Metal template reactions thermodynamic

Metal template reactions, 1, 416, 433 equilibrium kinetic, 1, 434 thermodynamic, 1, 434 Metal tolerance amino acid complexes, 2, 964 plants, 2, 963 Metal toxicity... 

Mercury, tris(l,10-phenanthroline)-structure, 64 Mercury(II) complexes masking agent, 536 Mercury electrodes potential range aqueous solution, 480 Metal carbonyls structure, 16 Metallocenes nomenclature, 126,127 Metallochromic indicators, 554 Metallofluorescent indicators, 558 Metallothionein proteins, 142 Mettd-metal bonding, 137,169 gravimetry, 525 history, 21,23 nomenclature, 122, 123 Metal nitrosyls structure, 16 Metal-phthalein metallochromic indicator, 557 Metal template reactions, 416,433 equilibrium kinetic, 434 thermodynamic, 434 Methane, dichloro-... 

Two possible roles for the metal ion in a template reaction have been delineated (Thompson Busch, 1964). First, the metal ion may sequester the cyclic product from an equilibrium mixture such as, for example, between products and reactants. In this manner the formation of the macrocycle is promoted as its metal complex. The metal ion is thus instrumental in shifting the position of an equilibrium - such a process has been termed a thermodynamic template effect. Secondly, the metal ion may direct the steric course of a condensation such that formation of the required cyclic product is facilitated. This process has been called the kinetic template effect. 

The template effect has been recognized to show two or three aspects. The thermodynamic template effect involves the removal of a product from an equilibrium by stabilization of its metal complex (Scheme 29). This phenomenon has also been termed the equilibrium template effect,112 but some authors5 draw a distinction between these two types of effects. They reserve the equilibrium template effect for reactions which result in the formation of different products in the metal-assisted and metal-free reactions. 

The synthesis of quadridentate imine chelates usually requires the combination of two equivalents of the carbonyl compound and a diamine, as in the formation of complexes of ligands (6),17 18 (7)19 and (8).20,21 In similar fashion, thermodynamic template reactions allow the very effective synthesis of quinquedentate and sexadentate metal complexes of ligands such as (9),22 (10),23 (ll),24 (12)25 and (13).26 Condensation of 1,1,1-tris(aminomethyl)ethane with pyridine-2-carbaldehyde alone yields... 

The thermodynamic stability of the macrocyclic complex provides one of the driving forces for cyclisation in template reactions. In a way, co-ordination of the macrocycle to the metal ion provides a thermodynamic sink into which the reaction product can fall. This is clearly of importance when we consider the reactions such as the formation of metal... 

In terms of template reactions, this combination of kinetic and thermodynamic stability usually means that the metal ion remains co-ordinated to the macrocyclic ligand and the isolation of the metal complex of the macrocycle provides strong circumstantial evidence for the existence of a metal-directed process. This is particularly easy to establish if the incorporation of the metal ion into the macrocyclic ligand can be shown to be slower than the metal-directed formation reaction. 

Metal ion template mediation in macrocyclic synthesis has been a part of the field since its inception, its importance having been realized early in the development of this area. Two specific roles for the metal ion in template reactions have been proposed. These are, in turn, kinetic and thermodynamic in origin." In the kinetic template effect, the arrangement of ligands already coordinated to the metal ion provides control in a subsequent condensation during which the macrocycle is formed. The thermodynamic effect serves to promote stabilization of a structure which would not be favored in the absence of a metal ion. Schiff base condensations tend to be dependent on this latter type of template effect. Some of the more routine and general synthetic procedures will be described here. A more in-depth treatment can be found in a review by Curtis, with particular emphasis on general methods as well as modifications of preformed macrocycles." ... 

Some believe that there are two main template effects kinetic and thermodynamic [8]. The latter is responsible for an increase in the yield of the complex with ligands formed in situ in the presence of metal ions, which bind products that result from ordinary reactions and to withdraw them from the reaction medium. These procedures are not true template reactions since they do not satisfy the above-mentioned conditions, and the metal ion causes equilibrium shift only. It is impossible to distinguish between kinetic and thermodynamic contributions to the template effect, since the coordination to the metal ion simultaneously causes both steric... 

The precatenate intermediate can be regarded as a threaded complex, which is thermodynamically stabilized by coordination bonds, from this simple consideration, a transition metal-templated synthesis of rotaxanes was devised, the principle of which is shown in Figure 28 [117]. The threading step (i) is a complexation reaction. 

Different roles for the metal ion in a template reaction have been dehneated and termed thermodynamic template effect and kinetic template effect In the first case, the metal ion picks out the macrocyclic ligand from an equilibrating mixture of products, thus driving the reaction equilibrium... 

The hexahydropyrimidine (58), formed from l-phenylpropane-l,2-dione and propane-1,3-diamine, is an excellent precursor for the a-diimine macrocyclic complexes (60), presumably via the amino ketone (59) (Scheme 36).126 In this case, intramolecular cyclization of (59) to (58) is reversible, so that the metal ion can exert a thermodynamic template effect in formation of the complex (60). This represents a further example of a long-known phenomenon in which a metal ion can stabilize an a-diimine structure by virtue of the formation of stable five-membered chelate rings. Many 2-hydroxy- or 2-mercapto-amines undergo reaction with a-dicarbonyl compounds to yield heterocyclic compounds rather than a-diimines. However, in the presence of suitable metal... 

We have already looked at three key Schiff base macrocycles (Figure 3.56), which were amongst the first artificial metal macrocycle compounds to be synthesised. These compounds are generally formed by thermodynamic template effects because, unless water is removed during the course of the reaction, the condensation is reversible, allowing complexation to sequester the most stable metal-product... 

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