The Reductive Addition Oxidative Elimination Mechanism

dc.contributor.affiliationInstituto Universitario Mixto de Tecnología Química
dc.contributor.authorLerma-Berlanga, Belén
dc.contributor.authorLeyva Perez, Antonio
dc.contributor.funderAgencia Estatal de Investigaciónes_ES
dc.date.accessioned2026-05-26T12:35:30Z
dc.date.available2026-05-26T12:35:30Z
dc.date.issued2025-03-10es_ES
dc.description.abstract[EN] The oxidative addition¿reductive elimination (OARE) mechanism of reactive molecules on metal atoms is a cornerstone of modern chemistry. However, the complementary reductive addition¿oxidative elimination (RAOE) mechanism is barely considered, despite a first reduction reaction between metal atoms and the incoming organic reactant makes chemical sense in a plethora of processes. Here we show, in a chronological order, early precedents in the literature which indicated the possibility of a general RAOE mechanism, the few systems explicitly reported so far (including a catalytic system) and some other reactions where a RAOE mechanism would satisfactorily explain the mechanistic evidences found. These examples, together, strongly suggest that researchers should consider the RAOE mechanism during their investigations, and not simply adjust their conclusions to the omnipresent OARE mechanism. This new line of thinking might open new avenues in the design of chemical reactions, particularly catalytic ones.es_ES
dc.description.accrualMethodSes_ES
dc.description.bibliographicCitationLerma-Berlanga, Belén; Leyva Perez, Antonio (2025). The Reductive Addition Oxidative Elimination Mechanism. ChemistryEurope. 3(2). https://doi.org/10.1002/ceur.202400086es_ES
dc.description.issue2es_ES
dc.description.referencesLabinger, J. A. (2015). Tutorial on Oxidative Addition. Organometallics, 34(20), 4784-4795. https://doi.org/10.1021/acs.organomet.5b00565es_ES
dc.description.referencesSouillart, L., & Cramer, N. (2015). Catalytic C–C Bond Activations via Oxidative Addition to Transition Metals. Chemical Reviews, 115(17), 9410-9464. https://doi.org/10.1021/acs.chemrev.5b00138es_ES
dc.description.referencesGarcı́a-Cárceles, J., Bahou, K. A., & Bower, J. F. (2020). Recent Methodologies That Exploit Oxidative Addition of C–N Bonds to Transition Metals. ACS Catalysis, 10(21), 12738-12759. https://doi.org/10.1021/acscatal.0c03341es_ES
dc.description.referencesCollman, J. P. (1968). Patterns of organometallic reactions related to homogeneous catalysis. Accounts of Chemical Research, 1(5), 136-143. https://doi.org/10.1021/ar50005a002es_ES
dc.description.referencesVaska, L. (1968). Reversible activation of covalent molecules by transition-metal complexes. The role of the covalent molecule. Accounts of Chemical Research, 1(11), 335-344. https://doi.org/10.1021/ar50011a003es_ES
dc.description.referencesSunley, G. J., & Watson, D. J. (2000). High productivity methanol carbonylation catalysis using iridium. Catalysis Today, 58(4), 293-307. https://doi.org/10.1016/s0920-5861(00)00263-7es_ES
dc.description.referencesDenisova, E. A., Kostyukovich, A. Yu., Fakhrutdinov, A. N., Korabelnikova, V. A., Galushko, A. S., & Ananikov, V. P. (2022). “Hidden” Nanoscale Catalysis in Alkyne Hydrogenation with Well-Defined Molecular Pd/NHC Complexes. ACS Catalysis, 12(12), 6980-6996. https://doi.org/10.1021/acscatal.2c01749es_ES
dc.description.referencesRuiz-Castillo, P., & Buchwald, S. L. (2016). Applications of Palladium-Catalyzed C–N Cross-Coupling Reactions. Chemical Reviews, 116(19), 12564-12649. https://doi.org/10.1021/acs.chemrev.6b00512es_ES
dc.description.referencesChu, T., & Nikonov, G. I. (2018). Oxidative Addition and Reductive Elimination at Main-Group Element Centers. Chemical Reviews, 118(7), 3608-3680. https://doi.org/10.1021/acs.chemrev.7b00572es_ES
dc.description.referencesGardner, B. M., Kefalidis, C. E., Lu, E., Patel, D., McInnes, E. J. L., Tuna, F., Wooles, A. J., Maron, L., & Liddle, S. T. (2017). Evidence for single metal two electron oxidative addition and reductive elimination at uranium. Nature Communications, 8(1). https://doi.org/10.1038/s41467-017-01363-0es_ES
dc.description.referencesChristmann, U., & Vilar, R. (2004). Monoligated Palladium Species as Catalysts in Cross‐Coupling Reactions. Angewandte Chemie International Edition, 44(3), 366-374. Portico. https://doi.org/10.1002/anie.200461189es_ES
dc.description.referencesWagschal, S., Perego, L. A., Simon, A., Franco‐Espejo, A., Tocqueville, C., Albaneze‐Walker, J., Jutand, A., & Grimaud, L. (2019). Formation of XPhos‐Ligated Palladium(0) Complexes and Reactivity in Oxidative Additions. Chemistry – A European Journal, 25(28), 6980-6987. Portico. https://doi.org/10.1002/chem.201900451es_ES
dc.description.referencesZhang, J., Bellomo, A., Trongsiriwat, N., Jia, T., Carroll, P. J., Dreher, S. D., Tudge, M. T., Yin, H., Robinson, J. R., Schelter, E. J., & Walsh, P. J. (2014). NiXantphos: A Deprotonatable Ligand for Room-Temperature Palladium-Catalyzed Cross-Couplings of Aryl Chlorides. Journal of the American Chemical Society, 136(17), 6276-6287. https://doi.org/10.1021/ja411855des_ES
dc.description.referencesBraun, T. (2005). Oxidative Addition of NH<sub>3</sub> to a Transition‐Metal Complex: A Key Step for the Metal‐Mediated Derivatization of Ammonia? Angewandte Chemie International Edition, 44(32), 5012-5014. Portico. https://doi.org/10.1002/anie.200501505es_ES
