Relevant bibliographies by topics / N-Heterocyclic carbenes complexes

Academic literature on the topic 'N-Heterocyclic carbenes complexes'

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Published: 4 June 2021
Last updated: 12 February 2022

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Journal articles on the topic "N-Heterocyclic carbenes complexes"

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Longevial, Jean-François, Mamadou Lo, Aurélien Lebrun, Danielle Laurencin, Sébastien Clément, and Sébastien Richeter. "Molecular complexes and main-chain organometallic polymers based on Janus bis(carbenes) fused to metalloporphyrins." Dalton Transactions 49, no. 21 (2020): 7005–14. http://dx.doi.org/10.1039/d0dt00594k.

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Janus bis(N-heterocyclic carbenes) composed of a porphyrin core with two N-heterocyclic carbene (NHC) heads fused to opposite pyrroles were used as bridging ligands for the preparation of metal complexes.
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Zhao, Shixian, Feifei Wu, Yuyu Ma, Wanzhi Chen, Miaochang Liu, and Huayue Wu. "Enhancement of N-heterocyclic carbenes on rhodium catalyzed olefination of triazoles." Organic & Biomolecular Chemistry 14, no. 8 (2016): 2550–55. http://dx.doi.org/10.1039/c5ob02397a.

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Frański, Rafał, Błażej Gierczyk, Grzegorz Schroeder, Stefan Pieper, Andreas Springer, and Michael Linscheid. "Electrospray ionization mass spectrometric study of mercury complexes of N-heterocyclic carbenes derived from 1,2,4-triazolium salt precursors." Open Chemistry 5, no. 1 (March 1, 2007): 316–29. http://dx.doi.org/10.2478/s11532-006-0050-0.

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AbstractBy mixing 1,2,4-triazolium salts (precursors of N-heterocyclic carbenes 1–6) with mercury acetate, a number of complexes have been obtained under electrospray ionization condition. Carbenes 1 and 2 contain one carbene center; therefore, they are able to bond only one mercury cation. Carbenes 3–5 contain two carbene centers; therefore, they can bond two mercury cations. Mercury complexes of 1–5 always contain an acetate anion attached to a mercury cation. Carbene 6 also contains two carbene centers; however, its structure allows formation of a complex containing mercury bonded simultaneously to both centers, therefore, the complex that does not contain an acetate anion. The MS/MS spectra taken for complexes of carbenes 1–5 have shown formation of a cation corresponding to N1 substituent (adamantyl or benzyl), and those of complexes of carbenes 3–5 (doubly charged ions) have also shown the respective complementary partner ions. Mercury complex of 2 has yielded some other interesting fragmentation pathways, e.g. a loss of the HHgOOCCH3 molecule. The fragmentation pathway of the mercury complexes of 6 was found to be complicated.
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Leitão, Maria Inês P. S., Giulia Francescato, Clara S. B. Gomes, and Ana Petronilho. "Synthesis of Platinum(II) N-Heterocyclic Carbenes Based on Adenosine." Molecules 26, no. 17 (September 4, 2021): 5384. http://dx.doi.org/10.3390/molecules26175384.

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Organometallic derivatization of nucleosides is a highly promising strategy for the improvement of the therapeutic profile of nucleosides. Herein, a methodology for the synthesis of metalated adenosine with a deprotected ribose moiety is described. Platinum(II) N-heterocyclic carbene complexes based on adenosine were synthesized, namely N-heterocyclic carbenes bearing a protected and unprotected ribose ring. Reaction of the 8-bromo-2′,3′,5′-tri-O-acetyladenosine with Pt(PPh3)4 by C8−Br oxidative addition yielded complex 1, with a PtII centre bonded to C-8 and an unprotonated N7. Complex 1 reacted at N7 with HBF4 or methyl iodide, yielding protic carbene 2 or methyl carbene 3, respectively. Deprotection of 1 to yield 4 was achieved with NH4OH. Deprotected compound 4 reacted at N7 with HCl solutions to yield protic NHC 5 or with methyl iodide yielding methyl carbene 6. Protic N-heterocyclic carbene 5 is not stable in DMSO solutions leading to the formation of compound 7, in which a bromide was replaced by chloride. The cis-influence of complexes 1–7 was examined by 31P{1H} and 195Pt NMR. Complexes 2, 3, 5, 6 and 7 induce a decrease of 1JPt,P of more than 300 Hz, as result of the higher cis-influence of the N-heterocyclic carbene when compared to the azolato ligand in 1 and 4.
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Wilhelm, René, Eduard Rais, and Ulrich Flörke. "Reactivity of Grubbs–Hoveyda II Complexes Including Extended N-Heterocyclic Carbenes with a Bicyclic Camphor-Based Framework." Synthesis 49, no. 13 (June 7, 2017): 2852–64. http://dx.doi.org/10.1055/s-0036-1588849.

