Gotowe bibliografie tematyczne / Amides

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Gotowa bibliografia na temat „Amides”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 25 lipca 2025

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Artykuły w czasopismach na temat "Amides"

Barham, Joshua P., та Jaspreet Kaur. "Site-Selective C(sp3)–H Functionalizations Mediated by Hydrogen Atom Transfer Reactions via α-Amino/α-Amido Radicals". Synthesis 54, № 06 (2021): 1461–77. http://dx.doi.org/10.1055/a-1677-6619.

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AbstractAmines and amides, as N-containing compounds, are ubiquitous in pharmaceutically-active scaffolds, natural products, agrochemicals, and peptides. Amides in nature bear a key responsibility for imparting three-dimensional structure, such as in proteins. Structural modifications to amines and amides, especially at their positions α to N, bring about profound changes in biological activity oftentimes leading to more desirable pharmacological profiles of small drug molecules. A number of recent developments in synthetic methodology for the functionalizations of amines and amides omit the n

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Zhou, Yongyun, Ruhima Khan, Baomin Fan, and Lijin Xu. "Ruthenium-Catalyzed Selective Reduction of Carboxylic Esters and Carboxamides." Synthesis 51, no. 12 (2019): 2491–505. http://dx.doi.org/10.1055/s-0037-1611524.

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Amines and alcohols are important classes of building blocks in organic synthesis. The synthesis of these compounds has been a topic of interest. A straightforward method for their synthesis is the reduction of esters and amides to alcohols and amines, respectively. Various transition-metal catalysts have been developed for the homogeneous hydrogenation of esters and amides to alcohols and amines. In this review, an overview of the ruthenium-catalyzed selective hydrogenation of esters and amides is provided.1 General Introduction2 Ru-Catalyzed Reduction of Esters3 Ru-Catalyzed Selective Reduct

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Zarecki, Adam P., Jacek L. Kolanowski, and Wojciech T. Markiewicz. "Microwave-Assisted Catalytic Method for a Green Synthesis of Amides Directly from Amines and Carboxylic Acids." Molecules 25, no. 8 (2020): 1761. http://dx.doi.org/10.3390/molecules25081761.

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Amide bonds are among the most interesting and abundant molecules of life and products of the chemical pharmaceutical industry. In this work, we describe a method of the direct synthesis of amides from carboxylic acids and amines under solvent-free conditions using minute quantities of ceric ammonium nitrate (CAN) as a catalyst. The reactions are carried out in an open microwave reactor and allow the corresponding amides to be obtained in a fast and effective manner when compared to other procedures of the direct synthesis of amides from acids and amines reported so far in the literature. The

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Orsy, György, Sayeh Shahmohammadi, and Enikő Forró. "A Sustainable Green Enzymatic Method for Amide Bond Formation." Molecules 28, no. 15 (2023): 5706. http://dx.doi.org/10.3390/molecules28155706.

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A sustainable enzymatic strategy for the preparation of amides by using Candida antarctica lipase B as the biocatalyst and cyclopentyl methyl ether as a green and safe solvent was devised. The method is simple and efficient and it produces amides with excellent conversions and yields without the need for intensive purification steps. The scope of the reaction was extended to the preparation of 28 diverse amides using four different free carboxylic acids and seven primary and secondary amines, including cyclic amines. This enzymatic methodology has the potential to become a green and industrial

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Khalimon, Andrey, Kristina Gudun, and Davit Hayrapetyan. "Base Metal Catalysts for Deoxygenative Reduction of Amides to Amines." Catalysts 9, no. 6 (2019): 490. http://dx.doi.org/10.3390/catal9060490.

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The development of efficient methodologies for production of amines attracts significant attention from synthetic chemists, because amines serve as essential building blocks in the synthesis of many pharmaceuticals, natural products, and agrochemicals. In this regard, deoxygenative reduction of amides to amines by means of transition-metal-catalyzed hydrogenation, hydrosilylation, and hydroboration reactions represents an attractive alternative to conventional wasteful techniques based on stoichiometric reductions of the corresponding amides and imines, and reductive amination of aldehydes wit

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Ding, Wen, Shaoyu Mai, and Qiuling Song. "Molecular-oxygen-promoted Cu-catalyzed oxidative direct amidation of nonactivated carboxylic acids with azoles." Beilstein Journal of Organic Chemistry 11 (November 11, 2015): 2158–65. http://dx.doi.org/10.3762/bjoc.11.233.

