Monomeric coupling products

Since one of the substrates is a cyclic alkene there is now the possibility of ring-opening metathesis polymerisation (ROMP) occurring which would result in the formation of polymeric products 34 (n >1). Since polymer synthesis is outside the scope of this review, only alkene cross-metathesis reactions resulting in the formation of monomeric cross-coupled products (for example 30) will be discussed here. 

With R = R = Ph and using complexes 1 or 2a, the central N -N single bond of the azine is cleaved by both metals. In this case, the bis(imido) complexes 81 were formed, treatment of which with complexes such as CpCo(C2H2)2 can give heterobimetallic bis(alkylideneamido)-bridged complexes such as 82. Mach has used this concept for the reaction of methyl-substituted titanocenes with acetoneazine. With 3, monomeric Ti(III) complexes 83 and, after activation of the methyl groups, coupled products such as 84 could be obtained [44],... 

Soluble heptapnicanortricyclane anions [Pny] (Fig. 3a) and trishomocubane-shaped (ufosane-like) anions [Pnn] (Fig. 3d) are very common and known as in the binary solids for Pn = P, As, Sb (Table 2). Oxidative coupling of these monomers leads to the dimers [Pny-Pny]" and [Pnn-Pnn]" for Pn = P and As (Fig. 3b, e), which - as observed for the tetrel element clusters - have an external homoatomic bond, but in this case the structures of the monomeric units are fully retained upon dimerization. A trimeric oxidative coupling product of [Py] is the... 

The abundance of CO2 makes it attractive as a carbon source (Cl chemistry), and consequently the utilization of CO2 as substrate in C-C bond-forming electrochemical reactions is of considerable interest. Direct reduction of CO2 takes place at rather low potentials (< —2.2 V in aprotic medium) and normally leads to mixtures of the C-C coupling product, oxalate, and CO + CO when carried out in aprotic solvents at inert electrodes such as Hg or Pb (Scheme 12). Monomeric products dominate when the reduction is carried out at electrodes at which either CO2 or the reduction products are chemisorbed. Numerous attempts have therefore been made to catalyze the reduction and optimize the yield of oxalate. 

The practice of using an insoluble polymer to isolate and kinetic-ally stabilize a reactive intermediate has been addressed in several reports, most commonly using DVB cross-linked polystyrene as a support. In these cases, the three dimensional structure of the polymer and rigidity of the polymer backbone diminish intramolecular reactivity between two sites on the same polymer bead. Physical constraints preclude any significant reaction between two different polymer beads. Similar, less dramatic reduced intramolecular reactivity has also been noted for reactive intermediates bound to linear polystyrene. For example, o-benzyne bound to linear polystyrene has been shown by Mazur to have enhanced stability relative to non-polymer-bound -benzyne (35). In this case, o-benzyne was generated by lead tetraacetate oxidation of a 2-aminobenzotriazole precursor, 1. Analysis of the reaction products after cleaving the benzyne derived products from the polymer by hydrolysis showed a 60% yield of aryl acetates was obtained (Equation 11). In contrast, the monomeric aryne forms only coupled products under similar conditions. Further comparisons of the reactivity of -benzyne bound to insoluble 2% or 20%... 

The mechanism of this transformation has explored by Hashmi, and postulated to proceed via a Pd(II)/Pd(IV) cycle, wherein palladium mediates cyclization to form 14 (Scheme 6.23), followed by either proton migration and reductive elimination (forming simple furans) or allene coupling via either a carbene or insertion. This approach can be employed to form exclusively monomeric cydoisomerization products with more sterically encumbered substituted allenes [34]. 

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