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This feature article discusses the synthesis of new asymmetric Grubbs–Hoveyda II complexes with extended N-heterocyclic carbenes containing a bicyclic camphor-based framework. The new enantiopure complexes can be prepared in a short route from the chiral pool. The extended carbene-based catalyst shows high activity in olefin metathesis reactions. The new complexes exhibited enantioselectivity in an asymmetric ROCM desymmetrization. Depending on the substituents on the nitrogen atoms of the carbenes, the opposite enantiomer was formed in excess.
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Michalak and Kośnik. "Chiral N-heterocyclic Carbene Gold Complexes: Synthesis and Applications in Catalysis." Catalysts 9, no. 11 (October 25, 2019): 890. http://dx.doi.org/10.3390/catal9110890.

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N-Heterocyclic carbenes have found many applications in modern metal catalysis, due to the formation of stable metal complexes, and organocatalysis. Among a myriad of N-heterocyclic carbene metal complexes, gold complexes have gained a lot of attention due to their unique propensity for the activation of carbon-carbon multiple bonds, allowing many useful transformations of alkynes, allenes, and alkenes, inaccessible by other metal complexes. The present review summarizes synthetic efforts towards the preparation of chiral N-heterocyclic gold(I) complexes exhibiting C2 and C1 symmetry, as well as their applications in enantioselective catalysis. Finally, the emerging area of rare gold(III) complexes and their preliminary usage in asymmetric catalysis is also presented.
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Ho, Luong Phong, Lukas Körner, Thomas Bannenberg, and Matthias Tamm. "Chalcogen complexes of anionic N-heterocyclic carbenes." Dalton Transactions 49, no. 38 (2020): 13207–17. http://dx.doi.org/10.1039/d0dt02392b.

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Mas-Marzá, Elena, Patrícia M. Reis, Eduardo Peris, and Beatriz Royo. "Dioxomolybdenum(VI) complexes containing N-heterocyclic carbenes." Journal of Organometallic Chemistry 691, no. 12 (June 2006): 2708–12. http://dx.doi.org/10.1016/j.jorganchem.2006.02.004.

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Weskamp, Thomas, Florian J. Kohl, and Wolfgang A. Herrmann. "N-heterocyclic carbenes: novel ruthenium–alkylidene complexes." Journal of Organometallic Chemistry 582, no. 2 (June 1999): 362–65. http://dx.doi.org/10.1016/s0022-328x(99)00163-1.

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Herrmann, Wolfgang A., Florian J. Kohl, and Jurgen Schwarz. "ChemInform Abstract: Complexes of N-Heterocyclic Carbenes." ChemInform 32, no. 1 (January 2, 2001): no. http://dx.doi.org/10.1002/chin.200101252.

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Dissertations / Theses on the topic "N-Heterocyclic carbenes complexes"

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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.

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Mungur, 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.

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McNally, 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.

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Silcock, 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.

