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Relevant bibliographies by topics / 8-hydroxyquinoline

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Academic literature on the topic '8-hydroxyquinoline'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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Journal articles on the topic "8-hydroxyquinoline"

1

MARRUGO-GONZALEZ, Alonso Jose, Valery D. ORLOV, and Roberto FERNANDEZ-MAESTRE. "1,3,5-TRIARYL 2-PYRAZOLINES WITH 8-HYDROXYQUINOLINIC SUBSTITUENT: SYNTHESES, PHOTOPHYSICAL PROPERTIES, AND BIOLOGICAL ACTIVITY." Periódico Tchê Química 12, no. 24 (2015): 51–62. http://dx.doi.org/10.52571/ptq.v12.n24.2015.51_p_24_pgs_51_62.pdf.

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1,3,5-triaryl-2-pyrazolines are organic luminophores with arylic radicals that show a wide biological activity and are used as liquid scintillators and electro-optic materials. Experimental. Eleven 2-pyrazolines were synthesized from phenylhidrazine and chalcones of the 8-hydroxyquinoline series: 3-(8-hydroxyquinolin-5-yl)-1-(3-R)-phenylprop-2-enone and 1-(8-hydroxyquinolin-5-yl)-3--(3-R)-phenylprop-2-enone, where R = H, CH3, OCH3, N(CH3)2, Cl, Br, and NO2. The structures were confirmed by elemental analysis, IR, 1H-NMR, and electronic spectroscopy. Results and discussion. The 1- and 3-aryl su

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Suwanjang, Wilasinee, Supaluk Prachayasittikul, and Virapong Prachayasittikul. "Effect of 8-hydroxyquinoline and derivatives on human neuroblastoma SH-SY5Y cells under high glucose." PeerJ 4 (August 31, 2016): e2389. http://dx.doi.org/10.7717/peerj.2389.

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8-Hydroxyquinoline and derivatives exhibit multifunctional properties, including antioxidant, antineurodegenerative, anticancer, anti-inflammatory and antidiabetic activities. In biological systems, elevation of intracellular calcium can cause calpain activation, leading to cell death. Here, the effect of 8-hydroxyquinoline and derivatives (5-chloro-7-iodo-8-hydroxyquinoline or clioquinol and 8-hydroxy-5-nitroquinoline or nitroxoline) on calpain-dependent (calpain-calpastatin) pathways in human neuroblastoma (SH-SY5Y) cells was investigated. 8-Hydroxyquinoline and derivatives ameliorated high

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Wang, Hong Liang, Jun Hao Zhang, Zhao Kun Qu, Liang Jia, and Jiao Long Wang. "Synthesis and Photoluminescence Property of Tris(8-hydroxyquinoline) Bismuth Rod-Like Structures at Room Temperature." Advanced Materials Research 415-417 (December 2011): 1382–86. http://dx.doi.org/10.4028/www.scientific.net/amr.415-417.1382.

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Tris(8-hydroxyquinoline) bismuth complex has been synthesized with a facile method in a mixed solvent system containing bismuth nitrate and 8-hydroxyquinolineat at room temperature. The molecular formula of the products is speculated by the C, H and N element analysis and thermal gravimetric analysis, and FTIR was also utilized to measure the structure, which further confirms the molecular formula of the products. The observation of FESEM and TEM shows that the morphology of tris(8-hydroxyquinoline) bismuth complexes is rod-like structure. The results of photoluminescence emission indicate tha

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MARRUGO-GONZALEZ, A. Jose, V. D. ORLOV, and Roberto FERNANDEZ-MAESTRE. "SYNTHESIS OF 2,3-DIHYDRO-1H-1,5-BENZODIAZEPINES CONTAINING THE 8- HYDROXYQUINOLINIC FRAGMENT." Periódico Tchê Química 13, no. 26 (2016): 14–32. http://dx.doi.org/10.52571/ptq.v13.n26.2016.14_periodico26_pgs_14_32.pdf.

