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Статті в журналах з теми "Supramolecular organic chemistry"
Sherburn, Michael. "Introduction to Supramolecular Chemistry By Helena Dodziuk." Australian Journal of Chemistry 55, no. 5 (2002): 357. http://dx.doi.org/10.1071/ch02004_br.
Повний текст джерелаBose, Anima, and Prasenjit Mal. "Mechanochemistry of supramolecules." Beilstein Journal of Organic Chemistry 15 (April 12, 2019): 881–900. http://dx.doi.org/10.3762/bjoc.15.86.
Повний текст джерелаHr. "Supramolecular Chemistry." Journal of Molecular Structure 274 (November 1992): 315. http://dx.doi.org/10.1016/0022-2860(92)80171-d.
Повний текст джерелаSerpe, Michael J., and Stephen L. Craig. "Physical Organic Chemistry of Supramolecular Polymers." Langmuir 23, no. 4 (February 2007): 1626–34. http://dx.doi.org/10.1021/la0621416.
Повний текст джерелаGasparini, Giulio, Eun-Kyoung Bang, Javier Montenegro, and Stefan Matile. "Cellular uptake: lessons from supramolecular organic chemistry." Chemical Communications 51, no. 52 (2015): 10389–402. http://dx.doi.org/10.1039/c5cc03472h.
Повний текст джерелаJolliffe, Katrina (Kate) A., and Philip A. Gale. "The supramolecular chemistry of anions." Organic & Biomolecular Chemistry 20, no. 4 (2022): 713–14. http://dx.doi.org/10.1039/d1ob90183d.
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 джерелаSaji, Viswanathan S. "Supramolecular concepts and approaches in corrosion and biofouling prevention." Corrosion Reviews 37, no. 3 (June 26, 2019): 187–230. http://dx.doi.org/10.1515/corrrev-2018-0105.
Повний текст джерелаHaino, Takeharu. "Supramolecular Chemistry: From Host-guest Complexes to Supramolecular Polymers." Journal of Synthetic Organic Chemistry, Japan 71, no. 11 (2013): 1172–81. http://dx.doi.org/10.5059/yukigoseikyokaishi.71.1172.
Повний текст джерелаLi, Zhan-Ting. "Supramolecular chemistry: from aromatic foldamers to solution-phase supramolecular organic frameworks." Beilstein Journal of Organic Chemistry 11 (November 2, 2015): 2057–71. http://dx.doi.org/10.3762/bjoc.11.222.
Повний текст джерелаДисертації з теми "Supramolecular organic chemistry"
Skabara, Peter John. "Functionalised tetrathiafulvalenes in supramolecular chemistry." Thesis, Durham University, 1994. http://etheses.dur.ac.uk/10491/.
Повний текст джерелаRather, Elisabeth. "Supramolecular metal-organic and organic materials." [Tampa, Fla.] : University of South Florida, 2004. http://purl.fcla.edu/fcla/etd/SFE0000267.
Повний текст джерелаRoshandel, Sahar. "Supramolecular devices as selective receptors." Thesis, California State University, Long Beach, 2015. http://pqdtopen.proquest.com/#viewpdf?dispub=1597789.
Повний текст джерелаWe have found that calixarenes are good receptors of choline (trimethylammonium group) and they have strong affinity to form host-guest complexes with a variety of molecules carrying this moiety. Furthermore, the ability of lower rim carboxylic acid calix[n]arenes and upper rim phosphonic acid functionalized calix[4]arene to transport choline-conjugated drugs through a liquid membrane was discovered. The results demonstrate that these systems are highly efficient toward transporting choline-conjugated targets, as well as neurotransmitters that possess ionizable amine termini. The breadth of compounds that are transported is significant, facing limitations only when the payloads become extremely lipophilic. These developments reveal new approaches towards attempting synthetic receptor mediated selective small molecule transport in vesicular and cellular systems.
Sisson, Thomas Michael 1966. "Crosslinking polymerization in supramolecular assemblies." Diss., The University of Arizona, 1997. http://hdl.handle.net/10150/282566.
Повний текст джерелаChilds, Laura Jennifer. "Supramolecular assemblies based on imine and azo chemistry." Thesis, University of Warwick, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.269076.
Повний текст джерелаYoung, Michael Christopher. "Self-Assembly of Functionalized Supramolecular Structures." Thesis, University of California, Riverside, 2014. http://pqdtopen.proquest.com/#viewpdf?dispub=3644049.
