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Lerma, Israel Consea. "Transformations Mediated by Palladium-(N-Heterocyclic)Carbenes Complexes". Thesis, University College London (University of London), 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.498701.
Pełny tekst źródłaMungur, Shaheed Ali. "Electropositive metal complexes of amino N-heterocyclic carbenes". Thesis, University of Nottingham, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.415893.
Pełny tekst źródłaMcNally, C. T. "Transition metal complexes of pyridyl functionalized n-heterocyclic carbenes". Thesis, Queen's University Belfast, 2012. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.546329.
Pełny tekst źródłaSilcock, Peter J. "Nickel and palladium complexes of di-N-heterocyclic carbenes". Thesis, University of Oxford, 1999. https://ora.ox.ac.uk/objects/uuid:679dade4-1d16-4918-b155-996250516783.
Pełny tekst źródłaBrayshaw, Simon Keith. "Metal complexes bearing pendant alkynes and metal complexes of N-heterocyclic carbenes". University of Western Australia. School of Biomedical and Chemical Sciences, 2004. http://theses.library.uwa.edu.au/adt-WU2005.0017.
Pełny tekst źródłaMartin, Thomas Antony. "Unravelling the photochemistry of organometallic N-heterocyclic carbene complexes". Thesis, University of Bath, 2011. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.547630.
Pełny tekst źródłaConti, Riccardo. "Synthesis of novel N-Heterocyclic Carbenes for chiral complexes and catalysis". Master's thesis, Alma Mater Studiorum - Università di Bologna, 2017. http://amslaurea.unibo.it/13374/.
Pełny tekst źródłaMokfi, Moloud [Verfasser]. "Xanthine-derived N-heterocyclic carbenes and their metal complexes / Moloud Mokfi". Wuppertal : Universitätsbibliothek Wuppertal, 2021. http://d-nb.info/1240266960/34.
Pełny tekst źródłaTurner, Zoe Rose. "Small molecule activation using electropositive metal N-heterocyclic carbene complexes". Thesis, University of Edinburgh, 2011. http://hdl.handle.net/1842/8210.
Pełny tekst źródłaHesler, Valerie Jane. "N-Heterocyclic carbene-metal complexes derived from imidazolium-linked cyclophane and biimidazolium salts". University of Western Australia. School of Biomedical, Biomolecular and Chemical Sciences, 2008. http://theses.library.uwa.edu.au/adt-WU2009.0088.
Pełny tekst źródłaPoulten, Rebecca. "Synthesis and reactivity of low coordinate nickel(I) complexes bearing ring expanded N-heterocyclic carbene ligands". Thesis, University of Bath, 2015. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.669038.
Pełny tekst źródłaDurmus, Semih. "Silver(I) and Gold(I) N-Heterocyclic Carbene Complexes". University of Akron / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=akron1165247084.
Pełny tekst źródłaHaque, Rosenani S. M. Anwarul. "Silver, mercury and ruthenium complexes of N-heterocyclic carbene linked cyclophanes". University of Western Australia. Chemistry Discipline Group, 2008. http://theses.library.uwa.edu.au/adt-WU2008.0236.
Pełny tekst źródłaDupuy, Stéphanie. "N-heterocyclic carbene gold hydroxide complexes as bond activation reagents". Thesis, University of St Andrews, 2014. http://hdl.handle.net/10023/6613.
Pełny tekst źródłaCharra, Valentine. "Coordination of multidentate N-heterocyclic carbene ligands to nickel". Thesis, Strasbourg, 2014. http://www.theses.fr/2014STRAF019/document.
Pełny tekst źródłaThe purpose of this work was the synthesis of bis-NHC (N-Heterocyclic carbene) ligands, theformation of the corresponding silver(I), copper(I) and nickel(II) complexes and the assessment ofthe catalytic activity of the bis-NHC nickel(II) complexes in ethylene oligomerization. A series of new bis-NHC silver(I) and copper(I) complexes was synthesized. Five different synthetic routes were tested for the formation of nickel(II) bis-NHC complexes. The most significant results were obtained by transmetalation from the silver(I) iodide or bromide complexes
Dyson, Gavin. "Synthesis of amine functionalised di-N-heterocyclic carbenes and chiral N-heterocyclic carbene-Schiff base transition metal complexes and their application to homogeneous catalysis". Thesis, University of York, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.440968.
