Ligands template synthesis

Although direct reaction of lanthanide mono-porphyrins with free phthalo-cyanine or its lithium derivatives is generally more efficient than the template synthesis, and gives rise to mixed-ligand complexes, the template strategy can also be applied for synthesis of phthalocyanine-porphyrin complexes, as in the case of unsymmetric bisphthalocyanine complexes (Scheme 8.2, B(b)) [106, 136, 145, 146]. Thus, metallation of free porphyrins with lanthanide salts in TCB or n-octanol leads to single-decker complexes, which then react with phthalonitriles under the action of DBU in alcoholic media to give the desired compounds. 

Apart from this one-reaction type, the routine use of metal template procedures for obtaining a wide range of macrocyclic systems stems from 1960 when Curtis discovered a template reaction for obtaining an isomeric pair of Ni(n) macrocyclic complexes (Curtis, 1960). Details of this reaction are discussed later in this chapter. The template synthesis of these complexes marked the beginning of renewed interest in macrocyclic ligand chemistry which continues to the present day. 

Studies involving 2,6-diacetylpyridine derivatives. Detailed studies by Nelson and coworkers supported by X-ray structural work by Drew and coworkers have elucidated many aspects of the template synthesis of metal complexes of a Schiff-base ligand series which includes the N4-donor system (83) and the N5-systems (84)-(86) (Nelson, 1980). Since... 

Three methods can be followed for the synthesis of a SIB catalyst (i) zeolite synthesis around the metal complex (ii) template synthesis and (iii) the flexible ligand method. 

The template synthesis method involves the diffusion of ligand precursors into the pores of a zeolite where they can assemble around an intrazeolite metal ion that acts as a template. This approach was first used in 1977 for the intrazeoHte synthesis of Cu, Co and Ni phthalocyanines by the condensation of four molecules of dicyanobenzene around the metal cation within the cages of NaY [132, 174]. 

Fe(CO)s], [Fe2(CO)g], [Co2(CO)8] and [Os3(CO)i2]) have been reacted with dicyanobenzene to form intrazeolite [M(Pc)] complexes [140]. Another class of materials prepared by the intrazeolite template synthesis method has been mixed ligand metal carbonyls and metal carbonyl clusters, frequently by reductive car-bonylation of metal ions in zeolite cages [175]. However, because these are frequently decomposed in situ to form, for example, nanoparticles, they are outside the scope of this chapter, and will be considered here only when they are used as precursors for metal complexes. 

Similar to the Cu(II) complex, direct synthesis afforded an unstable Ni(II) complex and precipitation of the starting ligand occurred. Template synthesis, even with HC104 produced the complex with the monoanionic Hdapsox- ligand (complex 6), and heating in alkaline... 

Only three PBP complexes of Fe(III) with acyclic ligands from the class of bis(acylhydrazone) of dap have been structurally characterized at present (41,49,53) and this prompted studies in that direction. Both direct and template synthesis afforded the complex [Fe(Hdapsox) Cl2] - 1/2H20 (9) with a monoanionic H2dapsox ligand (7). Protonation of the coordinated ligand was unsuccessful even upon addition of HC1 to the reaction mixture (Scheme 5). In spite of asymmetrical mono-deprotonation, the ligand was symmetrically pentadentately... 

The template synthesis has also been successfully employed for the preparation of macrocycles containing mixed donor atoms. Examples which refer to tetra- and bexa-dentate ligands are given in Schemes 42, 47 and 50.2649,2653 2654,2658 Apart from the template synthesis a number of nickel macrocycles have been prepared by direct combination of the appropriate nickel(II) salt with the preformed macrocyclic ligand in alcoholic medium, often MeOH (see also Tables 103, 106-108). 

Template syntheses of P macrocycles are a new area. In fact, a 1978 review93 of template synthesis made no mention of P macrocycles. Template syntheses have been developed by Stelzer and co-workers.94 Firstly, two molecules of the bidentate secondary phosphine are complexed with a nickel(II) or palladium(II) salt (Scheme 6) and the resultant secondary phosphine complex is then condensed with a diketone to form the macrocyclic metal complex. Unfortunately, these macrocycles are strong field ligands and no method has yet been devised to remove the metal from the ring. On the other hand, Cooper and co-workers95 have used a template synthesis to produce a [l4]aneP2N2 macrocycle (Scheme 7). 

Simple macrocyclic quadridentate complexes can be synthesized by template reactions from ethers derived from salicylaldehyde and diamines in the presence of appropriate metal ions such as nickel(II) (equation 3).35>36 However, these reactions can also be carried out quite effectively in the absence of metal ions to yield the free ligands, which can be obtained by hydrolysis of the complexes. An iron(II) macrocyclic quinquedentate chelate of this type has been produced by template synthesis (equation 4).37... 