dc.description.referencesDoherty, S., Knight, J. G., Alharbi, H. Y., Paterson, R., Wills, C., Dixon, C., Šiller, L., Chamberlain, T. W., Griffiths, A., Collins, S. M., Wu, K., Simmons, M. D., Bourne, R. A., Lovelock, K. R. J., & Seymour, J. (2022). Efficient Hydrolytic Hydrogen Evolution from Sodium Borohydride Catalyzed by Polymer Immobilized Ionic Liquid‐Stabilized Platinum Nanoparticles. ChemCatChem, 14(4). Portico. https://doi.org/10.1002/cctc.202101752es_ES
dc.description.referencesGhosh, T. K., & Nair, N. N. (2011). Oxidative Addition of Water to Rh<sub><i>n</i></sub> (<i>n</i> = 1–4) Clusters on Alumina Surfaces and Spontaneous Formation of H<sub>2</sub>. The Journal of Physical Chemistry C, 115(31), 15403-15409. https://doi.org/10.1021/jp202832ves_ES
dc.description.referencesAsensio, J. M., Bouzouita, D., van Leeuwen, P. W. N. M., & Chaudret, B. (2019). σ-H–H, σ-C–H, and σ-Si–H Bond Activation Catalyzed by Metal Nanoparticles. Chemical Reviews, 120(2), 1042-1084. https://doi.org/10.1021/acs.chemrev.9b00368es_ES
dc.description.referencesAdams, Richard D., & Captain, B. (2007). Hydrogen Activation by Unsaturated Mixed‐Metal Cluster Complexes: New Directions. Angewandte Chemie International Edition, 47(2), 252-257. Portico. https://doi.org/10.1002/anie.200702407es_ES
dc.description.referencesCorma, A., Ródenas, T., & Sabater, M. J. (2012). Aerobic oxidation of thiols to disulfides by heterogeneous goldcatalysts. Chem. Sci., 3(2), 398-404. https://doi.org/10.1039/c1sc00466bes_ES
dc.description.referencesShen, C., Zhang, P., Sun, Q., Bai, S., Hor, T. S. A., & Liu, X. (2015). Recent advances in C–S bond formation via C–H bond functionalization and decarboxylation. Chemical Society Reviews, 44(1), 291-314. https://doi.org/10.1039/c4cs00239ces_ES
dc.description.referencesGarnes-Portolés, F., Greco, R., Oliver-Meseguer, J., Castellanos-Soriano, J., Consuelo Jiménez, M., López-Haro, M., Hernández-Garrido, J. C., Boronat, M., Pérez-Ruiz, R., & Leyva-Pérez, A. (2021). Regioirregular and catalytic Mizoroki–Heck reactions. Nature Catalysis, 4(4), 293-303. https://doi.org/10.1038/s41929-021-00592-3es_ES
dc.description.referencesRobinson, P. S. D., Khairallah, G. N., da Silva, G., Lioe, H., & O’Hair, R. A. J. (2012). Gold‐Mediated CI Bond Activation of Iodobenzene. Angewandte Chemie International Edition, 51(16), 3812-3817. Portico. https://doi.org/10.1002/anie.201108502es_ES
dc.description.referencesBoronat, M., Leyva-Pérez, A., & Corma, A. (2013). Theoretical and Experimental Insights into the Origin of the Catalytic Activity of Subnanometric Gold Clusters: Attempts to Predict Reactivity with Clusters and Nanoparticles of Gold. Accounts of Chemical Research, 47(3), 834-844. https://doi.org/10.1021/ar400068wes_ES
dc.description.referencesTu, W., Ghoussoub, M., Singh, C. V., & Chin, Y.-H. C. (2017). Consequences of Surface Oxophilicity of Ni, Ni-Co, and Co Clusters on Methane Activation. Journal of the American Chemical Society, 139(20), 6928-6945. https://doi.org/10.1021/jacs.7b01632es_ES
dc.description.referencesPrasad Reddy, K. S. S. V., & Deshpande, P. A. (2022). DFT reveals the support effects in Pd nanoclusters over defect-ridden graphene for the oxidative addition of bromobenzene. Molecular Catalysis, 521, 112205. https://doi.org/10.1016/j.mcat.2022.112205es_ES
dc.description.referencesChaudret, B. Synthesis and Surface Reactivity of Organometallic Nanoparticles. En (editor), Surface and Interfacial Organometallic Chemistry and Catalysis (pp. 233-259). Springer-Verlag. https://doi.org/10.1007/b138079es_ES
dc.description.referencesAstruc, D. (2007). Palladium Nanoparticles as Efficient Green Homogeneous and Heterogeneous Carbon−Carbon Coupling Precatalysts:  A Unifying View. Inorganic Chemistry, 46(6), 1884-1894. https://doi.org/10.1021/ic062183hes_ES
dc.description.referencesDeraedt, C., & Astruc, D. (2013). “Homeopathic” Palladium Nanoparticle Catalysis of Cross Carbon–Carbon Coupling Reactions. Accounts of Chemical Research, 47(2), 494-503. https://doi.org/10.1021/ar400168ses_ES
dc.description.referencesRicciardi, R., Huskens, J., & Verboom, W. (2015). Dendrimer-encapsulated Pd nanoparticles as catalysts for C–C cross-couplings in flow microreactors. Organic &amp; Biomolecular Chemistry, 13(17), 4953-4959. https://doi.org/10.1039/c5ob00289ces_ES
dc.description.referencesPalazzolo, A., & Carenco, S. (2021). Phosphines Modulating the Catalytic Silane Activation on Nickel–Cobalt Nanoparticles, Tentatively Attributed to Frustrated Lewis Pairs in a Colloidal Solution. Chemistry of Materials, 33(19), 7914-7922. https://doi.org/10.1021/acs.chemmater.1c03105es_ES
dc.description.referencesHuang, Z., Sam, Q. P., & Dong, G. (2015). Palladium-catalyzed direct β-arylation of ketones with diaryliodonium salts: a stoichiometric heavy metal-free and user-friendly approach. Chemical Science, 6(10), 5491-5498. https://doi.org/10.1039/c5sc01636ces_ES
dc.description.referencesSheokand, S., & Balakrishna, M. S. (2023). Cationic and Neutral Pd<sup>II</sup> and Pt<sup>II</sup> Pincer Complexes of Phosphinamino-Triazolyl-Pyridine [PN(H)N]: Pincer Ligand-Stabilized Palladium Nanoparticles and Their Catalytic Annulation of Internal Alkynes to Indenones. Inorganic Chemistry, 62(31), 12317-12328. https://doi.org/10.1021/acs.inorgchem.3c01273es_ES
