Sunday, April 8, 2012

Double chemical action yields double success

Halogen elements such as chlorine or bromine can boost the synthetic capabilities of many once attached to their frameworks. Techniques known as substitution reactions can then switch the halogens for other groups, such as aromatic species. However, chemists have scarcely studied halogenated disilenes because theoretical calculations indicate that they are inherently volatile. 

Recently however, Tamao and colleagues developed compounds that are extraordinarily adept at stabilizing disilenes. Known as ‘Rind’ ligands, these molecules have a unique fused-ring structure that locks into place. They also have chemically tunable side chains that optimize compatibility with a variety of substrates and solvents. Based on these capabilities, Tamao and team postulated that their technique could capture the halogenated targets.

Experiments proved that their instincts were correct: combining a Rind-protected bromine–silicon precursor with a reducing agent successfully produced the sought-after dibromo-disilene crystals. But closer examination of the new product’s reactivity revealed a surprise. Simply mixing it with an acetylene derivative caused the disilene to cleave in half and join to both sides of the carbon triple bond, producing a triangle-shaped unsaturated ring.

According to co-author Tsukasa Matsuo, this reaction provided strong evidence that the halogenated disilene could easily dissociate. To confirm this behavior, Katsunori Suzuki, another co-author, dissolved two dibromo-disilenes, each protected by a different Rind ligand, into solution. After one day at room temperature, the researchers observed an extraordinary event: the spontaneously cleaved fragments, known as bromo-silylenes, had reconnected into new disilenes containing both Rind ligands (Fig. 1). This type of ‘cross-over’ reaction, also known as olefin metathesis, is extremely useful to chemists and normally requires expensive metal catalysts to proceed.

The researchers exploited the synthetic potential of the dynamic dibromo-disilenes by capturing the reactive silylene fragment with a base, and then used this complex to construct aromatic-substituted conjugated silicon molecules inaccessible through other techniques. “These results open a new platform for development of functional disilene materials and devices,” says Matsuo.

More information: Suzuki, K., Matsuo, T., Hashizume, D. & Tamao, K. Room-temperature dissociation of 1,2-dibromodisilenes to bromosilylenes. Journal of the American Chemical Society 133, 19710–19713 (2011).

Matsuo, T., et al. Synthesis and structures of a series of bulky “Rind-Br” based on a rigid fused-ring s-hydrindacene skeleton. Bulletin of the Chemical Society of Japan 84, 1178–1191 (2011).

Provided by RIKEN (news : web)

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