Protonated [4n] and [4n+2]π octaphyrins choose their möbius/hückel aromatic topology

Journal of the American Chemical Society

Volumn 132, Issue 9, 2010, Pages 3105-3114

  Lim, Jong Min ^a   Shin, Jae Yoon ^a   Tanaka, Yasuo ^b   Saito, Shohei ^b   Osuka, Atsuhiro ^b   Kim, Dongho ^a  

^a Yonsei University   (South Korea)

^b KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC STABILIZATION; AROMATICITIES; CONFORMATIONAL CHANGE; COUNTER ANIONS; INTERMOLECULAR HYDROGEN; INTRAMOLECULAR HYDROGEN BOND; MACROCYCLES; NMR ANALYSIS; OCTAPHYRINS; PENTAFLUOROPHENYL; PHOTOPHYSICAL PROPERTIES; PROTONATED; TWO-PHOTON ABSORPTIONS; X RAY CRYSTAL STRUCTURES;

AROMATIC COMPOUNDS; AROMATIZATION; MOLYBDENUM; MULTIPHOTON PROCESSES; NEGATIVE IONS; NITROGEN COMPOUNDS; PROTONATION; TOPOLOGY;

HYDROGEN BONDS;

FORMIC ACID; MACROCYCLIC COMPOUND; PYRROLE DERIVATIVE; PORPHYRIN; PROTON;

AROMATIZATION; ARTICLE; CONFORMATION; CRYSTAL STRUCTURE; ELECTRON; HYDROGEN BOND; LIGHT ABSORPTION; NUCLEAR MAGNETIC RESONANCE; PROTON TRANSPORT; X RAY CRYSTALLOGRAPHY; CHEMICAL STRUCTURE; CHEMISTRY; SYNTHESIS;

CRYSTALLOGRAPHY, X-RAY; MODELS, MOLECULAR; MOLECULAR STRUCTURE; PORPHYRINS; PROTONS;

EID: 77949366871     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja909744z     Document Type: Article

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