Relevant bibliographies by topics / Ionic and molecular recognition

Academic literature on the topic 'Ionic and molecular recognition'

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Published: 6 September 2023

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Journal articles on the topic "Ionic and molecular recognition"

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Liu, Zhilian, Lin Jiang, Zhi Liang, and Yunhua Gao. "Photo-switchable molecular devices based on metal-ionic recognition." Tetrahedron Letters 46, no. 5 (January 2005): 885–87. http://dx.doi.org/10.1016/j.tetlet.2004.11.164.

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Jha, Kshitij C., Hua Liu, Michael R. Bockstaller, and Hendrik Heinz. "Facet Recognition and Molecular Ordering of Ionic Liquids on Metal Surfaces." Journal of Physical Chemistry C 117, no. 49 (November 27, 2013): 25969–81. http://dx.doi.org/10.1021/jp4032404.

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Machado, Isabel, Veli Cengiz Özalp, Elixabete Rezabal, and Thomas Schäfer. "DNA Aptamers are Functional Molecular Recognition Sensors in Protic Ionic Liquids." Chemistry - A European Journal 20, no. 37 (July 25, 2014): 11820–25. http://dx.doi.org/10.1002/chem.201403354.

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Ta, Daniel D., and Sergei V. Dzyuba. "Squaraine-Based Optical Sensors: Designer Toolbox for Exploring Ionic and Molecular Recognitions." Chemosensors 9, no. 11 (October 25, 2021): 302. http://dx.doi.org/10.3390/chemosensors9110302.

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Small molecule-based chromogenic and fluorogenic probes play an indispensable role in many sensing applications. Ideal optical chemosensors should provide selectivity and sensitivity towards a variety of analytes. Synthetic accessibility and attractive photophysical properties have made squaraine dyes an enticing platform for the development of chemosensors. This review highlights the versatility of modular assemblies of squaraine-based chemosensors and chemodosimeters that take advantage of the availability of various structurally and functionally diverse recognition motifs, as well as utilizing additional recognition capabilities due to the unique structural features of the squaraine ring.
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Faul, Charl F. J., Philipp Krattiger, Bernd M. Smarsly, and Helma Wennemers. "Ionic self-assembled molecular receptor-based liquid crystals with tripeptide recognition capabilities." Journal of Materials Chemistry 18, no. 25 (2008): 2962. http://dx.doi.org/10.1039/b802690d.

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Rebek, J., and D. Nemeth. "Molecular recognition: ionic and aromatic stacking interactions bind complementary functional groups in a molecular cleft." Journal of the American Chemical Society 108, no. 18 (September 1986): 5637–38. http://dx.doi.org/10.1021/ja00278a052.

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Tlili, Amal, Ghada Attia, Sohayb Khaoulani, Zouhour Mazouz, Chouki Zerrouki, Nourdin Yaakoubi, Ali Othmane, and Najla Fourati. "Contribution to the Understanding of the Interaction between a Polydopamine Molecular Imprint and a Protein Model: Ionic Strength and pH Effect Investigation." Sensors 21, no. 2 (January 17, 2021): 619. http://dx.doi.org/10.3390/s21020619.

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Several studies were devoted to the design of molecularly imprinted polymer (MIP)-based sensors for the detection of a given protein. Here, we bring elements that could contribute to the understanding of the interaction mechanism involved in the recognition of a protein by an imprint. For this purpose, a polydopamine (PDA)-MIP was designed for bovine serum albumin (BSA) recognition. Prior to BSA grafting, the gold surfaces were functionalized with mixed self-assembled monolayers of (MUDA)/(MHOH) (1/9, v/v). The MIP was then elaborated by dopamine electropolymerization and further extraction of BSA templates by incubating the electrode in proteinase K solution. Three complementary techniques, electrochemistry, zetametry, and Fourier-transform infrared spectrometry, were used to investigate pH and ionic strength effects on a MIP’s design and the further recognition process of the analytes by the imprints. Several MIPs were thus designed in acidic, neutral, and basic media and at various ionic strength values. Results indicate that the most appropriate conditions, to achieve a successful MIPs, were an ionic strength of 167 mM and a pH of 7.4. Sensitivity and dissociation constant of the designed sensor were of order of (3.36 ± 0.13) µA·cm−2·mg−1·mL and (8.56 ± 6.09) × 10−11 mg/mL, respectively.
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SUGAWARA, Masao, Kazunori ODASHIMA, and Yoshio UMEZAWA. "Novel approaches to molecular recognition of ionic and neutral species by using membranes." membrane 15, no. 3 (1990): 112–20. http://dx.doi.org/10.5360/membrane.15.112.

