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Summary The following compounds were synthesized by the reaction of secondary aliphatic amines with 2-alkoxyl-and 2 phenoxy vinylphosphonic dichlorides: the bisdimethylamides of 2-ethoxy-, 2-isopropoxy-, 2-butoxy, and 2 phonoxy vinylphosphonic acids; teh bisdiethylamides of 2-ethoxy-, 2-isopropoxy-, 2-butoxy-, and 2-phenoxyvinylphosphonic acids; the bisdibutylamides of 2-ethoxy-, 2-propoxy-, 2-isopentyloxy-, and 2-phenoxyl-vinyl-phosphonic acids; and the dipiperidides of 2-ethoxy-, 2-butoxy-, and 2-phenoxyl-vinylphosphonic acids.  相似文献   

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Summary The following compounds were prepared and characterized: 2-(ethylthio)vinylphosphonie and 2-(butylthio)vinylphosphonis dichlorides, dipropyl, dibutyl, diallyl, dihexyl, bis(2-methoxyethyl), and bis(2-ethoxyethyl) 2-(ethylthio)vinylphosphonates; dibutyl, diallyl, and dihexyl 2-(butylthio)vinylphosphonates; and 2-(ethylthio)vinylphosphonic dipiperidide.  相似文献   

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Russian Chemical Bulletin -  相似文献   

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The P—O stretching force constants of the phosphonic acids of the type CHxCl3-xPO3H2, in which x varies from 0 to 3, and their anions are interpreted in terms of (dπpπ)—bonding. The behaviour of the P—C stretching force constants in these compounds is also discussed.  相似文献   

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《Tetrahedron letters》1986,27(16):1751-1754
Phosphonic monoesters are prepared in a two—step procedure by DCC—DMAP mediated esterification of phosphonous acids and oxidation of the resulting phosphonous monoester.  相似文献   

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The paper compares building and decomposition pathways of two phosphonic acids, amino trimethylene phosphonic acid (ATMP) and 1-hydroxy ethylidene-1,1-diphosphonic acid (HEDP).The theoretical formation reactions were composed using elementary reactions and compared to reaction routes published in literature. As result, summary reaction pathways for both phosphonic acids are proposed which only vary in the number of reaction steps required. These reaction steps include carbonyl reactions, SN2-reactions, and ionic reactions. The synthesis of ATMP proceeds in three reaction steps, whereas HEDP is formed in one reaction. The thermal decomposition of both phosphonic acids in solid state was examined by combination of thermogravimetry coupled with infrared spectroscopy as well as pyrolysis gas chromatography coupled with mass spectrometry. Decomposition mechanisms were deduced and compared to the theoretical findings resulting in the conclusion that the decomposition processes of ATMP and HEDP follows the formation mechanism.Thus, the suitability of theoretical considerations for the understanding of thermal decomposition processes is shown.  相似文献   

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Summary Polynuclear chromium(III) and iron(III) complexes with hydroxyethylidenediphosphonic acid (H4L1), ethylenediphosphonic acid (H4L2),o-phenylenediamine-N,N-bis(methylenephosphonic acid) (H4L3), ethylenediamine-N, N, N, N-tetrakis(methylenephosphonic acid) (H8L4) ando-phenylenediamine-N, N, N, N-tetrakis-(methylenephosphonic acid) (H8L5) have been prepared and characterised by elemental analyses, magnetic measurements, i.r., electronic Mössbauer spectra. The compounds are anti-ferromagnetic.  相似文献   

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1.  The formation of protonated and free Schiff's bases from S-alanine and salicylaldehyde was studied quantitatively by the PMR method in the interval of pD 9.0–12.0.
2.  The rate constants of the racemization of S-alanine and its Schiffs base with salicylaldehyde protonated at the nitrogen were determined, and they were compared with the analogous constants for N-salicyl-idene-S-alaninate complexes of Cr(III), Rh(III), and Co(III) and the Schiffs base from pyridoxal and S-alanine.
3.  The basic role of the metal in the model reactions consists of increasing the concentration of reactive particles in solution as a result of coordination of the Schiffs base with the metal ion.
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Conclusions The tetra- and dicyanoethylation products of the sodium bis-(N-salicylideneglycinato)cobaltate(III) complex were isolated and characterized. The condensation of the complex with methyl acrylate and aeetaldehyde respectively leads to the formation of glutamic acid and racemic threonine.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 12, pp. 2772–2776, December, 1972.  相似文献   

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1.  Diastereomeric complexes of - and -bis-[N-salicylidene-S-alaninato]chromate(III)K and - and -bis-[N-salicylidene-S-valinato]chromate(III)K were synthesized and chromatographically separated. The absolute configuration of the diastereomers was demonstrated with the aid of ORD curves.
2.  The kinetics of the epimerization of - and -bis-[N-salicylidene-S-alaninato]chromate(III)K and - and -bis-[N-salicylidene-S-valinato]chromate(III)K under the action of OH ions in water was studied: it was shown that the proton of the amino acid fragment is less labile in these complexes than in the isostructural complexes of Co3+ and Rh3+.
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