Cryptands metals

The hexacarbonylmetalates(-II) of group 4 can be synthesized by reducing the tetrachlorides with potassium in the presence of a cryptand. In the case of hafnium, the starting material is a tertiary-phosphine-carbonyl complex of the zerovalent metal (see equations 52 and 53). The cryptand/(metal cation) system, characterized by a large mass and a low charge density, presumably has a stabilizing effect on the carbonyl anion. Reactions of equations (52) and (53) are carried out with CO at atmospheric pressure. ... 

Jean-Marie Lehn et al. Cryptand metal complexes... 

Synthesis by high-dilution techniques requires slow admixture of reagents ( 8-24 hrs) or very large volumes of solvents 100 1/mmol). Fast reactions can also be carried out in suitable flow cells (J.L. Dye, 1973). High dilution conditions have been used in the dilactam formation from l,8-diamino-3,6-dioxaoctane and 3,6-dioxaoctanedioyl dichloride in benzene. The amide groups were reduced with lithium aluminum hydride, and a second cyclization with the same dichloride was then carried out. The new bicyclic compound was reduced with diborane. This ligand envelops metal ions completely and is therefore called a cryptand (B. Dietrich, 1969). 

In 1967, DuPont chemist Charles J. Pedersen (21) discovered a class of ligands capable of complexing alkaU metal cations, a discovery which led to the Nobel Prize in Chemistry in 1987. These compounds, known as crown ethers or cryptands, allow gready enhanced solubiUty of sodium and other alkaU metals in amines and ethers. About 50 crown ethers having between 9—60 membered oligoether rings were described (22). Two such stmctures, dibenzo-18-crown-6 (1) and benzo-9-crown-3 (2), are shown. 

Cryptands, 7, 731-761 alkali metal complexes NMR, 7, 740 reactivity, 7, 743-744 alkaline earth complexes reactivity, 7, 743-744 anion complexes, 7, 747-748 applications, 7, 753-761 as biological models, 7, 753-754 bis-tren... 

H-1,3,2- Diazaborole, 1,2-dihydro-reactions, 1, 641 synthesis, 1, 639, 640 transition metal complexes, 1, 641 Diazadiborine, tetrahydro-semi-empirical calculations, 1, 632 Diaza[2.2.2]cryptand synthesis, 7, 750 Diazacryptands bispyridine... 

A number of bridged crown ethers have been prepared. Although the Simmons-Park in-out bicyclic amines (see Sect. 1.3.3) are the prototype, Lehn s cryptands (see Chap. 8) are probably better known. Intermediates between the cryptands (which Pedersen referred to as lanterns ) and the simple monoazacrowns are monoazacrowns bridged by a single hydrocarbon strand. Pedersen reports the synthesis of such a structure (see 7, below) which he referred to as a clam compound for the obvious reason . Although Pedersen appears not to have explored the binding properties of his clam in any detail, he did attempt to complex Na and Cs ions. A 0.0001 molar solution of the clam compound is prepared in ethanol. The metal ions Na and Cs are added to the clam-ethanol solutions as salts. Ultraviolet spectra of these solutions indicate that a small amount of the Na is complexed by the clam compound but none of the Cs . 

The in-out bicyclic amines prepared by Simmons and Park bear a remarkable semblance to the cryptands but lack the binding sites in the bridges. As a result, these molecules interact with electrophiles in a fashion similar to other tertiary amines and generally do not exhibit strong interactions with alkali or alkaline earth metal ions. The in-out bicyclic amines are prepared by reaction of the appropriate acid chlorides and amines in two stages to yield the macrobicyclic amine after reduction of the amidic linkages. A typical amine is shown above as compound 18. 

In other sections in this chapter, we have referred to a variety of macropolycyclic structures which are more elaborate than the simple three-stranded bicyclic cryptands. This includes bridged double-macrocycles " , in-out bicyclic amines and the macrotricyclic quaternary ammonium salts of Schmidtchen. In addition to these, there are two other types of compounds which deserve special note. The first of these is a stacked twin-ring cryptand, but it is a hybrid molecule rather than a double-cryptand . The species shown below as 20 is a crowned porphyrin, and was designed to provide a pair of metal cation binding sites similar to those which might be available in natural biological systems . 

A particularly imaginative application of this concept has led to the isolation of compounds which contain monatomic alkali metal anions. For example, Na was reacted with cryptand in the presence of EtNHi to give the first example of a sodide salt of... 

Poly (macrocyclic) compounds. The analytical application of compounds such as crown polyethers and cryptands is based on their ability to function as ligands and form stable stoichiometric complexes with certain cations. Special importance is due to their preference for alkali metal ions which do not form complexes with many other ligands. A number of these compounds are commercially available and their properties and analytical applications have been described by Cheng et a/.11... 

Fig. 29. The pseudo-cryptand 110 can be transformed with boric acid and a metal hydroxide to the corresponding charge neutral pseudocryptates 111-116. 117 serves as precursor ligand for Li ...

In Chapter 3, we saw that cryptands specifically solvate the alkali metal portion of salts like KF, KOAc, and so on. Synthetic advantage can be taken of this fact to allow anions to be freer, thus increasing the rates of nucleophilic substitutions and other reactions (see p. 455). 

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