РОССИЙСКАЯ АКАДЕМИЯ НАУК УРАЛЬСКОЕ ОТДЕЛЕНИЕ ИНСТИТУТ ХИМИИ TBEPДОГО ТЕЛА |
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21.01.2010 | Карта сайта Language |
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'This is the first example of such a silicon-silicon bond,' says Kano. 'And it is quite stable [even under thermal conditions] despite the apparent electronic repulsion and bond dissociation tendency.' 'I find the paper very interesting indeed, and well carried out,' says Daniel Kost, a silicon chemistry expert at Ben-Gurion University in Israel. He explains that the reason why the electrostatic repulsion does not cause destruction of the molecule is that the negative charges are only formally on silicon. 'The charges are [actually] distributed among the many atoms surrounding the silicon atoms, leaving the [silicon] positively charged, with no Coulomb repulsions.' However, Kost remains puzzled at the stability of the dianionic disilicates. 'Neither hydrolysis nor warming up causes decomposition of the compounds, although other hypervalent mono-nuclear silicon compounds tend to decompose rapidly when exposed to air and moisture.' The team made the disilicate structures via a reductive coupling reaction of a silane bearing two electron-withdrawing bidentate ligands, used to stabilise the molecule. The result was two silicon atoms that are effectively surrounded by four sets of ligands and bind eight atoms. Kanoenvisages this kind of bond being useful for making new materials. 'If we can accumulate the bond in series to form a silicon wire made up of silicate moieties, the [highest occupied molecular orbital to lowest unoccupied molecular orbital] energy gap will be much more decreased which could be helpful in creating new conductive materials like doped polyacetylene.' Kano also suggests that such silicon wire could be useful for optical materials like polysilane. As well as aiming to connect several sets of the silicon-silicon bond chain to form a silicon-wire comprised of silicate chains, the team plans to look at the synthesis of similar bonding between other group 14 element compounds such as germanium and tin. James Urquhart
Interesting? Spread the word using the 'tools' menu on the left. ReferencesN Kano et al, Nature Chemistry, 2010, DOI: 10.1038/NCHEM.513
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