Pełny tekst źródłaMelaiye, Abdulkareem M. "Synthesis and Antimicrobial Properties of Silver(I) N-Heterocyclic Carbene Complexes". University of Akron / OhioLINK, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=akron1124310734.
Pełny tekst źródłaGlover, Leighton Paul. "Transition metal complexes of N-heterocyclic carbenes and their application in homogeneous catalysis". Thesis, University of Sheffield, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.482842.
Pełny tekst źródłaMcMullon, Max William. "Exploiting anionically-tethered N-heterocyclic carbene complexes for small molecule activation". Thesis, University of Edinburgh, 2018. http://hdl.handle.net/1842/31079.
Pełny tekst źródłaZinser, Caroline Magdalene. "Palladium and gold N-heterocyclic carbene complexes : synthesis and catalytic applications". Thesis, University of St Andrews, 2019. http://hdl.handle.net/10023/17066.
Pełny tekst źródłaGauthier, Étienne. "Chiral complexes based on helicenic N-heterocyclic carbenes : synthesis, structure, photophysical and chiroptical properties". Thesis, Rennes 1, 2020. http://www.theses.fr/2020REN1S083.
Pełny tekst źródłaMy PhD work was dedicated to the synthesis and the study of novel chiral transition metal complexes (rhenium, iridium, copper, gold) bearing NHC-helicenes ligands and to the study of their chiroptical and photophysical properties. The first subject focused on the preparation and the study of CP-phosphorescent complexes of cyclometalated rhenium(I) complexes bearing NHC-helicenic (N^C:) ligands. The influence of the ligand design, ancillary ligands and geometry of the complexes on the chiroptical and photophysical properties has been highlighted. In the second project, we have prepared novel chiral cyclometalated iridium complexes bearing one or multiple N-[6]helicenyl- benzimidazolylidene ligands.Then, the attention has been focused on monodentate complexes. Thus, in the third project, a chiral copper complex bearing a helicenic-NHC ligand which emits circularly polarized fluorescence was successfully obtained. Finally, chiral monodentate helicenic-NHC gold(I) complexes have been prepared. During this project, the electronic properties (sigma-donating et pi-accepting) of a helicenic-NHC were investigated
Duan, Gongping. "Design, synthesis, and photophysics and photochromic study of dithienylethene-containing heterocyclic derivatives and N-heterocyclic carbene-ruthenium (II) complexes". Click to view the E-thesis via HKUTO, 2010. http://sunzi.lib.hku.hk/hkuto/record/B44248246.
Pełny tekst źródłaHolmes, Michael R. II. "The Synthesis And Characterization Of Novel Chiral Gold(I) N-Heterocyclic Carbene Complexes". Miami University / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=miami1437737871.
Pełny tekst źródłaHe, Fan. "Transition metal complexes with N-heterocyclic carbene ligands : synthesis and reactivity". Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAF031/document.
Pełny tekst źródłaThe purpose of this work is the synthesis of complexes containing imine-functionalized protic NHC ligands in order to further develop synthetic methodologies giving access to pNHC, C-bound ‘anionic’ imidazolide, and homo- and heterodinuclear complexes. In the case of imidazoles without functional group, deprotonation with n-butyl lithium afforded (1-aryl-1H-imidazol-2-yl)lithium in good yield. Reaction of (1-aryl-1H-imidazol-2-yl)lithium with [Ir(cod)(μ-Cl)]2 or [Rh(cod)(μ-Cl)]2 yielded a doubly C2,N3-bridged dinuclear complex. In the case of imine-functionalized imidazole, the Ir(I) N-bound imidazole complex can tautomerize to Ir(I) imine-functionalized pNHC complex chloride abstraction at room temperature, while in the Rh(I) analog the tautomerization can be achieved at 110 °C. In situ deprotonation of the N-bound imidazole Ir(I) or Rh(I) complexes, followed by addition of [Ir(cod)(μ-Cl)]2 or [Rh(cod)(μ-Cl)]2 led to the isolation of homo- and heterodinuclear complexes. The metalation of imine-functionalized imidazolium salts is also an effective procedure for synthesis of pNHC metal complexes, and it was extended from bidentate to pincer-type pNHC complexes
Lesieur, Mathieu. "Cu and Pd complexes of N-heterocyclic carbenes : catalytic applications as single and dual systems". Thesis, University of St Andrews, 2015. http://hdl.handle.net/10023/7999.
