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931.
Potassium salts of aziridine-2-carboxylic acid derivatives are efficiently converted into esters of amides by reactions with alkyl halides, alkyl dihalides or by acylation with trimethylacetyl chloride followed by aminolyses. 相似文献
932.
The adducts NbCl5 · OPCl3 and NbCl5 · OPBr3 are observed in chloroform solution by 31P-NMR spectroscopy. The enthalpy and entropy of activation for the exchange reaction between bulk and coordinated OPCl3 are found equal to 17 ± 3 kcal/mole and 18 ± 10 cal/°mole. The stability of NbCl5 · OPCl3 is compared on a semi-quantitative basis to the stability of other adducts NbCl5 · OPR3 (R = Br, OMe, NMe2). 相似文献
933.
C. F. Parrish D. E. Harmer 《Journal of polymer science. Part A, Polymer chemistry》1967,5(5):1015-1020
The solid-state polymerization of 1,2,3,4-diepoxybutane appears to proceed “insource” by an ionic mechanism and has an overall activation energy of 0.4 kcal./mole with an intensity dependency of 0.99. There is a rapid increase in the rate of polymerization just prior to the melting point and a very low rate for the liquid-phase reaction. Limiting conversions of 5% polymer are observed at ?196°C. for irradiation in vacuo. No limiting conversion was observed when the monomer was polymerized in the presence of air or in vacuo at ?78°C. Under all polymerization conditions the reactions were characterized by the absence of an induction period. 相似文献
934.
The mass spectra of a series of 2-alkyl N-methyl pyrrolidines have been examined and fragments which may be pyrrole type structures are apparent. These ions are most prominent in the spectra of the long chain alkyl derivatives. 相似文献
935.
5-Methyl-4-phenyl-2-styryipyridine has been oxidized to 5-methyl-4-phenylpyridinie-2-carboxylic acid. The decarboxylation of this acid has given 3-methyl-4-phenylpyrldine. To prove the structure of -(5-methyl-4-phenyl-2-pyridyl)acetophenone, it has been converted into 2, 5-dimethyl-4-phenylpyridine. The reaction of benzyl chloride with the lithium derivative of 2, 5-dimethyl-4-phenylpyridine has been studied. 3,7-Dimethyl-2-azafluorene has been obtained from 2,5-dimethyl-4-p-tolylpyridine. 相似文献
936.
The use of a carbon rod atomizer for the analysis of lead in petroleum and petroleum products is described. Variables affecting sensitivity studied include: type of lead salt and type of solvent for standard and sample preparation, hydrogen diffusion flame, choice of analytical wavelength and interferences. For the 217.00-nm line, a sensitivity of 1·10-11 g (absolute) and for the 283.31-nm line, a detection limit of 2·10-12 g (absolute) are reported. Results of analysis of gasoline, used bunker heating oil, used jet engine lubricating oil, and crude oil for lead content are presented. An organic-to-aqueous solvent extraction system for lead is described. 相似文献
937.
A new redox titrant, Dibromamine-T (N,N'-dibromo-p-toluenesulphonamide) is introduced for use in acetic acid media. Potentiometric titrations of Sb(III), As(III), Tl(I), Fe(II), ferrocyanide, iodide, ascorbic acid, hydroquinone, hydrazine, aniline, phenol and oxine are described. Direct potentiometric titrations of oxinates of Mn, Fe, Co, Ni, Cu and Zn with Dibromamine-T as well as with Dichloramine-T are also described. 相似文献
938.
M.C. Lin 《Chemical physics》1975,7(3):442-448
CO laser emission was detected in the vacuum UV flash photolysis of CH2CO. The emission is attributed to the initial photodissociation reaction Addition of O2 to the CH2CO system caused a pronounced enhancement in the laser intensity. This effect is believed to be due to the removal of the CH2 + CH2CO reaction, which produces uninverted CO molecules. A greater laser output was obtained when SO2 was used instead of O2. In the O2-added system, a total of 16 transitions ranging from Δv(8→7) to (4→3) were identified. Addition of SO2 increased the total number of lines to 34, lasing in the range between (11→10) and (4→3). This enhancement is ascribed to the occurrence of the reaction In addition to these chemical effects, the effects of flash energy, inert gases and total pressures have been investigated. 相似文献
939.
S. Pandey K. A. Fletcher W. E. Acree Jr C. Fetzer 《Fresenius' Journal of Analytical Chemistry》1998,360(6):669-674
Applicability of the nitromethane selective quenching rule for discriminating between alternant versus nonalternant polycyclic
aromatic hydrocarbons (PAHs) is examined for 20 representative PAH solutes dissolved in micellar sodium dodecylsulfate (SDS)
+ cetyltrimethylammonium bromide (CTAB), SDS + dodecyltrimethylammonium bromide (DTAB), SDS + Brij-35, and SDS + sodium octanoate
(SO) mixed surfactant solvent media. Experimental results show that nitromethane quenched fluorescence of all 8 alternant
PAHs studied in the four different solvent systems. Unexpected quenching behavior was observed, however, in the case of nonalternant
PAHs. Nitromethane quenched fluorescence emission of nonalternant PAHs dissolved in the SDS + SO solvent media, which is contrary
to the selective quenching rule. In the case of the mixed anionic + cationic surfactant solvent media, nitromethane quenching
selectivity was restored at concentration ratios of approximately 4 : 1 (anionic:cationic) or less.
Received: 22 May 1997 / Revised: 29 September 1997 / Accepted: 3 October 1997 相似文献
940.
Nielsen MB Moonen NN Boudon C Gisselbrecht JP Seiler P Gross M Diederich F 《Chemical communications (Cambridge, England)》2001,(18):1848-1849
Novel extended tetrathiafulvalenes (TTFs) with hexa-2,4-diyne-1,6-diylidene spacers between the two 1,3-dithiole rings and laterally appended alkynyl moieties for one- and two-dimensional scaffolding were synthesised and investigated for their electronic properties. 相似文献