Discovery Early Career Researcher Award - Grant ID: DE210100065
Funder
Australian Research Council
Funding Amount
$423,808.00
Summary
Designing Organocatalysts to Achieve Hyperpolarised Magnetic Resonance. Magnetic resonance techniques (such as MRI scans) suffer from an inherent insensitivity problem. In medical imaging, this can hamper diagnosis and mean long scan times for patients. This project aims to chemically develop catalysts which dramatically increase sensitivity, producing a signal that is thousands of times more visible. This project is significant as these catalysts can turn common, harmless molecules in the body ....Designing Organocatalysts to Achieve Hyperpolarised Magnetic Resonance. Magnetic resonance techniques (such as MRI scans) suffer from an inherent insensitivity problem. In medical imaging, this can hamper diagnosis and mean long scan times for patients. This project aims to chemically develop catalysts which dramatically increase sensitivity, producing a signal that is thousands of times more visible. This project is significant as these catalysts can turn common, harmless molecules in the body - even water - into visible tracers. The expected outcomes of this project include the synthesis and understanding of these catalysts which will be chemically fine-tuned to maximise their effectiveness. Potential benefits include translation to MRI applications to improve diagnosis and treatment, or chemical monitoring.Read moreRead less
Designing reactivity of homogeneous and heterogeneous water-splitting catalysts using muti-dimensional site-selective spectroscopies. New classes of heterogeneous manganese-calcium water splitting catalysts analogous to the unique biological water splitting cofactor have recently emerged but with far lower catalytic rates than seen for the biological system. These new materials are promising targets for large-scale hydrogen fuel production with low cost, high efficiency and ease of manufacture. ....Designing reactivity of homogeneous and heterogeneous water-splitting catalysts using muti-dimensional site-selective spectroscopies. New classes of heterogeneous manganese-calcium water splitting catalysts analogous to the unique biological water splitting cofactor have recently emerged but with far lower catalytic rates than seen for the biological system. These new materials are promising targets for large-scale hydrogen fuel production with low cost, high efficiency and ease of manufacture. To achieve this, the performance gap between these materials and the homogenous biological catalyst must be bridged. Multi-dimensional site-selective spectroscopies, including magneto/optical resonance methods which are aimed to be developed in this project are expected to provide new, atomic level understanding of properties needed to achieve high catalytic efficiency, thus guiding rational catalyst design.Read moreRead less
Linkage Infrastructure, Equipment And Facilities - Grant ID: LE100100236
Funder
Australian Research Council
Funding Amount
$180,000.00
Summary
Facilities for spectroscopy and diffraction at high pressures. The provision of infrastructure for the study of novel materials under high pressures will enhance Australia's capability in creating new materials and in creating new devices that meet needs in communication, environment and medicine applications. The new facility will enable researchers to understand the response of structures to extreme pressures and will exploit the unique capabilities of the synchrotron light.
The role of low-energy excited states in solar-energy capture. This project aims to determine the nature and role of the lowest-energy excited states in most natural photosynthetic reaction centres and light-harvesting complexes. The lowest-energy states of bacterial reaction centres are critical to function and are used as a paradigm in artificial organic solar-energy capture, but for most photosystems their nature remains unknown. The project aims to answer the critical question of why they do ....The role of low-energy excited states in solar-energy capture. This project aims to determine the nature and role of the lowest-energy excited states in most natural photosynthetic reaction centres and light-harvesting complexes. The lowest-energy states of bacterial reaction centres are critical to function and are used as a paradigm in artificial organic solar-energy capture, but for most photosystems their nature remains unknown. The project aims to answer the critical question of why they do not actually prevent function. It is expected that both the outcomes obtained and techniques developed will be directly relevant to solar-energy device design. The project will apply five existing, complimentary and purposely built spectrometers as well as quantum electronic and nuclear simulation techniques to identify and characterise three key systems.Read moreRead less
Linkage Infrastructure, Equipment And Facilities - Grant ID: LE130100057
Funder
Australian Research Council
Funding Amount
$200,000.00
Summary
A diffractometer for small molecule structural elucidation by crystallographic analysis. X-ray diffractometry provides an unambiguous means of identifying the three-dimensional spatial arrangement of atoms within molecules affording important insights into the origins of chemical properties. A modern diffractometer will provide information to help develop new functional materials, therapeutic agents and environmentally sustainable processes.
