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Synthesis, characterisation and some chemistry of C- and B-substituted carboxylic acids of cobalt bis(dicarbollide)

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388980%3A_____%2F14%3A00428161" target="_blank" >RIV/61388980:_____/14:00428161 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1039/c3dt52870g" target="_blank" >http://dx.doi.org/10.1039/c3dt52870g</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c3dt52870g" target="_blank" >10.1039/c3dt52870g</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis, characterisation and some chemistry of C- and B-substituted carboxylic acids of cobalt bis(dicarbollide)

  • Original language description

    Low temperature reactions of lithiated cobalt bis(1,2-dicarbollide)(1-) (1(-)) in DME with carbon dioxide leads to the substitution of 1(-) at the C-atoms by carboxy function(s). This results in a good yield formation of monosubstituted and disubstitutedproducts of formulations [(1-HOOC-1,2-C2B9H10)(1', 2'-C2B9H11)3,3'-Co)](-) (2(-)) and [(HOOC)(2)-(1,2-C2B9H10)(2)-3,3'-Co](-)(3a, b(-)), respectively. Indeed, the latter compound is in fact a mixture of two diastereoisomers, denoted here as 1,1'-anti (3a(-)) and 1,2'-syn-isomer (3b(-)), from which only the former major species (3a(-)) could be isolated in pure form. Considerations about stereochemistry of these species are supported by geometry optimizations and calculations of 11B NMR shifts at the GIAO-DFT level. In addition, three monocarboxylic acids with three different linear spacers between the carboxy groups and the cage are reported. The first one of the formula [(1-HOOC-CH2-1,2-C2B9H10)(1', 2'-C2B9H11)-3,3'-Co]-(5-) results i

  • 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

    <a href="/en/project/IAAX00320901" target="_blank" >IAAX00320901: Functionalized boron clusters as viral enzyme inhihitors</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2014

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Dalton Transactions

  • ISSN

    1477-9226

  • e-ISSN

  • Volume of the periodical

    43

  • Issue of the periodical within the volume

    13

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    15

  • Pages from-to

    5106-5120

  • UT code for WoS article

    000332475300023

  • EID of the result in the Scopus database