected to each other by a third P(2)pz ligand. The electronic absorption spectra (CH(2)Cl(2)) of 1-4 show broad, nearly featureless absorption bands that tail into the visible with pi-pi bands at 296 nm and discernible shoulders at 314 nm for 2 and 334 nm for 3. Excitation into the low energy band of 2 produces only a modest emission in solution at 540 nm (lambda(ex) 468 nm) and 493 nm (lambda(ex) 403 nm). Under identical conditions, the P(2)pz ligand also emits at 540 and 493 nm.
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PMID:Three- and four-coordinate gold(I) complexes of 3,6-bis(diphenylphosphino)pyridazine: monomers, polymers, and a metallocryptand cage. 1263 53

An industrial prompt-gamma neutron activation analysis (PGNAA) system, originally designed for the real-time elemental analyses of bulk coal on a conveyor belt, has been studied to examine the feasibility of using such a system for body composition analysis. Experiments were conducted to measure nitrogen in a simple, tissue equivalent phantom comprised of 2.7 wt% of nitrogen. The neutron source for these experiments was 365 MBq (18.38 microg) of 252Cf located within an engineered low Z moderator and it yielded a dose rate in the measurement position of 3.91 mSv/h; data were collected using a 2780 cm(3) NaI(Tl) cylindrical detector with a digital signal processor and a 512 channel MCA. Source, moderator and detector geometries were unaltered from the system's standard configuration, where they have been optimized for considerations such as neutron thermalization, measurement sensitivity and uniformity, background radiation and external dose minimization. Based on net counts in the 10.8 MeV PGNAA nitrogen photopeak and its escape peaks the dose dependent nitrogen count rate was 11,600 counts/mSv with an uncertainty of 3.0% after 0.32 mSv (4.9 min), 2.0% after 0.74 mSv (11.4 min) and 1.0% after 3.02 mSv (46.4 min).
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PMID:Measurement of nitrogen in the body using a commercial PGNAA system--phantom experiments. 1468 37

Body composition has become the main outcome of many nutritional intervention studies including osteoporosis, malnutrition, obesity, AIDS, and aging. Traditional indirect body composition methods developed with healthy young adults do not apply to the elderly or diseased. Fast neutron activation (for N and P) and neutron inelastic scattering (for C and O) are used to assess in vivo elements characteristic of specific body compartments. Non-bone phosphorus for muscle is measured by the (31)P(n, alpha)(28)Al reaction, and nitrogen for protein via the (14)N(n,2n)(13)N fast neutron reaction. Inelastic neutron scattering is used to measure total body carbon and oxygen. Body fat is derived from carbon after correcting for contributions from protein, bone, and glycogen. Carbon-to-oxygen ratio (C/O) is used to measure the distribution of fat and lean tissue in the body and to monitor small changes of lean mass. A sealed, D-T neutron generator is used for the production of fast neutrons. Carbon and oxygen mass and their ratio are measured in vivo at a radiation exposure of less than 0.06 mSv. Gamma-ray spectra are collected using large BGO detectors and analyzed for the 4.43 MeV state of carbon and 6.13 MeV state of oxygen, simultaneously with the irradiation. P and N analysis by delayed fast neutron activation is performed by transferring the patient to a shielded room equipped with an array of NaI(Tl) detectors. A combination of measurements makes possible the assessment of the "quality" of fat-free mass. The neutron generator system is used to evaluate the efficacy of new treatments, to study mechanisms of lean tissue depletion with aging, and to investigate methods for preserving function and quality of life in the elderly. It is also used as a reference method for the validation of portable instruments of nutritional assessment.
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PMID:Use of D-T-produced fast neutrons for in vivo body composition analysis: a reference method for nutritional assessment in the elderly. 1474 91

The design, calibration, dosimetry and performance evaluation of a prompt-gamma neutron activation analysis facility for in vivo body composition studies in small animals (i.e. rats or rabbits) is discussed. The system design was guided by Monte Carlo transport calculations using MCNP-4C code. A system was built and performance evaluation was made using a 185-GBq Pu-Be neutron source. Prompt-gamma rays produced by neutron capture reactions were detected by a combination of a NaI(Tl) scintillation and a HPGe semiconductor detectors. Nitrogen and chlorine were quantified by analysis of the 10.83-MeV and 6.11-MeV peaks, respectively. Appropriate corrections for the animal body size were determined. The facility described allows the in vivo determination of protein and extracellular space in sets of experimental animals.
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PMID:Prompt-gamma neutron activation analysis facility for in vivo body composition studies in small animals. 1476 43

