Synthesis of thiophene-containing hybrid calixphyrins of the 5,10-porphodimethene type

Journal of Organic Chemistry

Volumn 73, Issue 13, 2008, Pages 5139-5142

  Matano, Yoshihiro ^a   Miyajima, Tooru ^a   Ochi, Noriaki ^a   Nakao, Yoshihide ^a   Sakaki, Shigeyoshi ^a   Imahori, Hiroshi ^a,b  

^a KYOTO UNIVERSITY   (Japan)

^b KYOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CHEMICAL PROPERTIES; CHEMICAL REACTIONS; SYNTHESIS (CHEMICAL); THIOPHENE;

(PL) PROPERTIES; CHEMICAL EQUATIONS; OPTICAL (PET) (OPET); SYNTHESIS (OF CHIRAL IONIC LIQUIDS);

ELECTROCHEMICAL PROPERTIES;

CARBON; HETEROCYCLIC COMPOUND; LIGAND; NITROGEN; PHOSPHOLE DERIVATIVE; PYRROLE DERIVATIVE; THIOPHENE DERIVATIVE;

ABSORPTION SPECTROSCOPY; ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; CYCLIC POTENTIOMETRY; DIFFERENTIAL PULSE VOLTAMMETRY; ELECTROCHEMICAL ANALYSIS; OXIDATION REDUCTION REACTION; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; ULTRAVIOLET SPECTROSCOPY; X RAY DIFFRACTION;

MODELS, MOLECULAR; MOLECULAR STRUCTURE; PORPHYRINS; THIOPHENES;

EID: 46849089739     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo800532n     Document Type: Article

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44. In ref 8b, we reported the reaction energies from 10Xm to 11Xm calculated without the solvation effect. The conclusion does not change at all.
45. 2, X-hybrids have been unsuccessful so far.