Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1432-1327
    Keywords: Key words Galactose oxidase ; Phenoxyl-copper complexes ; Resonance Raman spectroscopy ; Copper enzymes ; Copper model complexes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract  The reaction of the macrocycles 1,4,7-tris (3,5-di-tert-butyl-2-hydroxy-benzyl)-1,4,7-triazacyclononane, L1H3, or 1,4,7-tris(3-tert-butyl-5-methoxy-2-hydroxy-benzyl)-1,4,7-triazacyclononane, L2H3, with Cu(ClO4)2·6H2O in methanol (in the presence of Et3N) affords the green complexes [CuII(L1H)] (1), [CuII(L2H)]·CH3OH (2) and (in the presence of HClO4) [CuII(L1H2)](ClO4) (3) and [CuII(L2H2)] (ClO4) (4). The CuII ions in these complexes are five-coordinate (square-base pyramidal), and each contains a dangling, uncoordinated pendent arm (phenol). Complexes 1 and 2 contain two equatorially coordinated phenolato ligands, whereas in 3 and 4 one of these is protonated, affording a coordinated phenol. Electrochemically, these complexes can be oxidized by one electron, generating the phenoxyl-copper(II) species [CuII(L1H)]+ ·, [Cu(L2H)]+ ·, [CuII(L1H2)]2+ ·, and [CuII(L2H2)]2+ ·, all of which are EPR-silent. These species are excellent models for the active form of the enzyme galactose oxidase (GO). Their spectroscopic features (UV-VIS, resonance Raman) are very similar to those reported for GO and unambiguously show that the complexes are phenoxyl-copper(II) rather than phenolato-copper(III) species.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1259-1269 
    ISSN: 1434-1948
    Keywords: Metal dithiolenes ; Charge-transfer complexes ; Azo compounds ; Electrical conductivity ; High-resolution X-ray powder diffractometry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Combination of the planar redox-active ions [ML2]2- (L = mnt2- = maleonitrile-1,2- dithiolate; M = Ni (1), Pd (2), Pt (3); dmit2- = 2-thioxo-1,3-dithiol-4,5-dithiolate: M = Ni (4), Pd (5) and trans-4,4′-azobis(1-methyl-pyridinium), (a2+) affords 1:1 ion pairs exhibiting partial and complete electron transfer as evidenced by UV-Vis and EPR spectra. Replacement of planar a2+ by a non-planar dipyridinium ketone b2+ leads to the complexes 1b and 4b. 1a, 2a, and 3a are predominantly composed of dications and dianions while 4a, 5a, and 4b are rare examples of ion pairs consisting of two radical ions. Single crystal X-ray structural analyses was performed on 4a, a(PF6)2, and a(MeSO4)2 while the structure of 1a was resolved by powder X-ray diffractometry. The latter consists of mixed stacks of planar dianions and dications forming a slipped arrangement with the centers of the two ions displaced relative to each other by 250 pm. The short interplanar distances of 340 pm are in agreement with the presence of a weak charge-transfer interaction as indicated by the corresponding absorption band at about 1400 nm. A mean reorganization energy of 0.85 ±0.04 eV is calculated from the Hush equation for complexes 1a, 2a, and 3a. No ion pair charge-transfer band is observable for 4a, 5a, and 4b. Surprisingly, in the solid state structure of 4a the [Ni(dmit)2]- monoanions do not form segregated columns as found in the many ion pairs with redox inert counterions, but prefer a mixed stack arrangement as observed also for 1a.The specific electrical conductivity of pressed powder pellets of complexes exhibiting a charge-transfer band is in the range of 2 × 10-7 to 1 × 10-5 Ω-1cm-1, increasing with increasing driving force of electron transfer in accordance with previous results. Different to that, the conductivity of the other complexes does not depend on driving force and is much higher (2 × 10-4 to 4 × 10-4 Ω-1cm-1).
