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Double-C,N-chelated tri- and diorganotin(IV) fluorides

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F05%3A00002968" target="_blank" >RIV/00216275:25310/05:00002968 - isvavai.cz</a>

  • Alternative codes found

    RIV/61389013:_____/05:00029540 RIV/00216208:11310/05:00008391 RIV/00216208:11310/05:8391

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Double-C,N-chelated tri- and diorganotin(IV) fluorides

  • Original language description

    Attempts to fluorinate the compounds (L-CN)(SnPhCl)-Sn-2 (1), (L-CN)(2)SnCl2 (2), (L-CN)(2)SnBr2 (3), (L-CN)(2)SnI2 (4) and (LSnPhCl2)-Sn-CN (5), where LCN is {2-[(CH3)(2)NCH2]C6H4}(-), were made by four different methods. The fluorinated monomeric five-coordinated analogue of 1 was made by fluorination of I with KF/18-crown-6 ether and by metathetical fluorination with 10 ((LSnBu2F)-Sn-CN). The fluorinated monomeric six-coordinated analogue ((L-CN)(2)SnF2(7)) of diorganotin compounds 2-4 was made easily by all methods used in adequate yield. The fluorination of 5 by all methods did not lead to the monomeric product and phenyl group migrations were observed during the course of these reactions. The most clear is the reaction of 5 with two equivalents of 10 leading to, presumably, a fluorinated analogue of 5 having a trimeric structure, which reacts immediately with three equivalents of NH4F in methanol to give the complex compound NH4+[(LPhSnF3)-Ph-CN](-) in quantitative yield. Compoun

  • Czech name

    Double-C,N-chelated tri- and diorganotin(IV) fluorides

  • Czech description

    Attempts to fluorinate the compounds (L-CN)(SnPhCl)-Sn-2 (1), (L-CN)(2)SnCl2 (2), (L-CN)(2)SnBr2 (3), (L-CN)(2)SnI2 (4) and (LSnPhCl2)-Sn-CN (5), where LCN is {2-[(CH3)(2)NCH2]C6H4}(-), were made by four different methods. The fluorinated monomeric five-coordinated analogue of 1 was made by fluorination of I with KF/18-crown-6 ether and by metathetical fluorination with 10 ((LSnBu2F)-Sn-CN). The fluorinated monomeric six-coordinated analogue ((L-CN)(2)SnF2(7)) of diorganotin compounds 2-4 was made easily by all methods used in adequate yield. The fluorination of 5 by all methods did not lead to the monomeric product and phenyl group migrations were observed during the course of these reactions. The most clear is the reaction of 5 with two equivalents of 10 leading to, presumably, a fluorinated analogue of 5 having a trimeric structure, which reacts immediately with three equivalents of NH4F in methanol to give the complex compound NH4+[(LPhSnF3)-Ph-CN](-) in quantitative yield. Compoun

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CA - Inorganic chemistry

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2005

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    JOURNAL OF FLUORINE CHEMISTRY

  • ISSN

    0022-1139

  • e-ISSN

  • Volume of the periodical

  • Issue of the periodical within the volume

    126

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    9

  • Pages from-to

    1531-1538

  • UT code for WoS article

  • EID of the result in the Scopus database