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Dr Kanatzidis's group is developing new ways of making these compounds crystallise correctly.But even existing devices could become economically useful as fuel prices rise, Dr Kanatzidis argues.
However, these molecules present a poor solubility making these compounds poorly bioavailable.
Medicinal chemists have long sought an easier and cheaper route to making these compounds, in hopes that they might find new medicines.
This study demonstrates that both enzymes are inhibited by peptidyl (acyloxy methyl ketones (AOMKs), making these compounds the first documented dual specificity inhibitors of the CaaX proteases.
These materials exhibited excellent sensing characteristics; moreover, the two sensors exhibited cross-reactive response patterns, making these compounds very promising candidates for array-based vapor-sensing applications.
Experimental electrochemical and DFT estimation of the HOMO and LUMO levels revealed that the energy of the frontier orbitals is increased as compared to C60 making these compounds prospective for application as acceptor materials in polymer solar cells (PSCs).
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It is possible that such disorder is required to make these compounds thermodynamically stable.
The presence of a π bond in thioketones makes these compounds reactive in Diels-Alder reactions and related cycloaddition reactions.
One way to make these compounds is to reduce a nitro (NO2) group to an amino (NH2) group.
But the researchers did not know exactly how plants make these compounds.
The obvious enhancement in luminescence makes these compounds potential materials for optical use.
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