Relevant bibliographies by topics / Anions (Chemistry)

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Anions (Chemistry)'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 September 2023

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Journal articles on the topic "Anions (Chemistry)"

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Černý, Radovan, Matteo Brighi, and Fabrizio Murgia. "The Crystal Chemistry of Inorganic Hydroborates." Chemistry 2, no. 4 (September 29, 2020): 805–26. http://dx.doi.org/10.3390/chemistry2040053.

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The crystal structures of inorganic hydroborates (salts and coordination compounds with anions containing hydrogen bonded to boron) except for the simplest anion, borohydride BH4−, are analyzed regarding their structural prototypes found in the inorganic databases such as Pearson’s Crystal Data [Villars and Cenzual (2015), Pearson’s Crystal Data. Crystal Structure Database for Inorganic Compounds, Release 2019/2020, ASM International, Materials Park, Ohio, USA]. Only the compounds with hydroborate as the only type of anion are reviewed, although including compounds gathering more than one different hydroborate (mixed anion). Carbaborane anions and partly halogenated hydroborates are included. Hydroborates containing anions other than hydroborate or neutral molecules such as NH3 are not discussed. The coordination polyhedra around the cations, including complex cations, and the hydroborate anions are determined and constitute the basis of the structural systematics underlying hydroborates chemistry in various variants of anionic packing. The latter is determined from anion–anion coordination with the help of topology analysis using the program TOPOS [Blatov (2006), IUCr CompComm. Newsl. 7, 4–38]. The Pauling rules for ionic crystals apply only to smaller cations with the observed coordination number within 2–4. For bigger cations, the predictive power of the first Pauling rule is very poor. All non-molecular hydroborate crystal structures can be derived by simple deformation of the close-packed anionic lattices, i.e., cubic close packing (ccp) and hexagonal close packing (hcp), or body-centered cubic (bcc), by filling tetrahedral or octahedral sites. This review on the crystal chemistry of hydroborates is a contribution that should serve as a roadmap for materials engineers to design new materials, synthetic chemists in their search for promising compounds to be prepared, and materials scientists in understanding the properties of novel materials.
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Rashid, Ambreen, Sahidul Mondal, and Pradyut Ghosh. "Development and Application of Ruthenium(II) and Iridium(III) Based Complexes for Anion Sensing." Molecules 28, no. 3 (January 27, 2023): 1231. http://dx.doi.org/10.3390/molecules28031231.

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Improvements in the design of receptors for the detection and quantification of anions are desirable and ongoing in the field of anion chemistry, and remarkable progress has been made in this direction. In this regard, the development of luminescent chemosensors for sensing anions is an imperative and demanding sub-area in supramolecular chemistry. This decade, in particular, witnessed advancements in chemosensors based on ruthenium and iridium complexes for anion sensing by virtue of their modular synthesis and rich chemical and photophysical properties, such as visible excitation wavelength, high quantum efficiency, high luminescence intensity, long lifetimes of phosphorescence, and large Stokes shifts, etc. Thus, this review aims to summarize the recent advances in the development of ruthenium(II) and iridium(III)-based complexes for their application as luminescent chemosensors for anion sensing. In addition, the focus was devoted to designing aspects of polypyridyl complexes of these two transition metals with different recognition motifs, which upon interacting with different inorganic anions, produces desirable quantifiable outputs.
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Helal, Aasif, Mohd Yusuf Khan, Abuzar Khan, Muhammad Usman, and Md Hasan Zahir. "Reticular Chemistry for Optical Sensing of Anions." International Journal of Molecular Sciences 24, no. 17 (August 22, 2023): 13045. http://dx.doi.org/10.3390/ijms241713045.

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In the last few decades, reticular chemistry has grown significantly as a field of porous crystalline molecular materials. Scientists have attempted to create the ideal platform for analyzing distinct anions based on optical sensing techniques (chromogenic and fluorogenic) by assembling different metal-containing units with suitable organic linking molecules and different organic molecules to produce crystalline porous materials. This study presents novel platforms for anion recognition based on reticular chemistry with high selectivity, sensitivity, electronic tunability, structural recognition, strong emission, and thermal and chemical stability. The key materials for reticular chemistry, Metal-Organic Frameworks (MOFs), Zeolitic Imidazolate Frameworks (ZIFs), and Covalent-Organic Frameworks (COFs), and the pre- and post-synthetic modification of the linkers and the metal oxide clusters for the selective detection of the anions, have been discussed. The mechanisms involved in sensing are also discussed.
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Basappa, Suma, Ramesh Bhawar, D. H. Nagaraju, and Shubhankar Kumar Bose. "Recent advances in the chemistry of the phosphaethynolate and arsaethynolate anions." Dalton Transactions 51, no. 10 (2022): 3778–806. http://dx.doi.org/10.1039/d1dt03994f.

