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Case Study of N‐<sup>i</sup>Pr versus N‐Mes Substituted NHC Ligands in Nickel Chemistry: The Coordination and Cyclotrimerization of Alkynes at [Ni(NHC)<sub>2</sub>].
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- Chemistry - A European Journal, 2021, v. 27, n. 71, p. 17849, doi. 10.1002/chem.202103093
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[Ni(NHC)<sub>2</sub>] as a Scaffold for Structurally Characterized trans [H−Ni−PR<sub>2</sub>] and trans [R<sub>2</sub>P−Ni−PR<sub>2</sub>] Complexes.
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- Chemistry - A European Journal, 2021, v. 27, n. 52, p. 13221, doi. 10.1002/chem.202101484
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A General Synthetic Route to NHC‐Phosphinidenes: NHC‐mediated Dehydrogenation of Primary Phosphines.
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- Zeitschrift für Anorganische und Allgemeine Chemie, 2021, v. 647, n. 8, p. 881, doi. 10.1002/zaac.202000405
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Large vs. Small NHC Ligands in Nickel(0) Complexes: The Coordination of Olefins, Ketones and Aldehydes at [Ni(NHC)<sub>2</sub>].
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- European Journal of Inorganic Chemistry, 2020, v. 2020, n. 33, p. 3194, doi. 10.1002/ejic.202000493
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NHC‐Stabilized Nickel Olefin, Dialkyl, and Dicyanido Complexes.
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- European Journal of Inorganic Chemistry, 2019, v. 2019, n. 26, p. 3061, doi. 10.1002/ejic.201900484
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[Ni<sub>3</sub>(iPr<sub>2</sub>Im)<sub>3</sub>(µ<sup>2</sup>‐CO)<sub>3</sub>(µ<sup>3</sup>‐CO)] – A CO‐Stabilized NHC Analogue of the Parent Neutral Nickel Chini‐Type Cluster.
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- European Journal of Inorganic Chemistry, 2019, v. 2019, n. 21, p. 2618, doi. 10.1002/ejic.201900302
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NHC Nickel Catalyzed Hiyama‐ and Negishi‐Type Cross‐Coupling of Aryl Fluorides and Investigations on the Stability of Nickel(II) Fluoroaryl Alkyl Complexes.
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- European Journal of Inorganic Chemistry, 2019, v. 2019, n. 13, p. 1767, doi. 10.1002/ejic.201801477
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Investigation of Organonickel‐Pentafluoroorthotellurates.
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- Zeitschrift für Anorganische und Allgemeine Chemie, 2018, v. 644, n. 17, p. 1047, doi. 10.1002/zaac.201800177
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Isolation of a Reactive Cyclopropane Intermediate via a Unique Catalyst-Free Spontaneous Cyclopropanation Step at 0 °C.
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- Chemistry - A European Journal, 2017, v. 23, n. 25, p. 5953, doi. 10.1002/chem.201605514
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- Article
Regioselective Catalytic and Stepwise Routes to Bulky, Functional-Group-Appended, and Luminescent 1,2-Azaborinines.
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- Chemistry - A European Journal, 2016, v. 22, n. 25, p. 8603, doi. 10.1002/chem.201600653
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- Article