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Chemistry of cobalt bis(1,2-dicarbollide) ion; the synthesis of carbon substituted alkylamino derivatives from hydroxyalkyl derivatives via methylsulfonyl or p-toluenesulfonyl esters

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F15%3A10296754" target="_blank" >RIV/00216208:11310/15:10296754 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388980:_____/15:00445959

  • Result on the web

    <a href="http://www.sciencedirect.com/science/article/pii/S0022328X15300590" target="_blank" >http://www.sciencedirect.com/science/article/pii/S0022328X15300590</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.jorganchem.2015.06.032" target="_blank" >10.1016/j.jorganchem.2015.06.032</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Chemistry of cobalt bis(1,2-dicarbollide) ion; the synthesis of carbon substituted alkylamino derivatives from hydroxyalkyl derivatives via methylsulfonyl or p-toluenesulfonyl esters

  • Original language description

    In this paper we report the synthetic procedures providing the C-substitution of the cobalt bis(dicarbollide) sandwich anion [(1,2-C2B9H11)-3,30-Co] with primary, secondary and tertiary alkylamine groups of different length of the aliphatic spacer attached to the carbon C(1) or C(1) and C(10) cage positions. Reaction pathways leading to these compounds proceed via synthesis of mono [(1-X-O-(CH2)n- 1,2-C2B9H10) (10,20-C2B9H11)-3,30-Co]Me4N (where n 1/4 1e3 and X 1/4 eSO2CH3 or eSO2(-C6H4-4-CH3) esters (2aef) and diesters [(1,10-X-O-(CH2)n-1,2-C2B9H10)2-3,30-Co]Me4N (3a-c) (n 1/4 1 and 2). These compounds are readily accessible in good to excellent yields by reactions of trimethylammonium salts of alkylhydroxy derivatives (1aee) of the parent ion with methylsulfonyl or p-toluenesulfonyl chloride. The esterifications proceeded with lower conversions only for methylene hydroxy derivatives. The series of primary amines of general formulation [(1-1R2RN-(CH2)n-1,2-C2B9H10) (10,20-C2B9H11)-3,3

  • 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/GA15-05677S" target="_blank" >GA15-05677S: Novel metallacarborane derivatives that exhibit inhibitory properties towards carbonic anhydrase enzyme and potential applicability in cancer therapy</a><br>

  • Continuities

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

Others

  • Publication year

    2015

  • 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 Organometallic Chemistry

  • ISSN

    0022-328X

  • e-ISSN

  • Volume of the periodical

    798/1

  • Issue of the periodical within the volume

    december

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    9

  • Pages from-to

    112-120

  • UT code for WoS article

    000366155400018

  • EID of the result in the Scopus database

    2-s2.0-84949626362