[2]Catenanes decorated with porphyrin and [60]fullerene groups: Design, convergent synthesis, and photoinduced processes

Journal of the American Chemical Society

Volumn 132, Issue 11, 2010, Pages 3847-3861

  Megiatto Jr , Jackson D ^a   Schuster, David I ^a   Abwandner, Silke ^b   De Miguel, Gustavo ^b   Guldi, Dirk M ^b  

^a NEW YORK UNIVERSITY   (United States)

^b UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

1 ,3-DIPOLARCYCLOADDITION; [2]CATENANE; [2]CATENANES; [60] FULLERENE; BACK ELECTRON TRANSFER; CATENANES; CHARGE SHIFT; CHARGE-SEPARATED STATE; COMPUTATIONAL ANALYSIS; CONVERGENT SYNTHESIS; CU COMPLEXES; ELECTRON DONOR ACCEPTORS; H NMR SPECTROSCOPY; LONG DISTANCES; METAL-TO-LIGAND CHARGE TRANSFER; PHENANTHROLINES; PHOTOINDUCED PROCESS; PHOTOPHYSICAL INVESTIGATION; PHOTOPHYSICAL STUDIES; RADICAL PAIR; SINGLET EXCITED STATE; SYNTHETIC APPROACH; TIME-SCALES;

AROMATIC COMPOUNDS; CHARGE TRANSFER; CHROMOPHORES; CYCLOADDITION; EXCITED STATES; FREE RADICAL REACTIONS; FULLERENES; GROUND STATE; HYBRID MATERIALS; ION EXCHANGE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PORPHYRINS; ZINC;

ZINC COMPOUNDS;

CARBON; CATENANE; CUPROUS ION; FULLERENE DERIVATIVE; LIGAND; METAL; PHENANTHROLINE DERIVATIVE; PORPHYRIN DERIVATIVE;

ARTICLE; CHROMATOPHORE; CONFORMATION; COVALENT BOND; ELECTROCHEMICAL ANALYSIS; ELECTRON TRANSPORT; ENERGY TRANSFER; IRRADIATION; LIGHT; PROTON NUCLEAR MAGNETIC RESONANCE; SPECTROSCOPY; SYNTHESIS;

ABSORPTION; ALKYNES; AZIDES; CATALYSIS; CATENANES; COPPER; DRUG DESIGN; ELECTROCHEMISTRY; ENERGY TRANSFER; FULLERENES; METALLOPORPHYRINS; PHOTOCHEMICAL PROCESSES; PORPHYRINS; SPECTROMETRY, FLUORESCENCE; SPECTROPHOTOMETRY, ULTRAVIOLET;

EID: 77949867106     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja910149f     Document Type: Article

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