All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Reactivity of Organotin(I) Dimers RSnSnR (R = 2,6-(Me2NCH2)2C6H3, 4-t-Bu-2,6-{P(O)(O-i-Pr)2}2C6H2) with Diaryl Dichalcogenides, ArEEAr (E = S, Se, Te; Ar = Ph, 2-C5H4N): Control of Secondary Sn???Sn Interactions by Intramolecular Coordination and Identity of the Aryl Chalcogenate

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F13%3A39896813" target="_blank" >RIV/00216275:25310/13:39896813 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1021/om400694z" target="_blank" >http://dx.doi.org/10.1021/om400694z</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/om400694z" target="_blank" >10.1021/om400694z</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Reactivity of Organotin(I) Dimers RSnSnR (R = 2,6-(Me2NCH2)2C6H3, 4-t-Bu-2,6-{P(O)(O-i-Pr)2}2C6H2) with Diaryl Dichalcogenides, ArEEAr (E = S, Se, Te; Ar = Ph, 2-C5H4N): Control of Secondary Sn???Sn Interactions by Intramolecular Coordination and Identity of the Aryl Chalcogenate

  • Original language description

    The reactions of the in situ prepared organotin(I) compounds RSnSnR with diary! dichalcogenides ArEEAr provided, depending on the ratio of the reactants, the intramolecularly coordinated heteroleptic organotin(II) chalcogenoarylates RSnEAr (1, R = 2,6-(Me2NCH2)(2)C6H3, -E = S, Ar = Ph; 2, R = 2,6-(Me2NCH2)(2)C6H3, E = Se, Ar = Ph; 3, R = 2,6(Me2NCH2)(2)C6H3, E Te, Ar = Ph; 6, R = 4-t-Bu-2,6-{P(O)(O-i-ET)z}(2)C6H2, E = Se, Ar = Ph; 7, R = 4-t-Bu-2,6-{P(O)(O-i-Pr)(2)}(2)C6H2, E = Te, Ar = Ph; 8, R = 4-t-Bu-2,6-{P(O)(O-i-Pr)(2)}(2)C6H2, E = Se, Ar = 2-C5H4N) and the corresponding organotin(IV) compounds RSn(EAr)(3) (4, R = 2,6-(Me2NCH2)(2)C6H3, E = S, Ar = Ph; 5, R = 2,6-(Me2NCH2)(2)C6H3, E = Se, Ar = Ph; 10, R = 4-t-Bu-2,6-{P(O)(O-i-PO2}(2)C6H2, E = S, Ar = 2-C5H4N), respectively. Compound 1O undergoes a thermally initiated cyclization reaction to give the benzoxaphosphastannole derivative {1(P),3(Sn)-Sn(S-Py)2-OP(O)(O-i-Pr)-6-t-Bu-4-P(O)(Oi-Pr)2}C6H2 (11). The compounds were characteriz

  • Czech name

  • Czech description

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

  • Continuities

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • 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

    32

  • Issue of the periodical within the volume

    17

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    4973-4984

  • UT code for WoS article

    000330144900033

  • EID of the result in the Scopus database