{"title":"Ligand-enabled stabilisation of elusive copper metallocenes","authors":"Rajan Yadav, Susanta Hazra","doi":"10.1007/s12039-026-02548-1","DOIUrl":null,"url":null,"abstract":"<div><p>The synthesis and isolation of copper metallocenes have remained a long-standing challenge in organometallic chemistry due to the inherent propensity of copper to promote carbon–carbon bond formation rather than sustaining in the sandwich coordination. Evans and coworkers addressed this obstacle and reported a ligand-centric strategy for isolating bis(cyclopentadienyl) copper complexes using sterically encumbered tri-tert-butylcyclopentadienyl (Cp<sup>ttt</sup>) ligands. Computational and spectroscopic analyses suggest that, despite a change in formal oxidation states of copper from +1 to +3, the electronic charge at the copper centre remains largely invariant, highlighting the dominant role of ligand-based charge delocalisation and dynamic coordination. This work establishes a conceptual framework for stabilising electronically flexible, low-coordinate metal centres, and provides new insights into the interplay between steric confinement and electronic structure in transition-metal complexes.</p><h3>Graphical abstract</h3><p>A missing member of the 3d metallocene series has been realised through the synthesis and structural characterisation of Cp<sup>ttt</sup>₂Cu, the first neutral bis(cyclopentadienyl) copper complex, providing a true ‘cuprocene’ analogue and redefining bonding at copper. Importantly, the ligand has the flexibility of coordination to stabilise Cu in this set of three metallocenes, both in terms of structure and electron delocalisation.\n</p><div><figure><div><div><picture><source><img></source></picture><span>The alternative text for this image may have been generated using AI.</span></div></div></figure></div></div>","PeriodicalId":616,"journal":{"name":"Journal of Chemical Sciences","volume":"138 2","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2026-05-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chemical Sciences","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s12039-026-02548-1","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The synthesis and isolation of copper metallocenes have remained a long-standing challenge in organometallic chemistry due to the inherent propensity of copper to promote carbon–carbon bond formation rather than sustaining in the sandwich coordination. Evans and coworkers addressed this obstacle and reported a ligand-centric strategy for isolating bis(cyclopentadienyl) copper complexes using sterically encumbered tri-tert-butylcyclopentadienyl (Cpttt) ligands. Computational and spectroscopic analyses suggest that, despite a change in formal oxidation states of copper from +1 to +3, the electronic charge at the copper centre remains largely invariant, highlighting the dominant role of ligand-based charge delocalisation and dynamic coordination. This work establishes a conceptual framework for stabilising electronically flexible, low-coordinate metal centres, and provides new insights into the interplay between steric confinement and electronic structure in transition-metal complexes.
Graphical abstract
A missing member of the 3d metallocene series has been realised through the synthesis and structural characterisation of Cpttt₂Cu, the first neutral bis(cyclopentadienyl) copper complex, providing a true ‘cuprocene’ analogue and redefining bonding at copper. Importantly, the ligand has the flexibility of coordination to stabilise Cu in this set of three metallocenes, both in terms of structure and electron delocalisation.
The alternative text for this image may have been generated using AI.
期刊介绍:
Journal of Chemical Sciences is a monthly journal published by the Indian Academy of Sciences. It formed part of the original Proceedings of the Indian Academy of Sciences – Part A, started by the Nobel Laureate Prof C V Raman in 1934, that was split in 1978 into three separate journals. It was renamed as Journal of Chemical Sciences in 2004. The journal publishes original research articles and rapid communications, covering all areas of chemical sciences. A significant feature of the journal is its special issues, brought out from time to time, devoted to conference symposia/proceedings in frontier areas of the subject, held not only in India but also in other countries.