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  • Walter de Gruyter GmbH  (69)
  • Chemistry/Pharmacy  (69)
  • 1
    Online Resource
    Online Resource
    Walter de Gruyter GmbH ; 1983
    In:  Zeitschrift für Naturforschung B Vol. 38, No. 12 ( 1983-12-1), p. 1643-1651
    In: Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 38, No. 12 ( 1983-12-1), p. 1643-1651
    Abstract: Steady-state γ-radiolysis of 5 × 10 -4 M pyrimidine and purine 2′-deoxyribonucleosides in aqueous solutions saturated with N 2 , N 2 O and O 2 , respectively, have been carried out in the presence of 0.1 M KBr. The main final degradation products have been isolated and characterised by various spectroscopic measurements including 1 H and 13 C NMR, UV, C.D. and mass spectrometry. The radiation-induced decomposition of thymidine is mostly accounted for by an ionic mechanism involving Br 2 , the decay product of Br 2 -·, as the reactive oxidising specie. On the other hand the degradation of the purine ring of 2′-deoxy-adenosine and 2′-deoxyguanosine may be accounted for by the action of Br 2 -·or Br 3 ·2-
    Type of Medium: Online Resource
    ISSN: 1865-7117 , 0932-0776
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    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 1983
    detail.hit.zdb_id: 2078109-X
    detail.hit.zdb_id: 124635-5
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  • 2
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    Online Resource
    Walter de Gruyter GmbH ; 1967
    In:  Zeitschrift für Naturforschung B Vol. 22, No. 6 ( 1967-06-1), p. 587-596
    In: Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 22, No. 6 ( 1967-06-1), p. 587-596
    Abstract: Ethylpolyphosphates have been prepared by reacting P 4 O 10 with either triethylorthophosphate or with ethylether. Phenylpolyphosphates were prepared from P 4 O 10 and triphenylorthophosphate at 300 °C. By the same procedure, o-kresylpolyphosphates could also be obtained, but not p-nitro-phenylpolyphosphates. The various polyphosphate esters were subjected to nuclear magnetic resonance analysis to characterize the distribution of phosphate moieties present, branching groups, middle groups, end groups, and orthophosphates. A true equilibrium between the units was found for ethylpolyphosphates and the systems could be accurately described by the theory of van Wazer. This theory does not seem to hold for the present results with polyphenylphosphates. However, the experimental data can be described quantitatively with a modified form of the theory. Ethylpolyphosphates can either phosphorylate or alkylate nucleophilic groups and alkylation is favored by the presence of protons. Only phosphorylation is observed with phenylpolyphosphates. Solvolysis of the polyphosphate esters with water or n-butanol leads to a very rapid disappearance of branching groups and a slow disappearance of the middle groups. The amount of reactive phosphorus can be calculated from the nuclear magnetic resonance data. The application of phenylpolyphosphates for a number of synthetic procedures is discussed.
    Type of Medium: Online Resource
    ISSN: 1865-7117 , 0932-0776
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    Language: Unknown
    Publisher: Walter de Gruyter GmbH
    Publication Date: 1967
    detail.hit.zdb_id: 2078109-X
    detail.hit.zdb_id: 124635-5
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  • 3
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    Online Resource
    Walter de Gruyter GmbH ; 1971
    In:  Zeitschrift für Naturforschung B Vol. 26, No. 7 ( 1971-7-1), p. 694-700
    In: Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 26, No. 7 ( 1971-7-1), p. 694-700
    Abstract: Reaction rates of the ethanolysis and hydrolysis of the phenyl- and methylpolyphosphate-esters and of tetraphenylpyrophosphate were measured by potentiometric titration methods. Exceptionally high rate constants were obtained for the solvolysis of these compounds, some reactions occurring with half-times of less than 10 seconds. The phosphorylating activity of the phenylpolyphosphateester on polyfunctional nucleophilic compounds (SN 2P -reaction) was tested and shown to exceed the activity of the conventional agent diphenylphosphoro-chloridate considerably. The catalytic effects of dimethylformamide were measured under several conditions and were shown to be complex solvent phenomena rather than conventional catalysis. The reactivity of the polyphosphate-esters is discussed with respect to their structure as well as the reactivity of P -O -P-bonds as a function of their ligands.
