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Статті в журналах з теми "Supramolecular Self-assembly - Molecules"
BÖHRINGER, MATTHIAS, WOLF-DIETER SCHNEIDER, and RICHARD BERNDT. "TWO-DIMENSIONAL SELF-ASSEMBLY OF SUPRAMOLECULAR STRUCTURES." Surface Review and Letters 07, no. 05n06 (October 2000): 661–66. http://dx.doi.org/10.1142/s0218625x00000749.
Повний текст джерелаJana, Achintya, Puneet Mishra, and Neeladri Das. "Polymorphic self-assembly of pyrazine-based tectons at the solution–solid interface." Beilstein Journal of Nanotechnology 10 (February 18, 2019): 494–99. http://dx.doi.org/10.3762/bjnano.10.50.
Повний текст джерелаJames, Tony D. "Self and directed assembly: people and molecules." Beilstein Journal of Organic Chemistry 12 (March 1, 2016): 391–405. http://dx.doi.org/10.3762/bjoc.12.42.
Повний текст джерелаSaini, Ankita, and K. R. Justin Thomas. "Bis-naphthalimides bridged by electron acceptors: optical and self-assembly characteristics." RSC Advances 6, no. 75 (2016): 71638–51. http://dx.doi.org/10.1039/c6ra12776b.
Повний текст джерелаOkamoto, Ken, Parayalil Chithra, Gary Richards, Jonathan Hill, and Katsuhiko Ariga. "Self-Assembly of Optical Molecules with Supramolecular Concepts." International Journal of Molecular Sciences 10, no. 5 (April 27, 2009): 1950–66. http://dx.doi.org/10.3390/ijms10051950.
Повний текст джерелаGao, Yuxi, Jun Hu, and Yong Ju. "Supramolecular Self-Assembly Based on Natural Small Molecules." Acta Chimica Sinica 74, no. 4 (2016): 312. http://dx.doi.org/10.6023/a16010016.
Повний текст джерелаMi, Yong Sheng, Zhou Yang, Dong Wang, Peng Xia Liang, and Zhao Kui Jin. "Self-Assembly Micro-Nanostructures of Discotic Organic Molecules." Applied Mechanics and Materials 331 (July 2013): 567–71. http://dx.doi.org/10.4028/www.scientific.net/amm.331.567.
Повний текст джерелаHaino, Takeharu, Ryo Sekiya, Kentaro Harada, and Natsumi Nitta. "Resorcinarene-Based Supramolecular Capsules: Supramolecular Functions and Applications." Synlett 33, no. 06 (October 27, 2021): 518–30. http://dx.doi.org/10.1055/a-1679-8141.
Повний текст джерелаJIANG, DANFENG, YAN LU, JIE LING, XINLI LENG, XIAOQING LIU, and LI WANG. "CHIRAL SUPRAMOLECULAR SELF-ASSEMBLY OF 2,2’:6’,2”-TERPYRIDINE-4’-CARBOXYLIC ACID MOLECULES CHEMICALLY ADSORBED ON Cu(111)." Surface Review and Letters 23, no. 06 (November 17, 2016): 1650061. http://dx.doi.org/10.1142/s0218625x1650061x.
Повний текст джерелаWang, Jing, Xueliang Wang, Kai Yang, Sijun Hu, and Wanhe Wang. "Self-Assembly of Small Organic Molecules into Luminophores for Cancer Theranostic Applications." Biosensors 12, no. 9 (August 25, 2022): 683. http://dx.doi.org/10.3390/bios12090683.
Повний текст джерелаДисертації з теми "Supramolecular Self-assembly - Molecules"
Jin, Lun. "Synthesis and Self-assembly of Planar Giant Molecules Based on Polyhedral Oligomeric Silsesquioxanes(POSS)." University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1490653139392999.
Повний текст джерелаSmykalla, Lars. "Investigation of the supramolecular self-assembly, electronic properties, and on-surface reactions of porphyrin and phthalocyanine molecules." Doctoral thesis, Universitätsbibliothek Chemnitz, 2017. http://nbn-resolving.de/urn:nbn:de:bsz:ch1-qucosa-216602.
