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41.
Ke Jian Liu Jin Jie Jiang Li Li Ji Xianglin Shi Harold M. Swartz 《Research on Chemical Intermediates》1996,22(5):499-509
Application of the spin trapping technique in intact animals requires an understanding of the stability and distribution of the spin traps and their spin adducts in vivo. We studied the stability of DMPO in vivo in mice using HPLC and the stability of spin adducts of DMPO by EPR in plasma, whole blood, peritoneal fluid, and homogenized heart tissue of the rat. At 15 minutes after intraperitoneal injection DMPO had similar concentrations in the liver, heart, and blood of the mice and 40% remained in the organs 2 hours after the injection. In contrast, the spin adduct DMPO-OH was short lived, with a half-life of 3.0 minutes in plasma, and was not detectable 1 minute after formation in whole blood and homogenized heart tissue. The carbon centered spin adduct DMPO-CH(OH)CH3 was more stable, having half-lives of 16, 11, 3.6, and 0.79 minutes in plasma, peritoneal fluid, whole blood, and homogenized heart tissue, respectively. The spin adduct DMPO-SO3 was sufficiently stable for the adduct to be observed directly from living mice. 相似文献
42.
A rapid, sensitive, and convenient spectrophotometric assay was developed for the measurement of amino groups on solid supports.
This method is based on the reaction of amino groups of solids with an excess ofo-phthaldialdehyde (OPA) and subsequent quantitative determination of unreacted OPA by reaction with glycine. Four solids possessing
variable quantities of amino groups were examined. Results indicate that about 70% of the total surface amino concentration
(determined by the microKjeldahl method) are available for ligand attachment. Unlike the spectrophotometric 2,4,6-trinitrobenzenesulfonic
acid method, the OPA spectrophotometric assay is more rapid, sensitive, and convenient, and unlike the spectrofluorimetric
OPA, it does not require sophisticated instrumentation. 相似文献
43.
Yoel Tsur Harold H. Levine Moshe Levy 《Journal of polymer science. Part A, Polymer chemistry》1974,12(7):1515-1529
Polybenzimidazoles were prepared in poly(phosphoric acid) from isophthalic, m- and p-phenylene diacetic, succinic, adipic, suberic, and sebacic acids and 3,3′-diaminobenzidine, 3,3′,4,4′-tetraaminodiphenyl ether and 3,3′,4,4′-tetraaminodiphenylmethane. The thermal, mechanical, and bonding properties were studied. A 3:1 copolymer of isophthalic and m-phenylenediacetic acid with 3,3′-diaminobenzidine showed the best results as far as isothermal oxidation resistance and thermal and processing characteristics. 相似文献
44.
45.
Harold Basch 《Molecular physics》2013,111(4):683-689
Self-consistent field results for the excited electronic states of cyclopropene, with regard to the spatial extent of the π* orbital in the lowest energy 1(π, π*) state, are found to be identical with that for ethylene. Due to the forced planarity of the ring structure, dihedrally twisted conformers of the upper electronic state cannot contribute significantly to the oscillator strength which must therefore receive a substantial contribution from the vertical transition; this conclusion is contrary to the self-consistent field results. For a proper theoretical treatment of the problem the importance of a multi-configuration approach in an extended basis with 1(σ, σ*)-type states is emphasized. 相似文献
46.
Harold Williams 《Letters in Mathematical Physics》2013,103(4):389-419
We construct a family of integrable Hamiltonian systems generalizing the relativistic periodic Toda lattice, which is recovered as a special case. The phase spaces of these systems are double Bruhat cells corresponding to pairs of Coxeter elements in the affine Weyl group. In the process we extend various results on double Bruhat cells in simple algebraic groups to the setting of Kac–Moody groups. We also generalize some fundamental results in Poisson–Lie theory to the setting of ind-algebraic groups, which is of interest beyond our immediate applications to integrable systems. 相似文献
47.
One‐Pot Synthesis of Pomegranate‐Structured Fe3O4/Carbon Nanospheres‐Doped Graphene Aerogel for High‐Rate Lithium Ion Batteries
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Dr. Dafang He Lixian Li Fengjuan Bai Chenyang Zha Prof. Liming Shen Prof. Harold H. Kung Prof. Ningzhong Bao 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(13):4454-4459
A unique hierarchically nanostructured composite of iron oxide/carbon (Fe3O4/C) nanospheres‐doped three‐dimensional (3D) graphene aerogel has been fabricated by a one‐pot hydrothermal strategy. In this novel nanostructured composite aerogel, uniform Fe3O4 nanocrystals (5–10 nm) are individually embedded in carbon nanospheres (ca. 50 nm) forming a pomegranate‐like structure. The carbon matrix suppresses the aggregation of Fe3O4 nanocrystals, avoids direct exposure of the encapsulated Fe3O4 to the electrolyte, and buffers the volume expansion. Meanwhile, the interconnected 3D graphene aerogel further serves to reinforce the structure of the Fe3O4/C nanospheres and enhances the electrical conductivity of the overall electrode. Therefore, the carbon matrix and the interconnected graphene network entrap the Fe3O4 nanocrystals such that their electrochemical function is retained even after fracture. This novel hierarchical aerogel structure delivers a long‐term stability of 634 mA h g?1 over 1000 cycles at a high current density of 6 A g?1 (7 C), and an excellent rate capability of 413 mA h g?1 at 10 A g?1 (11 C), thus exhibiting great potential as an anode composite structure for durable high‐rate lithium‐ion batteries. 相似文献
48.
Meroquinene (1), a key degradation product of quinine and an important intermediate in the preparation of the cinchona and other alkaloids,1 has only recently been synthesized 2 even though attempts were made at its preparation for over thirty years. These early attempts were frustrated primarily by the difficulty encountered in the introduction of a potential vinyl group onto a piperidine ring. Alkylation of 3-car-bethoxy-N-benzoyl-4-piperidone (2) with either phenoxyethyl chloride3 or dimethylaminoethyl chloride (3)4 resulted in exclusive formation of the O-alkylated product, even though alkylation of the presumably analogous 2-carbethoxycyclohexanone with 3 gave nearly equal amounts of C- and O- alkylated materials.4 The use of other piperidone derivatives in this reaction was precluded by the report that attempts to alkylate 3-car-bethoxy-N-alkyl-4-piperidones gave only the quaternary nitrogen product.5 相似文献
49.
THE REACTIONS OF N3P3CL6 AND RELATED COMPOUNDS WITH DIFUNCTIONAL REAGENTS. COMPARISONS AND CONTRASTS
Abdulla H. Alkubaisi W. Francis Deutsch Michael B. Hursthouse Harold G. Parkes Leylacaron S. Shaw Robert A. Shaw 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-2):229-237
Abstract The reactions of N3P3Cl6 with a variety of difunctional reagents are discussed. NMR spectroscopic and X-ray crystallographic investigations are presented. 相似文献
50.
John K. Fincham Michael B. Hursthouse Harold G. Parkes Leylacaron S. Shaw Robert A. Shaw 《Phosphorus, sulfur, and silicon and the related elements》2013,188(1-2):185-194
Abstract Based on its reactions with various nucleophiles both geminal and non-geminal structures have been earlier proposed for N3P3Cl4(NH2)2, although its geminal structure is now considered established. The reactions of this compound with alcohols have been investigated and the products examined by NMR spectroscopy and X-ray crystallography. Evidence for both unrearranged as well as geminal → non-geminal rearranged alcoholysis products is presented. 相似文献