Relevant bibliographies by topics / Site-selectivity

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  2. Dissertations / Theses
  3. Books
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Academic literature on the topic 'Site-selectivity'

Author: Grafiati
Published: 4 June 2021
Last updated: 12 February 2022

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Journal articles on the topic "Site-selectivity"

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Roche, Camille J., James A. Thomson, and Donald M. Crothers. "Site selectivity of daunomycin." Biochemistry 33, no. 4 (1994): 926–35. http://dx.doi.org/10.1021/bi00170a011.

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Wilcock, Brandon C., Brice E. Uno, Gretchen L. Bromann, Matthew J. Clark, Thomas M. Anderson, and Martin D. Burke. "Electronic tuning of site-selectivity." Nature Chemistry 4, no. 12 (2012): 996–1003. http://dx.doi.org/10.1038/nchem.1495.

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Yeston, Jake. "Shaking up reaction-site selectivity." Science 363, no. 6427 (2019): 594.3–594. http://dx.doi.org/10.1126/science.363.6427.594-c.

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Wu, Bin, Peter Dröge, and Curt A. Davey. "Site selectivity of platinum anticancer therapeutics." Nature Chemical Biology 4, no. 2 (2007): 110–12. http://dx.doi.org/10.1038/nchembio.2007.58.

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Colloms, Sean D., Jonathan Bath, and David J. Sherratt. "Topological Selectivity in Xer Site-Specific Recombination." Cell 88, no. 6 (1997): 855–64. http://dx.doi.org/10.1016/s0092-8674(00)81931-5.

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Routbort, J. L., S. J. Rothman, Nan Chen, J. N. Mundy та J. E. Baker. "Site selectivity and cation diffusion inYBa2Cu3O7−δ". Physical Review B 43, № 7 (1991): 5489–97. http://dx.doi.org/10.1103/physrevb.43.5489.

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Baldinozzi, G., J.-F. Bérar, M. Gautier-Soyer, and G. Calvarin. "Segregation and site selectivity in Zr-doped." Journal of Physics: Condensed Matter 9, no. 45 (1997): 9731–44. http://dx.doi.org/10.1088/0953-8984/9/45/004.

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Andersen, Kristen A., Langdon J. Martin, Joel M. Prince, and Ronald T. Raines. "Intrinsic site-selectivity of ubiquitin dimer formation." Protein Science 24, no. 2 (2015): 182–89. http://dx.doi.org/10.1002/pro.2603.

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Chiavarino, Barbara, Maria Elisa Crestoni, Barbara Di Rienzo, Simonetta Fornarini, and Francesco Lanucara. "Site-selectivity of protonation in gaseous toluene." Physical Chemistry Chemical Physics 10, no. 36 (2008): 5507. http://dx.doi.org/10.1039/b808710e.

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Cromie, Sarah, Vickie McKee, and Frédéric Launay. "Site-selectivity in a heterotetranuclear macrocyclic complex." Chemical Communications, no. 19 (2001): 1918–19. http://dx.doi.org/10.1039/b106340p.

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Dissertations / Theses on the topic "Site-selectivity"

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Morley, Krista Louise. "Focusing mutagenesis into the active site to improve hydrolase selectivity." Thesis, McGill University, 2005. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=111830.

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Occasionally, researchers need to modify enzymes through amino acid substitutions to make them more efficient catalysts for organic synthesis. There is still debate over the best protein engineering strategy for improving enzyme enantioselectivity: rational design or directed evolution. Rational design experiments focus mutations close to the active site, while directed evolution experiments often find mutations far from the active site.<br>In this thesis, a combination of the two strategies improved Pseudomonas fluorescens esterase (PFE) for production of a useful synthetic building block for
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Korvorapun, Korkit. "Site-Selectivity in Ruthenium-Catalyzed C–H and C–C Activations." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2020. http://hdl.handle.net/21.11130/00-1735-0000-0005-148C-7.

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Korvorapun, Korkit [Verfasser]. "Site-Selectivity in Ruthenium-Catalyzed C–H and C–C Activations / Korkit Korvorapun." Göttingen : Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2020. http://d-nb.info/1218299231/34.

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Rengifo, Emérita Mendoza. "Exploring the selectivity of metal ions in the active site of the enzyme superoxide dismutase (SOD) using site-directed mutagenesis." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-05012017-114055/.

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Iron/Manganese superoxide dismutases (Fe/Mn-SODs) are metalloenzymes with highly conserved protein folds, active sites, and dimer interfaces. They protect cells against oxidative stress by catalyzing the conversion of the cytotoxic free radical superoxide to molecular oxygen and hydrogen peroxide. The majority are highly specific for the type of metal (iron or manganese) present within the active site. However, there are many key aspects of metal specificity and catalytic activity that lack a structural explanation. Computational analyses suggested that several residues are important for fine-
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Douglas, Ross Gavin. "Significance of active site residues in the n-domain selectivity of angiotensin-converting enzyme." Doctoral thesis, University of Cape Town, 2011. http://hdl.handle.net/11427/11786.