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Benzodiazepines are used as anxiolytic, hypnotic, sedative, and antidepressant drugs and to treat anxiety, insomnia, and epileptic seizures and show other types of biological activities. In this study, ten new 4(2)-(8-hydroxyquinolinil-5)-2(-4)-aryl-2,3-dihydro-1H-1,5-benzodiazepines and their rearrangement products, 2-substituted benzimidazoles, were synthesized from 1-aryl-3- (8-hydroxyquinolinil-5) propenone-1 (-3) and ophenylenediamine in methanol-triethylamine (1:1) solution. The reaction between the diamine and chalcones containing the 8-hydroxyquinoline fragment was carried out under mi

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Wang, Chengchao, Wei Zhang, Nianchen Zhou, Yansheng Qiu, Zhengping Cheng, and Xiulin Zhu. "Synthesis and Characterization of Well-Defined SolubleAlq3- andZnq2-Functionalized Polymers via RAFT Copolymerization." International Journal of Polymer Science 2010 (2010): 1–7. http://dx.doi.org/10.1155/2010/340926.

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The reversible addition-fragmentation chain transfer (RAFT) copolymerizations of 2-((8-hydroxyquinolin-5-yl)methoxy)ethyl methacrylate (HQHEMA) with styrene (St) or methyl methacrylate (MMA) were successfully carried out in the presence of 2-cyanoprop-2-yl dithionaphthalenoate (CPDN). The polymerization behaviors showed the typical living natures by the first-order polymerization kinetics, the linear dependence of molecular weights of the polymers on the monomer conversions with the relatively narrow molecular weight distributions(Mw/Mn), and the successful chain extension experiments. The sol

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Csuvik, Oszkár, and István Szatmári. "Synthesis of Bioactive Aminomethylated 8-Hydroxyquinolines via the Modified Mannich Reaction." International Journal of Molecular Sciences 24, no. 9 (2023): 7915. http://dx.doi.org/10.3390/ijms24097915.

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8-hydroxyquinoline (oxine) is a widely known and frequently used chelating agent, and the pharmacological effects of the core molecule and its derivatives have been studied since the 19th century. There are several synthetic methods to modify this core. The Mannich reaction is one of the most easily implementable examples, which requires mild reaction conditions and simple chemical reagents. The three components of the Mannich reaction are a primary or secondary amine, an aldehyde and a compound having a hydrogen with pronounced activity. In the modified Mannich reaction, naphthol or a nitroge

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Fung, Man Kin, Alan Man Ching Ng, Aleksandra B. Djurišić, Wai Kin Chan, and Hai Wang. "Preparation of 8-hydroxyquinoline wires by decomposition of tris(8-hydroxyquinoline) aluminium." Journal of Experimental Nanoscience 7, no. 5 (2012): 578–85. http://dx.doi.org/10.1080/17458080.2010.543992.

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RAGULIN, V. V., I. R. RAGULINA, and L. G. SHAKIROV. "ChemInform Abstract: Carboxylation of 8-Hydroxyquinoline to 8-Hydroxyquinoline-7-carboxylic Acid." ChemInform 26, no. 26 (2010): no. http://dx.doi.org/10.1002/chin.199526159.

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Ribeiro da Silva, Manuel A. V., Manuel João S. Monte, and M. Agostinha R. Matos. "Enthalpies of combustion, vapour pressures, and enthalpies of sublimation of 8-hydroxyquinoline, 5-nitro-8-hydroxyquinoline, and 2-methyl-8-hydroxyquinoline." Journal of Chemical Thermodynamics 21, no. 2 (1989): 159–66. http://dx.doi.org/10.1016/0021-9614(89)90127-4.

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Senchurin, V. S., S. A. Nayfert, A. A. Osipov, D. A. Zherebtsov, and R. Kantkhapazham. "Structures of Acylated 5-Iodo-8-Hydroxyquinoline and 5,7-Diiodo-8-Hydroxyquinoline Derivatives." Journal of Structural Chemistry 66, no. 3 (2025): 595–602. https://doi.org/10.1134/s0022476625030151.

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Dissertations / Theses on the topic "8-hydroxyquinoline"

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Curry, Richard James. "Luminescence characterisation of aluminium and erbium tris (8-hydroxyquinoline)." Thesis, Queen Mary, University of London, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312173.

