Recent Development in Coordination Compounds as a Sensor for Cyanide Ions in Biological and Environmental Segments

References

• Aspinall, H. C. Chiral Lanthanide Complexes: coordination Chemistry and Applications. Chem. Rev. 2002, 102, 1807–1850. DOI: 10.1021/cr010288q.
   PubMed Web of Science ®Google Scholar
• Hegg, E. L.; Burstyn, J. N. Toward the Development of Metal-Based Synthetic Nucleases and Peptidases: A Rationale and Progress Report in Applying the Principles of Coordination Chemistry. Coord. Chem. Rev. 1998, 173, 133–165. DOI: 10.1016/S0010-8545(98)00157-X.
   Web of Science ®Google Scholar
• Kumar, N.; Khullar, S.; Singh, Y.; Mandal, S. K. Hierarchical Importance of Coordination and Hydrogen Bonds in the Formation of Homochiral 2D Coordination Polymers and 2D Supramolecular Assemblies. CrystEngComm 2014, 16, 6730–6744. DOI: 10.1039/C4CE00387J.
   Web of Science ®Google Scholar
• Poli, R. Radical Coordination Chemistry and Its Relevance to Metal‐Mediated Radical Polymerization. Eur. J. Inorg. Chem. 2011, 2011, 1513–1530. DOI: 10.1002/ejic.201001364.
   Google Scholar
• Haque, A.; Ilmi, R.; Al-Busaidi, I. J.; Khan, M. S. Coordination Chemistry and Application of Mono-and Oligopyridine-Based Macrocycles. Coord. Chem. Rev. 2017, 350, 320–339. DOI: 10.1016/j.ccr.2017.07.008.
   Web of Science ®Google Scholar
• Holliday, B. J.; Mirkin, C. A. Strategies for the Construction of Supramolecular Compounds through Coordination Chemistry. Angew. Chem. Int. Ed. 2001, 40, 2022–2043. DOI: 10.1002/1521-3773(20010601)40:11<2022::AID-ANIE2022>3.0.CO;2-D.
   PubMed Web of Science ®Google Scholar
• Khan, E.; Ahmad, T.; Gul, Z.; Ullah, F.; Tahir, M. N.; Noor, A. Methyl-Substituted 2-Aminothiazole–Based Cobalt (II) and Silver (I) complexes: synthesis, X-Ray Structures, and Biological Activities. Turk. J. Chem. 2019, 43, 857–868. DOI: 10.3906/kim-1812-4.
   Web of Science ®Google Scholar
• Bernhardt, P. V.; Chin, P.; Sharpe, P. C.; Richardson, D. R. Hydrazone Chelators for the Treatment of Iron Overload Disorders: iron Coordination Chemistry and Biological Activity. Dalton Trans. 2007, 30, 3232–3244. DOI: 10.1039/b704102k.
   PubMed Web of Science ®Google Scholar
• Castillo-Blum, S. E.; Barba-Behrens, N. Coordination Chemistry of Some Biologically Active Ligands. Coord. Chem. Rev. 2000, 196, 3–30. DOI: 10.1016/S0010-8545(99)00153-8.
   Web of Science ®Google Scholar
• Donnelly, P. S. The Role of Coordination Chemistry in the Development of Copper and Rhenium Radiopharmaceuticals. Dalton Trans. 2011, 40, 999–1010. DOI: 10.1039/c0dt01075h.
   PubMed Web of Science ®Google Scholar
• Haas, K. L.; Franz, K. J. Application of Metal Coordination Chemistry to Explore and Manipulate Cell Biology. Chem. Rev. 2009, 109, 4921–4960. DOI: 10.1021/cr900134a.
   PubMed Web of Science ®Google Scholar
• Phillips, A. D.; Gonsalvi, L.; Romerosa, A.; Vizza, F.; Peruzzini, M. Coordination Chemistry of 1, 3, 5-Triaza-7-Phosphaadamantane (PTA): Transition Metal Complexes and Related Catalytic, Medicinal and Photoluminescent Applications. Coord. Chem. Rev. 2004, 248, 955–993. DOI: 10.1016/j.ccr.2004.03.010.
   Web of Science ®Google Scholar
• Ronconi, L.; Sadler, P. J. Using Coordination Chemistry to Design New Medicines. Coord. Chem. Rev. 2007, 251, 1633–1648. DOI: 10.1016/j.ccr.2006.11.017.
   Web of Science ®Google Scholar
• Tfouni, E.; Krieger, M.; McGarvey, B. R.; Franco, D. W. Structure, Chemical and Photochemical Reactivity and Biological Activity of Some Ruthenium Amine Nitrosyl Complexes. Coord. Chem. Rev. 2003, 236, 57–69. DOI: 10.1016/S0010-8545(02)00177-7.
   Web of Science ®Google Scholar
• Thompson, K. H.; Orvig, C. Coordination Chemistry of Vanadium in Metallopharmaceutical Candidate Compounds. Coord. Chem. Rev. 2001, 219-221, 1033–1053. DOI: 10.1016/S0010-8545(01)00395-2.
   Web of Science ®Google Scholar
• Gul, Z.; Din, N. U.; Khan, E.; Ullah, F.; Tahir, M. N. Synthesis, Molecular Structure, anti-Microbial, anti-Oxidant and Enzyme Inhibition Activities of 2-Amino-6-Methylbenzothiazole and Its Cu (II) and Ag (I) complexes. J. Mol. Struct. 2020, 1199, 126956. DOI: 10.1016/j.molstruc.2019.126956.
   Web of Science ®Google Scholar
• Allardyce, C. S.; Dyson, P. J. Metal-Based Drugs That Break the Rules. Dalton Trans. 2016, 45, 3201–3209. DOI: 10.1039/c5dt03919c.
   PubMed Web of Science ®Google Scholar
• Łakomska, I.; Fandzloch, M. Application of 1, 2, 4-Triazolo [1, 5-a] Pyrimidines for the Design of Coordination Compounds with Interesting Structures and New Biological Properties. Coord. Chem. Rev. 2016, 327-328, 221–241. DOI: 10.1016/j.ccr.2016.04.014.
