Crown ethers complex structures

Photolysis of the arene complexes in the presence of monodentate ligands, e.g. carbon monoxide, leads to new complexes of the type CpFe(L) whereas in pure aprotic solvents, ferrocene and iron salts are formed Investigation of the photo-lytic reaction of an iron arene complex with excess ethylene oxide in methylene chloride solution (Meier and Rhis ) showed that a crystalline crown ether complex (structure shown in Fig. 9) was obtained in high yield. Only traces of dioxane could be detected. 

Figure 4.11 Molecular structures of typical crown-ether complexes with alkali metal cations (a) sodium-water-benzo-I5-crown-5 showing pentagonal-pyramidal coordination of Na by 6 oxygen atoms (b) 18-crown-6-potassium-ethyl acetoacetate enolate showing unsymmelrical coordination of K by 8 oxygen atoms and (c) the RbNCS ion pair coordinated by dibenzo-I8-crown-6 to give seven-fold coordination about Rb.

An enormous variety of solvates associated with many different kinds of compounds is reported in the literature. In most cases this aspect of the structure deserved little attention as it had no effect on other properties of the compound under investigation. Suitable examples include a dihydrate of a diphosphabieyclo[3.3.1]nonane derivative 29), benzene and chloroform solvates of crown ether complexes with alkyl-ammonium ions 30 54>, and acetonitrile (Fig. 4) and toluene (Fig. 5) solvates of organo-metallic derivatives of cyclotetraphosphazene 31. In most of these structures the solvent entities are rather loosely held in the lattice (as is reflected in relatively high thermal parameters of the corresponding atoms), and are classified as solvent of crystallization or a space filler 31a). However, if the geometric definition set at the outset is used to describe clathrates as crystalline solids in which guest molecules... 

Figure 60 The structure of the crown ether complex of barium diphenylmethanide 116 (the dashed line is to a contact at 3.39 A). 

Cross-interaction constants and transition-state structure in solution, 27, 57 Crown-ether complexes, stability and reactivity of, 17,279 Crystallographic approaches to transition state structures, 29,87 Cyclodextrins and other catalysts, the stabilization of transition states by, 29,1... 

For sodium and potassium chalcogenolates, donor influence on structural pattern has been explored with a special emphasis in donor hapticity. Thus, crown ether complexation allows the isolation of monomeric species, such as [K(SCPh3)(18-crown-6)Lra] (L=thf, CgH6, hmpa, n = 0.5 L=toluene, n = l),36 [K(SMes )(dibenzo-18-crown-6)(thf)],45 [K(STrip)(dibenzo-18-crown-... 

The proportion of the /rans-O-alkylated product [101] increases in the order no ligand < 18-crown-6 < [2.2.2]-cryptand. This difference was attributed to the fact that the enolate anion in a crown-ether complex is still capable of interacting with the cation, which stabilizes conformation [96]. For the cryptate, however, cation-anion interactions are less likely and electrostatic repulsion will force the anion to adopt conformation [99], which is the same as that of the free anion in DMSO. This explanation was substantiated by the fact that the anion was found to have structure [96] in the solid state of the potassium acetoacetate complex of 18-crown-6 (Cambillau et al., 1978). Using 23Na NMR, Cornelis et al. (1978) have recently concluded that the active nucleophilic species is the ion pair formed between 18-crown-6 and sodium ethyl acetoacetate, in which Na+ is co-ordinated to both the anion and the ligand. 

In the preceding section it was shown that the stability of crown-ether complexes with alkylammonium salts depends on the relationship between the structures of the crown ethers and the ammonium ions. How critically this relationship determines the complex stability will become clear in this section, which deals with the discrimination between the two enantiomers of racemic salts by chiral macrocyclic ligands. 

All alkali and ammonium DNM salts have been prepared and characterized. Solid state structures of the potassium, cesium, tetramethylammonium and a potassium crown-ether complex of DNM are available . 

We now proceed to more complicated ionophores in order to testify the validity of this extrathermodynamic relationship and its hypothetical interpretation as an attempt to understand the nature of supramolecular interactions more generally and deeply. The thermodynamic parameters are plotted in Figures 16-19 for long glymes, (pseudo)cyclic ionophore antibiotics, lariat ethers with donating side-arm(s), and bis(crown ethers), whose structural changes upon complexation are schematically illustrated in Figure 20. 

Figure 5 Crystal structures of (a) [18]crown-6 complex with two malonodinitrile molecules (b) binaphthol crown ether complex with water (reproduced with permission from 77CB2249 and 78AX(B)3387)...

The structures of several related crown ether complexes have also been solved. Ligand (87) forms a 1 1 complex with KNCS. In this complex the cation is coordinated to all of the donor atoms of the ligand, with a further weak interaction with the NCS anion.422... 

The structure of [Cs(l8-crown-6)z]+e has been determined 109 Because the efectride anions are extremely poor scatterers compared to the large cesium cation (and to a lesser extent the C and O atoms of the crown ether), the structure has the odd appearance of complexed metal cations with no corresponding anions (Fig. 12.50b). However, the most likely position of the electrons can be inferred from the presence of cavities of 240-pm radius presumably the electrons are located in these cavities. 

Polar O—H bonds are found in molecules such as water and alcohols. Crystal structures of several crown ether complexes have indicated that the cavity need only be partially filled by water.260-262 Several host-guest complexes of alcohols with the pyridino crown (83) have been reported.263 Longer chain and branched alcohols do not in general form crystalline adducts with this ligand. 

Thuery, P., Nierlich, M., Bryan, J.C. et al. 1997. Crown ether conformations in 1,3-calix[4]arene bis(crown ether) Crystal structures of a cesium complex and solvent adducts and molecular dynamics simulations. J. Chem. Soc. Dalton Trans. 1997 (22) 4191 4202. 

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