Kinetic template effect

Hydration enthalpy Stability or formation constant Overall and stepwise stability constants Chelate effect Macrocyclic effect Preorganization Equilibrium template effect Kinetic template effect Self-assembly... 

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... 

In 1977, Mandolini and Masci reported clear kinetic evidence that a template effect was important to the cyclization of o-hydroxyphenyl-3,6,9,12-tetraoxa-14-bromotetra-decyl ether. The starting material and its subsequent reactions are illustrated in Eq. (2.4). 

There are also reports of template effects on reactivity ratios in copolymerization. For example, Polowinski20S has reported that both kinetics and reactivity ratios in MMA-MAA copolymerization in benzene arc affected by the presence of a PVA template. 

Hawthorne and co-workers have also produced a series of macrocyclic Lewis acid hosts called mercuracarborands (156, 157, and 158) (Fig. 84) with structures incorporating electron-withdrawing icosahedral carboranes and electrophilic mercury centers. They were synthesized by a kinetic halide ion template effect that afforded tetrameric cycles or cyclic trimers in the presence or absence of halide ion templates, respectively.163 These complexes, which can bind a variety of electron-rich guests, are ideal for catalytic and ion-sensing applications, as well as for the assembly of supramolecular architectures. 

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. 

Whereas Gold and Sghibartz showed that cation complexation depressed the rate of crown-ether disrupture, there is convincing evidence that crown ether formation is facilitated by the presence of cations. The template effect, presumably due to complexation of the open-chain precursor and formation of a crown-type conformation, clearly emerged from studies in which the yield of crown ethers was related to the type of cations present (Reinhoudt et al., 1976). Kinetic evidence for the template effect was presented by Mandolini and Masci (1977), who showed that the rate of cyclization of the precursor of benzo-18-crown-6 [2061 decreased in the order Ba2+ > SrJ+ > K+ > Na+ > Li+. This sequence is the same as the one found for the stability constants of the 1 1 complexes of these cations with 18-crown-6 in water (Table 3). 

In the associates, polymerization occurs according to the zip-propagation mechanism, and auto-acceleration takes place. In the range of temperatures from 10 to GO C, the system gradually changes from the system dominated by occlusion to the system where template effect determines the kinetic behavior. In this range of temperatures, a significant post-effect occurs. ... 

A seemingly similar process of polymerization - the radiation induced polymerization of methyl acrylate in n-hexane - shows also auto-acceleration and post-polymerization. Polymerization was carried out under precipitating conditions. Using the results of kinetics examination, the authors showed that all effects can be explained by the mechanism based on trapped radical reactions in particles of precipitated polymer. No influence of any template effect was detected in these systems. 

Reactions Predominantly Involving Kinetic Template Effects 439... 

The kinetic template effect is observed in reactions in which the metal ion acts by coordinating the reactants. This effect has also been described as a coordination template effect. A more direct description of a kinetic template reaction is one which involves Combination of two Ligands Attached to the same. Metal ion. Such a description leads to the useful acronym CLAM reaction , which graphically portrays the key reaction step. The process can be generalized and compared with the non-template reaction in Scheme 30. 

An essential feature of template reactions of both the thermodynamic and kinetic type is the formation of a new chelate ring. One of the main difficulties in a discussion of mechanistic aspects of template reactions is the inevitable mixture and overlap of mechanistic effects. Those reactions which clearly exhibit a kinetic template effect could also depend to some extent on a thermodynamic one. Also, in some multistep macrocyclization processes, for example, both effects could be involved. Despite the inherent difficulties, the following discussion in this section will be subdivided into two, to cope predominantly with the thermodynamic and kinetic template effects. A further subdivision of thermodynamic and equilibrium effects will not be made. 