   Web of Science ®Google Scholar
• Soobramoney, L.; Bala, M. D.; Friedrich, H. B. Coordination Chemistry of Co Complexes Containing Tridentate SNS Ligands and Their Application as Catalysts for the Oxidation of n-Octane. Dalton Trans. 2014, 43, 15968–15978. DOI: 10.1039/c4dt01750a.
   PubMed Web of Science ®Google Scholar
• Atkinson, R. C.; Gibson, V. C.; Long, N. J.; White, A. J.; Williams, D. J. Synthesis, Coordination Chemistry, and Catalytic Application of a Novel Unsymmetrical P/O Ferrocenediyl Ligand. Organometallics 2004, 23, 2744–2751. DOI: 10.1021/om0343768.
   Web of Science ®Google Scholar
• Rodríguez-Lugo, R.; Chacón-Terán, M.; De León, S.; Vogt, M.; Rosenthal, A.; Landaeta, V. Synthesis, Characterization and Pd(ii)-coordination chemistry of the ligand tris(quinolin-8-yl)phosphite. Application in the catalytic aerobic oxidation of amines . Dalton Trans. 2018, 47, 2061–2072. DOI: 10.1039/c7dt04000h.
   PubMed Web of Science ®Google Scholar
• Willms, H.; Frank, W.; Ganter, C. Coordination Chemistry and Catalytic Application of Bidentate Phosphaferrocene − Pyrazole and − Imidazole Based P, N-Ligands. Organometallics 2009, 28, 3049–3058. DOI: 10.1021/om8012025.
   Web of Science ®Google Scholar
• Müller, C.; López, L. G.; Kooijman, H.; Spek, A. L.; Vogt, D. Chiral Bidentate Phosphabenzene-Based Ligands: synthesis, Coordination Chemistry, and Application in Rh-Catalyzed Asymmetric Hydrogenations. Tetrahedron Lett. 2006, 47, 2017–2020. DOI: 10.1016/j.tetlet.2006.01.049.
   Web of Science ®Google Scholar
• Khusnutdinova, J. R.; Milstein, D. Metal-ligand cooperation. Angew. Chem. Int. Ed. Engl. 2015, 54, 12236–12273. DOI: 10.1002/anie.201503873.
   PubMed Web of Science ®Google Scholar
• Gunanathan, C.; Milstein, D. Metal-ligand cooperation by aromatization-dearomatization: a new paradigm in bond activation and "green" catalysis“”. Acc. Chem. Res. 2011, 44, 588–602. DOI: 10.1021/ar2000265.
   PubMed Web of Science ®Google Scholar
• Milstein, D. Discovery of Environmentally Benign Catalytic Reactions of Alcohols Catalyzed by Pyridine-Based Pincer Ru Complexes, Based on Metal–Ligand Cooperation. Top. Catal. 2010, 53, 915–923. DOI: 10.1007/s11244-010-9523-7.
   Web of Science ®Google Scholar
• Zell, T.; Milstein, D. Hydrogenation and Dehydrogenation Iron Pincer Catalysts Capable of metal-ligand cooperation by aromatization/dearomatization. Acc. Chem. Res. 2015, 48, 1979–1994. DOI: 10.1021/acs.accounts.5b00027.
   PubMed Web of Science ®Google Scholar
• Bureekaew, S.; Shimomura, S.; Kitagawa, S. Chemistry and Application of Flexible Porous Coordination Polymers. Sci. Technol. Adv. Mater. 2008, 9, 014108. DOI: 10.1088/1468-6996/9/1/014108.
   PubMed Web of Science ®Google Scholar
• Spokoyny, A. M.; Farha, O. K.; Mulfort, K. L.; Hupp, J. T.; Mirkin, C. A. Porosity Tuning of Carborane-Based Metal–Organic Frameworks (MOFs) via Coordination Chemistry and Ligand Design. Inorg. Chim. Acta 2010, 364, 266–271. DOI: 10.1016/j.ica.2010.08.007.
   Web of Science ®Google Scholar
• Murray, L. J.; Dincă, M.; Long, J. R. Hydrogen Storage in metal-organic frameworks. Chem. Soc. Rev. 2009, 38, 1294–1314. DOI: 10.1039/b802256a.
   PubMed Web of Science ®Google Scholar
• Collins, D. J.; Zhou, H.-C. Hydrogen Storage in Metal–Organic Frameworks. J. Mater. Chem. 2007, 17, 3154. DOI: 10.1039/b702858j.
   Web of Science ®Google Scholar
• He, Y.; Zhou, W.; Qian, G.; Chen, B. Methane Storage in metal-organic frameworks. Chem. Soc. Rev. 2014, 43, 5657–5678. DOI: 10.1039/c4cs00032c.
   PubMed Web of Science ®Google Scholar
• Zhao, X.; Wang, Y.; Li, D. S.; Bu, X.; Feng, P. Metal–Organic Frameworks for Separation. Adv. Mater. 2018, 30, 1705189. DOI: 10.1002/adma.201705189.
   PubMedGoogle Scholar
• Bao, Z.; Chang, G.; Xing, H.; Krishna, R.; Ren, Q.; Chen, B. Potential of Microporous Metal–Organic Frameworks for Separation of Hydrocarbon Mixtures. Energy Environ. Sci. 2016, 9, 3612–3641. DOI: 10.1039/C6EE01886F.
   Web of Science ®Google Scholar
• Krishna, R.; van Baten, J. M. In Silico Screening of metal-organic frameworks in separation applications. Phys. Chem. Chem. Phys. 2011, 13, 10593–10616. DOI: 10.1039/c1cp20282k.
   PubMed Web of Science ®Google Scholar
• Banerjee, D.; Cairns, A. J.; Liu, J.; Motkuri, R. K.; Nune, S. K.; Fernandez, C. A.; Krishna, R.; Strachan, D. M.; Thallapally, P. K. Potential of metal-organic frameworks for separation of xenon and krypton. Acc. Chem. Res. 2015, 48, 211–219. DOI: 10.1021/ar5003126.
   PubMed Web of Science ®Google Scholar
• Jiao, L.; Wang, Y.; Jiang, H. L.; Xu, Q. Metal–Organic Frameworks as Platforms for Catalytic Applications. Adv. Mater. 2018, 30, 1703663. DOI: 10.1002/adma.201703663.
