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Relevant bibliographies by topics / Ligand systems

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Academic literature on the topic 'Ligand systems'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 February 2022

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Journal articles on the topic "Ligand systems"

1

Oszwałdowski, Sławomir, Katarzyna Zawistowska-Gibuła, and Kenneth Roberts. "Characterization of CdSe quantum dots with bidentate ligands by capillary electrophoresis." Open Chemistry 9, no. 4 (August 1, 2011): 572–84. http://dx.doi.org/10.2478/s11532-011-0037-3.

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AbstractThe CdSe quantum dots (QDs) with bidentate ligands: a-diimine (NN) and dihydrolipoic acid (DHLA) were synthesized and characterized by UV-Vis, particle size and capillary electrophoretic techniques. Two systems were analyzed: CdSe with one ligand (CdSe/ligand) and CdSe with two different ligands (CdSe//ligand1/ligand2), where ligand = α-diimine or DHLA. Hydrodynamic features of functionalized QDs were characterized by zone capillary electrophoretic (CZE), and particle size techniques and these methods were consistent. It was established that CZE, micellar (MEKC) and microemulsion (MEEKC) modes were suitable for separating charged CdSe QDs and that no peaks were obtained for QDs passivated with electrically neutral ligands. For CdSe QDs with neutral (NN) ligands, a preconcentration method with the use of a micellar plug was introduced for visualizing these QDs. A sharp peak representing neutral QDs was obtained within the zone of micellar plug of a non-ionic surfactant, Here, a ligand character used for CdSe modification and the type of the electrophoretic method applied were the determining factors for the QDs peak visualization. Moreover, examples of visualization of charged and neutral QDs on the same run were presented, and for this purpose, dual mechanism (separation/preconcentration) was proposed.

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Denizli, Adil, and Erhan Pişkin. "Dye-ligand affinity systems." Journal of Biochemical and Biophysical Methods 49, no. 1-3 (October 2001): 391–416. http://dx.doi.org/10.1016/s0165-022x(01)00209-3.

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Wang, K. "Biological metal ligand systems." Pure and Applied Chemistry 60, no. 8 (January 1, 1988): 1279–84. http://dx.doi.org/10.1351/pac198860081279.

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Osguthorpe, D. J. "Modelling ligand-receptor systems." Neurochemistry International 21 (January 1992): S8. http://dx.doi.org/10.1016/0197-0186(92)91742-f.

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Ben-Shlomo, Izhar, Rami Rauch, Orna Avsian-Kretchmer, and Aaron J. W. Hsueh. "Matching Receptome Genes with Their Ligands for Surveying Paracrine/Autocrine Signaling Systems." Molecular Endocrinology 21, no. 8 (August 1, 2007): 2009–14. http://dx.doi.org/10.1210/me.2007-0087.

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Abstract Sequencing of genomes from diverse organisms facilitates studies on the repertoire of genes involved in intercellular signaling. Extending previous efforts to annotate most human plasma membrane receptors in the Human Plasma Membrane Receptome database, we matched cognate ligands with individual receptors by surveying the published literature. In the updated online database we called “liganded receptome,” users can search for individual ligands or receptors to reveal their pairing partners and browse through receptor or ligand families to identify relationships between ligands and receptors in their respective families. Because local signaling systems are prevalent in diverse normal and diseased tissues, we used the liganded receptome knowledgebase to interrogate DNA microarray datasets for genome-wide analyses of potential paracrine/autocrine signaling systems. In addition to viewing ligand-receptor coexpression based on precomputed DNA microarray data, users can submit their own microarray data to perform online genome-wide searches for putative paracrine/autocrine signaling systems. Investigation of transcriptome data based on liganded receptome allows the discovery of paracrine/autocrine signaling for known ligand-receptor pairs in previously uncharacterized tissues or developmental stages. The present annotation of ligand-receptor pairs also identifies orphan receptors and ligands without known interacting partners in select families. Because hormonal ligands within the same family usually interact with paralogous receptors, this genomic approach could also facilitate matching of orphan receptors and ligands. The liganded receptome is accessible at http://receptome.stanford.edu.

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Chen, Fang, Gangliang Huang, and Hualiang Huang. "Sugar ligand-mediated drug delivery." Future Medicinal Chemistry 12, no. 2 (January 2020): 161–71. http://dx.doi.org/10.4155/fmc-2019-0114.

