Library

Language
Preferred search index
Number of Hits per Page
Default Sort Criterion
Default Sort Ordering
Size of Search History
Default Email Address
Default Export Format
Default Export Encoding
Facet list arrangement
Maximum number of values per filter
Auto Completion
Feed Format
Maximum Number of Items per Feed
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
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Some copper(II) complexes of the types: Cu(HPPK)-(PPK)X, Cu(HMPK)(MPK)X (where HPPK = syn-phenyl-2-pyridylketoxime, HMPK = syn-methyl-2-pyridylketoxime and X = Cl−, Br−, I−, NO3 −, SCN− or SeCN−) Cu(HPPK)2SO4 3 H2O and Cu(HMPK)2SO4 · 3 H2O were synthesized and characterized by analysis, magnetic susceptibility, e.s.r., reflectance and i.r. spectral measurements. The spectral data suggest that Cu(HPPK)(PPK)X and Cu(HMPK)(MPK)X containcis square-coplanar [Cu(HPPK)(PPK)]+ and [Cu(HMPK)(MPK)]+ units respectively, linked by weakly coordinated anions, giving infinite polymeric highly distorted octahedral chain structures, whereas Cu(HPPK)2SO4 · 3H2O and Cu(HMPK)2SO4 · 3 H2O have acis distorted octahedral structure containing two ligand molecules of ketoxime and a bidentate sulphate group. The polycrystalline e.s.r. spectra suggest a distorted octahedral stereochemistry for the CuII ion involving a $$d_{x^2 - y^2 } $$ ground-state. By using e.s.r. and reflectance spectral data, the orbital reduction parameters, k11 and k1 were calculated and interpreted in terms of molecular orbital coefficients.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...