Chemiluminescence from osmium(ii) complexes with phenanthroline, diphosphine and diarsine ligands

The reaction of various [Os(L)2(L′)]2+ complexes (where L and L′ are phenanthroline, diphosphine or diarsine ligands) and organic reducing agents after chemical or electrochemical oxidation of the reactants produces an emission of light corresponding to MLCT transitions. In certain instances, the emission was greater than that of [Ru(bipy)3]2+, but the relative signals were dependent on many factors, including reagent concentration, mode of oxidation, reducing agent and the sensitivity of the photodetector over the wavelength range

A portable sensor for cell optical density measurement in microfluidic chips

This paper presents the development of a smartphone-controlled wireless device for cell optical density sensing in microfluidic chips. The footprint of the device is very compact relative to a classical laboratory spectrophotometer, making it a portable device. The cell optical density sensing device consists of an embedded microcontroller, optical sensing components, and a wireless transceiver performing cell optical density measurements in disposable microfluidic chips fabricated from poly(methylmethacrylate) polymers. The device is controlled by an Android application allowing for true portability and the possibility of remote or field operation of the device. The use of microfluidic chips as the sample carrier for optical density detection instead of a plastic cuvette allows users the flexibility to explore and/or conduct a variety of micro-scale chemical analysis using the device which would be difficult in a cuvette-based system. The function of the device is validated through a series of off-line and online optical density measurements using Saccharomyces cerevisae yeast cultures. The device is low cost, small enough to fit in most laboratory flow hood cabinets, and can be easily integrated into miniature bioreactor systems. Moreover, wireless communication enables the user to operate the device using smartphones or rapidly transfer the measured data to an online repository for analysis or storage

New perspectives on the annihilation electrogenerated chemiluminescence of mixed metal complexes in solution

Preliminary explorations of the annihilation electrogenerated chemiluminescence (ECL) of mixed metal complexes have revealed opportunities to enhance emission intensities and control the relative intensities from multiple luminophores through the applied potentials. However, the mechanisms of these systems are only poorly understood. Herein, we present a comprehensive characterisation of the annihilation ECL of mixtures of tris(2,2′-bipyridine)ruthenium(ii) hexafluorophosphate ([Ru(bpy)3](PF6)2) and fac-tris(2-phenylpyridine)iridium(iii) ([Ir(ppy)3]). This includes a detailed investigation of the change in emission intensity from each luminophore as a function of both the applied electrochemical potentials and the relative concentrations of the two complexes, and a direct comparison with two mixed (Ru/Ir) ECL systems for which emission from only the ruthenium-complex was previously reported. Concomitant emission from both luminophores was observed in all three systems, but only when: (1) the applied potentials were sufficient to generate the intermediates required to form the electronically excited state of both complexes; and (2) the concentration of the iridium complex (relative to the ruthenium complex) was sufficient to overcome quenching processes. Both enhancement and quenching of the ECL of the ruthenium complex was observed, depending on the experimental conditions. The observations were rationalised through several complementary mechanisms, including resonance energy transfer and various energetically favourable electron-transfer pathways

Analytically useful blue chemiluminescence from a water-soluble iridium(iii) complex containing a tetraethylene glycol functionalised triazolylpyridine ligand

We examine [Ir(df-ppy)2(pt-TEG)](+) as the first highly water soluble, blue-luminescent iridium(iii) complex for chemiluminescence detection. Marked differences in selectivity were observed between the new complex and the conventional [Ru(bpy)3](2+) reagent, which will enable this mode of detection to be extended to new areas of application

Iridium(III) N-heterocyclic carbene complexes: an experimental and theoretical study of structural, spectroscopic, electrochemical and electrogenerated chemiluminescence properties