dc.description.referencesTrzeciak, A. M., & Ziółkowski, J. J. (2007). Monomolecular, nanosized and heterogenized palladium catalysts for the Heck reaction. Coordination Chemistry Reviews, 251(9-10), 1281-1293. https://doi.org/10.1016/j.ccr.2006.11.013es_ES
dc.description.referencesHajipour, A., & Azizi, G. (2013). The [RPPh3]2[Pd2X6] as a Catalyst Precursor for the Heck Cross-Coupling Reaction by in situ Formation of Stabilized Pd(0) Nanoparticles. Synlett, 24(02), 254-258. https://doi.org/10.1055/s-0032-1317963es_ES
dc.description.referencesPolynski, M. V., Vlasova, Y. S., Solovev, Y. V., Kozlov, S. M., & Ananikov, V. P. (2024). Computational analysis of R–X oxidative addition to Pd nanoparticles. Chemical Science, 15(26), 9977-9986. https://doi.org/10.1039/d4sc00628ces_ES
dc.description.referencesSun, B., Ning, L., & Zeng, H. C. (2020). Confirmation of Suzuki–Miyaura Cross-Coupling Reaction Mechanism through Synthetic Architecture of Nanocatalysts. Journal of the American Chemical Society, 142(32), 13823-13832. https://doi.org/10.1021/jacs.0c04804es_ES
dc.description.referencesGNIEWEK, A., TRZECIAK, A., ZIOLKOWSKI, J., KEPINSKI, L., WRZYSZCZ, J., & TYLUS, W. (2005). Pd-PVP colloid as catalyst for Heck and carbonylation reactions: TEM and XPS studies. Journal of Catalysis, 229(2), 332-343. https://doi.org/10.1016/j.jcat.2004.11.003es_ES
dc.description.referencesGuo, D., Jiang, K., Gan, H., Ren, Y., Long, J., Li, Y., & Yin, B. (2023). Template‐Oriented Polyaniline‐Supported Palladium Nanoclusters for Reductive Homocoupling of Furfural Derivatives. Angewandte Chemie International Edition, 62(39). Portico. https://doi.org/10.1002/anie.202304662es_ES
dc.description.referencesTang, L., Wang, P., Fan, Y., Yang, X., Wan, C., & Zha, Z. (2016). Heterogeneous Palladium‐Catalyzed Hydrogen‐Transfer Cyclization of Nitroacetophenones with Benzylamines: Access to C−N Bonds. ChemCatChem, 8(23), 3565-3569. Portico. https://doi.org/10.1002/cctc.201601060es_ES
dc.description.referencesPrasad Reddy, K. S. S. V., & Deshpande, P. A. (2023). Insights into the surface catalysis of CeO<mml:math xmlns:mml=«http://www.w3.org/1998/Math/MathML» altimg=«si84.svg» display=«inline» id=«d1e394″><mml:msub><mml:mrow/><mml:mrow><mml:mn>2</mml:mn><mml:mo>−</mml:mo><mml:mi>δ</mml:mi></mml:mrow></mml:msub></mml:math> supported Pd<mml:math xmlns:mml=«http://www.w3.org/1998/Math/MathML» altimg=«si83.svg» display=«inline» id=«d1e406″><mml:msub><mml:mrow/><mml:mrow><mml:mi>n</mml:mi></mml:mrow></mml:msub></mml:math> clusters (<mml:math xmlns:mml=«http://www.w3.org/1998/Math/MathML» altimg=«si13.svg» display=«inline» id=«d1e415″><mml:mi>n</mml:mi></mml:math> = 3, 4) for the oxidative addition of bromobenzene. Applied Surface Science, 614, 156206. https://doi.org/10.1016/j.apsusc.2022.156206es_ES
dc.description.referencesLeyva-Pérez, A., Oliver-Meseguer, J., Cabrero-Antonino, J. R., Rubio-Marqués, P., Serna, P., Al-Resayes, S. I., & Corma, A. (2013). Reactivity of Electron-Deficient Alkynes on Gold Nanoparticles. ACS Catalysis, 3(8), 1865-1873. https://doi.org/10.1021/cs400362ces_ES
dc.description.referencesBudroni, G., Corma, A., García, H., & Primo, A. (2007). Pd nanoparticles embedded in sponge-like porous silica as a Suzuki–Miyaura catalyst: Similarities and differences with homogeneous catalysts. Journal of Catalysis, 251(2), 345-353. https://doi.org/10.1016/j.jcat.2007.07.027es_ES
dc.description.referencesLin, J., Abroshan, H., Liu, C., Zhu, M., Li, G., & Haruta, M. (2015). Sonogashira cross-coupling on the Au(1 1 1) and Au(1 0 0) facets of gold nanorod catalysts: Experimental and computational investigation. Journal of Catalysis, 330, 354-361. https://doi.org/10.1016/j.jcat.2015.07.020es_ES
dc.description.referencesBeaumont, S. K., Kyriakou, G., & Lambert, R. M. (2010). Identity of the Active Site in Gold Nanoparticle-Catalyzed Sonogashira Coupling of Phenylacetylene and Iodobenzene. Journal of the American Chemical Society, 132(35), 12246-12248. https://doi.org/10.1021/ja1063179es_ES
dc.description.referencesBoronat, M., Combita, D., Concepción, P., Corma, A., García, H., Juárez, R., Laursen, S., & de Dios López-Castro, J. (2012). Making C–C Bonds with Gold: Identification of Selective Gold Sites for Homo- and Cross-Coupling Reactions between Iodobenzene and Alkynes. The Journal of Physical Chemistry C, 116(47), 24855-24867. https://doi.org/10.1021/jp3071585es_ES
dc.description.referencesSánchez-Sánchez, C., Yubero, F., González-Elipe, A. R., Feria, L., Sanz, J. F., & Lambert, R. M. (2014). The Flexible Surface Revisited: Adsorbate-Induced Reconstruction, Homocoupling, and Sonogashira Cross-Coupling on the Au(100) Surface. The Journal of Physical Chemistry C, 118(22), 11677-11684. https://doi.org/10.1021/jp501321ues_ES
dc.description.referencesCandu, N., Dhakshinamoorthy, A., Apostol, N., Teodorescu, C., Corma, A., Garcia, H., & Parvulescu, V. I. (2017). Oriented Au nanoplatelets on graphene promote Suzuki-Miyaura coupling with higher efficiency and different reactivity pattern than supported palladium. Journal of Catalysis, 352, 59-66. https://doi.org/10.1016/j.jcat.2017.04.034es_ES
