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Jaime Martín

@jaimechem.bsky.social

Research Chemist. Postdoc at the University of Zurich

33 Followers  |  36 Following  |  3 Posts  |  Joined: 03.02.2025  |  1.4111

Latest posts by jaimechem.bsky.social on Bluesky

Check out our new work synthesizing (P^N^C)Gold(III) complexes, creating two new Au-C bonds in one pot! @chem.uzh.ch

07.09.2025 16:32 — 👍 3    🔁 0    💬 0    📌 0
Promotional graphic featuring the table of contents image along with the journal and article title.

Promotional graphic featuring the table of contents image along with the journal and article title.

'Synthesis of (P^N^C)Gold(III) Complexes via Tandem Oxidative Addition/C–H Auration' from ACS Organic & Inorganic Au is an open access #ACSEditorsChoice.

📖 Read the article: buff.ly/2UUBEnb

07.09.2025 12:01 — 👍 2    🔁 1    💬 0    📌 1
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Fantastic two weeks of science! Very happy to have participated at the Bienal @rseq-quimica.bsky.social and @eucomc2025.bsky.social sharing our advances in gold(III) chemistry, made at the @chem-uzh-ch.bsky.social. Thanks to the organisers for these great opportunities! @swisschemistry.bsky.social

11.07.2025 15:58 — 👍 10    🔁 3    💬 2    📌 0
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Interrogating the anti-Insertion of Alkynes into Gold(III) Alkyne hydrofunctionalizations are a powerful strategy to efficiently build up structural complexity. The selectivity of these reactions is typically governed by the interaction between the alkyne and...

Congrats for this nice work now available in @jacsau.bsky.social by the group of Cristina Nevado
Interrogating the anti-Insertion of Alkynes into Gold(III) | JACS Au pubs.acs.org/doi/10.1021/...

04.03.2025 23:48 — 👍 4    🔁 1    💬 0    📌 0
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Interrogating the anti-Insertion of Alkynes into Gold(III) Alkyne hydrofunctionalizations are a powerful strategy to efficiently build up structural complexity. The selectivity of these reactions is typically governed by the interaction between the alkyne and a metal-hydride, which commonly proceeds via a well-understood syn-insertion mechanism. In contrast, anti-insertions are far less common, with proposed mechanisms often extrapolated from literature precedents rather than grounded in direct experimental evidence. While gold complexes rank among the most efficient catalysts for such transformations, the mechanistic understanding of the key alkyne insertion step remains incomplete. In this study, we demonstrate that stable gold(III)-hydrides, featuring a (P∧N∧C) ligand, undergo selective insertion of alkynes to yield the corresponding anti-Markovnikov Z-vinyl complexes. A combination of control experiments, kinetic studies, and computational analyses reveals a nonradical, bimolecular insertion process, in which water plays a pivotal role by accelerating the reaction and potentially stabilizing a highly reactive, T-shaped gold(I) intermediate. Notably, this is the first demonstration of the insertion of both activated and unactivated terminal and internal alkynes into a gold(III)-hydride complex.

My first post here comes with my latest work at the University of Zurich: Interrogating the anti-Insertion of Alkynes into Gold(III)! We explore the complex mechanism behind this apparently simple two-component reaction. Check it out in JACS Au pubs.acs.org/doi/10.1021/...
@uzhchemistry.bsky.social

28.02.2025 07:58 — 👍 3    🔁 1    💬 0    📌 0

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