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Steric effects macrocyclic ligands

Schiff base 69 and sulfur-linked 70 ferrocene bjs-crown ether ligands have also been prepared and both were shown to be potassium ion selective, especially the S-linked macrocycle 70 [89]. Compound 69 did not behave well electrochemically and somewhat unexpectedly addition of to 70 resulted in a cathodic shift of the ferrocene redox couple, possibly due to conformational steric effects involving the electron lone pairs on sulfur, but certainly reminiscent of Sato s thia-ferrocenophanes discussed earlier. [Pg.304]


See other pages where Steric effects macrocyclic ligands is mentioned: [Pg.911]    [Pg.206]    [Pg.149]    [Pg.218]    [Pg.62]    [Pg.391]    [Pg.484]    [Pg.55]    [Pg.193]    [Pg.207]    [Pg.329]    [Pg.41]    [Pg.124]    [Pg.484]    [Pg.932]    [Pg.14]    [Pg.263]    [Pg.274]    [Pg.136]    [Pg.195]    [Pg.319]    [Pg.1184]    [Pg.1263]    [Pg.1267]    [Pg.49]    [Pg.2125]    [Pg.2177]    [Pg.76]    [Pg.104]    [Pg.55]    [Pg.395]    [Pg.121]    [Pg.147]    [Pg.911]    [Pg.645]    [Pg.260]    [Pg.2124]    [Pg.2176]    [Pg.1184]    [Pg.1263]    [Pg.1267]    [Pg.124]    [Pg.499]    [Pg.1578]    [Pg.3930]    [Pg.4638]    [Pg.4717]    [Pg.4721]   
See also in sourсe #XX -- [ Pg.64 ]




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