1989
DOI: 10.1002/9780470772232.ch4
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Crown ethers—complexes and selectivity

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Cited by 19 publications
(12 citation statements)
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“…Selectivity of crown ether not only sensitive toward cation diameter, macrocycle cavity size, donor atoms, electron donating and withdrawing group substitution but also the complementary counterion, solvent types and extraction temperatures. In the case of the charged metal complex and the counterion exist mainly in the same cage solvent, the counterion effects will be observed [3]. The EXAFS experiment showed that even in highly solvated environment, counterion still has influence.…”
Section: Introductionmentioning
confidence: 94%
“…Selectivity of crown ether not only sensitive toward cation diameter, macrocycle cavity size, donor atoms, electron donating and withdrawing group substitution but also the complementary counterion, solvent types and extraction temperatures. In the case of the charged metal complex and the counterion exist mainly in the same cage solvent, the counterion effects will be observed [3]. The EXAFS experiment showed that even in highly solvated environment, counterion still has influence.…”
Section: Introductionmentioning
confidence: 94%
“…F) Benzo[is]crown-5 and a series of derivatives modified with electron donating or withdrawing substituents. All structures are from Cox.& Schneider (1992) or from Vogtle & Weber (1980). Lehn & Sauvage (1975) and the cryptand structures are illustrated in Fig.…”
Section: Organic Chelators Useful As Models For Protein C a U Sitesmentioning
confidence: 99%
“…successively substituted with nitrogen, the cryptand affinities for Ca 2+ , Sr 2+ and Ba 2+ decrease modestly for the first nitrogen substitutions (oxygen: nitrogen ratio 5:3), but begin to drop dramatically when the subsequent nitrogen substitutions equalize the number of coordinating oxygens and nitrogens (oxygen: nitrogen ratio 4:4) (Lehn & Montavon, 1978;Arnaud-Neu et al 1977). Group la monovalent ions, including K + and Na + , exhibit even stronger preference for coordinating oxygen over nitrogen (reviewed by Vogtle & Weber, 1980). High affinity binding requires that the spatial features of the coordinating array be optimally configured in the metal binding cavity.…”
Section: Organic Chelators Useful As Models For Protein C a U Sitesmentioning
confidence: 99%
“…This is because monovalent ions usually exhibit a lower stability constant in crown ether or cryp-tand complexes. [8] Therefore, more detailed studies were focused on polymers 1 d and 1 c. The absolute molecular weight of the metal containing polymer was not determined because it is difficult to obtain reliable results for polymers that contain electronic charge on the main chain. [9] Fig.…”
Section: Polymer Synthesis and Structural Characterizationmentioning
confidence: 99%