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  • Platinum complexes  (5)
  • Tungsten complexes  (5)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 253-257 
    ISSN: 0009-2940
    Keywords: Palladium complexes ; Platinum complexes ; Thioglycinate ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal complexes with biologically important Ligands, IL. - Palladium and Platinum(II) complexes of Thioglycinate and ThioalaninateFrom chloro phosphane complexes and thioglycinate or thioalaninate the chelate complexes (1) (r2 = Et, Ph, n-Bu) and (2) (M = Pd, Pt) have been obtained. Spectroscopic data and the X-ray analysis of 1a (R1 = H; R2 = Et) indicate bonding of the α-Amino acylchloride complexes Cl2Pt(NH2CHRCOCl)2 react with thiophenol to give Cl2Pt(NH2CHRCOSPh)2 (4) (R = H, CHMe2).
    Notes: Aus Chloro-phosphan-Metallverbindungen werden mit Thioglycinat bzw. Thioalaninat die Chelat-Komplexe (1) (r2 = Et, Ph, n-Bu) und (2) (M = Pd, Pt) erhalten. Nach den spektroskopischen Daten und der Kristallstrukturbestimmung von 1a (R1 = H; R2 = Et) koordinieren die Anionen der α-Aminothiosäuren über die Aminogruppe und das S-Atom. Aus α-Aminosäure-chlorid-Komplexen Cl2Pt(NH2CHRCOCl)2 entstehen mit Thiophenol in heterogener Reaktion die Verbindungen Cl2Pt-(NH2CHRCOSPh)2 (4) (R = H, CHMe2) mit α-Aminothiosäure-S-phenylester-Liganden.
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  • 2
    ISSN: 0009-2940
    Keywords: Fischer carbene complexes, anionic ; Carbene, methoxy(pentacarbonylrheniopropyl) ; Chromium complexes ; Molybdenum complexes ; Tungsten complexes ; Rhenium complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydrocarbon-Bridged Metal Complexes, XXII1). - Addition of Anionic Fischer Carbene Complexes to Coordinated Unsaturated Hydrocarbons with C - C CouplingThe addition of [(OC)5MC(OMe)CH2]- (M = Cr,W) to the cationic complexes [(OC)5Re(C2H4)]+ and [(OC)3M' (λ7-C7H7)]+ (M' = Cr, Mo) affords the bimetallic hydrocarbon-bridged complexes (OC)5M = C(OMe)CH2CH2CH2Re(CO)5 (1) and (OC)5M = C(OMe)CH2C7H7 - λ6 - M'(CO)3 (2), respectively. The structures of 1a and 2d have been determined by X-ray diffraction.
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  • 3
    ISSN: 0009-2940
    Keywords: Tungsten complexes ; Rhenium complexes ; Iron complexes ; Ruthenium complexes ; Osmium complexes ; Cobalt complexes ; Vinyl ; Cyclohexadienyl ; Cycloheptadienyl ; Cyclooctatrienyl ; Hydrocarbon-bridged complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydrocarbon-Bridged Complexes, XXX.  -  Nucleophilic Addition of Carbonylmetallates to Cationic Vinyl, Diene, Dienyl and Triene Complexes of Iron, Ruthenium and Cobalt: Di-, Tri-, Tetra- and Pentametallic Complexes with σ,σ- and σ,π-Hydrocarbon BridgesHerrn Professor Ekkehard Lindner zum 60. Geburtstag gewidmet.The reactions of [Re(CO)5]-, [Ru(CO)2Cp]-, and [Os(CO)4]2- with [Cp2(OC)2Fe2(μ-CO)(μ-η1:η2-CH=CH2)]+, [Cp*Ru(η2:η4-1,3,7-octatriene)]+, [(OC)Fe(η4-diene)(η5-cycloheptadienyl)]+, and [CpCo(η5-cyclodienyl)]+ give the nucleophilic adducts whereas with [Mn(CO)5]-, [W(CO)3Cp]-, and [Fe(CO)2Cp]- formation of the corresponding C-C coupling products and of the metal-metal-bonded dimers is observed. The structures of Cp*Ru(μ-η1:η2:η3-1,5-octadienyl)Re(CO)5 (4), [Cp* Ru(μ-η1:η2:η3-1,5-octadienyl)]2Os(CO)4 (6), and of (OC)-Fe(η4-1,3-cyclohexadiene) (μ-η1:η4-1,3-cycloheptadiene)Re(CO)5 (9) have been determined by X-ray diffraction.