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Angiotensin-converting enzyme (ACE) is a zinc metallopeptidase that plays an important role in vascular function; with ACE inhibitors being clinically utilised in the treatment of cardiovascular disease and diabetic nephropathy. Somatic ACE consists of two homologous catalytically active domains (designated N- and C-domains) that share high overall sequence identity and structural topology. Despite the high degree of similarity between domains, each domain displays differences in substrate processing and inhibitor binding abilities. This suggests that active site residues differing between the
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Sun, Xixi. "Scaffolding Catalysis: Towards Regioselective Hydroformylation of Alkenes and Site-Selective Functionalization of Polyhydroxylated Molecules." Thesis, Boston College, 2013. http://hdl.handle.net/2345/3324.

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Thesis advisor: Kian L. Tan<br>Chapter 1. We reported the first synthesis of all-carbon quaternary centers via hydroformylations using a catalytic directing group. With the ability of reversibly and covalently binding to a substrate, and coordinating to a metal center, scaffolding catalyst 1.1 is able to direct the branch-selective hydroformylation of 1,1-disubstituted olefins under mild temperature. Chapter 2. We have designed and synthesized a chiral organocatalyst 2.11. This catalyst is able to covalently bind to one hydroxyl, and utilize the induced intramolecularity to stereoselectively f
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Milan, Michela. "Oxidation of unactivated C-H bonds catalyzed by manganese complexes: control over site-selectivity and enantioselectivity." Doctoral thesis, Universitat de Girona, 2018. http://hdl.handle.net/10803/664865.

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The oxidation of aliphatic C-H bonds is a very powerful reaction because it allows the functionalization of inert C-H bonds, converting them into a suitable sites for further chemical elaboration. It also represents one of the most challenging reactions in modern synthetic organic chemistry because the multitude of aliphatic C-H bonds in a molecule makes site selective oxidation particularly difficult. Moreover, the introduction of chirality represents an unmet but very appealing challenge, because the asymmetric oxidation of hydrocarbons produces chiral compounds of high value in organic synt
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Malmberg, Michelle. "Probing the G protein selectivity of FR900359 by means of molecular modeling and site directed mutagenesis." Thesis, Umeå universitet, Farmakologi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-132256.

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Okumura, Shogo. "Studies on Site-selective C-H Alkylation of Arenes with Alkenes." Kyoto University, 2019. http://hdl.handle.net/2433/242514.

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Yang, Lichen. "Studies on Site-Selective C-H Borylation Reactions of Arenes and Heteroarenes." Kyoto University, 2020. http://hdl.handle.net/2433/253291.

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Books on the topic "Site-selectivity"

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Bertole, Christopher Jason. Site-activity, active carbon coverage and methane selectivity of cobalt Fischer-Tropsch catalysts: Effects of catalyst composition and reaction conditions. 2002.

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Book chapters on the topic "Site-selectivity"

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Benavides, Jesús, Pascale Abadie, Jean Claude Baron, and Bernard Scatton. "Comparative In vivo and In vitro Selectivity of Zolpidem for ω (Benzodiazepine) Modulatory Site Subtypes." In PET for Drug Development and Evaluation. Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0429-6_10.

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Durland, Ross H., Donald J. Kessler, Madeleine Duvic, and Michael Hogan. "Triplex Forming Oligonucleotide Reagents: Rationalization of DNA Site Selectivity and Application in a Pharmaceutical Context." In The Jerusalem Symposia on Quantum Chemistry and Biochemistry. Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-3728-7_36.

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Liebmann, C., R. Bossé, and E. Escher. "Preparation of an iodinated bradykinin analogue with selectivity for a picomolar, high-affinity bradykinin binding site." In Peptides. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_138.

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Eisenman, George, and Osvaldo Alvarez. "Structure and Selectivity of Ca-Binding Sites in Proteins: The 5-Fold Site in an Icosahedral Virus." In Calcium Transport and Intracellular Calcium Homeostasis. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-83977-1_27.

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Simonton, Matthew. "The Manipulation of Information." In Classical Greek Oligarchy. Princeton University Press, 2017. http://dx.doi.org/10.23943/princeton/9780691174976.003.0005.

