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O,O′-Ditolylphosphorodithioates of phosphorus(III), [(o-, m-, or p-CH3C6H4O)2PS2] n PCl3−n , and phosphorus(V), [(o-, m-, or p-CH3C6H4O)2-PS2] n POCl3−n , (n = 1, 2, and 3) were isolated as colorless viscous liquids by the reaction of PCl3 and POCl3 with sodium ditolylphosphorodithioate, (o-, m-, or p-CH3C6H4O)2PS2Na, in 1:1, 1:2, and 1:3 molar ratios in toluene. These compounds were characterized by elemental analyses, molecular weight measurements, IR, and NMR (1H, 31P, and 13C) spectroscopic studies, which indicated a less common monodentate linkage of dithiophosphate moieties in both phosphorus(III) and phosphorus(V) derivatives leading to a tetrahedral geometry around the phosphorus atom.  相似文献   
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Relativistic α-particles have been studied in 423 interactions of Fe in emulsion at 1.7A GeV. Comparisons of the observed angular distribution with that from 16O-emulsion reactions at 2.1A GeV reveal that more α-particles are observed at large angles in the Fe-emulsion reactions. The α-particles at large angles cannot be explained by fragmentation from a clean-cut spectator. Comparison of the experimental data with moving relativistic Boltzmann distributions shows that a single Boltzmann distribution cannot fit the fragmentation peak and the tail simultaneously. A thermal source (fireball) explaining the tail part of the distribution needs to be formed by a mechanism other than a simple clean-cut participant-spectator process. A large transverse momentum transfer to the spectator before fragmentation may explain the tail.  相似文献   
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This is a continuation of our earlier investigation (Gurtuet al 1974Phys. Lett. 50 B 391) on multiparticle production in proton-nucleus collisions based on an exposure of emulsion stack to 200 GeV/c beam at the NAL. It is found that the ratioR em = 〈n s〉/〈n ch〉, where 〈n ch〉 is the charged particle multiplicity in pp-collisions, increases slowly from about 1 at 10 GeV/c to 1·6 at 68 GeV/c and attains a constant value of 1·71 ± 0·04 in the region 200 to 8000 GeV/c. Furthermore,R em = 1·71 implies an effectiveA-dependence ofR A =A 0.18,i.e., a very weak dependence. Predictions ofR em on various models are discussed and compared with the emulsion data. Data seem to favour models of hadron-nucleon collisions in which production of particles takes place through adouble step mechanism,e.g., diffractive excitation, hydrodynamical and energy flux cascade as opposed to models which envisage instantaneous production.  相似文献   
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Reactions of (m- and p-ClC 6 H 4 NH 2 ), (p-BrC 6 H 4 NO 2 ), and (p-ClCOC 6 H 4 NO 2 ) with sodium O,O′-ditolyl/dibenzylphosphorodithionates, (ArO) 2 PS 2 Na, (Ar = o?, m?, and p?CH 3 C 6 H 4 or –C 6 H 5 CH 2 ) in 1:1 molar ratio in refluxing toluene under anhydrous conditions resulted in the formation of the compounds (ArO) 2 PS 2 C 6 H 4 L and (ArO) 2 PS 2 COC 6 H 4 L (L = NH 2 or NO 2 ) in 87–94% yield. These viscous compounds were characterized by elemental analyses, molecular weight determination, and IR and NMR ( 1 H, 13 C, and 31 P) spectroscopic studies, which revealed a monodentate mode of bonding of the dithiophosphate moiety with the carbon of the phenyl ring of the organic moiety leading to a P–S–C linkage.  相似文献   
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Our previous work described the neural processes of motor response inhibition during a stop signal task (SST). Employing the race model, we computed the stop signal reaction time (SSRT) to index individuals' ability in inhibitory control. The pre-supplementary motor area (preSMA), which shows greater activity in individuals with short as compared to those with long SSRT, plays a role in mediating response inhibition. In contrast, the right inferior prefrontal cortex (rIFC) showed greater activity during stop success as compared to stop error. Here we further pursued this functional differentiation of preSMA and rIFC on the basis of an intra-subject approach.  相似文献   
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O,O′-Ditolylphosphorodithioates of phosphorus(III), [(o-, m-, or p-CH3C6H4O)2PS2] n PCl3−n , and phosphorus(V), [(o-, m-, or p-CH3C6H4O)2-PS2] n POCl3−n , (n = 1, 2, and 3) were isolated as colorless viscous liquids by the reaction of PCl3 and POCl3 with sodium ditolylphosphorodithioate, (o-, m-, or p-CH3C6H4O)2PS2Na, in 1:1, 1:2, and 1:3 molar ratios in toluene. These compounds were characterized by elemental analyses, molecular weight measurements, IR, and NMR (1H, 31P, and 13C) spectroscopic studies, which indicated a less common monodentate linkage of dithiophosphate moieties in both phosphorus(III) and phosphorus(V) derivatives leading to a tetrahedral geometry around the phosphorus atom. Correspondence: Sushil K. Pandey, Department of Chemistry, University of Jammu, Baba Saheb Ambedkar Road, Jammu 180 006 (J & K), India.  相似文献   
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