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Davis, Jeffery T., Philip A. Gale, and Roberto Quesada. "Advances in anion transport and supramolecular medicinal chemistry." Chemical Society Reviews 49, no. 16 (2020): 6056–86. http://dx.doi.org/10.1039/c9cs00662a.

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The development of discrete molecular carriers for anions and supramolecular anion channels are reviewed followed by an overview of the use of these systems in biological systems as putative treatments for diseases such as cystic fibrosis and cancer.
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Flood, Amar H. "Creating molecular macrocycles for anion recognition." Beilstein Journal of Organic Chemistry 12 (March 31, 2016): 611–27. http://dx.doi.org/10.3762/bjoc.12.60.

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The creation and functionality of new classes of macrocycles that are shape persistent and can bind anions is described. The genesis of triazolophane macrocycles emerges out of activity surrounding 1,2,3-triazoles made using click chemistry; and the same triazoles are responsible for anion capture. Mistakes made and lessons learnt in anion recognition provide deeper understanding that, together with theory, now provides for computer-aided receptor design. The lessons are acted upon in the creation of two new macrocycles. First, cyanostars are larger and like to capture large anions. Second is tricarb, which also favors large anions but shows a propensity to self-assemble in an orderly and stable manner, laying a foundation for future designs of hierarchical nanostructures.
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Dye, J. L. "CHEMISTRY: Electrons as Anions." Science 301, no. 5633 (August 1, 2003): 607–8. http://dx.doi.org/10.1126/science.1088103.

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Zhu, Xiaotian, Chang Liu, and Jie Liu. "Colorimetric Detection of Sulfide Anions via Redox-Modulated Surface Chemistry and Morphology of Au-Hg Nanorods." International Journal of Analytical Chemistry 2019 (May 2, 2019): 1–9. http://dx.doi.org/10.1155/2019/8961837.

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A new colorimetric assay for the detection of sulfide anions with high sensitivity and selectivity is reported, utilizing Au-Hg alloy nanorods (Au-HgNRs) as probe. Au-HgNRs were prepared by modifying gold nanorods (AuNRs) with reducing agent and mercury ions. In an aqueous solution with sulfide anions, the formation of mercuric sulfide due to redox reaction between the amalgams and sulfide anions greatly changed the surface chemistry and morphology of the Au-HgNRs, leading to a red shift of the localized surface plasmon resonance (LSPR) absorption peak, accompanied by a change in colorimetric response. A good linear relationship was obtained between the LSPR peak wavelength shift and concentration of sulfide anion in the range of 1 × 10−5−1 × 10−4 mol/L. The selectivity of this method has been investigated by other anions. The colorimetric sensing system successfully detected sulfide in wastewater from leather industry.
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Černý, Radovan, and Pascal Schouwink. "The crystal chemistry of inorganic metal borohydrides and their relation to metal oxides." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 71, no. 6 (December 1, 2015): 619–40. http://dx.doi.org/10.1107/s2052520615018508.

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The crystal structures of inorganic homoleptic metal borohydrides are analysed with respect to their structural prototypes found amongst metal oxides in the inorganic databases such as Pearson's Crystal Data [Villars & Cenzual (2015). Pearson's Crystal Data. Crystal Structure Database for Inorganic Compounds, Release 2014/2015, ASM International, Materials Park, Ohio, USA]. The coordination polyhedra around the cations and the borohydride anion are determined, and constitute the basis of the structural systematics underlying metal borohydride chemistry in various frameworks and variants of ionic packing, including complex anions and the packing of neutral molecules in the crystal. Underlying nets are determined by topology analysis using the program TOPOS [Blatov (2006). IUCr CompComm. Newsl. 7, 4–38]. It is found that the Pauling rules for ionic crystals apply to all non-molecular borohydride crystal structures, and that the latter can often be derived by simple deformation of the close-packed anionic lattices c.c.p. and h.c.p., by partially removing anions and filling tetrahedral or octahedral sites. The deviation from an ideal close packing is facilitated in metal borohydrides with respect to the oxide due to geometrical and electronic considerations of the BH4 − anion (tetrahedral shape, polarizability). This review on crystal chemistry of borohydrides and their similarity to oxides is a contribution which should serve materials engineers as a roadmap to design new materials, synthetic chemists in their search for promising compounds to be prepared, and materials scientists in understanding the properties of novel materials.
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Jolliffe, Katrina (Kate) A., and Philip A. Gale. "The supramolecular chemistry of anions." Organic & Biomolecular Chemistry 20, no. 4 (2022): 713–14. http://dx.doi.org/10.1039/d1ob90183d.