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A copper-catalyzed oxidative direct formation of amides from nonactivated carboxylic acids and azoles with dioxygen as an activating reagent is reported. The azole amides were produced in good to excellent yields with a broad substrate scope. The mechanistic studies reveal that oxygen plays an essential role in the success of the amidation reactions with copper peroxycarboxylate as the key intermediate. Transamidation occurs smoothly between azole amide and a variety of amines.

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Meerakrishna, Ramakrishnan Suseela, and Ponnusamy Shanmugam. "Synthesis of blue-red emissive amido-substituted di(het)aryl and tri(het)aryl amine derivatives via chemoselective N-mono and N,N-diarylation of (het) aryl amino amides using benzyne/arynes." New Journal of Chemistry 43, no. 6 (2019): 2550–58. http://dx.doi.org/10.1039/c8nj05823g.

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Chemoselective synthesis of amide-substituted triaryl and diaryl amines by N-mono and N,N-diarylation of (het)aryl amino amides using arynes has been reported. Selected triarylamines showed blue-red emission.

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Krieck, Sven, Philipp Schüler, Jan Peschel, and Matthias Westerhausen. "Straightforward One-Pot Syntheses of Silylamides of Magnesium and Calcium via an In Situ Grignard Metalation Method." Synthesis 51, no. 05 (2018): 1115–22. http://dx.doi.org/10.1055/s-0037-1610407.

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Calcium bis[bis(trimethylsilyl)amide] (Ca(HMDS)2) is a widely used reagent in diverse stoichiometric and catalytic applications. These processes necessitate a straightforward and large-scale access of this complex. Calcium does not react with primary and secondary amines, but the addition of excess bromoethane to a mixture of calcium turnings and amines in THF at room temperature yields the corresponding calcium bis(amides), calcium bromide and ethane. This in situ Grignard metalation method (iGMM) allows the preparation of calcium bis(amides) from secondary and primary trialkylsilyl-substitut

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Mohd Shah, Nursyahmira Farhana, Nur Zulaikha Adriana Shahrulnizam, Asiah Nusaibah Masri, Nik Nor Aznizam Nik Norizam, and Izni Mariah Ibrahim. "Effect of Temperatures on Green Synthesis of Amide-based Corrosion Inhibitors from Sustainable Source." Journal of Advanced Research in Fluid Mechanics and Thermal Sciences 125, no. 2 (2024): 120–28. https://doi.org/10.37934/arfmts.125.2.120128.

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This research addresses the critical need for effective anticorrosion solutions, focusing on the development of environmentally friendly coatings using Palm Fatty Acid Distillate (PFAD), a byproduct of crude palm oil production, as a key component in amide inhibitors. Traditional inorganic corrosion inhibitors pose environmental and economic concern due to their expense and toxicity while PFAD based amides promote a sustainable and cost-effective alternative. The synthesis of PFAD based amides using ethylenediamine in ethanol at reflux at various temperatures (25, 40, 60 and 90˚C) revealed tha

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Yao, Lei, Ming-Yi Wang, Xin-Ke Wang, et al. "Detection of atmospheric gaseous amines and amides by a high-resolution time-of-flight chemical ionization mass spectrometer with protonated ethanol reagent ions." Atmospheric Chemistry and Physics 16, no. 22 (2016): 14527–43. http://dx.doi.org/10.5194/acp-16-14527-2016.

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Abstract. Amines and amides are important atmospheric organic-nitrogen compounds but high time resolution, highly sensitive, and simultaneous ambient measurements of these species are rather sparse. Here, we present the development of a high-resolution time-of-flight chemical ionization mass spectrometer (HR-ToF-CIMS) method, utilizing protonated ethanol as reagent ions to simultaneously detect atmospheric gaseous amines (C1 to C6) and amides (C1 to C6). This method possesses sensitivities of 5.6–19.4 Hz pptv−1 for amines and 3.8–38.0 Hz pptv−1 for amides under total reagent ion signals of ∼ 0

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Rozprawy doktorskie na temat "Amides"

Kargina, Irina. "Topochemical reactions of amines and amides with titanium and vanadium oxychlorides." Thesis, University of Ottawa (Canada), 1995. http://hdl.handle.net/10393/10109.