   PubMed Web of Science ®Google Scholar
• Corma, A.; García, H.; Llabrés i Xamena, F. X. Llabrés i Xamena, F. Engineering Metal Organic Frameworks for Heterogeneous Catalysis. Chem. Rev. 2010, 110, 4606–4655. DOI: 10.1021/cr9003924.
   PubMed Web of Science ®Google Scholar
• Liu, J.; Chen, L.; Cui, H.; Zhang, J.; Zhang, L.; Su, C.-Y. Applications of metal-organic frameworks in heterogeneous supramolecular catalysis. Chem. Soc. Rev. 2014, 43, 6011–6061. DOI: 10.1039/c4cs00094c.
   PubMed Web of Science ®Google Scholar
• Gao, Q.; Xu, J.; Bu, X.-H. Recent Advances about Metal–Organic Frameworks in the Removal of Pollutants from Wastewater. Coord. Chem. Rev. 2019, 378, 17–31. DOI: 10.1016/j.ccr.2018.03.015.
   Web of Science ®Google Scholar
• Liu, C.; Yu, L.-Q.; Zhao, Y.-T.; Lv, Y.-K. Recent Advances in Metal-Organic Frameworks for Adsorption of Common Aromatic Pollutants. Mikrochim. Acta. 2018, 185, 342. DOI: 10.1007/s00604-018-2879-2.
   PubMed Web of Science ®Google Scholar
• Zhao, X.; Yu, X.; Wang, X.; Lai, S.; Sun, Y.; Yang, D. Recent Advances in Metal-Organic Frameworks for the Removal of Heavy Metal Oxoanions from Water. Chem. Eng. J. 2021, 407, 127221. DOI: 10.1016/j.cej.2020.127221.
   Web of Science ®Google Scholar
• Dias, E. M.; Petit, C. Towards the Use of Metal–Organic Frameworks for Water Reuse: A Review of the Recent Advances in the Field of Organic Pollutants Removal and Degradation and the Next Steps in the Field. J. Mater. Chem. A 2015, 3, 22484–22506. DOI: 10.1039/C5TA05440K.
   Web of Science ®Google Scholar
• Ojida, A.; Park, S-k.; Mito-Oka, Y.; Hamachi, I. Efficient Fluorescent ATP-Sensing Based on Coordination Chemistry under Aqueous Neutral Conditions. Tetrahedron Lett. 2002, 43, 6193–6195. DOI: 10.1016/S0040-4039(02)01317-5.
   Web of Science ®Google Scholar
• Alreja, P.; Kaur, N. Recent Advances in 1, 10-Phenanthroline Ligands for Chemosensing of Cations and Anions. RSC Adv. 2016, 6, 23169–23217. DOI: 10.1039/C6RA00150E.
   Web of Science ®Google Scholar
• Prodi, L.; Bolletta, F.; Montalti, M.; Zaccheroni, N. Luminescent Chemosensors for Transition Metal Ions. Coord. Chem. Rev. 2000, 205, 59–83. DOI: 10.1016/S0010-8545(00)00242-3.
   Web of Science ®Google Scholar
• Wu, D.; Sedgwick, A. C.; Gunnlaugsson, T.; Akkaya, E. U.; Yoon, J.; James, T. D. Fluorescent Chemosensors: The past, Present and Future. Chem. Soc. Rev. 2017, 46, 7105–7123. DOI: 10.1039/c7cs00240h.
   PubMed Web of Science ®Google Scholar
• Khan, E.; Khan, S.; Gul, Z.; Muhammad, M. Medicinal Importance, Coordination Chemistry with Selected Metals (cu, Ag, au) and Chemosensing of Thiourea Derivatives. A Review. Crit. Rev. Anal. Chem. 2020, 51, 812–834. DOI: 10.1080/10408347.2020.1777523.
   PubMed Web of Science ®Google Scholar
• Nural, Y.; Keleş, E.; Aydıner, B.; Seferoğlu, N.; Atabey, H.; Seferoğlu, Z. New Naphthoquinone-Imidazole Hybrids: Synthesis, Anion Recognition Properties, DFT Studies and Acid Dissociation Constants. J. Mol. Liq. 2021, 327, 114855. DOI: 10.1016/j.molliq.2020.114855.
   Web of Science ®Google Scholar
• Keleş, E.; Aydıner, B.; Nural, Y.; Seferoğlu, N.; Şahin, E.; Seferoğlu, Z. Cover Feature: A New Mechanism for Selective Recognition of Cyanide in Organic and Aqueous Solution (Eur. J. Org. Chem. 30/2020). Eur. J. Org. Chem. 2020, 2020, 4640–4640. DOI: 10.1002/ejoc.202001038.
   Web of Science ®Google Scholar
• Gul, Z.; Ullah, S.; Khan, S.; Ullah, H.; Khan, M. U.; Ullah, M.; Ali, S.; Altaf, A. A. Recent Progress in Nanoparticles Based Sensors for the Detection of Mercury (II) Ions in Environmental and Biological Samples. Crit. Rev. Anal. Chem. 2022. DOI: 10.1080/10408347.2022.2049676.
   Web of Science ®Google Scholar
• Ozawa, T.; Yoshimura, H.; Kim, S. B. Advances in Fluorescence and Bioluminescence Imaging. Anal. Chem. 2013, 85, 590–609. DOI: 10.1021/ac3031724.
   PubMed Web of Science ®Google Scholar
• Astruc, D.; Boisselier, E.; Ornelas, C. Dendrimers Designed for Functions: From Physical, Photophysical, and Supramolecular Properties to Applications in Sensing, Catalysis, Molecular Electronics, Photonics, and Nanomedicine. Chem. Rev. 2010, 110, 1857–1959. DOI: 10.1021/cr900327d.
   PubMed Web of Science ®Google Scholar
• Basabe-Desmonts, L.; Reinhoudt, D. N.; Crego-Calama, M. Design of Fluorescent Materials for Chemical Sensing. Chem. Soc. Rev. 2007, 36, 993–1017. DOI: 10.1039/b609548h.
   PubMed Web of Science ®Google Scholar
• Muhammad, M.; Khan, S.; Fayaz, H. Charge-Transfer Complex–Based Spectrophotometric Method for the Determination of Mesotrione in Environmental Samples. Environ. Monit. Assess. 2021, 193, 1. DOI: 10.1007/s10661-021-09432-0.
