Library

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: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By the use of the 1H—1H and 1H—31P coupling constants in two analogues of aspartic acid i.e. 3-amino-3-phosphonatopropionic and 3-amino-3-(methylphosphinato) propionic acids, it was shown that the six parameter formulation for the evaluation of mole fractions of three staggered ethanic rotamers is not necessarily better than the two parameter formulation in this system. The results allowed the recommendation of the following values for the two vicinal proton parameters i.e. J(HH)g=2.3, J(HH)t=13.9 and for the two vicinal proton-phosphorus parameters i.e. J(HP)g=4.2, J(HP)t=33.0 Hz.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 14 (1980), S. 431-433 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1H and 31P NMR spectra of 3-amino-3-phosphonatopropionic acid, a phosphonic derivative of aspartic acid, have been measured and completely analysed for 14 pH values. The vicinal coupling constants, 3J(HH) and 3J(HP), were used to obtain information on the rotational isomerism of the amino acid. The most stable conformer is the one where the phosphonic and β-carboxyl groups are in trans position to each other.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 30 (1992), S. 163-168 
    ISSN: 0749-1581
    Keywords: ESR ; Iminoxy radicals ; Diethyl phosphonate ; 31P hyperfine interaction ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Iminoxy radicals of a new type, having the general formula RC(=NO·)P(O)(OEt)2, were synthesized and characterized by means of ESR spectroscopy. The presence of two isomers due to the different position of the C=NO· fragment with respect to the R substituent and the P atom, and the relative stability of the isomers, was established. The influence of the R substituent on the relative population of the isomers was found. The nitrogen hyperfine constants for the isomers differ by about 10%, while the phosphorus hyperfine constant for the less populated isomer is about six time greater, reaching a value of 60 G. A linear correlation was found between the values of this hyperfine constant and Dimroth-Reichardt ET(30)solvent parameters. The solvent dependence of the 31P hyperfine constant was shown to be stronger than the dependence found for the 14N hyperfine constant of nitroxides and iminoxyls.
    Additional Material: 3 Ill.
    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...