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Overview
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Professor in the Department of Chemistry+44 (0) 191 33 42124

Biography

Prof J. A. Gareth Williams studied for an M.A. in Chemistry at Merton College, University of Oxford, including a year of research on the chemistry of dinuclear tungsten complexes in the group of Prof. Malcolm L. H. Green FRS. He then moved to the University of Durham to study for a PhD with Prof. David Parker FRS on the luminescence properties of macrocyclic metal complexes. That was followed by a postdoctoral fellowship at Universite Louis Pasteur, Strasbourg, with Prof. Jeane-Pierre Sauvage (Nobel Laureate 2016), working on the synthesis of multi-porphyin assemblies, and the study of energy- and electron-transfer processes within them, in collaboration with researchers at the C.N.R. Bologna, Italy.

Following further postdoctoral research, Williams was appointed to a lectureship at Durham University, promoted to Senior Lecturer, and then to full Professor in 2012.

He is author or co-author of around 240 publications, with an average of 75 citations per paper and an h index of 79 (data from Google scholar as of Jan 2025).  Recent publications from the Group are listed at the end of this page. A full list can be viewed from the "ORCID profile" link above.

Research Interests

The Group's interests are centred around the synthesis and excited-state properties of light-emitting molecules ... particularly where there's a metal ion involved! We have a multi-disciplinary team, in which group members are typically engaged both in synthesis and optical spectroscopy. Applications of our molecular materials include: (i) emitters for organic light-emitting diodes (OLEDs) for new flat-screen display technology, (ii) luminescent probes for bioimaging and as sensors for bioactive molecules in solution, and (iii) photosensitisers of energy- and electron-transfer for solar energy conversion.

Synthetic work includes both organic synthesis and the coordination chemistry of transition metal and lanthanide ions. Luminescence and other photophysical properties are studied using steady-state and time-resolved absorption and emission spectroscopy in solution, in polymer films, and in solids, over a range of temperatures. The work is multi-disciplinary in nature and embraces all three of the main branches of chemistry. We have close links with Universities in France, Italy and North America, and industrial laboratories in the UK and USA.

We are also interested in the bacteriostatic effects of ligands related to EDTA - how such chelants can interfere with the ability of bacteria to acquire the metal ions that they need to survive. Such research has huge implications for the shelf-life of many consumer products, ranging from mayonnaise to face cream. We are exploring a bio-inspired approach to the problem of the environmental impact of the EDTA that is added to such products to preserve them. PhD student Lucy Woods leads the Group's current efforts in this area.

Cyclometallated platinum(II) and iridium(III) complexes
image of a molecule and its emission spectrum

Organic light-emitting devices (OLEDs) are at the forefront of modern display screen technology. Luminescent, charge-neutral complexes of third-row transition metal ions like iridium and platinum function as "triplet-harvesting agents" in OLEDs. The high spin-orbit coupling constant of these heavy metal ions promotes emission from the triplet excited states that are normally non-emissive and otherwise wasted in such devices, leading to huge gains in efficiency and lower power consumption.

We have a particular interest in platinum(II) complexes. Being planar, they are able to undergo intermolecular face-to-face interactions that may lead to aggregates or excimers. These bimolecular excited states emit at lower energy than the isolated molecules, that is, further to the red and even into the near-infrared (NIR). We have been pioneering the use of such bimolecular states as a strategy to obtain efficient NIR OLEDs, and also for the red component that is needed to generate white light from an RGB display.

OLEDs emitting with different colours

For example, the figure shows four OLEDs prepared using different concentrations of one of our platinum(II) complexes and the different colours that result, superimposed on the CIE coordinates. The asterisk indicates the ideal position for ambient room lighting (a bit redder than pure white) – and we’re not far off! The complex in this instance features a tridentate NCN-coordinating ligand based on 2,6-di(2-pyridyl)benzene, a structural type that we have developed extensively in our laboratory. We've discovered that these complexes are exceptionally good at forming brightly-emitting excimers and aggregates. 

Meanwhile, we are also exploring the chemistry and excited states of platinum(IV) complexes with tridentate ligands. These are challenging to prepare due to the kinetic inertness of Pt(IV), but Yana Dikova, a PhD student in the group, has not been deterred!

films emitting red, orange or green according to oxygen concentration

We have also investigated the utility of these compounds as oxygen sensors. By immobilising them in an ethyl cellulose film also containing platinum octaethylporphyrin, a wide-range O2 sensor is obtained that responds as a kind of molecular traffic light - as seen in the photograph above.

Luminescent sensors for bioactive ions and molecules in solution
chemical structures of APDAP and APTRA

Although a large number of fluorescent sensors for a variety of species are commercially available, most rely on changes in the wavelength or intensity of the short-lived (nanosecond) emission. We are seeking to develop new light-emitting components for sensors, in which the emission is long-lived, in the microsecond-to-millisecond range. This allows time-resolved detection methods of analysis to be employed, which gets round the problem of background interference from other fluorescent material, and also offers the potential for lifetime-based sensing.

We're also interested in the challenging problem of designing fluorescent sensors for magnesium ions. There's been enormous progress over the past 30 years or so in the real-time detection of the biologically important metal ions Ca2+ and Zn2+. These metal ions can now be studied well in cellulo, using appropriate sensors in conjunction with fluorescence microscopy. But Mg2+ is difficult, because Ca2+ is usually a highly competitive ion: selectivity for Mg2+ is hard to achieve. We've found that by switching from the well-established ligand APTRA to a new phosphinate analogue APDAP (illustrated in the figure above), the affinity for Ca2+ is reduced far more than for Mg2+. The selectivity for Mg2+ is correspondingly enhanced greatly. This result offers a way to improved magnesium-selective fluorescent sensors.  PhD student Laura Duncan is working on this challenging but rewarding topic.

Research interests

  • Synthetic Chemistry
  • Metal Complexes
  • Luminescence and Bioimaging

Publications

Journal Article

Supervision students