dc.description.referencesTsuji, Y., Yoshida, M., Kamachi, T., & Yoshizawa, K. (2022). Oxidative Addition of Methane and Reductive Elimination of Ethane and Hydrogen on Surfaces: From Pure Metals to Single Atom Alloys. Journal of the American Chemical Society, 144(40), 18650-18671. https://doi.org/10.1021/jacs.2c08787es_ES
dc.description.referencesPolynski, M. V., & Ananikov, V. P. (2019). Modeling Key Pathways Proposed for the Formation and Evolution of “Cocktail”-Type Systems in Pd-Catalyzed Reactions Involving ArX Reagents. ACS Catalysis, 9(5), 3991-4005. https://doi.org/10.1021/acscatal.9b00207es_ES
dc.description.referencesChernyshev, V. M., & Ananikov, V. P. (2022). Nickel and Palladium Catalysis: Stronger Demand than Ever. ACS Catalysis, 12(2), 1180-1200. https://doi.org/10.1021/acscatal.1c04705es_ES
dc.description.referencesLi, Y., Zhang, Z., Fan, T., Li, X., Ji, J., Dong, P., Baines, R., Shen, J., & Ye, M. (2016). Magnetic Core–Shell to Yolk–Shell Structures in Palladium‐Catalyzed Suzuki–Miyaura Reactions: Heterogeneous versus Homogeneous Nature. ChemPlusChem, 81(6), 564-573. Portico. https://doi.org/10.1002/cplu.201600094es_ES
dc.description.referencesOndar, E. E., Kostyukovich, A. Yu., Burykina, J. V., Galushko, A. S., & Ananikov, V. P. (2023). Examination of Pt<sub>2</sub>dba<sub>3</sub> as a “cocktail”-type catalytic system for alkene and alkyne hydrosilylation reactions. Catalysis Science &amp; Technology, 13(20), 6022-6040. https://doi.org/10.1039/d3cy00865ges_ES
dc.description.referencesOliver‐Meseguer, J., Dominguez, I., Gavara, R., Leyva‐Pérez, A., & Corma, A. (2017). Disassembling Metal Nanocrystallites into Sub‐nanometric Clusters and Low‐faceted Nanoparticles for Multisite Catalytic Reactions. ChemCatChem, 9(8), 1429-1435. Portico. https://doi.org/10.1002/cctc.201700037es_ES
dc.description.referencesGonzález‐Arellano, C., Abad, A., Corma, A., García, H., Iglesias, M., & Sánchez, F. (2007). Catalysis by Gold(I) and Gold(III): A Parallelism between Homo‐ and Heterogeneous Catalysts for Copper‐Free Sonogashira Cross‐Coupling Reactions. Angewandte Chemie International Edition, 46(9), 1536-1538. Portico. https://doi.org/10.1002/anie.200604746es_ES
dc.description.referencesChinchilla, R., & Nájera, C. (2011). Recent advances in Sonogashira reactions. Chemical Society Reviews, 40(10), 5084. https://doi.org/10.1039/c1cs15071ees_ES
dc.description.referencesCorma, A., Juárez, R., Boronat, M., Sánchez, F., Iglesias, M., & García, H. (2011). Gold catalyzes the Sonogashira coupling reaction without the requirement of palladium impurities. Chem. Commun., 47(5), 1446-1448. https://doi.org/10.1039/c0cc04564kes_ES
dc.description.referencesElhage, A., Wang, B., Marina, N., Marin, M. L., Cruz, M., Lanterna, A. E., & Scaiano, J. C. (2018). Glass wool: a novel support for heterogeneous catalysis. Chemical Science, 9(33), 6844-6852. https://doi.org/10.1039/c8sc02115ees_ES
dc.description.referencesHong, K., Sajjadi, M., Suh, J. M., Zhang, K., Nasrollahzadeh, M., Jang, H. W., Varma, R. S., & Shokouhimehr, M. (2020). Palladium Nanoparticles on Assorted Nanostructured Supports: Applications for Suzuki, Heck, and Sonogashira Cross-Coupling Reactions. ACS Applied Nano Materials, 3(3), 2070-2103. https://doi.org/10.1021/acsanm.9b02017es_ES
dc.description.referencesCorma, A., & Garcia, H. (2008). Supported gold nanoparticles as catalysts for organic reactions. Chemical Society Reviews, 37(9), 2096. https://doi.org/10.1039/b707314nes_ES
dc.description.referencesLi, G., & Jin, R. (2013). Catalysis by gold nanoparticles: carbon-carbon coupling reactions. Nanotechnology Reviews, 2(5), 529-545. https://doi.org/10.1515/ntrev-2013-0020es_ES
dc.description.referencesFiordaliso, E. M., Murphy, S., Nielsen, R. M., Dahl, S., & Chorkendorff, I. (2012). H2 splitting on Pt, Ru and Rh nanoparticles supported on sputtered HOPG. Surface Science, 606(3-4), 263-272. https://doi.org/10.1016/j.susc.2011.10.004es_ES
dc.description.referencesLin, J. L., & Bent, B. E. (1993). Formation of methyl radicals during the oxidative addition of iodomethane to a single-crystal copper surface. Journal of the American Chemical Society, 115(7), 2849-2853. https://doi.org/10.1021/ja00060a036es_ES
dc.description.referencesLeyva‐Pérez, A., Oliver‐Meseguer, J., Rubio‐Marqués, P., & Corma, A. (2013). Water‐Stabilized Three‐ and Four‐Atom Palladium Clusters as Highly Active Catalytic Species in Ligand‐Free CC Cross‐Coupling Reactions. Angewandte Chemie International Edition, 52(44), 11554-11559. Portico. https://doi.org/10.1002/anie.201303188es_ES
dc.description.referencesRivero-Crespo, M. A., Rubio-Marqués, P., Hernández-Garrido, J. C., Mon, M., Oliver-Meseguer, J., & Leyva-Pérez, A. (2023). Intimate ruthenium–platinum nanoalloys supported on carbon catalyze the hydrogenation and one-pot hydrogenation-coupling reaction of oxidized amino derivatives. Catalysis Science &amp; Technology, 13(8), 2508-2516. https://doi.org/10.1039/d2cy01846bes_ES
dc.description.referencesJeddi, N., Scott, N. W. J., & Fairlamb, I. J. S. (2022). Well-Defined Pd<sub><i>n</i></sub> Clusters for Cross-Coupling and Hydrogenation Catalysis: New Opportunities for Catalyst Design. ACS Catalysis, 12(19), 11615-11638. https://doi.org/10.1021/acscatal.2c03345es_ES
