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31.
Conclusions The major pathways were established for the fragmentation of -allyliron tricarbonyl halides upon dissociative electron capture. The mechanisms for the formation of C3H5Fe(CO) 3 anions in the gas phase and under electrochemical reduction conditions on a dropping mercury electrode were shown to differ. A predominant effect was proposed for solvation factors on the electrochemical reduction in the condensed phase.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1428–1430.  相似文献   
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The thermochemistry of resonant dissociative electron attachment processes for furan, thiophene, selenophene, and pyrrole molecules has been studied. The structures of the dissociation products originating from negative molecular ions at energies ranging from 2 to 6 eV have been established using the measured appearance energies of fragment ions and the known thermodynamic functions of radical and molecular dissociation products. Heats of formation and electron affinities for some radicals and molecules have been assessed by calculations and estimated experimentally. It has been concluded that the majority of the fragment ions are formedvia rearrangement processes in molecular or fragment ions.

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33.
Specificity of the dissociative attachment of low-energy electrons to ecdysteroid molecules (viz., 20-hydroxyecdysone 2,3:20,22-diacetonide, 20-hydroxyecdysone 20,22-acetonide, and poststerone 2-acetate) was found, which is manifested as the formation of long-lived pseudo-molecular negative ions that appeared due to the elimination of the H2 and H2O molecules. These rearrangements are resulted from the formation of the system of conjugated double bonds in the ecdysteroid skeleton, stabilizing the lowest vacant molecular orbital.  相似文献   
34.
New resonance states were discovered for the negative molecular ions of thiophene and selenophene and a series of resonances was found for various heterocyclic compounds in the region 3.0–3.6 eV. The low-energy resonances at 1.65–2.3 eV are formed by a resonance mechanism of a form of the molecular ground state, while an electronically excited Feschbach resonance is responsible for the series of resonance states at 3.0–3.6 eV. The mother state for the latter resonance states is the first triplet state of these molecules. The first triplet state of selenophene is at 3.6±0.15 eV.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 925–927, April, 1990.  相似文献   
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Conclusions The stereospecific fragmentation of 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid -cyano-3-phenoxybenzyl ester was found under conditions of resonant capture of electrons of epithermal energies with dissociation of HCN. The stereospecific collection of fragment ions allows not only the identification of one of the diastereoisomers, but also the quantitative (5%) determination of it in a mixture of racemates.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 291–294, February, 1989.  相似文献   
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Two couples of low pressure multi-wire proportional chambers (MWPC) were located in the target chamber to detect fission fragments in a hypernuclei producing experiment at Thomas Jefferson National Laboratory (Jlab). In the experiment, a continuous wave (CW) electron beam was applied to form hypernuclei by electromagnetic interaction. In the target chamber, the high energy (1.853 GeV) and high intensity (500 nA) primary electron beam caused a high particle background, which influenced the detection of the fission fragments. This report described the design of the MWPCs and studied the fission-fragment detecting performance of them under such a high background. The efficiency of the MWPCs was given with the help of a high resolution kaon spectrometer. At the same time, the background particles were discussed with a Monte Carlo code based on GEANT4.  相似文献   
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