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Xu, Limin, Lingxiang Jiang, Markus Drechsler, Yu Sun, Zhirong Liu, Jianbin Huang, Ben Zhong Tang, Zhibo Li, Martien A. Cohen Stuart, and Yun Yan. "Self-Assembly of Ultralong Polyion Nanoladders Facilitated by Ionic Recognition and Molecular Stiffness." Journal of the American Chemical Society 136, no. 5 (January 23, 2014): 1942–47. http://dx.doi.org/10.1021/ja410443n.

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Gómez-González, Borja, Luis García-Río, Nuno Basílio, Juan C. Mejuto, and Jesus Simal-Gandara. "Molecular Recognition by Pillar[5]arenes: Evidence for Simultaneous Electrostatic and Hydrophobic Interactions." Pharmaceutics 14, no. 1 (December 28, 2021): 60. http://dx.doi.org/10.3390/pharmaceutics14010060.

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The formation of inclusion complexes between alkylsulfonate guests and a cationic pillar[5]arene receptor in water was investigated by NMR and ITC techniques. The results show the formation of host-guest complexes stabilized by electrostatic interactions and hydrophobic effects with binding constants of up to 107 M−1 for the guest with higher hydrophobic character. Structurally, the alkyl chain of the guest is included in the hydrophobic aromatic cavity of the macrocycle while the sulfonate groups are held in the multicationic portal by ionic interactions.
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Dissertations / Theses on the topic "Ionic and molecular recognition"

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Sen, Ananya. "Chiral recognition in neutral and ionic molecular complexes." Thesis, Paris 11, 2012. http://www.theses.fr/2012PA112163/document.

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L'objectif principal de cette thèse est l’étude spectroscopique de molécules ou de complexes portant plusieurs centres chiraux en phase gazeuse, pour comprendre les effets de la stéréochimie sur leurs propriétés structurales. Des alcaloïdes dérivés de la Cinchonine ont été introduits intacts en phase gazeuse par ablation laser. Ils ont été étudiés en combinant un jet supersonique avec de la spectroscopie laser. Les deux pseudo-énantiomères Quinine et Quinidine ont montré des spectres électroniques et vibrationnels similaires, en accord avec leur structure similaire. Leurs propriétés en solution diffèrent davantage, comme le montrent les expériences de dichroïsme circulaire vibrationnel (VCD). Cette différence est encore plus marquée dans l’Hydroquinine et l’Hydroquinidine. Enfin la reconnaissance chirale a été étudiée dans des complexes ioniques dans un piège à ions. La stabilité des complexes formés entre S-camphre et les R et S-Alanine protonées indique une préférence homochirale. Cependant, l'énergie d'interaction calculée ainsi que les spectres IRMPD dans la région des empreintes digitales sont identiques. Le rôle des conformères plus hauts en énergie dans la reconnaissance chirale a été discuté
The main objective of this thesis is a spectroscopic study of molecules or complexes bearing multiple chiral centres in the gas phase, to understand the effects of stereochemistry on their structural properties. Neutral cinchona alkaloids have been introduced intact in gas phase by laser-ablation. They have been studied by combining supersonic expansion with laser spectroscopy. The two pseudo-enantiomers Quinine and Quinidine show similar electronic and vibrational spectra, in line with similar structure. Their properties in solution differ more, as shown by Vibrational Circular Dichroism (VCD) experiments. This difference is further enhanced in Hydroquinine and Hydroquinidine. Lastly chiral recognition has been studied in ionic complexes in an ion trap. A homochiral preference has been shown in the stability of the complexes formed between S-Camphor and R and S protonated Alanine. However, the calculated interaction energy as well as the IRMPD spectrum in the fingerprint region are identical. The role of higher energy conformers in chiral recognition has been discussed
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Cheng, Shijing. "Synthesis and Characterization of Cation-Containing and Hydrogen Bonding Supramolecular Polymers." Diss., Virginia Tech, 2011. http://hdl.handle.net/10919/77185.