dc.description.referencesKirlikovali, K. O., Cho, E., Downard, T. J., Grigoryan, L., Han, Z., Hong, S., Jung, D., Quintana, J. C., Reynoso, V., Ro, S., Shen, Y., Swartz, K., Ter Sahakyan, E., Wixtrom, A. I., Yoshida, B., Rheingold, A. L., & Spokoyny, A. M. (2018). Buchwald–Hartwig amination using Pd( <scp>i</scp> ) dimer precatalysts supported by biaryl phosphine ligands. Dalton Transactions, 47(11), 3684-3688. https://doi.org/10.1039/c8dt00119ges_ES
dc.description.referencesDenisova, E. A., Eremin, D. B., Gordeev, E. G., Tsedilin, A. M., & Ananikov, V. P. (2019). Addressing Reversibility of R–NHC Coupling on Palladium: Is Nano-to-Molecular Transition Possible for the Pd/NHC System? Inorganic Chemistry, 58(18), 12218-12227. https://doi.org/10.1021/acs.inorgchem.9b01630es_ES
dc.description.referencesBriggs, B. D., Bedford, N. M., Seifert, S., Koerner, H., Ramezani-Dakhel, H., Heinz, H., Naik, R. R., Frenkel, A. I., & Knecht, M. R. (2015). Atomic-scale identification of Pd leaching in nanoparticle catalyzed C–C coupling: effects of particle surface disorder. Chemical Science, 6(11), 6413-6419. https://doi.org/10.1039/c5sc01424ges_ES
dc.description.referencesYang, Y., Unsworth, L. D., & Semagina, N. (2011). Size- and shape-controlled palladium nanoparticles in a fluorometric Tsuji–Trost reaction. Journal of Catalysis, 281(1), 137-146. https://doi.org/10.1016/j.jcat.2011.04.009es_ES
dc.description.referencesKyriakou, G., Beaumont, S. K., Humphrey, S. M., Antonetti, C., & Lambert, R. M. (2010). Sonogashira Coupling Catalyzed by Gold Nanoparticles: Does Homogeneous or Heterogeneous Catalysis Dominate? ChemCatChem, 2(11), 1444-1449. Portico. https://doi.org/10.1002/cctc.201000154es_ES
dc.description.referencesNorouzi, N., Das, M. K., Richard, A. J., Ibrahim, A. A., El-Kaderi, H. M., & El-Shall, M. S. (2020). Heterogeneous catalysis by ultra-small bimetallic nanoparticles surpassing homogeneous catalysis for carbon–carbon bond forming reactions. Nanoscale, 12(37), 19191-19202. https://doi.org/10.1039/d0nr04105jes_ES
dc.description.referencesEdwards, J. K., Pritchard, J., Lu, L., Piccinini, M., Shaw, G., Carley, A. F., Morgan, D. J., Kiely, C. J., & Hutchings, G. J. (2014). The Direct Synthesis of Hydrogen Peroxide Using Platinum‐Promoted Gold–Palladium Catalysts. Angewandte Chemie International Edition, 53(9), 2381-2384. Portico. https://doi.org/10.1002/anie.201308067es_ES
dc.description.referencesRai, R. K., Gupta, K., Tyagi, D., Mahata, A., Behrens, S., Yang, X., Xu, Q., Pathak, B., & Singh, S. K. (2016). Access to highly active Ni–Pd bimetallic nanoparticle catalysts for C–C coupling reactions. Catalysis Science &amp; Technology, 6(14), 5567-5579. https://doi.org/10.1039/c6cy00037aes_ES
dc.description.referencesBoekfa, B., Pahl, E., Gaston, N., Sakurai, H., Limtrakul, J., & Ehara, M. (2014). C–Cl Bond Activation on Au/Pd Bimetallic Nanocatalysts Studied by Density Functional Theory and Genetic Algorithm Calculations. The Journal of Physical Chemistry C, 118(38), 22188-22196. https://doi.org/10.1021/jp5074472es_ES
dc.description.referencesWang, J., Kondrat, S. A., Wang, Y., Brett, G. L., Giles, C., Bartley, J. K., Lu, L., Liu, Q., Kiely, C. J., & Hutchings, G. J. (2015). Au–Pd Nanoparticles Dispersed on Composite Titania/Graphene Oxide-Supports as a Highly Active Oxidation Catalyst. ACS Catalysis, 5(6), 3575-3587. https://doi.org/10.1021/acscatal.5b00480es_ES
dc.description.referencesHutchings, G. J., & Kiely, C. J. (2013). Strategies for the Synthesis of Supported Gold Palladium Nanoparticles with Controlled Morphology and Composition. Accounts of Chemical Research, 46(8), 1759-1772. https://doi.org/10.1021/ar300356mes_ES
dc.description.referencesNotar Francesco, I., Fontaine‐Vive, F., & Antoniotti, S. (2014). Synergy in the Catalytic Activity of Bimetallic Nanoparticles and New Synthetic Methods for the Preparation of Fine Chemicals. ChemCatChem, 6(10), 2784-2791. Portico. https://doi.org/10.1002/cctc.201402252es_ES
dc.description.referencesSon, S. U., Jang, Y., Park, J., Na, H. B., Park, H. M., Yun, H. J., Lee, J., & Hyeon, T. (2004). Designed Synthesis of Atom-Economical Pd/Ni Bimetallic Nanoparticle-Based Catalysts for Sonogashira Coupling Reactions. Journal of the American Chemical Society, 126(16), 5026-5027. https://doi.org/10.1021/ja039757res_ES
dc.description.referencesRaza, F., Yim, D., Park, J. H., Kim, H.-I., Jeon, S.-J., & Kim, J.-H. (2017). Structuring Pd Nanoparticles on 2H-WS<sub>2</sub> Nanosheets Induces Excellent Photocatalytic Activity for Cross-Coupling Reactions under Visible Light. Journal of the American Chemical Society, 139(41), 14767-14774. https://doi.org/10.1021/jacs.7b08619es_ES
dc.description.referencesSarina, S., Zhu, H., Jaatinen, E., Xiao, Q., Liu, H., Jia, J., Chen, C., & Zhao, J. (2013). Enhancing Catalytic Performance of Palladium in Gold and Palladium Alloy Nanoparticles for Organic Synthesis Reactions through Visible Light Irradiation at Ambient Temperatures. Journal of the American Chemical Society, 135(15), 5793-5801. https://doi.org/10.1021/ja400527aes_ES
dc.description.referencesKang, N., Wang, Q., Djeda, R., Wang, W., Fu, F., Moro, M. M., Ramirez, M. d. l. A., Moya, S., Coy, E., Salmon, L., Pozzo, J.-L., & Astruc, D. (2020). Visible-Light Acceleration of H<sub>2</sub> Evolution from Aqueous Solutions of Inorganic Hydrides Catalyzed by Gold-Transition-Metal Nanoalloys. ACS Applied Materials &amp; Interfaces, 12(48), 53816-53826. https://doi.org/10.1021/acsami.0c16247es_ES
