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  • 1
    ISSN: 0009-2940
    Keywords: Hexadeamino-hexaisocyano-neomycin B ; Organometallic complexes ; Gold ; Chromium ; Rhodium ; Iridium ; Ruthenium ; Palladium ; Platinum ; Hexanuclear carbene gold(I) complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: From the amino glycoside neomycin B, the acetate-protected hexaisocyanide 4 has been prepared. 4 forms the hexanuclear complexes [(4)(AuCl)6] (5), {(4)[Cr(CO)5]6}, {(4)[MCl2(η5-C5Me5)]6} (M = Rh, Ir), {(4)[RuCl2(p-cymene)]6}, {(4)-[MCl2(PR3)]6} (M=Pd, Pt), and 4{(4)[PdCl(C6H4CH2NMe2)]6). The hexaisocyanohexagold(I) complex 5 reacts with H2NtBu and PhNH2 to give the corresponding carbene complexes. The compounds have been characterized by IR, 13C- and 31P-NMR spectroscopy, and (partially) by FAB-MS data.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: Schiff bases ; Polyene dialdehydes ; α-Amino acids ; Pantamethylcyclopentadienyl complexes ; P ligands ; Iridium ; Palladium ; Platinum ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Schiff bases 1—11 were synthesized from α-amino acids or o-aminophenol and crocetindialdehyde, 2,7-dimethyloctatrienedial, terephthalaldehyde, or β,β′ -p-phenylendiacroleine. The reactions of these Schiff bases with chloro-bridged complexes [(R3P)(Cl)M(η-Cl)]2 (M = Pd, Pt) and [(C5Me5)(Cl)Ir(°Cl)]2 gave the dinuclear complexes 12-31.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1434-1948
    Keywords: α-Metallated amino acids ; Palladium ; Platinum ; Oxidative addition ; α-Bromoglycinate ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidative addition of methyl N-benzoyl-2-bromoglycinate to bis(dibenzylideneacetone)palladium, in the presence of 2,2′-bipyridyl, and to (Ph3P)2Pt(η2-C2H4) gives the α-metallated glycine esters 1a and 2a. Abstraction of bromide from 1a, 2a, using AgSbF6 or AgBF4, affords the cationic C,O-chelate complexes [(bpy)Pd-CH(CO2Me)NHC(Ph)O]+ (1b,c) and [(Ph3P)2Pt-CH(CO2Me)NHC(Ph)O]+ (2b), respectively, featuring coordination of the amide O atom. The complexes 1b and 2b have been characterized by X-ray diffraction.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 93-99 
    ISSN: 1434-1948
    Keywords: 2-Methyl-1,2,3,4-tetrazole-5-thiolates ; 2-Phenyl-1,2,3,4-tetrazole-5-thiolates ; Palladium ; Platinum ; Copper ; Silver ; Gold ; Molecular structures ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The molecular structures of nine transition metal tetrazolethiolates have been determined by X-ray structure determinations. The ligand is invariably coordinated through its sulfur atom to the metal center [M = PdII, CuI, AgI, AuI, AuIII, and Hg]. The M-S-C bond angles vary considerably, but this cannot be correlated with variations in the C-S bond lengths. Intermolecular association occurs for Ph3PAu(SCN4Me) via Au-S contacts, leading to dimeric strands in the solid state. The copper compound (Ph3P)3Cu4(SCN4Me)4 (5), possesses a rather asymmetric structure: one Cu atom is tricoordinated by 3 sulfur atoms, the other three are tetracoordinated by P and N as well as by S atoms.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 471-482 
    ISSN: 1434-1948