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  • 4
    ISSN: 0009-2940
    Keywords: Palladium complexes ; Platinum complexes ; Rhodium complexes ; Iridium complexes ; Glycine, C-allyl-, C-vinyl- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal Complexes of Biologically Important Ligands, LVIII. - C-Allylglycine and C-Vinylglycine Complexes of Palladium(II), Platinum(II), Rhodium(III), Iridium(III) and Reactions with NucleophilesThe synthesis of the complexes (R13P)(Cl2Pt(C-allylglycine ester) (1), (2) and of (η5-C5Me5)Ir(C-allylglycinate) (6) with tridentate O,N,η2;-C—C allylglycinate as ligand is described. Addition of enolates (Nu-) to the coordinated C=C bond of 2 gives the γ-C-metallated α-amino acid ester complexes (3). In most cases the platination occurs stereoselectively to yield the five-membered metallacycle with the substitutents CH2Nu and CO2R2 in trans position. From 3d the new α-amino acid H2NCH(CO2Me)-(CH2)3C(Ph)(CO2Et)21 (4) is cleaved. The structures of 3c and 6 have been determined by X-ray diffraction. C-Vinylglycinate can be stabilized at the metal atom in the complexes (10) (M=Rh, Ir).
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  • 5
    ISSN: 0009-2940
    Keywords: Heterobimetallic complexes ; Tungsten complexes ; Iron complexes ; Ruthenium complexes ; Manganese complexes ; Rhenium complexes ; Diene bridges, σ,π-C6, -C7, and -C8 ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydrocarbon-Bridged Metal Complexes, XX. - Nucleophilic Addition of Carbonyl Metallates to Cationic Hexadienyl, Cyclohexadienyl, Cycloheptadienyl, and Cyclooctadienyl Complexes of Iron and Ruthium: Heterobimetallic Complexes with η1:η4, -C6, -C7, and -C8 Hydrocarbon BridgesThe addition of Re(CO)-5, Mn(CO)-5, and [(η5-C5H5)W(CO)3]- to the cationic dienyl complexes [(η5-dienyl)M(CO)3]+ (M = Fe, Ru; dienyl = hexadienyl, cyclohexadienyl, cycloheptadienyl, cyclooctadienyl, bicyclo[5.1.0]octadienyl) gives the heterobimetallic η1:η4-hydrocarbon-bridged complexes 1 - 4, 6, 7. In solution the initial nucleophilic adduct 2e of [(η5-cyclo-hexadienyl)Ru(CO)3]+ and [Re(CO)5]- rearranges to the complex 3, in which the Re(CO)5 group is bound to a sp2 carbon atom. By using Mn(CO)-5 also the products of electron transfer between cation and anion have been observed. The crystal structures of (OC)3Fe(μ-η4:η1-hexadiene)Re(CO)5 (1), (OC)3Ru(μ-η4:η1-cyclohexadiene)Re(CO)5(3), (OC)3Fe(η4:η4-C7H9 - C7H9)Fe(CO)3 (5), (OC)3Ru(μ-η4:η1-cyclooctadiene)Re-(CO)5 (6b), and of (OC)3Fe(η4:η1-bicyclo[5.1.0]octadiene)-Re(CO)5 (7) have been determined by X-ray diffraction.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 61-66 
    ISSN: 0009-2940