   Web of Science ®Google Scholar
• Khan, S.; Chen, X.; Almahri, A.; Allehyani, E. S.; Alhumaydhi, F. A.; Ibrahim, M. M.; Ali, S. Recent Developments in Fluorescent and Colorimetric Chemosensors Based on Schiff Bases for Metallic Cations Detection: A Review. J. Environ. Chem. Eng. 2021, 9, 106381. DOI: 10.1016/j.jece.2021.106381.
   Web of Science ®Google Scholar
• Ali, S.; Shah, M. R.; Hussain, S.; Khan, S.; Latif, A.; Ahmad, M.; Ali, M. A Facile Approach Based on Functionalized Silver Nanoparticles as a Chemosensor for the Detection of Paraquat. J. Clust. Sci. 2022, 33, 413–420. DOI: 10.1007/s10876-021-01978-w.
   Web of Science ®Google Scholar
• Glasgow, H. B.; Burkholder, J. M.; Reed, R. E.; Lewitus, A. J.; Kleinman, J. E. Real-Time Remote Monitoring of Water Quality: A Review of Current Applications, and Advancements in Sensor, Telemetry, and Computing Technologies. J. Exp. Mar. Biol. Ecol. 2004, 300, 409–448. DOI: 10.1016/j.jembe.2004.02.022.
   Web of Science ®Google Scholar
• Ma, J.; Dasgupta, P. K. Recent Developments in Cyanide Detection: A Review. Anal. Chim. Acta. 2010, 673, 117–125. DOI: 10.1016/j.aca.2010.05.042.
   PubMed Web of Science ®Google Scholar
• Bhalla, V.; Singh, H.; Kumar, M. Triphenylene Based Copper Ensemble for the Detection of Cyanide Ions. Dalton Trans. 2012, 41, 11413–11418. DOI: 10.1039/c2dt31244a.
   PubMed Web of Science ®Google Scholar
• Xu, Z.; Chen, X.; Kim, H. N.; Yoon, J. Sensors for the Optical Detection of Cyanide Ion. Chem. Soc. Rev. 2010, 39, 127–137. DOI: 10.1039/b907368j.
   PubMed Web of Science ®Google Scholar
• Park, G. J.; You, G. R.; Choi, Y. W.; Kim, C. A Naked-Eye Chemosensor for Simultaneous Detection of Iron and Copper Ions and Its Copper Complex for Colorimetric/Fluorescent Sensing of Cyanide. Sens. Actuators, B 2016, 229, 257–271. DOI: 10.1016/j.snb.2016.01.133.
   Web of Science ®Google Scholar
• Mohammadi, A.; Ghasemi, Z. A Simple Pyrimidine Based Colorimetric and Fluorescent Chemosensor for Sequential Detection of Copper (II) and Cyanide Ions and Its Application in Real Samples. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2020, 228, 117730. DOI: 10.1016/j.saa.2019.117730.
   PubMed Web of Science ®Google Scholar
• Chandra, R.; Ghorai, A.; Patra, G. K. A Simple Benzildihydrazone Derived Colorimetric and Fluorescent ‘on–off-On’sensor for Sequential Detection of Copper (II) and Cyanide Ions in Aqueous Solution. Sens. Actuators, B 2018, 255, 701–711. DOI: 10.1016/j.snb.2017.08.067.
   Web of Science ®Google Scholar
• Khoshsoroor, S.; Mohammadi, A.; Khalili, B.; Mohammadi, S. A Novel Uracil-Based Chemosensor for Sequential Detection of Copper (II) and Cyanide Ions and Its Application in Real Samples. J. Photochem. Photobiol, A 2020, 388, 112208. DOI: 10.1016/j.jphotochem.2019.112208.
   Web of Science ®Google Scholar
• Mohammadi, A.; Zabihi, F. S.; Chaibakhsh, N. Chemical Sensor Using Metal-Organic Complex: Preparation, Characterization and Application for Highly Selective Detection of Cyanide Ions in Mixed Aqueous-Organic Media. J. Photochem. Photobiol, A 2018, 367, 384–389. DOI: 10.1016/j.jphotochem.2018.09.004.
   Web of Science ®Google Scholar
• Mukherjee, S.; Talukder, S. A Coumarin-Based Luminescent Chemosensor for Recognition of Cu2+ and its In-Situ Complex for CN- Sensing via Cu2+ Displacement Approach . J. Fluoresc. 2017, 27, 1567–1572. DOI: 10.1007/s10895-016-1974-1.
   PubMed Web of Science ®Google Scholar
• You, G. R.; Park, G. J.; Lee, J. J.; Kim, C. A Colorimetric Sensor for the Sequential Detection of Cu(2+) and CN(-) in fully aqueous media: practical performance of Cu(2+). Dalton Trans. 2015, 44, 9120–9129. DOI: 10.1039/c5dt00772k.
   PubMed Web of Science ®Google Scholar
• Wu, C.; Wang, J.; Shen, J.; Zhang, C.; Wu, Z.; Zhou, H. A Colorimetric Quinoline-Based Chemosensor for Sequential Detection of Copper Ion and Cyanide Anions. Tetrahedron 2017, 73, 5715–5719. DOI: 10.1016/j.tet.2017.08.010.
   Web of Science ®Google Scholar
• Sahu, M.; Manna, A. K.; Chowdhury, S.; Patra, G. K. A Novel Dihydro phenylquinazolinone-based two-in-one colourimetric chemosensor for nickel(ii), copper(ii) and its copper complex for the fluorescent colourimetric nanomolar detection of the cyanide anion. RSC Adv. 2020, 10, 44860–44875. DOI: 10.1039/d0ra09023a.
   PubMed Web of Science ®Google Scholar
• Bhardwaj, S.; Maurya, N.; Singh, A. K. Chromone Based Fluorescent Organic Nanoparticles for High-Precision in-Situ Sensing of Cu2+ and CN − Ions in 100% Aqueous Solutions. Sens. Actuators, B 2018, 260, 753–762. DOI: 10.1016/j.snb.2018.01.003.