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Dissertations / Theses on the topic "Anions (Chemistry)"

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Greenhall, Martin Paul. "Fluorinated anions." Thesis, Durham University, 1989. http://etheses.dur.ac.uk/6503/.

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Each of my four main areas of work is concerned with the formation and further reactions of organic fluorinated anions. a) We have investigated the fluoride ion induced reactions of 2H-pentafluoropropene with some perfluoro-aromatic compounds, forming a series of aryl substituted carbon acids and their corresponding carbanions. Also included is a study of an unusual product that was formed with pentafluoronitrobenzene as the aromatic substrate. b) Some fluorinated dienes have been generated from the fluoride ion induced reactions of dimethylacetylenedicarboxylate with a series of cyclic fluorinated alkenes. With perfluorocyclohexene, a variable temperature n.m.r. investigation indicated that one of the products was fluxional at room temperature. Products derived from, perfluorocyclopentene were then further reacted with mono- and bi-functional nucleophiles forming some new products including some interesting polycyclic compounds. c) We have studied the fluoride ion induced reactions of malononitrile and phenylsulphonylacetonitrile with a range of polyfluorinated aromatic and heteroaromatic systems. This study has yielded a series of stable fluorinated organic caesium salts which could be crystallised. Acidification of these salts yielded a series of conjugate acids and some acidity measurements were made. Analysis of n.m.r. data has shed some light on the n.m.r. consequences of tautomerisation which was observed in some of the conjugate acids. A highly unusual carbon-13 n.m.r. concentration effect was studied for several pyrimidyl salts in perdeuteroacetone solution. d) The reaction of bifunctional carbon acids with fluorinated dienes has been used to develop a route to new pentadienyl anions, cyclopentadienes, and cyclopentadienyl anions. FAB mass spectroscopy has proved to be an important tool in the study of our anionic species. Some unusual thermal isomerisation behaviour of the new cyclopentadienes has also been observed and investigated.
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Kawachi, Atsushi. "The Chemistry of Functionalized Silyl Anions." Kyoto University, 1995. http://hdl.handle.net/2433/77813.

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Morris, Daniel S. "Redox chemistry of perrhenate and other anions." Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/31480.

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This thesis discusses reduction and oxidation reactions catalysed by the perrhenate anion and oxidation reactions catalysed by other oxo-anions i.e. sulfate and nitrate. Chapter one introduces catalytic hydrosilylation, hydroboration, deoxydehydration and alkene epoxidation and some of their applications, with a focus on high oxidation state complexes. Chapter two describes the synthesis of a salt of perrhenate [N(hexyl)4][ReO4] which is highly soluble in organic solvents. The use of this salt as a catalyst for both the hydrosilylation and hydroboration of carbonyl compounds and carbon dioxide is discussed. Catalytic methylation of amines and anilines with carbon dioxide and hydrosilanes is also reported. Labelled carbon dioxide reactions and DFT calculations are conducted in order to understand the mechanism of carbon dioxide reduction using hydrosilanes. Chapter three outlines the synthesis of a number of alkylammonium and pyridinium perrhenate salts and their application in the deoxydehydration reaction, converting vicinal diols to alkenes. The role of the counterion is discussed with pyridinium perrhenates shown to be more effective catalysts. DFT calculations are conducted to identify the most likely pathway of the catalytic cycle. Alternative reducing agents to the triphenylphosphine initially used are also studied. Chapter four reports results of organic salts of perrhenate, sulfate and nitrate as oxidation catalysts, specifically their ability to catalyse epoxidations of alkenes. By the formation of supramolecular ion pairs (SIPs), these anions are made organic soluble which is found to significantly enhance their catalytic ability, however, the organic counterions used to form these SIPs were found to be of importance. Ionic liquids are also used for the epoxidation of alkenes. Solution studies are presented to further understanding of how these compounds interact with one another in solution. Chapter five contains experimental conditions and characterisation for compounds discussed in this work.
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Buck, J. "Vinyl anions in synthesis." Thesis, University of Nottingham, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.353565.