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Sugar ligand molecules, such as mannose, galactose and glucose, can bind to drug-delivery systems, making them targeted. These glycosylation ligands have the advantages of nontoxicity, no immunogenicity, good biocompatibility and biodegradation. They can be widely used in glycosylation-modified drug-delivery systems. Herein, the targeting mechanisms, synthesis methods and targeting characteristics of glycosylation-modified drug-delivery systems were reviewed.

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Gorzsás, András, Ingegärd Andersson, and Lage Pettersson. "Speciation in aqueous vanadate–ligand and peroxovanadate–ligand systems." Journal of Inorganic Biochemistry 103, no. 4 (April 2009): 517–26. http://dx.doi.org/10.1016/j.jinorgbio.2008.12.006.

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LIANG, G., and Q. YAO. "Ce 4f-LIGAND DEHYBRIDIZATION IN CeT2X2-BASED KONDO LATTICE/HEAVY FERMION SYSTEMS." International Journal of Modern Physics B 16, no. 19 (July 30, 2002): 2815–22. http://dx.doi.org/10.1142/s0217979202011378.

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The lattice parameters of two CeT2X2 ( T =3d transition elements and X=Si and Ge) based Kondo lattice systems, the CeNi2-xCux Si2 and Ce(NiSi)2-x (CuGe)x, have been studied. The analysis of the Ce-ligand distances indicates that the variation of the a-parameter dominantly affects Ce 4f-X ligandn orbital hybridization whereas the variation of c-parameter dominantly affects Ce 4f-T ligand orbital hybridization. The average Ce-ligand distance varies linearly with x across the whole series in spite of the abnormal increase of the c-parameter in the region 1.6 ≤ x ≤ 2.0. Thus, our analysis shows that the average Ce 4f-ligand orbital hybridization decreases uniformly with x across the entire range of x for the CeNi2-xCuxSi 2 and Ce(NiSi)2-x(CuGe)x series. The means that the Ce 4f-ligand orbital dehybridization may not be a key factor to the formation of the heavy-fermion ground state in CeCu2Si2.

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Martín-Mora, David, Matilde Fernández, Félix Velando, Álvaro Ortega, José Gavira, Miguel Matilla, and Tino Krell. "Functional Annotation of Bacterial Signal Transduction Systems: Progress and Challenges." International Journal of Molecular Sciences 19, no. 12 (November 26, 2018): 3755. http://dx.doi.org/10.3390/ijms19123755.

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Bacteria possess a large number of signal transduction systems that sense and respond to different environmental cues. Most frequently these are transcriptional regulators, two-component systems and chemosensory pathways. A major bottleneck in the field of signal transduction is the lack of information on signal molecules that modulate the activity of the large majority of these systems. We review here the progress made in the functional annotation of sensor proteins using high-throughput ligand screening approaches of purified sensor proteins or individual ligand binding domains. In these assays, the alteration in protein thermal stability following ligand binding is monitored using Differential Scanning Fluorimetry. We illustrate on several examples how the identification of the sensor protein ligand has facilitated the elucidation of the molecular mechanism of the regulatory process. We will also discuss the use of virtual ligand screening approaches to identify sensor protein ligands. Both approaches have been successfully applied to functionally annotate a significant number of bacterial sensor proteins but can also be used to study proteins from other kingdoms. The major challenge consists in the study of sensor proteins that do not recognize signal molecules directly, but that are activated by signal molecule-loaded binding proteins.

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Zahid, Kanwal, Shazia Nisar, Saima Imad, Shazia Perveen, Shazia Ghaffar, and Nasreen Fatima. "Synthesis and Characterization of Homo and Mixed Ligand Complexes of Fe(III) with Hydroxypyridinone and Hydroxypyranone Type Ligands." Pakistan Journal of Scientific & Industrial Research Series A: Physical Sciences 63, no. 1 (March 18, 2020): 12–17. http://dx.doi.org/10.52763/pjsir.phys.sci.63.1.2020.12.17.

