Auswahl der wissenschaftlichen Literatur zum Thema „Covalent functionalisation“
Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an
Inhaltsverzeichnis
Machen Sie sich mit den Listen der aktuellen Artikel, Bücher, Dissertationen, Berichten und anderer wissenschaftlichen Quellen zum Thema "Covalent functionalisation" bekannt.
Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.
Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.
Zeitschriftenartikel zum Thema "Covalent functionalisation"
Namasivayam, Muthuraman, Mats R. Andersson und Joseph Shapter. „Role of Molecular Weight in Polymer Wrapping and Dispersion of MWNT in a PVDF Matrix“. Polymers 11, Nr. 1 (17.01.2019): 162. http://dx.doi.org/10.3390/polym11010162.
Der volle Inhalt der QuelleNicks, Joshua, Jiawen Zhang und Jonathan A. Foster. „Tandem catalysis by ultrathin metal–organic nanosheets formed through post-synthetic functionalisation of a layered framework“. Chemical Communications 55, Nr. 60 (2019): 8788–91. http://dx.doi.org/10.1039/c9cc02061f.
Der volle Inhalt der QuelleClancy, Adam J., Heather Au, Noelia Rubio, Gabriel O. Coulter und Milo S. P. Shaffer. „Understanding and controlling the covalent functionalisation of graphene“. Dalton Transactions 49, Nr. 30 (2020): 10308–18. http://dx.doi.org/10.1039/d0dt01589j.
Der volle Inhalt der QuelleGromov, Andrei, Staffan Dittmer, Johannes Svensson, Oleg A. Nerushev, Sergio Alfonso Perez-García, Liliana Licea-Jiménez, Rodney Rychwalski und Eleanor E. B. Campbell. „Covalent amino-functionalisation of single-wall carbon nanotubes“. Journal of Materials Chemistry 15, Nr. 32 (2005): 3334. http://dx.doi.org/10.1039/b504282h.
Der volle Inhalt der QuelleMaitra, Urmimala, A. Gomathi und C. N. R. Rao. „Covalent and noncovalent functionalisation and solubilisation of nanodiamond“. Journal of Experimental Nanoscience 3, Nr. 4 (Dezember 2008): 271–78. http://dx.doi.org/10.1080/17458080802574155.
Der volle Inhalt der QuelleDa Silva Rodrigues, Rafael, David L. Marshall, John C. McMurtrie und Kathleen M. Mullen. „Dynamic covalent synthesis of [2]- and [3]rotaxanes both in solution and on solid supports“. New Journal of Chemistry 44, Nr. 26 (2020): 11231–36. http://dx.doi.org/10.1039/d0nj02137g.
Der volle Inhalt der QuelleJanaun, Jidon, Ong Carrie, S. M. Anisuzzaman und Duduku Krishnaiah. „Non-Covalent Functionalisation of Amorphous Carbon From D-Glucose as a Novel Catalyst for Renewable Fuels“. International Journal of Biomass and Renewables 9, Nr. 2 (30.12.2020): 6. http://dx.doi.org/10.61762/ijbrvol9iss2art10104.
Der volle Inhalt der QuelleHarismah, Kun, Mahmoud Mirzaei, Nahid Ghasemi und Mohammad Nejati. „Non-Covalent Functionalisation of C30 Fullerene by Pyrrole-n-Carboxylic Acid (n=2, 3): Density Functional Theory Studies“. Zeitschrift für Naturforschung A 73, Nr. 1 (20.12.2017): 51–56. http://dx.doi.org/10.1515/zna-2017-0233.
Der volle Inhalt der QuelleKim, HyunJeong, WungYeon Kim, Maria O'Brien, Niall McEvoy, Chanyoung Yim, Mario Marcia, Frank Hauke, Andreas Hirsch, Gyu-Tae Kim und Georg S. Duesberg. „Optimized single-layer MoS2 field-effect transistors by non-covalent functionalisation“. Nanoscale 10, Nr. 37 (2018): 17557–66. http://dx.doi.org/10.1039/c8nr02134a.
Der volle Inhalt der QuelleClavé, Guillaume, und Stéphane Campidelli. „Efficient covalent functionalisation of carbon nanotubes: the use of “click chemistry”“. Chemical Science 2, Nr. 10 (2011): 1887. http://dx.doi.org/10.1039/c1sc00342a.
Der volle Inhalt der QuelleDissertationen zum Thema "Covalent functionalisation"
Neate, Nigel Christopher. „Covalent functionalisation of carbon surfaces for biomedical applications“. Thesis, University of Nottingham, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.420434.
Der volle Inhalt der QuelleDavis, Holly. „Harnessing non-covalent interactions to control regioselectivity in the functionalisation of arene C-H bonds“. Thesis, University of Cambridge, 2018. https://www.repository.cam.ac.uk/handle/1810/277900.