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Downard, Kevin M. "Gas phase chemistry of organic anions involving isomerisation /." Title page, contents and abstract only, 1991. http://web4.library.adelaide.edu.au/theses/09PH/09phd748.pdf.

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Camiolo, Salvatore. "Anions in supramolecular chemistry : binding, sensing and assembly." Thesis, University of Southampton, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.252044.

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Allasia, Sara. "Dipyrromethane based receptors for anions." Thesis, University of Southampton, 2008. https://eprints.soton.ac.uk/67198/.

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This thesis is principally concerned with the synthesis of a range of dipyrromethane based receptors and their ability to bind anions, in particular carboxylates of amino acid derivatives. Chapter I provides a general introduction to the field of Supramolecular Chemistry and its applications. In this chapter a series of receptors for anions are presented their properties discussed. A particular attention is given to the aromatic heterocycles based receptors and to enantioselective receptors. Chapter II describes the synthesis of a series of acyclic receptors which are the results of subsequent modifications of a simple tweezer, based on a dipyrromethane unit coupled with two butyl amines, previously studied by the group.1 The binding properties with a series of anions are presented and, for the chiral receptors, the binding properties with Nprotected amino acids were investigated. Chapter III describes the synthesis and the binding properties of a series of macrocycles obtained by modifications of the tweezer receptors. The binding properties of the macrocyclic receptors with a series of anions and amino acids are also presented.
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Hiscock, Jennifer R. "Binding anions using simple neutral molecules." Thesis, University of Southampton, 2010. https://eprints.soton.ac.uk/171157/.

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This thesis reports a number of novel neutral, hydrogen bond donating anion receptors and describes their anion coordination properties in both the solution and solid states. A set of ten urea/thiourea linked indole/carbazole groups were found to have high affinities for a variety of oxo-anions in highly competitive DMSO solutions. Of these receptors, the diindolylurea motif was found to be excellent for the binding of dihydrogen phosphate. This group of receptors were found to form 1:1 complexes in solution with various anions but more complex 2:1 and 3:1 receptor:anion complexes were observed in the solid state. Deprotonation of the bound protonated oxo-anion was observed with these 2:1 and 3:1 complexes. The basic diindolylurea motif was then extended by the incorporation of further NH bond donor groups from amide, indole and carbazole functionalities. This group of receptors were found to form 1:1 complexes in both the solution and solid states, with the binding mode dependent of the geometry of the anion. These compounds also showed spontaneous crystallisation with sulfate in as little as 20 minutes. These receptors showed high affinities for the oxo-anions and gave the first examples of solution state deprotonation of bound protonated oxo-anions. A set of three dimensional indole-based receptors was also synthesised, utilising the TREN and pin-wheel scaffolds. These receptors contain between six and fifteen NH bond donor groups that give a range of anion binding modes, some too complex to be defined, that generally show a preference for the oxo-anions. Again, an example of deprotonation of the bound protonated oxo-anion was observed.
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Ogle, Mark Edward. "Spectroscopic studies of [alpha],[omega]-diphenylpolyenyl anions." Diss., Georgia Institute of Technology, 1990. http://hdl.handle.net/1853/30363.

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Timmons, Christopher L. "Fluorocarbon Post-Etch Residue Removal Using Radical Anion Chemistry." Diss., Georgia Institute of Technology, 2004. http://hdl.handle.net/1853/10583.