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Non-covalent interactions including nucleobase hydrogen bonding and phosphonium/ammonium ionic aggregation were studied in block and random polymers synthesized using controlled radical polymerization techniques such as nitroxide mediated polymerization (NMP) and reversible addition-fragmentation chain transfer polymerization (RAFT). Non-covalent interactions were expected to increase the effective molecular weight of the polymeric precursors through intermolecular associations and to induce microphase separation. The influence of non-covalent association on the structure/property relationships of these materials were studied in terms of physical properties (tensile, DMA, rheology) as well as morphological studies (AFM, SAXS). Ionic interactions, which possess stronger interaction energies than hydrogen bonds (~150 kJ/mol) were studied in the context of phosphonium-containing acrylate triblock (ABA) copolymers and random copolymers. Phosphonium-containing ionic liquid monomers with different alkyl substituent lengths and counterions enabled an investigation of the effects of ionic aggregation of phosphonium cations on the polymer physical properties. The polymerization of styrenic phosphonium-containing ionic liquid monomers using a difunctional alkoxyamine initiator, DEPN2, afforded an ABA triblock copolymer with an n-butyl acrylate soft center block and symmetric phosphonium-containing external reinforcing blocks. Small-angle X-ray scattering (SAXS) and transmission electron microscopy (TEM) of triblock copolymers revealed pronounced microphase separation at the nanoscale. Phosphonium aggregation governed block copolymer flow activation energies. In random copolymers, the phosphonium cations only weakly aggregated, which strongly depended on the length of alkyl substituents and the type of counterions. Acrylate random copolymers consisting of quaternary ammonium functionalities were synthesized using reversible addition-fragmentation chain transfer polymerization (RAFT). The obtained copolymers possessed controlled compositions and narrow molecular weight distributions with molecular weights ranging from Mn =50,000 to 170,000 g/mol. DMA evidenced the weak aggregation of ammonium cations in the solid state. Additionally, this ionomer was salt-responsive in NaCl aqueous solutions. Hydrogen bonding, a dynamic interaction with intermediate enthalpies (10-40 kJ/mol) was introduced through complementary heterocyclic DNA nucleobases such as adenine, thymine and uracil. Our investigations in this field have focused on the use of DNA nucleobase pair interactions to control polymer self-assembly and rheological behavior. Novel acrylic adenine- and thymine-containing monomers were synthesized from aza-Michael addition reaction. The long alkyl spacers between nucleobase and polymer backbone afforded structural flexibility in self-assembly process. Adenine-containing polyacrylates exhibited unique morphologies due to adenine-adenine π-π interactions. The complementary hydrogen bonding of adenine and thymine resulted in disruption of adenine-adenine π-π interactions, leading to lower plateau modulus and lower softening temperatures. Moreover, hydrogen bonding interactions enabled the compatibilization of complementary hydrogen bonding guest molecules such as uracil phosphonium chloride.
Ph. D.
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Benedek, Nicole Ann, and n. benedek@gmail com. "Interactions in ionic molecular crystals." RMIT University. Applied Sciences, 2006. http://adt.lib.rmit.edu.au/adt/public/adt-VIT20070109.161440.

