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101.
Toby Chapman 《Europhysics News》1998,28(5-6):151-151
102.
M. Derrick K. K. Gan P. Kooijman J. S. Loos B. Musgrave L. E. Price J. Repond K. Sugano M. Valdata-Nappi D. Blockus B. Brabson J. -M. Brom C. Jung H. Ogren D. R. Rust C. Akerlof J. Chapman D. Errede M. T. Ken D. I. Meyer D. Nitz R. Thun R. Tschirhart S. Abachi P. Baringer B. G. Bylsma R. DeBonte D. Koltick F. J. Loeffler E. H. Low R. L. McIlwain D. H. Miller C. R. Ng L. K. Rangan E. I. Shibata B. Cork 《Zeitschrift fur Physik C Particles and Fields》1987,35(3):323-328
The charged particle multiplicity distributions for two-jet events ine + e ? annihilation at 29 GeV have been measured using the High Resolution Spectrometer at PEP. A Poisson distribution describes the data for both the complete event and for the single jets. In addition, no correlation is observed between the multiplicities in the two jets of an event. For fixed values of the prong number of the complete event, the multiplicity sharing between the two jets is in good agreement with a binomial distribution. The rapidity gap distribution is exponential with a slope equal to the mean rapidity density. These observations, which are consistent with a picture of independent emission of single particles, are contrasted to the results from soft hadronic collisions and conclusions are drawn about the nature of clusters. 相似文献
103.
LetD be a Dedekind domain. It is well known thatD is then an atomic integral domain (that is to say, a domain in which each nonzero nonunit has a factorization as a product
of irreducible elements). We study factorization properties of elements in Dedekind domains with finite class group. IfD has the property that any factorization of an elementα into irreducibles has the same length, thenD is called a half factorial domain (HFD, see [41]). IfD has the property that any factorization of an elementα into irreducibles has the same length modulor (for somer>1), thenD is called a congruence half factorial domain of orderr. In Section I we consider some general factorization properties of atomic integral domains as well as the interrelationship
of the HFD and CHFD property in the Dedekind setting. In Section II we extend many of the results of [41], [42] and [36] concerning
HFDs when the class group ofD is cyclic. Finally, in Section III we consider the CHFD property in detail and determine some basic properties of Dedekind
CHFDs. IfG is any Abelian group andS any subset ofG−[0], then {G, S} is called a realizable pair if there exists a Dedekind domainD with class groupG such thatS is the set of nonprincipal classes ofG which contain prime ideals. We prove that for a finite abelian groupG there exists a realizable pair {G, S} such that any Dedekind domain associated to {G, S} is CHFD for somer>1 but not HFD if and only ifG is not isomorphic toZ
2,Z
2,Z
2 ⊕Z
2, orZ
3 ⊕Z
3.
The first author received support under the John M. Bennett Fellowship at Trinity University and also gratefully acknowledges
the support of The University of North Carolina at Chapel Hill. 相似文献
104.
R. Hyndman P. Warin J. Gierak J. N. Chapman J. Ferr J. P. Jamet V. Mathet C. Chappert 《Journal of magnetism and magnetic materials》2002,240(1-3):50-52
We present a study of the structural and magnetic effects induced by focused 30 keV Ga+ ion beam irradiation on a Pt(2.8 nm)/[Pt(0.6 nm)/Co(0.3 nm)]6/Pt(6.5 nm) ferromagnetic multilayer, using transmission electron microscopy, optical and magneto-optical microscopy. The work is of relevance to high-density data-storage applications, where media planarity is crucial for device reliability. 相似文献
105.
Synthesis and pH‐Dependent Spectroscopic Behavior of 2,4,6‐Trisubstituted Pyridine Derivatives 下载免费PDF全文
Gala Chapman Isaac Solomon Gabor Patonay Maged Henary 《Journal of heterocyclic chemistry》2015,52(3):861-872
Seven 2,4,6‐trisubstituted pyridine derivatives with N,N‐diethylaniline substituents at the 4‐position were synthesized, and their spectroscopic properties in the absence and presence of acid were studied. The spectral effects of protonation, molar absorptivities, pKa values, and the structural origins of the observed spectral behavior were ascertained. The pyridine nitrogen was found to be more basic than the diethylamino nitrogen atom. Protonation of the pyridine ring nitrogen is associated with the appearance of a red‐shifted intramolecular charge transfer peak in the UV‐visible spectra. Favorable color indicating properties result from electron‐donating substitution at the 2 and 6 positions of pyridine, which provide a greater absorptivity of the red‐shifted peak associated with protonation of the pyridine nitrogen. These findings will assist in the design and optimization of these compounds for ion‐indicating and pH‐sensing applications. 相似文献
106.