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The intercalation of primary, secondary, tertiary, and aromatic amines into layered TiOCl have been investigated by a variety of methods. The intercalation reaction does not appear to be a redox process. A key step for intercalation of amines into host TiOCl is proposed to be a coordination via nitrogen lone electron pair to Ti$\sp{3+}$ metal centres. Subsequent substitution of the interlayer chloride ions of TiOCl by the amine molecules is strongly dependent on the properties of the organic compounds and their ability to form ammonium salts. Based on X-ray diffraction, fluorescence, elemental

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Rofouei, Mohammad Kazem. "The preparation, characterisation and reactivity of derivatives of a novel sterically demanding amido ligand." Thesis, University of Sussex, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.361401.

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Li, Haiying. "A study on grafting poly(p-phenylene terephthalamide) with aliphatic amines and amides." Thesis, Georgia Institute of Technology, 1999. http://hdl.handle.net/1853/8594.

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Muller, Catherine R. "Lithium amides in synthesis." Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.413176.

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Richardson, J. "Corrosion inhibition with amides." Thesis, University of Nottingham, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.381056.

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Ledingham, Lyndsay A. "Sustainable methods for the chemical synthesis of amides and amide-containing aromatic compounds." Thesis, University of York, 2016. http://etheses.whiterose.ac.uk/16191/.

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Described in this thesis is work based on silica and palladium catalysis which focusses on the formation of amide-containing compounds. Efforts were made towards expanding the substrate scope of direct amide bond formation reactions catalysed by an activated K60 silica catalyst. Two of the resulting amides were then investigated as substrates in single and oxidative C–H functionalisation reactions to form phenanthridin-6(5H)-ones.

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Lauck, Maximilian Thomas Johannes [Verfasser]. "Cobaltocenium Amides - Photoinduced Electron Transfer Processes in Donor-Acceptor Amides / Maximilian Thomas Johannes Lauck." Mainz : Universitätsbibliothek Mainz, 2020. http://d-nb.info/1205943900/34.

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Farrell, Emma K. "Biosynthesis of fatty acid amides." Scholar Commons, 2010. http://scholarcommons.usf.edu/etd/1629.

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Primary fatty acid amides (PFAMs) and N-acylglycines (NAGs) are important signaling molecules in the mammalian nervous system, binding to many drug receptors and demonstrating control over sleep, locomotor activity, angiogenesis, vasodilatation, gap junction communication, and many other processes. Oleamide is the best-studied of the PFAMs, while the in vivo activity of the others is largely unstudied. Even less is known about the NAGs, as their discovery as novel compounds is much more recent due to low endogenous levels. Herein is described extraction and quantification techniques for PFAMs

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Lineswala, Jayana P. "Total synthesis of lavendamycin amides." Virtual Press, 1996. http://liblink.bsu.edu/uhtbin/catkey/1036197.

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The synthesis of 7-N-acetyldemethyllavendamycin butyl amide (47), 7-Nacetyldemethyllavendamycin isopropyl amide (48), 7-N-acetyldemethyllavendamycin amide of piperidine (49), 7-N-acetyldemethyllavendamycin amide of pyrrolidine (50), 7N-acetyldemethyllavendamycin amide of morpholine (51), demethyllavendamycin butyl amide (52), demethyllavendamycin amide of pyrrolidine (53), and demethyllavendamycin amide of morpholine (54) are described. Pictet Spengler condesation of 7-acetamido-2formylquinoline-5,8-dione (28) with tryptophan butyl amide (66), tryptophan isopropyl amide (67), tryptophan amide

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McCarthy, Sean Joseph. "Strained amides as potential antibacterials." Thesis, University of Sussex, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296003.

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Książki na temat "Amides"

Arthur, Greenberg, Breneman Curt M, and Liebman Joel F, eds. The amide linkage: Structural significance in chemistry, biochemistry, and materials science. Wiley-Interscience, 2003.

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Westlund, Neil Edward. Atropisomerism in hindered tertiary amides. University of Manchester, 1996.

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Relihan, Colette. 1-Hydroxy-1-aminoalkenes: Enols of amides. University College Dublin, 1998.

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Hickey, Kenneth. A study of amides in aqueous and non-aqueous solution. University College Dublin, 1995.

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Mazurkiewicz, Roman. Studium reakcji imidoilowania amidów. Politechnika Śląska, 1989.

