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Thiaborane clusters with an exoskeletal B-H group

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F19%3A39915528" target="_blank" >RIV/00216275:25310/19:39915528 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388980:_____/19:00503673 RIV/61388963:_____/19:00503673

  • Result on the web

    <a href="https://pubs.rsc.org/en/content/articlelanding/2019/CC/C9CC00952C#!divAbstract" target="_blank" >https://pubs.rsc.org/en/content/articlelanding/2019/CC/C9CC00952C#!divAbstract</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c9cc00952c" target="_blank" >10.1039/c9cc00952c</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Thiaborane clusters with an exoskeletal B-H group

  • Original language description

    The thiaboranes closo-1-SB11H11 (1a) and 12-I-closo-1-SB11H10 (1b) react with 4-(dimethylamino) pyridine under inert conditions upon the formation of the nido-type thiaboranes 9-B{(4-Me2N)C5NH4}(2)(H)-7-SB10H11 and 9-B{(4-Me2N)C5NH4}(2)(H)-5-I-7-SB10H10 containing an exoskeletal B-Hgroup. The same type of B-Hmoiety is also stabilised by one bipyridine molecule in a chelating fashion. These complexes are unstable in solution, and in air and hydrolyse to monodeboronated ionic compounds having [nido-7-SB10H11]- or [5-I-nido-7-SB10H10]- anions which are also products of the reactions of 1a and 1b with other N-bases such as pyridine, ammonia and DABCO. The extrusion of one boron and one sulphur atom takes place when 1a reacts with 2,6-di-tert-butylpyridine to yield decaborane.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10402 - Inorganic and nuclear chemistry

Result continuities

  • Project

    <a href="/en/project/GA17-08045S" target="_blank" >GA17-08045S: Getting stronger together: exo-substituted heteroboranes and their adducts as suitable motifs for exploration of non-covalent interactions</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2019

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Chemical Communications

  • ISSN

    1359-7345

  • e-ISSN

  • Volume of the periodical

    55

  • Issue of the periodical within the volume

    23

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    4

  • Pages from-to

    3375-3378

  • UT code for WoS article

    000461397500012

  • EID of the result in the Scopus database