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Hydroxypyridinone and hydroxypyranone are known to be used for the treatment of iron overload by chelation therapy for a long time. Both the ligands have their own side effects when used as medicines. In the present study homo and mixed ligand complexes of both the ligands with iron were prepared and characterized by UV-visible spectrophotometry, Potentiometric study, IR spectroscopy, SEM/EDX and XRD. Overlay spectra obtained from UV-visible spectroscopy of our studied system show the formation of different types of species and confirm that mixed ligand complex is different from the other two systems. Potentiometric titration curves of homo and mixed ligand complexes show the formation of different types of species at different pH and confirm the formation of mixed ligand complex. The comparative results of SEM images of these systems show different surface topologies and hence conform to the formation of mixed ligand complex.

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Dissertations / Theses on the topic "Ligand systems"

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Freundlich, Joel Stephen. "Metal-ligand multiple bonds in organometallic complexes containing triamidoamine ligand systems." Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/38782.

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Taylor, Steven John. "Exploratory studies of novel ligand systems." Thesis, Rhodes University, 1992. http://hdl.handle.net/10962/d1004973.

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A range of novel ligand systems have been developed in three distinct phases and preliminary studies have been initiated to evaluate their complexation potential. Phase I incorporated the synthesis of single strand ligand systems, which were mainly based on amino acid residues. Techniques have been developed for the attachment of these ligand systems onto, firstly, a styrene monomer, and then later onto a pseudo-styrene linking group, viz. the p-toluoyl group. The linking reactions were based on the formation of amides or esters by the reaction of an acid chloride system with an amine or alcohol. Phase II involved the synthesis of bis-chain ligand systems and their attachment onto the p-toluoyl linking group. A further linking group was also developed at this stage, viz. the xylyl group. In the preparation of phase II ligand systems, use was made of malonic ester and iminodiacetic acid derivatives. Phase III has involved the synthesis of cyclic ligand systems, with skeletons based upon the structures used in phase I and phase II and two crown ether type systems have been prepared.

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Kidd, Sara Jean. "Studies of group 15/nitrogen ligand systems." Thesis, University of Cambridge, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.621394.

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Paul, Diana Rachel. "The development of new organolead reagents in organic synthesis." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.320635.

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Bujotzek, Alexander [Verfasser]. "Molecular Simulation of Multivalent Ligand-Receptor Systems / Alexander Bujotzek." Berlin : Freie Universität Berlin, 2013. http://d-nb.info/1041255721/34.

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Peace, Richard John. "Bulky ligand systems containing pi-acidic aryl and carboranyl groups." Thesis, Durham University, 1996. http://etheses.dur.ac.uk/5388/.

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This thesis describes studies into the synthesis and coordination chemistry of ligands containing bulky π-acidic groups. Both π-acidic aryl and carboranyl groups have been investigated. Chapter One highlights electronic and structural aspects of ligands investigated and computational techniques employed. Chapter Two describes the synthesis of aromatic systems bearing nitrogen substituents and trifluoromethyl groups, with a view to their use in the synthesis of new ligands. The π -interaction between the nitrogen substituent and aromatic ring has been investigated and is found to vary considerably with the nature of the substituent and position of the CF(_3) groups on the ring. Chapter Three describes the synthesis of molybdenum compounds containing CF3 substituted aryl-imido ligands. The presence of the π-acidic group is found to decrease π-bonding from the ligand to the metal which results in changes in the reactivity of such complexes. Chapter Four describes the synthesis of nitrogen-substituted carboranes 1- NHX-2-R-l,2-C(_2)B (_10)H(_10) (R = Me, Ph; X = 2-R-l,2-C(_2)B(_10)H(_10), NHAr, OH, H) and 1- NX-2-R-C(_2)B(_10)H(_10) (R = Me, Ph; X = 0, NAr). The structures of many of these compounds are described and the π-interaction between the cage and substituent investigated. This 7t-interaction determines the orientation of the substituent relative to the cage and causes changes in the geometry of the cage. The "B NMR shift of the atom directly opposite the nitrogen substituent is found to give an accurate indication of the exo π-bond order. In light of these observations data from other systems have been re-examined. Chapter Five describes the incorporation of carborane containing ligands into metal systems. The π-acidic carboranyl group reduces 7i-bonding from the ligand to the metal. The consequences of this on the structure and reactivity of these complexes are discussed. Chapter Six gives experimental details for Chapters Two to Five. Richard John Peace (August 1996).

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Li, Aixiao. "Molecular modeling of non-bonding interactions in biomolecules-ligand systems." Paris 7, 2009. http://www.theses.fr/2009PA077032.

