Topotactic reactions, solids

Keywords Crystal engineering Solid-state photoreaction Topochemical polymerization Controlled radical polymerization Dimerization Isomerization Topotactic reaction... 

Thus, the solid-state photoisomerization of 10 proceeds via a topotactic reaction mechanism, while some (Z,Z)-muconic esters (e.g., 13 and 15) can pho-toisomerize to the corresponding ( , )-muconic esters (14 and 16) without any change in the space group, i.e., proceed via topochemical EZ isomerization (Scheme 13, Fig. 15) [115]. 

When the reactivity of a solid is controlled by the crystal structure, rather than by the chemical constituents of the crystal, the reaction is said to be topochemically controlled. The nature of products obtained in a decomposition reaction is frequently decided by topochemical factors, particularly when the reaction occurs within the solid without separation of a new phase (Thomas, 1974 Manohar, 1974). A topotactic reaction is a solid state reaction where the atomic arrangement in the reactant crystal remains largely unaffected during the course of the reaction, except for changes in dimension in one or more directions. Dehydration of Mo03-2H20 is a typical example of a topotactic reaction ... 

Reactivity in the solid-state is always connected with specific motions which allow the necessary contact between the reacting groups. In most cases solid-state reactions proceed by diffusion of reactions to centers of reactivity or by nucleation of the product phase at certain centers of disorder. This leads to the total destruction of the parent lattice. If the product is able to crystallize it is highly probable that nucleation of the crystalline product phase at the surface of the parent lattice will lead to oriented growth under the influence of surface tension. In such topotactic reactions certain crystallographic directions of parent and daughter phases will coincide. Typical examples for this behaviour are the solid-state polymerizations of oxacyclic compounds such as trioxane, tetroxane or 3-propiolactone... 

Crystalline trithiane, the sulfur containing analog of trioxane polymerizes in a topotactic reaction after irradiation on subsequent heating to 180° C 93). Again the crystal structure is twinned and differential thermal analysis has shown a higher melting point for polymers produced by solid state polymerization than for solution polymerized trithiane... 

Combined VIM and X-ray Diffraction [39]. The crystallographic phase of (solid) products generated immediately by VIM experiments can be studied when performing both experiments simultaneously. The reduction of PbO and Pb(OH)Cl served as an example of this combination, showing strong evidence for a topotactic electrochemical solid-state reaction. 

These characteristics can be derived from a polymerization of crystalline monomers controlled topochemically. Topotactic reaction geno-ally involve a strong correspondence between the lattices of the monomer crystal and the resulting polymer crystal. Hence, the topochemical solid state reaction occurs when sufficiently intense thermal mobility of molecules takes place in the lattice, and the distance between active centers for the polymerization in the neighboring molecules should not exceed 3.7 A for C — O interactions All monomers mentioned above show quite close C — O interactions. 

Solid-state chemistry is less widely used than solution chemistry but the particular molecular configuration and interaction imposed by the crystal lattice leads to a well defined reaction product. The very specific nature of the lattice packing required for reaction, however, makes the solid-state route less predictable than solution chemistry. Solid-state polymerization has been observed to occur by bulk, topotactic and topochemical reactions. In bulk reactions the product is amorphous because the crystal lattice is destroyed during the reaction. Topotactic reactions produce a product phase which has a small number of orientations, possibly only one, with respect to the initial crystal. Topochemical reactions are those in which the reaction path is determined by the crystal structure and may lead to a topotactic product. 

X-Ray and electron diffraction measurements have been most usually used to characterize the phases present in any reactant mixture, and provide a means of identification of solid reactants, intermediates and products. In addition to such qualitative analyses, the method can also be used quantitatively, with suitable systems, to determine the amounts of particular solids present [111], changes in lattice parameters during reaction, topotactical relationships between reactants and products, the presence of finely divided or strained material, crystallographic transformations, etc. 

Bruce PG, Irvine ITS (2001) Insertion Compounds. In Encyclopedia of Materials Science and Technology, Elsevier Science Ltd Oxford ISBN 0-08-0431526, pp. 4115-4121 SchoUhom R (1980) Reversible topotactic redox reactions of solids by electron/ion transfer. Angew Chem Int Ed Engl 19 983-1003... 

Toda et al. reported that the topotactic and enantioselective photodimerization of coumarin and thiocoumarin takes place in single crystals without significant molecular rearrangements [49]. Molecular motion needs to be called upon to explain the photochemically activated cycloaddition reaction of 2-benzyl-5-benzylidenecyclopentanone. The dimer molecules, once formed, move smoothly in the reactant crystal to form the product crystal [50]. Harris et al. investigated the reactivity of 10-hydroxy-10,9-boroxophenanthrene in the solid state and the mechanism of the solid-state reaction was characterized by both X-ray diffraction and thermal analysis [51]. It was demonstrated that the solution chemistry of 10-hydroxy-10,9-boroxophenanthrene is different from that in the solid state, where it undergoes dimerization and dehydration to form a monohydride derivative. 

Solid-state reactions are known from thermal intracrystalline conversions (isomerizations or loss of volatile fragments), photoreactions, gas-solid reactions, and solid-solid reactions. As all of these relate strictly to the crystal packing (unifying solid-state mechanism) and are not separated in the various sections. Also, nontopotactic (normal) and topotactic (very rare) reactions are not separated in different sections. 

It may be suspected that the genuinely topotactic (as secured by the molecular precision of the AFM [18]) photodimerization of 2-benzyl-5-benzyli-denecyclopentanone [118] might be a good candidate for a quantitative preparative photo dimerization to give the head-to-tail anti-[2+2] dimer. Early quantitative solid-state [2-1-2] photodimerizations (most of the published mechanistic interpretations of which can no longer be accepted) are listed in [110]. These deal with the anti dimerization of acenaphthylene-1,2-dicarboxylic anhydride, the head-to-head syn dimerization of acenaphthylene-1-carboxylic acid, the syn dimerization of 5,6-dichloroacenaphthylene, and the thermally reversible head-to-tail anti dimerization of seven ( )-2,6-di-f-butyl-4-(2-aryl-ethenyl)pyrylium-trifluoromethanesulfonates. All of these reactions proceed fully specific. On the other hand, quantitative photoconversions of a 1 1 mixed crystal of ethyl and propyl a-cyano-4-[2-(4-pyridyl)ethenyl]cinnamates gives mixtures of diesters with one (A>410 nm) or two cyclobutane rings (no cutoff filter). 

Convincing evidence for phase separation was obtained from the photopolymerization behavior of 6 in the mixed 6/DSPE monolayer films. Photopolymerization of diacetylenes is a topotactic process which requires the proper alignment of the 1,3-diyne moieties [35]. Thus diacetylenes typically polymerize rapidly in the solid state but not in solution. Polymerization is triggered by ultraviolet irradiation and proceeds via a 1,4-addition mechanism yielding a conjugated ene-yne backbone (Fig. 5). The reaction can be followed by the growth of the visible absorption band of the polymer. 

A topotactic solid state polymerization reaction has been reported for the Ni complex with tris(2-cyanoethyl)phosphine, P(CH2CH2CN)3 the square planar NiBr2 P(CH2CH2CN)3 2 com-... 

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