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The Cyclization of Alkyl Side Chains of Naphthalenes: GC/Potential Energies/FTIR Approach
- 1.0434445 - ÚSMH 2015 RIV US eng J - Journal Article
Straka, Pavel - Novotná, M. - Buryan, P. - Bičáková, Olga
The Cyclization of Alkyl Side Chains of Naphthalenes: GC/Potential Energies/FTIR Approach.
American Journal of Analytical Chemistry. Roč. 5, č. 14 (2014), s. 957-968. ISSN 2156-8251
Institutional support: RVO:67985891
Keywords : alkyl naphtalenes * retention times * molecular mechanics * Van der Waals forces
Subject RIV: CC - Organic Chemistry
http://www.scirp.org/journal/AJAC/
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.
Permanent Link: http://hdl.handle.net/11104/0238505
Number of the records: 1