Relevant bibliographies by topics / Diazonium salts chemistry

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  2. Dissertations / Theses
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Academic literature on the topic 'Diazonium salts chemistry'

Author: Grafiati
Published: 4 June 2021
Last updated: 11 February 2022

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Journal articles on the topic "Diazonium salts chemistry"

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Kasprzak, Artur, Agnieszka Zuchowska, and Magdalena Poplawska. "Functionalization of graphene: does the organic chemistry matter?" Beilstein Journal of Organic Chemistry 14 (August 2, 2018): 2018–26. http://dx.doi.org/10.3762/bjoc.14.177.

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Reactions applying amidation- or esterification-type processes and diazonium salts chemistry constitute the most commonly applied synthetic approaches for the modification of graphene-family materials. This work presents a critical assessment of the amidation and esterification methodologies reported in the recent literature, as well as a discussion of the reactions that apply diazonium salts. Common misunderstandings from the reported covalent functionalization methods are discussed, and a direct link between the reaction mechanisms and the basic principles of organic chemistry is taken into
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Oger, Nicolas, Erwan Le Grognec, and François-Xavier Felpin. "Handling diazonium salts in flow for organic and material chemistry." Organic Chemistry Frontiers 2, no. 5 (2015): 590–614. http://dx.doi.org/10.1039/c5qo00037h.

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Ahmad, Ahmad A. L., Bizuneh Workie, and Ahmed A. Mohamed. "Diazonium Gold Salts as Novel Surface Modifiers: What Have We Learned So Far?" Surfaces 3, no. 2 (2020): 182–96. http://dx.doi.org/10.3390/surfaces3020014.

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The challenges of diazonium salts stabilization have been overcome by their isolation as metal salts such as tetrachloroaurate(III). The cleavage of molecular nitrogen from diazonium salts even at very low potential or on reducing surfaces by fine tuning the substituents on the phenyl ring expanded their applications as surface modifiers in forensic science, nanomedicine engineering, catalysis and energy. The robustness of the metal–carbon bonding produced from diazonium salts reduction has already opened an era for further applications. The integration of experimental and calculations in this
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Huang, Jing, Zhenyao Yin, and Jinggao Wu. "Covalent attachment of chitosan to graphene via click chemistry for superior antibacterial activity." Materials Advances 1, no. 4 (2020): 579–83. http://dx.doi.org/10.1039/d0ma00082e.

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Ledenyova, I. V., V. V. Didenko, and Kh S. Shikhaliev. "Chemistry of Pyrazole-3(5)-Diazonium Salts (Review)*." Chemistry of Heterocyclic Compounds 50, no. 9 (2014): 1214–43. http://dx.doi.org/10.1007/s10593-014-1585-1.

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Servinis, Linden, Kathleen M. Beggs, Thomas R. Gengenbach, et al. "Tailoring the fibre-to-matrix interface using click chemistry on carbon fibre surfaces." Journal of Materials Chemistry A 5, no. 22 (2017): 11204–13. http://dx.doi.org/10.1039/c7ta00922d.

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A convenient and effective strategy to control the surface chemistry of carbon fibres is presented, comprising electro-chemical reduction of aryl diazonium salts onto the surface, followed by ‘click chemistry’ to tether the desired surface characteristic of choice.
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Luo, Yun, Yu Xiao, Delphine Onidas, et al. "Raman reporters derived from aryl diazonium salts for SERS encoded-nanoparticles." Chemical Communications 56, no. 50 (2020): 6822–25. http://dx.doi.org/10.1039/d0cc02842h.

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Josefík, František, Markéta Svobodová, Valerio Bertolasi, and Petr Šimůnek. "A simple, enaminone-based approach to some bicyclic pyridazinium tetrafluoroborates." Beilstein Journal of Organic Chemistry 9 (July 23, 2013): 1463–71. http://dx.doi.org/10.3762/bjoc.9.166.