Повний текст джерелаEnzymes are capable of exquisite selectivity in catalysis chemical reactions because of a well-evolved mechanism that binds substrates in internal active sites based on size and shape complementarity. The cavities of these enzymes are decorated with organic or inorganic groups which can promote reactivity once the substrate is non-covalently bound. Synthetic molecular hosts to date have been able to bind to substrates in a similar, biomimetic fashion, but functionalized molecular hosts are still virtually unknown.
One convenient way to prepare molecular hosts is by the self-assembly of organic coordinating ligands with suitable metal salts. The reversible dative bonds holding these cage structures together allow incorrect products to break apart and reform, favoring creation of the most thermodynamically stable product. This leads to discrete, solution phase cages that can function as cavity-containing hosts. Some of these hosts have shown efficacy as catalysts for pericyclic reactions due to favorable transition states of the bound substrates. These cages, however, fail to orient reactive functional groups into their interiors. Truly biomimetic cages will require modifying traditional self-assembled targets to incorporate these reactive functionalities.
This work explores the self-assembly of metal-organic cages displaying covalent modifications on their interior. Incorporation of unreactive and poorly reactive groups was found to have a significant impact on the outcome of the self-assembly process. Cages with endohedral alcoholic functionality were found to have different binding properties than unfunctionalized analogs. Cages with introverted alcohol groups were also exploited for their ability to self-catalyze reactions on the interior of the hosts. The metal vertices themselves could also be used as functional groups, and showed the ability to sense neutral analytes in hybrid dative/hydrogen bonded self-assemblies.
Lee, Youn-Sik. "Supramolecular assemblies of polymerizable phospholipids." Diss., The University of Arizona, 1992. http://hdl.handle.net/10150/185929.
Повний текст джерелаFrankel, David Alan. "Supramolecular assemblies of diacetylenic amphiphiles." Diss., The University of Arizona, 1993. http://hdl.handle.net/10150/186384.
Повний текст джерелаLin, Xiang. "The supramolecular chemistry of metal-organic coordination oligomers and polymers." Thesis, University of Nottingham, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.416395.
Повний текст джерелаBarker, Philip. "The introduction of supramolecular architectures into macromolecular arrays." Thesis, University of Warwick, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.250967.
Повний текст джерелаКниги з теми "Supramolecular organic chemistry"
L, Atwood J., ed. Comprehensive supramolecular chemistry. Oxford: Pergamon, 1996.
Знайти повний текст джерелаSiegel, Jay S. Supramolecular Stereochemistry. Dordrecht: Springer Netherlands, 1995.
Знайти повний текст джерелаTsoucaris, George. Current Challenges on Large Supramolecular Assemblies. Dordrecht: Springer Netherlands, 1999.
Знайти повний текст джерелаL, Atwood J., Szejtli József, and Osa Tetsuo, eds. Comprehensive supramolecular chemistry. Oxford: Pergamon, 1996.
Знайти повний текст джерелаWipff, Georges. Computational Approaches in Supramolecular Chemistry. Dordrecht: Springer Netherlands, 1994.
Знайти повний текст джерела1935-, Schneider Hans-Jörg, and Dürr Heinz, eds. Frontiers in supramolecular organic chemistry and photochemistry. Weinheim, Federal Republic of Germany: VCH, 1991.
Знайти повний текст джерелаPifat-Mrzljak, Greta. Supramolecular Structure and Function. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986.
Знайти повний текст джерелаK, Yatsimirsky Anatoly, ed. Principles and methods in supramolecular chemistry. New York: Wiley, 2000.
Знайти повний текст джерелаMacrocyclic chemistry: Aspects of organic and inorganic supramolecular chemistry. Weinheim: VCH, 1993.
Знайти повний текст джерелаSchalley, Christoph A. Analytical methods in supramolecular chemistry. Weinheim: Wiley-VCH, 2007.
Знайти повний текст джерелаЧастини книг з теми "Supramolecular organic chemistry"
Sun, Wei-Yin, Zheng-Shuai Bai, and Jin-Quan Yu. "Supramolecular Chemistry of Silver." In Silver in Organic Chemistry, 329–55. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470597521.ch11.
Повний текст джерелаCraig, Stephen L., and Donghua Xu. "Physical Organic Chemistry of Supramolecular Polymers." In Supramolecular Polymer Chemistry, 269–91. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639786.ch12.
Повний текст джерелаBerscheid, R., I. Lüer, C. Seel, and F. Vögtle. "Molecules with Large Cavities -Selective Complexation of Inorganic and Organic Guests." In Supramolecular Chemistry, 71–86. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2492-8_5.
Повний текст джерелаSchoedel, Alexander, and Omar M. Yaghi. "Porosity in Metal-Organic Compounds." In Macrocyclic and Supramolecular Chemistry, 200–219. Chichester, UK: John Wiley & Sons, Ltd, 2016. http://dx.doi.org/10.1002/9781119053859.ch9.