Signature of vibrational motions encoded into small polyatomic spectra. Using revolutionary state-of-the-art spectrometers, the project plans to search for signatures of large-amplitude vibrational motions that transform one chemical species to another. Bond-breaking chemical reactions necessarily involve highly vibrationally excited reactants and/or products that move the energy of the system away from equilibrium. It is now possible for direct measurements to be made of the changes that a mole ....Signature of vibrational motions encoded into small polyatomic spectra. Using revolutionary state-of-the-art spectrometers, the project plans to search for signatures of large-amplitude vibrational motions that transform one chemical species to another. Bond-breaking chemical reactions necessarily involve highly vibrationally excited reactants and/or products that move the energy of the system away from equilibrium. It is now possible for direct measurements to be made of the changes that a molecule undergoes as it transits across a chemical potential energy barrier. The project plans to examine the long-standing problem of vinylidene-acetylene isomerisation in order to verify the long-suspected existence of large amplitude vibrational motion in small molecules, which are thought to be the signatures of a particular class of chemical dynamics. These would provide a rational basis for future control of unimolecular chemical reactions.Read moreRead less
The Quantum Dot SPASER. Can we replace electrons with photons in future computers? This project provides two steps toward this goal. By combining advanced materials with ultra-small metallic structures, a new nano-sized form of a laser, called the spaser will be realised. Furthermore, a key component of a computer, a nanoscale modulator, will be demonstrated.
Benchmarking of advanced scattering probes for materials characterisation. The project seeks to establish the accuracy and validity of different methods of nanoscale structure determination. Nanoscale structure is crucial to the properties of many modern materials with diverse applications: e.g. sensors and actuators in cell phones; smart shock absorbers and fuel injectors in cars; memory devices; drug delivery devices.
Expanding the molecular tool set for structural studies of proteins and their complexes. Many applications in medical science and drug development depend on our ability to determine the 3D structures of proteins, protein assemblies and protein-ligand complexes. This project will develop novel lanthanide-binding tags and crosslinking agents that can be coupled to unnatural amino acids introduced into proteins with advanced protein chemistry techniques. These new tools will facilitate the collecti ....Expanding the molecular tool set for structural studies of proteins and their complexes. Many applications in medical science and drug development depend on our ability to determine the 3D structures of proteins, protein assemblies and protein-ligand complexes. This project will develop novel lanthanide-binding tags and crosslinking agents that can be coupled to unnatural amino acids introduced into proteins with advanced protein chemistry techniques. These new tools will facilitate the collection of structure restraints by nuclear magnetic resonance (NMR), electron paramagnetic resonance (EPR) and mass spectrometry, which are needed to generate accurate models of proteins and their complexes with other molecules. Major beneficial outcome will include an increase in the number of protein targets amenable to rational drug design and improved methods for generating new drug leads.Read moreRead less
Voltage-dependent structural changes in voltage-gated sodium channels. This project aims to provide insights into the structural rearrangements experienced by Nav channels, which are key components of animal nervous systems. Voltage-gated sodium (Nav) channels initiate action potentials in excitable cells. They open in response to membrane depolarisation then rapidly inactivate. Eukaryotic Nav channels contain four unique voltage-sensor domains (VSDs) that control how the channel responds to mem ....Voltage-dependent structural changes in voltage-gated sodium channels. This project aims to provide insights into the structural rearrangements experienced by Nav channels, which are key components of animal nervous systems. Voltage-gated sodium (Nav) channels initiate action potentials in excitable cells. They open in response to membrane depolarisation then rapidly inactivate. Eukaryotic Nav channels contain four unique voltage-sensor domains (VSDs) that control how the channel responds to membrane potential changes. Recently reported crystal structures of bacterial Nav channels have greatly advanced the field, but these channels contain four identical VSDs and have different inactivation properties. Thus, much remains to be learnt about the conformational plasticity of eukaryotic Nav channel VSDs. The project plans to use animal toxins to capture eukaryotic VSDs in defined states of the gating cycle for detailed structural analysis using nuclear magnetic resonance and X-ray crystallography.Read moreRead less