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      A brief review on novel pyrene based fluorometric and colorimetric chemosensors for the detection of Cu 2+

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          Abstract

          This review article provides a detailed overview of pyrene containing colorimetric and fluorometric chemosensors based on different binding mechanisms which fulfill the criteria of affinity, selectivity and sensitivity.

          Abstract

          The development of colorimetric and fluorometric chemosensors that capable of detecting Cu 2+ ions by a change in colour and fluorescence intensity has been described. Herein, chemosensors having pyrene functional groups as a signaling moiety are discussed in detail as pyrene derivatives show significant photophysical properties being superior to those of other commonly used scaffolds. This review article provides a detailed overview of pyrene containing chemosensors based on fluorescence mechanisms, such as excimer/exciplex formation, photoinduced electron transfer (PET), photoinduced charge transfer (PCT), aggregation induced emission (AIE), ligand to metal charge transfer process (LMCT), chelation enhanced quenching mechanism (CHEQ), Cu 2+-selective reactions for the selective and sensitive detection of Cu 2+. Potential future applications are also discussed because of the fact Cu 2+ ion recognition has a great significance in the biological, environmental and medical sectors.

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          Most cited references180

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          Aggregation-induced emission.

          Luminogenic materials with aggregation-induced emission (AIE) attributes have attracted much interest since the debut of the AIE concept in 2001. In this critical review, recent progress in the area of AIE research is summarized. Typical examples of AIE systems are discussed, from which their structure-property relationships are derived. Through mechanistic decipherment of the photophysical processes, structural design strategies for generating new AIE luminogens are developed. Technological, especially optoelectronic and biological, applications of the AIE systems are exemplified to illustrate how the novel AIE effect can be utilized for high-tech innovations (183 references). This journal is © The Royal Society of Chemistry 2011
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            Neurodegenerative diseases and oxidative stress.

            Oxidative stress has been implicated in the progression of Alzheimer's disease, Parkinson's disease and amyotrophic lateral sclerosis. Oxygen is vital for life but is also potentially dangerous, and a complex system of checks and balances exists for utilizing this essential element. Oxidative stress is the result of an imbalance in pro-oxidant/antioxidant homeostasis that leads to the generation of toxic reactive oxygen species. The systems in place to cope with the biochemistry of oxygen are complex, and many questions about the mechanisms of oxygen regulation remain unanswered. However, this same complexity provides a number of therapeutic targets, and different strategies, including novel metal-protein attenuating compounds, aimed at a variety of targets have shown promise in clinical studies.
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              The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene.

              Wilson disease (WD) is an autosomal recessive disorder of copper transport, resulting in copper accumulation and toxicity to the liver and brain. The gene (WD) has been mapped to chromosome 13 q14.3. On yeast artificial chromosomes from this region we have identified a sequence, similar to that coding for the proposed copper binding regions of the putative ATPase gene (MNK) defective in Menkes disease. We show that this sequence forms part of a P-type ATPase gene (referred to here as Wc1) that is very similar to MNK, with six putative metal binding regions similar to those found in prokaryotic heavy metal transporters. The gene, expressed in liver and kidney, lies within a 300 kb region likely to include the WD locus. Two WD patients were found to be homozygous for a seven base deletion within the coding region of Wc1. Wc1 is proposed as the gene for WD.
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                MCFAC5
                Materials Chemistry Frontiers
                Mater. Chem. Front.
                Royal Society of Chemistry (RSC)
                2052-1537
                March 8 2021
                2021
                : 5
                : 5
                : 2173-2200
                Affiliations
                [1 ]Department of Applied Chemistry
                [2 ]Faculty of Science and Engineering
                [3 ]Saga University
                [4 ]Saga 840-8502
                [5 ]Japan
                [6 ]Department of Chemistry
                [7 ]The University of Hull
                [8 ]UK
                Article
                10.1039/D0QM01008A
                a370b588-f5b4-49ac-aa1d-06f4d48673e2
                © 2021

                http://rsc.li/journals-terms-of-use

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