   Web of Science ®Google Scholar
• Jung, K. H.; Lee, K.-H. Efficient Ensemble System Based on the Copper Binding Motif for Highly Sensitive and Selective Detection of Cyanide Ions in 100% Aqueous Solutions by Fluorescent and Colorimetric Changes. Anal. Chem. 2015, 87, 9308–9314. DOI: 10.1021/acs.analchem.5b01982.
   PubMed Web of Science ®Google Scholar
• Zhang, Y.-M.; Su, J.-X.; Li, Q.; Qu, W.-J.; Zhu, X.; Leng, Y.-L.; Xin, S.-F.; Yao, H.; Lin, Q.; Wei, T.-B. Novel Fluorescent Cyanide-Selective Chemosensor Based on a Functionalised Pillar [5] Arene Copper (II) Complex. Supramol. Chem. 2017, 29, 411–416. DOI: 10.1080/10610278.2016.1253843.
   Web of Science ®Google Scholar
• Kaushik, R.; Ghosh, A.; Singh, A.; Gupta, P.; Mittal, A.; Jose, D. A. Selective Detection of Cyanide in Water and Biological Samples by an off-the-Shelf Compound. ACS Sens. 2016, 1, 1265–1271. DOI: 10.1021/acssensors.6b00519.
   Web of Science ®Google Scholar
• Sebastian, A.; Prasad, E. Cyanide Sensing in Water Using a Copper Metallogel through “Turn-on” Fluorescence. Langmuir 2020, 36, 10537–10547. DOI: 10.1021/acs.langmuir.0c01803.
   PubMed Web of Science ®Google Scholar
• Kaushik, R.; Sakla, R.; Ghosh, A.; Dama, S.; Mittal, A.; Jose, D. A. Copper Complex-Embedded Vesicular Receptor for Selective Detection of Cyanide Ion and Colorimetric Monitoring of Enzymatic Reaction. ACS Appl. Mater. Interfaces . 2019, 11, 47587–47595. DOI: 10.1021/acsami.9b17316.
   PubMed Web of Science ®Google Scholar
• Hotta, H.; Kurihara, S.; Johno, K.; Kitazume, M.; Sato, K.; Tsunoda, K-i. New Determination Methods of Halides and Cyanide Ions by Electrospray Ionization Mass Spectrometry Based on Ternary Complex Formation. Anal. Sci. 2011, 27, 953–956. DOI: 10.2116/analsci.27.953.
   PubMed Web of Science ®Google Scholar
• Shahid, M.; Chawla, H. M.; Bhatia, P. A Calix [4] Arene Based Turn off/Turn on Molecular Receptor for Cu2+ and CN − Ions in Aqueous Medium. Sens. Actuators, B 2016, 237, 470–478. DOI: 10.1016/j.snb.2016.06.102.
   Web of Science ®Google Scholar
• Sharma, P.; Singh, P. A Perylene Diimide-Based near-IR Ratiometric Sensor for Detection of Cu 2+ Ions: ensemble for Discrimination of CN − and S 2− Ions. Anal. Methods 2020, 12, 758–767. DOI: 10.1039/C9AY02726B.
   Web of Science ®Google Scholar
• Teerasarunyanon, R.; Watchasit, S.; Suksai, C.; Tuntulani, T.; Ruangpornvisuti, V. U. Vis and Theoretical Studies on an Ensemble of Dinuclear Cu (II) Complex of Anthracene–Based Tripodal Tetramine with Pyrogallol Red for Cyanide Detection and Species Distribution in Aqueous Solution. Inorg. Chem. Commun. 2019, 108, 107502. DOI: 10.1016/j.inoche.2019.107502.
   Web of Science ®Google Scholar
• Mondal, P.; Parua, S. P.; Pattanayak, P.; Das, U.; Chattopadhyay, S. Synthesis and Structure of Copper (II) Complexes: Potential Cyanide Sensor and Oxidase Model. J. Chem. Sci. 2016, 128, 803–813. DOI: 10.1007/s12039-016-1063-7.
   Web of Science ®Google Scholar
• Wang, L.; Wei, Z.-L.; Chen, Z.-Z.; Liu, C.; Dong, W.-K.; Ding, Y.-J. A Chemical Probe Capable for Fluorescent and Colorimetric Detection to Cu2+ and CN − Based on Coordination and Nucleophilic Addition Mechanism. Microchem. J. 2020, 155, 104801. DOI: 10.1016/j.microc.2020.104801.
   Web of Science ®Google Scholar
• Khatua, S.; Samanta, D.; Bats, J. W.; Schmittel, M. Rapid and Highly Sensitive dual-channel detection of cyanide by bis-heteroleptic ruthenium(II) complexes. Inorg. Chem. 2012, 51, 7075–7086. DOI: 10.1021/ic2022853.
   PubMed Web of Science ®Google Scholar
• Li, M.-J.; Lin, Z.; Chen, X.; Chen, G. Colorimetric and Luminescent Bifunctional Ru(II) complexes for rapid and highly sensitive recognition of cyanide. Dalton Trans. 2014, 43, 11745–11751. DOI: 10.1039/c4dt00231h.
   PubMed Web of Science ®Google Scholar
• Bar, M.; Maity, D.; Das, K.; Baitalik, S. Asymmetric Bimetallic Ruthenium (II) Complexes Selectively Sense Cyanide in Water through Significant Modulation of Their Ground and Excited State Properties. Sens. Actuators, B 2017, 251, 208–223. DOI: 10.1016/j.snb.2017.05.025.
   Web of Science ®Google Scholar
• Zhu, J.-W.; Ou, H.-D.; Xu, N.; Deng, W.; Yao, Z.-J. Ruthenium-Based Phosphorescent Probe for Selective and Naked-Eye Detection of Cyanide in Aqueous Media. Dyes Pigm. 2020, 176, 108196. DOI: 10.1016/j.dyepig.2020.108196.
   Web of Science ®Google Scholar
• Karmakar, S.; Maity, D.; Mardanya, S.; Baitalik, S. Pyrene and Imidazole Functionalized Luminescent Bimetallic Ru(II) terpyridine complexes as efficient optical chemosensors for cyanide in aqueous, organic and solid media. Dalton Trans. 2015, 44, 18607–18623. DOI: 10.1039/c5dt02585k.