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Knight, Cheryl Lynn. "Application of IR and NMR spectroscopy to certain complexes of 8-hydroxyquinoline and 8-aminoquinoline." Master's thesis, University of Cape Town, 1987. http://hdl.handle.net/11427/22001.

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The IR spectra of twenty-one transition metal complexes of 8-hydroxyquinoline over the range 700 - 50 cm⁻¹ are discussed in relation to their known or inferred structures. The complexes are of three types: (a) the bis(aquo) complexes of the first row transition metal(II) ions, [M(ox)₂(H₂O)₂] (M =Mn, Fe, Co, Ni, Cu, Zn); (b) the corresponding anhydrous complexes, [M(ox)₂]n (M=Mn, Co, Ni, Cu, Zn) and (c) the complexes of the metal(III) ions, [M(ox)₃] (M = Sc, V, Cr, Mn, Fe, Co, Ga, Rh and In). Deuterated 8-hydroxyquinoline was. synthesized by the Skraup synthesis and has been used to assist in t

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Pretorius, Alet. "A preliminary investigation of the potential anticancer properties of 8-hydroxyquinoline derivatives." Diss., University of Pretoria, 2011. http://hdl.handle.net/2263/24884.

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Derivatives of the quinoline moiety have been shown to exert a range of biological activities, including anti-neoplastic activity. The clinical application of quinoline derivatives in the treatment of malignancies has been limited due to non-selectivity. Four novel hydroxyquinoline derivatives were synthesised as potential anticancer agents. Each of these compounds contains the characteristic quinoline nucleus: a heterocyclic moiety containing a nitrogen atom. A hydroxyl group is present on C-8 and an azo bond links the heterocyclic quinoline core to a monocyclic benzene ring with various subs

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Tarverdi, Karnik. "Preparation and testing of lanthanum and neodymium with 8-hydroxyquinoline as potential biocide." Thesis, Brunel University, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.332067.

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McDonald, F. Crisp. "The study of 8-Hydroxyquinoline-2-Carboxyllic acid and its metal ion complexing properties /." Electronic version (PDF), 2005. http://dl.uncw.edu/etd/2005/mcdonaldf/fcrispmcdonald.pdf.

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Vu, Thi huyen. "Synthesis and Development New 8-Hydroxyquinoline Derivatives for the Treatment of Chlamydia trachomatis Infection." Thesis, Université de Paris (2019-....), 2020. https://wo.app.u-paris.fr/cgi-bin/WebObjects/TheseWeb.woa/wa/show?t=4392&f=28906.

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Chlamydia trachomatis, une bactérie à Gram négatif, est responsable, à la fois, de l'infection bactérienne sexuellement transmissible la plus diagnostiquée dans le monde et du trachome, une cause importante de cécité. Aucun vaccin n'est disponible mais deux antibiotiques (Azithromycine, Doxycycline) sont recommandés par l'Organisation Mondiale de la Santé. Toutefois, un échec du traitement est signalé chez 10 à 20% des patients et résulte probablement d'un manque de sensibilité des formes persistantes de la bactérie et des modestes concentrations intracellulaires des médicaments conventionnell

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Joaquim, Angélica Rocha. "Síntese de derivados de 8-hidroxiquinolina e avaliação da atividade antimicrobiana." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2018. http://hdl.handle.net/10183/181465.

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A prospecção e síntese de novos derivados de 8-hidroxiquinolina está em ascensão devido às suas diversas atividades biológicas. Neste trabalho é relatada a síntese e avaliação da atividade antimicrobiana de novos derivados contendo uma sulfonamida substituída na posição 5 da 8-hidroxiquinolina ou um grupamento aminossubstituído na posição 7 da 5-cloro-8-hidroxiquinolina ou 5-cloro-8-metoxiquinolina. Os derivados 5-sulfonamidas foram preparados por clorossulfonação seguida da reação com a amina apropriada. Os derivados 7-aminossubstituído foram sintetizados através da metilação da hidroxila da

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Gregušová, Michaela. "Modifikace techniky difúzních gelů (DGT) pro charakterizaci přírodních systémů." Doctoral thesis, Vysoké učení technické v Brně. Fakulta chemická, 2010. http://www.nusl.cz/ntk/nusl-233319.