dc.description.referencesSingh, A., Kumar, M., & Bhalla, V. (2022). Phenazine‐based supramolecular photosensitizing assemblies: A “smart” selectivity control on catalytic activity of Pd(II) nanoparticles. Aggregate, 4(1). Portico. https://doi.org/10.1002/agt2.192es_ES
dc.description.referencesZhang, S., Chang, C., Huang, Z., Ma, Y., Gao, W., Li, J., & Qu, Y. (2015). Visible-Light-Activated Suzuki–Miyaura Coupling Reactions of Aryl Chlorides over the Multifunctional Pd/Au/Porous Nanorods of CeO<sub>2</sub> Catalysts. ACS Catalysis, 5(11), 6481-6488. https://doi.org/10.1021/acscatal.5b01173es_ES
dc.description.referencesVerma, P., Kuwahara, Y., Mori, K., & Yamashita, H. (2016). Pd/Ag and Pd/Au bimetallic nanocatalysts on mesoporous silica for plasmon-mediated enhanced catalytic activity under visible light irradiation. Journal of Materials Chemistry A, 4(26), 10142-10150. https://doi.org/10.1039/c6ta01664bes_ES
dc.description.referencesLyu, P., Espinoza, R., Khan, Md. I., Spaller, W. C., Ghosh, S., & Nguyen, S. C. (2022). Mechanistic insight into deep holes from interband transitions in Palladium nanoparticle photocatalysts. iScience, 25(2), 103737. https://doi.org/10.1016/j.isci.2022.103737es_ES
dc.description.referencesJoy, J., Stuyver, T., & Shaik, S. (2020). Oriented External Electric Fields and Ionic Additives Elicit Catalysis and Mechanistic Crossover in Oxidative Addition Reactions. Journal of the American Chemical Society, 142(8), 3836-3850. https://doi.org/10.1021/jacs.9b11507es_ES
dc.description.referencesDavis, J. J., Coleman, K. S., Busuttil, K. L., & Bagshaw, C. B. (2005). Spatially Resolved Suzuki Coupling Reaction Initiated and Controlled Using a Catalytic AFM Probe. Journal of the American Chemical Society, 127(38), 13082-13083. https://doi.org/10.1021/ja043235+es_ES
dc.description.referencesCarrettin, S., Guzman, J., & Corma, A. (2005). Supported Gold Catalyzes the Homocoupling of Phenylboronic Acid with High Conversion and Selectivity. Angewandte Chemie International Edition, 44(15), 2242-2245. Portico. https://doi.org/10.1002/anie.200462560es_ES
dc.description.referencesWillis, N. G., & Guzman, J. (2008). Influence of the support during homocoupling of phenylboronic acid catalyzed by supported gold. Applied Catalysis A: General, 339(1), 68-75. https://doi.org/10.1016/j.apcata.2008.01.019es_ES
dc.description.referencesBanerjee, S., Basheer, C., & Zare, R. N. (2016). A Study of Heterogeneous Catalysis by Nanoparticle‐Embedded Paper‐Spray Ionization Mass Spectrometry. Angewandte Chemie International Edition, 55(41), 12807-12811. Portico. https://doi.org/10.1002/anie.201607204es_ES
dc.description.referencesBavaro, L. M., Montangero, P., & Keister, J. B. (1983). Kinetics and mechanism of oxidative addition and reductive elimination of hydrogen on triruthenium clusters. Journal of the American Chemical Society, 105(15), 4977-4981. https://doi.org/10.1021/ja00353a022es_ES
dc.description.referencesSafarowic, F. J., Bierdeman, D. J., & Keister, J. B. (1996). Kinetics and Mechanism of Reversible Oxidative Addition of Hydrogen across the Metal−Metal Bond of (μ-H)<sub>2</sub>Ru<sub>3</sub>(CO)<sub>8</sub>(μ-P(<i>t</i>-Bu)<sub>2</sub>)<sub>2</sub>. Steric Promotion of Metal−Metal Bond Cleavage But a CO Dissociative Mechanism. Journal of the American Chemical Society, 118(47), 11805-11812. https://doi.org/10.1021/ja9628819es_ES
dc.description.referencesCrabtree, R. H., & Morehouse, S. M. (1982). Carbon-13 NMR spectra of some new iridium(I) complexes: evidence for reductive character in hydrogen addition and the cis and trans influences of nitriles. Inorganic Chemistry, 21(12), 4210-4213. https://doi.org/10.1021/ic00142a019es_ES
dc.description.referencesWatzky, M. A., & Finke, R. G. (1997). Transition Metal Nanocluster Formation Kinetic and Mechanistic Studies. A New Mechanism When Hydrogen Is the Reductant:  Slow, Continuous Nucleation and Fast Autocatalytic Surface Growth. Journal of the American Chemical Society, 119(43), 10382-10400. https://doi.org/10.1021/ja9705102es_ES
dc.description.referencesOtt, L. S., & Finke, R. G. (2006). Nanocluster Formation and Stabilization Fundamental Studies: Investigating “Solvent-Only” Stabilization En Route to Discovering Stabilization by the Traditionally Weakly Coordinating Anion BF<sub>4</sub><sup>-</sup>Plus High Dielectric Constant Solvents. Inorganic Chemistry, 45(20), 8382-8393. https://doi.org/10.1021/ic060876ses_ES
dc.description.referencesStegemann, F., Benndorf, C., Zhang, Y., Bartsch, M., Zacharias, H., Fokwa, B. P. T., Eckert, H., & Janka, O. (2017). Network Formation by Condensed Tetrahedral [Au<sub>3</sub>Al] Units in Na<sub>2</sub>Au<sub>3</sub>Al: Crystal and Electronic Structure, Spectroscopic Investigations, and Physical Properties of an Ordered Ternary Auride. Inorganic Chemistry, 56(4), 1919-1931. https://doi.org/10.1021/acs.inorgchem.6b02480es_ES
dc.description.referencesXia, Z., Corcé, V., Zhao, F., Przybylski, C., Espagne, A., Jullien, L., Le Saux, T., Gimbert, Y., Dossmann, H., Mouriès-Mansuy, V., Ollivier, C., & Fensterbank, L. (2019). Photosensitized oxidative addition to gold(i) enables alkynylative cyclization of o-alkylnylphenols with iodoalkynes. Nature Chemistry, 11(9), 797-805. https://doi.org/10.1038/s41557-019-0295-9es_ES
