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DC Field | Value | Language |
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dc.contributor.advisor | Granell Sanvicente, Jaime Ramón | - |
dc.contributor.author | Ates Ceresuela, Ulunay | - |
dc.date.accessioned | 2019-02-25T14:23:52Z | - |
dc.date.available | 2019-02-25T14:23:52Z | - |
dc.date.issued | 2019-01 | - |
dc.identifier.uri | http://hdl.handle.net/2445/128822 | - |
dc.description | Treballs Finals de Grau de Química, Facultat de Química, Universitat de Barcelona, Any: 2019, Tutor: Jaume Granell Sanvicente | ca |
dc.description.abstract | The treatment of 4-fluorobenzylamine with 4-chlorobenzaldehyde or 2,3-difluorobenzaldehyde in acetone at 80ºC afforded the corresponding imines (1), 4-ClC6H4CH=NCH2(4’-FC6H4) and 2,3-F2C6H3CH=NCH2(4’-FC6H4) respectively, which were isolated in a yield >90%. The same reaction was performed in milder conditions obtaining similar results. The imines (1) reacted with a stoichiometric amount of Pd(OAc)2 in acetic acid affording the corresponding acetato-bridged five-membered ortho-cyclopalladated dimers (2) in 44-69% yield. The reaction was reproduced in different conditions to improve the yield, obtaining the best results at 85ºC for 1h. Compounds 2 were converted by a metathesis reaction with an excess of LiCl and LiBr in acetone into the corresponding chloro- or bromo-bridged dinuclear cyclopalladated compounds. The stoichiometric amount of PPh3 and dppe was added to the halogen-bridge compounds to obtain the mononuclear compounds trans-N,L-[Pd{RHC=NCH2(4’-FC6H4)}(X)(L)] [3-A (R= 4-ClC6H4, X= Br, L= PPh3); 3-B (R= 2,3-F2C6H3, X = Br, L = PPh3); 4-A (R= 4-ClC6H4, X= Cl, L= PPh3); and the dinuclear compounds 5-A (R= 4-ClC6H4, X= Br, L= dppe); 5-B (R= 2,3-F2C6H3, X= Br, L= dppe)] in 50-90% yield. The compounds obtained were characterized by 1H NMR, 31P NMR spectroscopy −in CDCl3 solution−, elemental analyses, mass spectrometry, and IR spectroscopy. Some tendencies have been found in this work: i) the E isomer of the imine was isolated in all reactions; ii) the ortho-fluoro atoms show an interaction with the imine proton; iii) the endo-palladacycle is the thermodynamic control isomer; iv) the aromatic protons of the metallated ring are high field shifted in compounds containing phosphines, showing a trans arrangement between the phosphines and the nitrogen atom in agreement with the transphobia; v) the methinic proton signal in proton NMR spectra is displaced toward high fields confirming the nitrogen-metal bond. | ca |
dc.format.extent | 51 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | ca |
dc.rights | cc-by-nc-nd (c) Ates, 2019 | - |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/es/ | * |
dc.source | Treballs Finals de Grau (TFG) - Química | - |
dc.subject.classification | Imines | cat |
dc.subject.classification | Fosfina | cat |
dc.subject.classification | Treballs de fi de grau | cat |
dc.subject.other | Imines | eng |
dc.subject.other | Phosphine | eng |
dc.subject.other | Bachelor's theses | - |
dc.title | Synthesis and characterization of cyclometallated complexes of imines: 4-ClC6H4CH=NCH2(4’-FC6H4) and 2,3-F2C6H3CH=NCH2(4’-FC6H4). Expanding the scope of cyclopalladations | eng |
dc.title.alternative | Síntesis y caracterización de los complejos ciclometalados de las iminas: 4-ClC6H4CH=NCH2(4’-FC6H4) y 2,3-F2C6H3CH=NCH2(4’-FC6H4). Ampliando horizontes en el ámbito de las ciclopaladaciones | ca |
dc.type | info:eu-repo/semantics/bachelorThesis | ca |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | ca |
Appears in Collections: | Treballs Finals de Grau (TFG) - Química |
Files in This Item:
File | Description | Size | Format | |
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TFG_QU Ates Ceresuela, Ulunay.pdf | 1.28 MB | Adobe PDF | View/Open |
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