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Ce travail est consacré à la modélisation des interactions entre des inhibiteurs et des molécules impliquées dans la cancérisation, dans le but notamment d'établir de manière précise les modes d'interaction biomolécules-ligand. Dans la famille des CDK (cyclin dépendant kinases) nous nous sommes intéressés à la sélectivité que présente un nouvel inhibiteur (2PU) vis-à-vis de CDK4 par rapport à CDK2. Les méthodes employées : dynamique moléculaire, calculs d'énergies d'interaction, docking et méthodes mixtes du type ONIOM ont permis d'établir les raisons précises de la sélectivité en mettant en évidence des interactions privilégiées (notamment des liaisons H) entre l'inhibiteur et CDK4. Sur le plan méthodologique la méthode ONIOM (à deux ou trois couches) a fait l'objet d'une étude minutieuse et originale quant à la procédure de définition de la partition du système. Une nouvelle approche est proposée. La stabilisation du DNA G-quadruplex par un nouveau ligand (TQMP) a également été étudiée par dynamique moléculaire, ce qui a permis de préciser les modes d'interaction et de démontrer la sélectivité de l'un des deux sites possibles d'interaction
This work is devoted to modelling the interactions between some inhibitors and molecules involved in cancer development and aims at precisely establishing the interactions modes between the ligands and the biomolecules. In the CDK (cyclin dependant kinases) family we have examined the selectivity of a new inhibitor (2PU) towards CDK4 as compared to CDK2. The techniques we have used : molecular dynamics interaction energies calculation, molecular docking and mixed methods of the ONIOM type allowed us to establish the precise causes of this selectivity, showing the existence of specific interactions (H bonds, among others) between the inhibitor and CDK4. From a methodological point of view, the ONIOM method (with 2 or 3 layers) has been carefully examined with respect to the System partitioning procedure. A new approach is proposed. The stabilisation of G-quadruplex DNA by a new ligand (TQMP) has also been studied with molecular dynamics, which allowed establishing the interaction modes and show the selectivity of one of the 2 possible interaction sites

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Tran, Anh. "Ruthenium-Manganese Complexes as Model Systems for Artificial Photosynthesis." Doctoral thesis, KTH, Chemistry, 2001. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-3169.

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Larsson, Rikard. "Dynamic Systems for Screening, Control and Identification of Protein-Ligand Interactions." Doctoral thesis, Stockholm : Kemi, Chemistry, Kungliga Tekniska högskolan, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-4709.

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Bunn, Natalie R. "Synthetic and structural studies of low coordinate group 13 ligand systems." Thesis, Cardiff University, 2005. http://orca.cf.ac.uk/56114/.

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A new generation of diode lasers is being developed using quantum dots as the gain generating medium. A detailed understanding of the carrier recombination mechanisms and optical gain generation is essential for optimisation of their performance. The aim of this work is to further understand the optical processes occurring in quantum dots. In particular, the effect of the localisation of the energy states in the dots on the recombination mechanisms and the gain/absorption is studied. It is often assumed that the rates of nonradiative recombination via defects, radiative recombination and Auger recombination are proportional to linear, quadratic and cubic functions of the carrier number respectively. The derivation of these functional forms is possible in quantum well and bulk structures because the extended electronic states make it meaningful to talk of a global carrier population. In a quantum dot system the dependence of the recombination processes on the total number of electrons populating the dots is modified by the localisation of all the recombination processes. In this thesis a computer model has been developed in which the dots are occupied by integer numbers of electrons and holes, with electron and hole occupancies controlled by Fermi-Dirac statistics. The recombination processes have similar dependences on the electron number and there is no clear transition from one process to another as the injection level is increased. These dependences cannot be represented by simple power law functions of the carrier number. An alternative model, in which each dot is electrically neutral, has also been studied, and the two models show significant differences for the hole distribution as the injection is increased. It is found that analyses based on power law relations between recombination rates and carrier number, as used for extended state systems, cannot be applied to localised recombination in dots.

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Books on the topic "Ligand systems"

1

Tucs, Eric R. Ligand and proton transfer reactions in a series of RePt and MnPt bimetallic systems. Ottawa: National Library of Canada, 1990.

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N, Dʹi͡a︡chkov P., ed. Heteroligand molecular systems: Bonding, shapes and isomer stabilities. London: Taylor & Francis, 2002.

