Gotowa bibliografia na temat „Cyclophanes”
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Artykuły w czasopismach na temat "Cyclophanes"
Rajakumar, Perumal, i Ramar Padmanabhan. "Synthesis, Anti-Arthritic, and Anti-Inflammatory Activity of N-Tosyl aza Cyclophanes". Australian Journal of Chemistry 65, nr 2 (2012): 186. http://dx.doi.org/10.1071/ch11435.
Pełny tekst źródłaMageed, Ahmed Hassoon, i Karrar Al-Ameed. "Synthesis, structural studies and computational evaluation of cyclophanes incorporating imidazole-2-selones". RSC Advances 13, nr 25 (2023): 17282–96. http://dx.doi.org/10.1039/d3ra02913a.
Pełny tekst źródłaRühe, Jessica, David Bialas, Peter Spenst, Ana-Maria Krause i Frank Würthner. "Perylene Bisimide Cyclophanes: Structure–Property Relationships upon Variation of the Cavity Size". Organic Materials 02, nr 02 (kwiecień 2020): 149–58. http://dx.doi.org/10.1055/s-0040-1709998.
Pełny tekst źródłaZhang, Xing-Xing, Jian Li i Yun-Yin Niu. "A Review of Crystalline Multibridged Cyclophane Cages: Synthesis, Their Conformational Behavior, and Properties". Molecules 27, nr 20 (20.10.2022): 7083. http://dx.doi.org/10.3390/molecules27207083.
Pełny tekst źródłaKotha, Sambasivarao, Mukesh Eknath Shirbhate i Gopalkrushna T. Waghule. "Selected synthetic strategies to cyclophanes". Beilstein Journal of Organic Chemistry 11 (29.07.2015): 1274–331. http://dx.doi.org/10.3762/bjoc.11.142.
Pełny tekst źródłaJabłoński, Mirosław. "Determining Repulsion in Cyclophane Cages". Molecules 27, nr 13 (21.06.2022): 3969. http://dx.doi.org/10.3390/molecules27133969.
Pełny tekst źródłaVermeij, Rudolf J., David O. Miller, Louise N. Dawe, Ivan Aprahamian, Tuvia Sheradsky, Mordecai Rabinovitz i Graham J. Bodwell. "Mixed [2.2]Cyclophanes of Pyrene and Benzene". Australian Journal of Chemistry 63, nr 12 (2010): 1703. http://dx.doi.org/10.1071/ch10356.
Pełny tekst źródłaSalazar-Medina, Alex J., Enrique F. Velazquez-Contreras, Rocio Sugich-Miranda, Hisila Santacruz, Rosa E. Navarro, Fernando Rocha-Alonzo, Maria A. Islas-Osuna i in. "Immune response of human cultured cells towards macrocyclic Fe2PO and Fe2PC bioactive cyclophane complexes". PeerJ 8 (20.04.2020): e8956. http://dx.doi.org/10.7717/peerj.8956.
Pełny tekst źródłaBenniston, Andrew C., Philip R. Mackie, Louis J. Farrugia, Simon Parsons, William Clegg i Simon J. Teat. "Metallo-Based Cyclophanes and [2]Catenanes". Platinum Metals Review 42, nr 3 (1.07.1998): 100–105. http://dx.doi.org/10.1595/003214098x423100105.
Pełny tekst źródłaPatel, Suraj, Tyson N. Dais, Paul G. Plieger i Gareth J. Rowlands. "Breaking paracyclophane: the unexpected formation of non-symmetric disubstituted nitro[2.2]metaparacyclophanes". Beilstein Journal of Organic Chemistry 17 (29.06.2021): 1518–26. http://dx.doi.org/10.3762/bjoc.17.109.
Pełny tekst źródłaRozprawy doktorskie na temat "Cyclophanes"
Turner, Peter D. "Organic materials for nonlinear optics /". Title page, contents and abstract only, 1999. http://web4.library.adelaide.edu.au/theses/09PH/09pht951.pdf.
Pełny tekst źródłaRobbins, Steven Joseph, i University of Lethbridge Faculty of Arts and Science. "Cyclophanes from kinetically stabilized bis(isobenzofuran)s". Thesis, Lethbridge, Alta. : University of Lethbridge, Deptartment of Chemistry and Biochemistry, 2009, 2009. http://hdl.handle.net/10133/781.
Pełny tekst źródłaxxii, 122 leaves : ill. ; 29 cm.
Arifhodzic, Lejla. "Novel bis-quinolinium cyclophanes as SKca channel blockers". Thesis, University College London (University of London), 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.248484.
