Deeksha Setia, Patrick Weis, Manfred Kappes, Jana Roithová
{"title":"Rare-Earth Metal Triflates Inclusion Complexes with Cobalt(II) Hemicryptophane Tren Cage","authors":"Deeksha Setia, Patrick Weis, Manfred Kappes, Jana Roithová","doi":"10.1021/acsorginorgau.6c00049","DOIUrl":null,"url":null,"abstract":"<p>Rare-earth metal\r\ntriflates can modulate the structure, redox properties,\r\nand reactivity of transition-metal complexes when confined in supramolecular\r\nhosts. In this paper, we have investigated the inclusion of rare-earth\r\nmetal triflates (Ln(OTf)<sub>3</sub>, Ln = Dy, Yb, La, Lu) into a\r\ncobalt(II) hemicryptophane tren cage (<strong>CoCage</strong><sup><strong>HCPT</strong></sup>) using high-resolution electrospray ionization\r\nmass spectrometry (ESI-MS), cyclic traveling wave ion mobility mass\r\nspectrometry (cIM-TWIMS), host–guest exchange experiments,\r\nand examined the electrochemical properties using cyclic voltammetry.\r\nESI-MS reveals the formation of dicationic inclusion complexes [Co<sup>II</sup>(Cage<sup><strong>HCPT</strong></sup>)(Ln(OTf)<sub>3</sub>)]<sup>2+</sup> with additional solvated adducts. Ion mobility measurements\r\nrevealed the conformational flexibility of the empty cage complex,\r\nshowing a broad distribution of isomers. In contrast, guest encapsulation\r\nyields defined geometries with only two dominant isomers, each with\r\nsimilar abundance and a close collisional cross-section in the range\r\nof 371–374 Å<sup>2</sup>. The DFT calculations revealed\r\nthat the cap of the cage creates an attractive pocket for the lanthanum\r\nion, while the side openings of the cage accommodate the coordinated\r\ntriflate ions. In addition, one triflate anion is bridging, anchoring\r\nLa(OTf)<sub>3</sub> to the cobalt center. This rigid structure leads\r\nto the formation of two diastereoisomers of the inclusion complex,\r\ncorresponding to the experimentally detected isomers. Equilibration\r\nexperiments demonstrated fast host–guest exchange kinetics\r\n(k<sub>MS</sub> ≥ 0.5 s<sup>–1</sup>), indicating dynamic\r\nbinding of Ln(OTf)<sub>3</sub> within the cage cavity. Furthermore,\r\ncyclic voltammetry studies showed anodic shifts of the Co<sup>II/I</sup> (0.6 V) and Co<sup>I/0</sup> (0.5 V) reduction waves upon Dy(OTf)<sub>3</sub> inclusion, indicating strong\r\nLewis-acid effects on the cobalt center. Overall, the combined results\r\nreveal that lanthanoid triflates form dynamic yet structurally defined\r\ninclusion complexes that substantially tune the redox properties of\r\nthe cobalt cage system.</p>","PeriodicalId":29797,"journal":{"name":"ACS Organic & Inorganic Au","volume":"6 5","pages":"616–623"},"PeriodicalIF":5.2000,"publicationDate":"2026-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Organic & Inorganic Au","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsorginorgau.6c00049","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/4 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Rare-earth metal
triflates can modulate the structure, redox properties,
and reactivity of transition-metal complexes when confined in supramolecular
hosts. In this paper, we have investigated the inclusion of rare-earth
metal triflates (Ln(OTf)3, Ln = Dy, Yb, La, Lu) into a
cobalt(II) hemicryptophane tren cage (CoCageHCPT) using high-resolution electrospray ionization
mass spectrometry (ESI-MS), cyclic traveling wave ion mobility mass
spectrometry (cIM-TWIMS), host–guest exchange experiments,
and examined the electrochemical properties using cyclic voltammetry.
ESI-MS reveals the formation of dicationic inclusion complexes [CoII(CageHCPT)(Ln(OTf)3)]2+ with additional solvated adducts. Ion mobility measurements
revealed the conformational flexibility of the empty cage complex,
showing a broad distribution of isomers. In contrast, guest encapsulation
yields defined geometries with only two dominant isomers, each with
similar abundance and a close collisional cross-section in the range
of 371–374 Å2. The DFT calculations revealed
that the cap of the cage creates an attractive pocket for the lanthanum
ion, while the side openings of the cage accommodate the coordinated
triflate ions. In addition, one triflate anion is bridging, anchoring
La(OTf)3 to the cobalt center. This rigid structure leads
to the formation of two diastereoisomers of the inclusion complex,
corresponding to the experimentally detected isomers. Equilibration
experiments demonstrated fast host–guest exchange kinetics
(kMS ≥ 0.5 s–1), indicating dynamic
binding of Ln(OTf)3 within the cage cavity. Furthermore,
cyclic voltammetry studies showed anodic shifts of the CoII/I (0.6 V) and CoI/0 (0.5 V) reduction waves upon Dy(OTf)3 inclusion, indicating strong
Lewis-acid effects on the cobalt center. Overall, the combined results
reveal that lanthanoid triflates form dynamic yet structurally defined
inclusion complexes that substantially tune the redox properties of
the cobalt cage system.
期刊介绍:
ACS Organic & Inorganic Au is an open access journal that publishes original experimental and theoretical/computational studies on organic organometallic inorganic crystal growth and engineering and organic process chemistry. Short letters comprehensive articles reviews and perspectives are welcome on topics that include:Organic chemistry Organometallic chemistry Inorganic Chemistry and Organic Process Chemistry.