ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Articles  (1,595)
  • Articles: DFG German National Licenses  (1,595)
  • Springer  (1,595)
  • American Meteorological Society
  • American Physical Society (APS)
  • Cambridge University Press
  • De Gruyter
  • Springer Nature
  • Wiley
  • 2000-2004
  • 1980-1984  (1,041)
  • 1960-1964  (259)
  • 1955-1959  (202)
  • 1935-1939  (93)
  • 1930-1934
  • 1983  (1,041)
  • 1962  (259)
  • 1956  (202)
  • 1936  (93)
  • Geosciences  (1,595)
Collection
  • Articles  (1,595)
Source
Publisher
Years
  • 2000-2004
  • 1980-1984  (1,041)
  • 1960-1964  (259)
  • 1955-1959  (202)
  • 1935-1939  (93)
  • +
Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 13 (1983), S. 221-229 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract C18H10S2,M=290.34, monoclinic,P21,a=20.556(5),b=15.843(3),c=3.963(1) Å,β=92.79(2)° at 18°C,Z=4,D x =1.496 g cm−3,μ(Cu Kα)=3.53 mm−1. Full-matrix least-squares refinement resulted in a final conventionalR value of 0.036 for 2030 observed reflections. The average C-S bond distance is 1.747(16) Å, the S-S bond length is 2.074(1) Å. The torsion angles at the disulfide group are close to zero, at 3.5 and 0.8°. The carbon frameworks are nearly planar, and closely approximate symmetrymmm. Bond distances are comparable with those in related molecules.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 13 (1983), S. 231-239 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The results of an X-ray structure determination of one of the three possible chloride salts of [Cr(en) F2(OH2)2]+ show the two fluoro ligands to betrans to each other. The purple crystals are monoclinic in the space groupC2/c-C 2h 6 , witha=11.409(3),b=9.319(2),c=10.260(3) Å,β=128.73(2)° andD c =1.73 g cm−3 forZ=4. Least-squares refinement based on 1341 independent observed reflections resulted in a finalR of 0.026. The molecule lies on a crystallographic two-fold axis, and the Cr-F, Cr-N, and Cr-O bond lengths are 1.885(1), 2.044(2), and 1.997(2) Å respectively. It is suggested that the ill-defined shoulder in the visible electronic spectrum of this complex is indicative of atrans dihalo geometry.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 13 (1983), S. 263-272 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The X-ray crystal structure of 3-ammonium-4-hydroxyphenylarsonic acid chloride dihydrate has been determined from single-crystal diffraction data. The compound crystallizes in the orthorhombic space groupPna 21 with four molecules in a unit cell of dimensionsa=17.712(7),b=13.468(4), andc=4.798(2) Å. The structure was solved by the Patterson method and refined to a finalR value of 2.1%. The average C-C phenyl distance is 1.393 Å, but two bonds are somewhat shorter than the others. This, coupled with the fact that the C-O and C-As bonds are shorter than normal, makes it appear as if there is a minor resonance contributor of a keto form. The C-N bond length of 1.443 Å is intermediate between values found in aminophenols and other ammoniumphenols. The H2AsO3 group is nearly tetrahedral, with the double-bonded oxygen rotated 9° out of the phenyl plane about the C-As bond. There is an extensive hydrogen-bonding system, involving every one of the OH and NH hydrogens, through the chloride and the waters of crystallization.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 13 (1983), S. 279-292 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The crystal and molecular structure of white (MNA-1) and yellow (MNA-3) forms of 4-methyl-2-nitroacetanilide have been determined by X-ray diffraction techniques. The crystals of MNA-1 are monoclinic,a=10.421(2),b=9.980(2),c=9.568(2) Å,β=99.51(2)°, space groupP21/c,Z=4. Crystals of MNA-3 are triclinic,a=17.956(2),b=12.908(2),c=4.039(1) Å,α=93.13(2)°,β=83.71(2)°, γ=90.77(2)°, space groupP¯1,Z=4. Both structures were solved by direct methods using theShelx-76 system of programs, and refined using full-matrix least squares. The number of unique reflections used in refinement and the finalR values are: MNA-1, 1545, 0.067; MNA-3, 3127, 0.065. The two distinct molecules in MNA-3 have intramolecular hydrogen bonds and different molecular conformations, although both are fairly planar, and each type is closely packed in columns of parallel molecules along thec direction. In MNA-1 the C=O⋯H-N geometry is indicative of intermolecular hydrogen bonding and the molecules adopt a conformation in which the nitro and amide groups lie in planes at approximately 45° to the benzene ring.