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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.
  • 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. (en)
Title
  • The Cyclization of Alkyl Side Chains of Naphthalenes: GC/Potential Energies/FTIR Approach
  • The Cyclization of Alkyl Side Chains of Naphthalenes: GC/Potential Energies/FTIR Approach (en)
skos:prefLabel
  • The Cyclization of Alkyl Side Chains of Naphthalenes: GC/Potential Energies/FTIR Approach
  • The Cyclization of Alkyl Side Chains of Naphthalenes: GC/Potential Energies/FTIR Approach (en)
skos:notation
  • RIV/67985891:_____/14:00434445!RIV15-AV0-67985891
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  • I
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  • 14
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  • 9513
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  • RIV/67985891:_____/14:00434445
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  • alkyl naphtalenes; retention times; molecular mechanics; Van der Waals forces (en)
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  • US - Spojené státy americké
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  • [1A3E74861E18]
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  • American Journal of Analytical Chemistry
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  • 5
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  • Bičáková, Olga
  • Buryan, P.
  • Straka, Pavel
  • Novotná, M.
issn
  • 2156-8251
number of pages
http://bibframe.org/vocab/doi
  • 10.4236/ajac.2014.514103
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