Добірка наукової літератури з теми "Synthetic Oligomers"
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Статті в журналах з теми "Synthetic Oligomers"
Bazaco, Raúl Blanco, José L. Segura, and Carlos Seoane. "Recent advances in the design, synthesis and study of covalent conjugated oligomer–C60 ensembles." Collection of Czechoslovak Chemical Communications 74, no. 6 (2009): 857–86. http://dx.doi.org/10.1135/cccc2008218.
Повний текст джерелаKayama, Kotetsu, Hibiki Hashizume, Gerry Amor Camer, and Daiji Endoh. "An improved gene synthesis method with asymmetric directions of oligonucleotides designed using a simulation program." BioTechniques 69, no. 3 (September 2020): 211–19. http://dx.doi.org/10.2144/btn-2020-0062.
Повний текст джерелаAli, Dildar, Zaheer Ahmed, Peter M. Kazmaier, and Erwin Buncel. "Synthesis and characterization of low-molecular-weight azo-acetoxystyrene and azo-naphthalene oligomers via stable free radical polymerization (SFRP)." Canadian Journal of Chemistry 88, no. 9 (September 2010): 910–21. http://dx.doi.org/10.1139/v10-072.
Повний текст джерелаPils, Marlene, Alexandra Dybala, Fabian Rehn, Lara Blömeke, Tuyen Bujnicki, Victoria Kraemer-Schulien, Wolfgang Hoyer, Detlev Riesner, Dieter Willbold, and Oliver Bannach. "Development and Implementation of an Internal Quality Control Sample to Standardize Oligomer-Based Diagnostics of Alzheimer’s Disease." Diagnostics 13, no. 10 (May 11, 2023): 1702. http://dx.doi.org/10.3390/diagnostics13101702.
Повний текст джерелаOrlov, Y. N. "The impact of the of cationic polyelectrolyte polymerization degree in latexes coagulation dosage of synthetic emulsion rubbers." Proceedings of the Voronezh State University of Engineering Technologies 81, no. 1 (July 18, 2019): 318–24. http://dx.doi.org/10.20914/2310-1202-2019-1-318-324.
Повний текст джерелаMao, Jialin, Wei Zhang, Stephen ZD Cheng, and Chrys Wesdemiotis. "Analysis of monodisperse, sequence-defined, and POSS-functionalized polyester copolymers by MALDI tandem mass spectrometry." European Journal of Mass Spectrometry 25, no. 1 (February 2019): 164–74. http://dx.doi.org/10.1177/1469066719828875.
Повний текст джерелаWalsh, D. M., I. Klyubin, G. M. Shankar, M. Townsend, J. V. Fadeeva, V. Betts, M. B. Podlisny та ін. "The role of cell-derived oligomers of Aβ in Alzheimer's disease and avenues for therapeutic intervention". Biochemical Society Transactions 33, № 5 (26 жовтня 2005): 1087–90. http://dx.doi.org/10.1042/bst0331087.
Повний текст джерелаUrrego-Riveros, Sara, Matthias Bremer, Jonas Hoffmann, Anne Heitmann, Thibault Reynaldo, Janek Buhl, Paul J. Gates, et al. "Conjugated oligomers with alternating heterocycles from a single monomer: synthesis and demonstration of electroluminescence." Organic Chemistry Frontiers 6, no. 21 (2019): 3636–43. http://dx.doi.org/10.1039/c9qo00947g.
Повний текст джерелаNúñez-Villanueva, Diego, and Christopher A. Hunter. "Controlled mutation in the replication of synthetic oligomers." Chemical Science 12, no. 11 (2021): 4063–68. http://dx.doi.org/10.1039/d0sc06770a.
Повний текст джерелаBianco, Alberto. "ChemInform Abstract: Combinatorial Synthetic Oligomers." ChemInform 32, no. 41 (May 24, 2010): no. http://dx.doi.org/10.1002/chin.200141275.
Повний текст джерелаДисертації з теми "Synthetic Oligomers"
Szczypiński, Filip Tomasz. "Ester-based synthetic information oligomers." Thesis, University of Cambridge, 2019. https://www.repository.cam.ac.uk/handle/1810/289396.
Повний текст джерелаStross, Alexander. "Synthetic H-bonding information oligomers." Thesis, University of Sheffield, 2016. http://etheses.whiterose.ac.uk/12365/.
Повний текст джерелаSwain, Jonathan. "Phenylacetylene oligomers as synthetic information molecules." Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/279084.
