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Pyridinium-based receptors

Ghosh K, Sarkar AR, Patra A (2009) Pyridinium amide-based simple synthetic receptor for selective recognition of dihydrogenphosphate. Tetrahedron Lett 50 6557-6561... [Pg.100]

The anion templated syntheses by Beer afforded receptors 60-62 by reacting the chloride salt of the starting pyridinium precursor with an appropriately chosen 1,3-diamidobenzene derivative. Based on 1H NMR spectroscopic titrations carried out in acetone-d6, the structure Cl 60 was found to form with a 1 1 stoichiometry and with an association constant of 2400 M-1. [Pg.339]

The Bronsted acid/base pair pyridinium/pyridine is unusual because redox potentials are available for both partners in an accessible range [35]. This allows detailed anticipation of the sensory behaviour of systems containing pyridine receptors. (49), whose fluorescence properties have received some attention before [113], is a member of a family of PET sensors for protons whose excitation and emission wavelengths spread over a substantial fraction of the accessible optical spectrum without compromising sensory action [114]. [Pg.246]


See other pages where Pyridinium-based receptors is mentioned: [Pg.1]    [Pg.34]    [Pg.1]    [Pg.34]    [Pg.1095]    [Pg.1112]    [Pg.48]    [Pg.766]    [Pg.114]    [Pg.459]    [Pg.757]    [Pg.171]    [Pg.733]    [Pg.757]    [Pg.58]    [Pg.1969]    [Pg.2923]    [Pg.370]    [Pg.17]   
See also in sourсe #XX -- [ Pg.34 ]




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