The profiles of the interaction of antimycobacterial drugs with macrophage (MPhi) antimicrobial mechanisms have yet to be elucidated in detail. We examined the effects of various antimycobacterial drugs on the anti-Mycobacterium avium complex (MAC) antimicrobial activity of reactive oxygen intermediates (ROIs), especially of an H(2)O(2)-halogen (H(2)O(2)-Fe(2+)-NaI)-mediated bactericidal system, reactive nitrogen intermediates (RNIs), and free fatty acids (FFAs), which are known as central antimicrobial effectors of host MPhis against mycobacterial pathogens. We have found that certain drugs, such as rifampin (RIF), rifabutin (RFB), isoniazid (INH), clofazimine (CLO), and some fluoroquinolones, strongly or moderately reduced the anti-MAC activity of the H(2)O(2)-Fe(2+)-NaI system, primarily by inhibiting the generation of hypohalite ions and in part by interfering with the halogenation reaction of bacterial cell components due to the H(2)O(2)-Fe(2+)-NaI system. This phenomenon is specific to the H(2)O(2)-Fe(2+)-NaI system, since these drugs did not reduce the anti-MAC activity of RNIs and FFAs. From the perspective of the chemotherapy of MAC infections, the present findings indicate an important possibility that certain antimycobacterial drugs, such as rifamycins (RIF and RFB), INH, CLO, and also some types of fluoroquinolones, may interfere with the ROI-mediated antimicrobial mechanisms of host MPhis against intracellular MAC organisms.
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PMID:Interaction of antimycobacterial drugs with the anti-Mycobacterium avium complex effects of antimicrobial effectors, reactive oxygen intermediates, reactive nitrogen intermediates, and free fatty acids produced by macrophages. 1515 11

A germanium (Ge) detector system has been installed in a whole-body counting facility at NIRS (Japan). The system employs five detectors that have relative efficiencies of more than 80%. A basic performance of the Ge detectors was tested and compared with that of the former NaI(Tl) detector system. Although the Ge detector system has advantages of improved radionuclide identification capability and MDA values, it also has disadvantages of high operation costs and demanding maintenance such as supply of liquid nitrogen.
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PMID:Performance of a whole-body counter with five high-purity germanium detectors. 1630 14

Because of the nitrogen functionality, the azido group plays an important role in the synthesis of amines, and numerous reduction methods of azides to primary amines are reported. Recent reports have highlighted the capability of NaI as a useful reagent for this transformation when it is used in combination with a Lewis acid promoter. However, these methods often suffer from harsh reaction conditions; for this reason, the development of a simple and efficient protocol using NaI in presence of inexpensive and readily available cerium salts Lewis acids would extend the scope of this organic transformation. In continuation of our interest on the use of the CeCl3.7H2O/NaI system, in this paper we report how azides undergo reduction by NaI in the presence of CeCl3.7H2O in refluxing acetonitrile under neutral conditions to produce the corresponding primary amines. The rate and yield of the reaction are considerably improved by employing this microwave-assisted procedure, and this may be of value for the preparation of densely functionalized molecules having biological and pharmaceutical activities.
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PMID:Efficient transformation of azides to primary amines using the mild and easily accessible CeCl3.7H2O/NaI system. 1826 85

A novel electron cyclotron resonance x-ray source is constructed based on the ECR technique. In this paper, the possibility of using the ECR x-ray source for producing UV rays by optimizing the plasma parameters is explored. X-ray and UV emissions from the ECR x-ray source are carried out for argon, nitrogen, and CO(2) plasma. The x-ray spectral and dose measurements are carried with NaI(Tl) based spectrometer and dosimeter, respectively. For UV measurement, a quartz window arrangement is made at the exit port and the UV intensity is measured at 5 cm from the quartz plate using UV meter. The x-ray and UV emissions are carried out for different microwave power levels and gas pressures. The x-ray emission is observed in the pressure range < or =10(-5) Torr, whereas the UV emission is found to be negligible for the gas pressures <10(-5) Torr and it starts increasing in the pressure range between 10(-5) and 10(-3) Torr. At high-pressure range, collision frequency of electron-atom is large which leads to the higher UV flux. At low pressure, the electron-atom collision frequency is low and hence the electrons reach high energy and by hitting the cavity wall produces higher x-ray flux. By choosing proper experimental conditions and plasma gas species, the same source can be used as either an x-ray source or an UV source.
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PMID:Studies on x-ray and UV emissions in electron cyclotron resonance x-ray source. 1831 55

Glancing angle laser-induced fluorescence was used to follow the kinetics of chlorophyll loss at the air-salt water interface under the influence of visible radiation. Aqueous solutions of NaCl, NaBr, NaI, KNO(3), and NaNO(2) in a range of concentrations up to approximately 1 M were used as substrates. The first-order reaction rate depends linearly on salt concentration for the halide salts but does not vary with concentration for nitrate or nitrite salts. At the same salt concentration, the chlorophyll loss rate is greatest for the bromide-containing solutions, followed by those containing chloride and then iodide. The results are consistent with a mechanism in which photoproduced chlorophyll cations are reduced by halide anions and subsequently react with the halogen atoms thus produced. This mechanism gives a novel route for gas-phase halogenated species, and possibly nitrogen oxides, to be released to the marine boundary layer.
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PMID:Photooxidation of halides by chlorophyll at the air-salt water interface. 1971 14

Gamma-ray spectra produced in carbon, nitrogen, oxygen, sodium, aluminium, silicon, chlorine, calcium, chromium, iron, nickel, copper, zinc, and lead by 14 MeV tagged neutrons have been collected with NaI(Tl) detectors of the EURITRACK system, which low-energy threshold has been reduced to 0.6 MeV to detect gamma rays of major elements like iron. The spectra have been compared with Monte Carlo simulations to check the tabulated gamma-ray production data. A quantitative approach to subtract the scattered neutron background is also reported.
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PMID:Acquisition of prompt gamma-ray spectra induced by 14 MeV neutrons and comparison with Monte Carlo simulations. 2129 86


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