596 research outputs found

    Kinematic differences between NLS1 and BLAGN sources

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    It is well-known that the higher policyclic aromatic hydrocarbon (PAH) abundance, lower black hole mass, higher accretion rate and lower luminosities are among the major characteristics of Narrow-Line Seyfert galaxies (NLS1), when they are compared to Broad line Seyfert galaxies (BLS1). NLS1s may be normal Seyfert galaxies at an early stage of evolution, their black holes may still be growing and/or they could be special for some other reason. In this work we discuss the findings that NLS1s have most of line and continuum luminosities correlated with FWHM(HĪ²\beta), which may be the trace of their rapid black hole mass grow. BLS1 do not show such trends. Also, PAHs may be destroyed as the black hole grows and the starbursts are removed, for NLS1 objects.Comment: Revisiting narrow-line Seyfert 1 galaxies and their place in the Universe - NLS1 Padov

    RXJ 0921+4529: a binary quasar or gravitational lens?

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    We report the new spectroscopic observations of the gravitational lens RXJ 021+4529 with the multi-mode focal reducer SCORPIO of the SAO RAS 6-m telescope. The new spectral observations were compared with the previously observed spectra of components A and B of RXJ 0921+4529, i.e. the same components observed in different epochs. We found a significant difference in the spectrum between the components that cannot be explained with microlensing and/or spectral variation. We conclude that RXJ 0921+4529 is a binary quasar system, where redshifts of quasars A and B are 1.6535 +/- 0.0005 and 1.6625 +/- 0.0015, respectively.Comment: 6 pages, 5 figures, accepted for publication in The Astrophysical Journal Letter

    The Action of Hydrazines upon \u27Thiazolidine-4-carboxylic Acids I. Preparation of D-Penicillamine from D-Benzylpenilloic Acid

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    In the reaction of phenylhydrazine with n-benzylpenilloic acids (Ia or Ila) n-penicillamine was obtained in high yield and purity. The lack of reactivity of N-acyl derivatives (Ib or Ub) with phenylhydrazine indicated that the above reaction proceeded through the open chain imine tautomer of Ia or Ila (IV). The epim~risation of n-benzylpenilloic acid (Ia and Ha) in aprotic solvents was studied by using PMR spectroscopy

    Ring Expansion of Thiazolidine and Nucleophilic Substitution in N-Acyl Derivatives of 6-Thia-3,8-diazabicyclo[3.2.1. ]octan-2-one

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    Reaction of N3,N8-diacyl 6-thia-3,8-diazabicyclo/3.2. l./octan-2- -one (I) with PC15 or S02Cl2 gave 6-chloro substituted N2,N5-diacyl 7-thia-2,5-diazabicyclo/2.2.2./octan-3-one (II). Treatment of II with water yielded the 6-hydroxy derivative (III) while reaction with methanol gave the 6-methoxy derivative (IV). Under the same reaction conditions the mono N8-acyl derivative (V) gave a mixture of 6-substituted 7-thia-2,5-diazabicyclo/2.2.2./octan-3-one and 4- -su bsti tuted 6-thia-3,8-diazabicyclo/3.2. l ./octan-2-one derivatives (XIV and XV; VI and VII; VIII and IX). It was proposed that ring expansion of thiazolidine and nucleophilic substitution occured vi a the thiiranium ion XIII as a common intermediate

    Preparation and lsomerization of 3S-Benzylpenicilloamides

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    The isomerization of 3S-benzylpenicillobenzylamide in aprotic solvents was studied by using 1H NMR spectroscopy. The lack of isomerization of the N-acetyl derivative of I indicated that the epimerization at C-5 and C-6 positipn2 proceeded through the open chain imine tautomer (III) of I or II. Since the isomerization at the C-6 position occurred after the opening of the thiazolidine ring, it was concluded that isomerization at this centre preceeded through penamaldic acid (IV) as an intermediate. All four isomersĀ· of 3S- benzylpenicillobenzylamide were prepared and isolated as methyl esters (II)
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