   PubMed Web of Science ®Google Scholar
• Lee, J. H.; Jeong, A. R.; Shin, I.-S.; Kim, H.-J.; Hong, J.-I. Fluorescence Turn-on Sensor for Cyanide Based on a cobalt(II)-coumarinylsalen complex. Org. Lett. 2010, 12, 764–767. DOI: 10.1021/ol902852g.
   PubMed Web of Science ®Google Scholar
• Maurya, N.; Singh, A. K. Effective Ensemble System for the Identification of CN − Based on a Cobalt (ii) Complex: A Logic Gate Mimic. New J. Chem. 2017, 41, 4814–4819. DOI: 10.1039/C6NJ03926J.
   Web of Science ®Google Scholar
• Bhowmick, I.; Boston, D. J.; Higgins, R. F.; Klug, C. M.; Shores, M. P.; Gupta, T. Naked Eye Detection of Cyanide in Water with CoII Bis (Terpyridine) Complexes. Sens. Actuators, B 2016, 235, 325–329. DOI: 10.1016/j.snb.2016.05.053.
   Web of Science ®Google Scholar
• Collins, C. C.; Regalado‐Love, S.; Portillo, R. I.; Boston, D. J.; Shores, M. P.; Bhowmick, I. Functionalized Cellulose‐Co (II)‐Bis‐Terpyridine Hybrid Material as Colorimetric Sensor for Micromolar Aqueous Cyanide. Adv. Mater. Technol. 2019, 4, 1800406. DOI: 10.1002/admt.201800406.
   Web of Science ®Google Scholar
• Gabr, M. T.; Pigge, F. C. A Fluorescent Turn-on Probe for Cyanide Anion Detection Based on an AIE Active cobalt(ii) complex. Dalton Trans. 2018, 47, 2079–2085. DOI: 10.1039/c7dt04242f.
   PubMed Web of Science ®Google Scholar
• Lvova, L.; Pomarico, G.; Mandoj, F.; Caroleo, F.; Di Natale, C.; Kadish, K. M.; Nardis, S. Smartphone Coupled with a Paper-Based Optode: Towards a Selective Cyanide Detection. J. Porphyrins Phthalocyanines 2020, 24, 964–972. DOI: 10.1142/S1088424620500091.
   Web of Science ®Google Scholar
• Mukherjee, S.; Pal, P.; Bar, M.; Baitalik, S. Chromogenic and Fluorogenic Detection of Selected Anions by Bis-Terpyridine Fe (II) Complex through Displacement Approach. J. Chem. Sci. 2018, 130, 1. DOI: 10.1007/s12039-018-1484-6.
   Web of Science ®Google Scholar
• Hu, Z.-Q.; Du, M.; Zhang, L.-F.; Guo, F.-Y.; Liu, M.-D.; Li, M. A Novel Colorimetric and Fluorescent Chemosensor for Cyanide Ion in Aqueous Media Based on a Rhodamine Derivative in the Presence of Fe3+ Ion. Sens. Actuators, B 2014, 192, 439–443. DOI: 10.1016/j.snb.2013.10.138.
   Web of Science ®Google Scholar
• Lozano-Torres, B.; Marcos, M. D.; Pardo, T.; Sancenón, F.; Martínez-Máñez, R.; Rurack, K. Anilinopyridine–Metal Complexes for the Selective Chromogenic Sensing of Cyanide Anion. J. Coord. Chem. 2018, 71, 786–796. DOI: 10.1080/00958972.2018.1434719.
   Web of Science ®Google Scholar
• Jayasudha, P.; Manivannan, R.; Elango, K. P. Simple Colorimetric Chemodosimeters for Selective Sensing of Cyanide Ion in Aqueous Solution via Termination of ICT Transition by Michael Addition. Sens. Actuators, B 2015, 221, 1441–1448. DOI: 10.1016/j.snb.2015.08.017.
   Web of Science ®Google Scholar
• Niu, Q.; Sun, T.; Li, T.; Guo, Z.; Pang, H. Highly Sensitive and Selective Colorimetric/Fluorescent Probe with Aggregation Induced Emission Characteristics for Multiple Targets of Copper, Zinc and Cyanide Ions Sensing and Its Practical Application in Water and Food Samples. Sens. Actuators, B 2018, 266, 730–743. DOI: 10.1016/j.snb.2018.03.089.
   Web of Science ®Google Scholar
• Kim, Y.; Huh, H. S.; Lee, M. H.; Lenov, I. L.; Zhao, H.; Gabbaï, F. P. Turn-on fluorescence sensing of cyanide ions in aqueous solution at parts-per-billion concentrations. Chemistry 2011, 17, 2057–2062. DOI: 10.1002/chem.201002861.
   PubMed Web of Science ®Google Scholar
• Li, W.-T.; Qu, W.-J.; Zhu, X.; Li, Q.; Zhang, H.-L.; Yao, H.; Lin, Q.; Zhang, Y.-M.; Wei, T.-B. A Highly Selective Colorimetric and “off-on” Fluorescence Sensor for CN − Based on Zn (Salphenazine) Complex. Sci. China Chem. 2017, 60, 754–760. DOI: 10.1007/s11426-016-0438-4.
   Web of Science ®Google Scholar
• Rosales-Vázquez, L. D.; Valdes-García, J.; Bazany-Rodríguez, I. J.; German-Acacio, J. M.; Martinez-Otero, D.; Vilchis-Nestor, A. R.; Morales-Luckie, R.; Sanchez-Mendieta, V.; Dorazco-Gonzalez, A. A Sensitive Photoluminescent Chemosensor for Cyanide in Water Based on a Zinc Coordination Polymer Bearing Ditert-Butyl-Bipyridine. Dalton Trans. 2019, 48, 12407–12420. DOI: 10.1039/c9dt01861a.
   PubMed Web of Science ®Google Scholar
• Parthiban, C.; Ciattini, S.; Chelazzi, L.; Elango, K. P. Colorimetric Sensing of Anions by Cu (II), Co (II), Ni (II) and Zn (II) Complexes of Naphthoquinone-Imidazole Hybrid—Influence of Complex Formation on Selectivity and Sensing Medium. Sens. Actuators, B 2016, 231, 768–778. DOI: 10.1016/j.snb.2016.03.106.