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Lemmerer, Miran. Chemoselective Nucleophilic α-Amination of Amides. Springer Fachmedien Wiesbaden, 2020. http://dx.doi.org/10.1007/978-3-658-30020-3.

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Pirilä-Honkanen, Päivi. Physicochemical properties of 2-pyrrolidinone and n-methylbenzenesulfonamide in binary solution mixtures. Oulun Yliopisto, 1996.

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Hutchby, Marc. Novel Synthetic Chemistry of Ureas and Amides. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32051-4.

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Bukowska, Jolanta. Spektroskopia oscylacyjna roztworów amidowych. Wydawnictwa Uniwersytetu Warszawskiego, 1986.

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Kolev, Tsonko. Quantum chemical, spectroscopic and structural study of hydrochlorides, hydrogens squarates and ester amides of squaric acid of amina. Nova Science Publishers, 2008.

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Części książek na temat "Amides"

Paulus, Wilfried. "Amides." In Microbicides for the Protection of Materials. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2118-7_10.

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Gooch, Jan W. "Amides." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_546.

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Paulus, Wilfried. "Amides." In Directory of Microbicides for the Protection of Materials. Springer Netherlands, 2004. http://dx.doi.org/10.1007/1-4020-2818-0_33.

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Smith, Robert M., and Arthur E. Martell. "Amides." In Critical Stability Constants. Springer US, 1989. http://dx.doi.org/10.1007/978-1-4615-6764-6_23.

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Sonke, Theo, and Bernard Kaptein. "Hydrolysis of Amides." In Enzyme Catalysis in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639861.ch15.

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Lappert, M. F. "From Organotin Amides." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145234.ch139.

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Lappert, M. F. "From Organolead Amides." In Inorganic Reactions and Methods. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145234.ch160.

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Carmalt, Claire J., Neville A. Compton, R. John Errington, et al. "Homoleptic Bismuth Amides." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132623.ch15.

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Ouellette, Robert J., and J. David Rawn. "Amines and Amides." In Organic Chemistry. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-12-812838-1.50024-4.

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Ouellette, Robert J., and J. David Rawn. "Amines and Amides." In Principles of Organic Chemistry. Elsevier, 2015. http://dx.doi.org/10.1016/b978-0-12-802444-7.00012-4.

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Streszczenia konferencji na temat "Amides"

Wu, Jing, Shelley Zhou, and Jeremy Moloney. "A Study of Ethoxylated Amide as an Intermediate for Corrosion Inhibition." In CONFERENCE 2025. AMPP, 2025. https://doi.org/10.5006/c2025-00136.

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Abstract Amide is a common intermediate used in the formulation of corrosion inhibitors for various applications in oil and gas production fields. In many cases, due to its oil solubility nature of the amide, it is often used to form a film on metal surfaces to mitigate corrosion. In this work, ethoxylated amides with varying moles of Ethylene Oxide (EO) were synthesized to study the impact of ethoxylation on water solubility, water partitioning as well as corrosion inhibition performance under specific test conditions. The laboratory test results showed an improvement on water solubility and

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Jovancicevic, V., S. Ramachandran, and P. Prince. "Inhibition of CO2 Corrosion of Mild Steel by Imidazolines and Their Precursors." In CORROSION 1998. NACE International, 1998. https://doi.org/10.5006/c1998-98018.

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Abstract A study of the mechanism of corrosion inhibition of mild steel by imidazolines and their precursors in a CO2 containing environment is carried out using Rotating Cylinder Electrode (RCE) and Linear Polarization Resistance (LPR) technique. Corrosion rate-time/concentration profiles (LPR) and minimum effective concentrations (MEC) obtained for a series of imidazolines and amides are discussed in terms of the respective contributions of their constituent parts (imidazoline ring, amide/amine group, hydrocarbon chain) to the overall corrosion inhibition. The formation of the inhibitor film

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Matherly, Ron M., Jian Jiao, David J. Blumer, and Jeffery S. Ryman. "Determination of Imidazoline and Amido-Amine Type Corrosion Inhibitors in Both Crude Oil and Produced Brine from Oilfield Production." In CORROSION 1995. NACE International, 1995. https://doi.org/10.5006/c1995-95543.