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During fabrication of integrated circuits, fluorocarbon plasma etching is used to pattern dielectric layers. As a byproduct of the process, a fluorocarbon residue is deposited on exposed surfaces and must be removed for subsequent processing. Conventional fluorocarbon cleaning processes typically include at least one plasma or liquid treatment that is oxidative in nature. Oxidative chemistries, however, cause material degradation to next generation low-dielectric constant (low-k) materials that are currently being implemented into fabrication processes. This work addresses the need for alternative fluorocarbon-residue removal chemistries that are compatible with next generation low-k materials. Radical anion chemistries are known for their ability to defluorinate fluorocarbon materials by a reductive mechanism. Naphthalene radical anion solutions, generated using sodium metal, are used to establish cleaning effectiveness with planar model residue films. The penetration rate of the defluorination reaction into model fluorocarbon film residues is measured and modeled. Because sodium is incompatible with integrated circuit processing, naphthalene radical anions are alternatively generated using electrochemical techniques. Using electrochemically-generated radical anions, residue removal from industrially patterned etch structures is used to evaluate the process cleaning efficiency. Optimization of the radical anion concentration and exposure time is important for effective residue removal. The efficiency of removal also depends on the feature spacing and the electrochemical solvent chosen. The synergistic combination of radical anion defluorination and wetting or swelling of the residue by the solvent is necessary for complete removal. In order to understand the interaction between the solvent and the residue, the surface and interfacial energy are determined using an Owens/Wendt analysis. These studies reveal chemical similarities between specific solvents and the model residue films. This approach can also be used to predict residue or film swelling by interaction with chemically similar solvents.
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Books on the topic "Anions (Chemistry)"

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1956-, Bianchi Antonio, Bowman-James Kristin 1946-, and García-España Enrique, eds. Supramolecular chemistry of anions. New York: Wiley-VCH, 1997.

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A, Gale Philip, and Cho Won-Seob, eds. Anion receptor chemistry. Cambridge: Royal Society of Chemistry, 2006.

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Helmut, Stache, ed. Anionic surfactants: Organic chemistry. New York: Marcel Dekker, 1996.

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Gale, Philip A., W. Dehaen, and E. Alcade. Anion recognition in supramolecular chemistry. Heidelberg: Springer, 2010.

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Dianion chemistry in organic synthesis. Boca Raton: CRC Press, 1994.

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Determination of anions: A guide for the analytical chemist. Berlin: Springer, 1996.

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P, Gulʹti͡a︡ĭ V., ed. Teoreticheskie osnovy khimii organicheskikh anion-radikalov. Moskva: "Nauka", 1990.

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Determination of anions in natural and treated waters. New York: Spon Press, 2002.

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1937-, Cross John, ed. Anionic surfactants: Analytical chemistry. 2nd ed. New York: Marcel Dekker, 1998.

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James, Preer, Edwards Pamela J, and United States. Forest Service. Northeastern Research Station, eds. Geologic and tributary influences on the chemistry of a headwater stream. Radnor, PA: U.S. Dept. of Agriculture, Forest Service, Northeastern Research Station, 1999.

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Book chapters on the topic "Anions (Chemistry)"

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Gale, Philip A. "Anions in Supramolecular Chemistry." In Fundamentals and Applications of Anion Separations, 1–30. Boston, MA: Springer US, 2004. http://dx.doi.org/10.1007/978-1-4419-8973-4_1.

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Stibor, Ivan, and Petra Zlatušková. "Chiral Recognition of Anions." In Topics in Current Chemistry, 31–63. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/b101161.

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Kubik, Stefan. "Receptors for Biologically Relevant Anions." In Anion Coordination Chemistry, 363–464. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527639502.ch7.

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Pope, Michael T. "Polyoxometallate Cluster Anions." In From Simplicity to Complexity in Chemistry — and Beyond, 137–47. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-49368-3_11.

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Liebau, Friedrich. "Crystal Chemical Classification of Silicate Anions." In Structural Chemistry of Silicates, 52–68. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-50076-3_4.

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Rabinovitz, Mordecai, and Yoram Cohen. "NMR Studies of 4nπ-Conjugated Polycyclic Anions." In Advances in Chemistry, 53–72. Washington, DC: American Chemical Society, 1987. http://dx.doi.org/10.1021/ba-1988-0217.ch004.

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Schmidtchen, Franz P. "Artificial Host Molecules for the Sensing of Anions." In Topics in Current Chemistry, 1–29. Berlin, Heidelberg: Springer Berlin Heidelberg, 2005. http://dx.doi.org/10.1007/b101160.

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Lee, Semin, and Amar H. Flood. "Binding Anions in Rigid and Reconfigurable Triazole Receptors." In Topics in Heterocyclic Chemistry, 85–107. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/7081_2011_70.

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Tuck, D. G. "Structures and Properties of HX2 - and HXY- Anions." In Progress in Inorganic Chemistry, 161–94. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470166109.ch2.

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Darensbourg, Marcetta York. "Ion Pairing Effects on Transition Metal Carbonyl Anions." In Progress in Inorganic Chemistry, 221–74. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470166345.ch5.