Four cationic heteroleptic iridium(III) complexes have been prepared from methyl- or benzyl-substituted chelating imidazolylidene or benzimidazolylidene ligands using a Ag(I) transmetallation protocol. The synthesised iridium(III) complexes were characterised by elemental analysis, (1)H and (13)C NMR spectroscopy and the molecular structures for three complexes were determined by single crystal X-ray diffraction. A combined theoretical and experimental investigation into the spectroscopic and electrochemical properties of the series was performed in order to gain understanding into the factors influencing photoluminescence and electrochemiluminescence efficiency for these complexes, with the results compared with those of similar NHC complexes of iridium and ruthenium. The N^C coordination mode in these complexes is thought to stabilise thermally accessible non-emissive states relative to the case with analogous complexes with C^C coordinated NHC ligands, resulting in low quantum yields. As a result of this and the instability of the oxidised and reduced forms of the complexes, the electrogenerated chemiluminescence intensities for the compounds are also low, despite favourable energetics. These studies provide valuable insights into the factors that must be considered when designing new NHC-based luminescent complexes

Chemiluminescence detection with water-soluble iridium(III) complexes containing a sulfonate-functionalised ancillary ligand

The chemiluminescence from four cyclometalated iridium(III) complexes containing an ancillary bathophenanthroline-disulfonate ligand exhibited a wide range of emission colours (green to red), and in some cases intensities that are far greater than the commonly employed benchmark reagent, [Ru(bpy)3](2+). A similar complex incorporating a sulfonated triazolylpyridine-based ligand enabled the emission to be shifted into the blue region of the spectrum, but the responses with this complex were relatively poor. DFT calculations of electronic structure and emission spectra support the experimental findings

Erratum to: 36th International Symposium on Intensive Care and Emergency Medicine

[This corrects the article DOI: 10.1186/s13054-016-1208-6.]

Titanium in biomedical applications—properties and fabrication: a review

Ti and Ti-based alloys have unique properties such as high strength, low density and excellent corrosion resistance. These properties are essential for the manufacture of lightweight and high strength components for biomedical applications. In this paper, Ti properties such as metallurgy, mechanical properties, surface modification, corrosion resistance, biocompatibility and osseointegration in biomedical applications have been discussed. This paper also analyses the advantages and disadvantages of various Ti manufacturing processes for biomedical applications such as casting, powder metallurgy, cold and hot working, machining, laser engineering net shaping (LEN), superplastic forming, forging and ring rolling. The contributions of this research are twofold, firstly scrutinizing the behaviour of Ti and Ti-based alloys in-vivo and in-vitro experiments in biomedical applications to determine the factors leading to failure, and secondly strategies to achieve desired properties essential to improving the quality of patient outcomes after receiving surgical implants. Future research will be directed toward manufacturing of Ti for medical applications by improving the production process, for example using optimal design approaches in additive manufacturing and investigating alloys containing other materials in order to obtain better medical and mechanical characteristics

MiniStat: development and evaluation of a mini-potentiostat for electrochemical measurements

As high-precision instrumentation is becoming more portable and cost-effective, an opportunity has arisen to move the electrochemical analysis techniques out of the laboratory and into novel application environments. The increased demand in electrochemical systems driven by a new age of technology sees the need for devices that are adaptive to the following: 1) portable, allowing for handheld and user-friendly field-based testing; 2) embeddable, allowing for long-term in situ assays; and 3) low cost, allowing for large-scale, parallel simultaneous experiments. To address these needs, we propose a potentiostat platform which allows for a variety of electrochemical assays to be performed on a miniaturized, battery-powered, low-cost device. This device incorporates the three key components of a potentiostat: output stage, input stage, and control/communications, into a single 27 mm $\times20$ mm footprint. The device is evaluated through several bench tests which confirmed the accuracy of both the precision voltage output and current measurement input of the device. Subsequently, three electrochemical experiments were conducted to evaluate the real-world performance and application of the device. These experiments allowed for the confirmation of the devices capability to accurately perform chronoamperometry, cyclic voltammetry, and anodic stripping square wave voltammetry. These experiments clearly indicated that the device operates as an analytically useful potentiostat, outputting accurate voltages, and precisely measuring the resulting current