Relevant bibliographies by topics / Supramolecular chemistry; Molecular recognition

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

Academic literature on the topic 'Supramolecular chemistry; Molecular recognition'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Supramolecular chemistry; Molecular recognition"

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Safarnejad Shad, Mastaneh, Pulikkal Veettil Santhini, and Wim Dehaen. "1,2,3-Triazolium macrocycles in supramolecular chemistry." Beilstein Journal of Organic Chemistry 15 (September 12, 2019): 2142–55. http://dx.doi.org/10.3762/bjoc.15.211.

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In this short review, we describe different pathways for synthesizing 1,2,3-triazolium macrocycles and focus on their application in different areas of supramolecular chemistry. The synthesis is mostly relying on the well-known “click reaction” (CuAAC) leading to 1,4-disubstituted 1,2,3-triazoles that then can be quaternized. Applications of triazolium macrocycles thus prepared include receptors for molecular recognition of anionic species, pH sensors, mechanically interlocked molecules, molecular machines, and molecular reactors.
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Liu, Yu, and Shizhao Kang. "Molecular recognition on supramolecular systems (XXXV)." Science in China Series B: Chemistry 44, no. 3 (2001): 260–67. http://dx.doi.org/10.1007/bf02879616.

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Lehn, Jean-Marie. "Towards Complex Matter: Supramolecular Chemistry and Self-organization." European Review 17, no. 2 (2009): 263–80. http://dx.doi.org/10.1017/s1062798709000805.

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Chemistry has developed from molecular chemistry, mastering the combination and recombination of atoms into increasingly complex molecules, to supramolecular chemistry, harnessing intermolecular forces for the generation of informed supramolecular systems and processes through the implementation of molecular information carried by electromagnetic interactions. Supramolecular chemistry is actively exploring systems undergoing self-organization, i.e. systems capable of spontaneously generating well-defined functional supramolecular architectures by self-assembly from their components, on the bas
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Haino, Takeharu. "Supramolecular Polymerization Engineered with Molecular Recognition." Chemical Record 15, no. 5 (2015): 837–53. http://dx.doi.org/10.1002/tcr.201500012.

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Schalley, Christoph A. "Molecular recognition and supramolecular chemistry in the gas phase." Mass Spectrometry Reviews 20, no. 5 (2001): 253–309. http://dx.doi.org/10.1002/mas.10009.

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Zimmerman, Steven C. "A journey in bioinspired supramolecular chemistry: from molecular tweezers to small molecules that target myotonic dystrophy." Beilstein Journal of Organic Chemistry 12 (January 25, 2016): 125–38. http://dx.doi.org/10.3762/bjoc.12.14.

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This review summarizes part of the author’s research in the area of supramolecular chemistry, beginning with his early life influences and early career efforts in molecular recognition, especially molecular tweezers. Although designed to complex DNA, these hosts proved more applicable to the field of host–guest chemistry. This early experience and interest in intercalation ultimately led to the current efforts to develop small molecule therapeutic agents for myotonic dystrophy using a rational design approach that heavily relies on principles of supramolecular chemistry. How this work was infl
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Spaniol, Jacqueline M., and Kraig A. Wheeler. "Accessing Centnerszwer's quasiracemate – molecular shape controlled molecular recognition." RSC Advances 6, no. 69 (2016): 64921–29. http://dx.doi.org/10.1039/c6ra08131b.

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Yu, Liu, and You Changcheng. "Molecular recognition studies on supramolecular systems (XXIV)." Science in China Series B: Chemistry 43, no. 1 (2000): 27–33. http://dx.doi.org/10.1007/bf03028846.

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Zeng, Fanwen, and Steven C. Zimmerman. "Dendrimers in Supramolecular Chemistry: From Molecular Recognition to Self-Assembly." Chemical Reviews 97, no. 5 (1997): 1681–712. http://dx.doi.org/10.1021/cr9603892.

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Newkome, George R., Barry D. Woosley, Enfei He, et al. "Supramolecular chemistry of flexible, dendritic-based structures employing molecular recognition." Chem. Commun., no. 24 (1996): 2737–38. http://dx.doi.org/10.1039/cc9960002737.

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Dissertations / Theses on the topic "Supramolecular chemistry; Molecular recognition"

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Kerdelhue, Jean-Luc. "The higher paracyclophanes : potential receptors for the molecular recognition of molecular halogens and benzenes." Thesis, University of Nottingham, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307819.