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We have used ab initio computational simulation techniques to investigate both intra- and intermolecular interactions in a novel family of ionic organophosphonate molecular crystals. We have examined the influence of various numerical approximations on the computed geometry and binding energies of a selection of well-characterised hydrogen bonded systems. It was found that numerical basis sets provided the efficiency required to study the large hydrogen bonded dimer anions present in the organophosphonate system, while also producing accurate geometries and binding energies. We then calculated the relaxed structures and binding energies of phenylphosphonic acid dimer in the two arrangements in which it is present in the bulk crystal. The computed geometries were in excellent agreement with the experimental structures and the binding energies were consistent with those found for other ionic hydrogen bonded systems. Electron density maps were used to gain insight into the nature of the hydrogen bonding interaction between phenylphosphonic acid dimers. We also examined the effect of aromatic ring substituents on the geometry and energetics of the hydrogen bonding interaction. The nitro-substituted dimer was predicted to have a stronger binding energy than its unsubstituted parent while the methyl-substituted dimer was predicted to have a similar binding energy to its unsubstituted parent. An analysis of crystal field effects showed that the structure of the phenylphosphonic acid dimers in the organophosphonates is a complex product of competing intra- and intermolecular forces and crystal field effects. Cooperative effects in the organophosphonate system were also investigated and it was found that the interactions were mostly one-body (local) in nature. We have examined the intramolecular charge-transfer interaction between copper-halogen cations in the organophosphonate materials. The origin of geometric differences between the Cu(I) starting material and Cu(II) product cations was attributed to the electronic configuration of the Cu ion, not crystal field effects. To gain further insight into the difference in electronic structure between the starting material and product, we attempted to simulate the step-by-step dissociation of the [CuI]+ system. Although this investigation was not successful, we were able to expose some of the pitfalls of simulating dissociating odd-electron systems. We also analysed and compared the charge-transfer interaction in the chloro-, bromo- and iodo-forms of the organophosphonate family. The charge-transfer interaction was predicted to increase on going from the chloro- to the iodo-form, consistent with solid-state UV-visible data. Finally, we used the highly accurate Quantum Monte Carlo (QMC) method to investigate the hydrogen bonding interaction in water dimer and to calculate the dissociation energy. The accuracy of the experimental estimate for the dissociation energy has recently been questioned and an alternative value has been put forward. Our results lend support to the validity of the alternative value and are also in excellent agreement with those from other high-level calculations. Our results also indicate that QMC techniques are a promising alternative to traditional wavefunction techniques in situations where both high accuracy and efficiency are important.
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Yang, Junhong. "GLASS FORMATION BEHAVIOR AND IONIC CONDUCTIVITY OF IONIC LIQUIDS AND POLYMERIC IONIC LIQUID: INSIGHT FROM MOLECULAR SIMULATION." University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1494886213137829.

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Ong, Tien Teng. "Crystal Engineering of Molecular and Ionic Cocrystals." Scholar Commons, 2011. http://scholarcommons.usf.edu/etd/3270.

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Solubility enhancement of poorly-soluble active pharmaceutical ingredients (APIs) remains a scientific challenge and poses a practical issue in the pharmaceutical industry. The emergence of pharmaceutical cocrystals has contributed another dimension to the diversity of crystal forms available at the disposal of the pharmaceutical scientist. That pharmaceutical cocrystals are amenable to the design principles of crystal engineering means that the number of crystal forms offered by pharmaceutical cocrystals is potentially greater than the combined numbers of polymorphs, salts, solvates and hydrates for an API. The current spotlight and early-onset dissolution profile ("spring-and-parachute" effect) exhibited by certain pharmaceutical cocrystals draw attention to an immediate question: How big is the impact of cocrystals on aqueous solubility? The scientific literature and in-house data on pharmaceutical cocrystals that are thermodynamically stable in water are reviewed and analyzed for trends in aqueous solubility and melting point between the cocrystal and the cocrystal formers. There is poor correlation between the aqueous solubility of cocrystal and cocrystal former with respect to the API. The log of the aqueous solubility ratio between cocrystal and API has a poor correlation with the melting point difference between cocrystal and API. Structure-property relationships between the cocrystal and the cocrystal formers remain elusive and the actual experiments are still necessary to investigate the desired physicochemical properties. Crystal form (cocrystals, polymorphs, salts, hydrates and solvates) diversity is and will continue to be a contentious issue for the pharmaceutical industry. That the crystal form of an API dramatically impacts its aqueous solubility (a fixed thermodynamic property) is illustrated by the histamine H2-receptor antagonist ranitidine hydrochloride and HIV protease inhibitor ritonavir. For more than a century, the dissolution rate of a solid has been shown to be directly dependent on its solubility, cçterîs paribus. A century later, it remains impossible to predict the properties of a solid, given its molecular structure. If delivery or absorption of an API are limited by its aqueous solubility, aqueous solubility then becomes a critical parameter linking bioavailability and pharmacokinetics of an API. Since the majority of APIs are Biopharmaceutical Classification System (BCS) Class II (low solubility and high permeability) compounds, crystal form screening, optimization and selection have thus received more efforts, attention and investment. Given that the dissolution rate, aqueous solubility and crystal form of an API are intricately linked, it remains a scientific challenge to understand the nature of crystal packing forces and their impact upon physicochemical properties of different crystal forms. Indeed, the selection of an optimal crystal form of an API is an indispensable part of the drug development program. The impact of cocrystals on crystal form diversity is addressed with molecular and ionic targets in ellagic acid and lithium salts. A supramolecular heterosynthon approach was adopted for crystal form screening. Crystal form screening of ellagic acid yields molecular cocrystals, cocrystal solvates/hydrates and solvates. Crystal form screening of lithium salts (chloride, bromide and nitrate salts) afforded ionic cocrystals and cocrystal hydrates.
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Chen, Long-Qing 1962. "Molecular dynamics study of ionic grain boundaries." Thesis, Massachusetts Institute of Technology, 1990. https://hdl.handle.net/1721.1/128799.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 1990.
Includes bibliographical references (leaves 240-244).
by Long-Qing Chen.
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 1990.
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Yu, Shu W. "Ionic and molecular diffusion in cementitious materials." Thesis, Aston University, 1990. http://publications.aston.ac.uk/14273/.

