Macrocycles valinomycin

For example, potassium-selective electrodes can be constructed with the natural macrocycle valinomycin as a neutral carrier in diphenyl ether. This membrane has a much... 

Neutral carriers are organic complexing agents which are capable of sequestering and transporting ionic species in a hydrophobic organic phase. The antibiotics, valino-mycin and nonactin were the first neutral carriers to be incorporated in an ISE These macrocyclic neutral carriers contain a polar internal cavity and an outer hydro-phobic shell. The excellent selectivity exhibited by valinomycin for potassium ions is... 

Impetus was given to work in the field of selective cation complex-ation by the observation of Moore and Pressman (5) in 1964 that the macrocyclic antibiotic valinomycin is capable of actively transporting K+ across mitochondrial membranes. This observation has been confirmed and extended to numerous macrocyclic compounds. There is now an extensive literature on the selective complexation and transport of alkali metal ions by various macrocyclic compounds (e.g., valinomycin, mo-nactin, etc.) (2). From solution spectral (6) and crystal X-ray (7) studies we know that in these complexes the alkali metal cation is situated in the center of the inwardly oriented oxygen donor atoms. Similar results are found from X-ray studies of cyclic polyether complexes of alkali metal ions (8) and barium ion (9). These metal macrocyclic compound systems are especially noteworthy since they involve some of the few cases where alkali metal ions participate in complex ion formation in aqueous solution. 

Valinomycin (137) is a macrocyclic dodecadepsipeptide and has shown an unequalled K+/Na discrimination.5" As a consequence of this prime ionophorous behaviour many studies have been carried out on both the free ligand and on its metal complexes, and here discussion is restricted to the nature of the metal complexes. 

Natural macrocycles displaying antibiotic propenies are also very efficient in the recognition of alkali metal ions. For instance, valinomycin (5 in Fig, 3) gives a strong and selective complex in which a K+ ion is included in the macrocyclic cavity in octahedral environment of six carbonyl oxygens (Fig. 4). 

Although some scattered examples of binding of alkali cations (AC) were known (see [2.13,2.14]) and earlier observations had suggested that polyethers interact with them [2.15], the coordination chemistry of alkali cations developed only in the last 30 years with the discovery of several types of more or less powerful and selective cyclic or acyclic ligands. Three main classes may be distinguished 1) natural macrocycles displaying antibiotic properties such as valinomycin or the enniatins [1.21-1.23] 2) synthetic macrocyclic polyethers, the crown ethers, and their numerous derivatives [1.24,1.25, 2.16, A.l, A.13, A.21], followed by the spherands [2.9, 2.10] 3) synthetic macropolycyclic ligands, the cryptands [1.26, 1.27, 2.17, A.l, A.13], followed by other types such as the cryptospherands [2.9, 2.10]. 

The question of carrier design was first addressed for the transport of inorganic cations. In fact, selective alkali cation transport was one of the initial objectives of our work on cryptates [1.26a, 6.4]. Natural acyclic and macrocyclic ligands (such as monensin, valinomycin, enniatin, nonactin, etc.) were found early on to act as selective ion carriers, ionophores and have been extensively studied, in particular in view of their antibiotic properties [1.21, 6.5]. The discovery of the cation binding properties of crown ethers and of cryptates led to active investigations of the ionophoretic properties of these synthetic compounds [2.3c, 6.1,6.2,6.4-6.13], The first step resides in the ability of these substances to lipophilize cations by complexation and to extract them into an organic or membrane phase [6.14, 6.15]. 

Until the late 1960s, whereas there had been considerable interest in the transition metal complexes of natural and synthetic macrocyclic ligands (1—4), relatively few reports described complexes of alkaline earth and more particularly alkali metal cations. Research in this area was stimulated by the recognition of the importance of the biological role of Na+, K, Ca2 , and Mg2 and also the discovery and characterization of the natural antibiotic ionophores (5, 6). These macrocyclic antibiotics, such as valinomycin and nonactin, were shown to complex alkali metal cations with remarkable selectivity (7-9). 

A host of carriers, with a wide variety of ion selectivities, have been proposed for this task. Most of them have been used for the recognition of alkali and alkaline metal cations (e.g., clinically relevant electrolytes). A classical example is the cyclic depsipeptide valinomycin (Fig. 5.13), used as the basis for the widely used ISE for potassium ion (38). This doughnut-shaped molecule has an electron-rich pocket in the center into which potassium ions are selectively extracted. For example, the electrode exhibits a selectivity for K+ over Na+ of approximately 30,000. The basis for the selectivity seems to be the fit between the size of the potassium ion (radius 1.33 A) and the volume of the internal cavity of the macrocyclic molecule. The hydrophobic sidechains of valinomycin stretch into the lipophilic part of the membrane. In addition to its excellent selectivity, such an electrode is well behaved and has a wide working pH range. Strongly acidic media can be employed because the electrode is 18,000 times more responsive to K+ than to H+. A Nernstian response to potassium ion activities, with a slope of 59mV/pK+, is commonly observed... 

In the case of a neutral non-ionic chelating agent we have neutral carrier-selective electrodes transport is achieved by selective complexa-tion of certain ions. The best-known electrode of this kind is the potassium-selective electrode, whose membrane consists of a valinomycin macrocycle immobilized in phenylether. The important criterion appears to be the size of the cavity in the centre of the macrocycle and interferences are from cations with similar hydrated ionic radius, such as Rb+ and Cs+. 

Polarography of alkaline metals and ammonium ion has proved successful for studying complexes of alkali metals with biologically important macrocyclic compounds such as valinomycin [18], macrotetrolides [19,20] and polyethers [20,21]. 

In 1955, Brockmann and Schmidt-Kastner isolated valinomycin from extracts of streptomyces fulvissimus33). The antibiotic was found to be active against a number of bacteria, yeasts, and fungi205). Valinomycin has a macrocyclic molecular structure consisting of three identical tetradepsipeptide fragments with alternating amino and hydroxy acid residues (Fig. 21). Its synthesis was first achieved by Shemyakin and... 

The X-ray crystal structures of many of the.se complexes have now been determined representative examples are. shown in Fig. 4.11 from which it is clear that, at least for the larger cations, coordinative saturation and bond directionality are far less significant factors than in many transition element complexes. - Further interest in these ligands stems from their use in biochemical modelling since they sometimes mimic the behaviour of naturally occurring, neutral, macrocyclic antibiotics such as valinomycin, monactin, nonactin, nigericin... 

We have already introduced the hole-fit concept for a macrocyclic ligand in Chapter 4 (see Figure 4.38), which effectively means that the most stable complexes form where the internal diameter of the ring cavity matches the size of the entering cation. The effect can be significant for example, the natural antibiotic valinomycin is a macrocycle that binds potassium ion to form a complex 104 times more stable than that formed with the smaller... 

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