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Rajbanshi, Arbin. "Supramolecular interactions from small-molecule selectivity to molecular capsules." Diss., Manhattan, Kan. : Kansas State University, 2010. http://hdl.handle.net/2097/3879.

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Agostini, Alessandro. "Supramolecular and heterosupramolecar chemistry in controlled release and molecular recognition processes." Doctoral thesis, Universitat Politècnica de València, 2013. http://hdl.handle.net/10251/29397.

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La presente tesis doctoral titulada ¿Supramolecular and heterosupramolecular chemistry in controlled release and molecular recognition processes¿ está centrada en los dos aspectos principales de la química supramolecular que han experimentado un gran auge en los últimos años: el reconocimiento molecular y los procesos de liberación controlada. En particular la primera parte de la tesis se focaliza en el diseño y síntesis de moléculas orgánicas que pueden ser empleados cómo sensores para especies aniónicas y neutras. El paradigma seleccionado para los procesos de reconocimiento mo
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South, Clinton Ray. "Polymer side-chains as arms for molecular recognition." Diss., Atlanta, Ga. : Georgia Institute of Technology, 2008. http://hdl.handle.net/1853/22667.

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Thesis (Ph. D.)--Chemistry and Biochemistry, Georgia Institute of Technology, 2008.<br>Committee Chair: Weck, Marcus; Committee Member: Beckham, Haskell; Committee Member: Bunz, Uwe; Committee Member: Jones, Christopher; Committee Member: Marder, Seth.
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Welideniya, Dhanushi Thathsara. "Supramolecular chemistry of small molecular fundamentals to drug–receptor applications." Diss., Kansas State University, 2015. http://hdl.handle.net/2097/19106.

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Doctor of Philosophy<br>Department of Chemistry<br>Christer B. Aakeroy<br>A family of bis-pyridine based pharmaceutical active ingredients were synthesized and co-crystallized with four iodoperfluoroalkanes. Thirteen new crystal structures that are driven by I‧‧‧N(py) halogen bonds, are presented and compared with that of their hydrogen-bonded analogues. Halogen bonded co-crystals exhibit two different structural arrangements, as opposed to layered architectures observed in hydrogen bonded co-crystals. In order to explore the effect of aromatic stacking interactions on hydrogen and halogen b
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D'Souza, Lawrence Joseph. "Bile Acid Based Molecular Tweezers And Crown Ethers." Thesis, Indian Institute of Science, 1995. http://hdl.handle.net/2005/114.

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Chapter 1. Introduction to Molecular Tweezers Whitlock and Zimmerman developed a class of molecular hosts, popularly known as molecular tweezers, which sandwich aromatic guests by ii=ii interaction. Chapter 1 summarizes molecular tweezers of various kinds which have recently been synthesized. Chapter 2. Design and synthesis of "Bile Acid-Based Molecular Tweezers" Bile acids have a rigid backbone, and the array of hydroxyl groups separated by 5-7 A provides opportunities for the attachment of binding surfaces such as two extended chromophoric units.
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Gardlik, Matthew Michael. "Design, synthesis, and encapsulation processes of molecular baskets." Columbus, Ohio : Ohio State University, 2009. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1243536105.

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Tiwari, Laxmikant. "Design and synthesis of novel anion receptors." Thesis, University of Oxford, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.312677.

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Shade, Matthew. "Redox-active calixarenes as receptors for anions and neutral molecules." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.242875.

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De, la Torre Paredes Cristina. "Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications"." Doctoral thesis, Universitat Politècnica de València, 2018. http://hdl.handle.net/10251/94043.

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La presente tesis doctoral, titulada "Nanotecnología y química supramolecular en procesos de liberación controlada y reconocimiento molecular para aplicaciones biomédicas", se centra en dos temas importantes: el reconocimiento molecular y los procesos de liberación controlada. Esta tesis doctoral está estructurada en cuatro capítulos. El primer capítulo introduce el concepto de materiales híbridos orgánicos-inorgánicos funcionalizados con puertas moleculares y sus aplicaciones biomédicas como nanomateriales para dirigir y controlar la liberación controlada de fármacos. Además se introduce
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Books on the topic "Supramolecular chemistry; Molecular recognition"

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Weber, E., ed. Supramolecular Chemistry II — Host Design and Molecular Recognition. Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/3-540-58800-0.

