Louis Rendina

Prof. Louis Rendina


Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 June 2022 in Nature Reviews Chemistry
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Journal Article
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AMAnita Marfavi
Anita Marfavi
PKPoya Kavianpour
Poya Kavianpour
LRLouis Rendina
Louis Rendina

3 April 2014 in ACS Chemical Neuroscience
Verified
Journal Article
Open access
SWShane M. Wilkinson
Shane M. Wilkinson
Hendra GunosewoyoHendra Gunosewoyo
Hendra Gunosewoyo
MBMelissa L. Barron
Melissa L. Barron
ABAurelie Boucher
Aurelie Boucher
MMMichelle McDonnell
Michelle McDonnell
MKMichael Kassiou
Michael Kassiou
Relative to other polycyclic frameworks (1–3), a carborane cage (4 and Cs·5) exerts a significant biological effect as an inhibitor of the purinergic P2X7 receptor (P2X7R) which allows one to target depression in vivo and thus demonstrate, for the first time, that a carborane has the capacity to modify CNS activity.

1 May 2015 in Drug Discovery Today
Verified
Journal Article
Closed access
CAChristopher J.D. Austin
Christopher J.D. Austin
LRLouis Rendina
Louis Rendina

18 February 2021 in Chemical Society Reviews
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Journal Article
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ARAmy G. Robertson
Amy G. Robertson
LRLouis Rendina
Louis Rendina
Combining therapeutic and diagnostic tools into a single ‘theranostic’ platform lies at the forefront of cancer research. Some of the most promising theranostics exploit the unique nuclear and electronic properties of the lanthanoid metal gadolinium.

15 December 2023 in ACS Polymers Au
Verified
Journal Article
Open access
XZXinyi Zhang
Xinyi Zhang
LRLouis Rendina
Louis Rendina
MMMarkus Muellner
Markus Muellner
Carboranes are an important class of electron-delocalized icosahedral carbon-boron clusters with unique physical and chemical properties, which can offer various functions to polymers including enhanced heat-resistance, tuned electronic properties and hydrophobicity, special ability of dihydrogen bond formation, and thermal neutron capture. Carborane-containing polymers have been synthesized mainly by means of step-growth polymerizations of disubstituted carborane monomers, with chain-growth polymerizations of monosubstituted carborane monomers including ATRP, RAFT, and ROMP only utilized recently. Carborane-containing polymers may find application as harsh-environment resistant materials, ceramic precursors, fluorescent materials with tuned emissive properties, novel optoelectronic devices, potential BNCT agents, and drug carriers with low cytotoxicity. This review highlights carborane-containing polymer synthesis strategies and potential applications, showcasing the versatile properties and possibilities that this unique family of boron compounds can provide to the polymeric systems.

15 July 2013 in Australian Journal of Chemistry
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Journal Article
Closed access
PDF file
JKJan Kahlert
Jan Kahlert
CAChristopher J. D. Austin
Christopher J. D. Austin
MKMichael Kassiou
Michael Kassiou
LRLouis Rendina
Louis Rendina
The unique chemistry of boron allows for the utilisation of novel building-blocks which are not traditionally found in medicinal chemistry. The pharmaceutical industry has begun to exploit boronic acid derivatives as new drugs and several research groups are also exploring 1,2-azaborines and icosahedral boranes known as carboranes as boron-based structural motifs, with great promise for innovative drug design. Recent advances in the medicinal chemistry of these three important boron moieties are highlighted and illustrated with selected examples.