Pełny tekst źródłaSantoro, Orlando. "Copper(I)-N-heterocyclic carbene (NHC) complexes : synthesis, characterisation and applications in synthesis and catalysis". Thesis, University of St Andrews, 2016. http://hdl.handle.net/10023/8409.
Pełny tekst źródłaDeblock, Michael C. "The Synthesis, In Vitro and In Vivo Testing of Silver N-Heterocyclic Carbenes and Imidazolium Complexes". University of Akron / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=akron1353951003.
Pełny tekst źródłaJagenbrein, Martin. "Complexes of Bi, Pd, Ir and Hg and N-heterocyclic ligands". Thesis, Strasbourg, 2014. http://www.theses.fr/2014STRAF023.
Pełny tekst źródłaThe purpose of this thesis was the synthesis of novel pro-ligands to NHCs and their corresponding metal complexes, notably of iridium. While the attempt to find a new pathway to obtain NHC complexes starting from the corresponding imidazole-2-thiones did not yield the expected result, it was possible to obtain interesting coordination compounds from those imidazole-2-thiones themselves:A dinuclear Bi complex was prepared that served as an effective transmetallation agent toward Pd. Novel pincer-type NHC pro-ligands were obtained, and several iridium complexes of their corresponding NHC ligands were prepared. Furthermore, several mercury complexes of these ligands were synthesized. Finally, a series of imidazolium salts bearing potentially hemilabile functionalities were prepared and their reactivity toward Ir was studied
Brucka, Marta Anna. "N-Heterocyclic carbene complexes of silver, rhodium and iron: structures, dynamics and catalysis". Master's thesis, Alma Mater Studiorum - Università di Bologna, 2012. http://amslaurea.unibo.it/3873/.
Pełny tekst źródłaReade, Steven Peter. "Ruthenium dihydride and hydride fluoride complexes with N-heterocyclic carbenes : a route to C-F bond activation". Thesis, University of Bath, 2009. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.507754.
Pełny tekst źródłaMaftei, Catalin-Vasile Verfasser], i Matthias [Akademischer Betreuer] [Tamm. "Cytotoxic Metal Complexes With N-Heterocyclic Carbenes Containing 1,2,4-Oxadiazole Substituents / Catalin-Vasile Maftei ; Betreuer: Matthias Tamm". Braunschweig : Technische Universität Braunschweig, 2018. http://d-nb.info/1175816043/34.
Pełny tekst źródłaLiu, Ming [Verfasser], i Andreas [Akademischer Betreuer] Schmidt. "Formation of borane adducts and some complexes starting from N-heterocyclic carbenes / Ming Liu ; Betreuer: Andreas Schmidt". Clausthal-Zellerfeld : Technische Universität Clausthal, 2017. http://d-nb.info/1231364963/34.
Pełny tekst źródłaHoughton, Jennifer M. "Synthesis and catalytic applications of transition metal complexes of di-N-heterocyclic carbenes incorporating an amine functionality". Thesis, University of York, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.421500.
Pełny tekst źródłaGutiérrez, Blanco Ana María. "Tetrametallic (Gold, Iridium and Rhaodium) complexes based on N-Heterocyclic carbenes. From luminescent properties to supramolecular assemblies". Doctoral thesis, Universitat Jaume I, 2021. http://dx.doi.org/10.6035/14104.2021.164087.
Pełny tekst źródłaLa investigación llevada a cabo en esta Tesis doctoral puede resumirse como la preparación de diferentes complejos multimetálicos que contienen ligandos carbeno N-heterocíclico (NHC). Con este propósito, el objetivo principal es la obtención de nuevos ligandos basados en poli-NHC con sistemas poliaromáticos extendidos para la preparación de estos complejos, con una combinación de características que pueden dar acceso a aplicaciones fotofísicas y catalíticas muy interesantes.
Programa de Doctorat en Ciències
Simler, Thomas. "New transition metal complexes with functional N-heterocyclic carbene ligands for molecular activation". Thesis, Strasbourg, 2016. http://www.theses.fr/2016STRAF005.