dc.description.referencesOliver‐Meseguer, J., Doménech‐Carbó, A., Boronat, M., Leyva‐Pérez, A., & Corma, A. (2017). Partial Reduction and Selective Transfer of Hydrogen Chloride on Catalytic Gold Nanoparticles. Angewandte Chemie International Edition, 56(23), 6435-6439. Portico. https://doi.org/10.1002/anie.201700282es_ES
dc.description.referencesOliver-Meseguer, J., Boronat, M., Vidal-Moya, A., Concepción, P., Rivero-Crespo, M. Á., Leyva-Pérez, A., & Corma, A. (2018). Generation and Reactivity of Electron-Rich Carbenes on the Surface of Catalytic Gold Nanoparticles. Journal of the American Chemical Society, 140(9), 3215-3218. https://doi.org/10.1021/jacs.7b13696es_ES
dc.description.referencesOhmura, T., Morimasa, Y., & Suginome, M. (2015). Organocatalytic Diboration Involving “Reductive Addition” of a Boron–Boron σ-Bond to 4,4′-Bipyridine. Journal of the American Chemical Society, 137(8), 2852-2855. https://doi.org/10.1021/jacs.5b00546es_ES
dc.description.referencesKang, J., Wang, Y.-X., Peng, F., Zhang, N.-N., Xue, Y., Yang, Y., Kumacheva, E., & Liu, K. (2022). Oxidative Elimination and Reductive Addition of Thiol‐Terminated Polymer Ligands to Metal Nanoparticles. Angewandte Chemie International Edition, 61(35). Portico. https://doi.org/10.1002/anie.202202405es_ES
dc.description.referencesLerma‐Berlanga, B., Orlando, F., Merino, E., & Leyva‐Pérez, A. (2024). Au Clusters Catalyze The Disulfide Metathesis Reaction By A Reductive Addition‐Oxidative Elimination Mechanism. ChemCatChem, 16(23). Portico. https://doi.org/10.1002/cctc.202400909es_ES
dc.description.referencesBai, Y., He, S., Lv, Y., Zhu, M., & Yu, H. (2021). Redox-Induced Interconversion of Two Au<sub>8</sub> Nanoclusters: the Mechanism and the Structure–Bond Dissociation Activity Correlations. Inorganic Chemistry, 60(8), 5724-5733. https://doi.org/10.1021/acs.inorgchem.0c03828es_ES
dc.description.referencesKamei, Y., Shichibu, Y., & Konishi, K. (2011). Generation of Small Gold Clusters with Unique Geometries through Cluster‐to‐Cluster Transformations: Octanuclear Clusters with Edge‐sharing Gold Tetrahedron Motifs. Angewandte Chemie International Edition, 50(32), 7442-7445. Portico. https://doi.org/10.1002/anie.201102901es_ES
dc.description.referencesOliver-Meseguer, J., Dominguez, I., Gavara, R., Doménech-Carbó, A., González-Calbet, J. M., Leyva-Pérez, A., & Corma, A. (2017). The wet synthesis and quantification of ligand-free sub-nanometric Au clusters in solid matrices. Chemical Communications, 53(6), 1116-1119. https://doi.org/10.1039/c6cc09119aes_ES
dc.description.referencesArisawa, M., & Yamaguchi, M. (2003). Rhodium-Catalyzed Disulfide Exchange Reaction. Journal of the American Chemical Society, 125(22), 6624-6625. https://doi.org/10.1021/ja035221ues_ES
dc.description.referencesArisawa, M., Suwa, A., & Yamaguchi, M. (2006). RhCl3-catalyzed disulfide exchange reaction using water solvent in homogeneous and heterogeneous systems. Journal of Organometallic Chemistry, 691(6), 1159-1168. https://doi.org/10.1016/j.jorganchem.2005.11.049es_ES
dc.description.referencesGuo, J., Zha, J., Zhang, T., Ding, C.-H., Tan, Q., & Xu, B. (2021). PdCl<sub>2</sub>/DMSO-Catalyzed Thiol–Disulfide Exchange: Synthesis of Unsymmetrical Disulfide. Organic Letters, 23(8), 3167-3172. https://doi.org/10.1021/acs.orglett.1c00858es_ES
dc.description.referencesGary, S., & Bloom, S. (2022). Peptide <i>Carbo</i>cycles: From −SS– to −CC– via a Late-Stage “Snip-and-Stitch”. ACS Central Science, 8(11), 1537-1547. https://doi.org/10.1021/acscentsci.2c00456es_ES
dc.description.referencesBlack, S. P., Sanders, J. K. M., & Stefankiewicz, A. R. (2014). Disulfide exchange: exposing supramolecular reactivity through dynamic covalent chemistry. Chem. Soc. Rev., 43(6), 1861-1872. https://doi.org/10.1039/c3cs60326aes_ES
dc.description.referencesArce, A. J., Arrojo, P., De Sanctis, Y., Deeming, A. J., & West, D. J. (1992). Addition of diselenides RSe2R to [Os3(CO)10(MeCN)2] to give isomers of [Os3(μ-SeR)2(CO)10]. Polyhedron, 11(9), 1013-1021. https://doi.org/10.1016/s0277-5387(00)84468-xes_ES
dc.description.referencesSonawane, A. D., Sonawane, R. A., Ninomiya, M., & Koketsu, M. (2021). Diorganyl diselenides: a powerful tool for the construction of selenium containing scaffolds. Dalton Transactions, 50(37), 12764-12790. https://doi.org/10.1039/d1dt01982aes_ES
dc.description.referencesJones, D. J., Lautens, M., & McGlacken, G. P. (2019). The emergence of Pd-mediated reversible oxidative addition in cross coupling, carbohalogenation and carbonylation reactions. Nature Catalysis, 2(10), 843-851. https://doi.org/10.1038/s41929-019-0361-0es_ES
dc.description.referencesHe, Z., Song, F., Sun, H., & Huang, Y. (2018). Transition-Metal-Free Suzuki-Type Cross-Coupling Reaction of Benzyl Halides and Boronic Acids via 1,2-Metalate Shift. Journal of the American Chemical Society, 140(7), 2693-2699. https://doi.org/10.1021/jacs.8b00380es_ES
dc.description.referencesKovach, J. S., Svingen, P. A., & Schaid, D. J. (1992). Levamisole Potentiation of Fluorouracil Antiproliferative Activity Mimicked by Orthovanadate, an Inhibitor of Tyrosine Phosphatase. JNCI Journal of the National Cancer Institute, 84(7), 515-519. https://doi.org/10.1093/jnci/84.7.515es_ES