   Web of Science ®Google Scholar
• Jang, H. J.; Kang, J. H.; Lee, M.; Lim, M. H.; Kim, C. Fluorescent Sensor for Sequentially Monitoring Zinc (II) and Cyanide Anion in near-Perfect Aqueous Media. Ind. Eng. Chem. Res. 2018, 57, 54–62. DOI: 10.1021/acs.iecr.7b03826.
   Web of Science ®Google Scholar
• Bouhadir, K. H.; Elaridi, J.; Sonji, G. Selective and Sensitive Turn on Fluorescence Cyanide Recognition in Aqueous Medium Based on Zn(II)-hydrazone metal complex chemosensor . Luminescence 2021, 36, 1608–1620. DOI: 10.1002/bio.4102.
   PubMed Web of Science ®Google Scholar
• Kumar, A.; Ahmed, N. Indirect Approach for CN–Detection: Development of “Naked-Eye” Hg2+-Induced Turn-Off Fluorescence and Turn-On Cyanide Sensing by the Hg2+ Displacement Approach. Ind. Eng. Chem. Res. 2017, 56, 6358. DOI: 10.1021/acs.iecr.7b00188.
   Web of Science ®Google Scholar
• Gupta, R. C.; Razi, S. S.; Ali, R.; Dwivedi, S. K.; Srivastava, P.; Singh, P.; Koch, B.; Mishra, H.; Misra, A. An Efficient Hg2+ Ensemble Based on a Triazole Bridged Anthracene and Quinoline System for Selective Detection of Cyanide through Fluorescence Turn-off–on Response in Solution and Live Cell. Sens. Actuators, B 2017, 251, 729–738. DOI: 10.1016/j.snb.2017.04.096.
   Web of Science ®Google Scholar
• Isaad, J.; El Achari, A. Colorimetric and Fluorescent Probe Based on Coumarin for Sequential Sensing of Mercury (II) and Cyanide Ions in Aqueous Solutions. J. Lumin. 2022, 243, 118668. DOI: 10.1016/j.jlumin.2021.118668.
   Web of Science ®Google Scholar
• Misra, R.; Jadhav, T.; Dhokale, B.; Mobin, S. M. Colorimetric and Fluorimetric Detection of Fluoride and Cyanide Ions Using Tri and Tetra Coordinated Boron Containing Chromophores. Dalton Trans. 2015, 44, 16052–16060. DOI: 10.1039/c5dt02356d.
   PubMed Web of Science ®Google Scholar
• Lin, N.; Ou, H.-D.; Xu, Q.; Jin, Y.; Deng, W.; Yao, Z.-J. An Efficient Probe of Cyclometallated Phosphorescent Iridium Complex for Selective Detection of Cyanide. ACS Omega. 2020, 5, 4636–4645. DOI: 10.1021/acsomega.9b04364.
   PubMed Web of Science ®Google Scholar
• Kumar, R.; Chaudhri, N.; Sankar, M. Ratiometric and Colorimetric “Naked Eye” Selective Detection of CN − Ions by Electron Deficient Ni (ii) Porphyrins and Their Reversibility Studies. Dalton Trans. 2015, 44, 9149–9157. DOI: 10.1039/C5DT00937E.
   PubMed Web of Science ®Google Scholar
• Salomón-Flores, M. K.; Bazany-Rodriguez, I. J.; Martinez-Otero, D.; Garcia-Eleno, M. A.; Guerra-Garcia, J. J.; Morales-Morales, D.; Dorazco-Gonzalez, A. Bifunctional Colorimetric Chemosensing of Fluoride and Cyanide Ions by nickel-POCOP Pincer Receptors. Dalton Trans. 2017, 46, 4950–4959. DOI: 10.1039/c6dt04897h.
   PubMed Web of Science ®Google Scholar
• Wang, K.; Zhao, C.; Guo, S.; Lu, Y.; Shen, Y.; Wang, C. A Coumarin-Based near-Infrared Fluorescent Probe with a Large Stokes Shift for the Sequential Recognition of Ni2+ and CN−: Performance Research and Quantum Calculation. J. Photochem. Photobiol. A 2019, 382, 111943. DOI: 10.1016/j.jphotochem.2019.111943.
   Web of Science ®Google Scholar
• Holaday, M. D.; Tarafdar, G.; Adinarayana, B.; Reddy, M.; Srinivasan, A. Chemodosimetric Cyanide Sensing in a 5,15-porphodimethene Pd(II) complex . Chem. Commun. (Camb.) 2014, 50, 10834–10836. DOI: 10.1039/c4cc04775c.
   PubMed Web of Science ®Google Scholar
• Singh, H.; Wasi, N.; Mehra, M. Detection and Determination of cyanide-a review. Int. J. Environ. Anal. Chem. 1986, 26, 115–136. DOI: 10.1080/03067318608077109.
   PubMed Web of Science ®Google Scholar
• Ebadinia, L.; Darabi, H. R.; Ramazani, A. Optical Detection of Cyanide by Palladium (II)-Dithiazolopyridine Probe at the Parts per Billion Level. Phosphorus Sulfur Silicon Relat. Elem. 2020, 195, 620–627. DOI: 10.1080/10426507.2019.1702987.
   Web of Science ®Google Scholar
• Slone, R. V.; Yoon, D. I.; Calhoun, R. M.; Hupp, J. T. Luminescent Rhenium/Palladium Square Complex Exhibiting Excited State Intramolecular Electron Transfer Reactivity and Molecular Anion Sensing Characteristics. J. Am. Chem. Soc. 1995, 117, 11813–11814. DOI: 10.1021/ja00152a027.
   Web of Science ®Google Scholar
• Huynh, L.; Wang, Z.; Yang, J.; Stoeva, V.; Lough, A.; Manners, I.; Winnik, M. A. Evaluation of Phosphorescent Rhenium and Iridium Complexes in Polythionylphosphazene Films for Oxygen Sensor Applications. Chem. Mater. 2005, 17, 4765–4773. DOI: 10.1021/cm047794r.