Pełny tekst źródłaThe purpose of this work is the synthesis and study of hybrid and potentially “pincer” ligands featuring an N-heterocyclic carbene (NHC) donor. The phosphine-NHC ligands based on the m-phenylene framework led to di- or tetranuclear Ag, Cu, Au and Ir complexes, and to bimetallic Ag/Cu and Ag/Ir complexes by selective transmetallation of the NHC. With the phosphino-picoline-NHC (PNC) ligands, transmetallation from the corresponding Li or K salts led to dearomatised Cr, Fe and Co “pincer” complexes. Deprotonation of the bis(phosphinomethyl)pyridine (PNP) ligand was also examined. The corresponding dearomatised mono- and bis-anionic ligands were isolated as Li or K salts and further used in transmetallation reactions towards Cr(II) and Zr(IV). Different coordination modes of the dearomatised ligands, including side-arm metallation, were observed. Substitution of the phosphine group in PNC by an imine donor led to a hybrid and “redox non-innocent” ligand
Kaplan, Hilan. "A General Approach to Cis-Fused Sesquiterpene Quinones and Synthesis, Characterization, and Catalytic Applications of Bis(Imino)-N-Heterocyclic Carbene Complexes of Iron". Thesis, Boston College, 2014. http://hdl.handle.net/2345/3862.
Pełny tekst źródłaSesquiterpene quinones are a prolific class of marine natural products that are particularly interesting due to their antibacterial, antiviral, and anti-inhibitory properties. Hundreds of these biologically active molecules are based on decalin frameworks, both cis- as well as trans-fused, however, significantly less synthetic work has focused on targeting the cis-fused series of compounds. In this chapter, progress towards an asymmetric, general route to various sesquiterpene quinones in the cleordane family of natural products will be described. The key steps of the synthesis include a highly convergent and diastereoselective reductive alkylation to forge both the requisite cis-ring fusion well as the all carbon quaternary center, as well as a scandium-catalyzed ring expansion of a 6,5-ring system to deliver the decalin core of the molecule. Additionally, the chapter includes the development and substrate scope of both methodologies utilized in the key complexity building reactions. Iron complexes ligated by bis(imino)pyridine ligands are remarkably active catalysts for a vast range of organic transformations including polymerization, hydrogenation, hydrosilylation, and hydroboration. Whereas much work has been done to probe the importance of the imine-substituents on catalysis, significantly less information is known about the nature of the central pyridine donor. To study the effects of a more donating ligand in which the pyridine is replaced with an N-heterocyclic carbene, a series of novel ligands and their corresponding iron complexes were synthesized and characterized. Whereas imidazole-derived complexes exhibited exclusively bidentate binding modes, 4,5,6-trihydropyrimidylidene-based ligands adopted a tridentate pincer conformation analogous to complexes of bis(imino)pyridines. Bonding in the five-coordinate bis(imino)-N-heterocyclic carbene complex displayed considerably contracted iron-ligand bond distances compared to the analogous bis(imino)pyridine iron complex. The study of physical and electronic structure and bonding in organometallic compounds is a critical for understanding and predicting complex behavior and reactivity. Having synthesized a completely new type of N-heterocyclic carbene (NHC) ligand and the corresponding iron complex, a rigorous study of metal-NHC bonding, magnetism, and redox activity in bis(imino)-NHC (or carbenodiimine, CDI) complexes of iron was carried out. A series of oxidation and reduction reactions on CDI complexes of iron were performed, enabling access to complexes spanning from formally iron(0) to iron (III) oxidation states. A battery of spectroscopic and computational methods, including X-ray crystallography, Mössbauer spectroscopy, SQUID magnetometry, and EPR spectroscopy established the CDI ligand as a redox active chelator. Additionally, a unique iron-carbene interaction was discovered, in which the metal center antiferromagnetically couples with the carbon of the NHC. Intent on developing CDI complexes of iron into practical catalysts for both synthetic organic transformations and polymerization, a series of stoichiometric as well as catalytic reactions were carried out to evaluate the reactivity profile of the novel complexes. Halide atom abstraction generated a new cationic species, which demonstrated different coordination chemistry compared to the bis(imino)pyridine analogue. Furthermore, the addition of a hydride or alkyl lithium reagent to the parent (CDI)FeCl2 species resulted in interesting and unexpected reactivity involving the carbene ligand. Preliminary catalytic hydrogenation experiments established (CDI)FeCl2 as a competent catalyst for the reduction of simple alkenes in the presence of Na(Hg) as a reductant under 80 psi of hydrogen. Additionally, the dichloride species could be readily converted into bis(aryloxide) complexes that were active for the polymerization of lactide to produce poly(lactic acid). The polymerization is very controlled (PDI values are <1.3), and polymers with molecular weights of around 35 kDa can be obtained after 3 hours at room temperature
Thesis (PhD) — Boston College, 2014
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Robishaw, Nikki K. "Encapsulating N-heterocyclic carbene complexes into biodegradable nanoparticles and the antimicrobial and antitumor effects". University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1530222031725709.
