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  Oligooxa[3n.3]paracyclophane Quinhydrones — Cation-Induced Charge-Transfer Absorptions and Structures of the Metal Complexes

Bauer, H., Matz, V., Lang, M., Krieger, C., & Staab, H. A. (1994). Oligooxa[3n.3]paracyclophane Quinhydrones — Cation-Induced Charge-Transfer Absorptions and Structures of the Metal Complexes. Chemische Berichte, 127(10), 1993-2008. doi:10.1002/cber.19941271024.

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 Urheber:
Bauer, Helmut1, Autor           
Matz, Volker2, Autor           
Lang, Martina3, Autor           
Krieger, Claus1, Autor           
Staab, Heinz A.1, Autor           
Affiliations:
1Department of Organic Chemistry, Max Planck Institute for Medical Research, Max Planck Society, ou_1497706              
2Max Planck Institute for Medical Research, Max Planck Society, ou_1125545              
3Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Max Planck Society, ou_1497704              

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Schlagwörter: Electron donor-acceptor cyclophanes; Charge-transfer compounds; Crown ethers; Oligooxaparacyclophane metal complexes, charge-transfer absorption of, crystal structures of; Cyclophanes, electron donor-acceptor
 Zusammenfassung: The intramolecular oligooxa[3n.3]paracyclophane quinhy-drones 2–5 (with n = 3 to 6) were synthesized and their interactions with alkali and alkaline earth metal and mercury(II) ions were studied by electron absorption and NMR spectroscopy. Remarkable enhancements of the CT absorptions were observed by complexation with metal ions of the pentaoxa[15.3]paracyclophane quinhydrone 4 and the hexaoxa[18.3]paracyclophane quinhydrone 5 to the corresponding complexes 6a–e and 7, respectively. The various donor-acceptor orientations and the crown ether-like complexation in the calcium complex 6d, the mercury complex 6e and the barium complex 7 were determined by X-ray analysis. Moreover, the X-ray structures of the tetramethoxy-2,5,8-trioxa[9.3]paracyclophane 8a, a precursor of the quinhydrone 2, and of the pentaoxa[15.3](2,5)-p-benzoquinonophane 20, the product of oxidative demethylation of the quinhydrone 4, are given. For comparison with the cyclic quinhydrones acyclic analogs are also described.

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Sprache(n): eng - English
 Datum: 1994-03-242006-01-261994-10
 Publikationsstatus: Erschienen
 Seiten: 16
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: eDoc: 666741
DOI: 10.1002/cber.19941271024
Anderer: 4138
 Art des Abschluß: -

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Titel: Chemische Berichte
  Andere : Chem. Ber.
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Weinheim : VCH Verlagsgesellschaft mbH
Seiten: - Band / Heft: 127 (10) Artikelnummer: - Start- / Endseite: 1993 - 2008 Identifikator: ISSN: 0009-2940
CoNE: https://pure.mpg.de/cone/journals/resource/954926940716