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The work described in this thesis is an attempt to provide improved understanding of the effects of several factors affecting diffusion in hydrated cement pastes and to aid the prediction of ionic diffusion processes in cement-based materials. Effect of pore structure on diffusion was examined by means of comparative diffusion studies of quaternary ammonium ions with different ionic radii. Diffusivities of these ions in hydrated pastes of ordinary portland cement with or without addition of fly ash were determined by a quasi-steady state technique. The restriction of the pore geometry on diffusion was evaluated from the change of diffusivity in response to the change of ionic radius. The pastes were prepared at three water-cement ratios, 0.35, 0.50 and 0.65. Attempts were made to study the effect of surface charge or the electrochemical double layer at the pore/solution interface on ionic diffusion. An approach was to evaluate the zeta potentials of hydrated cement pastes through streaming potential measurements. Another approach was the comparative studies of the diffusion kinetics of chloride and dissolved oxygen in hydrated pastes of ordinary portland cement with addition of 0 and 20% fly ash. An electrochemical technique for the determination of oxygen diffusivity was also developed. Non-steady state diffusion of sodium potassium, chloride and hydroxyl ions in hydrated ordinary portland cement paste of water-cement ratio 0.5 was studied with the aid of computer-modelling. The kinetics of both diffusion and ionic binding were considered for the characterization of the concentration profiles by Fick's first and second laws. The effect of the electrostatic interactions between ions on the overall diffusion rates was also considered. A general model concerning the prediction of ionic diffusion processes in cement-based materials has been proposed.
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Raskatov, Jevgenij A. "Rational design of chiral ionic recognition for asymmetric catalysis." Thesis, University of Oxford, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.497082.

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Brown, Susan Elizabeth. "Molecular recognition by cyclodextrins /." Title page, contents and abstract only, 1994. http://web4.library.adelaide.edu.au/theses/09PH/09phb8798.pdf.

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Westwell, Martin Stuart. "Cooperativity in molecular recognition." Thesis, University of Cambridge, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.388343.

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Books on the topic "Ionic and molecular recognition"

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Bartsch, Richard A., and Mizuo Maeda, eds. Molecular and Ionic Recognition with Imprinted Polymers. Washington, DC: American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0703.

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A, Bartsch Richard, Maeda Mizuo, American Chemical Society. Division of Industrial and Engineering Chemistry., and American Chemical Society Meeting, eds. Molecular and ionic recognition with imprinted polymers. Washington, DC: American Chemical Society, 1998.

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S, Agnew William, Claudio Tonio, Sigworth F, Yale University. Dept. of Physiology., and Conference on Membrane Transport Processes (12th : 1988 : Yale University. School of Medicine), eds. Molecular biology of ionic channels. San Diego: Academic Press, 1988.

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Buckingham, A. D., A. C. Legon, and S. M. Roberts, eds. Principles of Molecular Recognition. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2168-2.

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Coleman, A. W., ed. Molecular Recognition and Inclusion. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4.