Surface and Structural Investigation of a MnOx Birnessite‐Type Water Oxidation Catalyst Formed under Photocatalytic Conditions 下载免费PDF全文
Benjamin J. Deibert Jingming Zhang Paul F. Smith Dr. Karena W. Chapman Dr. Sylvie Rangan Debasis Banerjee Kui Tan Hao Wang Nicholas Pasquale Prof. Feng Chen Prof. Ki‐Bum Lee Prof. G. Charles Dismukes Prof. Yves J. Chabal Prof. Jing Li 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(40):14218-14228
Catalytically active MnOx species have been reported to form in situ from various Mn‐complexes during electrocatalytic and solution‐based water oxidation when employing cerium(IV) ammonium ammonium nitrate (CAN) oxidant as a sacrificial reagent. The full structural characterization of these oxides may be complicated by the presence of support material and lack of a pure bulk phase. For the first time, we show that highly active MnOx catalysts form without supports in situ under photocatalytic conditions. Our most active 4MnOx catalyst (~0.84 mmol O2 mol Mn?1 s?1) forms from a Mn4O4 bearing a metal–organic framework. 4MnOx is characterized by pair distribution function analysis (PDF), Raman spectroscopy, and HR‐TEM as a disordered, layered Mn‐oxide with high surface area (216 m2g?1) and small regions of crystallinity and layer flexibility. In contrast, the SMnOx formed from Mn2+ salt gives an amorphous species of lower surface area (80 m2g?1) and lower activity (~0.15 mmol O2 mol Mn?1 s?1). We compare these catalysts to crystalline hexagonal birnessite, which activates under the same conditions. Full deconvolution of the XPS Mn2p3/2 core levels detects enriched Mn3+ and Mn2+ content on the surfaces, which indicates possible disproportionation/comproportionation surface equilibria. 相似文献
107.
Development and application of sub‐2‐μm particle CO2‐based chromatography coupled to mass spectrometry for comprehensive analysis of lipids in cottonseed extracts 下载免费PDF全文
108.
Novel extracellular polymeric substances produced by Cupriavidus necator IPT 027 grown on glucose and crude glycerol originated from biodiesel 下载免费PDF全文
The aim of this study was to evaluate the production and properties of novel extracellular polymeric substances (EPS) from glucose (EPS 1) and crude glycerol (CG) from castor beans oil (EPS 2). Cupriavidus necator IPT 027 cultivated with glucose and CG (35 °C, 150 rpm, 72 hr, pH 7, shaker) produced approximately 1.60 ± 0.01 and 2.83 ± 0.02 g l?1 EPS, respectively, with high‐molecular weight (3.89 × 105 and 1.89 × 107 Da) and constituted of different functional groups such as uronic acid, monosaccharides (glucose, mannose, arabinose, and fucose) and primary amine group. The composition of the fermentable substrate influenced the melting temperature (221.11 and 230.18 °C), crystallinity (34.36% and 37.11%), degradation temperature (255.06 and 296.62 °C) and morphology. EPS showed pseudoplastic non‐Newtonian fluid behavior in the aqueous solutions, presenting potential applicability biotechnological and industrial mainly in food industry as emulsifiers and biosurfactants. This is the first study on the production and characterization of EPS obtained by C. necator IPT 027 in culture with glucose and CG. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
109.
Janice CalzavaraJames McNulty 《Tetrahedron letters》2011,52(43):5672-5675
A short, convergent synthesis of the immunosuppressant FTY720 is described involving the use of 4-hydroxymethylbenzaldehyde as a pivotal intermediate. A double Wittig strategy was developed to connect this dual-functional aldehyde with an alkyl-tether and to a readily available TRIS-derivative leading to an efficient synthesis of the target molecule. 相似文献
110.
A directing/protecting group designed for regioselective functionalization of partially-protected glucopyrannosides has been successfully used to prepare disaccharides in high yields. Most importantly, it has been demonstrated that highly regioselective and stereoselective glycosylation can be achieved when disarmed donors are employed. This study demonstrates the ability of directing/protecting group to induce regioselective glycosylation of carbohydrates and opens the field to the design of other DPGs for other monosaccharides. 相似文献