    Keywords: Benzimidazoline, 2-(1,3-dioxo-2-indanylidene)-, as chelate ligand ; Copper complexes ; Nickel complexes ; Palladium complexes ; Platinum complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal Complexes of Dyes  -  Transition Metal Complexes of Mono- and Dianions of 2-(1,3-Dioxo-2-indanylidene)-benzimidazolines2-(1,3-Dioxo-2-indanylidene)benzimidazolines (L) (1 - 6) react with metal salts and chloro-bridged complexes in the presence of NaH to give the mono and bis-N,O-chelate complexes (L  -  H+)2M (M=Cu, Pd, Ni) (7 - 9), (L  -  H+)M(PR3)Cl (M=Pd, Pt; 10 - 15 and (L  -  2H+)[Pt(PEt3)Cl]2 (16, 17). The electronic spectra of the bis(chelate) complexes show a large bathochromic shift of the absorptions in the visible region as compared to the free ligands. The structures of (L  -  H+)Pd(Cl)-(PnBu3) (10) and of (L  -  2H+)[Pt(Cl)PEt3)]2 (16) have been determined by X-ray crystallography. The two heterocyclic planes in 16 are bent along the elongated central C=C bond [143.2(12)pm] which gives a hip-roof-like structure.
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  • 7
    ISSN: 0009-2940
    Keywords: Manganese complexes ; Chromium complexes ; Molybdenum complexes ; Tungsten complexes ; Cycloheptatriene ; Cyclooctatriene ; Cyclooctatetraene ; Hydrocarbon-bridged complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydrocarbon-Bridged Complexes, XXV[1]. - C-C Coupling of Anionic Tricarbonyl Manganese Complexes of Cyclic Polyenes with Cationic Tropylium Metal Compounds; Preparation and Structure of (OC)3Mn(μ-η5:η6-C7H8-C7H7)M(CO)3, (OC)3Mn(μ-η5:η6-C8H10-C7H7)M(CO)3, and (OC)3Mn(μ-η5:η5-C8H8-C7H7)M(CO)3 (M = Cr, Mo, W)The addition of the anionic complexes [(η4-C7H8)Mn(CO)3]-, [(η4-C8H10)Mn(CO)3]- and [(η4-C8H8)Mn(CO)3]- to the cations [(η7-C7H7)M(CO)3]+ (M = Cr, Mo, W) gives the hydrocarbon-bridged complexes (OC)3Mn(μ-η5:η6-C7H8-C7H7)M(CO)3, (OC)3Mn(μ-η5:η6-C8H10-C7H7)M(CO)3, and (OC)3Mn(μ-η5:η6-C8H8-C7H7)M(CO)3 (M = Cr, Mo, W). The structures of 4b and 6a have been determined by X-ray diffraction.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 2347-2350 
    ISSN: 0009-2940
    Keywords: Indigo, octahydro- ; Pyrrole indigo, 4,4′-dibutyl-5,5′-dimethyl- ; Zinc complexes ; Copper complexes ; Rhodium complexes ; Iridium complexes ; Palladium complexes ; Platinum complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal Complexes of Dyes, III[1,2]. - Transition Metal Complexes of Pyrrole Indigo The dianions of octahydroindigo and 4,4′-dibutyl-5,5′-dimethylpyrrole indigo (L) react with metal salts and chloro-bridged complexes [(μ-Cl)M(Cl)PR3]2 (M = Pd, Pt; R = nBu, Et), [(μ-Cl)M(Cl)(η5-C5Me5)]2 (M = Rh, Ir) to give the bis-N,O chelate complexes [M(L - 2H+)]n (M = Cu, Zn), (L - 2H+)[M(Cl)(PR3)]2 (M = Pd, Pt), and (L - 2H+)[M(Cl)(η5-C5Me5)]2 (M = Rh, Ir). The electronic spectra of the soluble complexes with phosphane or C5Me5 ligands show a large bathochromic shift of the absorptions in the visible region compared to the free neutral ligands which is in accordance with PPP calculations of model compounds.
