期刊
CHEMICAL SCIENCE
卷 9, 期 1, 页码 181-188出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7sc04123c
关键词
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资金
- Ministero dell'Istruzione, dell'Universita e della Ricerca (MIUR) [PRIN 2010CX2TLM]
- Universita di Roma La Sapienza (Progetti di Ricerca)
This work deals with the use of 2-cyano-2-arylpropanoic acids as chemical fuels for an acid-base operated molecular switch that consists of a Sauvage-type catenand composed of two identical macrocycles incorporating a phenanthroline unit. When used as a base promoter of the decarboxylation of propanoic acid derivatives, the switch undergoes large amplitude motion from the neutral catenand to a protonated catenate and back again to the neutral state. The rate of back proton transfer, which determines the rate of the overall process, was markedly affected by para-substituents in the order Cl > H > CH3 > OCH3 ( rho = + 5.2). Thus, the time required to complete a full cycle was almost two days for the OCH3 derivative and dropped to a few minutes for the Cl derivative. These results show for the first time that the rate of operation of a molecular switch can be regulated by variations in the fuel structure.
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