Повний текст джерелаIadevaia, Giulia. "A synthetic approach to H-bonding information oligomers." Thesis, University of Sheffield, 2014. http://etheses.whiterose.ac.uk/6370/.
Повний текст джерелаTrinh, Thanh Tam. "Synthèse itérative supportée de macromolécules à séquences contrôlées." Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAF006/document.
Повний текст джерелаIn this thesis, iterative syntheses of sequence-controlled oligonylons and oligo(triazole-amide)s by protecting group-free approaches have been described. Oligonylons have been prepared by an «AA+BB» approach i.e. by stepwise couplings of a large excess of diacids (AA) and diamines (BB) monomers. This strategy was interesting but could not prevent the formation of bridged molecules. Therefore, an «AB+CD» strategy has been adopted for the synthesis of oligo(triazole-amide)s. In this case, the growth of oligomers was controlled by consecutive chemoselective couplings of AB (A = acid, B = alkyne) and CD (C = amine, D = azide) monomers. This approach was found to be efficient for the preparation of encoded monodisperse oligo(triazole-amide)s whose sequence is based on a binary code (0, 1). However, this iterative approach is slow and is not adapted to longer sequences. Consequently, a strategy based on trimers couplings has been developed in order to simplify the process. This new approach has enabled the synthesis of long code sequences containing a molecular byte
Lightowler, Stephen. "Palladium-catalysed cross-coupling reactions in the synthesis of novel organic polymers and monodisperse oligomers." Thesis, University of Hull, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.342874.
Повний текст джерелаHenry, Brian Lawrence. "Novel Sulfated 4-Hydroxycinnamic Acid Oligomers as Potent Anticoagulants." VCU Scholars Compass, 2007. http://scholarscompass.vcu.edu/etd/1462.
Повний текст джерелаSprafke, Johannes Klaus. "Supramolecular control of synthesis and electronic structure of porphyrin oligomers." Thesis, University of Oxford, 2011. http://ora.ox.ac.uk/objects/uuid:520bfa69-8cd5-4615-96fb-487651dd557a.
Повний текст джерелаSun, Xiaohua. "Synthesis and properties of monodisperse oligomer-substituted calix[4]arene assemblies and related oligomers." HKBU Institutional Repository, 2006. http://repository.hkbu.edu.hk/etd_ra/706.
Повний текст джерелаYao, Dandan. "Synthesis of new conjugated meso porphyrin dendrimers and oligomers and study of their optical properties." Thesis, Rennes, INSA, 2015. http://www.theses.fr/2015ISAR0008/document.
Повний текст джерелаDuring this thesis, we have worked on the synthesis and characterization of new compounds using the porphyrin macrocycle as a starting material. The aim, after synthesis, was to study the photophysical properties of these new molecules. More precisely, we have synthesized and characterized three groups of fluorenyl-porphyrin dendrimers and two oligomers in conjugated structures. Their correlation on optical property-structure have been discussed in detail, as well as the energy transfer processes from the conjugated dendron donor to porphyrin acceptor. In the first chapter, we introduce the general background of the porphyrin chemistry based on three aspects: (i) structure, (ii) optical properties and (iii) synthetic methods. We further review prior porphyrin studies done in our group and propose new molecular designs based on these results. In the second chapter, we study the influence of substitution position and nature of the antennae on the central core. Two groups of new TPP-cored porphyrin dendrimers were synthesized according to different substituted positions on the peripheral phenyl rings: para-substituted series TPP1, TPP2 and TPP3, and meta-substituted ones TPP4, TPP5 and TPP6. All have conjugated dendrons with bridged phenyl-alkynyl and are terminated by fluorenyl groups. In the third chapter, we study the influence of positions of light absorbers. To this aim, a series of TFP-cored porphyrin dendrimers presenting fluorenyls in conjugated dendrons on different positions is reported (core fluorenyl, bridging fluorenyl and terminal fluorenyl): TFP1, TFP2 and TFP3. The core fluorenyl mainly influences emission peaks and quantum yield, while the bridging fluorenyl and terminal fluorenyl have a large effect on the dendron absorption and on the energy transfer efficiency. Thus, for the largest dendrimer TFP3, dendron emission is not totally quenched by long distance energy transfer process when exciting the peripheral dendrons. In the fourth chapter, we study the influence of linkages in the Dendron. Thus, two new porphyrin dendrimers with bridged vinyl, TPP-D and TFP-D, were synthesized and compared to analogues with alkynyl bridged TPP-T and TFP-T. Vinyl and alkynyl bridges are shown to influence the optical properties of the porphyrin dendrimers to a certain extent depending on the substituted positions. Finally, in the last chapter, two oligomers with n-butyl substituted TFP as terminal group, a linear dimer and a star – shaped trimer, were synthesized from the same porphyrin monomer
Книги з теми "Synthetic Oligomers"
Uglea, Constantin V. Synthesis and characterization of oligomers. Boca Raton, Fla: CRC Press, 1991.