Повний текст джерелаWang, Yongfeng. "SYNTHESIS AND STRUCTURE-PROPERTY STUDIES OF ORGANIC MATERIALS CONTAINING FLUORINATED AND NON-FLUORINATED # SYSTEMS (SMALL MOLECULES AND POLYMERS)." UKnowledge, 2008. http://uknowledge.uky.edu/gradschool_diss/593.
Повний текст джерелаZhang, Ruimeng. "Design, Synthesis, and Self-assembly of Dendritic Rod-like Molecules with Precisely Controlled Compositions, Interactions, and Topologies." University of Akron / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron157231026041301.
Повний текст джерелаBorder, Sarah Elaine Border. "Light Responsive Molecular Baskets." The Ohio State University, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1543329849092005.
Повний текст джерелаSmykalla, Lars [Verfasser], Michael [Akademischer Betreuer] Hietschold, Michael [Gutachter] Hietschold, and Thomas [Gutachter] Seyller. "Investigation of the supramolecular self-assembly, electronic properties, and on-surface reactions of porphyrin and phthalocyanine molecules / Lars Smykalla ; Gutachter: Michael Hietschold, Thomas Seyller ; Betreuer: Michael Hietschold." Chemnitz : Universitätsbibliothek Chemnitz, 2017. http://d-nb.info/1214648851/34.
Повний текст джерелаBofinger, Robin. "Photocontrolled biomimetic communication between molecules and nanosystems in confined compartments." Thesis, Bordeaux 1, 2013. http://www.theses.fr/2013BOR14933/document.
Повний текст джерелаThe thesis focuses on the study and design of novel photoactive molecules and their application as labeling agents, fluorescent molecular Ca2+-sensors and photolabile Ca2+-decaging agents in aqueous media and organized supramolecular assemblies. The designed fluorophores are based on boron-dipyrromethene (BODIPY) bearing hydrophobic chains or a reactive group like an azide or a perfluorophenyl moiety. Biocompatible calcium receptors have been prepared harnessing the fluorescence properties of BODIPY, naphthalimide and furan fluorophores. The development of self-assembled multicompartmentalized architectures, namely fluorocarbon vesicles in giant polymersomes is reported and the system has been used to create white light emission in confined microdomains. The Ca2+-based ion transfer ion the confined polymer compartments between individual fluorinated vesicles has been studied. The ion transfer in between vesicles in polymer microcompartments has been established as an artificial prototype system for cellular communication
Iden, Hassan. "From molecular tweezers to metallocavitands : self-assembly and supramolecular chemistry." Thesis, Université Laval, 2014. http://www.theses.ulaval.ca/2014/30840/30840.pdf.
Повний текст джерелаThis thesis described the synthesis of organic and organometallic hosts containing electron rich units in particularly tetrathiafulvalene (TFF) to bind fullerenes C60 and C70. Chapter two illustrates the different analysis techniques used in this thesis. Chapter three described new method for the synthesis of tweezers-like TTF and tripodal TTF molecules in addition to their binding affinity towards fullerenes C60 and C70. The tweezers-like TTF were prepared by click chemistry from azide-TTF and 1,3 substituted benzene. Similarly, the reaction of azide-TTF and 1,3, 5 substituted benzene yielded the tripodal-TTF receptor. The affinity toward fullerenes C60 and C70 were studied in four different solvents. The highest binding constant was calculated for host 4 in chlorobenzene toward fullerene C70. Moreover, solvent dependant behavior was observed with the studied host. However, the tripodal receptor did not showed significant affintity towards fullerenes. Chapter four described the synthesis of new TTF-Zr3 metallocavitand by coordination method; two hosts were isolated and characterized. In this chapter we present the binding study toward fullerenes by monitoring the UV-vis response to increasing amount of fullerenes added to the solution of the host. Chapter five described the synthesis of new Zr3 metallocavitand in one pot reaction from the reaction of zirconocene dichloride with carboxylic acid in aqueous media. Four Zr3 metallocavitand were prepared and the crystallography was presented in addition to the photophysical properties and their potential uses as blue emissive materials. The last chapter is separated into three sections. The first section described our early work on tantalum (V) metallocavitand in addition to their hosting capability toward fullerenes. The second section illustrate the tentative has been committed to the design and synthesis of Zr3 library using cross-coupling reaction in addition to the synthesis of extended Zr3-cinnamate metallocavitand. Lastly, the last section illustrates the synthesis of new Ta3-Carbox achieved by aggregation method from reaction of Cp*TaMe4 with 4-iodobenzoic acid. The single X-ray structure revealed a new structure with trimetallic core comparable to the core observed for tantalum metallocavitand.