The most important reaction of this type is the formation of imine bonds and Schiff bases. For example, salicylaldehyde and a variety of primary amines undergo reaction to yield the related imines, which can be used as ligands in the formation of metal complexes. However, it is often more desirable to prepare such metal complexes directly by reaction of the amine and the aldehyde in the presence of the metal ion, rather than preform the imine.113 As shown in Scheme 31, imine formation is a reversible process and isolation of the metal complex results from its stability, which in turn controls the equilibrium. It is possible, and quite likely, that prior coordination of the salicylaldehyde to the metal ion results in activation of the carbonyl carbon to amine nucleophilic attack. But it would be impossible for a precoordinated amine to act as a nucleophile and consequently no kinetic template effect could be involved. Numerous macrocyclic chelate systems have been prepared by means of imine bond formation (see Section 61.1.2.1). In mechanistic terms, the whole multistep process could occur without any geometrical influence on the part of the metal ion, which could merely act to stabilize the macrocycle in complex formation. On the other hand,... 

New chelate rings can be formed by the nucleophilic addition of alcohols to imine complexes. For example, the nickel(II) TAAB complex is susceptible to attack by bis-alkoxides (equation 31).127 It is not clear whether or not a kinetic template effect operates by prior coordination of the central oxygen or sulfur atom. However, such an effect is not necessary, as simple alkoxides undergo a similar addition reaction.128... 

Many reactions in this section probably owe a thermodynamic template effect for part of their success, but it is the kinetic effect which is most clearly illustrated. Reactions have been chosen to display a range of geometrical features and also various types of bond formation. The coverage will be selective and many topics will be developed more fully in Chapter 61.1 The present section will be subdivided according to the involvement or otherwise of donor atoms. 

Kinetic template effects have been involved in the formation of crown ethers, with respect to the cyclization step involving a nucleophilic displacement of halide or tosylate by alkoxide ions. It has been proposed that cyclization of the linear bifunctional precursor is enhanced by a cyclic conformation in which the alkoxide cation brings the two ends of the molecule into close proximity... 

The situation is even more clear cut in the formation of thioethers by alkylation of thiolate complexes. Such reactions have been described in Section 7.4.2.1.2, but in those examples new chelate rings were not formed. The reaction which led Busch to propose the kinetic template effect is a thiolate complex alkylation, which does indeed produce a new chelate ring (equation 40).110 162 163 This reaction is an example of the general type shown in equation (35) and it has been established clearly that the sulfur atoms remain coordinated to the metal ion throughout the... 

This reaction process is depicted in general terms in equations (51) and (52). It includes the majority of reactions which exhibit a kinetic template effect. A selection of reactions will be given but many areas will be developed further in Chapter 61.1. 

Kinetic template effects have been postulated in more typical organic aldol condensations, where metals such as lithium and zinc are likely to coordinate both the enolate or enamine nucleophile and the aldehyde in the transition state. The examples shown in Schemes 58184 and 59185 are illustrative of these reactions and the degree of selectivity obtained. The carboxylation of ketones and nitroalkanes by methyl magnesium carbonate to produce P-keto acids and a-nitro acids respectively provides early examples of similar reactions (Scheme 60).186 187 See also Section 61.1.4.4. 

What should we do to observe a three-dimensional template effect First, we should choose a reaction type that we know to be effective for the formation of macrocyclic ligands and extend the methodology to a kinetically inert cP or d6 metal centre. Let us reconsider the reaction, that we first encountered in Fig. 6-11. In this reaction, a dioximato complex reacted with BF3 to give the nickel(n) complex of a dianionic macrocycle (Fig. 7-1). 

Figure 3.45 Kinetic studies of the template effects of metal ions on cyclisation to form benzo [18] crown-6. ( Wiley-VCH Verlag GmbH Co. Reproduced with permission).

A library of vancomycin analogues has been prepared using ring closing metathesis reactions in aqueous solution (Nicolaou, K. C., Hughes, R., Cho, S. Y., Wissinger, N., Labischinski, H., Endermann, R. Chem. Eur. J. 2001, 7, 3824) a kinetic template effect was observed when the library was prepared in the presence of a dipeptide trap. 

A reaction is described as proceeding by a kinetic template effect if it provides a route to a product that would not be formed in the absence of the metal ion and where the metal ion acts by coordinating the reactants. An alternative description for this process is the coordination template effect that more aptly describes how the stereochemistry imposed by the metal ion, through coordination, promotes a series of controlled steps in a multistep reaction, e.g., Scheme 1 17, 136, 137). 

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