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Volumn 15, Issue 11, 2009, Pages 2486-2490

Toward volatile and nonvolatile molecular memories: Fluorescence switching based on fluoride-triggered interconversion of simple porphyrin derivatives

Author keywords

Fluoride; Molecular devices; Oxoporphyrinogen; Porphyrinoids; Switching

Indexed keywords

ALDEHYDES; DATA STORAGE EQUIPMENT; DICHLOROMETHANE; FATTY ACIDS; FLUORESCENCE; NITROGEN COMPOUNDS; OPTICAL PROPERTIES; PORPHYRINS; SWITCHING;

EID: 62349121594     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200802469     Document Type: Article
Times cited : (33)

References (64)
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    • Oxoporphyrinogen 3 is related to meso-tetraoxoporphyrinogen (see C Otto, E. Breitmaier, Liebigs Ann. Chem. 1991, 1347-1349)
    • Oxoporphyrinogen 3 is related to meso-tetraoxoporphyrinogen (see C Otto, E. Breitmaier, Liebigs Ann. Chem. 1991, 1347-1349)
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    • and to the calix[4]pyrroles (see: J. L. Sessler, P. J. Gale in The Porphyrin Handbook, 6 (Eds.: K. M. Radish, K. M. Smith, R. Guilard), Academic Press, Burlington, 2000, pp. 257-277).
    • and to the calix[4]pyrroles (see: J. L. Sessler, P. J. Gale in The Porphyrin Handbook, Vol.6 (Eds.: K. M. Radish, K. M. Smith, R. Guilard), Academic Press, Burlington, 2000, pp. 257-277).
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    • Compound 3 is capable of binding anions, yielding the 3/anions complex with 1:2 stoichiometry and giving a spectrum identical to that shown in Figure 3 A,b, see: J. P. Hill, A. L. Schumacher, F. D'Souza, J. Labuta, C. Redshaw, M. R. J. Elsegood, M. Aoyagi, T. Nakanishi, K. Ariga, Inorg. Chem. 2006, 45, 8288-8296.
    • Compound 3 is capable of binding anions, yielding the 3/anions complex with 1:2 stoichiometry and giving a spectrum identical to that shown in Figure 3 A,b, see: J. P. Hill, A. L. Schumacher, F. D'Souza, J. Labuta, C. Redshaw, M. R. J. Elsegood, M. Aoyagi, T. Nakanishi, K. Ariga, Inorg. Chem. 2006, 45, 8288-8296.
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    • Under these conditions, ascorbic acid is fully dissolved as indicated by the homogeneity of the solution. Judging from the spectra obtained, no scattering occurred and isosbestic points were unaffected during monitoring of the reduction process
    • Under these conditions, ascorbic acid is fully dissolved as indicated by the homogeneity of the solution. Judging from the spectra obtained, no scattering occurred and isosbestic points were unaffected during monitoring of the reduction process.
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    • The two-electron aerial oxidation of 1. in basic solutions was reported and studied previously, see reference [11] and a L. R. Milgrom, W. D. Flitter, E. L. Short, J. Chem. Soc. Chem. Commun. 1991, 788-790;
    • The two-electron aerial oxidation of 1. in basic solutions was reported and studied previously, see reference [11] and a) L. R. Milgrom, W. D. Flitter, E. L. Short, J. Chem. Soc. Chem. Commun. 1991, 788-790;
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    • -) permit determination of the quantity of F required and can be used to prove that dioxygen operates as the oxidant for deprotonated 1. However, immediate oxidation prevents these experiments, see : a) J. Alvarez, A. E. Kaifer, Organometallics 1999, 18, 5733-5734;
    • -) permit determination of the quantity of F required and can be used to prove that dioxygen operates as the oxidant for deprotonated 1. However, immediate oxidation prevents these experiments, see : a) J. Alvarez, A. E. Kaifer, Organometallics 1999, 18, 5733-5734;


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