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Canceill, J., J. C. Chambron, A. Collet, et al. Supramolecular Chemistry I — Directed Synthesis and Molecular Recognition. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/bfb0111279.

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L, Atwood J., ed. Supramolecular chemistry. 2nd ed. Wiley, 2008.

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

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Gale, Philip A., and Wim Dehaen, eds. Anion Recognition in Supramolecular Chemistry. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-642-15444-7.

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Simon, J. Design of molecular materials: Supramolecular engineering. Wiley, 2000.

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Marguerettaz, Xavier. Supramolecular chemistry at the semiconductor-liquid electrolyte interface. University College Dublin, 1997.

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Functional supramolecular architectures: For organic electronics and nanotechnology. Wiley-VCH, 2011.

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D, Försterling H., ed. Principles of physical chemistry: Understanding molecules, molecular assemblies, supramolecular machines. Wiley, 2000.

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service), SpringerLink (Online, ed. Molecular networks. Springer, 2009.

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Book chapters on the topic "Supramolecular chemistry; Molecular recognition"

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Arduini, A., A. Casnati, M. Fabbi, et al. "New Shapes For Selective Molecular Recognition From Calixarenes." In Supramolecular Chemistry. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2492-8_3.

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Dearden, David V. "Host-Guest Molecular Recognition Without Solvents." In Physical Supramolecular Chemistry. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0317-3_15.

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Knipe, Peter C., Sam Thompson, and Andrew D. Hamilton. "Molecular Recognition in Biomimetic Receptors." In Macrocyclic and Supramolecular Chemistry. John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.ch7.

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Buergi, H. B. "On Molecular Recognition in Fullerene Chemistry." In Crystallography of Supramolecular Compounds. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-1692-0_3.

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Bampos, Nick, Zöe Clyde-Watson, Joanne C. Hawley, et al. "NMR Studies of Molecular Recognition by Metalloporphyrins." In NMR in Supramolecular Chemistry. Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4615-9_3.

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Jorgensen, William L., Wolfgang Damm, Antonio Frontera, and Michelle L. Lamb. "Molecular Recognition of Carbohydrates: Interaction of Diols with Acetate Ion." In Physical Supramolecular Chemistry. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0317-3_8.

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de Vink, Pim J., and Luc Brunsveld. "Chapter 17. Molecular Recognition of Proteins by Cucurbiturils." In Monographs in Supramolecular Chemistry. Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788015967-00464.

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Brodbelt, J. S. "Evaluation of Hydrogen-Bonding Interactions in Molecular Recognition By Ion Trap Mass Spectrometry." In Physical Supramolecular Chemistry. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0317-3_16.

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Becher, Jan, Zhan-Ting Li, Philippe Blanchard, et al. "Tetrathiafulvalenes in Macrocyclic and Supramolecular Chemistry: Self Assembly with Tetrathiafulvalenes." In Molecular Recognition and Inclusion. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4_9.

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Desiraju, Gautam R., and C. V. Krishnamohan Sharma. "Crystal Engineering and Molecular Recognition-Twin Facets of Supramolecular Chemistry." In Perspectives in Supramolecular Chemistry. John Wiley & Sons, Ltd., 2007. http://dx.doi.org/10.1002/9780470511459.ch2.

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Conference papers on the topic "Supramolecular chemistry; Molecular recognition"

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Long, Timothy E., Casey L. Elkins, Lars Kilian, et al. "“Reversible Macromolecules” as Scaffolds for Adaptive Structures." In ASME 2003 International Mechanical Engineering Congress and Exposition. ASMEDC, 2003. http://dx.doi.org/10.1115/imece2003-43010.

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Self-healing macromolecular structures, submicron capsules and fibers with molecular recognition, stimuliresponsive molecules, solvent-free rheological reversibility, multivalency in rational drug design, and the emergence of new fields of adaptive and evolutive chemistry will require a predictive synergy of tailored non-covalent and covalent bonding in molecular design. Supramolecular chemistry has emerged as a stimulating focal point that will enable these scientific and technological discoveries, and biorecognition and biomolecular organization often serve as the inspiration for the future
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Jorobekova, Sh. "Molecular recognition in supramolecular systems of humic substances." In Fifth International Conference of CIS IHSS on Humic Innovative Technologies «Humic substances and living systems». CLUB PRINT ltd., 2019. http://dx.doi.org/10.36291/hit.2019.jorobekova.030.

