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  • 1
    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.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 1023-1030 
    ISSN: 0009-2940
    Keywords: Metal dithiolenes ; Viologens ; Charge-transfer complexes ; Electrical conductivity ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Charge-Transfer Complexes of Metal Dithiolenes, IV. - Viologens as Redoxactive Acceptors - Synthesis and Electrical ConductivityTitle compounds of the type [G]n+m [ML2]m-n are prepared from viologens or related bipyridylium halides GXn and mono- or dianionic metal dithiolenes [ML2]m- (M = Ni, Pd, Pt; L = a substituted or unsubstituted 1,2-ethenedithiolate; m = 1,2). IR and UV-VIS spectra essentially exhibit absorption bands of the components whereas all dianionic complexes additionally show ion pair charge-transfer bands in the long wavelength region (850-1250 nm). All complexes show semiconducting behaviour with electrical conductivities ranging from 7.5 · 10-3 〈 1 · 10-10 S/cm (measured as compacted pellets at 293 K) depending on the nature of the ligand, metal, anion charge, and the cation size. The conductivity of monoanionic dithiolene complexes is influenced by the steric properties of the viologen cations while charge-transfer interaction seems to be more important in the case of dianionic dithiolenes.
    Notes: Die Titelverbindungen vom Typ [G]n+m [ML2]m-n werden aus Viologenen oder verwandten Bipyridyliumhalogeniden GXn und mono- oder dianionischen Metalldithiolenen [ML2]m- (M = Ni, Pd, Pt; L = ein substituiertes oder unsubstituiertes 1,2-Ethendithiolat; m = 1,2) synthetisiert. IR- und UV-VIS-Spektren spiegeln im wesentlichen das Absorptionsverhalten der Komponenten wider, darüber hinaus zeigen alle dianionischen Komplexe Ionenpaar-Charge-Transfer-Banden im langwelligen Spektralbereich (800-1250 nm). Alle Verbindungen besitzen Halbleiter-eigenschaften. Die bei 293 K an Pulverpreßlingen gemessenen elektrischen Leitfähigkeiten variieren in Abhängigkeit von Ligand, Zentralmetall, Anionenladung und Kationengröße von 7.5 · 10-3 bis 〈 1 · 10-10 S/cm. Während die Leitfähigkeitseigenschaften der monoanionischen Dithiolenkomplexe weitgehend durch den sterischen Einfluß der Viologen-Kationen bestimmt werden, scheint im Falle der dianionischen Dithiolenkomplexe die Charge-Transfer-Wechselwirkung ausschlaggebend zu sein.
    Additional Material: 3 Ill.
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  • 3
    ISSN: 0009-2940
    Keywords: Metal dithiolenes ; Dipyridinioethylene dihalides ; Charge-Transfer complexes ; Electrical conductivity ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Charge-Transfer Complexes of Metal Dithiolenes, XIII[1]. - cis-trans-Photoisomerisable Viologens as Redoxactive Acceptors  -  Synthesis and Electrical ConductivityIon Pair Charge-Transfer (IPCT) complexes of the type [A2+[ML2]2-} (1a-f to 4a-f) are synthesized from dianionic metal dithiolenes [M = Ni, Zn, L = cis-1,2-dicyano-1,2-ethene-dithiolate (mnt2-), 2-thioxo-1,3-dithiol-4,5-dithiolate (dmit2-)] and dicationic viologens [A2+ = 4,4′-(1,2-ethenediyl)bis(1-alkylpyridinium)]. The acceptors can exist as cis/trans isomers and may have coordinating properties in the case of 1-cyanoalkyl groups. The IPCT bands are in the range of 500 to 1200 nm and their energy follows the Hush-Marcus relation. For the nickel complexes the reorganization energy amounts to 73, for the zinc compounds to 115 kJ/mol. As shown by X-ray analysis of {A2+[Ni(mnt)2]2-} (2d), A2+ = trans-4,4′-(1,2-ethenediyl)-bis[1-(3-cyanopropyl)pyridinium], the structure consists of stacks of alternating donors and acceptors with a typical plane-to-plane distance of 350 pm. There is no interaction between the cyano group of the acceptor and the nickel atom of the donor. The electrical conductivities of the nickel compounds are in the range of 5 · 10-6 to 3 · 10-11 Ω-1 cm-1, and the corresponding activation energies vary from 0.24 to 0.61 eV. For the dmit complexes these values agree well with the free activation enthalpy of the electron transfer reaction A2+ + [ML2]2- → A+ + [ML2]- calculated from the Hush-Marcus model. This suggests that charge carrier generation occurs by electron transfer. When a trans acceptor is replaced by its cis isomer in [A2+[NiL2]2-}, conductivity changes from 5 · 10-7 to 5 · 10-6 Ω-1 cm-1 and the activation energy from 0.43 to 0.24 eV, when L - dmit2- but stays at about 1 · 10-8 Ω-1 cm-1 for L = mnt2-.
    Additional Material: 6 Ill.
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