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Rotello, Vincent M., and S. Thayumanavan, eds. Molecular Recognition and Polymers. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470384053.

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D, Buckingham A., Legon A. C, and Roberts Stanley M, eds. Principles of molecular recognition. London: Blackie Academic & Professional, 1993.

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Weber, E., ed. Molecular Inclusion and Molecular Recognition — Clathrates II. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/3-540-19338-3.

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Weber, E., ed. Molecular Inclusion and Molecular Recognition — Clathrates I. Berlin/Heidelberg: Springer-Verlag, 1987. http://dx.doi.org/10.1007/bfb0003833.

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E, Weber, and Gerdil R, eds. Molecular inclusion and molecular recognition: Clathrates I. Berlin: Springer-Verlag, 1987.

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Book chapters on the topic "Ionic and molecular recognition"

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Kricka, L. J. "Molecular and ionic recognition by biological systems." In Chemical Sensors, 3–14. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-010-9154-1_1.

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Beer, P. D. "Molecular and ionic recognition by chemical methods." In Chemical Sensors, 17–72. Dordrecht: Springer Netherlands, 1988. http://dx.doi.org/10.1007/978-94-010-9154-1_2.

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Maeda, Mizuo, and Richard A. Bartsch. "Molecular and Ionic Recognition with Imprinted Polymers: A Brief Overview." In ACS Symposium Series, 1–8. Washington, DC: American Chemical Society, 1998. http://dx.doi.org/10.1021/bk-1998-0703.ch001.

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Hall, George G. "Ionic Crystals." In Molecular Solid State Physics, 16–37. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-84461-4_2.

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Cleaves, Henderson James. "Molecular Recognition." In Encyclopedia of Astrobiology, 1079–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1019.

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Cleaves, Henderson James. "Molecular Recognition." In Encyclopedia of Astrobiology, 1613. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1019.

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Donato, Laura. "Molecular Recognition." In Encyclopedia of Membranes, 1–2. Berlin, Heidelberg: Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-40872-4_1613-1.

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Cleaves, Henderson James. "Molecular Recognition." In Encyclopedia of Astrobiology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_1019-3.

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Cleaves, Henderson James. "Molecular Recognition." In Encyclopedia of Astrobiology, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-642-27833-4_1019-4.

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Cleaves, Henderson James. "Molecular Recognition." In Encyclopedia of Astrobiology, 1993. Berlin, Heidelberg: Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-65093-6_1019.

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Conference papers on the topic "Ionic and molecular recognition"

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Borner, Arnaud, Zheng Li, and Deborah Levin. "Ionic Liquid Electrospray Modeling using Molecular Dynamics." In 47th AIAA/ASME/SAE/ASEE Joint Propulsion Conference & Exhibit. Reston, Virigina: American Institute of Aeronautics and Astronautics, 2011. http://dx.doi.org/10.2514/6.2011-5524.

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Adams, Nigel G. "Ionic Processes in Low Temperature Interstellar Molecular Plasmas." In ATOMIC PROCESSES AND PLASMAS: 13th APS Topical Conference on Atomic Processes in Plasmas. AIP, 2002. http://dx.doi.org/10.1063/1.1516309.

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Srinivasan, H., P. S. Dubey, V. K. Sharma, R. Biswas, S. Mitra, and R. Mukhopadhyay. "Molecular dynamics of acetamide based ionic deep eutectic solvents." In DAE SOLID STATE PHYSICS SYMPOSIUM 2017. Author(s), 2018. http://dx.doi.org/10.1063/1.5029015.

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LIU, ZHIPING, XIAOPING WU, SHIPING HUANG, and WENCHUAN WANG. "MOLECULAR DYNAMICS SIMULATION OF IONIC LIQUIDS WITH IMIDAZOLIUM CATIONS." In Proceedings of the 4th International Conference. WORLD SCIENTIFIC, 2004. http://dx.doi.org/10.1142/9789812702623_0084.

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Song, K. S., and Chun-Rong Fu. "RELAXATION OF EXCITONS IN IONIC HALIDES: MOLECULAR DYNAMICS STUDY." In Proceedings of 2000 International Conference. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812811387_0022.