Der volle Inhalt der QuelleNikolaievskyi, Dmytro. „Searching for spatial and chemical control of graphene modification : atomic force microscopy assisted folding and covalent functionalisation“. Electronic Thesis or Diss., Aix-Marseille, 2022. http://www.theses.fr/2022AIXM0263.
Der volle Inhalt der QuelleMany efforts are put in manipulating graphene with local and chemical control to tune its electronic properties, enabling its application in device fabrication. We have used atomic force microscopy (AFM) to investigate catalytic scanning probe lithography (cSPL) as a method to functionalise covalently a supported chemical vapour deposition graphene. We have shown that supported graphene is cut at smaller tip forces in liquid than in air. So far, the cSPL epoxidation with a manganese-based catalytic system was inefficient to functionalise graphene, but AFM scanning has opened the way for studying graphene folding by the “cut and fold” method. We have explored contact mode AFM scanning of micrometric zones of few-layer graphene (FLG), where graphene is cut and pushed at the top of scanned zones, forming wide folded stacks. Transmission electron microscopy and Raman analyses have revealed the creation of a turbostratic multilayer graphene (MLG), consisting of folded stacks of 10–20 layers, with an interlayer distance of 0.36 nm. Linear defects are introduced by folding, likely due to loops and folding edges. Thus, the cut and fold method creates a particular kind of MLG from initial FLG, sharing properties of free-standing and free-stacked graphene, and electronically different from the FLG. Finally, we have done preliminary tests of the reversible distortion of graphene by covalently grafted bridged azobenzene structures, using photoinduced E/Z isomerisation. We have confirmed functionalisation by Raman and XPS and observed UV-induced electric resistance changes
Sun, Anil. „Chemistry of single-wall carbon nanotubes : studies in purification, non-covalent modifîcation by tertiary phosphines and covalent functionalisation via nucleophilic reduction“. Thesis, Durham University, 2007. http://etheses.dur.ac.uk/2425/.
Der volle Inhalt der QuelleLee, Kuen-Chan. „New strategies for non-covalent chemical functionalisation and dispersion of single-wall carbon nanotubes“. Thesis, University of Oxford, 2010. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.526495.
Der volle Inhalt der QuelleGupta, Jaipal. „Compatibilisation of 1D/2D graphitic nanomaterials and poly(propylene) via non-covalent functionalisation with poly(acrylate)s“. Thesis, University of Warwick, 2018. http://wrap.warwick.ac.uk/109406/.
Der volle Inhalt der QuelleSalem, Diana. „Synthèse de nanotubes de carbone monofeuillets individuels et composites modèles polymères - nanotubes de carbone : application à l’effet photovoltaïque“. Thesis, Strasbourg, 2012. http://www.theses.fr/2012STRAE001/document.
Der volle Inhalt der QuelleThe aim of this work is to develop composite materials carbon nanotubes/polymers to take advantage of properties of carbon nanotubes at macroscopic scale. To get such materials, homogeneous functionalization between carbon nanotubes and polymers is required, carbon nanotubes must be individual with the same chemical reactivity, therefore the same diameter. Thus, they must be synthesized by CVD from monodispersed and supported catalyst nanoparticles. In the first part, we developed a new universal method for the synthesis of metal oxide supported nanoparticles. We mainly detailed the synthesis of Fe2O3 nanoparticles with size distribution of 1.1 ± 0.3 nm. In the second part, after studying the thermal stability of these nanoparticles, we used them to catalyze the growth of individual single wall carbon nanotubes by CVD. The caracterisation of the obtained nanotubes by Raman show exceptionally narrow diameter distribution of 1.27 ± 0.15 nm. In the third section, we first studied the dispersion of carbon nanotubes by noncovalent functionalization withhydro-soluble polymer POE with pyrene as end group and revealed depletion phenomena that limit the solubilization of nanotubes. Then we developed composite materials carbon nanotubes/rrP3HT by covalent and noncovalent functionalisation and we studied the efficiency of charge separation in both cases of functionalization
Buchteile zum Thema "Covalent functionalisation"
Ingrosso, C., N. Depalo, E. Fanizza, A. Panniello, R. Comparelli, A. Agostiano, M. Striccoli und M. L. Curri. „In Situ Synthesis of Multifunctional Hybrid Nanocomposites Based on Graphene Derivatives and Inorganic Nanoparticles for Advanced Applications“. In Unconventional Green Synthesis of Inorganic Nanomaterials, 252–314. Royal Society of Chemistry, 2024. http://dx.doi.org/10.1039/9781839165757-00252.
Der volle Inhalt der Quelle