Dehydration of ortho-, meta- and para-Alkoxy Phenylboronic Acids to their Corresponding Boroxines

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F18%3A10386132" target="_blank" >RIV/00216208:11310/18:10386132 - isvavai.cz</a>
Alternative codes found
RIV/61389013:_____/18:00488791
Result on the web
<a href="https://doi.org/10.1002/ejic.201701485" target="_blank" >https://doi.org/10.1002/ejic.201701485</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/ejic.201701485" target="_blank" >10.1002/ejic.201701485</a>

Result language
angličtina
Original language name
Dehydration of ortho-, meta- and para-Alkoxy Phenylboronic Acids to their Corresponding Boroxines
Original language description
Isomeric isobutoxy phenylboronic acids (ortho-, meta-, para-) were synthesized and their properties such as pK(a) and thermal stability have been compared. Molecular and crystal structures of the para isomer were determined by single crystal XRD methods. DSC and TGA measurements have been carried out on all isomers to study their dehydration as well as thermal stability. The results show that the position of the substituent in phenylboronic acids influences their acidity as well as possible formation of the corresponding boroxines.
Czech name
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Czech description
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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

Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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