Cryptates alkali metal complexes

The kinetics and dynamics of crvptate formation (75-80) have been studied by various relaxation techniques (70-75) (for example, using temperature-jump and ultrasonic methods) and stopped-flow spectrophotometry (82), as well as by variable-temperature multinuclear NMR methods (59, 61, 62). The dynamics of cryptate formation are best interpreted in terms of a simple complexation-decomplexation exchange mechanism, and some representative data have been listed in Table III (16). The high stability of cryptate complexes (see Section III,D) may be directly related to their slow rates of decomplexation. Indeed the stability sequence of cryptates follows the trend in rates of decomplexation, and the enhanced stability of the dipositive cryptates may be related to their slowness of decomplexation when compared to the alkali metal complexes (80). The rate of decomplexation of Li" from [2.2.1] in pyridine was found to be 104 times faster than from [2.1.1], because of the looser fit of Li in [2.2.1] and the greater flexibility of this cryptand (81). At low pH, cation dissociation apparently... 

Adenosine triphosphate alkali metal complexes, 34 vanadyl complexes, 568 Alane, 123 amine adducts, 107 phosphine adducts, 111 Alane, alkoxy-, 124 Alane, amino-, 109 Alane, imino-, 109 Alkali metal complexes, 1-70 acid anions, 30 acid salts, 30 bipyridyl, 13 crown ethers cavity size, 38 cryptates... 

Weber, E., and Vogtle, E, Crown-type compounds—an introductory overview, in Host-Guest Complex Chemistry, Vogtle, E, Ed., Springer Verlag, Berlin, 1981, 11. Hemery, E, Warzelhan, V, and Boileau, S., Kinetics of ring opening of propylene sulfide. 1. Alkali metal and cryptated metal carbonyl. Polymer, 21, 77, 1980. 

Modem work on these and related bare post-transition element clusters began in the 1960s after Corbett and coworkers found ways to obtain crystalline derivatives of these post-transition element clusters by the use of suitable counterions. Thus, crystalline derivatives of the cluster anions had cryptate or polyamine complexed alkali metals as countercations [8]. Similarly, crystalline derivatives of the cluster cations had counteractions, such as AlCLj, derived from metal halide strong Lewis acids [9]. With crystalhne derivatives of these clusters available, their structures could be determined definitively using X-ray diffraction methods. 

Table 10 Rates and Selectivities of Alkali Metal Cation Transport via Cryptate Complexes...

Of particular significance in this respect has been the ability to prepare, characterize and study most intriguing species, the alkalides [2.79, 2.80] and the electrides [2.80, 2.81] containing an alkali metal anion and an electron, respectively, as counterion of the complexed cation. Thus, cryptates are able to stabilize species such as the sodide [Na+ c 9]Na- and the electride [K+ c 9]e-. They have also allowed the isolation of anionic clusters of the heavy post-transition metals, as in ([K+ c cryp-tand]2 Pb52-) [2.82]. 

With alkali metal cryptates, cations and anions are well separated (except for the KNCS complex of [2.2.1] in which the ligand is too small to effectively shield the cation). Indeed the cryptated cation may be regarded as a very large, spheroidal cation (—10 A in diameter) of low surface charge density. 

Cryptands were found to react with metal solutions in basic solvents to generate the alkali metal cryptate and an alkali anion (alkalide), for example (Na[2.2.2])+Na (62, 63). 23Na-NMR measurements of this salt in methylamine, tetrahydrofuran, and ethylamine solutions showed that the Na resonance is shifted strongly upheld from the Na resonance (free or complexed) as shown in Fig. 7. The anion resonates at approximately the same frequency as that calculated for the free... 

Kirch and Lehn have studied selective alkali metal transport through a liquid membrane using [2.2.2], [3.2.2], [3.3.3], and [2.2.C8] (146, 150). Various cryptated alkali metal picrates were transported from an in to an out aqueous phase through a bulk liquid chloroform membrane. While carrier cation pairs which form very stable complexes display efficient extraction of the salt into the organic phase, the relative rates of cation transport were not proportional to extraction efficiency and complex stability (in contrast to antibiotic-mediated transport across a bulk liquid membrane). Thus it is [2.2.Ca] which functions as a specific potassium ion carrier, while [2.2.2] is a specific potassium ion receptor (Table VI). 

Some molecular transition-metal complexes of P , As3-, and Sb3 have been isolated as salts of cryptated alkali metal ions. The structures of the complex anions are shown in Fig. 15.3.9. The bond valence b and bond number of these complex anions are as follows ... 

In general, discrete Zintl anions, whether they obey the simple octet rule or are electronically more complex, can often be obtained intact from the initial Zintl phase by substituting tetraalkylammonium ions for the alkali metal cations or by encapsulating the latter in a cryptand such as cryptate-222 (see 1-XXII).25... 

Crown ethers have particularly large complexing constants for alkali metals equilibrium constants for cyclohexyl-crown-6, for example, are in the order K+ > Rb+ > Cs+ > Na+ > Li+. The cryptates have high complexing ability especially for M2+ ions and will render even BaS04 soluble. They also have good complexing ability for transition metal ions (e.g., for lanthanides). 

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