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Conference papers on the topic "Anions (Chemistry)"

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Pye, Cory. "Computational Chemistry Applied to Solutions: Anions." In Goldschmidt2022. France: European Association of Geochemistry, 2022. http://dx.doi.org/10.46427/gold2022.9429.

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TERANISHI, KATSUNORI. "RED-CHEMILUMINESCENT PROBES FOR DETECTING SUPEROXIDE ANIONS." In Chemistry, Biology and Applications. WORLD SCIENTIFIC, 2007. http://dx.doi.org/10.1142/9789812770196_0038.

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Campo-Cacharrón, Alba, Jesús Rodríguez-Otero, and Enrique Cabaleiro-Lago. "Interaction between anions and naphthalendiimides." In The 14th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00472.

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Carles, S., J. L. Le Garrec, J. C. Guillemin, and L. Biennier. "Chemistry of nitrile anions in the interstellar medium." In INTERNATIONAL CONFERENCE OF COMPUTATIONAL METHODS IN SCIENCES AND ENGINEERING 2015 (ICCMSE 2015). AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4938817.

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Agúndez, Marcelino, José Cernicharo, and Michel Guélin. "The chemistry of molecular anions in circumstellar sources." In PROCEEDINGS OF THE INTERNATIONAL CONFERENCE OF COMPUTATIONAL METHODS IN SCIENCES AND ENGINEERING 2010 (ICCMSE-2010). AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4906694.

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Peña-Gallego, Ángeles, Jesús Rodríguez-Otero, and Enrique Cabaleiro-Lago. "Interaction between anions and substituted molecular bowls." In The 13th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2009. http://dx.doi.org/10.3390/ecsoc-13-00250.

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Carminati, S., L. Del Gaudio, F. Zausa, and M. Brignoli. "How do Anions in Water-Based Muds Affect Shale Stability?" In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 1999. http://dx.doi.org/10.2118/50712-ms.

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Barthorpe, R. T. "The Impairment of Scale Inhibitor Function by Commonly Used Organic Anions." In SPE International Symposium on Oilfield Chemistry. Society of Petroleum Engineers, 1993. http://dx.doi.org/10.2118/25158-ms.

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CAI, JIWEN, XIAO-PENG HU, JUN FENG, and XIAO-LONG FENG. "POROUS CRYSTALLINE MATERIALS CONSTRUCTED BY COMPLEX CATIONS AND BULKY ARENEDISULFONATE COUNTER ANIONS." In Proceedings of the International Symposium on Solid State Chemistry in China. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812776846_0049.

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Pirh, Rok, Primož Šket, and Janez Plavec. "NMR study of a potential role of anions on folding of dimeric G-quadruplex in aqueous solution." In XVth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2011. http://dx.doi.org/10.1135/css201112226.

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Reports on the topic "Anions (Chemistry)"

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Jonathan L. Sessler. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), September 2007. http://dx.doi.org/10.2172/891664.

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Moyer, Bruce a., Debra A. Bostick, Christopher J. Fowler, Hyun-Ah Kang, Alexandre Ruas, Laetitia H. Delmau, Tamara J. Haverlock, et al. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), September 2005. http://dx.doi.org/10.2172/893098.

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Bowman-James, Kristin, George S. Wilson, and Bruce Moyer. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), June 2001. http://dx.doi.org/10.2172/834750.

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Bowman-James, Kristin, George S. Wilson, and Bruce Moyer. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), June 2002. http://dx.doi.org/10.2172/834752.

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Bowman-James, Kristin, and George S. Wilson. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), June 2003. http://dx.doi.org/10.2172/834754.

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Bowman-James, K., G. Wilson, and B. A. Moyer. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), December 2004. http://dx.doi.org/10.2172/835027.

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Bowman-James, Kristin, and Bruce A. Moyer. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), June 2004. http://dx.doi.org/10.2172/838638.

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Bowman-James, Kristen. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), December 2004. http://dx.doi.org/10.2172/850320.

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Chamberlin, R. M., K. D. Abney, G. J. Balaich, and S. A. Fino. Advanced polymer chemistry of organometallic anions. Office of Scientific and Technical Information (OSTI), November 1997. http://dx.doi.org/10.2172/554744.

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Sessler, Jonathan L. The Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), June 2005. http://dx.doi.org/10.2172/884859.

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