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This thesis is concerned with the synthesis of two di-N-heterocyclic carbene ligands, and their reactivity towards nickel and palladium precursors in order to synthesise new organometallic pre-catalysts for a number of important reactions. The catalytic properties of a new rhodium C60 compound are also investigated, with relevance to the evaluation of C60 as a hydrogen storage medium. Chapter 1 reviews the preparation and chemistry of N-heterocyclic carbenes, emphasising their organometallic reactivity and role as ancillary ligands in homogeneous transition metal catalysis. An overview of relevant nickel and palladium catalysis is also presented, including olefin polymerisation, olefm / CO copolymerisation and Heck coupling reactions. Chapter 2 describes the synthesis and characterisation of the dicarbene ligands tBuCCmeth and tBuCCeth and their reactions with various nickel precursors in attempts to prepare chelating dicarbene nickel cis-dihalide complexes. The synthesis, characterisation and chemical reactivity of the cations [Ni(tBuCCmeth)2]2+, [(tBuCCmeth)NiCl(PMe3)] + and [(tBuCCeth)NiCl(PMe3)]+ is detailed, and their X-ray structures are compared. The unsuccessful preparation of [Ni(tBuCCeth)2] 2+ and the relative stability of the monocations with respect to dicarbene substitution is discussed and attributed to steric factors. Chapter 3 describes the synthesis, characterisation, reactivity and catalytic studies of simple nickel and palladium cis-dimethyl complexes of the chelating dicarbene ligands. Variable temperature 1H NMR spectroscopy showed contrasting rates of thermal hydrocarbon elimination from Ni(tBuCCmeth)Me2 and Ni(tBuCCeth)Me2, which has previously been observed for chelating bis-phosphine analogues with various P,P' linkages (CH2)n . These observations further corroborate the analogy between dicarbene and 6/s-phosphine ligands. It was demonstrated that the compounds Pd(tBuCCmeth)Me2and Pd(tBuCCeth)Me2 are effective pre-catalysts for the Heck coupling of 4-bromoanisole and n-butyl acrylate. In addition cations of the type [(tBuCCmeth/eth)PdMe(L)]+ (L = pyridine, THF) which are relevant to olefin / CO copolymerisation were prepared. The X-ray structures of M(tBuCCeth)Me2 (M = Ni, Pd) are discussed as well as the synthesis and structural characterisation of [(|Li-tBu CC meth){Ni(PMe3)Me2}2]. Chapter 4 presents a brief introduction to some relevant C60 chemistry and to the concept of hydrogen storage. The synthesis and characterisation of a new rhodium Ceo compound is described. The compound catalysed the hydrogenation and hydroformylation of simple alkenes as well as the hydrogenation of C60 to C60H36 . The recovery of hydrogen gas from C60H36 was investigated in order to evaluate C60 as a hydrogen storage medium. Chapter 5 outlines the experimental details for the synthesis, characterisation, reactions and catalytic studies of the new compounds described in the preceding three chapters. Chapter 6 presents the characterising data for the new compounds described in chapters 2 and 3. Appendices contain details of the crystallographic data for the eight structurally characterised compounds described in chapters 2 and 3.
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Brayshaw, 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.

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This thesis is comprised of two parts. The first part describes the synthesis of cyclopentadienyltungsten complexes containing a pendant alkyne group (I), and the subsequent photo-induced intramolecular coordination of the alkyne, forming complexes such as II. Compounds containing intramolecularly coordinated alkynes are rare, and this is the first example using cyclopentadiene as the core ligand. The second part describes the synthesis and structural characterisation of a number of novel metal complexes containing N-heterocyclic carbene ligands, some containing particular functionality for taylored applications. New methods were used to form complexes of rhodium, iridium, silver and gold (eg. III, IV). Structural and spectroscopic properties of the complexes were correlated with electronic characteristics of the ancillary ligands. A number of rhodium and iridium complexes (eg. IV) derived from imidazolium-linked cyclophanes were synthesised and structurally characterised. Complexes of N-heterocyclic carbenes with pendant ionic groups were synthesised, and a preliminary examination of their catalytic activity in water was performed. N-Heterocyclic carbenes complexes containing an electron withdrawing nitro group were synthesised and the effect of the nitro group on metal-ligand bonding was examined.
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Martin, 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.