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Abstract The classical method for the determination of corrosion inhibitors in oilfield brines is the dye transfer method. Within this method are many variations which the analyst may use to determine the amount of corrosion inhibitor in either water or crude oil. These methods, however, suffer from many interferences which result in both false positive and negatives for corrosion inhibitor content. These methods essentially detect all amines as corrosion inhibitors. Improved high pressure liquid chromatography (HPLC) methods have been developed for the analysis of quaternary salt type corrosi

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Miksic, Boris M., Alla Y. Furman, and Margarita A. Kharshan. "Effectiveness of the Corrosion Inhibitors for the Petroleum Industry under Various Flow Conditions." In CORROSION 2009. NACE International, 2009. https://doi.org/10.5006/c2009-09573.

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Abstract Several types of corrosion inhibitors were evaluated. Active ingredients of those inhibitors included long chain amines, fatty amides, imidazolines, fatty acids and their salts. Inhibitors were tested at the concentration range of 50 - 200 ppm in the electrolyte and electrolyte/hydrocarbon mixture in the presence of CO2 and H2S in static and dynamic conditions. Several evaluations were performed when corrosion inhibitors were added into electrolyte containing flow modifiers. The results, which include the corrosion and electrochemical testing data, show that generally tested corrosion

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Groysman, Alec, Joseph Penner, Liran Mizrahi, and Naphtali Brodsky. "Examination of a "Green" Corrosion Inhibitor and Corrosion Resistant Alloys for the Overhead of the Crude Oil Distillation Unit." In CORROSION 2013. NACE International, 2013. https://doi.org/10.5006/c2013-02134.

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Abstract The aim of this work is to examine a new "green" corrosion inhibitor and nine different alloys for use in the overhead of the crude oil distillation unit. Ammonia, organic amines, amides, and imidazolines are injected in the overhead. In order to avoid using unfriendly ammonia, a new "green" corrosion inhibitor was examined in a model aggressive solution (pH=3.2) during a distillation procedure under laboratory conditions and showed 87-93% efficiency at concentrations of 30-40 ppm. This new inhibitor was compared with two commercial inhibitor systems, and revealed similar efficiency,

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Cao, Fang, Shuji Luo, Anthony Mennito, et al. "A Mechanistic Study of Corrosion Inhibitor Partitioning and Performance in Sweet Corrosion Environments." In CORROSION 2017. NACE International, 2017. https://doi.org/10.5006/c2017-09399.

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Abstract Nitrogen containing surfactants (e.g. amines, amides, imidazolines, and quaternary ammonium salts) have been commonly used as active corrosion inhibitors in commercial corrosion inhibitor (CI) packages for many years to control corrosion of carbon steel pipelines in the oil and gas industry. However, in the literature, not many systematic studies have been done to compare the partitioning behavior and corrosion performance of nitrogen-based CIs with different functional groups, and their inhibition mechanisms are currently not fully understood. In this study, nitrogen-based model CI c

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Son, Adelina J., and Jayant Chakravarty. "Analysis of Residual Corrosion Inhibitors by Fluorescence and Ultraviolet Spectrophotometry." In CORROSION 1996. NACE International, 1996. https://doi.org/10.5006/c1996-96344.

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Abstract The paper describes the development of a fully automated instrumental procedure for testing residual corrosion inhibitors in production waters in the field. Initial investigations were conducted in the laboratory to evaluate the suitability of ultraviolet and fluorescence spectrophotometric techniques to different types of corrosion inhibitors. Parameters for comparison included selectivity, sensitivity, speed, accuracy and precision of the methods under flowing conditions as in high performance liquid chromatography and static conditions as encountered in stand alone instruments. For

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Abdullayeva, E. H., L. I. Aliyeva, and Garry Keilty. "Suppression of SRB Growth by Biocides on the Base of Amino-Alcohols." In CORROSION 2010. NACE International, 2010. https://doi.org/10.5006/c2010-10259.

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Abstract Corrosion destroying of equipment manifests itself in a later stage during exploration of oil fields, when extracted oil is watered and properties of separating stratal water, during extraction, collection and preparation of oil, significantly change, particularly increases in sulfate reducing bacteria (SRB) and concentrations of corrosion aggressive gas products from their activity – hydrogen sulfide. As we know, most corrosion inhibitors and biocides which are applied in oil-gas extraction, consist of nitrogen containing substances, as amino alcohols, imidozolines, amides, etc. The

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Soriaga, Manuel P., G. M. Berry, C. Bhardwaj, et al. "Chemisorption of Organic Molecules on Metal Electrode Surfaces." In CORROSION 1990. NACE International, 1990. https://doi.org/10.5006/c1990-90300.

