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Solvent-Controlled Ring Size in Double C,N-Chelated Stannoxanes

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F08%3A00007538" target="_blank" >RIV/00216275:25310/08:00007538 - isvavai.cz</a>

  • Alternative codes found

    RIV/61389013:_____/08:00316901

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Solvent-Controlled Ring Size in Double C,N-Chelated Stannoxanes

  • Original language description

    The stannylene (L-CN)(2)Sn where L-CN is a chelating ligand (2-(N,N-dimethylaminomethyl)phenyl-) was oxidized by an excess of oxygen, nitrous oxide, or TEMPO free radical, giving dimeric stannoxane [(L-CN)(2)Sn](2)(mu-O)(2) in dynamic equilibrium with its monomeric form in solution. In the solid state, an unusual tetraoxatetrastannacycle cyclo-[(L-CN)(2)SnO](4) can be crystallized from diethyl ether and the trioxatristannacyclic complex of formula cyclo-[(L-CN)(2)SnO](3) from the hexane solution. The same result has been obtained when C,N-chelated organotin(IV) dihalides ((L-CN)(2)SnX2, where X = Cl or Br) were hydrolyzed with an excess of sodium hydroxide and than dehydrated by azeotropic distillation. The oxobridged dihydroxide [(L-CN)(2)Sn(OH)(2)(mu-O) has been isolated during the course of this hydrolysis.

  • Czech name

    Solvent-Controlled Ring Size in Double C,N-Chelated Stannoxanes

  • Czech description

    The stannylene (L-CN)(2)Sn where L-CN is a chelating ligand (2-(N,N-dimethylaminomethyl)phenyl-) was oxidized by an excess of oxygen, nitrous oxide, or TEMPO free radical, giving dimeric stannoxane [(L-CN)(2)Sn](2)(mu-O)(2) in dynamic equilibrium with its monomeric form in solution. In the solid state, an unusual tetraoxatetrastannacycle cyclo-[(L-CN)(2)SnO](4) can be crystallized from diethyl ether and the trioxatristannacyclic complex of formula cyclo-[(L-CN)(2)SnO](3) from the hexane solution. The same result has been obtained when C,N-chelated organotin(IV) dihalides ((L-CN)(2)SnX2, where X = Cl or Br) were hydrolyzed with an excess of sodium hydroxide and than dehydrated by azeotropic distillation. The oxobridged dihydroxide [(L-CN)(2)Sn(OH)(2)(mu-O) has been isolated during the course of this hydrolysis.

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

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2008

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Organometallics

  • ISSN

    0276-7333

  • e-ISSN

  • Volume of the periodical

    27

  • Issue of the periodical within the volume

    20

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

  • UT code for WoS article

  • EID of the result in the Scopus database