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71.
L. Lammich S. Altevogt H. Buhr H. Kreckel S. Krohn M. Lange D. Strasser R. Repnow M. Grieser R. Schinke Z.-W. Qu H. Zhu D. Schwalm D. Zajfman A. Wolf 《The European Physical Journal D - Atomic, Molecular, Optical and Plasma Physics》2007,41(1):103-111
The fragmentation of LiH2
- anions after electron
impact was investigated at the heavy-ion storage ring TSR.
The main reaction channel was found to be electron detachment followed by a
breakup into LiH + H.
In the first ms after production of the molecular ions in a cesium
sputtering ion source, additional
contributions were observed in the Li + H2 and Li- + H2 channels,
hinting at an initial population of a short-lived state of the anion.
To gain a better understanding of the mechanisms underlying the observed
behavior of the system, ab initio calculations of relevant potential
energy surfaces were performed at selected geometries.
The experimental findings are discussed in the
light of these calculations. 相似文献
72.
73.
74.
Fifty MR scans conducted at 1.5 T were evaluated to assess how well the pancreas could be identified. A total of 128 sets of images were reviewed. The pancreatic head was identified in 81%, 82% and 74% of scans with T1, intermediate and T2-weighting, respectively. The body was identified in 100%, 96% and 70% and tail in 96%, 87% and 54% on those respective sequences. Relative contrast was calculated between pancreas and: liver, spleen, muscle, fat, stomach and small bowel. The variability seen in contrast compared to stomach and small bowel suggests that consistent MR visualization of the pancreas will probably necessitate the use of an oral contrast agent. 相似文献
75.
Krystyna Wejroch Jerzy Lange Anna Kielak Janina Karolak‐Wojciechowska Jacek Sonicki Tadeusz Jagodziski 《Journal of heterocyclic chemistry》2001,38(4):877-884
Bis(ethoxycarbonyl)alkylidene derivatives 4 and 5 of the respective title hydrazones were obtained in the reactions with diethyl oxomalonate, diethyl oxosuccinate, diethyl 2‐oxoglutarate, and diethyl oxalo‐propionate as mixtures of geometric isomers with high predominance of one of them. On heating at 160‐200° without any solvent or on refluxing in ethanol 4 cyclized to yield the corresponding pyri‐dazino[6, 1‐c]triazines 6 , whereas heating of 5 gave, depending on the chain length, the corresponding pyra‐zolylpyridazines 8b and 8d or the pyridazinylpyridazine 8c . X‐ray analysis was used to determine the structures of 6 and 8 ; the unit cell of 6c was found to accommodate 16 molecules representing four conforma‐tional varieties. The different behavior of 4 and 5 in the cyclization reactions was interpreted in terms of the tautomeric equilibrium which was shifted towards the enamine form in 4 , and towards the imine form, in 5 . Transmission of a long‐range chirality effect in 4d and 5a‐d manifested itself in the 1H nmr spectra as the magnetic non‐equivalence of the CH2 protons in one or both ester ethyl groups. 相似文献
76.
I. Lange G. F. Nadeau L. E. Branchen D. G. Kerr A. E. Hill W. M. Malisoff S. I. Schodzew und E. M. Johansen 《Fresenius' Journal of Analytical Chemistry》1937,109(1-2):55-59
Ohne Zusammenfassung 相似文献
77.
Bailey und Lange 《Fresenius' Journal of Analytical Chemistry》1899,38(6):399-400
Ohne Zusammenfassung 相似文献
78.
L. Grünhut Neumann Wender G. Ambühl J. C. A. S. Thomas G. Holste und H. Lange 《Fresenius' Journal of Analytical Chemistry》1900,39(4):242-245
Ohne Zusammenfassung 相似文献
79.
80.
Gwenaelle Pound Zaskia Eksteen Rueben Pfukwa Jean M. McKenzie Ronald F. M. Lange Bert Klumperman 《Journal of polymer science. Part A, Polymer chemistry》2008,46(19):6575-6593
The monomer N‐vinylpyrrolidone (NVP) undergoes side reactions in the presence of R group functional xanthates and impurities. The fate of the monomer NVP and a selection of six O‐ethyl xanthates during xanthate‐mediated polymerization were studied via NMR spectroscopy. A high number of by‐products were identified. Significant side reactions affecting NVP include the formation of an unsaturated dimer and hydration products in bulk or in solution in C6D6. In addition, the xanthate adjacent to a NVP unit was found to undergo elimination at moderate temperature (60–70 °C), resulting in unsaturated species and the formation of new xanthate species. The presence of the chlorinated compound α‐chlorophenyl acetic acid, ethyl ester, a precursor in the synthesis of the xanthate S‐(2‐ethyl phenylacetate) O‐ethyl xanthate, resulted in a dramatic increase in the rate of side reactions such as unsaturated dimer formation and a high ratio of unsaturated chain ends. The conditions for the occurrence of such side reactions are discussed in this article, with relevance to increasing the control over the polymerization kinetics, endgroup functionality, and control over the molar mass distribution. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 6575–6593, 2008 相似文献