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    Publication Date: 1998-01-01
    Print ISSN: 0044-2313
    Electronic ISSN: 1521-3749
    Topics: Chemistry and Pharmacology
    Published by Wiley
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  • 3
    ISSN: 0044-2313
    Keywords: Metal complexes ; 2,2′-dihydroxyazoarenes complexes of phosphine nickel, palladium, platinum, pentamethylcyclopentadienyl rhodium, pentamethylcyclopentadienyl iridium ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal Complexes of Dyes. Phosphine-Nickel, Palladium, Platinum Complexes and Pentamethylcyclopentadienyl Rhodium and Iridium Complexes of 2,2′-DihydroxyazoarenesThe terdentate dianions of 2,2′-dihydroxyazobenzene (L1H), 1-(2-hydroxy-4-nitrophenylazo)-2-naphthol (L2H), 1-(2-hydroxy-5-nitrophenylazo)-2-naphthol (L3H) and 1-phenyl-3-methyl-4-(2-hydroxy-5-nitrophenylazo)-5-pyrazolone (L4H) form with chloro bridged complexes [(R3P)MCl2]2 (M = Pd, Pt; R = Ph, nBu), [(n5-C5Me5)MCl2]2 (M = Rh, Ir) and with (nBu3P)2NiCl2 the metal dye complexes (R3P)ML (M = Ni, Pd, Pt) and (C5Me5)ML (M = Rh, Ir). The structures of (Ph3P)PtL1 and (nBu3P)PdL3 have been determined by X-ray diffraction. For the complexes (n5-C5Me5)ML (M = Rh, Ir) with asymmetric metal centers two diastereoisomers are detected by nmr spectroscopy which points to the „hydrazone“ form of the azo ligand with a pyramidalized N-atom.
    Notes: Die dreizähnigen Dianionen von 2,2′-Dihydroxyazobenzol (L1H2), 1-(2-Hydroxy-4-nitrophenylazo)-2-naphthol (L2H2), 1-(2-Hydroxy-5-nitrophenylazo)-2-naphthol (L3H2) und 1-Phenyl-3-methyl-4-(2-hydroxy-5-nitrophenylazo)-5-pyrazolon (L4H2) bilden mit den chloroverbrückten Komplexen [(R3P)MCl2]2 (M = Pd, Pt; R = Ph, nBu), [(n5-C5Me5)MCl2]2 (M = Rh, Ir) sowie mit (nBu3P)2NiCl2 die Farbstoff-Komplexe (R3P)ML (M = Ni, Pd, Pt) und (n5-C5H5)ML (M = Rh, Ir). Die Strukturen von (Ph3P)PtL1 und (nBu3P)PdL3 wurden röntgenographisch bestimmt. Für die Komplexe (n5-C5Me5)ML (M = Rh, Ir) mit „asymmetrischem“ Metallatom lassen sich NMR-spektroskopisch zwei Diastereoisomere nachweisen, was für den „Hydrazon“-Charakter der Azoliganden mit pyramidalisiertem N-Atom spricht.
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  • 4
    ISSN: 0044-2313
    Keywords: Metal dye complexes ; curcumin and curcuminoides complexes of transition metals ; organo transition metal compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal Complexes of Dyes. IX. Transition Metal Complexes of Curcumin and DerivativesThe bidentate monoanions of curcumin[CU, (1, 7-bis(4-hydroxy-3-methoxyphenyl)-hepta-1,6-diene-3,5-dione)], diacetylcurcumin[DACU, (1,7-bis(4-acetyl-3-methoxyphenyl)-hepta-1,6-diene-3,5-dione)], dihydroxycurcumin[DHCU, (1,7-bis(4-hydroxiphenyl)-hepta-1,6-diene-3,5-dione)], dimethylcurcumin [DMCU, (1,7-bis(3,4-dimethoxyphenyl)-hepta-1, 6-diene-3,5-dione)] and trimethylcurcumin[TMCU, (1,7-bis(3,4-dimethoxyphenyl)-4-methylhepta-1,6-diene-3,5-dione)] form with chloro bridged complexes [(R3P)MCl2]2 (M=Pd, Pt; R=phenyl, n-butyl, ethyl, tolyl), [η5-C5Me5)MCl2]2 (M=Rh, Ir), [(η6-p-cymene)RuCl2]2, [(η3-C3H5)PdCl]2, di-μ-chlorobis[N-(diphenylmethylene)-glycinethylester-(C,N)]-dipalladium(II) and with [(η5-C5Me5)Co(CO)I2] monochelate dye complexes. The structure of [(η6-p-cymene)(Cl)Ru(DMCU)] was determined by X-ray diffraction. The dichelates (DMCU)2M with M=Cu, Ni, (CU)2Pd and the trichelate (CU)3Fe were obtained. Cationic bipyridine copper(II) complexes with CU, DHCU, and DMCU were sythesized by treating the dye ligands with copper(II) acetate, 2,2′-bipyridine and ammoniumtetrafluoroborate. In comparison to the free 1.3-diketones the dye complexes show a bathochromic shift in the UV/VIS spectra.
