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It is possible that such disorder is required to make these compounds thermodynamically stable.
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 multifunctional properties make these compounds potential candidates for application in organic light-emitting materials and two-photon bioimaging.
The ability to tune pore size at the Angstrom scale and to design accessible metallic nanoclusters in a highly porous structure, make these compounds very attractive for Catalysis.
The ease of synthesis and the remarkable biological activities make these compounds promising new frameworks for the development of cancer therapeutics.
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The presence of a π bond in thioketones makes these compounds reactive in Diels-Alder reactions and related cycloaddition reactions.
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.
The obvious enhancement in luminescence makes these compounds potential materials for optical use.
Presence of conjugated bis-dienone functionality makes these compounds sensitive to attack by nucleophiles and light energy.
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