Знайти повний текст джерелаCenter, Langley Research, and United States. National Aeronautics and Space Administration., eds. Synthesis and characterization of modified phenylethynyl terminated polyimides. Hampton, Va: National Aeronautics and Space Administration, Langley Research Center, 1998.
Знайти повний текст джерелаS, Minkin Vladimir, and Deberdeev Timur R, eds. Polysulfide oligomer sealants: Synthesis, properties, and applications. Oakville, ON, Canada: Apple Academic Press, 2015.
Знайти повний текст джерела1942-, Pethrick R. A., Zaikov Gennadiĭ Efremovich, and Pielichowski Jan, eds. Monomers, oligomers, polymers, composites and nanocomposites research: synthesis, properties and applications. Hauppauge, N.Y: Nova Science Publishers, 2009.
Знайти повний текст джерелаMalkin, A. Ya. Rheokinetics: Rheological transformations in synthesis and reactions of oligomers and polymers. Heidelberg: Hüthig & Wepf, 1996.
Знайти повний текст джерелаMalkin, Aleksandr I͡Akovlevich. Rheokinetics: Rheological transformations in synthesis and reactions of oligomers and polymers. Zug: Huthig & Wepf, 1996.
Знайти повний текст джерелаElsadig, Hwaida Misbah. Synthesis of pyrrolo[2,1-c][1,4]benzodiazepine peptoid oligomer libraries. [Portsmouth]: [University of Portsmouth], 2000.
Знайти повний текст джерелаKontes, Ferenc. Strategies for the Controlled Synthesis of Oligomeric Natural Products. [New York, N.Y.?]: [publisher not identified], 2011.
Знайти повний текст джерелаLyet, Karine Andree. Experiments leading towards the synthesis by the solid phase method of inositol oligomers. Birmingham: University of Birmingham, 1994.
Знайти повний текст джерелаStudies towards Selective Synthesis of Resveratrol-based Oligomeric Natural Products. [New York, N.Y.?]: [publisher not identified], 2011.
Знайти повний текст джерелаЧастини книг з теми "Synthetic Oligomers"
Gray, Gary M., Keith E. Branham, Lung-Hua Ho, Jimmy W. Mays, Prakash C. Bharara, Andreas Hajipetrou, and James B. Beal. "Poly(alkylene Phosphates): Synthetic Strategies." In Inorganic and Organometallic Oligomers and Polymers, 249–62. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-011-3214-5_20.
Повний текст джерелаOhgi, Tadaaki, and Junichi Yano. "Development of a Novel Synthetic Method for RNA Oligomers." In Pharmaceutical Process Chemistry, 345–61. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527633678.ch17.
Повний текст джерелаSillion, Bernard. "Polymerization of Reactive Telechelic Oligomers. Formation of Thermostable Networks." In Recent Advances in Mechanistic and Synthetic Aspects of Polymerization, 237–54. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3989-9_18.
Повний текст джерелаGoossens, Remko, and Annemieke Aartsma-Rus. "In Vitro Delivery of PMOs in Myoblasts by Electroporation." In Methods in Molecular Biology, 191–205. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2010-6_12.
Повний текст джерелаEntelis, S. G., V. V. Evreinov, A. I. Kuzaev, V. M. Divid, and Yu U. Rajabov. "Synthesis of Reactive Oligomers and the Formation of Functionally-Defective Macromolecules." In Reactive Oligomers, 11–51. London: CRC Press, 2023. http://dx.doi.org/10.1201/9780429087561-3.
Повний текст джерелаEbdon, J. R. "Terminally reactive oligomers: telechelic oligomers and macromers." In New Methods of Polymer Synthesis, 162–96. Dordrecht: Springer Netherlands, 1991. http://dx.doi.org/10.1007/978-94-010-9552-5_6.