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This thesis describes the synthesis, characterisation and reactivity of new manganese and rhenium(I) NHC complexes, which have been investigated both thermally and photochemically and the results contrasted with existing phosphine analogues in the literature. Cp’Mn(CO)2(NHC) (NHC = IEt2Me2 1, IMes 2, IiPr2Me2 3 and IPr 4) were synthesised and investigated by TRIR spectroscopy. Loss of CO was observed after 355 nm irradiation to form agostically stabilised intermediates, which reformed the parent species by recombination with CO on the nanosecond timescale. Loss of NHC was not observed, in contrast to Cp’Mn(CO)2(PPh3) which lost both CO and PPh3 upon photolysis. [Re(NHC)(Bpy)(CO)3]BAr4F (NHC = IEt2Me2 5, IMes 6) were synthesised and investigated by TRIR spectroscopy and UV/Vis absorption and emission spectrometry. Inclusion of an NHC altered the excited state manifold of the complexes, favouring population of the 3MLCT over the 3IL excited state. The lowest energy excited state for both 5 and 6 proved to be a 3MLCT excited state at 298 and 77 K. In contrast, [Re(PPh3)(Bpy)(CO)3]BAr4F exhibited 3MLCT at 298 K, but 3IL at 77 K. A series of complexes, M(NHC)(CO)4X and M(NHC)2(CO)3X (M = Re, X = Cl; M = Mn, X = Br) formed upon reaction of the corresponding M(CO)5X species and free NHC. The substitution pattern was dictated by the steric bulk of the NHC. Generation of the corresponding cations by halide abstraction was investigated. M(NHC)2(CO)3X was found to form agostic stabilised species upon halide abstraction by NaBAr4F in CH2Cl2. Under the same conditions, Re(IPr)(CO)4Cl was found to form the dichloromethane complex, [Re(IPr)(CO)4(η1-CH2Cl2)]BAr4F. In C6H5F solution under an atmosphere of dihydrogen, the CH2Cl2 ligand could be displaced by H2 to form the dihydrogen species, [Re(IPr)(CO)4(H2)]BAr4F.
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Conti, 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/.

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The aim of my training period has been the synthesis of new chiral N-heterocyclic carbene precursors starting from camphoric diacid and the employment of imidazolium salts derived NHC as linker to dendrimers supports for organometallic catalysis. New chiral ligands are needed to develop new catalytic systems for enantioselective transformations. The new type of ligand described was developed starting from camphoric diacid, a cheap chiral molecule, following different synthetic strategies. Asymmetric functionalized chiral NHCs are readily available by methods developed and two of the precursors obtained were employed in preliminary tests with Aluminium and Palladium. An NHC derived from imidazolium salt has been investigated as linker to dendrimeric supports for tetraarylciclopentadienone-Ruthenium complexes with the aim to combine advantages of homogeneous catalysis to advantages of heterogeneous one, in particular easy recover of catalyst. The functionalized dendrimers obtained have been used in transfer hydrogenation and dehydrogenation reactions. Moreover a new class of functionalized dendrimer was obtained employing a new tetraarylciclopentadienone-Ruthenium complex with trimethyl silyl groups on cyclopentadienone ligand with the aim to change solubility of the system.
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Mokfi, Moloud [Verfasser]. "Xanthine-derived N-heterocyclic carbenes and their metal complexes / Moloud Mokfi." Wuppertal : Universitätsbibliothek Wuppertal, 2021. http://d-nb.info/1240266960/34.

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Turner, Zoe Rose. "Small molecule activation using electropositive metal N-heterocyclic carbene complexes." Thesis, University of Edinburgh, 2011. http://hdl.handle.net/1842/8210.

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The versatility of N-heterocyclic carbenes (NHCs) is demonstrated by numerous practical applications in homogeneous transition metal catalysis, organocatalysis and materials science. There remains a paucity of electropositive metal NHC complexes and so this chemistry is poorly developed with respect to that of the late transition metal and main group elements. This thesis describes the synthesis of new alkoxy-tethered NHC proligands, their use in the synthesis of reactive metal amide and metal alkyl complexes, and finally small molecule activation using these complexes. Chapter One introduces NHCs and discusses their use as supporting ligands for early transition metal and f-block complexes. Small molecule activation using organometallic complexes is examined alongside the use of electropositive metal NHC complexes in catalysis. Chapter Two contains the synthesis and characterisation of new alkoxy-tethered NHC proligands and a variety of electropositive MII (M = Mg and Zn), MIII (M = Y, Sc, Ce and U) and MIV (M = Ce and U) amide complexes. X-ray diffraction studies and a DFT study are used to probe the extent of covalency in the bonding of the MIV complexes. Chapter Three investigates the reactivity of the amide complexes prepared in Chapter Two. The MII complexes are shown to be initiators for the polymerisation of raclactide into biodegradable polymers. The MIII complexes are used to demonstrate additionelimination reactivity of polar substrates across the M-Ccarbene bond which allows the formation of new N-E (E = Si, Sn, P or B) bonds. Treatment of the UIII silylamide complex U(N{SiMe3}2)3 with CO results in the reductive coupling and homologation of CO to form an ynediolate core -OC≡CO- and the first example of subsequent reactivity of the ynediolate group. The MIV complexes are used to examine the potential for forming MIV cationic species and alkyl complexes. Chapter Four examines the synthesis of MIII (M = Ce and Sc) aminobenzyl complexes and MIII (M = Y, Sc and U) neosilyl and neopentyl alkyl complexes. The addition-elimination reactivity discussed in Chapter Three is extended to include C-E bond formation (E = Si, Sn, P, B, I or C). Chapter Five provides overall conclusions to the work presented within this thesis. Chapter Six gives experimental and characterising data for all complexes and reactions in this work.
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Hesler, 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.