   Web of Science ®Google Scholar
• Xiao, Y.; Chu, W.-K.; Ng, C.-O.; Cheng, S.-C.; Tse, M.-K.; Yiu, S.-M.; Ko, C.-C. Design and Synthesis of Luminescent Bis (Isocyanoborato) Rhenate (I) Complexes as a Selective Sensor for Cyanide Anion. Organometallics 2020, 39, 2135–2141. DOI: 10.1021/acs.organomet.0c00204.
   Google Scholar
• Wu, H.; Li, R.; Dong, J.; Sun, F.; Jiang, Y.; Shen, Q. Synthesis, Structure and Electrochemical H2O2-Sensing of Two Silver (I) complexes with Bisbenzimidazole Ligands. Inorg. Chim. Acta 2022, 535, 120847. DOI: 10.1016/j.ica.2022.120847.
   Web of Science ®Google Scholar
• Jin, J.-C.; Jiang, C.; Chang, W.-G.; Xu, G.-N.; Fu, X.-C. A Luminescent Novel Octanuclear Silver (I) cluster Framework with Potential Cr2O72− Sensing. Inorg. Chem. Commun. 2016, 70, 157–159. DOI: 10.1016/j.inoche.2016.06.009.
   Web of Science ®Google Scholar
• Maurya, N.; Bhardwaj, S.; Singh, A. K. Selective Colorimetric and Fluorescence 'turn-on' sensor for Ag + and in-situ sensing of CN- (off-on-off) via displacement approach. Mater. Sci. Eng. C Mater. Biol. Appl. 2017, 74, 55–61. DOI: 10.1016/j.msec.2016.12.131.
   PubMed Web of Science ®Google Scholar
• Worlinsky, J. L.; Halepas, S.; Brückner, C. PEGylated Meso-Arylporpholactone Metal Complexes as Optical Cyanide Sensors in Water. Organic & Biomolecular Chemistry 2014, 12, 3991–4001. DOI: 10.1039/C4OB00697F.
   PubMed Web of Science ®Google Scholar
• Kumar, S. P.; Suresh, R.; Giribabu, K.; Manigandan, R.; Munusamy, S.; Muthamizh, S.; Narayanan, V. Synthesis and Characterization of chromium(III) Schiff base complexes: antimicrobial activity and its electrocatalytic sensing ability of catechol. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2015, 139, 431–441. DOI: 10.1016/j.saa.2014.12.012.
   PubMed Web of Science ®Google Scholar
• Weerasinghe, A. J.; Oyeamalu, A. N.; Abebe, F. A.; Venter, A. R.; Sinn, E. Rhodamine Based Turn-on Sensors for Ni(2+) and Cr(3+) in Organic Media: Detecting CN(-) via the Metal Displacement Approach. J. Fluoresc. 2016, 26, 891–898. DOI: 10.1007/s10895-016-1777-4.
   PubMed Web of Science ®Google Scholar
• Zheng, Z.-B.; Huang, Q.-Y.; Han, Y.-F.; Zuo, J.; Ma, Y.-N. Ruthenium (II) Complex-Based Chemosensors for Highly Sensitive and Selective Sequential Recognition of Copper Ion and Cyanide. Sens. Actuators, B 2017, 253, 203–212. DOI: 10.1016/j.snb.2017.06.145.
   Web of Science ®Google Scholar
• Christianson, A. M.; Gabbaï, F. P. Fluoride and Cyanide Anion Sensing by an Sb (V)-Substituted Cyclometalated Ru Polypyridyl Complex. J. Organomet. Chem. 2017, 847, 154–161. DOI: 10.1016/j.jorganchem.2017.03.012.
   Web of Science ®Google Scholar
• Chow, C. F.; Ho, P. Y.; Wong, W. L.; Gong, C. B. A Multifunctional Bimetallic Molecular Device for Ultrasensitive Detection, Naked-Eye Recognition, and Elimination of Cyanide Ions. Chemistry 2015, 21, 12984–12990. DOI: 10.1002/chem.201501448.
   PubMed Web of Science ®Google Scholar
• Christianson, A. M.; Gabbaï, F. P. Anion Sensing with a Lewis Acidic BODIPY-antimony(v) derivative . Chem. Commun. (Camb.) 2017, 53, 2471–2474. DOI: 10.1039/c6cc09205e.
   PubMed Web of Science ®Google Scholar
• Promchat, A.; Rashatasakhon, P.; Sukwattanasinitt, M. A Novel Indolium Salt as a Highly Sensitive and Selective Fluorescent Sensor for Cyanide Detection in Water. J. Hazard. Mater. 2017, 329, 255–261. DOI: 10.1016/j.jhazmat.2017.01.024.
   PubMed Web of Science ®Google Scholar
• Tsui, Y.-K.; Devaraj, S.; Yen, Y.-P. Azo Dyes Featuring with Nitrobenzoxadiazole (NBD) Unit: A New Selective Chromogenic and Fluorogenic Sensor for Cyanide Ion. Sens. Actuators, B 2012, 161, 510–519. DOI: 10.1016/j.snb.2011.10.069.
   Web of Science ®Google Scholar
• Wu, W.-N.; Wu, H.; Wang, Y.; Zhao, X.-L.; Xu, Z.-Q.; Xu, Z.-H.; Fan, Y.-C. A NIR Sensor for Cyanide Detection and Its Application in Cell Imaging. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2018, 199, 141–145. DOI: 10.1016/j.saa.2018.03.044.
   PubMed Web of Science ®Google Scholar
• Niu, Q.; Lan, L.; Li, T.; Guo, Z.; Jiang, T.; Zhao, Z.; Feng, Z.; Xi, J. A Highly Selective Turn-on Fluorescent and Naked-Eye Colorimetric Sensor for Cyanide Detection in Food Samples and Its Application in Imaging of Living Cells. Sens. Actuators, B 2018, 276, 13–22. DOI: 10.1016/j.snb.2018.08.066.
   Web of Science ®Google Scholar
• Cheng, S.; Pan, X.; Shi, M.; Su, T.; Zhang, C.; Zhao, W.; Dong, W. A Coumarin-Connected Carboxylic Indolinium Sensor for Cyanide Detection in Absolute Aqueous Medium and Its Application in Biological Cell Imaging. Spectrochim. Acta A Mol. Biomol. Spectrosc. 2020, 228, 117710. DOI: 10.1016/j.saa.2019.117710.
   PubMed Web of Science ®Google Scholar