    Type of Medium: Online Resource
    ISSN: 1865-7117 , 0932-0776
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    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 1971
    detail.hit.zdb_id: 2078109-X
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  • 4
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    Walter de Gruyter GmbH ; 2014
    In:  Zeitschrift für Kristallographie - Crystalline Materials Vol. 229, No. 5 ( 2014-5-1), p. 353-367
    In: Zeitschrift für Kristallographie - Crystalline Materials, Walter de Gruyter GmbH, Vol. 229, No. 5 ( 2014-5-1), p. 353-367
    Abstract: The atomic structure of the incommensurate Pd 5 B 1-z phase has been analysed in detail by selected area electron diffraction and neutron-powder diffraction. That structure is based on a close-packed cubic arrangement of Pd atoms with the B atoms occupying the octahedral sites in a long-range ordered fashion. The ordering pattern of B is an incommensurately modulated one with a modulation vector of a length which changes with the B content ( ~ PdB 0.18-0.19 ) to adapt the ordering pattern continuously to the actual composition. The structure can be conceived to be constituted from “isolated” BPd 6 units (also occurring in the previously reported Pd 6 B phase) and edge-sharing B 2 Pd 10 octahedra units, which occur in a ratio reflecting the actual B content. As predicted on the basis of elastic interactions between B atoms, nearest neighbour B-B pairs occur (the B 2 Pd 10 double octahedra units) in the structure of the Pd 5 B 1-z phase, whereas occurrence of second-nearest neighbour B-B pairs is avoided. For the ideal composition Pd 5 B the crystal structure of the Pd 5 B 1-z phase corresponds to that of monoclinic UCl 5 with U playing the role of B and Cl that of Pd.
    Type of Medium: Online Resource
    ISSN: 2196-7105 , 2194-4946
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    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2014
    SSG: 13
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  • 5
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    Walter de Gruyter GmbH ; 1969
    In:  Zeitschrift für Naturforschung B Vol. 24, No. 6 ( 1969-6-1), p. 722-728
    In: Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 24, No. 6 ( 1969-6-1), p. 722-728
    Abstract: Inactivation cross sections of infectious ΦΧ-174-DNA in the extreme vacuum-ultraviolet were determined by irradiation of thin layers with monochromatic light down to 584 Å by means of a powerful grating-monochromator, the elements of which are described. Comparison of inactivation and light-induced electron emission shows that light of quantum energies below 7 eV inactivates by excitation only, whereas above 10.2 eV ionization is the predominant inactivation mechanism. Because of the satisfactory agreement of the curves for inactivation and electron emission, it is conducted that the remarkable increase of the inactivation cross section in the region of the short wavelength vacuum-uv is due to increasing ionization probability.
    Type of Medium: Online Resource
    ISSN: 1865-7117 , 0932-0776
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    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 1969
    detail.hit.zdb_id: 2078109-X
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  • 6
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    Walter de Gruyter GmbH ; 1979
    In:  Zeitschrift für Naturforschung B Vol. 34, No. 11 ( 1979-11-1), p. 1606-1611
    In: Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 34, No. 11 ( 1979-11-1), p. 1606-1611
    Abstract: A low temperature X-ray study of the enol of benzoylacetone indicates fixed positions of the C and O atoms within the enolic ring system and an extensive bond delocalisation over these atoms. The distribution of electron density between the two oxygen atoms shows that the enolic hydrogen is spread over a wide range. This is in accordance with a structural model proposed by de la Vega, whereupon the C and O atoms are kept fixed in their average positions during a tunneling process of the hydrogen between the two oxygen atoms. With this conception, the chemical shifts in the 17 O and 13 C NMR spectra, the 13 C 13 C spin coupling constants and the temperature independance of these values can be explained.
    Type of Medium: Online Resource
    ISSN: 1865-7117 , 0932-0776
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    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 1979
    detail.hit.zdb_id: 2078109-X
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  • 7
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    Walter de Gruyter GmbH ; 2014
    In:  Zeitschrift für Naturforschung B Vol. 69, No. 11-12 ( 2014-12-1), p. 1061-1072
    In: Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 69, No. 11-12 ( 2014-12-1), p. 1061-1072
    Abstract: 5,11,17,23-Tetrakis(trimethylsilylethynyl)-25,26,27,28-tetra-n-propoxycalix[4]arene (1) was synthesised in two steps starting from 25,26,27,28-tetra-n-propoxycalix[4] arene, and the structure of 1 was determined by X-ray diffraction. Compound 1 was desilylated (K 2 CO 3 ) to give 5,11,17,23- tetrakis(ethynyl)-25,26,27,28-tetra-n-propoxycalix[4]arene (2), which was tetra-aurated under basic conditions (NaOEt, THF) with a series of phosphane-gold chlorides (o-Tol 3 PAuCl, Ph 3 PAuCl, Ph 2 MePAuCl, PhMe 2 PAuCl, Me 3 PAuCl, Cy 3 PAuCl, t-Bu 3 PAuCl) to afford in good to excellent yields the tetra-aurated tetraethynylcalix[4]arene species 3-9 in one step [with phosphane ligands o-Tol 3 P (3), Ph 3 P (4), Ph 2 MeP (5), PhMe 2 P (6), Me 3 P (7), Cy 3 P (8), t-Bu 3 P (9)]. All compounds were characterised by 1 H NMR and infrared spectroscopy, mass spectrometry and by elemental analyses, additionally 3, 4, 5, 8 and 9 by 13 C{ 1 H}, and 3-6, 8 and 9 by 31 P{ 1 H} NMR spectroscopy. The molecular structures of complexes 3 and 9 were determined by X-ray diffraction and show pinched-cone conformations, but neither intra- nor intermolecular attractive aurophilic Au···Au contacts. The acceptor ability of complexes 3 and 9 was investigated by complexation attempts with various phosphane-gold chlorides and xenon gas under pressure, but interactions could not be determined experimentally. The formation of a complex between xenon and gilded calix[4]arene could, however, be predicted for fluorine-substituted species and with very small phosphane ligands (PH 3 ) on the basis of quantum-chemical calculations; the energy of formation is 9:6 kJ mol -1 . The crystal structure of Ph 2 MePAuCl was also determined and shows Au···Au-bonded dimers.