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This thesis presents an investigation into the synthesis of metal complexes of (Nheterocyclic carbene)-based cyclophanes. There were three main areas of focus: synthesis and complexation of bis(4,5-dihydroimidazolium) salts; the synthesis and complexation of phenol-functionalised imidazolium cyclophanes; and the synthesis and complexation of (N-heterocyclic carbene)-based cyclophanes by C-C bond activation of biimidazolium salts with electron-rich metals. The synthesis of xylyl-linked bis(4,5-dihydroimidazolium) salts was investigated. Attempts to prepare these compounds by the cyclisation of a tetraamine (linear or macrocyclic) were unsuccessful due difficulties in preparing the tetraamines. The target compounds could be prepared by adapting the methods developed for the synthesis of bis(imidazolium) salts however problems associated with purification and stability of the products prevented complexation studies. A series of phenol-, phenoxide- and anisole-functionalised imidazolium cyclophanes were prepared. Their structural properties were investigated using dynamic nmr studies and X-ray crystallography. Complexation of the functionalised cyclophanes was investigated. The phenol cyclophane I formed a dinuclear complex with mercury(II). This complex is the first example of a complex derived from a phenol-functionalised imidazolium cyclophane. However the anisole cyclophane II and the unsymmetrical phenol/ortho cyclophane III were unable to form complexes possibly due to steric hindrance and instability of the cyclophane respectively. Preliminary complexation studies of the bis(imidazolium)phenol V suggested that complexation with palladium(II) and mercury(II) were possible but more work is required to determine the optimum reaction conditions. A series of biimidazolium salts VI (both new and known) were prepared. Previously reported biimidazolium salts have very low solubility in common solvents therefore the incorporation of long alkyl chains to the bridging group was investigated as a means to improve the solubility. The structure of the salts was explored using a range of techniques including dynamic nmr spectroscopy, cyclic voltammetry, UV/Visible spectroscopy, X-ray crystallography and mass spectrometry. Some of the biimidazolium salts were able to rotate about the C2-C2' bond and the free energy of activation for this process was estimated using dynamic nmr studies. C-C bond activation of the biimidazolium salts with palladium(0) was used to form a series of palladium(II) complexes (VII) of (NHC)-based cyclophanes. These reactions are the first examples of the synthesis of bis(NHC) complexes by C-C bond activation. The reactivity of the biimidazolium salts with palladium(0) was compared to their solution structure and it was found that only the biimidazolium that were able to rotate about the C2-C2' bond could react with palladium(0).
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Books on the topic "N-Heterocyclic carbenes complexes"

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Fedorkiw, Terry William. Study of new ruthenium and iridium hydride complexes bearing N-heterocyclic carbenes as ligands. Ottawa: National Library of Canada, 2003.

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Kühl, Olaf. Functionalised N-heterocyclic carbene complexes. Hoboken, N.J: Wiley, 2009.

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Kühl, Olaf. Functionalised N-heterocyclic carbene complexes. Chichester, U.K: Wiley, 2010.

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Functionalised N-heterocyclic carbene complexes. Hoboken, N.J: Wiley, 2009.

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Kühl, Olaf. Functionalised N-heterocyclic carbene complexes. Hoboken, N.J: Wiley, 2009.

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Vogel, Carola S. High- and Low-Valent tris-N-Heterocyclic Carbene Iron Complexes. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-27254-7.

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Zou, Taotao. Anti-Cancer N-Heterocyclic Carbene Complexes of Gold(III), Gold(I) and Platinum(II). Singapore: Springer Singapore, 2016. http://dx.doi.org/10.1007/978-981-10-0657-9.

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service), SpringerLink (Online, ed. High- and Low-Valent tris-N-Heterocyclic Carbene Iron Complexes: A Study of Molecular and Electronic Structure. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012.

