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81.
82.
Interesting competitive oxygen migrations from the nitro group to the nitrogen and to the sulfur have been noticed during the mass spectral decomposition of ortho nitro aromatic thioamides on electron impact. The migration of the oxygen to the nitrogen of the thioamide function results in the formation of stable o-nitrosothiobenzoyl cation. The other novel ortho effect noticed in the ortho isomers is the transfer of an oxygen from the nitro group to the sulfur followed by the ejection of SO from the molecular ions. A mechanism involving the initial oxygen migration to the sulfur through a favourable 6-membered transition state followed by cyclization with the concomitant expulsion of SO is proposed for this process. Other interesting decomposition processes occurring as a consequence of this ortho effect have also been noticed. The proposed mechanisms for these processes are supported by mass analysed ion kinetic energy spectra and high voltage scans. 相似文献
83.
The mass spectrum of o-picolinotoluidide gives rise to three major fragments at m/z 184, m/z 169 and m/z 168, corresponding to the loss of CO from the molecular ion followed by the loss of ?H2 and ?H3 by independent pathways. It has been shown that the ortho methyl group and the nitrogen of the pyridine ring in the 2-position are involved in the formation of these three major fragments observed in the mass spectrum of o-picolinotoluidide. The mass spectrum of 2-(o-toluidino) pyridine, the molecular ion of which can resemble the [M? CO]+ ion in o-picolinotoluidide, also shows loss of CH3 and NH2 radicals from the molecular ions. Based on these observations coupled with the high resolution data, the mass analysed ion kinetic energy spectrometry and high voltage scans of these fragments in both the compounds, two mechanistic pathways have been proposed for the formation of these ions in o-picolinotoluidide. 相似文献
84.
Grilli S Lunazzi L Mazzanti A Pinamonti M Anderson JE Ramana CV Koranne PS Gurjar MK 《The Journal of organic chemistry》2002,67(18):6387-6394
Variable-temperature NMR studies of tetraethylmethane (1a), tetrapropylmethane (1b), tetrachloromethylmethane (1c), tetrabromomethylmethane (1d), tetracyclopropylmethylmethane (1e), and tetrabenzylmethane (1f) show a range of dynamic behavior. Separate signals for two types of conformation are observed for 1a, 1c, and 1d at low temperatures, with more than 95% of the molecules in a time-averaged D2d conformation, and the S4 conformation as the minor populated alternative. Compound 1e populates only S4-type conformations but equilibrates slowly between degenerate versions of these at low temperatures. Compounds 1b and 1f show a temperature-dependent spectrum but the low-temperature limit spectrum could not be observed. Ab initio calculations agree well with experiment on the conformational equilibria and suggest in particular that compounds 1b and 1f behave similarly to compounds 1a and 1e, respectively. A crystal structure of compound 1f is reported. 相似文献
85.
Trivalent thallium is precipitated in the presence of 0.1 M HNO3 (or 0.05 M H2SO4) and O.1 M NH4NO3 (or 0.05 M (NH4)2SO4) with oxalic acid. The chemical analysis of the salt obtained correspondens to the formula, NH4[Tl(C2O4)2]·3H2O. The thermal decomposition studies of the complex indicate the formation of the intermediates ammonium thallous oxalate (stable from 150° to 160°C) and thallous oxalate (stable up to 290°C) and the final product to be a mixture of 25% of thallous oxide and 75% of thallic oxide (stable from 450° to 650°C). The infrared absorption spectra, X-ray diffraction patterns, microscopic observations and the electrical resistance measurements are used to characterise the complex and the intermediates of its thermal decomposition. 相似文献
86.
Ahmed Kamal A. Venkata Ramana K. Srinivasa Reddy K. Venkata Ramana A. Hari Babu B. Rajendra Prasad 《Tetrahedron letters》2004,45(44):8187-8190
Sodium iodide in acidic media has been employed for the synthesis of N-arylformamides and N-arylacetamides. The NaI/acetic acid reagent system has also been extended for the synthesis of 1,4-benzodiazepine-2,5-diones, pyrrolo[2,1-c][1,4]benzodiazepine-5,11-diones, and fused [2,1-b]quinazolinones. 相似文献
87.
Oxygen transfers to both the acetylenic carbons and sulphur are noticed in parallel fragmentation pathways during the electron-impact induced decompositions of 2-nitrophenylphenylethynylsulphides. Single oxygen transfer to acetylinic carbons leads to the most abundant ion corresponding to the benzoyl cation whilst double oxygen transfers to both the acetylenic carbons followed by the ejection of two CO units from the M+˙ ion afford another abundant fragment corresponding to the phenothiazine radical cation. However, the oxygen transfers to sulphur yield a less abundant [M ? SO2H]+ ion. The proposed fragmentation pathways and the ion structures are sup ported by high-resolution data, collision-induced dissociation Linked-scan spectra and chemical substitution. 相似文献
88.
89.
基于快速傅立叶变换的二阶可靠度分析方法 总被引:2,自引:0,他引:2
建立了一种基于快速傅立叶变换的二阶可靠度分析方法。状态函数在利用两点近似技术近似为二阶多项式后,进一步变换为统计上独立的中间变量之和。对于中间变量的线性形式表示的状态函数,其概率密度的傅立叶变换是各中间变量的概率密度的傅立叶变换之积。因此,状态函数的概率密度可由其傅立叶变换函数的逆变换求得。文中的傅立叶变换和相应的逆变换均由高效的快速傅立叶变换技术完成。该方法可应用于正态和非正态分布问题。由于在构造二阶近似中采用了近似技术,因而具有很好的计算效率。数值算例验了该方法的应用、效率和精度。 相似文献
90.