    Type of Medium: Online Resource
    ISSN: 1865-7117 , 0932-0776
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    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 2014
    detail.hit.zdb_id: 2078109-X
    detail.hit.zdb_id: 124635-5
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  • 8
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    Online Resource
    Walter de Gruyter GmbH ; 1996
    In:  Zeitschrift für Naturforschung B Vol. 51, No. 1 ( 1996-1-1), p. 1-8
    In: Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 51, No. 1 ( 1996-1-1), p. 1-8
    Abstract: Ba 2 Na(CN 2 )(CN) 3 was obtained by the reaction of Ba 2 N with melamine and NaCN at 700 °C. The compound was structurally characterized by single-crystal X-ray investigations (Fd3̄m, a = 1518.8(3) pm, Z = 16). In the crystal structure the Ba 2+ ions form a cubic close packed arrangement, the Na + and the CN 2- 2 ions occupy the octahedral interstices. The CN - ions are located within the close packed Ba 2+ layers. The unit cell of Ba 2 Na(CN 2 )(CN) 3 contains two interpenetrating substructures of the zinc-blende structure type, building up a variant of NaTl. A reversible phase transition has been observed during cooling of the compound. Whereas the Ba 2 (CN 2 )(CN) 3 sublattice remains nearly unaffected in this process, the Na + ions of the low-temperature phase are statistically distributed on two crystallographic positions.
    Type of Medium: Online Resource
    ISSN: 1865-7117 , 0932-0776
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    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 1996
    detail.hit.zdb_id: 2078109-X
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  • 9
    In: Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 50, No. 2 ( 1995-2-1), p. 159-167
    Abstract: The crystal structures of the thioether complexes [MCl 4 (SEt 2 ) 2 ] with M = Mo and W have been solved by X-ray methods. Both compounds crystallize isotypically in the triclinic space group P1̄ with two formula units per cell unit. The metal atoms are octahedrally coordinated by four chlorine atoms and by the two sulfur atoms of the thioether molecules in transposition (symmetry C i ) with bond lengths (average): Mo-Cl 233.1, Mo-S 253.4, W-Cl 233.1, and W-S 251.7 pm. Both complexes were also characterized by 1 H and 13 C NMR spectroscopy as well as by measurement of the magnetic susceptibilities in the temperature range from 1.8 to 350 K.
    Type of Medium: Online Resource
    ISSN: 1865-7117 , 0932-0776
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    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 1995
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  • 10
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    Online Resource
    Walter de Gruyter GmbH ; 1996
    In:  Zeitschrift für Naturforschung B Vol. 51, No. 2 ( 1996-2-1), p. 172-174
    In: Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 51, No. 2 ( 1996-2-1), p. 172-174
    Abstract: Single crystals of strontium danburite, SrB 2 Si 2 O 8 , were found after high-pressure treatment of SrSiO 3 /SiO 2 /Al 2 O 3 mixtures at 40 kbar and 1400°C, obviously formed by an unwanted side reaction with the boron oxide-containing boron nitride capsules used. The crystals are orthorhombic, space group Pnma, with a = 8.1891 (5), b = 7.9311 (6), c = 8.9284(5) Å and Z = 4. The structure was refined to R = 0.031, R w = 0.028 for 590 independent, absorption-corrected reflections. SrB 2 Si 2 O 8 is isostructural with danburite (CaB 2 Si 2 O 8 ). The structure comprises a tetrahedral framework of ordered B 2 O 7 and Si 2 O 7 groups which contains Sr in irregular coordination.
    Type of Medium: Online Resource
    ISSN: 1865-7117 , 0932-0776
    RVK:
    RVK:
    Language: English
    Publisher: Walter de Gruyter GmbH
    Publication Date: 1996
    detail.hit.zdb_id: 2078109-X
    detail.hit.zdb_id: 124635-5
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