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Fedorkiw, Terry William. Study of new ruthenium and iridium hydride complexes bearing N-heterocyclic carbenes as ligands. 2003, 2003.

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Vogel, Carola S. S. High- and Low-Valent tris-N-Heterocyclic Carbene Iron Complexes: A Study of Molecular and Electronic Structure. Springer, 2016.

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Book chapters on the topic "N-Heterocyclic carbenes complexes"

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Haynes, M. Taylor, Evan P. Jackson, and John Montgomery. "Nickel Complexes ofN-Heterocyclic Carbenes." In N-Heterocyclic Carbenes, 371–96. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch13.

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Lazreg, Faïma, and Catherine S. J. Cazin. "NHC-Copper Complexes and their Applications." In N-Heterocyclic Carbenes, 199–242. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch08.

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Hoyos, Mario, Daniel Guest, and Oscar Navarro. "(N-Heterocyclic Carbene)-Palladium Complexes in Catalysis." In N-Heterocyclic Carbenes, 85–110. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch04.

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Lazreg, Faïma, and Catherine S. J. Cazin. "Medical Applications of NHC-Gold and -Copper Complexes." In N-Heterocyclic Carbenes, 173–98. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch07.

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Wurm, Thomas, Abdullah Mohamed Asiri, and A. Stephen K. Hashmi. "NHC-Au(I) Complexes: Synthesis, Activation, and Application." In N-Heterocyclic Carbenes, 243–70. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch09.

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Wagers, Patrick O., Kerri L. Shelton, Matthew J. Panzner, Claire A. Tessier, and Wiley J. Youngs. "Synthesis and Medicinal Properties of Silver-NHC Complexes and Imidazolium Salts." In N-Heterocyclic Carbenes, 151–72. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch06.

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Mavila, Sudheendran, and N. Gabriel Lemcoff. "N-Heterocyclic Carbene-Ruthenium Complexes: A Prominent Breakthrough in Metathesis Reactions." In N-Heterocyclic Carbenes, 307–40. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch11.

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Schwartsburd, Leonid, and Michael K. Whittlesey. "RutheniumN-Heterocyclic Carbene Complexes for the Catalysis of Nonmetathesis Organic Transformations." In N-Heterocyclic Carbenes, 341–70. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch12.

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Murphy, Luke J., Katherine N. Robertson, Jason D. Masuda, and Jason A. C. Clyburne. "NHC Complexes of Main Group Elements: Novel Structures, Reactivity, and Catalytic Behavior." In N-Heterocyclic Carbenes, 427–98. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch15.

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Dierick, Steve, and István E. Markó. "NHC Platinum(0) Complexes: Unique Catalysts for the Hydrosilylation of Alkenes and Alkynes." In N-Heterocyclic Carbenes, 111–50. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527671229.ch05.

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Conference papers on the topic "N-Heterocyclic carbenes complexes"

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Vo-Thanh, Giang, Audrey Aupoix, and Chloée Bournaud. "Asymmetric transfer hydrogenation of aromatic ketones using rhodium complexes of chiral N-heterocyclic carbenes derived from (S)-pyroglutamic acid." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a005.

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Silbestri, Gustavo, Gabriela Fernández, María Vela Gurovic, Nelda Olivera, and Alicia Chopa. "Synthesis and Antimicrobial Activities of Gold(I) N-heterocyclic Carbene Complexes." In The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01015.

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Su, Qingzhi, Chaoyang Chai, and Feng Zhao. "Synthesis and Photophysical Properties of Four-Coordinate N-heterocyclic Carbene Copper(Ⅰ) Complex Emitting Material with Brightly Luminescence." In 2018 7th International Conference on Energy and Environmental Protection (ICEEP 2018). Paris, France: Atlantis Press, 2018. http://dx.doi.org/10.2991/iceep-18.2018.277.

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Hussaini, Sunusi Y., Rosenani A. Haque, Mohd R. Razali, and A. M. S. Abdul Majid. "Effects of supramolecular interactions in nitrile functionalized silver(I)-N-heterocyclic carbene complexes and investigation into their enhancement of antitumor metallodrugs." In 4TH INTERNATIONAL CONFERENCE ON THE SCIENCE AND ENGINEERING OF MATERIALS: ICoSEM2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0027461.

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