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Acid-Base Switching of Tautomerism and Conformation of a Dioxoporphyrin for Integrated Binary Subtraction

Y. Ding ; X. Li ; J. P. Hill ; K. Ariga ; H Ågren ; Joakim Andréasson (Institutionen för kemi- och bioteknik, Fysikalisk kemi) ; W-H Zhu ; H Tian ; Y Xie
Chemistry - A European Journal (0947-6539). Vol. 20 (2014), 40, p. 12910-12916.
[Artikel, refereegranskad vetenskaplig]

Compared with most of the reported logic devices based on the supramolecular approach, systems based on individual molecules can avoid challenging construction requirements. In this work, a novel dioxoporphyrin DPH22 was synthesized, and two of its tautomers were characterized by single crystal X-ray diffraction analyses. DPH22 exhibits multichannel controllable stepwise tautomerization, protonation and deprotonation processes by its interactions with H+ and F-. Using the addition of H+ and F- as the inputs and UV-vis absorption values at 412, 510, 562 and 603 nm as outputs, the controlled tautomerism of DPH22 has been successfully used for the construction of an integrated molecular level half-subtractor and comparator. Besides, this acid and base switched tautomerism turns out to be reversible, endowing the system with ease of reset and recycling, and there is no need to modulate complicated intermolecular interactions and electron/charge transfer processes.

Nyckelord: half-subtractars, logic gates, organic electronic, porphyrinoids, tautamerism

Denna post skapades 2014-10-10. Senast ändrad 2017-09-14.
CPL Pubid: 204074


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Institutioner (Chalmers)

Institutionen för kemi- och bioteknik, Fysikalisk kemi (2005-2014)


Fysikalisk kemi

Chalmers infrastruktur