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Diffusive gradient in thin film technique (DGT) represents a relatively new approach for in situ determinations of labile metal-species in aquatic systems. The DGT device passively accumulates labile species from the solution while deployed in situ, and therefore contamination problems associated with conventional collection and filtration procedures are eliminated. This study deals with a possible modification of DGT technique. The key of using DGT technique for speciation analysis of metals is to find out suitable binding phase and diffusion layer. The new resin gel based on Spheron Oxin (5

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Aprahamian, Vicken Haroutiun. "The behaviour and control of impurities during the solvent extraction of platinum metals with an alkylated 8-hydroxyquinoline /." Thesis, McGill University, 1992. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=61135.

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In order to understand and control the deportment of common impurity elements in the Pt(IV)-Pd(II)-HCl-8-hydroxyquinoline (TN 1911)$ sp{ rm a}$ system, their solvent extraction chemistry in chloride solution has been studied. The investigated elements were Fe(III), Cu(II), Ni(II), Zn(II), Pb(II), Sn(IV), Ag(I), As(V), Sb(V), Bi(III), Se(IV) and Te(IV). Extraction experiments carried out using multi-element and single element feed solutions helped to elucidate the extraction behaviour of the elements with the extractant TN 1911. From the collected data it was deduced that the majority formed an

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AVILA, HAROLD JOSE CAMARGO. "DEVELOPMENT AND CHARACTERIZATION OF ORGANIC ELECTROLUMINESCENT DEVICES (OLEDS) BASED ON NEWS TETRAKIS 8-HYDROXYQUINOLINE OF RARE-EARTH COMPLEXES." PONTIFÍCIA UNIVERSIDADE CATÓLICA DO RIO DE JANEIRO, 2012. http://www.maxwell.vrac.puc-rio.br/Busca_etds.php?strSecao=resultado&nrSeq=20308@1.

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PONTIFÍCIA UNIVERSIDADE CATÓLICA DO RIO DE JANEIRO<br>COORDENAÇÃO DE APERFEIÇOAMENTO DO PESSOAL DE ENSINO SUPERIOR<br>CONSELHO NACIONAL DE DESENVOLVIMENTO CIENTÍFICO E TECNOLÓGICO<br>PROGRAMA DE SUPORTE À PÓS-GRADUAÇÃO DE INSTS. DE ENSINO<br>O Alq3 é um dos mais importantes semicondutores orgânicos utilizados como transportador de elétrons e emissor em dispositivos eletroluminescentes (OLEDs). Este trabalho apresenta o estudo das propriedades ópticas, eletroquímicas, elétricas e morfológicas de três complexos baseados em íons de terras raras (TR) ligados à 8-hidroxiquinolina (q), Li[TR(q)4] (T

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Books on the topic "8-hydroxyquinoline"

1

Cölle, Michael. The electroluminescent material Alq3: Thermal, structural and photophysical propertires. Logos Verlag, 2004.

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Karim, Salma. Synthesis and study of metal-ion capacities of 8-hydroxyquinoline immobilised on different grades of silica gel. Brunel University, 1988.

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Khangura, Ranjit Singh. Charge injection properties of aluminum tris(8-hydroxyquinoline) based devices . 2005.

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Stary, J. Critical Evaluation of Equilibrium Constants Involving 8-Hydroxyquinoline and Its Metal Chelates : Critical Evaluation of Equilibrium Constants in Solution : Part B: Equilibrium Constants of Liquid-Liquid Distribution Systems. Elsevier Science & Technology Books, 2013.

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Book chapters on the topic "8-hydroxyquinoline"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetracyanonotrosylchromate(I) complex with 8-hydroxyquinoline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_460.

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Haesebroek, G. "Purity and long-term stability of 8-hydroxyquinoline-based metal extractants." In EMC ’91: Non-Ferrous Metallurgy—Present and Future. Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3684-6_32.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetranuclear manganese(III)-oxo-acetate complex with 8-hydroxyquinoline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_520.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetranuclear manganese(III)-oxo-acetate complex with 8-hydroxyquinoline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_521.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetranuclear manganese(III)-oxo-acetate complex with 8-hydroxyquinoline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_522.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetranuclear manganese(III)-oxo-benzoate complex with 8-hydroxyquinoline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_523.