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 13 (1983), S. 303-310 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound has been synthesized and its structure at room temperature has been solved. It crystallizes in the space groupP21/c, witha=9.581(5),b=13.746(4),c=8.869(1) Å, β=101.000(5)°, andZ=2. The structure was refined toR=0.029 from 1738 reflections. It consists of centrosymmetric dimeric units with two asymmetric end-to-end azido bridges. Each copper(II) ion is fivefold coordinated in the form of a slightly distorted square-based pyramid CuN5. The apical position is occuped by a nitrogen atom of the azido bridge with a Cu-N apical bond of 2.456(6) Å. The Cu-N bond with the azido bridge in the basal plane is 1.979(5) Å. The intradimer Cu⋯Cu distance is 5.004(2) Å. The magnetic properties and the X-band EPR spectrum are interpreted in the light of these structural data.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 13 (1983), S. 333-353 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The X-ray crystal structure of a racemic mixture of D- and L-penicillamine has been determined. Crystals are monoclinic,P21/c (No. 14), with cell dimensionsa=11.624(3),b=5.919(1),c=11.482(2) Å,β=114.48(2)°, andZ=2, based on the racemate. The structure was determined by standard methods and refined toR 1=0.0666,R 2=0.0726 for 985 independent reflections. Bond lengths and bond angles do not differ from those in similar structures. Mass spectra and1H and13C NMR spectra are reported ford-penicillamine, and detailed infrared and Raman spectra are reported for solidd-penicillamine hydrochloride,d 5-d-penicillamine hydrochloride,d-penicillamine,d 4-d-penicillamine, anddl-penicillamine. The Raman spectrum ofd-penicillamine in H2O solution as a function of pH is also reported.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 13 (1983), S. 1-7 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The crystal structure of SnBr[N(SiMe3)2]3 has been determined from three-dimensional X-ray diffraction data collected by counter methods. This compound crystallizes in the rhombohedral space groupR3c witha=11.970(3) Å, α=99.06(3)°, andZ=2forD c〉 =1.37 g cm−3. The finalR value was 0.027 based on 608 independent observed reflections. The molecule lies on a crystallographic three-fold axis which contains the Sn and Br atoms. The bromine atom is covalently coordinated to the tin atom at a Sn-Br separation of 2.519(2) Å. The three nitrogen atoms complete the bonding to tin with an Sn-N bond length of 2.056(7) Å.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 13 (1983), S. 19-29 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract C26H38O4,Mr=414.6, is monoclinic,P21/c, witha=15.059(2),b=7.348(2),c=23.164(3) Å,β=90.35(16)°,V c =2563.13(85) Å3,D x =1.07(4) g cm−3,μ(CuKα)=5.28 cm−1. The structure was determined by direct methods and refined by full-matrix least squares toR=0.074 for 2479 observed reflections. The two cyclohexane rings both adopt a chair conformation.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 13 (1983), S. 31-41 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract 13α-Hydroxy-α-isolupanine (I) and 13β-hydroxy-α-isolupanine (II) crystallize in the space groupP212121 witha=13.123(2),b=13.221(3),c=8.224(1) Å,Z=4 anda=9.745(2),b=11.383(1),c=12.710(2) Å,Z=4, respectively. Structural differences between the epimeric molecules are concentrated around ringA. In (I) ringA has a half-chair conformation, and in (II) it is a distorted sofa. TheA/B ring junction configuration isquasi-trans in the case of (I) andquasi-cis in (II). The above differences can be explained by the different intermolecular interactions observed in these two structures.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 13 (1983), S. 61-70 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...