Constructing a four-input molecular keypad lock with a multi-stimuli-responsive phthalocyanine
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AbstractA novel conjugate of a zinc(II) phthalocyanine with three 2,4-dinitrobenzenesulfonate (DNBS) substituents, a bis(ferrocenylethenyl) boron dipyrromethene (BODIPY) and a pyrene connected respectively via an acid-sensitive ketal bridge and a singlet oxygen-cleavable thioketal linker has been designed and synthesised. It is responsive towards four stimuli, including glutathione (GSH), acid and light sources at a wavelength of >610 nm and 345 nm in a sequence-dependent manner, enabling it to function as a molecular keypad lock with the four inputs. This work represents a proof-of-concept study using specially designed molecules to perform complicated sequential logic operations.
Acceptance Date02/11/2020
All Author(s) ListSummer Y. Y. Ha, Dennis K. P. Ng
Journal nameChemical Communications
Year2020
Month12
Volume Number56
Issue Number93
Pages14601 - 14604
ISSN1359-7345
eISSN1364-548X
LanguagesEnglish-United Kingdom

Last updated on 2021-27-02 at 23:24