Morris, Kyle. "The assembly and structure of self-assembling peptides : molecular to supramolecular." Thesis, University of Sussex, 2012. http://sro.sussex.ac.uk/id/eprint/39707/.
Повний текст джерелаBludin, Alexey O. "Peptide-Porphyrin Self-Assembled Materials." Bowling Green State University / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1308097842.
Повний текст джерелаКниги з теми "Supramolecular Self-assembly - Molecules"
Frédéric, Fages, and Araki K, eds. Low molecular mass gelators: Design, self-assembly, function. Berlin: Springer, 2005.
Знайти повний текст джерелаFrederic, Fages, and Araki K, eds. Low molecular mass gelators: Design, self-assembly, function. Berlin: Springer, 2005.
Знайти повний текст джерелаM, Rotello Vincent, and Thayumanavan Sankaran, eds. Molecular recognition and polymers: Control of polymer structure and self-assembly. Hoboken, N.J: Wiley, 2008.
Знайти повний текст джерелаLindoy, L. F., and I. M. Atkinson. Self-Assembly in Supramolecular Systems (Monographs in Supramolecular Chemistry). Royal Society of Chemistry, 2001.
Знайти повний текст джерелаFages, Frederic. Low Molecular Mass Gelators: Design, Self-Assembly, Function. Springer Berlin / Heidelberg, 2010.
Знайти повний текст джерелаFages, Frederic. Low Molecular Mass Gelators : Design, Self-Assembly, Function (Topics in Current Chemistry) (Topics in Current Chemistry). Springer, 2005.
Знайти повний текст джерелаFujita, Makoto. Molecular Self-Assembly: Organic Versus Inorganic Approaches. Springer, 2013.
Знайти повний текст джерелаMolecular Self-Assembly: Organic Versus Inorganic Approaches. Springer, 2000.
Знайти повний текст джерелаFujita, Makoto. Molecular Self-Assembly: Organic Versus Inorganic Approaches. Springer London, Limited, 2003.
Знайти повний текст джерелаЧастини книг з теми "Supramolecular Self-assembly - Molecules"
Li, Sheng-Hua, Yong Chen, and Yu Liu. "Mechanically Self-Locked Molecules." In Handbook of Macrocyclic Supramolecular Assembly, 83–106. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-2686-2_5.
Повний текст джерелаLi, Sheng-Hua, Yong Chen, and Yu Liu. "Mechanically Self-Locked Molecules." In Handbook of Macrocyclic Supramolecular Assembly, 1–25. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1744-6_5-1.
Повний текст джерелаYang, Ji, Jean-Luc Marendez, Abdullah Zafar, Steven J. Geib, and Andrew D. Hamilton. "Hydrogen Bonding Control of Molecular Self-Assembly." In Supramolecular Stereochemistry, 141–46. Dordrecht: Springer Netherlands, 1995. http://dx.doi.org/10.1007/978-94-011-0353-4_16.
Повний текст джерелаBissell, Richard A., and J. Fraser Stoddart. "Molecular and Supramolecular Self-Assembly Processes." In Computations for the Nano-Scale, 141–52. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1956-6_11.
Повний текст джерелаLin, Xiankun, Zhiguang Wu, and Qiang He. "Controlled Molecular Assembly Toward Self-propelled Micro-/Nanomotors." In Supramolecular Chemistry of Biomimetic Systems, 259–81. Singapore: Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-6059-5_11.
Повний текст джерелаBrand, Guy, Mir Wais Hosseini, Olivier Félix, Patrick Schaeffer, and Romain Ruppert. "Molecular Tectonics: Self-Assembly of Charged Molecular Tectons into One- and Two-Dimensional Solids." In Magnetism: A Supramolecular Function, 129–42. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-015-8707-5_8.
