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Journal of the Operational Research Society -  相似文献   
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Isobaric daughter ions formed from a common metastable ion have been analysed at high mass resolution. A three-dimensional representation is used to summarize the data for competitive CO and C2H4 losses and competitive CHO˙ and C2H5˙ losses from metastable molecular ions of cyclohexanone.  相似文献   
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Depending on their method of preparation, polyvinylamides can have nitrogen contents which vary from the theoretical value to considerably lower values. Cyanamer P-250, a polyacrylamide, manufactured by American Cyanamid Corporation, had a nitrogen content of 17.67% compared to the theoretical value of 19.7%. A polyacrylamide prepared in dioxane at 60°C and initiated by benzoyl peroxide, had a nitrogen content of only 15.5%. These low values are ascribed to loss of ammonia via intramolecular imide formation. We have found that when the intramolecular imidization reaction in poly acrylamide and in polymethacrylamide is driven to completion by heating the polymers in dilute solution, very close to 33% of the amide groups remain unreacted. Thus, unlike poly(methyl vinyl ketone) and poly(vinyl chloride), the poly-vinylamides do not obey Flory's statistical calculation for the random reaction of 1,3 groups in a head-to-tail polymer which predicts isolation of only 13.53% of the vinyl residues. Of the various possible explanations, the hypothesis of larger ring formation seems the most plausible, since specific interactions have been shown to exist between widely spaced amide groups in low molecular weight diamides. The infrared spectra of polyacrylimide and polymethacrylimide are presented and compared with those of the corresponding polyvinylamides. When the nitrogen content of polyacrylamide falls to the 14.9–15.4% N range due to imide formation, the polymer becomes water-insoluble. Because imidization stiffens the polymer chain and introduces weakly acidic groups, the imide content of a polyvinylamide should affect its compatibility with other polymeric systems.  相似文献   
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The lithiated (organo)sulfonylacetonitrile complex [MeSO(2)CHCNLi.THF] (3) has been prepared and structurally characterized in order to demonstrate that well-known molecular aggregates of s-block metals may be used as building blocks in the controlled assembly of complex supramolecular architectures. The solid state structure of 3 can be described as a novel basket-weaved, 2-D network, composed of (SO(2)Li)(2) "dimeric" rings joined via "interdimer" donation of nitrile units.  相似文献   
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We present what is to our knowledge the first experimental study of light-induced reflectivity changes at an alpha-Ga/Si interface irradiated by femtosecond and picosecond laser pulses. After exposure, the reflectivity can increase from R?0.55 , which is typical for alpha-Ga , to R?0.8 , which is close to that of liquid Ga. The initial step in the reflectivity change of 2-4 ps is resolved with 150-fs laser pulses. The light-induced reflectivity change relaxes during 100ns-10 mus , depending strongly on the background temperature of the Ga mirror and the laser fluence.  相似文献   
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