Повний текст джерелаLi, Zhan-Ting, Peter J. Stang, Liang Zhao, Mei-Xiang Wang, and Chen-Ho Tung. "Supramolecular Organic Chemistry: The Foldamer Approach." In Organic Chemistry - Breakthroughs and Perspectives, 477–535. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527664801.ch13.
Повний текст джерелаSugiyasu, Kazunori, and Seiji Shinkai. "Supra-Macromolecular Chemistry: Toward Design of New Organic Materials from Supramolecular Standpoints." In Supramolecular Polymer Chemistry, 51–70. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527639786.ch3.
Повний текст джерелаAriga, Katsuhiko, Gary J. Richards, Jonathan P. Hill, Ajayan Vinu, and Toshiyuki Mori. "Supramolecular Chemistry at the Mesoscale." In The Supramolecular Chemistry of Organic-Inorganic Hybrid Materials, 11–36. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470552704.ch2.
Повний текст джерелаVančik, Hrvoj. "Organic Supramolecular and Supermolecular Structures." In Basic Organic Chemistry for the Life Sciences, 187–96. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-92438-6_12.
Повний текст джерелаHathwar, Venkatesha R. "CHAPTER 5. Experimental Charge Density Analysis in Organic Solids." In Monographs in Supramolecular Chemistry, 159–88. Cambridge: Royal Society of Chemistry, 2018. http://dx.doi.org/10.1039/9781788013086-00159.
Повний текст джерелаAakeröy, Christer B., and Kanishka Epa. "Controlling Supramolecular Assembly Using Electronic Effects." In Electronic Effects in Organic Chemistry, 125–47. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/128_2011_155.
Повний текст джерелаТези доповідей конференцій з теми "Supramolecular organic chemistry"
Tato, José, Mercedes Alcalde, Aida Jover, Francisco Meijide, Luciano Galantini, Nicolae Pavel, and Alvaro Antelo. "Host-Guest Supramolecular Dendrimers." In The 11th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01357.
Повний текст джерелаAntelo, Alvaro, Mercedes Alcalde, Aida Jover, Francisco Meijide, Luciano Galantini, and José Tato. "Supramolecular polymer formed by ditopic cyclodextrin and ditopic adamantane derivatives." In The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01270.
Повний текст джерелаNovo, Mercedes, and Wajih Al-Soufi. "Fluorescence Study of the Supramolecular Interactions between Coumarins and Serum Albumin." In The 11th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01358.
Повний текст джерелаMargetic, Davor, Douglas Butler, and Ronald Warrener. "Theoretical Study of Bis-Porphyrin-Fullerene Supramolecular Complex Designed for Photovoltaic Devices." In The 9th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01646.
Повний текст джерелаNovo, Mercedes, Jorge Bordello, Daniel Granadero, Sonia Freire, and Wajih Al-Soufi. "Supramolecular host-guest complexes between coumarin 460 and cyclodextrins: a matter of size." In The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01267.
Повний текст джерелаIsz, S., Maria-Victoria Martinez, S. Palacin, H. Perez, and A. Ruaudel-Teixier. "New molecules for supramolecular architecture in Langmuir-Blodgett films." In The proceedings of the 53rd international meeting of physical chemistry: Organic coatings. AIP, 1996. http://dx.doi.org/10.1063/1.49435.
Повний текст джерелаMoral, M., A. de la Hoz, and A. Sánchez-Migallón. "Microwave Assisted Organic Synthesis of 1,3,5-triazine Dimmers with Their Application in Supramolecular Chemistry." In The 9th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01638.
Повний текст джерелаHagar, Mohamed E., and Hoda Ahmed. "Experimental and theoretical approaches of new nematogenic chair architectures of supramolecular H-bonded liquid crystals." In The 23rd International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2019. http://dx.doi.org/10.3390/ecsoc-23-06713.
Повний текст джерелаRomero, María J., Luis M. González-Barcia, Manuel R. Bermejo, M. Isabel Fernández, and Esther Gómez-Fórneas. "Supramolecular self-assembly of a symmetric imine ligand functionalized with a dansyl fluorophore moiety." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-d002.
Повний текст джерелаAl-Soufi, Wajih, Mercedes Novo, Belén Reija, and Claus Seidel. "Fluorescence Correlation Spectroscopy as a Tool for the Study of the Dynamics of Supramolecular and Organized Systems." In The 9th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2005. http://dx.doi.org/10.3390/ecsoc-9-01651.
Повний текст джерела