Pełny tekst źródłaRichard, Jimmy. "Cyclophanes de viologènes adressables pour stockage de charges". Thesis, Strasbourg, 2019. http://www.theses.fr/2019STRAF021.
Pełny tekst źródłaStoring data on a molecule is a fundamental challenge in developing a system that can store a large amount of data in a minimum of space. The project of this thesis is part of this theme, namely the design of molecular switches oscillating by redox stimuli and being readable without altering the different states to allow the creation of molecular memory. The bis-viologen cyclophanes are therefore potential candidates for the creation of information storage devices that could be reversibly written and read in many ways thanks to the magnetic, optical and conductive properties of the π-dimer. The first chapter of this thesis is devoted to an introduction to the chemistry of cyclophanes and the use of surfaces in the chemistry of cyclophanes and molecular switches. The second chapter deals with the synthesis of viologenes and bis-viologen cyclophanes. The third chapter is devoted to the synthesis of diazapyrenium-viologenes cyclophanes, possible alternatives for bis-viologen cyclophanes
Auffray, Morgan. "Cyclophanes, a bridge between photophysics and supramolecular chemistry". Thesis, Paris 6, 2017. http://www.theses.fr/2017PA066285/document.
Pełny tekst źródłaIn this work and due to their unique electronic properties, 3D-dithia[3.3]paracyclophane-based molecules have been studied for surface nanostructuration applications and as new fluorophore. First, the supramolecular self-assembly of molecules is used to create well-organised 2D-networks on conducting surfaces. However, the use of such substrates tends to quench any electronic properties of the adsorbed molecules. In this context, 3D-dithia[3.3]paracyclophane-based molecules were employed to lift up the active moiety from the surface. In this work, new pyridyl end-capped molecules were designed to self-assemble on any substrate. Preliminary characterisations were performed to study the supramolecular self-assembly of such molecules alone or with co-adsorbers, and the first images of organised 2D-networks on graphite and gold have been obtained by scanning probe microscopy. Second, the design of new and efficient emitter is a hot topic for the fabrication of OLED devices. A new type of compounds is currently investigated for their high electroluminescence efficiency due to thermally activated delayed fluorescence (TADF). This phenomenon is expected from molecules showing low electronic gap between singlet and triplet excited states, which is related to a low overlap of the HOMO and LUMO, localised on the electron-door and acceptor moieties of the molecule, respectively. In this sense, we propose a new design of donor-acceptor molecules where the HOMO (donor) and LUMO (acceptor) are separated by a cyclophane core. We synthesised a couple of emitters and their photophysics properties were studied in solution and in solid state
Auffray, Morgan. "Cyclophanes, a bridge between photophysics and supramolecular chemistry". Electronic Thesis or Diss., Paris 6, 2017. http://www.theses.fr/2017PA066285.
Pełny tekst źródłaIn this work and due to their unique electronic properties, 3D-dithia[3.3]paracyclophane-based molecules have been studied for surface nanostructuration applications and as new fluorophore. First, the supramolecular self-assembly of molecules is used to create well-organised 2D-networks on conducting surfaces. However, the use of such substrates tends to quench any electronic properties of the adsorbed molecules. In this context, 3D-dithia[3.3]paracyclophane-based molecules were employed to lift up the active moiety from the surface. In this work, new pyridyl end-capped molecules were designed to self-assemble on any substrate. Preliminary characterisations were performed to study the supramolecular self-assembly of such molecules alone or with co-adsorbers, and the first images of organised 2D-networks on graphite and gold have been obtained by scanning probe microscopy. Second, the design of new and efficient emitter is a hot topic for the fabrication of OLED devices. A new type of compounds is currently investigated for their high electroluminescence efficiency due to thermally activated delayed fluorescence (TADF). This phenomenon is expected from molecules showing low electronic gap between singlet and triplet excited states, which is related to a low overlap of the HOMO and LUMO, localised on the electron-door and acceptor moieties of the molecule, respectively. In this sense, we propose a new design of donor-acceptor molecules where the HOMO (donor) and LUMO (acceptor) are separated by a cyclophane core. We synthesised a couple of emitters and their photophysics properties were studied in solution and in solid state
Collins, Shawn K. "Design, synthesis, and applications of novel phenyl/acetylenic cyclophanes". Thesis, University of Ottawa (Canada), 2001. http://hdl.handle.net/10393/9015.
Pełny tekst źródłaHoughton, Tom J. "Synthesis and study of some novel and interesting cyclophanes". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1999. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape7/PQDD_0023/NQ54838.pdf.
