Transition metals template-controlled

Rigby, J.H. and Henshilwood, J.A. (1991) Transition metal template controlled cydoaddition reactions. An efficient chromium(0)-mediated [6it + 2it] cydoaddition. Journal of the American Chemical Society, 113, 5122—5123. 

Some radical reactions occur under the control of transition metal templates. The first example of asymmetric creation of an asymmetric carbon with a halogen atom is shown by the a DIOP-Rh(I) complex-catalyzed addition of bromotrichloromethane to styrene, which occurs with 32% enantioselectivity (Scheme 99) (233). Ru(II) complexes with DIOP or BINAP ligands promote addition of arenesulfonyl chlorides to afford the products in 25-40% ee (234). A reaction mechanism involving radical redox transfer chain process has been proposed. 

The earliest syntheses of rotaxanes were largely based on the statistical or directed methods.2,3 Statistical methods require very precise reaction conditions, and directed methods involve numerous chemicals steps. However, the use of templates allows high control of these synthetic methods resulting in efficient and precise assemblies of rotaxanes that incorporate a wide range of chemical functionalities. Two types of interactions occur in synthetic template methods (1) purely organic and (2) transition-metal-templated. In this latter case, the template can easily be removed at the end of the synthesis, whereas in the former, the interactions between the template and the components of the final rotaxane will often be maintained. Selected examples will now illustrate the statistical, the directed, and templated strategies outlined above. The transition-metal-templated route will be developed separately. 

Fig. 11 Principle of transition metal-templated synthesis of a [2]rotaxane. A thick line represents a dpp chelate, a black dot represents a metal cation, a hatched diamond represents a Au(III) porphyrin and an empty diamond represents a Zn(II) porphyrin. The transition metal controls the threading of Au(III) porphyrin-pendant macrocycle (A) onto chelate (B), to form prerotaxane (C). Construction of the porphyrin stoppers at the X functions leads to the metal complex [2]rotaxane (D). Removal of the template cation forms the free rotaxane (E)...

Although random and irregular type GaN nanorods have been prepared by using transition metal nanoparticles, such as Ni, Co, and Fe as catalysts and carbon nanotubes as the template, the preparation of controllable regular array of strai t GaN nanorods has not yet been reported. Fabrication of well-ordered nano-structures with high density is very important for the application of nano-structures to practical devices. 

Currently the main interest in template reactions lies in their key role in the controlled synthesis or the self-assembly of a variety of supramole-cular entities (449). One needs a combination of intuition, conjecture, and serendipity (450) a recent example of successfully combining serendipity and rational design is provided by the silver(I)-promoted assembly of one-dimensional stranded chains (451). One also needs an understanding of mechanism in order to optimize the selection and design of building blocks and templates for the generation of yet more sophisticated supramolecular structures references cited in this present review contain at least some kinetic or mechanistic information or speculation. Template routes to interlocked molecular structures have been reviewed (452), while a discussion of switching by transition metal contains a little about the kinetics and mechanisms of this aspect of template... 

Transition-metal nanopartides are of fundamental interest and technological importance because of their applications to catalysis [22,104-107]. Synthetic routes to metal nanopartides include evaporation and condensation, and chemical or electrochemical reduction of metal salts in the presence of stabilizers [104,105,108-110]. The purpose of the stabilizers, which include polymers, ligands, and surfactants, is to control particle size and prevent agglomeration. However, stabilizers also passivate cluster surfaces. For some applications, such as catalysis, it is desirable to prepare small, stable, but not-fully-passivated, particles so that substrates can access the encapsulated clusters. Another promising method for preparing clusters and colloids involves the use of templates, such as reverse micelles [111,112] and porous membranes [106,113,114]. However, even this approach results in at least partial passivation and mass transfer limitations unless the template is removed. Unfortunately, removal of the template may re-... 

Both 2-azido [184] and 2-nitrophenyl isocyanides [185] are suitable synthons for the generation of the freely unstable 2-aminophenyl isocyanide and they have been used (Fig. 23) in the template-controlled preparation of NH,NH-stabilized benzim-idazolin-2-ylidene hgands. Both phenyl isocyanides coordinate readily to transition metal centers. The isocyanide ligand in complex 65 reacts with PPhs and the... 

The rhodium containing hybrid materials prepared with the BINOL bicarbamate moieties are less active and enantioselective than the previous hybrid catalyst. The observed enantioselectivity was attributed to supramolecular effect of the chiral tridimensional network owing to the weakness of the interaction of the transition metal and the chiral ligand. The control of the texture and morphology of these solids by templating methods firstly reported by Macquarrie39 and Mann40 with suitable surfactants would improve the catalytic performance of this new class of chiral materials. 

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