Pełny tekst źródłaHickey, James Laurence. "Synthetic approaches towards gold (I) and silver (I) complexes of functionalised N-heterocyclic carbene ligands". University of Western Australia. School of Biomedical, Biomolecular and Chemical Sciences, 2009. http://theses.library.uwa.edu.au/adt-WU2009.0090.
Pełny tekst źródłaStander-Grobler, Elzet. "Carbene ligand and complex design directed towards application in synthesis and homogeneous catalysis". Thesis, Stellenbosch : Stellenbosch University, 2008. http://hdl.handle.net/10019.1/1139.
Pełny tekst źródłaAlkylated acetonitrile that forms during the synthesis of the sulfonium salt, [(Me3)2(MeS)S][BF4], is involved in the formation of new , -unsaturated Fischer-type carbene complexes from (CO)5M=C(OMe)CH2Li (M = Cr, W). Metal migration observed when the substitution product obtained from the reaction of the anionic carbene complexes (CO)5M=C(NMe2)CºC¯ (M = Cr, W) with Ph3PAu+ was left in solution, was also kinetically and theoretically investigated. 1H NMR and quantum mechanical (at the B3LYP level of theory) data indicated a complicated mechanism. The a,b-unsaturated Fischer-type carbene complex, (CO)5Cr=C(OMe)CH=C(Me)NH(Me), obtained from the reaction of (CO)5M=C(OMe)CH2¯ with alkylated acetonitrile, was transformed into the new remote one-N, six-membered, carbene ligand (rN1HC6) complex, (CO)5Cr=C(CH=C(Me)N(Me)CH=C(nBu). The carbene ligand unprecedentedly preferred the softer Rh(CO)2Cl moiety to the Cr(CO)5 metal fragment and transferred readily. A new series of remote and abnormal square planar compounds [r/a(NHC)(PPh3)2MCl]CF3SO3 (M = Pd or Ni) was prepared by oxidative substitution. The various positions for metal-carbon bond formation on a pyridine ring to furnish various ligand types i.e. C2 for nN1HC6, C3 for aN1HC6 or C4 for rN1HC6 received attention. The ligands were arranged in increasing order of carbene character, aNHC < nNHC < rNHC and trans influence, nN2HC5 ~ aN1HC6 ~ nN1HC6 < rN1HC6. In competitive situations, oxidative substitution occurred selectively at C4 of the pyridine ring rather than at C2 and on the aromatic ring containing the heteroatom (C4), rather than on an annealed aromatic ring (C7). Crystal and molecular structure determinations confirmed the preferred coordination sites. Quantum mechanical calculations (at the RI-BP86/SV level of theory) indicated that the chosen carbene ligand has a much larger influence than the metal on the BDE of the M-Ccarbene bond; the farther away the N-atom is from the carbene carbon, the stronger the bond. In complexes that also contain additional external nitrogen atoms, e.g. trans-chloro(N-methyl-1,2,4- trihydro-2-dimethylaminepyrid-4-ylidene)bis(triphenylphosphine)palladium(II) triflate and transchloro( N-methyl-1,2,4-trihydro-2-dimethylaminepyrid-4-ylidene)bis(triphenylphosphine)nickel(II) triflate, stabilisation originates from both the nitrogens. 