Pełny tekst źródłaMoody, T. S. "Switches based on crown ethers, cyclophanes and amino acids". Thesis, Queen's University Belfast, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390876.
Pełny tekst źródłaBartlett, Stephen James. "Synthesis, conformational studies and biological activity of bisindolylmaleimide cyclophanes". Thesis, University of Leeds, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.424060.
Pełny tekst źródłaKsiążki na temat "Cyclophanes"
Weber, E., red. Cyclophanes. Berlin/Heidelberg: Springer-Verlag, 1994. http://dx.doi.org/10.1007/bfb0025265.
Pełny tekst źródłaDiederich, François. Cyclophanes. London: Royal Society of Chemistry, 1991.
Znajdź pełny tekst źródłaDiederich, François. Cyclophanes. Cambridge [England]: Royal Society of Chemistry, 1994.
Znajdź pełny tekst źródłaF, Vögtle. Cyclophan-Chemie: Synthesen, Strukturen, Reaktionen : Einführung und Überblick. Stuttgart: Teubner, 1990.
Znajdź pełny tekst źródłaKostermans, Gerardus Botje Maria. Synthesis and properties of very small [n]cyclophanes. [s.l.]: [s.n.], 1989.
Znajdź pełny tekst źródłaVögtle, Fritz. Cyclophan-Chemie. Wiesbaden: Vieweg+Teubner Verlag, 1990. http://dx.doi.org/10.1007/978-3-322-92788-0.
Pełny tekst źródłaCyclophanes. Cambridge: Royal Society of Chemistry, 2016. http://dx.doi.org/10.1039/9781788010924.
Pełny tekst źródłaCyclophanes. Springer, 1994.
Znajdź pełny tekst źródłaHart, H. Cyclophanes. Springer, 2013.
Znajdź pełny tekst źródłaWeber, E. Cyclophanes. Springer-Verlag, 1994.
Znajdź pełny tekst źródłaCzęści książek na temat "Cyclophanes"
Benniston, Andrew C., i Anthony Harriman. "Photoactive Cyclophanes". W Physical Supramolecular Chemistry, 179–97. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0317-3_12.
Pełny tekst źródłaTsuji, Takashi. "Highly Strained Cyclophanes". W Modern Cyclophane Chemistry, 81–104. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603964.ch3.
Pełny tekst źródłaSpeiser, Bernd. "Molecular Electrochemistry of Cyclophanes". W Modern Cyclophane Chemistry, 359–79. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603964.ch14.
Pełny tekst źródłaErnst, Ludger, i Kerstin Ibrom. "NMR Spectra of Cyclophanes". W Modern Cyclophane Chemistry, 381–414. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603964.ch15.
Pełny tekst źródłaHopf, Henning. "Intramolecular Reactions in Cyclophanes". W Modern Cyclophane Chemistry, 189–210. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603964.ch7.
Pełny tekst źródłaSander, Wolfram. "Reactive Intermediates from Cyclophanes". W Modern Cyclophane Chemistry, 211–27. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603964.ch8.
Pełny tekst źródłaMuchall, Heidi M. "Ultraviolet Photoelectron Spectra of Cyclophanes". W Modern Cyclophane Chemistry, 259–74. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603964.ch10.
Pełny tekst źródłaRademacher, Paul. "UV/Vis Spectra of Cyclophanes". W Modern Cyclophane Chemistry, 275–310. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603964.ch11.
Pełny tekst źródłaFlood, Amar H., Yi Liu i J. Fraser Stoddart. "From Cyclophanes to Molecular Machines". W Modern Cyclophane Chemistry, 485–518. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603964.ch19.
Pełny tekst źródłaGleiter, Rolf, Bernhard J. Rausch i Rolf J. Schaller. "Endohedral Metal Complexes of Cyclophanes". W Modern Cyclophane Chemistry, 159–88. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603964.ch6.
Pełny tekst źródłaStreszczenia konferencji na temat "Cyclophanes"
Scherer, P. O. J. "Noise induced intramolecular electron transfer processes in polar media." W International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1992. http://dx.doi.org/10.1364/up.1992.fc4.
Pełny tekst źródłaRaporty organizacyjne na temat "Cyclophanes"
Li, Shulong, Henry S. White i Michael D. Ward. Scanning Tunneling Microscopy of the Organic Semiconductor ((Eta-C5Me5) 2Ru(1,4-(2(2))-cyclophane)) (TCNQ)4. Fort Belvoir, VA: Defense Technical Information Center, luty 1992. http://dx.doi.org/10.21236/ada246848.
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