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P. Chiappetta F. M. Renard C. Verzegnassi 《Zeitschrift fur Physik C Particles and Fields》1996,71(1):673-677
We consider the virtual signals of aZ′ of very general type in the processe + e ?→W + W ? at a future linear collider (NLC). We show that possible deviations from the SM predictions in this channel are related to similar deviations in the purely leptonic one in a way that is only characteristic of thisZ′ model, and not in general of possible competitor models with anomalous gauge couplings. 相似文献
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F. Boudjema B. W. Lynn F. M. Renard C. Verzegnassi 《Zeitschrift fur Physik C Particles and Fields》1990,48(4):595-603
We develop a simple and realistic strategy to identify the theoretical origin of aZ′ of massM z′ ? 400 GeV if the latter were directly produced at a futuree + e ? collider. A measurement of the muonic width and of two ratios of hadronic to muonic widths would lead to an almost complete identification within a very general class of extraU(1) models. Alternative models, though, would be better classified by measuring three longitudinal polarization asymmetries. 相似文献
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Ludovica Verzegnassi Catherine Riffé-Chalard Werner Kloeti F. O. Güla?ar 《Fresenius' Journal of Analytical Chemistry》1999,364(3):249-253
A new application is described of the on-line high-performance liquid chromatography/positive and negative ion atmospheric
pressure chemical ionization mass spectrometry (APCI(+/–)-MS) to the identification of tetrapyrrolic compounds in sediment
samples containing complex mixtures of natural pigments and their diagenetic products. The method relies on the production
of radical anions in order to determine the molecular masses of the molecules which yield abundant fragment ions when analyzed
in the positive mode. This approach allows to verify the occurrence of coeluting components by examining their negative ion
spectra and to complete their identification on the basis of their fragment ions produced in the positive ion spectra.
Received: 24 September 1998 / Revised: 23 December 1998 / Accepted: 29 December 1998 相似文献
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Ludovica Verzegnassi Catherine Riffé-Chalard Werner Kloeti F. O. Gülaçar 《Analytical and bioanalytical chemistry》1999,364(3):249-253
A new application is described of the on-line high-performance liquid chromatography/positive and negative ion atmospheric
pressure chemical ionization mass spectrometry (APCI(+/–)-MS) to the identification of tetrapyrrolic compounds in sediment
samples containing complex mixtures of natural pigments and their diagenetic products. The method relies on the production
of radical anions in order to determine the molecular masses of the molecules which yield abundant fragment ions when analyzed
in the positive mode. This approach allows to verify the occurrence of coeluting components by examining their negative ion
spectra and to complete their identification on the basis of their fragment ions produced in the positive ion spectra.
Received: 24 September 1998 / Revised: 23 December 1998 / Accepted: 29 December 1998 相似文献
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Verzegnassi L Riffé-Chalard C Gülaçar FO 《Rapid communications in mass spectrometry : RCM》2000,14(7):590-594
On-line high performance liquid chromatography/atmospheric pressure chemical ionization mass spectrometry (HPLC/APCI-MS) has been applied to the identification of a number of tetrapyrrolic pigments as well as several magnesium-free analogs. Mass spectra, acquired both in positive (+) and negative (-) ionization mode, allow not only the determination of the structural features of the pigments, but also a very easy differentiation of the Mg-chelated pigments from the free bases. In the positive ionization mode, all pigments show mainly a [M + H]+ ion and a [M + H - C20H38]+ fragment ion corresponding to the loss of the phytyl chain via a hydrogen rearrangement. In the negative ionization mode, on the other hand, although all pigments give an abundant molecular anion [M]-*, only the Mg-chelated chlorin spectra show a prominent fragment [M - C20H39]- produced by a formal loss of the phytyl radical. 相似文献