Carl Redshaw

Prof. Carl Redshaw

University of Hull
+1
orcid
Professor, Tokyo Metropolitan University

Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

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

Representative Publications

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1 September 1999 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
GBGeorge J. P. Britovsek
George J. P. Britovsek
MBMichael Bruce
Michael Bruce
VGVernon C. Gibson
Vernon C. Gibson
BKBrian S. Kimberley
Brian S. Kimberley
PMPeter J. Maddox
Peter J. Maddox
DWDavid J. Williams
David J. Williams

1 May 2007 in Chemical Reviews
Verified
Journal Article
Closed access
VGVernon C. Gibson
Vernon C. Gibson
CRCarl Redshaw
Carl Redshaw
Gregory SolanGregory Solan
Gregory Solan

29 October 2008 in Chemical Reviews
Verified
Journal Article
Closed access
DHDamien M. Homden
Damien M. Homden
CRCarl Redshaw
Carl Redshaw

11 September 2023 in Chemical Society Reviews
Verified
Journal Article
Closed access
PDF file
XFXing Feng
Xing Feng
XWXiaohui Wang
Xiaohui Wang
CRCarl Redshaw
Carl Redshaw
Ben Zhong TangBen Zhong Tang
Ben Zhong Tang
Molecular aggregates are self-assembled from multiple molecules via weak intermolecular interactions, and new chemical and physical properties can emerge compared to their individual molecule. With the development of aggregate science, much research has focused on the study of the luminescence behaviour of aggregates rather than single molecules. Pyrene as a classical fluorophore has attracted great attention due to its diverse luminescence behavior depending on the solution state, molecular packing pattern as well as morphology, resulting in wide potential applications. For example, pyrene prefers to emit monomer emission in dilute solution but tends to form a dimer via π–π stacking in the aggregation state, resulting in red-shifted emission with quenched fluorescence and quantum yield. Over the past two decades, much effort has been devoted to developing novel pyrene-based fluorescent molecules and determining the luminescence mechanism for potential applications. Since the concept of “aggregation-induced emission (AIE)” was proposed by Tang et al. in 2001, aggregate science has been established, and the aggregated luminescence behaviour of pyrene-based materials has been extensively investigated. New pyrene-based emitters have been designed and synthesized not only to investigate the relationships between the molecular structure and properties and advanced applications but also to examine the effect of the aggregate morphology on their optical and electronic properties. Indeed, new aggregated pyrene-based molecules have emerged with unique properties, such as circularly polarized luminescence, excellent fluorescence and phosphorescence and electroluminescence, ultra-high mobility, etc. These properties are independent of their molecular constituents and allow for a number of cutting-edge technological applications, such as chemosensors, organic light-emitting diodes, organic field effect transistors, organic solar cells, Li-batteries, etc. Reviews published to-date have mainly concentrated on summarizing the molecular design and multi-functional applications of pyrene-based fluorophores, whereas the aggregation behaviour of pyrene-based luminescent materials has received very little attention. The majority of the multi-functional applications of pyrene molecules are not only closely related to their molecular structures, but also to the packing model they adopt in the aggregated state. In this review, we will summarize the intriguing optoelectronic properties of pyrene-based luminescent materials boosted by aggregation behaviour, and systematically establish the relationship between the molecular structure, aggregation states, and optoelectronic properties. This review will provide a new perspective for understanding the luminescence and electronic transition mechanism of pyrene-based materials and will facilitate further development of pyrene chemistry.

13 January 2010 in Polymer Chemistry
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Journal Article
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AAAbdessamad Arbaoui
Abdessamad Arbaoui
CRCarl Redshaw
Carl Redshaw
Economic pressure, environmental issues and ever increasing demand are driving the shift from oil-based polymers to those available from renewable resources. Ring opening polymerisation of cyclic esters is currently a topical field with metal complex-induced coordination/insertion type polymerisation leading the way. Such a polymerisation method offers a wide range of advantages from control over the polymer structure to kinetic enhancement; however industrially available catalysts based on tin suffer from inherent toxicity and as a result a policy change from the Food and Drug Administration (FDA) is not unrealistic. This review underlines the efforts made in the past five years or so, and shows how low toxicity metals are attracting increasing attention in the field of ε-caprolactone polymerisation.

20 March 2019 in Materials Chemistry Frontiers
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Journal Article
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PDF file
Md. Monarul IslamMd. Monarul Islam
Md. Monarul Islam
ZHZhen Hu
Zhen Hu
QWQingsong Wang
Qingsong Wang
CRCarl Redshaw
Carl Redshaw
XFXing Feng
Xing Feng
“Unity is force” – Aesop. It is a common phenomenon that traditional chromophores exhibit high fluorescence in dilute solutions, yet luminescence is quenched at high concentrations or in the aggregate state, i.e. “aggregation-caused quenching” (ACQ). Tang reported the unusual photophysical observation that luminogens can exhibit weak or no fluorescence in solution, yet they are highly emissive in the aggregate or solid state; this is defined as aggregation-induced emission (AIE). The discovery of AIE helped solve the ACQ effect in traditional luminophores. Pyrene is an important polycyclic aromatic hydrocarbon (PAH), which exhibits very different photophysical behavior in solution versus the aggregate state, and the ACQ effect has played a dominant role in pyrene chemistry. The ACQ effect is harmful for some practical applications and is a challenge in organic light-emitting diodes (OLEDs) and light-emitting electrochemical cells, for which the effect is more severe in the solid state. Thus, how to overcome the ACQ effect observed in pyrene chemistry still remains a challenge. In this review, we discuss how following basic AIE mechanisms such as the restriction of intramolecular motion (RIM), excited-state intramolecular proton transfer (ESIPT), and twisted intramolecular charge transfer (TICT), can transform pyrene-based ACQ luminogens to AIE luminogens with excellent optical properties. Furthermore, prospective applications of pyrene-based AIEgens are discussed, as is the potential for designing new organic functional materials.