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131.
We report the measurement of the strong interaction shifts and widths of the pionic 3d → 2p transitions in separated isotopes of 50,52,54Cr and natural Sc, V, Mn, and Fe. Using these new data in combination with earlier low-Z pionic data (6 ? Z ? 20) we have studied the phenomenological pion-nuclear potential. Employing nuclear structure information from measured charge densities and Hartree-Fock calculations, we have fitted the pion-nuclear potential parameters to the pionic-atom data. We have explored the sensitivity of these data to the value of the Lorentz-Lorenz parameter ξ. The addition of an isovector dependence to the s- and p-wave two-nucleon terms is shown to be unnecessary at the present level of experimental accuracy. We have used the deduced optical potentials to determine the neutron radii of the nuclei 20 ? Z ? 26 and find reasonable agreement with Hartree-Fock predictions and with the results of other hadronic probes for 20 ? Z ? 23 but poor agreement for 24 ? Z ? 26. 相似文献
132.
Ranasinghe RT Rusling DA Powers VE Fox KR Brown T 《Chemical communications (Cambridge, England)》2005,(20):2555-2557
Substituted 3H-pyrrolo[2,3-d]pyrimidin-2(7H)-one nucleoside analogues have been synthesised from 5-alkynyl-uridine derivatives, incorporated into triplex forming oligonucleotides (TFOs) and found to selectively bind CG inversions with enhanced affinity compared to T. 相似文献
133.
A. S. Ahmad MD N. Hoda M. Ahmad F. Islam S. Z. Qureshi 《Journal of Analytical Chemistry》2006,61(9):870-874
A simple, sensitive, and selective kinetic spectrophotometric method for the determination of kanamycin in pure form and pharmaceutical
formulations is described. The method is based on the measurement of the intensity of the yellow chromogen formed by the reaction
between kanamycin and acetylacetone-formaldehyde reagent in a N,N′-dimethyl formamide medium. The variable-time method was used to evaluate the rate of reaction of the colored chromogen formed
at 410 nm. The reaction conditions were optimized and the calibration graph was found to be linear in the range 60–160 μg/mL.
The results obtained by the developed and reference methods are in good agreement. Various statistical parameters were evaluated
to establish the precision, accuracy, repeatability, and reproducibility of the proposed method.
The text was submitted by the authors in English. 相似文献
134.
A J Banes G W Link W C Beckman J L Camps S K Powers 《Journal of chromatography. A》1986,356(2):301-309
Rhodamine 123 is a fluorescent vital dye which has potential for therapeutic use in cancer treatment. The dye concentrates in mitochondria of normal and neoplastic cells but accumulates in and is toxic to neoplastic cells. When dye-treated cells are irradiated with blue laser light at 514 nm, mitochondrial injury or cell death results. Rhodamine concentration in cultured cells and tumor tissue was quantitated to correlate cell or tumor death with drug dose. A reversed-phase separation of rhodamine 123 was accomplished using a gradient of 0.05 M phosphate buffer pH 2.85 (mobile phase A) and acetonitrile (mobile phase B), 10-80% B in 15 min with a DuPont Golden Series C8 column. Effluent was monitored with a fluorescence detector at 295 nm excitation and 520 nm emission. Stock rhodamine 123 contained approximately 6-8% of rhodamine 110, the parent compound, which eluted at 9.8 min whereas rhodamine 123 eluted at 11.7 min. Structural verification of both compounds by field desorption mass spectrometry was performed. This is the first report of the chemical separation and quantitation of rhodamine 123 from cultured tumor cells or tumor tissue. 相似文献
135.
[reaction: see text] At 275 degrees C, 8-exo-methylbicyclo[4.2.0]oct-2-ene (1a) undergoes a [1,3] sigmatropic rearrangement to 5-methylbicyclo[2.2.2]oct-2-enes, of which the orbital symmetry-allowed si product is only marginally favored over the forbidden sr product; that is, si/sr is 2.4. Accompanying the [1,3] shift are significant amounts of epimerization and fragmentation. The 8-endo epimer 1b, which yields no [1,3] product, experiences primarily direct fragmentation and secondarily epimerization. A diradical intermediate can account for all such observations. 相似文献
136.