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Seela, Frank, Xiaohua Peng, Hong Li, et al. "Modified DNA: From synthesis to molecular recognition." In XIIIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2005. http://dx.doi.org/10.1135/css200507001.

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Higgins, M. J., M. Polcik, T. Fukuma, J. E. Sader, and S. P. Jarvis. "Direct Mechanical Measurement of Organised Water and the Influence of Adjacent Surface Chemistry Using Atomic Force Microscopy (Keynote)." In World Tribology Congress III. ASMEDC, 2005. http://dx.doi.org/10.1115/wtc2005-64383.

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Directly measuring structural changes in water with a mechanical probe of lateral dimensions comparable to that of a single molecule provides an invaluable insight into how and why bio-molecules behave with high selectivity or why certain surfaces promote or inhibit bio-molecular adhesion. In the immediate vicinity of the molecule, continuum models break down and the aqueous environment will often form a discrete layered structure depending on the nature of the molecule. The absence or presence of such structure may be fundamental in influencing the promotion or inhibition of protein adsorptio
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Veličković, Suzana, and Xianglei Kong. "„Superalkali” clusters, production, potential application like energy storage materials." In 8th International Conference on Renewable Electrical Power Sources. SMEITS, 2020. http://dx.doi.org/10.24094/mkoiee.020.8.1.15.

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One of the major developments of the past century was the recognition of clusters as building blocks of new materials. “Superalkali” clusters because of their ionization energies which lower than alkaline atoms, present the excellent reducing agents; hence, they are recognized as good can-didates for the synthesis of unusually compounds. “Superalkalis”, plays an important role in the chemistry and material science because of their potential to serve as structural units for the assem-bly of novel nanostructured functional materials, such as nonlinear optical materials, hydrogen storage material
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Chen, Kok Hao, and Jong Hyun Choi. "DNA Oligonucleotide-Templated Nanocrystals: Synthesis and Novel Label-Free Protein Detection." In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-11958.

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Semiconductor and magnetic nanoparticles hold unique optical and magnetic properties, and great promise for bio-imaging and therapeutic applications. As part of their stable synthesis, the nanocrystal surfaces are usually capped by long chain organic moieties such as trioctylphosphine oxide. This capping serves two purposes: it saturates dangling bonds at the exposed crystalline lattice, and it prevents irreversible aggregation by stabilizing the colloid through entropic repulsion. These nanocrystals can be rendered water-soluble by either ligand exchange or overcoating, which hampers their wi
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Chen, Kok Hao, and Jong Hyun Choi. "Nanoparticle-Aptamer: An Effective Growth Inhibitor for Human Cancer Cells." In ASME 2009 International Mechanical Engineering Congress and Exposition. ASMEDC, 2009. http://dx.doi.org/10.1115/imece2009-11966.

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Semiconductor nanocrystals have unique optical properties due to quantum confinement effects, and a variety of promising approaches have been devised to interface the nanomaterials with biomolecules for bioimaging and therapeutic applications. Such bio-interface can be facilitated via a DNA template for nanoparticles as oligonucleotides can mediate the aqueous-phase nucleation and capping of semiconductor nanocrystals.[1,2] Here, we report a novel scheme of synthesizing fluorescent nanocrystal quantum dots (NQDs) using DNA aptamers and the use of this biotic/abiotic nanoparticle system for gro
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Reports on the topic "Supramolecular chemistry; Molecular recognition"

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Moyer, Bruce a., Debra A. Bostick, Christopher J. Fowler, et al. Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), 2005. http://dx.doi.org/10.2172/893098.

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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), 2007. http://dx.doi.org/10.2172/891664.

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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), 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), 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), 2003. http://dx.doi.org/10.2172/834754.

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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), 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), 2004. http://dx.doi.org/10.2172/850320.

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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), 2004. http://dx.doi.org/10.2172/835027.

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Bowman-James, Kristin, and Bruce Moyer. Title: Supramolecular Chemistry of Selective Anion Recognition for Anions of Environmental Relevance. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/827243.

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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), 2004. http://dx.doi.org/10.2172/850321.

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