Flash Communication: Copper Complexes Supported by Macrocyclic N-Heterocyclic Carbene Ligands with Ether or Secondary Amine Donors

Abstract Metal complexes featuring secondary amine donors have been extensively studied in the context of hydrogen-bonding or metal–ligand cooperative interactions. In this regard, pincer-type ligand frameworks have been described, but macrocyclic variants remain rare. Herein, we describe the synthesis of macrocyclic carbene ligand frameworks featuring a carbazolide backbone and an ether or secondary amine donor. While the ether was synthesized through conventional methods, the amine variant required microwave heating. Carbazolide-bis(imidazolium) pro-ligands were isolated as air-stable compounds. Metalation with Cu(acac)2 led to the formation of square-planar Cu(II) complexes characterized by single-crystal X-ray diffraction and cyclic voltammetry. A significantly more cathodic Cu(I)/Cu(II) wave by 330 mV was observed for the amine complex. Combined, the results highlight new macrocyclic carbene platforms with variable coordination environments.

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Publication Details

Journal
Organometallics
Published
2026-09-22
DOI
https://doi.org/10.1021/acs.organomet.6c00208
Primary Topic
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
Type
article
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Flash Communication: Copper Complexes Supported by Macrocyclic N-Heterocyclic Carbene Ligands with Ether or Secondary Amine Donors

Yunping Zhoujin, Heui Beom Lee, Hans‐Conrad zur Loye, Brenna Lawrence et al.
Organometallics
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
article

Flash Communication: Copper Complexes Supported by Macrocyclic N-Heterocyclic Carbene Ligands with Ether or Secondary Amine Donors

Yunping Zhoujin, Heui Beom Lee, Hans‐Conrad zur Loye, Brenna Lawrence, Soumyadip Sharangi, Mark D. Smith, Matthew O. Ariwoola, Paul Bekai, Kaden Moracco
article en

Abstract

Abstract Metal complexes featuring secondary amine donors have been extensively studied in the context of hydrogen-bonding or metal–ligand cooperative interactions. In this regard, pincer-type ligand frameworks have been described, but macrocyclic variants remain rare. Herein, we describe the synthesis of macrocyclic carbene ligand frameworks featuring a carbazolide backbone and an ether or secondary amine donor. While the ether was synthesized through conventional methods, the amine variant required microwave heating. Carbazolide-bis(imidazolium) pro-ligands were isolated as air-stable compounds. Metalation with Cu(acac)2 led to the formation of square-planar Cu(II) complexes characterized by single-crystal X-ray diffraction and cyclic voltammetry. A significantly more cathodic Cu(I)/Cu(II) wave by 330 mV was observed for the amine complex. Combined, the results highlight new macrocyclic carbene platforms with variable coordination environments.

Organometallics
University of South Carolina (US), University of South Carolina Sumter (US)
Clean water and sanitation
Openalex Percentile: Top 21%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
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Flash Communication: Copper Complexes Supported by Macrocyclic N-Heterocyclic Carbene Ligands with Ether or Secondary Amine Donors — Yunping Zhoujin, Heui Beom Lee, et al. · Organometallics (2026) | TGRS Research Map | TGRS