Richard J. Sundberg Rita Broome Claudia Powers Walters Dora Schnur 《Journal of heterocyclic chemistry》1981,18(4):807-809
Benzenesulfonylindole is converted to a dilithio derivative by 2.2 equivalents of lithiating reagent. The dilithio derivative gives rise to sultones on reaction with carbonyl compounds. This reaction proceeds by an intramolecular displacement of the indole group from the bis-adduct. Fair to poor yields of the 2-indolycarbinols can also be isolated. Benzoyl chloride forms a thiazine dioxide ring by addition at both the 2-indolyl and 2′-phenylsulfonyl positions. 3-Methyl-1-benzenesulfonylindole is also easily dilithiated. 相似文献
137.
Christopher M. Lemon Michael Huynh Andrew G. Maher Bryce L. Anderson Dr. Eric D. Bloch Prof. Dr. David C. Powers Prof. Dr. Daniel G. Nocera 《Angewandte Chemie (International ed. in English)》2016,55(6):2176-2180
The ground state electronic structure of copper corroles has been a topic of debate and revision since the advent of corrole chemistry. Computational studies formulate neutral Cu corroles with an antiferromagnetically coupled CuII corrole radical cation ground state. X‐ray photoelectron spectroscopy, EPR, and magnetometry support this assignment. For comparison, CuII isocorrole and [TBA][Cu(CF3)4] were studied as authentic CuII and CuIII samples, respectively. In addition, the one‐electron reduction and one‐electron oxidation processes are both ligand‐based, demonstrating that the CuII centre is retained in these derivatives. These observations underscore ligand non‐innocence in copper corrole complexes. 相似文献
138.
A simple difference frequency generation (DFG) scheme based on two seeded optical parametric generators is presented as a tunable terahertz (THz) source. Using the nonlinear optical crystal 4-dimethylamino-N-methyl-4-stilbazolium-tosylate (DAST) as the DFG crystal, our system has demonstrated continuous and seamless tunable operation from 1.6 to 4.5 THz. The output bandwidth of the THz source is 2.4 GHz. The utility of the source over this spectral range is demonstrated by measuring a high-resolution transmission spectrum of water vapor in air. 相似文献
139.
Molecular recognition in water is challenging but water-soluble molecularly imprinted nanoparticle (MINP) receptors were produced readily by double cross-linking of surfactant micelles in the presence of suitable template molecules. When the micellar surface was decorated with different polyhydroxylated ligands, significant interactions could be introduced between the surface ligands and the template. Flexible surface ligands worked better than rigid ones to interact with the polar moiety of the template, especially for those template molecules whose water-exposed surface is not properly solvated by water. The importance of these hydrophilic interactions was examined in the context of different substrates, density of the surface ligands, and surface-cross-linking density of the MINP. Together with the hydrophobic interactions in the core, the surface hydrophilic interactions can be used to enhance the binding of guest molecules in water. 相似文献
140.
Chen‐Hao Wang Anuvab Das Dr. Wen‐Yang Gao Prof. Dr. David C. Powers 《Angewandte Chemie (International ed. in English)》2018,57(14):3676-3681
Metal–organic frameworks (MOFs) have garnered substantial interest as platforms for site‐isolated catalysis. Efficient diffusion of small‐molecule substrates to interstitial lattice‐confined catalyst sites is critical to leveraging unique opportunities of these materials as catalysts. Understanding the rates of substrate diffusion in MOFs is challenging, and few in situ chemical tools are available to evaluate substrate diffusion during interstitial MOF chemistry. Herein, we demonstrate nitrogen atom transfer (NAT) from a lattice‐confined Ru2 nitride to toluene to generate benzylamine. We use the comparison of the intramolecular deuterium kinetic isotope effect (KIE), determined for amination of a partially deuterated substrate, with the intermolecular KIE, determined by competitive amination of a mixture of perdeuterated and undeuterated substrates, to establish the relative rates of substrate diffusion and interstitial chemistry. We anticipate that the developed KIE‐based experiments will contribute to the development of porous materials for group‐transfer catalysis. 相似文献