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Biochemical Pharmacology Symposium (4th 1989 New Haven, Conn.). NMR methods for elucidating macromolecule-ligand interactions: An approach to drug design : proceedings of the Fourth Biochemical Pharmacology Symposium, New Haven, CT, 27-29 July 1989. Edited by Handschumacher Robert E, Armitage Ian M, and Welch Arnold D. Oxford, U.K: Pergamon Press, 1990.

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Conference on Neuroimmunophilins (1st 1999 Schlangengad, Germany). Immunophilins in the brain: FKBP Ligands: novel strategies for the treatment of neurodegenerative disorders. Barcelona, Spain: Prous Science, 2000.

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Online information hunting. Blue Ridge Summit PA: Windcrest/McGraw-Hill, 1992.

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United States. Environmental Protection Agency. U.S. EPA nonpoint source information exchange computer bulletin board system (BBS): User's manual. Washington, DC: U.S. Environmental Protection Agency, Office of Water, 1992.

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International Online Information Meeting (9th 1985 London). 9th International Online Information Meeting: London, 3-5 December 1985 : organized by Learned Information (Europe) Ltd. Oxford: Learned Information, 1985.

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européenne, Commission. Les bases de données de l'Union européenne: Un répertoire des produits et des services d'informatin électroniques. Luxembourg: Office des publications officielles des Communautés européennes, 1996.

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Lennie, Stovel, and Bales Kathleen, eds. Bibliographic displays in the online catalog. White Plains, NY: Knowledge Industry Publications, 1986.

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Issues in online database searching. Englewood, Colo: Libraries Unlimited, 1989.

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Book chapters on the topic "Ligand systems"

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Kemp, Melissa L. "Ligand." In Encyclopedia of Systems Biology, 1126. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-9863-7_1247.

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Keller, Heiko, Remigiusz Worch, and Petra Schwille. "Model Membrane Systems." In Protein-Ligand Interactions, 417–38. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-398-5_15.

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Frostell, Åsa, Lena Vinterbäck, and Hans Sjöbom. "Protein–Ligand Interactions Using SPR Systems." In Protein-Ligand Interactions, 139–65. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-398-5_6.

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Hicks, Matthew R., Sarah R. Dennison, Adewale Olamoyesan, and Alison Rodger. "Flow Linear Dichroism of Protein–Membrane Systems." In Protein-Ligand Interactions, 449–63. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1197-5_21.

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Jellinek, J. "Theoretical Dynamical Studies of Metal Clusters and Cluster-Ligand Systems." In Metal-Ligand Interactions, 325–60. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0155-1_12.

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Chuev, G. N., M. V. Fedorov, and N. Russo. "DFT-IET Method for Quantum-Classical Systems: Treatment of Solvated Quasiparticles." In Metal-Ligand Interactions, 385–408. Dordrecht: Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-010-0191-5_18.

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Pawar, Prasad V., Abraham J. Domb, and Neeraj Kumar. "Systemic Targeting Systems-EPR Effect, Ligand Targeting Systems." In Advances in Delivery Science and Technology, 61–91. Boston, MA: Springer US, 2013. http://dx.doi.org/10.1007/978-1-4614-9434-8_3.

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Kim, Seji, Yeong-Eun Kim, and Yunho Lee. "Correction to: Metal-Ligand Cooperativity of Phosphorus-Containing Pincer Systems." In Metal-Ligand Co-operativity, 451. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/3418_2020_74.

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Johansson, G. "Dye-ligand Aqueous Two-phase Systems." In Reactive Dyes in Protein and Enzyme Technology, 101–24. London: Macmillan Education UK, 1987. http://dx.doi.org/10.1007/978-1-349-06582-0_6.

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Yoneya, Makoto. "Simulation Studies of Metal-Ligand Self-Assembly." In Self-Assembling Systems, 186–207. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119113171.ch7.

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Conference papers on the topic "Ligand systems"

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Alper, Joshua, Aaron Schmidt, and Kimberly Hamad-Schifferli. "Thermal Transport From Gold Nanorod to Solvent, an Investigation of Ligand Effects by Ultrafast Laser Spectroscopy." In ASME 2008 International Mechanical Engineering Congress and Exposition. ASMEDC, 2008. http://dx.doi.org/10.1115/imece2008-67266.

