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<dc:creator>Sacristán Martín, Adriana</dc:creator>
<dc:creator>Miguel San José, Daniel</dc:creator>
<dc:creator>Barbero San Juan, Héctor</dc:creator>
<dc:creator>Álvarez González, Celedonio Manuel</dc:creator>
<dc:date>2022</dc:date>
<dc:description>Producción Científica</dc:description>
<dc:description>Addressing control over molecular machines resulting in variable output modulation by mimicking nature mechanisms is a current hot topic. The exploitation of reversibility in thiol/disulfide motifs in chemical systems flanked by nonplanar corannulene moieties capable to recognize fullerenes is presented herein. Two redox-based machines have been conceived for this purpose: an ON/OFF switch that activates its binding properties upon dimerization and a self-resetting (i.e., with an automated backward process) host that substantially modulates its affinity.</dc:description>
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<dc:identifier>https://uvadoc.uva.es/handle/10324/54595</dc:identifier>
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<dc:publisher>American Chemical Society</dc:publisher>
<dc:title>Self-resetting bistable redox molecular machines for fullerene recognition</dc:title>
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