dc.description.referencesAmery, W. K. P., & Bruynseels, J. P. J. M. (1992). Levamisole, the story and the lessons. International Journal of Immunopharmacology, 14(3), 481-486. https://doi.org/10.1016/0192-0561(92)90179-oes_ES
dc.description.referencesHigashihara, G., Terada, M., Inagaki, A., & Akita, M. (2006). C−C Coupling of a Permetalated Ethene, (μ<sub>4</sub>-CC)Ru<sub>2</sub>(FeCp*)<sub>2</sub>(CO)<sub>10</sub>, with Alkynes, and Isolation of a Labile MeCN Adduct, (μ<sub>4</sub>-CC)Ru<sub>2</sub>(FeCp*)<sub>2</sub>(CO)<sub>8</sub>(NCMe)<sub>2</sub>. Organometallics, 26(2), 439-444. https://doi.org/10.1021/om0609160es_ES
dc.description.referencesArce, A. J., De Sanctis, Y., Karam, A., & Deeming, A. J. (1994). Desulfurization of Benzo[<i>b</i>]thiophene by S/Ru Exchange: Formation and Structure of the Cluster [Ru<sub>3</sub>(CO)<sub>8</sub>(C<sub>8</sub>H<sub>6</sub>)]. Angewandte Chemie International Edition in English, 33(13), 1381-1383. Portico. https://doi.org/10.1002/anie.199413811es_ES
dc.description.referencesCabeza, J. A., García-Álvarez, P., & Pruneda, V. (2012). Reaction of [Ru<sub>3</sub>(CO)<sub>12</sub>] with Phenazine: Synthesis of C-Metalated Derivatives That Formally Arise from a C–H Oxidative Addition or a Long-Distance C-to-N Prototropy. Organometallics, 31(3), 941-946. https://doi.org/10.1021/om200983aes_ES
dc.description.referencesFernández, E., Rivero-Crespo, M. A., Domínguez, I., Rubio-Marqués, P., Oliver-Meseguer, J., Liu, L., Cabrero-Antonino, M., Gavara, R., Hernández-Garrido, J. C., Boronat, M., Leyva-Pérez, A., & Corma, A. (2019). Base-Controlled Heck, Suzuki, and Sonogashira Reactions Catalyzed by Ligand-Free Platinum or Palladium Single Atom and Sub-Nanometer Clusters. Journal of the American Chemical Society, 141(5), 1928-1940. https://doi.org/10.1021/jacs.8b07884es_ES
dc.description.referencesBigi, F., Cauzzi, D., Della Ca’, N., Malacria, M., Maggi, R., Motti, E., Wang, Y., & Maestri, G. (2022). Evolution of Triangular All-Metal Aromatic Complexes from Bonding Quandaries to Powerful Catalytic Platforms. ACS Organic &amp; Inorganic Au, 2(5), 373-385. https://doi.org/10.1021/acsorginorgau.2c00029es_ES
dc.description.referencesPerego, L. A., Payard, P.-A., Haddou, B., Ciofini, I., & Grimaud, L. (2018). Evidence for a Cooperative Mechanism Involving Two Palladium(0) Centers in the Oxidative Addition of Iodoarenes. Chemistry – A European Journal, 24(9), 2192-2199. Portico. https://doi.org/10.1002/chem.201704899es_ES
dc.description.referencesMcCallum, T. (2023). Heart of gold: enabling ligands for oxidative addition of haloorganics in Au(<scp>i</scp>)/Au(<scp>iii</scp>) catalysed cross-coupling reactions. Organic &amp; Biomolecular Chemistry, 21(8), 1629-1646. https://doi.org/10.1039/d3ob00002hes_ES
dc.description.referencesWang, C., Tuninetti, J., Wang, Z., Zhang, C., Ciganda, R., Salmon, L., Moya, S., Ruiz, J., & Astruc, D. (2017). Hydrolysis of Ammonia-Borane over Ni/ZIF-8 Nanocatalyst: High Efficiency, Mechanism, and Controlled Hydrogen Release. Journal of the American Chemical Society, 139(33), 11610-11615. https://doi.org/10.1021/jacs.7b06859es_ES
dc.description.sponsorshipWe thank the Ministerio de Ciencia e Innovación Spain (MICIIN), for grant numbers PID2023-148441NB I00 and Severo Ochoa program CEX2021-001230-S. B. L.-B. thanks Juan de la Cierva grant (JDC2022 048323 I).es_ES
dc.description.volume3es_ES
dc.identifier.doi10.1002/ceur.202400086es_ES
dc.identifier.eissn2751-4765es_ES
dc.identifier.urihttps://riunet.upv.es/handle/10251/235428
dc.languageIngléses_ES
dc.publisherWiley-VCHes_ES
dc.relation.ispartofChemistryEuropees_ES
dc.relation.pasarelaS\584469es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2023-148441NB-I00/ES/NANORREACTORES SOLIDOS MODULABLES A ESCALA DE SUB-ANGSTROMS PARA REACCIONES ORGANICAS REGIO-IRREGULARES/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI//CEX2021-001230-S/es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI//JDC2022-048323-I/es_ES
dc.relation.publisherversionhttps://doi.org/10.1002/ceur.202400086es_ES
dc.rightsReconocimiento (by)es_ES
dc.rights.accessRightsAbiertoes_ES
dc.subjectOxidative addition-reductive eliminationes_ES
dc.subjectReductive addition-oxidative eliminationes_ES
dc.subjectOrganometallic chemistryes_ES
dc.subjectCatalytic processeses_ES
dc.subjectMetal-mediated reactionses_ES
dc.subjectReaction mechanismses_ES
dc.titleThe Reductive Addition Oxidative Elimination Mechanismes_ES
dc.typeArtículoes_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_ES
dspace.entity.typePublication
person.identifier735346
person.identifier250316
person.identifier.orcid0000-0003-3686-8576
person.identifier.orcid0000-0003-1063-5811
relation.isAuthorOfPublication8b444811-cc26-483b-95c2-9dc5ad94c654
relation.isAuthorOfPublication710dfb4f-4429-4ad0-9a2c-10a4c568f6c0
relation.isAuthorOfPublication.latestForDiscovery8b444811-cc26-483b-95c2-9dc5ad94c654
relation.isOrgUnitOfPublicationb97c2806-5147-442a-a1a8-a2c75cc2a941
relation.isOrgUnitOfPublication.latestForDiscoveryb97c2806-5147-442a-a1a8-a2c75cc2a941
upv.uuid65365e04-e869-422e-af41-305d5d17d2f2es_ES

Archivos

Bloque original

Mostrando 1 - 1 de 1
Cargando...
Miniatura
Nombre:
Lerma-BerlangaLeyva - The Reductive AdditionOxidative Elimination Mechanism.pdf
Tamaño:
6.98 MB
Formato:
Adobe Portable Document Format
Descripción:
Versión editorial