2-Chloro-1-methyl-1H-pyrid-4-ylidenephenylammonium triflate afforded complexes with both remote as well as normal nitrogen atoms. New azole complexes of palladium and nickel with remote heteroatoms were also prepared from N-methyl-4',4'-dimethyl-2'-thiophen-3-chloro-2-yl-4,5-dihydro-oxazole. Employing the compound 1,5-dichloroanthraquinone, the product of a double oxidative substitution on two Pd centra could be isolated but not alkylated. The fact that the chemical shift of the metal bonded carbon in the 13C NMR spectrum can not be used as absolute measure of carbene character, was emphasised in a compound where the heteroatom was situated seven bonds away from the carbon donor. In efforts to synthesise a sulphur-bridged complex that contains carbene ligands, crystals of transdi- iodobis(1,3-dimethyl-imidazoline-2-ylidene)palladium were obtained. Bridged thiolato complexes with N1HC6 ligands were unexpectedly found in the attempt to substitute the halogen on chosen square planar carbene complexes of palladium, widening the application possibilities of N1HC6 ligands in organometallic chemistry beyond that of catalysis. A trinuclear cluster, [(PdPPh3)3(μ-SMe)3]BF4 was isolated as a by-product of these reactions. A series normal and abnormal thiazolylidene complexes of nickel and palladium were prepared by oxidative substitution of the respective 2-, 4- and 5-bromothiazolium salts with M(PPh3)4 (M = Pd or Ni), and unequivocally characterised. In a preliminary catalytic investigation, all the thiazolinium and simple pyridinium derived palladium complexes showed activity in the Suzuki-Miyaura coupling reaction. Little variation in activity in the order a (N next to carbon donor) > n > a (S next to carbon donor) was found for the former series, whereas decreased activity was exhibited in the sequence r > a > n of the latter group. The pyridinium derived complexes showed superior activity to the thiazolinium ones. The rNHC complex, trans-chloro(N-methyl-1,2,4-trihydro-2- dimethylaminepyrid-4-ylidene)bis(triphenylphosphine)palladium(II) triflate, showed similar Suzuki-Miyaura activity to the standard N2HC5 carbene complex precatalyst, trans-chloro[(1,3- dimethyl-imidazol-2-ylidene)triphenylphosphine]palladium(II) triflate.
Duan, Gongping, i 段公平. "Design, synthesis, and photophysics and photochromic study of dithienylethene-containing heterocyclic derivatives and N-heterocycliccarbene-ruthenium (II) complexes". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B44248246.
Pełny tekst źródłaAksın, Özge Artok Levent. "The activity of silica immobilized palladium N-heterocyclic carbene complexes toward Mizoro-Heck reaction and their characterization/Özge Aksın;thesis advisor Levent Artok". [s.l.]: [s.n.], 2005. http://library.iyte.edu.tr/tezler/master/kimya/T000341.pdf.
Pełny tekst źródłaKeywords: Palladium, Immobilization, Heck Reaction, Palladium-N-Heterocyclic Carbene, Carbon-Carbon Coupling. Includes bibliographical references (leaves. 89-104).
Au, Ka-man, i 區嘉雯. "Luminescent cyclometalated gold (III) complexes with ancillary N-heterocyclic carbene and alkynyl ligands : from design, synthesis, photophysics to supramolecular assembly and functions". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hdl.handle.net/10722/207995.
Pełny tekst źródłapublished_or_final_version
Chemistry
Doctoral
Doctor of Philosophy
Ai, Pengfei. "Synthesis and reactivity of metal complexes containing functionalized N-heterocyclic carbene ligands for catalytic applications". Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAF025/document.
