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  • 1
    ISSN: 1434-4475
    Keywords: Bis(diphenylarsino)maleic acid, derivatives ; Bis(diphenylstibino)maleic anhydride, synthesis, crystal structure ; Bis(phenylthio)maleic acid, derivatives ; Maleic acid derivatives, synthesis, molecular structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The unusual properties of bis(diphenylphosphino)maleic anhydride and similar ditertiary phosphines has prompted the synthesis of analogous arsines and stibines. Bis(diphenylarsino)maleic anhydride,-maleic thioanhydride and-N-methyl maleic imide, bis(diphenylstibino)maleic anhydride (5) and-maleic thioanhydride are obtained as crystalline yellow or red compounds by the reaction of the corresponding 2,3-dichloromaleic acid derivatives with diphenyl(trimethylsilyl)arsine and-stibine resp. The uv/vis spectra and characteristic i.r. bands of selected compounds are given and compared with those of the corresponding phosphines. The strong shift of νC=C to lower wavenumbers observed in all compounds has caused the determination of crystal and molecular structure of5 by x-ray diffraction. Bond distances and angles are given. The complex formation of the new diarsine ligands has been examined by the preparation of Ni-, Cr- and Mo-carbonyl derivatives. As the first organylsulfane substituted maleic acid derivatives bis(phenylthio)maleic thioanhydride,-N-methyl-maleic imide and-maleic acid dimethylester are synthesized and described.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-4475
    Keywords: Crystal structure ; Electronic transitions and structure ; Oxalic acid phosphides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The unexpected violet colour of P,P′-tetraphenyl-oxalic acid diphosphide (3) stimulated the synthesis of the following derivatives: P,P′-tetra-t-butyl-oxalic acid diphosphide (2), N,P-tetraphenyl-oxalic acid amide phosphide (4) and P, α-triphenyl-glyoxylic acid phosphide (5). The compounds could be prepared by the reaction of the corresponding acyl chlorides with diorganyl-(trimethylsilyl) phosphine; (organyl=t-butyl and phenyl). The electronic transitions of green-blue2 and red5 in the 450–700 nm region are discussed, also theirv C=O in the ir spectrum. These results are interpreted in connection with the molecule structures of2 and3 which have been determined by X-ray crystal structure analysis. In2 the framework P−C(O)−C(O)−P is only slightly distorted from a coplanartrans-position, in3 somewhat more. The bonds at P have the expected pyramidal arrangement. The direction of the lone pairs at the P-atoms, derived from this bond arrangement, is discussed with respect to the electronic transitions in acyl phosphides.
    Type of Medium: Electronic Resource
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