Chemical technology news from across RSC Publishing.
Computer-aided nanoparticle synthesis
04 October 2007
Fed up with having to optimise your own reactions? Ever wondered why you can't get a computer to do it for you? Thanks to researchers from the UK, this possibility is not as far away as you may think.

Nanoparticles are finding uses in all manner of interesting applications from photonics to bioanalysis, but to be able to exploit them properly, it is essential to be able to carefully control their properties.
John deMello and colleagues from Imperial College London set about designing a microfluidic system that would automatically optimise the emission wavelength of fluorescent nanoparticles. 'A spectrometer monitors the particles as they exit the microfluidic chip. The spectra are fed to a computer which assigns a "dissatisfaction coefficient" to the particles depending on how far they are from some pre-set goal. The computer repeatedly updates the reaction conditions to minimise this coefficient and in so doing forces the chip to produce particles with the desired properties,' said deMello.
The next step will be to try and apply this kind of set up to other synthetic systems. 'The control routines we use are fairly versatile and should be easy to adapt to other types of materials,' deMello continued. 'All that's needed is some property of the product that can be measured directly at the point of production and two or three reaction parameters to optimise.'
- John deMello, Imperial College, London
Stephen Davey
Link to journal article
Intelligent routes to the controlled synthesis of nanoparticles
S. Krishnadasan, R. J. C. Brown, A. J. deMello and J. C. deMello, Lab Chip, 2007, 7, 1434
DOI: 10.1039/b711412e
Also of interest
Pushing the boundaries of nanoparticle detection
Smaller than ever nanoparticles can be studied using new microscopy methods.
Rapid reactions using microfluidic devices
A glass microchip has been used for the first time to carry out fast carbonylative cross-coupling reactions of arylhalides to form secondary amides.