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Easily obtainable cyclic enaminones (piperidin-2-ylidenealkanones) can be transformed into substituted bicyclic pyridazinium tetrafluoroborates upon treatment with corresponding diazonium salts. The transformation can be performed either in a one-pot way or in a two-step process with the isolation of single azo-coupled enaminone as the intermediate. The former method is superior. Under the optimized conditions, a number of pyridazinium salts substituted with both electron-donating and electron-withdrawing substituents was easily synthesized. A mechanism of the formation of the pyridazinium sal
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Habraken, Evi, Andrew Jupp, and J. Slootweg. "Diazonium Salts as Nitrogen-Based Lewis Acids." Synlett 30, no. 08 (2019): 875–84. http://dx.doi.org/10.1055/s-0037-1612109.

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Aryldiazonium salts are widely used in many organic transformations with displacement of N2 or through addition to the terminal nitrogen. Such aryldiazonium salts can be viewed as N-based Lewis acids that can react with Lewis bases to synthesize a wide variety of azo compounds. Additionally, diazonium salts are known to undergo single-electron transfer and release N2, forming an aryl radical, which results in different reactivity. Herein, we provide a concise overview of the reactivity of aryldiazonium salts undergoing classical donor-acceptor reactivity or single-electron transfer.
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Paulus, Geraldine L. C., Qing Hua Wang, and Michael S. Strano. "Covalent Electron Transfer Chemistry of Graphene with Diazonium Salts." Accounts of Chemical Research 46, no. 1 (2012): 160–70. http://dx.doi.org/10.1021/ar300119z.

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Dissertations / Theses on the topic "Diazonium salts chemistry"

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Akwi, Faith Mary. "Scalable chemistry involving diazonium salts." Thesis, Nelson Mandela Metropolitan University, 2016. http://hdl.handle.net/10948/6909.

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Herein an alternative approach aimed at reducing the cost of numbering up technique as a scale up strategy for chemical processes from the laboratory bench top to the industry is explored. The effect of increasing channel size on the reaction conversion of the synthesis of azo compounds is investigated. This was achieved via a systematic investigative understanding of the synthesis in microreactors where a proof of concept study was performed to determine the optimum reaction parameters in azo coupling reactions involving couplers with aminated or hydroxylated groups in Little Things Factory-M
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Schotten, Christiane. "Investigating multistep continuous flow processes using diazonium salts." Thesis, Cardiff University, 2018. http://orca.cf.ac.uk/113812/.

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This thesis describes the investigation of continuous flow processes that incorporate the generation and use of diazonium salts. In this manner, processes for the preparation of triazenes, indoles and acridones have been developed. Diazonium salts are potentially unstable and hazardous and have to be handled with care. The use of continuous flow processes enables the safe synthesis avoiding accumulation of large quantities. This is due to the possibility to intercept intermediates at a precise point in time within a closed system. Diazonium salts were prepared via in situ diazotization of anil
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Zhang, Lin. "Co-immobilisation du complexe (2,2'-bipyridyl) (pentaméthylcyclopentadiényl)-rhodium et de déshydrogénases NAD-dépendantes pour l’électrosynthèse enzymatique énantiosélective." Thesis, Université de Lorraine, 2016. http://www.theses.fr/2016LORR0283/document.

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Dans ce travail, nous avons développé différentes méthodes pour la co-immobilisation sur des électrodes poreuses de carbone de déshydrogénases NAD-dépendantes avec le complexe (2,2'-bipyridyle)(pentaméthylcyclopentadiényl)-rhodium ([Cp*Rh(bpy)Cl]+) pour des applications de synthèse électroenzymatique d’alcools et de sucres chiraux. L'objectif était d'éviter la dégradation de l'activité enzymatique provenant de l'interaction entre les groupes fonctionnels de surface de l'enzyme (-SH, -NH2) et le complexe [Cp*Rh(bpy)Cl]+, et également de permettre le recyclage des catalyseurs. L’électrogreffage
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Felipe-Blanco, Diego. "Salicylic Acid-Catalyzed Radical Arylations from In-situ Formed Arenediazonium Salts." Doctoral thesis, Universidad de Alicante, 2020. http://hdl.handle.net/10045/112757.