Pyridine-2,6-dicarbaldehyde and 2,6-diacetylpyridine have been widely used in the template synthesis of imine chelates ranging in complexity from linear tridentates, such as (17),38 39 to macrocyclic structures with a range of ring sizes, such as (18).40-42 The in situ formation of macrocyclic ligands of this type depends upon the ring size and the strength of complexation of the triamine by the metal ion at the pH of the reaction. Related complexes with an additional donor atom attached to R2 have been synthesized also.43 44... 

Template reactions between malonaldehydes and diamines in the presence of copper(II), nickel(II) or cobalt(II) salts yield neutral macrocyclic complexes (equation 15).99-102 Both aliphatic102 and aromatic101 diamines can be used. In certain cases, non-macrocyclic intermediates can be isolated and subsequently converted into unsymmetrical macrocyclic complexes by reaction with a different diamine (Scheme ll).101 These methods are more versatile and more convenient than an earlier template reaction in which propynal replaces the malonaldehyde (equation 16).103 This latter method can also be used for the non-template synthesis of the macrocyclic ligand in relatively poor yield. A further variation on this reaction type allows the use of an enol ether (vinylogous ester), which provides more flexibility with respect to substituents (equation 17).104 The approach illustrated in equation (15), and Scheme 11 can be extended to include reactions of (3-diketones. The benzodiazepines, which result from reaction between 1,2-diaminobenzenes and (3-diketones, can also serve as precursors in the metal template reaction (Scheme 12).101 105 106 The macrocyclic complex product (46) in this sequence, being unsubstituted on the meso carbon atom, has been shown to undergo an electrochemical oxidative dimerization (equation 18).107... 

As we considered above, one of the fundamental problems associated with the preparation of macrocyclic ligands is concerned with the orientation of reactive sites such that they give intramolecular (cyclic) rather than intermolecular (acyclic) products. This is associated with the conformation of the reactants and the reactive sites, and so we might expect that judicious location of donor atoms might allow for metal ion control over such a cyclisation process. This is known as a template synthesis, and the metal ion may be viewed as a template about which the macrocyclic product is formed. This methodology was first developed in the 1960s, and has been very widely investigated since that time. At the present, template reactions usually prove to be the method of choice for the synthesis of many macrocyclic complexes (with the possible exceptions of those of crown ethers and tetraazaalkanes). When the reactions are successful, they provide an extremely convenient method of synthesis. 

Probably one of the commonest reactions encountered in the template synthesis of macrocycles is the formation of imine C=N bonds from amines and carbonyl compounds. We have seen in the preceding chapters that co-ordination to a metal ion may be used to control the reactivity of the amine, the carbonyl or the imine. If we now consider that the metal ion may also play a conformational role in arranging the reactants in the correct orientation for cyclisation, it is clear that a limitless range of ligands can be prepared by metal-directed reactions of dicarbonyls with diamines. The Tt-acceptor imine functionality is also attractive to the co-ordination chemist as it gives rise to strong-field ligands which may have novel properties. All of the above renders imine formation a particularly useful tool in the arsenal of preparative co-ordination chemists. Some typical examples of the templated formation of imine macrocycles are presented in Fig. 6-12. 

Schiff bases of 2-mercaptobenzaldehyde, which can be used as ligands to obtain ICC of type 467, are unstable for this purpose. So, the stable compounds 469 are mostly used as ligands for the syntheses of chelates 467 an alternative way for their synthesis is carried out through the method of template synthesis starting from thiosali-cylialdehydates 470 (see Sec. 3.3 on template syntheses) ... 

One of the most important synthetic routes to produce di- and polynuclear complexes is the immediate interaction of metal-containing ligands and metal salts or carbonyls [130a]. However, in this case, the reactions of coordinated ligands practically take place, so such transformations will be discussed in Sec. 3.3.2.3, dedicated to template synthesis. 

Template synthesis has long since [2,314a,315-325] foreseen two aspects formation of the ligand system on a metal matrix and the reaction of mainly organic compounds, connected with the central atom (ion) (reactions of coordinated ligands). 

At the same time, this method has a series of disadvantages. Among them, we note the possibiity of contamination of the final product not only by the excess of one of the reactants [2], but also by complexes of the components of the ligand system. So, to carry out strictly template synthesis experiments, it is necessary to take into account a comparative stability of coordination compounds, obtained on the basis of initial components-precursors and the ligand itself. Not only the thermodynamic characteristics of complex-formation processes should be taken into consideration [326,327], but also the influence of solvolysis processes (especially hydrolysis) and the type of atmosphere (air oxygen). 

The interesting variant of template synthesis, yielding (3.167) the different-ligand complex 718, is examined [314a] ... 

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