Crown ethers binding constants

Although the principal application for 9 has been in the synthesis of cryptands (see Chap. 8), this material has also served as precursor to a number of nitrogen based lariat ethers , sometimes referred to as crown complexanes . Binding constants for such compounds have been measured for a few examples in a few cases , but... 

The concept of matching ligand hole size to the size of the metal ion has played a role in discussions of the apparent selectivity of particular ligands for particular metal ions. The selectivity (such as that discussed above for [M(18-crown-b)]" complexes, equation 11.20) is based on measured stabihty constants. It has, however, also been pointed out that the stability constants for [KL] complexes are often higher than for corresponding [ML] complexes where M = Li, Na, Rb or Cs, even when hole-matching is clearly not the all-important factor. An alternative explanation focuses on the fact that, when a crown ether binds M" ", the... 

It was noted early by Smid and his coworkers that open-chained polyethylene glycol type compounds bind alkali metals much as the crowns do, but with considerably lower binding constants. This suggested that such materials could be substituted for crown ethers in phase transfer catalytic reactions where a larger amount of the more economical material could effect the transformation just as effectively as more expensive cyclic ethers. Knbchel and coworkers demonstrated the application of open-chained crown ether equivalents in 1975 . Recently, a number of applications have been published in which simple polyethylene glycols are substituted for crowns . These include nucleophilic substitution reactions, as well as solubilization of arenediazonium cations . Glymes have also been bound into polymer backbones for use as catalysts " " . 

The binding constants are also influenced by the number of ion-dipole interactions present involving the metal and the ether oxygen donors. As the ring size increases, so will the number of available dipoles this effect will be superimposed (and may dominate) the metal-ion binding pattern along a series of crowns. 

For monocyclic crown ethers the data presented in Table 4 and the stability constants for glymes [43]—[46] determined by Chaput et al. (1975) can be combined to calculate the macrocyclic effect (Table 7). The data indicate that the gain in binding energy on ring closure shows the same pattern as the ion selectivity of the crown ether, being highest for Na+/15-crown-5, K+/18-... 

Sr2+ so well that it was selectively extracted from a bulk sample of a barium salt (Helgeson et al., 1973a). Binding constants for metal-cation complexes of 1,3-xylyl-crown ethers [66]—[69] carrying an additional carboxylate binding... 

The cation affinity of aza-crown ethers depends on the type of substituent attached to the nitrogen. Wester and Vogtle (1978) have determined the cation binding constants for substituted [2.2]-cryptands 138] and [89]—191 ] in... 

Rates of decomplexation (kJ2) of cation complexes can also be determined by nmr spectroscopy on the cation. Rates of complex formation are then calculated from kn and the binding constant. The results for several ligands, cations, and solvents are given in Table 20. Despite the wide variations, the rates of complex formation are all in the range 2 x 107 to 8 x 10 M 1 s 1. In contrast, rates of decomplexation for crown-ether complexes span a much broader range 6.1 x 102 to 2 x 105 s 1. Comparison of crown-ether data with data for [2.2.2]-cryptand [37] and the linear polyether [92] also shows that the... 

The relative order of the catalytic activities of the crown ethers ([20] + [21]) > [9] > [ 11 ] > [ 13] > [8]) is the same as the relative order of their capacities to bind K+ (Table 4). However, the intrinsic reactivities of the ion pairs were also dependent on crown-ether structure, as was shown by experiments in which the alkylation rates were determined at various crown/phenoxide molar ratios. The curve obtained (Fig. 2) is similar to the curves found in titration experiments (Live and Chan, 1976 De Jong et al., 1976b), and shows that the rate constant reaches a maximum (called plateau kinetics in the literature) when all of the salt is complexed. 

The t-butylammonium cation forms a relatively weak complex, which was attributed to steric repulsion. The stability of anilinium complexes is about the same as that of alkylammonium complexes. The introduction of substituents at the 2- and 6-positions increases the steric repulsion which results in a drop in binding constant. This effect is enthalpic in origin. These results show that variations in the group R have only a minor effect on the stability of complexes in which the crown ether has a fully exposed cavity. Furthermore, there is no relationship between the p-K.-value of RNHJ and the stability of the complex. 

Association constant (M-1) for the binding of water by crown ethers to form a 1 1 complex. Estimated accuracy 10% c Molar ratio solubilized water/crown ether... 

Initially, on addition of sodium cations to a solution of the ligand, two distinct CV waves were observed, corresponding to the uncomplexed and complexed compound [1] (Fig. 4) (Chariot et al., 1962). Hie wave at the higher positive potential corresponds to the solution complexed species. Hie oxidized ferrocene crown ether has a lower binding constant with sodium than the... 

Intramolecularity in lariat ether complexation was demonstrated in three ways. First, when solution cation binding constants were determined. Kg was shown to be independent of cation and macrocycle concentrations (within certain limits). The efficacy of complexation of a single cation by two macrorings [(ML2) complex formation] should be concentration dependent. Second, ammonium cation binding constants were determined for the series (see above) of monoaza-15-crown-5 and -18-crown-6 compounds having (CH2CH20)jiClH3 (n 0 to 8) sidearms (31). 

In our initial studies of the polymerization of butyl acrylate by solid potassium persulfate in acetone solution (2), we attempted to relate the rate of polymerization to the ability of various crown ethers to complex the potassium cation. A reasonable correlation was discovered between log Rp and log K, where K represents the binding constant of the crown ether for in methanol solution (Figure 1). This finding provided some support for the idea that a typical phase transfer process was occurring in these reacti ons. 

The presence of two crown ether moieties in the baskets allows the simultaneous binding of two ammonium groups. Organic diammonium salts of type H3N(CH2)nNH3 are bound very strongly, as is evident from the high association constants in Table 5 [19]. 

As noted earlier, the similarities between H+ and alkali metal cations have led to the use of the former as a probe in biological studies, including studies with various macrocydic ligands, especially those with oxygen donor atoms. The thallium(I) cryptates behave kinetically like the potassium compounds, and the binding constants to 18-crown-6 have been measured by 205T1 NMR methods.347 Several Tl1 compounds with crown ethers (L) have been prepared in... 

---