Rare-Earth Metal Triflates Inclusion Complexes with Cobalt(II) Hemicryptophane Tren Cage

IF 5.2 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Organic & Inorganic Au Pub Date : 2026-10-07 Epub Date: 2026-08-04 DOI:10.1021/acsorginorgau.6c00049
Deeksha Setia, Patrick Weis, Manfred Kappes, Jana Roithová
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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.

稀土金属与钴的三氟化包合物(II)半透明笼
稀土金属三酸盐可以调节过渡金属配合物的结构、氧化还原性质和反应性,当它们被限制在超分子宿主体内时。本文采用高分辨率电喷雾电离质谱法(ESI-MS)、循环行波离子迁移质谱法(im - twims)、主-客交换实验研究了稀土金属三氟化物(Ln(OTf)3、Ln = Dy、Yb、La、Lu)在钴(II)半氪烷笼(CoCageHCPT)中的包合,并利用循环伏安法检测了其电化学性能。ESI-MS揭示了与附加溶剂化加合物形成的指示包合物[CoII(CageHCPT)(Ln(OTf)3)]2+。离子迁移率测量揭示了空笼配合物的构象灵活性,显示出异构体的广泛分布。相比之下,客体封装只产生两个主要异构体的定义几何形状,每个异构体具有相似的丰度和在371-374 Å2范围内的接近碰撞横截面。DFT计算表明,笼的盖子为镧离子创造了一个吸引人的口袋,而笼的侧面开口容纳了协调的三氟化离子。另外,一个三酸盐阴离子起桥接作用,将la (OTf)3锚定在钴中心。这种刚性结构导致包合物形成两个非对映异构体,与实验检测到的异构体相对应。平衡实验显示了快速的主客体交换动力学(kMS≥0.5 s-1),表明Ln(OTf)3在笼腔内的动态结合。此外,循环伏安法研究表明,Dy(OTf)3包合后CoII/I (0.6 V)和CoI/0 (0.5 V)还原波发生阳极位移,表明钴中心受到强刘易斯酸的影响。总的来说,综合结果表明,类镧三酸盐形成动态的、结构明确的包合物,极大地调节了钴笼体系的氧化还原性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Organic & Inorganic Au
ACS Organic & Inorganic Au 有机化学、无机化学-
CiteScore
4.10
自引率
0.00%
发文量
0
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.
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