Pełny tekst źródłaThe purpose of this work was the synthesis of N,N'-diphosphanyl-functionalized NHC ligands andtheir coordination chemistry. The novel stable and rigid tridentate N,N'-diphosphanyl-imidazol-2-ylidene was synthesized and experimental and computational information on its stability weregained. It served as a unique platform for the synthesis of novel mono-, di-, tri-, penta-, hexanuclear complexes with the coinage metals (Cu, Ag and Au), exhibiting rare structural features. The mono- and dinuclear complexes with one or two dangling P-donors provided rational access to heterotrinuclear complexes. All these coinage metal complexes have short metal-metalseparations, indicating the presence of d10-d10 interactions, and display excellent luminescentproperties. Partial or complete transmetallation of the homotrinuclear Cu or Ag complexes withPd(0) precursors led to hetero-trinuclear complexes with d10-d10 interactions. In addition to itsbridging behavior, this ligand also showed its chelating behavior in Pd or Cr(III) complexes. Thelatter displayed superior performance in ethylene oligomerization than the Cr(II) complexes andgave mostly oligomers
Herrmann, Dirk [Verfasser], i Robert [Akademischer Betreuer] Wolf. "Synthesis, Characterization, and Reactivity of Transition Metal Complexes Stabilized by Naphthalene and Naphthyl-substituted N-heterocyclic Carbenes / Dirk Herrmann ; Betreuer: Robert Wolf". Regensburg : Universitätsbibliothek Regensburg, 2019. http://d-nb.info/1196873437/34.
Pełny tekst źródłaKnapp, Amanda R. "Antimicrobial and Antitumor Properties of Free and Poly(Ethylene Glycol)-Poly(Lactic Acid) Encapsulated Silver N-Heterocyclic Carbene Complexes". University of Akron / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=akron1309211795.
Pełny tekst źródłaMay, Tricia Lee. "Copper-Based N-Heterocyclic Carbene Complexes for Catalytic Enantioselective Conjugate Additions of Alkyl-, Aryl- and Vinyl-Based Nucleophiles to Form All-Carbon Quaternary Stereogenic Centers". Thesis, Boston College, 2011. http://hdl.handle.net/2345/2650.
Pełny tekst źródłaChapter 1 Enantioselective Conjugate Additions of Carbon Nucleophiles to Activated Olefins: Preparation of Enantioenriched Compounds Containing All-Carbon Quaternary Stereogenic Centers. Methods for enantioselective conjugate addition of nucleophiles to activated olefins generating products containing all-carbon quaternary stereogenic centers are critically reviewed. Enantioselective conjugate addition has been shown to be a powerful and concise approach to construct carbon-carbon bonds to prepare compounds containing sterically hindered stereogenic centers and has seen great advances in the past several years. Owing to the difficult nature of additions to relatively unreactive conjugate acceptors, compared to additions generating tertiary stereogenic centers, and construction of a sterically-hindered bond, in many cases, new and active catalysts had to be developed. The review discusses the areas where significant advances have been made as well as current limitations and future outlook. Chapter 2 Development of New and Active Catalysts for Cu-Catalyzed Enantioselective Conjugate Addition of Alkyl- and Arylzinc Reagent. Through development of new chiral catalysts, we have found an active and enantiodiscriminating bidentate, sulfonate-containing NHC-Cu catalyst that effects enantioselective conjugate addition of alkyl- and arylzinc reagents on notoriously difficult trisubstituted cyclic enones. Products are prepared with high levels of selectivity and participate in a variety of further functionalizations. The enantioselective additions are efficient and practical, not requiring rigorously anhydrous or oxygen-free conditions. Chapter 3 Cu-Catalyzed Enantioselective Conjugate Addition of Alkyl- and Arylaluminum Reagents to Trisubstituted Enones. Outlined in this chapter is the first effective solution for Cu-catalyzed enantioselective addition of alkyl and aryl nucleophiles to trisubstituted cyclopentenones generating products bearing a β-all-carbon quaternary stereogenic center. Products are obtained in up to 97% yield and 99:1 er, only requiring 5 mol % of an in situ generated Cu-NHC catalyst. The methodology was highlighted as one of the key steps in the total synthesis of clavirolide C. Not only five-membered rings, but six- and seven-membered rings serve as proficient partners in the enantioselective process. Moreover, in cases for the enantioselective aryl addition, in situ prepared Me2AlAr can be used without purification, filtration, or isolation, only requiring the corresponding aryl halides. The additions have also been extended to trisubstituted unsaturated lactones and chromones. Chapter 4 Cu-Catalyzed Enantioselective Conjugate Addition of Vinylaluminum Reagents to Cyclic Trisubstituted Enones. An enantioselective protocol for the formation of β,β-disubstituted cyclic ketones containing a synthetically versatile vinylsilane is disclosed. Enantioselective conjugate addition of in situ prepared silyl-substituted vinylaluminum reagents to β,β-unsaturated ketones promoted by 5 mol % of chiral Cu-NHC complexes delivers desired products with high efficiency (up to 95% yield after purification) and enantioselectivities (up to >98:<2 er). Several functionalizations utilizing the vinylsilanes, vicinal to an all-carbon quaternary stereogenic center, are shown, including an oxidative rearrangement, vinyl iodide formation and protodesilylation, accessing products not previously attainable. Furthermore, the enantioselective protocol is demonstrated as the key transformation in the total synthesis of riccardiphenol B
Thesis (PhD) — Boston College, 2011
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Hameury, Sophie. "Oxygen-functionalized NHC ligands and their nickel(II), silver(I) and palladium(II) complexes". Thesis, Strasbourg, 2014. http://www.theses.fr/2014STRAF010.
