Highly sensitive conformational switching of ethane-bridged mono-zinc bis-porphyrin as an application tool for rapid monitoring of aqueous ammonia and acetone
Abstract
The spectroscopic behavior of mono-zinc ethane-bridged bis-porphyrin (ZnH2Po2) was studied as a solidfilm upon deposition from a chloroform solution by means of the spin-coating method. The angular speedused during the deposition strongly influences the conformational arrangement of bis-porphyrin. A preferentialarrangement as the anti- (opened) conformer was obtained when high speeds were used. Theobtained thin film was successfully employed to detect ammonia and acetone as the relevant analytes inaqueous solutions. This was a result of the supramolecular interaction between each of these two compoundsused and the bis-porphyrin active layer, inducing the corresponding conformational switchingeasily detectable by UV-vis absorption spectroscopy. The spectral variations of ZnH2Po2 were evident inthe range of concentrations between 1 ppm and 20 ppm for both the analytes. This is particular importantin light of the fact that ammonia and acetone concentrations are changed within this limit throughoutthe menstrual women's cycle, reaching their maximum during the fertility days. Hence, ZnH2Po2 canbe effectively applied as a potential active layer for medical devices to monitor the hormonal variationsduring the women's menstrual cycle.Additionally, the reversible sensing mechanism with reusable up to 8 cycles, makes this ZnH2Po2 basedactive layer practically efficient
Autore Pugliese
Tutti gli autori
-
Buccolieri A.; Manno D.; Serra A.; Santino A.; Hasan M.; Borovkov V.; Giancane G.
Titolo volume/Rivista
Sensors and actuators. B, Chemical
Anno di pubblicazione
2017
ISSN
0925-4005
ISBN
Non Disponibile
Numero di citazioni Wos
Nessuna citazione
Ultimo Aggiornamento Citazioni
Non Disponibile
Numero di citazioni Scopus
Non Disponibile
Ultimo Aggiornamento Citazioni
Non Disponibile
Settori ERC
Non Disponibile
Codici ASJC
Non Disponibile
Condividi questo sito sui social