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This chapter examines how Classical Greek oligarchs manipulated information in the specific context of the polis. In ancient Greece, “official” information was capable of being monopolized and manipulated, depending upon how many people were present at the site of its original production and circulation. The chapter argues that it was characteristic of a successful oligarchy to restrict this primary audience as much as possible to the members of the political class and to oversee how the information produced at their own secret political meetings was later promulgated. Three types of information manipulation were used by Classical Greek oligarchs: secrecy, projection, and selectivity. An example of oligarchic polis that deployed selectivity to its long-term advantage was the Thessalian city of Pharsalus.
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Bietti, M., and F. Dénès. "1.12 Intermolecular Radical C—H Functionalization." In Free Radicals: Fundamentals and Applications in Organic Synthesis 1. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-234-00262.

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AbstractThe generation of carbon-centered radicals via intermolecular hydrogen-atom transfer (HAT) from C—H bonds to an abstracting species (HAT reagent) represents a significant challenge in terms of reactivity, site-selectivity and stereoselectivity. The radical species resulting from such a transfer can then engage in carbon—carbon or carbon—heteroatom bond formation, possibly through the intervention of transition-metal catalysts, leading to a variety of functionalized products. This chapter aims to provide the reader with useful guidelines to understand, predict, and design selective radical transformations based upon initial HAT from a C—H bond coupled to different radical-capture strategies. A selection of examples that illustrate different approaches to implement HAT reactions in synthetically useful procedures are presented.
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Levitan, Irwin B., and Leonard K. Kaczmarek. "Receptors and Transduction Mechanisms I: Receptors Coupled Directly to Ion Channels." In The Neuron. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199773893.003.0011.

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The common feature that allows neurons and other cells to respond to extracellular signals is the presence of specific receptors in the plasma membrane, which may be similar in their structure and functional properties in different kinds of cells. There may be several different kinds of receptors for individual neurotransmitters. Many receptors can be grouped into families based on structural, functional, and regulatory homologies that are far more extensive than had been appreciated previously. One such family is that of the ligand-gated ion channels, whose members were first linked on the basis of a functional criterion—direct coupling between the receptor and the ion channel whose activity it regulates. Evolution has allowed the ligand specificity of the receptor site and the ion selectivity of the channel pore to diverge. However, the essential overall structural design of the ligand-gated receptor–channel complex has been preserved.
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K., Muddukrishnaiah. "Current Therapies and Future Prospects." In Handbook of Research on Nano-Strategies for Combatting Antimicrobial Resistance and Cancer. IGI Global, 2021. http://dx.doi.org/10.4018/978-1-7998-5049-6.ch015.

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Due to drug resistance, lack of cancer cell selectivity, and solubility, conventional cancer treatments lose their therapeutic uses, and as such, new therapeutic agents need to be developed. Nanomaterials and peptides are increasingly being used in the fields of cancer diagnosis, biomarker discovery due to their therapeutic values and novel way of targeting and curing the disease. Synergism among the peptide-conjugated nanoparticles is an exhilarating group of materials, not only sharing the benefits of conventional nanomedicine, but also possessing the unique properties of excellent biocompatibility, biodegradability, versatile sensitivity, specific biological purpose, and synthetic feasibility. These virtues inspired by the scientists and have taken advantage in the peptide-conjugated nano drugs for the accurate delivery of drugs reliably to the site of the lesion. This chapter offers a summary of emerging technologies that have recently been developed in the broad field of peptide-conjugated nanoparticles and offers guidance for targeted drug delivery and cancer therapy.
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Miletić Vukajlović, Jadranka, and Tanja Panić-Janković. "Mass Spectrometry in Clinical Laboratories." In Mass Spectrometry in Life Sciences and Clinical Laboratory. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96745.

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The analyses performed in clinical laboratories require a high level of precision, selectivity, and sensitivity. The rising number of therapeutic agents from both the field of small and large molecules and the increasing use of modern screening approaches have brought mass spectrometry into almost every clinical laboratory. The need to screen the patients and to follow the therapy’s success can often be fulfilled only by the highly selective and sensitive targeted approach with mass spectrometry. With improving instrument design and miniaturization of the separation technologies, mass spectrometry is no longer an exotic analytical approach. The use of mass spectrometry is now not restricted to the use in a clinical laboratory, but it is used in operating rooms for instant and on-site helping the surgeons with defining the margin of the tissue to be extracted. In this manuscript, we describe the use of mass spectrometry for selected clinical applications and show the possible way of future applications.
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Zhao, Zheng, and Philip E. Bourne. "Using the Structural Kinome to Systematize Kinase Drug Discovery." In Biochemistry. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.100109.