    Keywords: Quinine ; Cinchonine ; Palladium ; Platinum ; Silver ; Gold ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of metal complexes in which quinine (L1) and cinchonine (L2) are coordinated via the four possible donor atoms was prepared and characterized. Coordination of the tertiary N atom of quinine is observed in [L1MPPh3]+NO3- [M = Au (1), Ag (2)], [L1Pd(COD)(Cl)]+ NO3- (3) and L1Pd(Cl)(allyl) (4). The mono anion of quinine functions as N,O chelate ligand in (L1-H+)M(Cl)(PR3) (M = Pd, Pt, 5-10), [(L1-H+)Pd(en)]+NO3- (11) and (L1-H+)2TiCl2 (12). Protection of the tertiary N atom of quinine by methylation or protonation allows the synthesis of the quinoline complexes [(L1CH3+)M(Cl)2(PR3)]+ BF4- (M = Pd, Pt, 14-18), [(L1CH3+)Ir(Cl)2(Cp*)]+ BF4- (19), [(L1+H+)M(Cl)2(PR3)]+ CF3SO3- (M = Pd, Pt, 20-22) and (L2+H+)(ZnCl3-) (23). Quinine and cinchonine act as N,O-N bridge in the complexes (R3P)(Cl)M(μ-L1-H+)M(Cl)2(PR3) (M = Pd, Pt, 24, 25, 27, 28), (Cp*)(Cl)Ir(μ-L1-H1)Ir(Cl)2(Cp*) (29), (EtP3)(Cl)Pd(μ-L2-H+)Pd(Cl)2(PEt3) (26), and as N-N bridge in the complexes [(Ph3P)Au(μ-L1)Au(PPh3)]+NO3- (30) and (allyl)(Cl)Pd(μ-L1)Pd(Cl)(allyl) (31). Coordination of quinine via the C=C double bond occurs in [(L1+2 H+)PtCl3]+Cl- (32). The structures of 11, 13, 19, 23, 26 and 32 were determined by X-ray diffraction. In most cases the coordination mode and the conformation of quinine can also be derived from the 1H-NMR spectra.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1434-1948
    Keywords: Palladium ; Azide ; Pyridine ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Palladium(II) azide (1) was synthesized by reaction of palladium nitrate and sodium azide. 1 was characterized by AAS, IR, and 14N-NMR spectroscopy. Bis(azido)bis(pyridine)palladium(II) (2) and tetramminepalladium tetraazidopalladate(II) (3) were synthesized by a high-yield reaction. Both were characterized by X-ray structural analysis, IR, Raman, and NMR spectroscopy.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1434-1948
    Keywords: 2-Phenyl-4-R-5(4H)-oxazolones ; Iridium ; Palladium ; Platinum ; Iron ; Chromium ; C-o,N-Bridging 2-phenyloxazolone ; Peptide labelling ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of 2-phenyl-4-R-5(4H)-oxazolones (R = Me, CH2Ph, CHMeEt) with [(η5-C5Me5)IrCl2]2 afforded the cyclometallated complexes (η5-C5Me5)(Cl)Ir(L) (1-3) [L = 2-phenyl-4-R-5(4H)-oxazolone(C-o,N)]. 2-Phenyl-5(4H)-oxazolone reacts with [(η5-C5Me5)IrCl2]2 and palladium(II) acetate to give complexes with a C-o,N-bridging oxazolone [(η5-C5Me5)(Cl)Ir]2(μ-Cl)(μ-L-H+) (4) and Pd3(μ-ac)5(μ-L-H+) (5). 2-Phenyloxazolone anions were added to the π ligands of [(η5-C6H7)Fe(CO)3]+ and [(η7-C7H7)Cr(CO)3]+ to give the adducts 6-11. Dipeptide derivatives 12-18 were obtained by reaction of 1, 2 and by reaction of the adduct 6 from [(η5-C6H7)Fe(CO)3]+; and the anion of 2-phenyloxazolone with α-amino acid esters. These reactions may be used for the labelling of peptides. Saponification of 15-18 yields the organometallic substituted peptide acids 19-22. Their dianions (deprotonation of COOH and peptide amide) were used as ligands towards (Ph3P)2PtCl2 to yield the bimetallic complexes 23-25. The structures of 4, 5, 9 and 10 were determined by X-ray diffraction.
    Type of Medium: Electronic Resource
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