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Mir, M. Amin, Samar Dernayka, Anuj Kumar, Shailendra Prakash, Anita Bisht, and Minakshi. "Synthesis structural analysis and antimicrobial properties of Fe, V, Cr and 8-hydroxyquinoline complexes." In Advances in Electronics, Computer, Physical and Chemical Sciences. CRC Press, 2025. https://doi.org/10.1201/9781003616252-8.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of tetranuclear manganese(III)-oxo-acetate complex with 5-chloro-8-hydroxyquinoline." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_524.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mixed ligand ruthenium(III) complex with 8-hydroxyquinoline and 4-picoline." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 7. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65895-6_164.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of mixed ligandcomplex of cobalt(II) with malonic acid and 8-hydroxyquinoline." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_177.

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Conference papers on the topic "8-hydroxyquinoline"

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Wang, Junbo, Xinpei Cao, and Hanting Wang. "Tris-(8-hydroxyquinoline) lanthanide based UV photovoltaic diodes." In Fourth International Conference on Optics and Image Processing (ICOIP 2024), edited by Xiaotao Hao and Chuan Qin. SPIE, 2024. http://dx.doi.org/10.1117/12.3039126.

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Mir, M. Amin, Minakshi Memoria, Anuj Kumar, et al. "Preparation, Structure analysis and Antibacterial Properties of Iron Complexes mixed with 8-Hydroxyquinoline and Some Amino Acids." In 2024 International Conference on Smart Devices (ICSD). IEEE, 2024. http://dx.doi.org/10.1109/icsd60021.2024.10751600.

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Kepeňová, Martina, Michaela Benediková, Mária Vilková, Miroslava Litecká, and Ivan Potočňák. "Ionic palladium(II) complexes with nitro and halogen derivatives of 8-hydroxyquinoline." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.443k.

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Four commercially unavailable derivatives of 8-hydroxyquinoline with different functional groups (nitro and halogen) in positions 5 and 7 were prepared: 5-nitro-7-iodo-8-hydroxyquinoline (HNIQ), 5-nitro-7-bromo-8-hydroxyquinoline (HNBrQ), 5-iodo-7-bromo-8-hydroxyquinoline (HIBrQ) and 5-chloro-7-bromo-8-hydroxyquinoline (HClBrQ). Their characterization was performed by IR and NMR spectroscopy, elemental analysis and in the case of HIBrQ and HClBrQ by single crystal X-ray structure analysis. Prepared compounds were used for the synthesis of new palladium(II) complexes NH2(CH3)2[PdCl2(XQ)], where

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Potočňák, Ivan, Miroslava Litecká, Jitka Prachařová, Monika Hreusová, and Jana Kašpárková. "Anticancer gallium(III) complexes with halogen- and nitroderivatives of 8- hydroxyquinoline." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.451p.

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Six gallium(III) complexes with halogen- or nitroderivatives of 8-hydroxyquinoline, [Ga(ClQ)3] (1), [Ga(BrQ)3] (2), [Ga(dIQ)3] (3), [Ga(CQ)3] (4), [Ga(NQ)3] (5) and [Ga(ClNQ)3]·MeOH were prepared as possible anticancer drugs (HClQ = 5-chloro-8-hydroxyquinoline, HBrQ = 7-bromo-8-roxyquinoline, HdIQ = 5,7-diiodo-8-hydroxyquinoline, HCQ = 5-chloro-7-iodo-8-ydroxyquinoline, HNQ = 5-nitro-8-hydroxyquinoline and HClNQ = 5-chloro-7-nitro-8-hydroxyquinoline). X-ray single crystal structure analysis of [Ga(ClQ)3]·MeOH (1 – MeOH) and 5 showed that both complexes are molecular complexes with Ga(III) coor

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Roy, V. Arul Lenus, Chung Yin Kwong, Aleksandra B. Djurisic, Ramachandra B. Pode, T. K. Gundu Rao, and Wai Kin Chan. "Improvement in the environmental stability of tris(8-hydroxyquinoline) aluminum by substitution of sulphonic acid in 8-hydroxyquinoline ligand." In Optical Science and Technology, SPIE's 48th Annual Meeting, edited by Zakya H. Kafafi and Paul A. Lane. SPIE, 2004. http://dx.doi.org/10.1117/12.503009.