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Abstract The chemisorption of various organic functional groups from aqueous solutions onto smooth single-crystal and polycrystalline electrodes, and the resistance of the resulting monolayer intermediates towards electrochemical oxidation have been studied; these investigations were motivated by the need to understand, at the atomic level, metal passivation by monolayer organic coatings. The electrodes employed were Rh, Pd, Ir, Pt, and Au whose anodic dissolution is preceded by surface-oxide formation even in highly acidic media. Resistance towards anodic oxidation can thus be associated with

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Tomoe, Y., M. Shimizu, and H. Kaneta. "Active Dissolution and Natural Passivation of Carbon Steel in Carbon Dioxide-Loaded Alkanolamine Solutions." In CORROSION 1996. NACE International, 1996. https://doi.org/10.5006/c1996-96395.

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Abstract Corrosion rates of carbon steel specimens were measured in carbon dioxide(CO2)-loaded alkanolamine(amine) solutions by weight-loss tests and by the polarization resistance method. In dilute amine solutions, lower than 10[[illegible]] M, corrosion rates were controlled by the formation of protective FeCO3 scale as in hot, CO2 -H2O environments. Tested amines inhibited CO2 induced corrosion in the concentration range between 10-2 and 2M. In concentrated amine solutions, higher than 3M, primary and tertiary amines showed markedly different effects on carbon steel corrosion. The corrosion

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Raporty organizacyjne na temat "Amides"

Jiang, Zhiping, Leonard V. Interrante, Daekeun Kwon, Fook S. Tham, and Rudy Kullnig. Synthesis, Structure and Pyrolysis of Organoaluminum Amides Derived from the Reaction of Trialkylaluminum Compounds with Ethylenediamine in a 3:2 Ration. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada225758.

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Castner, E. W. Temperature-dependence of the ultrafast intermolecular dynamics of Amides: Formamide, N-methylformamide, N,N-dimethylformamide, N- methylacetamide, and N-methylpropionamide from 290-370 K. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/249036.

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Lin, Terri C. Poly(amido amine) Dendrimers in Supercapacitors. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1091321.

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Fernando, P. U. Ashvin Iresh, Gilbert Kosgei, Matthew Glasscott, Garrett George, Erik Alberts, and Lee Moores. Boronic acid functionalized ferrocene derivatives towards fluoride sensing. Engineer Research and Development Center (U.S.), 2022. http://dx.doi.org/10.21079/11681/44762.

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Streszczenie:

In this technical report (TR), a robust, readily synthesized molecule with a ferrocene core appended with one or two boronic acid moieties was designed, synthesized, and used toward F- (free fluoride) detection. Through Lewis acid-base interactions, the boronic acid derivatives are capable of binding with F- in an aqueous solution via ligand exchange reaction and is specific to fluoride ion. Fluoride binding to ferrocene causes significant changes in fluorescence or electrochemical responses that can be monitored with field-portable instrumentation at concentrations below the WHO recommended l

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Selig, W. Determination of equivalent weight of amines. Office of Scientific and Technical Information (OSTI), 1987. http://dx.doi.org/10.2172/6881693.

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Whitaker, Craig, Jay R. Heckert, and Ian C. Uber. Synthesis of Amide Functionalized Carbon Nanotubes. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada519137.

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Thomson, J. S., J. B. Green, T. B. McWilliams, and S. K. T. Yu. GC/MS determination of amines following exhaustive trifluoroacetylation. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10180988.

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Hameka, Hendrik F., George R. Famini, James O. Jensen, and E. I. Newhouse. Computations of Vibrational Infrared Frequencies of Selected Amines. Defense Technical Information Center, 1990. http://dx.doi.org/10.21236/ada218840.

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Mossine, Valerie V. Multivalent Lactulose-amines as Inhibitors of Prostate Cancer Metastasis. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada406249.

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Hameka, H. F., G. R. Famini, J. O. Jensen, and J. L. Jensen. Theoretical Prediction of Vibrational Infrared Frequencies of Tertiary Amines. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada232880.

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