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
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CA - Inorganic chemistry
OECD FORD branch
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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
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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
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