    Notes: Die zweizähnigen Monoanionen von Curcumin[CU, (1,7-bis(4-hydroxy-3-methoxyphenyl)-hepta-1,6-dien-3,5-dion)], Diacetylcurcumin[DACU, (1,7-bis(4-acetyl-3-methoxyphenyl)-hepta-1,6-dien-3,5-dion)], Dihydroxycurcumin[DHCU, (1,7-bis(4-hydroxiphenyl)-hepta-1,6-dien-3,5-dion)], Dimethylcurcumin[DMCU, (1,7-bis(3,4-dimethoxyphenyl)-hepta-1,6-dien-3,5-dion)] und Trimethylcurcumin[TMCU, (1,7-bis(3,4-dimethoxyphenyl)-4-methylhepta-1,6-dien-3,5-dion] bilden mit den chloroverbrückten Komplexen [(R3P)MCl2]2 (M=Pd, Pt; R=Phenyl, n-Butyl, Ethyl, Tolyl), [η5-C5Me5MCl2]2, M=Rh, Ir, [(η6-p-Cymol)RuCl2]2, [(η3-C3H5)PdCl]2, Di-μ-chlorobis[N-(diphenylmethylen)-glycinethylester-(C, N)]-dipalladium(II) sowie [(η5-C5Me5)Co(CO)I2] Monochelat-Komplexe. Die Struktur von [(η6-p-Cymol)(Cl)Ru(DMCU)] wurde röntgenographisch bestimmt. Die Bischelate der Form (DMCU)2M mit M=Cu, Ni, (CU)2Pd sowie ein Trischelat (CU)3Fe konnten erhalten werden. Kationische Bipyridinkupfer(II)-Komplexe mit CU, CHCU und DMCU bilden sich durch Umsetzung der Farbstoffliganden mit Kupfer(II)-acetat, 2,2′-Bipyridin und Ammoniumtetrafluoroborat. Eine Rotverschiebung der längstwelligen Absorptionsbande im UV/VIS Spektrum der Komplexe gegenüber den freien 1,3-Diketonen wird beobachtet.
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  • 5
    ISSN: 0044-2313
    Keywords: Metal dye complexes ; 1-, 1,4-substituted anthraquinone dyes as ligands in organo transition metal complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal Complexes of Dyes. X. New Transition Metal Complexes of Anthraquinone DyesThe chloro-bridged compounds [(R3P)MCl2]2 (M = Pd, Pt; R = ethyl, phenyl, n-butyl), [(Ph3P)2PdCl]2(BF4)2, [(η5-C5Me5)MCl2]2 (M = Rh, Ir), [(η6-p-cymene)RuCl2]2, react with mono- and dianions of several 9,10-anthracene-dione dyes [1-amino-9,10-anthracene-dione, Disperse Blue 19 (1-amino-4-anline-9,10-anthracene-dione), 1,4-diamino-9,10-anthracene-dione, Solventgreen 3 [1,4-bis(4′-methylaniline)-9,10-anthracene-dione], dianthrimide [1,1′-dianthraquinonylamin], 1-azo-β-naphtol-9,10-anthracene-dione, 1-anilido-o-carboxy-9,10-anthracene-dione and Quinizarin (1,4-dihydroxy-9,10-anthracene-dione)] to give N,O-, O,O- and O,N,O-chelate complexes. Copper(II)- and palladium(II) acetate and the anion of 1-aminoanthraquinone afford N,O-bischelates. Spectroscopic data are discussed. In comparision to the free anthraquinones the dye complexes show a bathochromic shift in the UV/VIS spectra. The structures of (ethyl)3P(Cl)Pt(1-aminoanthraquinone-H+), (η-C5Me5)(Cl)Ir(1-azo-β- #naphtolanthraquinone-H+) and (η-C5Me5)Rh(1-anilido-o-carboxyanthraquinone-2 H+) were determined by X-ray diffraction.
    Notes: Die zwei- bzw. dreizähnigen Farbstoffanionen von 1-Aminoanthrachinon, Oracetblau (1-Amino-4-anilinoanthrachinon), 1,4-Diaminoanthrachinon, Solventgreen 3 [1,4-Bis(4′-methylanilino)anthrachinon], 1,1′-Dianthrimid [Di-(1-anthrachinonyl)-amin], 1-Azo-β-naphtolanthrachinon, 1-Anilido-o-carbonsäure-anthrachinon und Chinizarin (1,4-Dihydroxyanthrachinon) bilden mit den chloroverbrückten Komplexen [(R3P)MCl2]2 (M = Pd, Pt; R = Ethyl, Phenyl, n-Butyl), [(Ph3P)2PdCl]2(BF4)2, [(η5-C5Me5)MCl2]2 (M = Rh, Ir), [(η6-p-Cymol)RuCl2]2, Mono- bzw. Bischelat-Komplexe. 2:1 Metallkomplexe des 1-Aminoanthrachinon-Anions entstehen mit CuII und PdII. Die spektroskopischen Daten der Komplexe werden vergleichend beschrieben. In allen Fällen wird ein bathochromer Shift der langwelligsten Absorptionsbande der Komplexe im Vergleich zu den freien Liganden im UV-VIS Spektrum beobachtet. Die Strukturen von (Ethyl)3P(Cl)Pt(1-Amino-anthrachinon-H+), (η-C5Me5)(Cl)Ir(1-Azo-β- #naphtolanthrachinon-H+) und (η-C5Me5)Rh(1-Anilido-o-carbonsäure-anthrachinon-2 H+) wurden röntgenographisch bestimmt.
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