Повний текст джерелаBecher, Jan, Zhan-Ting Li, Philippe Blanchard, Niels Svenstrup, Jesper Lau, Mogens Brøndsted Nielsen, and Klaus B. Simonsen. "Tetrathiafulvalenes in Macrocyclic and Supramolecular Chemistry: Self Assembly with Tetrathiafulvalenes." In Molecular Recognition and Inclusion, 85–95. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4_9.
Повний текст джерелаKrische, Michael J., and Jean-Marie Lehn. "The Utilization of Persistent H-Bonding Motifs in the Self-Assembly of Supramolecular Architectures." In Molecular Self-Assembly Organic Versus Inorganic Approaches, 3–29. Berlin, Heidelberg: Springer Berlin Heidelberg, 2000. http://dx.doi.org/10.1007/3-540-46591-x_1.
Повний текст джерелаTiekink, Edward R. T., and Ionel Haiduc. "Stereochemical Aspects of Metal Xanthate Complexes: Molecular Structures and Supramolecular Self-Assembly." In Progress in Inorganic Chemistry, 127–319. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471725560.ch3.
Повний текст джерелаBaroncini, Massimo. "Self-Assembly of Calix[6]arene-Diazapyrenium Pseudorotaxanes: Interplay of Molecular Recognition and Ion-Pairing Effects." In Design, Synthesis and Characterization of new Supramolecular Architectures, 55–70. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-19285-2_6.
Повний текст джерелаТези доповідей конференцій з теми "Supramolecular Self-assembly - Molecules"
Li, DeQuan, Xiaoguang Yang, and Duncan McBranch. "Molecular Architectural Approaches to Nonlinear Optical Materials." In Nonlinear Optics: Materials, Fundamentals and Applications. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/nlo.1996.nthe.12.
Повний текст джерелаPark, Jiyong, Byungnam Kahng та Wonmuk Hwang. "Supramolecular Structure and Stability of the GNNQQNY β-Sheet Bilayer Filament: A Computational Study". У ASME 2007 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2007. http://dx.doi.org/10.1115/sbc2007-175588.
Повний текст джерелаDrzewiecki, Kathryn, Ian Gaudet, Douglas Pike, Jonathan Branch, Vikas Nanda, and David Shreiber. "Temperature Dependent Reversible Self Assembly of Methacrylated Collagen Gels." In ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14705.
Повний текст джерелаChen, S. G., X. D. Chai, Y. W. Cao, R. Lu, Y. Y. Zhao, Y. S. Jiang, and T. J. Li. "Formation of non-centrosymmetric supramolecular structure by hydrogen-bonding control of molecular self-assembly." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835777.
Повний текст джерелаCha, J. M., D. G. Won, E. H. Jeong, T. Arakawa, S. Shoji, K. C. Kim, J. S. Boo, and J. S. Go. "Application of In-Channel Micro Chemical Plant to the Production of Functional Microcapsules." In ASME 2007 International Mechanical Engineering Congress and Exposition. ASMEDC, 2007. http://dx.doi.org/10.1115/imece2007-41795.
Повний текст джерелаDemangeat, Catherine, Yixuan Dou, Bin Hu, Yann Bretonniere, Chantal Andraud, Anthony D'Aleo, Jeong Weon Wu, Eunkyoung Kim, Tangui Le Bahers, and André-Jean Attias. "Rational design of metal-free organic chromophores to form efficient room temperature persistent luminescent molecular crystals via H-bond-directed supramolecular self-assembly." In Organic and Hybrid Light Emitting Materials and Devices XXV, edited by Tae-Woo Lee, Franky So, and Chihaya Adachi. SPIE, 2021. http://dx.doi.org/10.1117/12.2594420.
Повний текст джерелаDemangeat, Catherine, Yixuan Dou, Bin Hu, Yann Bretonniere, Chantal Andraud, Anthony D'Aleo, Jeong Weon Wu, Eunkyoung Kim, Tangui Le Bahers, and André-Jean Attias. "Rational design of metal-free organic chromophores to form efficient long-lived room-temperature phosphorescent molecular crystals via H-bond-directed supramolecular self-assembly." In Organic Photonic Materials and Devices XXIII, edited by Ileana Rau, Okihiro Sugihara, and William M. Shensky. SPIE, 2021. http://dx.doi.org/10.1117/12.2576848.
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