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  • 9
    ISSN: 0009-2940
    Keywords: Gold complexes ; Palladium complexes ; Platinum complexes ; Rhodium complexes ; Iridium complexes ; 3′-Azido-3′-deoxythymidine ; 3′-Isocyano-3′-deoxythymidine ; Anti-HIV ; Antiinflammatory activity ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Metal Complexes of Biologically Important Ligands, LX.  -  Metal Complexes of 3′-Azido-3′-deoxythymidine (AZT) and 3′-Isocyano-3′-deoxythymidineMetal complexes of N-3-deprotonated 3′-azido-3′-deoxythymidine (AZT  -  H+), (AZT  -  H+)AuPR3 (R = Me, Et, Ph) (2, 3, 4), trans-(AZT  -  H+)2Pd(NH3)2 (5), [(n-Bu3P)(AZT  -  H+) M(μ-Cl)2M(AZT  -  H+)(n-Bu3P)] (M = Pd, Pt) (6, 7), trans-(Ph3P)2Pd(AZT  -  H+)2 (8), cis-(Ph3P)2Pt(AZT -  H+)(Cl) (9), and complexes of 3′-isocyano-3′-deoxythymidine (L), (Et3P)(L)- PdCl, (11), (12), (n-Bu3P)(L)PtCl2 (13), [(Ph3P)2(L)PtCl](BF4) (14), (η5-C5Me5)(L)RhCl2 (15), and (η5-C5Me5)(L)IrCl2 (16) have been prepared and characterized by IR and NMR spectra, 2 by X-ray crystallography. 2, 4, and 9 show an anti-HIV activity very similar to AZT; 2 exhibits antiinflammatory activity.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 729-734 
    ISSN: 0009-2940
    Keywords: Lewis acids, organometallic ; 12-e- Systems ; Alkyne complexes ; Molybdenum complexes ; Tungsten complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organometallic Lewis Acids, LIV.  -  Mo(CO)2(PPh3)2(O3SCF3)2: A New Precursor for an Organometallic Dicationic Lewis Acid with Three Accessible Coordination SitesThe reaction of Mo(CO)2(PPh3)2Br2 (1) with AgO3SCF3 gives the bis(triflate) complex Mo(CO)2(PPh3)2(O3SCF3)2 (3) which can be considered as a precursor for the 12-e- system “Mo-(CO)2(PPh3)2+2”. According to the spectroscopic data one of the two coordinated CF3SO-3 anions is acting as a chelate ligand. Treatment of 3 and of the in situ generated W(CO)2(PPh3)2(O3SCF3)2 (4) with H2O affords the dinuclear hydroxo-bridged complexes [M2(μ-OH)3(CO)4(PPh3)4][CF3SO3] (5: M = Mo; 6: M = W). Acetonitrile replaces the CF3SO-3 ligands in 3 and 4 to afford the cationic complexes [M(CO)2(PPh3)2(NCMe)3][CF3SO3]2 (7: M = Mo; 8: M = W). The reaction of 3 with an excess of 2-butyne and 1-phenyl-1-propyne leads to the monoalkyne complexes Mo(CO)(MeC≡CR)(PPh3)2(O3SCF3)2 (9: R = Me; 10: R = Ph) in moderate yield. In contrast, the bisalkyne complexes [M(CO)(MeC≡CMe)2(PPh3)2(O3SCF3)][CF3SO3] (11: M = Mo; 12: M = W) are formed in high yield when a CH2Cl2 solution of 2-butyne is added to 1 and 2 in the presence of AgO3SCF3. At room temperature, 11 and 12 are highly fluxional in solution, while 9 and 10 are stereochemically rigid. Treatment of 11 with acetonitrile yields [Mo(CO)(MeC≡CMe)2(PPh3)2(NCMe)][CF3SO3]2 (13). Compounds 3-13 (except 4) are characterized by IR, 1H-, 13C-, 19F-, and 31P-NMR spectrescopy.
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