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Stearns, Jaime, Jerry Boatz, Alexander Zolot, David Sporleder, and Russell Cooper. "ION PAIR STRUCTURE AND PHOTODISSOCIATION DYNAMICS OF IONIC LIQUID [EMIM][TF2N]." In 69th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2014. http://dx.doi.org/10.15278/isms.2014.rg08.

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Young, Justin, Jaime Stearns, Christopher Annesley, and Ryan Booth. "INFRARED AND ULTRAVIOLET SPECTROSCOPY OF GAS-PHASE IMIDAZOLIUM AND PYRIDINIUM IONIC LIQUIDS." In 70th International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2015. http://dx.doi.org/10.15278/isms.2015.rg10.

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Delaporte, Philippe C., Bernard L. Fontaine, Marc L. Sentis, Olivier P. Uteza, and M. Voitik. "Kinetics and spectroscopy of alkali rare-gas ionic excimers." In International Conference on Atomic and Molecular Pulsed Lasers III, edited by Victor F. Tarasenko, Georgy V. Mayer, and Gueorgii G. Petrash. SPIE, 2000. http://dx.doi.org/10.1117/12.383451.

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Liang, Mengbing, Hongyu Yu, Miranda Ngan, Stella Nickerson, Elizabeth Nofen, and Lenore L. Dai. "MEMS accelerometer based on Molecular Electronic Transducers using Ionic Liquid." In 2015 IEEE 15th International Conference on Nanotechnology (IEEE-NANO). IEEE, 2015. http://dx.doi.org/10.1109/nano.2015.7388833.

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Qiu, Yinghua, Jian Ma, Weichuan Guo, Wei Si, Qiyan Tan, and Yunfei Chen. "Ionic current investigation in silicon nanochannels with molecular dynamics simulations." In 2013 International Conference on Manipulation, Manufacturing and Measurement on the Nanoscale (3M-NANO). IEEE, 2013. http://dx.doi.org/10.1109/3m-nano.2013.6737442.

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Reports on the topic "Ionic and molecular recognition"

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Alexandratos, S. D. Polymer-based separations: Synthesis and application of polymers for ionic and molecular recognition. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/7017486.

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Alexandratos, S. Polymer-based separations: Synthesis and application of polymers for ionic and molecular recognition. Office of Scientific and Technical Information (OSTI), April 1990. http://dx.doi.org/10.2172/6975900.

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Alexandratos, S. D. Polymer-based separations: Synthesis and application of polymers for ionic and molecular recognition. Triennial performance report, August 1, 1989--July 31, 1992. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/10188150.

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Alexandratos, S. D. Polymer-based separations: Synthesis and application of polymers for ionic and molecular recognition. Annual performance report, August 1, 1993--July 31, 1994. Office of Scientific and Technical Information (OSTI), April 1994. http://dx.doi.org/10.2172/10173307.

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Atassi, Zouhair M. Molecular Recognition of Alpha-Neurotoxins. Fort Belvoir, VA: Defense Technical Information Center, November 1990. http://dx.doi.org/10.21236/ada230342.

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Tiede, D. M., A. C. Vashista, and M. R. Gunner. Electrostatic basis for molecular recognition in photosynthesis. Office of Scientific and Technical Information (OSTI), November 1994. http://dx.doi.org/10.2172/10194615.

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Tan, Weihong. Ultrasensitive Biosensors for Molecular Recognition and Manipulation. Fort Belvoir, VA: Defense Technical Information Center, February 2003. http://dx.doi.org/10.21236/ada410625.

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Hardy, John R. Studies on the Microwave Optics of Ionic Molecular Solids. Fort Belvoir, VA: Defense Technical Information Center, March 2002. http://dx.doi.org/10.21236/ada413643.

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Wasielewski, Michael R. SENSORS USING MOLECULAR RECOGNITION IN LUMINESCENT, CONDUCTIVE POLYMERS. Office of Scientific and Technical Information (OSTI), September 1999. http://dx.doi.org/10.2172/828084.

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Pless, Jason, Tina Maria Nenoff, Terry J. Garino, and Marlene Axness. Tunable ionic-conductivity of collapsed Sandia octahedral molecular sieves (SOMS). Office of Scientific and Technical Information (OSTI), November 2006. http://dx.doi.org/10.2172/899364.

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