We investigated Xe binding in a previously reported paramagnetic metal-organic tetrahedral capsule, [CoL], where L = 4,4'-bis[(2-pyridinylmethylene)amino][1,1'-biphenyl]-2,2'-disulfonate. The Xe-inclusion complex, [XeCoL], was confirmed by H NMR spectroscopy to be the dominant species in aqueous solution saturated with Xe gas. The measured Xe dissociation rate in [XeCoL], = 4.45(5) × 10 s, was at least 40 times greater than that in the analogous [XeFeL] complex, highlighting the capability of metal-ligand interactions to tune the capsule size and guest permeability. The rapid exchange of Xe nuclei in [XeCoL] produced significant hyperpolarized Xe chemical exchange saturation transfer (hyper-CEST) NMR signal at 298 K, detected at a concentration of [XeCoL] as low as 100 pM, with presaturation at -89 ppm, which was referenced to solvated Xe in HO. The saturation offset was highly temperature-dependent with a slope of -0.41(3) ppm/K, which is attributed to hyperfine interactions between the encapsulated Xe nucleus and electron spins on the four Co centers. As such, [XeCoL] represents the first example of a paramagnetic hyper-CEST (paraHYPERCEST) sensor. Remarkably, the hyper-CEST Xe NMR resonance for [XeCoL] (δ = -89 ppm) was shifted 105 ppm upfield from the diamagnetic analogue [XeFeL] (δ = +16 ppm). The Xe inclusion complex was further characterized in the crystal structure of (C(NH))[XeCoL]·75 HO (). Hydrogen bonding between capsule-linker sulfonate groups and exogenous guanidinium cations, (C(NH)), stabilized capsule-capsule interactions in the solid state and also assisted in trapping a Xe atom (∼42 Å) in the large (135 Å) cavity of . Magnetic susceptibility measurements confirmed the presence of four noninteracting, magnetically anisotropic high-spin Co centers in . Furthermore, [CoL] was found to be stable toward aggregation and oxidation, and the CEST performance of [XeCoL] was unaffected by biological macromolecules in HO. These results recommend metal-organic capsules for fundamental investigations of Xe host-guest chemistry as well as applications with highly sensitive Xe-based sensors.
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http://dx.doi.org/10.1021/acs.inorgchem.9b03634 | DOI Listing |
Nat Commun
December 2024
Department of Psychiatry, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong SAR, China.
Biological systems are complex, encompassing intertwined spatial, molecular and functional features. However, methodological constraints limit the completeness of information that can be extracted. Here, we report the development of INSIHGT, a non-destructive, accessible three-dimensional (3D) spatial biology method utilizing superchaotropes and host-guest chemistry to achieve homogeneous, deep penetration of macromolecular probes up to centimeter scales, providing reliable semi-quantitative signals throughout the tissue volume.
View Article and Find Full Text PDFJ Sep Sci
December 2024
College of Chemistry and Chemical Engineering, Yunnan Normal University, Kunming, China.
Chiral macrocycles have emerged as attractive media for chromatographic enantioseparation due to their excellent host-guest recognition properties. In this study, a new chiral stationary phase (CSP) based on 1,1'-binaphthyl chiral polyimine macrocycle (CPM) was reported. The CPM was synthesized by one-step aldehyde-amine condensation of (S)-2,2'-dihydroxy-[1,1'-binaphthalene]-3,3'-dicarboxaldehyde with 1,2-phenylenediamine and bonded on thiolated silica via the thiol-ene click reaction to afford the CSP.
View Article and Find Full Text PDFJ Hazard Mater
December 2024
College of Materials Science and Engineering, State Key Laboratory of Bio-Fiber and Eco-textiles, Collaborative Innovation Center for Marine Biobased Fibers and Ecological Textile Technology Institute of Marine Biobased Materials, Qingdao University, Qingdao 266071, China; College of Chemical Engineering and Technology, Yantai Nanshan University, Yantai 265713, China. Electronic address:
Selective autonomous enrichment of micropollutants in the aquatic media has attracted increasing attention because of their low concentration characteristics and diverse coexisting species. Herein, the gradient hydrogels were prepared via free redical polymerization of AA and NH-β-CD under the induction of unilateral UV illumination (P(AA-NH-β-CD)). The gradient hydrogels present autonomous enrichment towards Sb(III) with a higher selectivity both in single and binary solutions.
View Article and Find Full Text PDFJ Chem Theory Comput
December 2024
Changping Laboratory, No. 28 Life Science Park Rd., Beijing 102206, China.
Accurate modeling of host-guest systems is challenging in modern computational chemistry. It requires intermolecular interaction patterns to be correctly described and, more importantly, the dynamic behaviors of macrocyclic hosts to be accurately modeled. Pillar[]arenes as a crucial family of macrocycles play a critical role in host-guest chemistry and biomedical applications.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Laboratório Associado para a Química Verde (LAQV), Rede de Química e Tecnologia (REQUIMTE), Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, 2829-516 Caparica, Portugal.
The photoswitching of supramolecular host-guest complexes is the basis of numerous molecularly controlled macroscopic functions, such as sol-gel transition, photopharmacology, the active transport of ions or molecules, light-powered molecular machines, and much more. The most commonly used systems employ photoactive azobenzene guests and synthetic host molecules, which bind as the stable isomers and dissociate as the forms after exposure to UV light. We present a new, extraordinarily efficient cucurbit[7]uril (CB7)/diazocine host/guest complex with inverted stability that self-assembles under UV irradiation and dissociates in the dark.
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