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To facilitate analysis of nanoscale heat transfer in nanoparticle systems the thermal properties of ligand layers must be understood. To this end, we use an optical pump-probe technique to study the thermal transport across ligands on gold nanorods and into the solvent. We find that varying properties of the ligand can have large impacts on the thermal decay of a nanorod after exposure to a laser pulse. By raising the concentration of free CTAB from 1 mM and 10 mM in solutions, the CTAB layer’s effective thermal interface conductance increases three fold. The transition occurs near the CTAB critical micelle concentration. Similar results are found for other ligand layers.

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Wang, Dong Hwan, Jin Young Kim, MinSeong Kim, Byung-Gi Kim, and Woongsik Jang. "Split-ligand re-precipitation via selective ligand capping for stable perovskite quantum dots in efficient photovoltaic application." In Quantum Nanophotonic Materials, Devices, and Systems 2020, edited by Mario Agio, Cesare Soci, and Matthew T. Sheldon. SPIE, 2020. http://dx.doi.org/10.1117/12.2572290.

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Wei, Alexander, and Ji-Xin Cheng. "Ligand-functionalized gold nanorods as theragnostic agents." In 2009 IEEE/NIH Life Science Systems and Applications Workshop (LiSSA) Formerly known as LSSA and. IEEE, 2009. http://dx.doi.org/10.1109/lissa.2009.4906697.

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Atilgan, Emrah, and Jianjun Hu. "Efficient protein-ligand docking using sustainable evolutionary algorithms." In 2010 10th International Conference on Hybrid Intelligent Systems (HIS 2010). IEEE, 2010. http://dx.doi.org/10.1109/his.2010.5600082.

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Zhou, Weiqiang, and Hong Yan. "Analysis of ligand binding sites using alpha shapes." In 2012 IEEE International Conference on Systems, Man and Cybernetics - SMC. IEEE, 2012. http://dx.doi.org/10.1109/icsmc.2012.6377780.

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Pakpahan, M. T., M. Rusmerryani, K. Kawaguchi, H. Saito, and H. Nagao. "Evaluation of scoring functions for protein-ligand docking." In 4TH INTERNATIONAL SYMPOSIUM ON SLOW DYNAMICS IN COMPLEX SYSTEMS: Keep Going Tohoku. American Institute of Physics, 2013. http://dx.doi.org/10.1063/1.4794652.

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Ahuja, Muskan, Ankit, and Manav R. Bhatnagar. "Capacity of Ligand Receptor Channel with Markovian Symbol Detection." In 2020 IEEE International Conference on Advanced Networks and Telecommunications Systems (ANTS). IEEE, 2020. http://dx.doi.org/10.1109/ants50601.2020.9342784.

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Tavares, Jorge, Alexandru-Adrian Tantar, Nouredine Melab, and El-Ghazali Talbi. "The Impact of Local Search on Protein-Ligand Docking Optimization." In 2008 8th International Conference on Hybrid Intelligent Systems (HIS). IEEE, 2008. http://dx.doi.org/10.1109/his.2008.14.

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Bahi, Meriem, and Mohamed Batouche. "Deep Learning for Ligand-Based Virtual Screening in Drug Discovery." In 2018 3rd International Conference on Pattern Analysis and Intelligent Systems (PAIS). IEEE, 2018. http://dx.doi.org/10.1109/pais.2018.8598488.

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Obliosca, Judy M., Fan-Gang Tseng, Ching-Mao Huang, Leu-Wei Lo, and Pen-Cheng Wang. "Ligand-exchange of TOPO-capped CdSe quantum dots with quinuclidines." In 2012 7th IEEE International Conference on Nano/Micro Engineered and Molecular Systems (NEMS). IEEE, 2012. http://dx.doi.org/10.1109/nems.2012.6196789.

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Reports on the topic "Ligand systems"

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Arnold, John. Potential New Ligand Systems for Binding Uranyl Ions in Seawater Environments. Office of Scientific and Technical Information (OSTI), December 2014. http://dx.doi.org/10.2172/1166963.

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Nolan, Steven. Synthetic and Thermodynamic Investigations of Ancillary Ligand Influence on Catalytic Organometallic Systems. Final Report. Office of Scientific and Technical Information (OSTI), March 2003. http://dx.doi.org/10.2172/821151.

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