0000000000040349

AUTHOR

Chang-cheng You

showing 2 related works from this author

Calix[4]arene-functionalized naphthalene and perylene imide dyes.

2002

[reaction: see text] Calix[4]arenes bearing one, two, or four 1,8-naphthyl imide groups at the wide rim and bis-calix[4]arenes connected via perylene-bisimide dye spacers have been synthesized. The low-temperature NMR spectrum of the tetranaphthylimide suggests, in agreement with a crystal structure, a C2-symmetrical pinched cone conformation stabilized via face-to-face pi-pi interactions between opposite naphthylimide groups. UV-vis and fluorescence studies have been carried out for the perylene bis-calix[4]arene dyes.

Molecular StructureChemistryOrganic ChemistryCrystal structureNuclear magnetic resonance spectroscopyNaphthalenesPhotochemistryImidesBiochemistryFluorescencechemistry.chemical_compoundPhenolsPolymer chemistryCalixareneMoleculePhysical and Theoretical ChemistryCalixarenesImideColoring AgentsPerylenePeryleneNaphthaleneFluorescent DyesOrganic letters
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CCDC 194904: Experimental Crystal Structure Determination

2002

Related Article: M.O.Vysotsky, V.Bohmer, F.Wurthner, Chang-Cheng You, K.Rissanen|2002|Org.Lett.|4|2901|doi:10.1021/ol026402o

Space GroupCrystallography25262728-tetrakis(Pentyloxy)-5111723-tetrakis(13-dioxo-23-dihydro-2-azaphenalen-2-yl)calix[4]arene chloroform solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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