Library

X
feed icon rss

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Calixarenes as second-sphere ligands for transition metal ions. Synthesis and crystal structure of [(H2O)5 Ni(NC5H5)]2(Na)[calix[4]arene sulfonate] · 3.5 H2O and [(H2O)4Cu(NC5H5)2]-(H3O)3 [calix[4]arene sulfonate] · 10 H2O (1992)
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 14 (1992), S. 37-46 
    Details
    ISSN: 1573-1111
    Keywords: Calix[4]arene ; crystal structure ; second-sphere coordination ; nickel(II) ; copper(II) ; pyridine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The title compounds crystallize such that bilayers of calixarenes are separated by hydrophilic layers. In each case the transition metal has, in addition to a primary sphere of ligands, a second-sphere coordination by a calixarene. [(H2O)5Ni(NC5H5)]2(Na)[calix[4]arene sulfonate]·3.5 H2O,1, crystallizes in the triclinic space groupP $$\bar 1$$ witha = 12.487(4),b = 14.281(2),c = 15.055(5) Å, α = 85.66(2), β = 80.07(2), γ = 80.48(2)°, andD c = 1.64 g cm−3 forZ = 2. Refinement based on 2441 observed reflections led to a finalR value of 0.066. There are two different environments for the nickel-containing cations: one is positioned within the hydrophilic layer with the pyridine ligand intercalated into the hydrophobic calixarene bilayer and the other is also positioned within the hydrophilic layer, but the pyridine ligand is inserted into the hydrophobic cavity of the calix[4]arene. [(H2O)4Cu(NC5HS)2](H3O)3[calix[4]arene sulfonate]·10 H2O,2, crystallizes in the triclinic space groupP $$\bar 1$$ witha = 15.438(4),b = 15.727(6),c = 12.121(9) Å, α = 112.74(4), β = 102.02(4), γ = 85.34(4)°, andD c = 1.57 g cm−3 forZ = 2. Refinement based on 3925 observed reflections led to a finalR value of 0.107. The structure is similar to that of 1 except that the one copper-containing cation spans the hydrophilic layer and is intercalated into the bilayer of calixarenes on one side and positioned into the calixarene cavity on the other.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01041364
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Thiocalix[4] arenes. I. Synthesis and structure of ethylthiocalix[4]arene methyl ether and the related structure of bromocalix[4]arene methyl ether (1990)
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 9 (1990), S. 195-206 
    Details
    ISSN: 1573-1111
    Keywords: Calix[4]arene ; thiocalixarene ; bromocalixarene ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Bromocalix[4]arene methyl ether serves as a precursor in the synthesis of the title thiocalixarene via the reagent CuSEt. Ethylthiocalix[4]arene methyl ether crystallizes in the monoclinic space groupP21/c witha = 20.577(9),b, = 10.722(5),c = 20.315(9) Å, β = 120.46(4)°, andD c = 1.24 g cm−3 forZ = 4. Refinement based on 1441 observed reflections led toR = 0.080. The configuration of the calixarene lies between the partial cone and the 1,3-altemate conformations. Bromocalix[4]arene methyl ether crystallizes in the triclinic space groupPI witha = 12.283(7),b = 17.658(9),c = 18.118(6) Å, α = 90.25(6), β = 105.95(4), γ = 105.11(6)°, andD c = 1.68 g cm−3 forZ = 4. Refinement based on 3028 observed reflections led toR = 0.083. The unit cell also contains four CHCl3 molecules which exist pairwise enclathrated by six calixarenes. The partial cone conformation of the bromocalixarene is identical to that of ethylthiocalix[4]arene methyl ether.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01053117
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Alternative methods of modifying the calixarene conformation. The synthesis and molecular structures oft-butylcalix[4]arene methyl ether complexed with aluminum alkyl species (1987)
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 5 (1987), S. 747-758 
    Details
    ISSN: 1573-1111
    Keywords: Calix[4]arene ; aluminum alkyl ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The configurations of calix[4]arenes may be modified by the formation of donor-acceptor complexes which make use of the basicity of the oxygen atoms of the macrocycle. The complex [t-butylcalix[4]arene methyl ether][AlMe3]2,2, exhibits the previously unseen ‘1,2-alternate’ geometry, while [t-butylcalix[4]arene methyl ether][MeAlCl2]2,3, and [t-butylcalix[4]arene methyl ether][EtAlCl2]2,4, show the ‘1,3-alternate’ configuration.2 crystallizes in the triclinic space groupPl witha=11.14(1),b=11.60(1),c=12.02(1) Å, α=77.32(8), β=67.91(8), and γ=69.34(8)o withD c =1.06 g cm−3 forZ=1. Refinement based on 1270 observed reflections led toR=0.106.3 as the benzene solvate belongs to the monoclinic space groupC2/c witha=12.116(2),b=21.557(7),c=23.470(6) Å, and β=104.05(2)o withD c =1.13 g cm−3 forZ=4. Refinement based on 2335 observed reflections led toR=0.075.4 crystallizes in the monoclinic space groupC2/c witha=12.062(4),b=21.175(6),c=21.596(5) Å, and β=100.78(4)o withD c =1.18 g cm−3 forZ=4. Refinement based on 2529 observed reflections gaveR=0.082. The Al-O lengths in all three complexes are normal for donor-acceptor interactions.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00656595
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    Organic clays. Synthesis and structure of Na5[calix[4] arene sulfonate] · 12 H2O, K5[calix[4]arene sulfonate]·8 H2O, Rb5[calix[4]arene sulfonate]·5 H2O, and Cs5[calix[4] arene sulfonate] ·4 H2O (1989)
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 7 (1989), S. 203-211 
    Details
    ISSN: 1573-1111
    Keywords: Calix[4]arene ; crystal structure ; clay mineral ; alkali metal ion ; layered structure ; water soluble ; sulfonate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The title calixarenes all exist in the solid state as bilayers of anionic calixarenes in the cone configuration. These layers alternate with inorganic regions which contain the cations and the water molecules. The overall structures bear a close resemblance to those found for clay minerals. The sodium salt crystallizes in the triclinic space groupPĪ witha = 10.998(6),b = 13.582(5),c = 14.472(5) Å,α = 74.01(3),β = 89.09(4),γ = 86.50(4)°, andZ = 2 forD calc = 1.72 g cm−3. Refinement based on 4727 observed reflections led to a conventionalR = 0.050. The potassium salt crystallizes in the triclinic space groupPĪ witha = 11.815(9),b = 13.636(6),c = 14.040(9) Å,α = 100.24(5),β = 111.86(9),γ = 95,14(9)°, andZ = 2 forD calc = 1.77 g cm−3. Refinement based on 2977 observed reflections led toR = 0.15. The rubidium and cesium salts are isostructural and crystallize in the monoclinic space groupP21/n with parameters for Rb[Cs]a = 11.603(5) [11.704(3)],b = 28.607(8) [29.747(9)],c = 12.512(5) [12.604(4)] Å,β = 91.70(4) [91.63(2)°], andZ = 4 forD calc = 2.01 [2.24] g cm−3. Refinement based on 1750 [4257] observed reflections led toR = 0.108 [0.075]. Disorder of the cations was observed for the rubidium and cesium salts.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01060722
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...