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  • 1
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 7 (1993), S. 437-441 
    ISSN: 0268-2605
    Schlagwort(e): Triorganotin ; triphenyltin ; tributyltin ; sediments ; Mössbauer spectroscopy ; speciation ; benthos ; Chesapeake Bay ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Triorganotin compounds can interact with various segments of natural water systems. In sediments, for example, these compounds can undergo speciation, and can also become injurious to benthos. The interaction of tributyltin (TBT) and triphenyltin (TPT) compounds with sediments have been studied using extraction techniques in addition to directly observing these compounds in sediments using Mössbauer spectroscopy. The effect of these compounds on benthos has also been examined. The results of these studies are reviewed with particular regard to studies on sediments from the Chesapeake Bay, USA.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    ISSN: 0268-2605
    Schlagwort(e): Adducts ; C. ulmi ; thiazolidin-4-ones ; Dutch elm disease ; IR spectroscopy ; Mössbauer spectroscopy ; toxicity ; triphenyltin Chloride ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Several 1:1 addition compounds between triphenyltin chloride and 2,3-disubstituted thiazolidin-4-one ligands have been synthesized. Their molecular structure has been deduced using far IR and Mössbauer spectroscopies. In addition, molecular modeling of several of the complexes was used to explain the variation of the quadrupole splitting values in the Mössbauer spectra. The structures of the complexes were determined to be trigonal-bipyramidal with the three phenyl groups in the equatorial plane. However, the phenyl groups are not co-planar, on the basis of the observation of both the Sn-C (phenyl) symmetric and asymmetric stretching vibrations. The adducts were screened against the fungus Ceratocystis ulmi, the agent responsible for Dutch elm disease, and found to be effective in the inhibition of this fungus. The toxicity of the adducts varied with the hydrophobicity of the molecule. A direct correlation between substitution on the phenyl group on the thiazolidine ring and the toxicity of the compound was not observed.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 12 (1998), S. 25-30 
    ISSN: 0268-2605
    Schlagwort(e): adduct ; carboxylate ; Ceratocystis ulmi ; Dutch elm disease ; far-infrared spectroscopy ; fungicide ; Mossbauer spectroscopy ; organotins ; QSAR ; thiazolidin-4-ones ; triphenyltin ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In the interest of developing a more effective fungicide to combat Dutch elm disease, our laboratories have synthesized several triphenyltin carboxylates and some 1:1 addition compounds of triphenyltin chloride using 2,3-disubstituted thiazolidin-4-ones as the ligand and screened them in vitro against Ceratocystis ulmi, the causative agent of Dutch elm disease, using a shake culture method. Elemental analyses and spectroscopic data indicate that the structures of the carboxy- lates in the solid state are monomeric with a tetrahedral tin atom with the exception of the furan-2-carboxylic acid derivative, which was found to be polymeric. The triphenyltin chloride adducts are trigonal-bipyramidal with the three phenyl groups in the equatorial plane. Far-infrared data indicate that the three phenyl groups are not co-planar. Screening results for both series of organotins indicate that these two classes of compounds are effective inhibitors of Ceratocystis ulmi, with the adducts having a higher activity. The furan-2-carboxylic acid derivative has a markedly decreased activity compared with the other carboxylates and this is attributed to its polymeric structure. © 1998 John Wiley & Sons, Ltd.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 8 (1994), S. 445-449 
    ISSN: 0268-2605
    Schlagwort(e): Organotin ; aryltin ; triaryltin ; tetraaryltin ; toxicity ; Mössbauer ; QSAR ; quantitative structure-activity ; fungus ; Ceratocystis ulmi ; fungicide ; Dutch elm disease ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The effect of aryltin compounds (Ar4Sn and Ar3SnCl) on the growth of Ceratocystis ulmi, the causative agent of Dutch elm disease, was studied in shake culture. In all cases, the triaryltins were more effective than the tetra-aryltins as inhibitors of C. ulmi in vitro. Furthermore, substitution on the phenyl ring at the meta- and para- positions in the triaryltins did not have a major effect on the biocidal activity for the substituted triaryltins. Quantitative structure-activity relationships (QSARs) gave support to the idea that the species responsible for the inhibition of the fungus is the triaryltin cation. The QSARs further suggest that the interaction of the triaryltin cation with the fungal cell wall of C. ulmi is by a non-specific mechanism.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    ISSN: 0268-2605
    Schlagwort(e): triphenyltin ; carboxylate ; spectroscopy ; crystal structure ; fungitoxicity ; Ceratocystis ulmi ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Four triphenyltin carboxylates formulated as o-Ph3SnOCOC6H4CH=N-Ar (Ar=C6H5; p-CH3C6H4; o-CH3C6H4; o-HOC6H4) were prepared and spectroscopically characterized. The crystal structure of o-Ph3SnOCOC6 H4CH=NC6H5 indicates that the tin atom, in each of the two molecules comprising the asymmetric unit, exists in a distorted tetrahedral geometry owing to an intramolecular acyl O. . .Sn contact. These new triphenyltin carboxylates display marked toxicity against the fungus Ceratocystis ulmi.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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