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In this thesis, it has been studied the deamination of aromatic amines, through in situ formed diazonium salts as reaction intermediates, catalyzed by salicylic acid, a nontoxic, eco-friendly and economic catalyst. In the early part of the thesis (Chapter I) it has studied the deamination process using THF as solvent as hydrogen donor and anilines as radical source, to carry the hydrodeamination reaction, as well as the process in its deuterodeamination manner using deuterated solvent. Following with this study in Chapter II and Chapter III, it has been studied the addition of the aromatic rad
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Doublet, Aurélien. "Développement d’un primaire d’adhésion anticorrosion sans Cr VI pour l’alliage aéronautique Al2024-T3." Thesis, Université Paris-Saclay (ComUE), 2019. http://www.theses.fr/2019SACLS280.

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L’utilisation du chrome hexavalent pour le traitement de surface des matériaux de l’aéronautique est en passe d’être interdite par la réglementation REACH. Dans l’objectif de trouver une solution alternative, PROTEC industrie et le CEA travaillent en collaboration sur le développement d’une nouvelle solution sans-chrome permettant de remplacer les revêtements classiquement utilisés. Le travail de thèse présenté dans ce manuscrit s’inscrit dans le cadre du laboratoire commun MESTREL financé par le programme ANR Labcom, réunissant les deux entités citées ci-dessus. La solution proposée est basée
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Fioresi, Flavia. "Modification de surface de différents matériaux pour les applications biologiques et environnementales Electrografting of diazonium salt for SPR application Atmospheric solid analysis probe-ion mobility mass spectrometry : an original approach to characterize grafting on cyclic olefin copolymer surfaces Chemical modification of the cocoa shell surface using diazonium salts Cobalt nanoparticles embedded into polydimethylsiloxane-grafted cocoa shell : functional agrowaste for CO2 capture." Thesis, Normandie, 2020. http://www.theses.fr/2020NORMR062.

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Depuis près d'un siècle, les chercheurs déploient des efforts importants pour apporter de nouvelles propriétés aux matériaux et aujourd'hui la modification de surface des matériaux est plus que jamais un sujet de recherche très attractif lié à une variété d'applications industrielles prometteuses. Le développement d'une méthodologie simple pour caractériser les interactions biomoléculaires a été, au fil des ans, une technologie indispensable pour soutenir les recherches dans les domaines de la biologie et de la microbiologie en raison de son haut degré de sensibilité. La fonctionnalisation de
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Naturale, Guillaume. "Approches radicalaires pour la fonctionnalisation directe de quinones à visée anticancereuse." Thesis, Bordeaux 1, 2012. http://www.theses.fr/2012BOR14635/document.

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Dans le cadre d’un programme de recherche dédié à la découverte de petites molécules à visée anticancéreuse, nous avons envisagé de concevoir des composés originaux dérivés de quinones. Notre premier objectif a été d’élaborer des mimes non-peptidiques de la protéine Smac, susceptibles de participer à relancer le phénomène d’apoptose, dont la structure est rigidifiée par des contraintes conformationnelles. Par ailleurs, les kinases et les phosphatases, jouant des rôles complémentaires de phosphorylation / déphosphorylation dans le cadre du contrôle du cycle cellulaire notamment, apparaissent au
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Kist, Madelyn M. "Light-induced surface site manipulation of gold nanoparticles using diazonium salt." Kent State University / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=kent1626960076521484.

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Lenoir, Isabelle. "Radical cascade reactions with isonitriles and dual lanthitide-transition metal catalysis : an approach to hidden diazoalkane and diazonium salt chemistry." Thesis, Imperial College London, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343737.

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Books on the topic "Diazonium salts chemistry"

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Chehimi, Mohamed Mehdi. Aryl Diazonium Salts: New Coupling Agents in Polymer and Surface Science. Wiley-VCH Verlag GmbH, 2012.