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Djurisic, Aleksandra B., Chung Yin Kwong, Weiling Guo, et al. "Optical funtions of tris (8-hydroxyquinoline) aluminum (Alq3)." In Symposium on Integrated Optoelectronic Devices, edited by Bernard Kippelen and Donal D. C. Bradley. SPIE, 2002. http://dx.doi.org/10.1117/12.470447.

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Derkowska-Zielinska, Beata. "Nonlinear optical properties of tris-(8-hydroxyquinoline)-aluminum." In 2016 18th International Conference on Transparent Optical Networks (ICTON). IEEE, 2016. http://dx.doi.org/10.1109/icton.2016.7550426.

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Petit, S., G. Coquerel, J. Langlet, and E. Kassab. "Theoretical study of intramolecular proton transfer in 8-hydroxyquinoline." In The first European conference on computational chemistry (E.C.C.C.1). AIP, 1995. http://dx.doi.org/10.1063/1.47682.

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Lougdali, M., A. Korcala, P. Plociennik, et al. "Physical Properties of Bis-(8-hydroxyquinoline) Magnesium Thin Films." In 2019 21st International Conference on Transparent Optical Networks (ICTON). IEEE, 2019. http://dx.doi.org/10.1109/icton.2019.8840182.

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Jampilek, Josef, Jiri Kos, Petra Machalova, et al. "Preparation and Herbicidal Activity of Halogenated 8-Hydroxyquinoline-2-carboxanilides." In The 17th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-b013.

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Reports on the topic "8-hydroxyquinoline"

1

Yang, Zhaoxia, Jerald S. Bradshaw, Paul B. Savage, Krzysztof E. Krakowiak, and Reed M. Izatt. Synthesis of Tetraazacrown Ethers Containing Two 8-Hydroxyquinoline Side Arms. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada361693.

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Song, H. C., J. S. Bradshaw, Y. W. Chen, G. P. Xue, and J. A. Chiara. Syntheses of Diazadithiacrown Ethers Containing Two 8-Hydroxyquinoline Side Arms. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada389900.

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Su, Ning, Jerald S. Bradshaw, Paul B. Savage, Guoping Xue, Krzysztof E. Krakowiak, and Reed M. Izaft. Synthesis of Novel 8-Hydroxyquinoline-Containing Diaz-18-Crown-6 Ligands and Analogues. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada370492.

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Zhang, Xian X., Jerald S. Bradshaw, R. T. Bronson, Paul B. Savage, and Reed M. Izatt. Preliminary Complexation Studies of Bis-(8-Hydroxyquinoline)-substituted Tetraaza-15-crown-5 with Various Metal Ions. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada361705.

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Bronson, R. T., Jerald S. Bradshaw, Paul B. Savage, Krzysztof E. Krakowiak, and Reed M. Izatt. Synthesis of Bis-8-Hydroxyquinoline-Armed Diazatrithia-15-Crown-5 and Diazatrithia-16-Crown-5 Ligands. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada389716.

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Bronson, R. T., Jerald S. Bradshaw, Paul B. Savage, Saowarux Fuangswasdi, and Sang C. Lee. Photophysical Properties of Bis-8-Hydroxyquinoline-Armed Diazatrithia-15-Crown-5 and Diazatrithia-16-Crown-5 Ligands. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada389688.

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Kawakami, J., R. T. Bronson, G. Xue, J. S. Bradshaw, and R. M. Izatt. Characterization of Bis-8-hydroxyquinoline-Armed Diazatrithia-16-crown-5 and Diazadibenzo-18-crown-6 Ligands as Fluorescent Chemosensors for Zinc. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada406097.

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