Повний текст джерелаEbdon, J. R. "Terminally reactive oligomers: telechelic oligomers and macromers." In New Methods of Polymer Synthesis, 162–96. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4684-1530-8_6.
Повний текст джерелаChan-Seng, Delphine, and Jean-François Lutz. "Solid-Phase Synthesis as a Tool for the Preparation of Sequence-Defined Oligomers Based on Natural Amino Acids and Synthetic Building Blocks." In ACS Symposium Series, 103–16. Washington, DC: American Chemical Society, 2014. http://dx.doi.org/10.1021/bk-2014-1170.ch007.
Повний текст джерелаSaito, Nozomi. "Synthesis of Ethynylhelicene Oligomers." In Springer Theses, 7–10. Tokyo: Springer Japan, 2013. http://dx.doi.org/10.1007/978-4-431-54514-9_2.
Повний текст джерелаKudaibergenov, Sarkyt, Werner Jaeger, and Andre Laschewsky. "Polymeric Betaines: Synthesis, Characterization, and Application." In Supramolecular Polymers Polymeric Betains Oligomers, 157–224. Berlin, Heidelberg: Springer Berlin Heidelberg, 2006. http://dx.doi.org/10.1007/12_078.
Повний текст джерелаТези доповідей конференцій з теми "Synthetic Oligomers"
Kim, Y. H., F. Li, and H. Zimmer. "Charged states of thiophene oligomers." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.834786.
Повний текст джерелаPoplawski, J., E. Ehrenfreund, R. Pugh, M. Ibrahim, A. J. Frank, J. Cornil, and J. L. Bredas. "Photogeneration of polarons in sexithiophene oligomers." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.834699.
Повний текст джерелаMatsuda, N., T. Shimura, K. Aramaki, and H. Nishihara. "Synthesis of soluble cobaltacyclopentadiene oligomers and polymers." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835311.
Повний текст джерелаRobins, K. A., S. J. Kim, J. L. Toto, M. Hasan, T. T. Toto, C. P. de Melo, and B. Kirtman. "Ab-initio nonlinear optical properties of finite polyacetylene oligomers." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.836119.
Повний текст джерелаFichou, D., J. M. Nunzi, F. Charra, and N. Pfeffer. "Molecular engineering of thiophene oligomers for efficient spatial light modulation." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835674.
Повний текст джерелаde Leeuw, D. M., and E. J. Lous. "Metal-insulator-semiconductor Schottky-type diodes of doped thiophene oligomers." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.836009.
Повний текст джерелаGraupner, W., S. Eder, M. Mauri, G. Leising, W. Fischer, and F. Stelzer. "Excited states in conjugated polymers and oligomers probed by photinduced absorption." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835200.
Повний текст джерелаXjangli Wu, J. P. Parakka, Yeon-Taik Kim, M. P. Cava, and R. M. Metzger. "Molecular ordering in scanning tunneling micrographs of thiophene-alkylpyrrole oligomers on graphite." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835399.
Повний текст джерелаCornil, J., D. A. dos Santos, D. Beljonne, R. Lazzaroni, and U. Bredas. "Theoretical investigation of the electronic structure of donor/acceptor substituted phenylene vinylene oligomers." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835221.
Повний текст джерелаUnderhill, A. E., C. A. S. Hill, A. Charlton, S. Oliver, and S. Kershami. "Third order NLO properties of PMMA films co-dispersed with metal dithiolene oligomers." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835741.
Повний текст джерелаЗвіти організацій з теми "Synthetic Oligomers"
Feng, J., W. Zhang, A. G. MacDiarmid, and A. J. Epstein. Synthesis and Characterization of Oligomeric Anilines. Fort Belvoir, VA: Defense Technical Information Center, September 1997. http://dx.doi.org/10.21236/ada330138.
Повний текст джерелаFreeman, J. In vitro synthesis and purification of PhIP-deoxyguanosine and PhIP-DNA oligomer covalent complexes. Office of Scientific and Technical Information (OSTI), December 1994. http://dx.doi.org/10.2172/98639.
Повний текст джерелаStone, Rebecca L., Joseph M. Mabry, and Timothy S. Haddad. Synthesis and Characterization of Long-Chain Fluorinated Polyhedral Oligomeric Silsesquioxane (F-POSS). Fort Belvoir, VA: Defense Technical Information Center, October 2010. http://dx.doi.org/10.21236/ada533419.
Повний текст джерела