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Chehimi, Mohamed Mehdi. Aryl Diazonium Salts: New Coupling Agents in Polymer and Surface Science. Wiley & Sons, Incorporated, John, 2012.

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Chehimi, Mohamed Mehdi. Aryl Diazonium Salts: New Coupling Agents in Polymer and Surface Science. Wiley & Sons, Incorporated, John, 2012.

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Chehimi, Mohamed Mehdi. Aryl Diazonium Salts: New Coupling Agents in Polymer and Surface Science. Wiley & Sons, Incorporated, John, 2012.

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Chehimi, Mohamed Mehdi. Aryl Diazonium Salts: New Coupling Agents in Polymer and Surface Science. Wiley & Sons, Limited, John, 2012.

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Book chapters on the topic "Diazonium salts chemistry"

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Went, C. "Amines, Amino Acids and Diazonium Salts." In Work Out Organic Chemistry. Macmillan Education UK, 1988. http://dx.doi.org/10.1007/978-1-349-09726-5_11.

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Coxon, James M., Juliet A. Gerrard, Sir Richard Norman, and James M. Coxon. "Aromatic diazonium salts." In Worked Solutions in Organic Chemistry. Routledge, 2018. http://dx.doi.org/10.1201/9780203733677-15.

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"Aromatic amines and diazonium salts." In Aromatic Chemistry, edited by John D. Hepworth, David R. Waring, and Michael J. Waring. Royal Society of Chemistry, 2007. http://dx.doi.org/10.1039/9781847550163-00088.

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"Electrode Surface Modication Using Diazonium Salts." In Electroanalytical Chemistry. CRC Press, 2015. http://dx.doi.org/10.1201/b19196-7.

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Berisha, Avni, Mohamed Chehimi, Jean Pinson, and Fetah Podvorica. "Electrode Surface Modification Using Diazonium Salts." In Electroanalytical Chemistry: A Series of Advances. CRC Press, 2015. http://dx.doi.org/10.1201/b19196-4.

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Kovács, Szabolcs, Giulia Bertoli, and Lukas J. Goossen. "Fluoroalkylation, Fluoroalkylthiolation and Fluoroalkylselenolation of Diazonium Salts and Diazo Compounds." In Frontiers of Organofluorine Chemistry. WORLD SCIENTIFIC (EUROPE), 2020. http://dx.doi.org/10.1142/9781786347336_0004.

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Gilbraith, W., and K. S. Booksh. "Strategies for Designing Chemical Functionalities for Biochemical Sensing With Diazonium Salts." In Encyclopedia of Interfacial Chemistry. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-12-409547-2.13180-4.

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Vrána, J., and A. Růžička. "5.2.24.10 Arylstannanes (Update 2021)." In Knowledge Updates 2021/2. Georg Thieme Verlag KG, 2021. http://dx.doi.org/10.1055/sos-sd-105-00330.

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AbstractThis chapter is an update to the earlier Science of Synthesis contribution describing methods for the synthesis and uses of arylstannanes. The focus is on the literature published in the period 2001–2020. Novel synthetic methods for the formation of the target compounds are reviewed, including reactions of aryl anions with aryltin halides, reactions of diazonium salts or aryl azo sulfones with distannanes, and various catalyzed processes. The use of arylstannanes as substrates in organic chemistry and radiochemistry is also discussed; these compounds can undergo coupling reactions, destannylations, metal–tin exchange reactions, electrophilic substitutions, and oxidative addition processes.
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"34. Diazotization (Diazonium Salt)." In Organic Chemistry: 100 Must-Know Mechanisms. De Gruyter, 2020. http://dx.doi.org/10.1515/9783110608373-035.

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"34. Diazotization (Diazonium Salt)." In Organic Chemistry: 100 Must-Know Mechanisms. De Gruyter, 2020. http://dx.doi.org/10.1515/9783110608373-034.

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