Ivana Murković Steinberg

Miniaturised wireless smart tag for optical chemical analysis applications

A novel miniaturised photometer has been developed as an ultra-portable and mobile analytical chemical instrument. The low-cost photometer presents a paradigm shift in mobile chemical sensor instrumentation because it is built around a contactless smart card format. The photometer tag is based on the radio-frequency identification (RFID) smart card system, which provides short-range wireless data and power transfer between the photometer and a proximal reader, and which allows the reader to also energise the photometer by near field electromagnetic induction. RFID is set to become a key enabling technology of the Internet-of-Things (IoT), hence devices such as the photometer described here will enable numerous mobile, wearable and vanguard chemical sensing applications in the emerging connected world. In the work presented here, we demonstrate the characterisation of a low-power RFID wireless sensor tag with an LED/photodiode-based photometric input. The performance of the wireless photometer has been tested through two different model analytical applications. The first is photometry in solution, where colour intensity as a function of dye concentration was measured. The second is an ion-selective optode system in which potassium ion concentrations were determined by using previously well characterised bulk optode membranes. The analytical performance of the wireless photometer smart tag is clearly demonstrated by these optical absorption-based analytical experiments, with excellent data agreement to a reference laboratory instrument.

Chromogenic radical based optical sensor membrane for screening of antioxidant activity

Solid-state optical sensor membranes based on immobilised chromogenic radicals for the assessment of antioxidant activity have been studied. Two stable lipophilic chromogenic radicals, DPPH (2,2-diphenyl-1-picrylhydrazyl radical) and galvinoxyl radical, GV, (2,6-di-tert-butyl-alpha-(3,5-di-tert-butyl-oxo-2,5-cyclohexadien-1-ylidene)-p-tolyloxy radical), were immobilised in plasticised PVC films and screened for suitability as indicators of antioxidative activity. The spectrophotometric characterisation of the polymer films containing immobilised free radicals was performed, and the response of the immobilised free radicals toward standard antioxidants was studied. It has been demonstrated that the immobilised radicals retain their reactivity towards antioxidants and the results suggest that the reactivity of immobilised radicals is comparable to standard solution-based DPPH assays. Polymer films containing immobilised DPPH radical respond to standard antioxidants in aqueous solutions by changing colour irreversibly from purple (absorption maximum at 520nm) to yellow. The initial slopes of the response curves to the phenolic antioxidant gallic acid, obtained in the 1-50mM concentration range, gave a linear calibration plot in a 1min exposure cuvette test. The polymer films were used to screen antioxidative activity of beverage and food samples known to contain antioxidants, such as black and green tea, coffee, red wine, fruit juice, olive oil and sunflower oil. It has been demonstrated that a rapid and simple qualitative screening test of untreated samples is possible using a test strip based on immobilised DPPH radical.

Fluorescent benzimidazo[1,2-a]quinolines: synthesis, spectroscopic and computational studies of protonation equilibria and metal ion sensitivity

We describe the UV-Vis and fluorescence spectroscopic characterization of newly synthesised amino and diamino substituted benzimidazo[1,2-a]quinolines and their various 1 : 1 metal complexes together with the related computational analysis of their acid/base properties and metal binding affinities. The work was performed in order to evaluate the photophysical features of these compounds and assess their potential chemosensor activity towards pH and metal ions in several polar and non-polar organic solvents. In addition, pH titrations and titration with metal chloride salts were carried out to determine the selectivity towards Co2+, Cu2+, Ni2+ and Zn2+ cations and explore their potential as chemosensors and pH probes. While all systems exhibit notable but impractical differences in sensitivities and spectral responses with the used metals, computational analysis aided in identifying benzimidazo[1,2-a]quinolines mono- and disubstituted with the piperazine fragment as very promising and efficient pH sensors in the acidic environment, particularly in the range of pH ≈ 3, which is extended to pH ≈ 6 upon the addition of metal cations. Their analytical features are significantly better than those involving the chain amino substituents, and their further development is strongly suggested.

Hybrid sol–gel thin films doped with a pH indicator: effect of organic modification on optical pH response and film surface hydrophilicity

Optical sensors for application in innovative wearable sensing systems such as textile-integrated systems and wireless sensor platforms rely on the development of low-cost multifunctional materials compatible with standard fabrication technologies. We are developing optically responsive pH sensitive sol–gel coatings for integration with a mobile wireless smart tag sensing system. For this application, we have fabricated a range of thin pH sensitive films using bromocresol green (BCG) indicator immobilised in inorganic–organic silica hybrid matrices prepared by a sol–gel method and deposited by spin-coating onto glass substrates. The surface hydrophilicity of the films were varied by using the inorganic sol–gel precursor tetraethoxysilane together with either methyltriethoxysilane, ethyltriethoxysilane, phenyltrimethoxysilane or glycidoxypropyltrimethoxysilane as organically modified sol–gel precursors, co-polymerised in different ratios. Spectral characterisation of the films was performed using visible absorption spectroscopy. The shift in absorption maxima and other spectral changes of the different matrices have been identified, and the apparent pKapp values of the immobilised BCG pH indicator determined. The surface wettability properties of the films have been studied by measuring the contact angle of water, formamide and diiodomethane which has allowed the estimation of the surface free energy (SFE) using three different models: Owens–Wendt, Wu and van Oss-Chaudhury-Good. It is shown that the SFE of the hybrid films is directly related to the type and the degree of organic modification, which in turn has a significant effect on the pH response-time of these sensing films.

