A5007174765- Crystallization and Solubility Studies
- X-ray Diffraction in Crystallography
- Organometallic Complex Synthesis and Catalysis
- Molecular Sensors and Ion Detection
- Mass Spectrometry Techniques and Applications
- Supramolecular Chemistry and Complexes
- Fluorine in Organic Chemistry
- Organometallic Compounds Synthesis and Characterization
- Lanthanide and Transition Metal Complexes
- Organic and Molecular Conductors Research
- Inorganic Fluorides and Related Compounds
- Catalytic Processes in Materials Science
- CO2 Reduction Techniques and Catalysts
- Magnetism in coordination complexes
- Synthesis and characterization of novel inorganic/organometallic compounds
- Electrocatalysts for Energy Conversion
UNSW Sydney
2013-2023
Shahid Chamran University of Ahvaz
2008
A new ruthenium(<sc>ii</sc>) complex capable of catalysing both CO<sub>2</sub> reduction and water oxidation was designed synthesised.
Embracing complexity in design, metallo-supramolecular self-assembly presents an opportunity for fabricating materials of economic significance. The array accessible supramolecules is alluring, along with favourable energy requirements. Implementation hampered by inability to efficiently characterise complex mixtures. stoichiometry, size, shape, guest binding properties and reactivity individual components combinations thereof are inherently challenging resolve. A large combinatorial library...
Abstract Foremost, practical applications of spin‐crossover (SCO) materials require control the nature spin‐state coupling. In existing SCO materials, there is a single, well‐defined dimensionality relevant to switching behavior. A new material, consisting 1,2,4‐triazole‐based trimers coordinated into 1D chains by [Au(CN) 2 ] − and spaced anions exchangeable guests, underwent defined elastic coupling across multiple dimensional hierarchies. Detailed structural, vibrational, theoretical...
Abstract The reactions of bis(anilino)phosphine oxide (C 6 H 5 NH) 2 P(O) with )2TiCl2 or Me2SiCl2 in a 1:1 molar ratio THF results the isolation new phosph(V)azane complexes (C5H5)2Ti[(N C6H5)2P(O)H] (1) Cl Si[(N C )2P(O)H] (2), respectively. In these reactions, HCl CH4 elimination occurs and N-Ti N-Si bonds form directly between ligand organotitanium organosilicon compounds. products(1) (2) have been fully characterized by elemental analysis as well 1 H, 31 P, 29 Si NMR, IR spectroscopy....
In the title complex salt, [{(η(5)-C5Me5)Rh}2(μ-Cl)3]PF6, dinuclear, single-charged cation is formed by cojoining of two classic (η(5)-C5Me5)RhCl3 'piano-stool' units bridging three choride ligand 'legs'. The crystal structure shows several close H⋯F contacts between hexa-fluorido-phosphate counter-ions and C5Me5 ligands.
Abstract Embracing complexity in design, metallo‐supramolecular self‐assembly presents an opportunity for fabricating materials of economic significance. The array accessible supramolecules is alluring, along with favourable energy requirements. Implementation hampered by inability to efficiently characterise complex mixtures. stoichiometry, size, shape, guest binding properties and reactivity individual components combinations thereof are inherently challenging resolve. A large...