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Kinase-targeted drug design is challenging. It requires designing inhibitors that can bind to specific kinases, when all kinase catalytic domains share a common folding scaffold that binds ATP. Thus, obtaining the desired selectivity, given the whole human kinome, is a fundamental task during early-stage drug discovery. This begins with deciphering the kinase-ligand characteristics, analyzing the structure–activity relationships and prioritizing the desired drug molecules across the whole kinome. Currently, there are more than 300 kinases with released PDB structures, which provides a substantial structural basis to gain these necessary insights. Here, we review in silico structure-based methods – notably, a function-site interaction fingerprint approach used in exploring the complete human kinome. In silico methods can be explored synergistically with multiple cell-based or protein-based assay platforms such as KINOMEscan. We conclude with new drug discovery opportunities associated with kinase signaling networks and using machine/deep learning techniques broadly referred to as structural biomedical data science.
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Conference papers on the topic "Site-selectivity"

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Lee, P. J., M. Anderlini, B. L. Brown, J. Sebby-Strabley, W. D. Phillips, and J. V. Porto. "Site-selectivity and spin exchange in a double-well optical lattice." In 2007 Quantum Electronics and Laser Science Conference. IEEE, 2007. http://dx.doi.org/10.1109/qels.2007.4431677.

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Sundaram, Krithika, Ian Jennings, Alexandre Arcaro та Philip Thompson. "Abstract 4246: Probing the inhibitor selectivity site of class II PI3KC2β". У Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-4246.

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Cordova, Daniel. "Diamide insecticides: Understanding the basis for insect selectivity and target-site resistance." In 2016 International Congress of Entomology. Entomological Society of America, 2016. http://dx.doi.org/10.1603/ice.2016.91186.

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Penn, Samson Tafon, Zackery Fleischman, and Volkmar Dierolf. "The Site Selectivity of the E-beam Excitation of Eu ion in GaN." In 2007 European Conference on Lasers and Electro-Optics and the International Quantum Electronics Conference. IEEE, 2007. http://dx.doi.org/10.1109/cleoe-iqec.2007.4386220.

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Denifl, Stephan, Sylwia Ptasińska, Fabio Zappa, et al. "Dissociative Electron Attachment to Thymine: Bond and Site Selectivity in Different Molecular Environments." In ATOMIC AND MOLECULAR DATA AND THEIR APPLICATIONS: 5th International Conference on Atomic and Molecular Data and Their Applications (ICAMDATA). AIP, 2007. http://dx.doi.org/10.1063/1.2727364.

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Agianian, Paul (Bogos), Xiomaris M. Cotto-Rios, Nadege Gitego, Emmanouil Zachariouadakis, and Evripidis Gavathiotis. "Abstract LB-B10: Targeting a new allosteric site modulates selectivity of BRAF dimer inhibition." In Abstracts: AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics; October 26-30, 2019; Boston, MA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1535-7163.targ-19-lb-b10.

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TALWAR, DEVKI N. "SITE SELECTIVITY OF DEFECTS IN III-V COMPOUNDS BY LOCAL MODE SPECTROSCOPY AND MODEL CALCULATIONS." In Proceedings of the 16th Course of the International School of Atomic and Molecular Spectroscopy. WORLD SCIENTIFIC, 2001. http://dx.doi.org/10.1142/9789812810960_0021.

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"On Comparative Analysis of Two Ant Colony's Optimal Selectivity Decisions for Best Food Source Versus Migration to Well Protected Nest Site." In March 21-23, 2018 Istanbul (Turkey). Dignified Researchers Publication, 2018. http://dx.doi.org/10.17758/dirpub1.dir0318402.

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Al Ezzi, Amged, and Hongbin Ma. "Equilibrium Adsorption Isotherm Mechanism of Water Vapor on Zeolites 3A, 4A, X, and Y." In ASME 2017 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/imece2017-72601.

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Many researchers have analyzed the equilibrium adsorption isotherm mechanism of water vapor molecules on 4A, 3A, Y and X zeolites for decades. The demand for moisture removal continues to increase along with the increasing stringency of requirements for product quality control and production energy efficiency. Due to the negative charge of the zeolite framework, exchangeable compensation cations such as Na+, Li+, K+, Ba2+, Mg2+, and Ca2+ might be added. These cations are located at different sites within the framework and with different concentrations. Each cation shows a strong affinity to bo
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Ryu, Sang-gil, David J. Hwang, Eunpa Kim, Jae-hyuck Yoo, and Costas P. Grigoropoulos. "Laser-Assisted on Demand Growth of Semiconducting Nanowires." In ASME 2013 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/imece2013-65696.

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We present laser-assisted direct synthesis of nanowires with site-, composition-, and shape-selectivity on a single substrate by employing a spatially confined laser heat source. Laser-assisted nanowire growth based on vapor-liquid-solid mechanism is conveniently studied with multiple growth parameters such as temperature, time, and illumination direction. On-demand direct integration of silicon and germanium nanowires are demonstrated in a hetero-array configuration by simply switching the reactant gases as the growth of nanowires is limited within the heat-affected zone induced by the laser.
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Reports on the topic "Site-selectivity"

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Wang, Xin. High resolution x-ray fluorescence spectroscopy - a new technique for site- and spin-selectivity. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/456318.

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