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 0947-6539
    Keywords: gallium ; iron ; scandium ; spectroelectrochemistry ; manganese ; phenoxyl radicals ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hexadentate macrocyclic ligands 1,4,7-tris(3,5-dimethyl-2-hydroxybenzyl)-1,4,7-triazacyclononane (LCH3H3), 1,4,7-tris(3,5-di-tert-butyl-2-hydroxybenzyl)-1,4,7-triazacyclononane (LBuH3) and 1,4,7-tris(3-tert-butyl-5-methoxy-2-hydroxybenzyl)-1,4,7-triazacyclononane (LOCH3-H3) form very stable octahedral neutral complexes LMIII with trivalent (or tetravalent) metal ions (GaIII, ScIII, FeIII, MnIII, MnIV). The following complexes have been synthesized: [LBuM], where M = Ga (1), Sc (2), Fe (3); [LBuMnIV]PF6 (4′); [LOCH3M], where M = Ga (1 a), Sc (2 a), Fe (3 a); [LOCH3MnIV]PF6 (4 a'); [LCH3M], where M = Sc (2 b), Fe (3 b), MnIII (4 b); [LCH3MnIV]2(ClO4)3(H3O)(H2O)3 (4 b'). An electrochemical study has shown that complexes 1, 2, 3, 1 a, 2 a and 3 a each display three reversible, ligand-centred, one-electron oxidation steps. The salts [LOCH3FeIII]ClO4 and [LOCH3GaIII]ClO4, have been isolated as stable crystalline materials. Electronic and EPR spectra prove that these oxidations produce species containing one, two or three coordinated phenoxyl radicals. The Mössbauer spectra of 3 a and [3 a]+ show conclusively that both compounds contain high-spin iron(III) central ions. Temperature-dependent magnetic susceptibility measurements reveal that 3 a has an S = 5/2 and [3a]+ an S = 2 ground state. The latter is attained through intramolecular antiferromagnetic exchange coupling between a high-spin iron(III) (S1 = 5/2) and a phenoxyl radical (S2 = 1/2) (H = - 2JS1S2; J = - 80 cm-1). The manganese complexes undergo metal- and ligand-centred redox processes, which were elucidated by spectroelectrochemistry; a phenoxyl radical MnIV complex [MnIVLOCH3]2+ is accessible.
    Additional Material: 17 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 90 (1978), S. 639-639 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Hydroxyl radicals were generated radiolytically in N2O- or N2O/O2(4:1)-saturated aqueous solutions of poly(vinyl alcohol) (PVAL) or its low-molecular-weight model compound pentane-2,4-diol (PD). Using the pulse radiolysis technique, the rate constant of OH with PD and PVAL has been determined to be 2,3 · 109 dm3 · mol-1 · s-1 and 1,5 · 108 dm3 · mol-1 · s-1, respectively. Upon OH attack two kinds of radicals are generated: (i) tertiary α-hydroxyalkyl radicals and (ii) alkyl radicals. The former rapidly reduce tetranitromethane yielding the stable nitroform anion, and from its yield it is calculated that 70-75% of the radicals are α-hydroxyalkyl radicals in both systems. In the presence of oxygen, the carbon-centered radicals are converted into the corresponding peroxyl radicals. The α-hydroxyalkylperoxyl radicals eliminate HO2·/O2· in spontaneous and base-catalyzed reactions (rate constants ≈700 s-1 and ≈2,3 · 109 dm3 · mol-1 · s-1, respectively). There are marked differences in the rates of the bimolecular radical decay reactions. The carbon-centered radicals of PD decay with a rate constant of 5 · 108 dm3 · mol-1 · s-1, whereas those of PVAL decay, under pulse-radiolytic conditions, mainly intramolecularly (loop formation), with rate constants which reach, at high radical numbers per macromolecule, values as high as 1010 dm3 · mol-1 · s-1. With PD it was shown by product studies that the radicals mainly (90%) disproportionate and dimerize only to 10%, thus limiting the yield of crosslinks in PVAL to the latter value. The bimolecular decay rates of the organic peroxyl radicals in O2· containing solutions are more difficult to investigate because of the effective unimolecular HO2·-elimination reaction. However, it is estimated that the peroxyl radicals of both compounds decay (under otherwise equal conditions) more than one order of magnitude slower than the carbon-centered radicals. The measured yields of strand breaks in oxygenated solutions as well as the yields of intermolecular crosslinks under anoxia, determined with PVAL by low-angle laser light-scattering at different dose-rates and pH values, support these conclusions.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 88 (1976), S. 413-413 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 604-605 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 15 (1976), S. 380-381 
    ISSN: 0570-0833
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...