The Cyclization of Alkyl Side Chains of Naphthalenes: GC/Potential Energies/FTIR Approach
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985891%3A_____%2F14%3A00434445" target="_blank" >RIV/67985891:_____/14:00434445 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.4236/ajac.2014.514103" target="_blank" >http://dx.doi.org/10.4236/ajac.2014.514103</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.4236/ajac.2014.514103" target="_blank" >10.4236/ajac.2014.514103</a>
Alternative languages
Result language
angličtina
Original language name
The Cyclization of Alkyl Side Chains of Naphthalenes: GC/Potential Energies/FTIR Approach
Original language description
Computational, GC- and FTIR analyses have shown that longer alkyl side chains of alkyl naphthalenes are cyclized through an interaction between the terminal CH3 group and the aromatic ring. Conventional aromatic-aliphatic molecules thus become new molecules with quasi-alicyclic rings.
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
CC - Organic chemistry
OECD FORD branch
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Result continuities
Project
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Continuities
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
American Journal of Analytical Chemistry
ISSN
2156-8251
e-ISSN
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Volume of the periodical
5
Issue of the periodical within the volume
14
Country of publishing house
US - UNITED STATES
Number of pages
12
Pages from-to
957-968
UT code for WoS article
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EID of the result in the Scopus database
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