Pełny tekst źródłaThe purpose of this work was the synthesis of complexes bearing O-functionalized NHC ligands in order to test their catalytic properties in ethylene oligomerization. In order to have access to alcohol-functionalized complexes, the corresponding silver complexes were synthesized for transmetallation purpose. Whereas no concluding results were obtained with the alcohol function in association with nickel, it was possible to access an alcoholate-functionalized NHC ligand by deprotonation of the corresponding pro-ligand. Thus, polynuclear nickel complexes were prepared, some of them included in their structure a lithium cation originating from the base. For comparison, alcohol- and alcoholate-functionalized NHC palladium complexes were synthesized by direct reaction of the pro-ligand with Pd(acac)2 followed by acidobasic reactions. Because of the complexity of the chemistry of NHC-alcohol ligands associated with nickel, the ether functionality was explored. A library of nickel complexes was synthesized and tested in the catalytic ethylene oligomerization
Zou, Taotao, i 邹滔滔. "Anti-cancer N-heterocyclic carbene complexes of gold(III), gold(I) and platinum(II) : thiol "switch-on" fluorescent probes, thioredoxin reductase inhibitors and endoplasmic reticulum targeting agents". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2015. http://hdl.handle.net/10722/208614.
Pełny tekst źródłaMartínez, Agramunt Víctor. "Nickel and palladium supramolecular organometallic complexes based on NHC-ligands with polyaromatic moieties for host-guest chemistry studies". Doctoral thesis, Universitat Jaume I, 2020. http://dx.doi.org/10.6035/14104.2020.366143.
Pełny tekst źródłaThree nickel-based and one palladium-based supramolecular organometallic cages have been prepared. These four cages are based on a N-heterocyclic carbene ligand with a pyrene tag, that has been key in the subsequent applications of the cage together with the inner cavity. By pi-stacking interactions, it has been possible to encapsulate both polycylic aromatic hydrocarbons and fullerenes. The interest on first group of compounds is based on their accurate toxicity while the fullerenes are interesting due to their added value. It was possible to extract the first group of molecules from an organic media through the encapsulation inside the supramolecular cages. The host-guest adduct formed with fullerenes encapsulated inside the palladium cage was used as photocatalyst of aromatic, cyclic and acyclic substrates via singlet oxygen generation. The same palladium cage was used as receptor for multiple stacks of polyaromatic compounds.
Programa de Doctorat en Ciències
Ren, Xiaoyu. "Synthèse et réactivité de complexes métalliques porteurs de ligands carbéniques N-hétérocycliques fonctionnels". Thesis, Strasbourg, 2017. http://www.theses.fr/2017STRAF081/document.
Pełny tekst źródłaPotentially bidentate hybrid ligands (containing a NHC donor associated with an ether or an amine) and tridentate NCN pincer-type ligands (containing a central NHC donor flancked by two chemically-different nitrogen donors (Nimine and Namine)) have been prepared and used for coordination to transition metals, such as Ni, Cr, Cu, Ir. The influence of the length of the alkyl chain, -(CH2)2- or -(CH2)3- connecting the ether or the amine group to the heterocycle NHC was examined. In order to have access to the transition metal complexes, several methodologies were adopted: a) deprotonation of the corresponding imidazolium salts followed by addition of transition metal precursors; b) transmetalation from NHC silver complexes; c) oxidative-addition reaction of Ni(0) with imidazolium salts or the corresponding protonated salts. A series of Ni(II), Cr(III) complexes were tested in the catalytic ethylene oligomerization reaction