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  • Articles: DFG German National Licenses  (3)
  • N ligands  (2)
  • 2-Aminoethyl phosphate complexes  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 509-513 
    ISSN: 0009-2940
    Keywords: 2-Aminoethyl phosphate complexes ; Magnesium complexes ; Calcium complexes ; Zinc complexes ; Hydrogen bonding ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crystalline magnesium, calcium, and zinc 2-aminoethyl phosphate complexes containing the monoanions PEAH⊖ have been prepared as the tetrahydrates (Ca, Zn) and the hexahydrate (Mg), and their structures determined by single-crystal X-ray methods. The structures of monoclinic Ca(PEAH)2·4 H2O and Zn(PEAH)2·4 H2O (space group C2/c) both contain polymeric chains with metal ions connected by bridging phosphate groups. The zinc atoms are in a tetrahedral environment of four oxygen atoms, while the calcium atoms are found to be hexacoordinated with two additional oxygen atoms from water molecules in axial positions. The triclinic Mg(PEAH)2·6 H2O (space group \documentclass{article}\pagestyle{empty}\begin{document}$ P\bar 1 $\end{document}) contains discrete complex units with hexacoordinate magnesium atoms octahedrally surrounded by six oxygen atoms, four of which from water molecules in the equatorial plane and two from phosphate groups in axial positions.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 647-650 
    ISSN: 0009-2940
    Keywords: Gold(I) coordination ; 2-(Diphenylphosphanyl)aniline ; Ambidentate P ; N ligands ; P Ligands ; Ligand effects ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of 2-(diphenylphosphanyl)aniline (1) with (tetrahydrothiophene)gold(I) chloride in the molar ratio 1:1 gives a stable molecular complex 2, in which the gold atom is bonded to the phosphorus atom. Reaction of two equivalents of ligand 1 with one equivalent of the salt [(tht)2Au]ClO4 results in the displacement of both thioether ligands, affording the ionic complex {[(2-NH2C6H4)PPh2]2Au}+ ClO-4 (3a), in which the metal center is exclusively P-coordinated. Treatment of [(tht)2Au]ClO4 with ligand 1 (1:1) affords the mixed P/S-coordinated complex 4, the structure of which has been confirmed by single-crystal X-ray diffraction. The reaction of ligand 1 with [(Ph3P)Au]+ BF-4 leads to a mixture of products which are components of an equilibrium between the unsymmetrical salt {[(2-NH2C6H4)PPh2]Au(PPh3)} BF-4 with the two symmetrical species 3b (the BF-4 analogue of 3a) and [(Ph3P)2Au]+ BF-4, With {[(Ph3P)Au]3O}+ BF-4 as the aurating agent, the ligand 1 (molar ratio 1:1) is converted into a polynuclear complex 7, which is tentatively assigned a structure with intimate aggregation of six gold atoms.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 1417-1422 
    ISSN: 0009-2940
    Keywords: Gold ; N ligands ; Gold(I) complexes ; (Imine)gold(I) complexes ; Guanidines ; Ketimines ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: (Tetramethylguanidine)gold(I) chloride (1) and bromide (2) are readily prepared in high yield from (Me2N)2C=NH and [AuCl(Me2S)] or [AuBr(tht) (tht = tetrahydrothiophene), repectively. NMR spectra of chloroform solutions of the two products indicate equilibria of the type 2 LAuX = L2Au+AuX2-. The cationic complex [Au(NH=C(NMe2)2)(PPh3)]+ is obtained as the triflate salt 3 from tetramethylguanidine and [Au(PPh3)]+O3SCF3-. In solution at low temperature (-60°C), this compound adopts a rigid structure whereby the NMe2 groups are rendered non-equivalent, but at ambient temperature there is coalescence of the NMe2 signals in the 1H- and 13C-NMR spectra. The related benzophenoneimine complex [Au{NH=CPh2}(PPh3)]+BF4- (4), which was synthesized as a reference3 compound, exhibits similar behaviour. In solution at low temperature (-60°C) the two phenyl rings of the ligand are diastereotopic. In contrast, the triisopropylphosphane derivative [Au[NH=CPh2](PiPr3)]+BF4- (5) is rigid on the NMR time scale, even at 25°C. Thbe solid-state structures of 2, 3, 4, and 5 have been determined by single-crystal X-ray diffraction. Compound 2 crystallizes in the ionic form with discrete Au … Au bonded ion pairs [Au[NH=C(NMe2)2]2]+ [AuBr2]- [Au … Au 3.1413(8) Å]. The cations of 3, 4, and 5 show the [Au(PPh3)]+ units N-coordinated to the imino groups, with the nitrogen atoms in a trigonal-planar configuration.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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