Benzimidazole acrylonitriles as multifunctional push-pull chromophores: Spectral characterisation, protonation equilibria and nanoaggregation in aqueous solutions

Heterocyclic donor-π-acceptor molecular systems based on an N,N-dimethylamino phenylacrylonitrile benzimidazole skeleton have been characterised and are proposed for potential use in sensing applications. The benzimidazole moiety introduces a broad spectrum of useful multifunctional properties to the system including electron accepting ability, pH sensitivity and compatibility with biomolecules. The photophysical characterisation of the prototropic forms of these chromophores has been carried out in both solution and on immobilisation in polymer films. The experimental results are further supported by computational determination of pKa values. It is noticed that compound 3 forms nanoaggregates in aqueous solutions with aggregation-induced emission (AIE) at 600nm. All the systems demonstrate spectral pH sensitivity in acidic media which shifts towards near-neutral values upon immobilisation in polymer films or upon aggregation in an aqueous environment (compound 3). The structure-property relationships of these functional chromophores, involving their spectral characteristics, acid-base equilibria, pKa values and aggregation effects have been determined. Potential applications of the molecules as pH and biomolecular sensors are proposed based on their pH sensitivity and AIE properties.

Paper-based ion-selective optodes for continuous sensing: Reversible potassium ion monitoring

A simple, low-cost paper-based potassium ion-selective optode that exhibits fully reversible sensing properties is presented. A classic optode formulation consisting of valinomycin as the ionophore and a lipophilic pH indicator has been successfully transferred to a paper substrate and characterised in a flow-through cell with reflectometric optical detection. The optode exhibits high repeatability, reversibility, and stability and can detect potassium in the physiologically relevant concentration range from 10-4 to 10-1 M. This new paper-based optode shows high potential for general application in paper microfluidic systems and for integration into wearable systems for perspiration monitoring due to its reversible and repeatable response. In general, we have demonstrated that ionophore-based optical sensors on paper can successfully be used for continuous ion-concentration monitoring.

Colourimetric and fluorimetric metal ion chemosensor based on a benzimidazole functionalised Schiff base

Abstract Herein we present the interaction of benzimidazole based Schiff base 1 with different metal ions studied by absorption and fluorescence spectroscopies and computational modelling. Compound 1 exhibits changes in spectroscopic properties upon chelation with specific metal ions. Its strong absorption band at 425 nm is significantly red shifted (Δλ = 30 nm) only upon the complexation with Al3+, an effect observable by a naked eye as a colour change from light- to dark-yellow. Of the metal ions investigated, only Al3+ caused any increase in the fluorescence intensity of 1. All other metal ions, including K(I), Na(I), Ag(I), Li(I), Zn(II), Co(II) and Hg(II), showed a negligible fluorescence response, while Cu(II) and Fe(III) significantly decreased the fluorescence intensity. Therefore, system 1 is a promising colourimetric sensor for Al3+, and a fluorescence sensor for Cu2+ and Fe3+ ions. Computational analysis revealed that 1 is unionized in ethanol solution, while it becomes di-deprotonated to 1 2– upon the complexation with Al3+. This changes the electronic structure of 1 and leaves no acidic hydrogen atoms to allow the ESIPT process. On the other hand, the presence of monovalent metal cations induces only mono-deprotonation to 1 – , which turns out to be an insufficient electronic change to be spotted in the recorded spectra.

Benzimidazole as a structural unit in fluorescent chemical sensors: the hidden properties of a multifunctional heterocyclic scaffold

Abstract Benzimidazole (BI) derivatives are structurally similar to naturally occurring nucleotides, a fact that enables their use as scaffolds in biologically active organic synthetic compounds. However, BI can serve as a multifunctional unit in heteroaromatic molecular systems for optoelectronics and non-linear optics, photovoltaics, and in sensing and bioimaging. Its many structure-related properties such as electron accepting ability, π-bridging, chromogenic pH sensitivity/switching and metal-ion chelating properties, also make BI an exceptional structural candidate for optical chemical sensors. The design of novel benzimidazole-based chemosensors is a challenging task. In this review, molecular sensing systems based on intramolecular charge transfer, photoinduced electron transfer and excited-state intramolecular proton transfer mechanisms are systematically examined and the role of the benzimidazole unit is discussed. Novel and emerging developments such as sensors based on aggregation-induced emission phenomena are also included. Conclusions are made on the advantages and disadvantages of existing fluorophores and chemosensors and guidelines are given for further design and development of new sensing systems based on benzimidazole.