Search results for "Two step"
showing 10 items of 34 documents
The Two‐Step Spin Conversion in a Supramolecular Triple Helicate Dinuclear Iron(II) Complex Studied by Mössbauer Spectroscopy
2006
The triple helicate dinuclear iron(II) complex, [Fe-2(L)(3)](ClO4)(4)center dot 2H(2)O (1), previously reported by Tuna et al. (Chem. Eur. J. 2004, 10, 5737), was prepared and characterised by detailed SQUID and Fe-57 Mbssbauer measurements. Compound 1 exhibits a thermochromic two-step spin conversion at T-SC((1)) ca. 240 K and T-SC((2)) ca. 120 K, but does not switch its spin state further below 20 K as proven by Mossbauer spectroscopy. The sharp variation of the susceptibility below 20 K is due to zero-field splitting of the remaining iron(II) high-spin species. Applied field Fe-57 Mossbauer spectroscopy experiments at 4.2 K indicate that the gradual thermal spin conversion from [HS-HS] p…
Two-step spin crossover behaviour in the chiral one-dimensional coordination polymer [Fe(HAT)(NCS)2]∞
2015
Solvated and unsolvated forms of the complex [Fe(HAT)(NCS)2]∞·(nMeOH) (1) (n = 1.5, 0; HAT = 1,4,5,8,9,12-hexaazatriphenylene) were prepared. The structure of 1·(1.5MeOH), measured at 120 K, showed that this system crystallizes in the homochiral P43 tetragonal space group. The solid is constituted of stacks of one-dimensional coordination polymers running along c-axis. All the FeII centres have the same Λ or Δ conformation and are in the LS state at 120 K. In the range of temperatures 10–300 K the magnetic properties of 1·(1.5MeOH) shows the occurrence of reversible spin crossover behaviour. However, above ca. 310 K complete desolvation of 1·(1.5MeOH) to give 1 was observed from crystal str…
A two-step synthesis of new macrobicyclic aza-ligands starting from “trans”dioxocyclam as diprotected macrocycle
1997
Abstract A rapid and convenient synthesis of two small aza-cryptands containing a 1,4,8,11-tetraazacyclotetradecane backbone is reported. This strategy can be applied to the preparation of many other aza-cages by varying the nature of the cross linker. Moreover, the two remaining secondary amine sites may allow the functionalization of these ligands or their grafting on a polymer.
Polyenolates of unsaturated carboxylic acids in synthesis. A straightforward synthesis of retinoic acids.
1990
Abstract Retinoic acids are prepared in a two step procedure by addition of lithium trienediolates of sorbic acid and 3-methyl-sorbic acid to β-ionone.
Two-Step Synthesis of 2-Aminoindolizines from 2-Alkylpyridines
2014
An efficient method for the synthesis of 2-aminoindolizines by the 5-exo-dig cyclization of 2-alkyl-1-(1-cyanoalkyl)pyridinium salts has been developed. These substrates were prepared by N-alkylation of 2-alkylpyridines with readily available cyanohydrin triflates. The method allows the introduction of various substituents at the 1-, 3-, 6-, 7-, and 8-positions and leaves no undesired acceptor groups in the products.
Die stufenweise Syntheseo,o?-methylenverbr�ckter Cyclohexamerer mitp-Kresol- oderP-Kresol- und 4-tert-Butylphenol-Bausteinen Vergleich mit �hnlich st…
1981
Two phenolic alcohols with six phenolic units in their molecules have been obtained by stepwise syntheses starting from simple phenolic derivatives. The phenolic alcohols were cyclized in a one step cyclization by boiling in a very diluted acetic acid solution. A two step cyclization of a phenolic alcohol with three phenolic units to a cyclohexamer proceeds only with poor yields. The cyclic compounds were compared with chainlike oligomers containing six phenolic units in their molecules.
Polymere ester von Säuren des phosphors, 5. Ringöffnende polymerisation des 2-phenoxy-1,3,2-dioxaphospholan durch Michaelis-Arbuzov-reaktion
1977
2-Phenoxy-1,3,2-dioxaphospholane (14) was polymerized by benzyl halogenides at temperatures between 120 and 200°C. It was found that the main chain consists predominantly of unexpected ethylene 1,2-ethanediphosphonate units 7; only about 10% of the monomer was incorporated as the expected 2-hydroxyethanephosphonate structure. An insertion mechanism, proposed by Harwood and Patel for the analogous polymerization of 2-phenyl-1,3,2-dioxaphospholane, does not agree with our experimental results. A hypothesis is developed involving a two step addition process, which exclusively occurs at the chain end. Alternating, one monomer molecule is added by a normal Michaelis-Arbuzov-reaction, and then a …
ChemInform Abstract: Two-Step Synthesis of 2-Aminoindolizines from 2-Alkylpyridines.
2015
5-Exo-dig cyclization of 2-alkyl-1-(1-cyanoalkyl)pyridinium triflates offers a convenient method for the synthesis of 2-aminoindolizines.
Zeitlicher Ablauf der ACTH-induzierten Stimulierung der Corticosteroidbiosynthese
1969
The time course of ACTH action was studied during incubation of quartered rat adrenals by estimation of corticosterone production and secretion rates. The results suggest a two step action of ACTH during the acute stimulation of corticosteroid biosynthesis: A modest initial stimulation was observed within the first 30 min of exposure to ACTH which was overlapped by a marked secondary stimulation between 30 and 60 min.
Simple two-step synthesis of 2,4-disubstituted pyrroles and 3,5-disubstituted pyrrole-2-carbonitriles from enones
2014
The cyclocondensation of enones with aminoacetonitrile furnishes 3,4-dihydro-2H-pyrrole-2-carbonitriles which can be readily converted to 2,4-disubstituted pyrroles by microwave-induced dehydrocyanation. Alternatively, oxidation of the intermediates produces 3,5-disubstituted pyrrole-2-carbonitriles.