Probing rotaxane dynamics with F NMR/MRI: Unveiling the roles of mechanical bond and steric hindrance.

Background: Deciphering the molecular dynamics (MD) of rotaxanes is crucial for designing and refining their applications in molecular devices. This study employed fluorine-19 nuclear magnetic resonance (F NMR) and magnetic resonance imaging (MRI) to unveil the interplay between mechanical bonds and steric hindrance in a series of fluorinated rotaxanes.

Results: H/F NMR revealed stable "Z"-shaped wheel conformations minimizing steric clashes and favoring π-π interactions with the axle.

Precise Distance Control and Functionality Adjustment of Frustrated Lewis Pairs in Metal-Organic Frameworks.

We report the construction of frustrated Lewis pairs (FLPs) in a metal-organic framework (MOF), where both Lewis acid (LA) and Lewis base (LB) are fixed to the backbone. The anchoring of a tritopic organoboron linker as LA and a monotopic linker as LB to separate metal oxide clusters in a tetrahedron geometry allows for the precise control of distance between them. As the type of monotopic LB linker varies, pyridine, phenol, aniline, and benzyl alcohol, a series of 11 FLPs were constructed to give fixed distances of 7.

Effect of Co-Adsorbed Guest Adsorbates on the Separation of Ethylene/Ethane Mixtures on Metal-Organic Frameworks with Open Metal Sites.

Direct determination of the equilibrium adsorption and spectroscopic observation of adsorbent-adsorbate interaction is crucial to evaluate the olefin/paraffin separation performance of porous adsorbents. However, the experimental characterization of competitive adsorption of various adsorbates at atomic-molecular level in the purification of multicomponent gas mixtures is challenging and rarely conducted. Herein, solid-state NMR spectroscopy is employed to examine the effect of co-adsorbed guest adsorbates on the separation of ethylene/ethane mixtures on Mg-MOF-74, Zn-MOF-74 and UTSA-74.

Surface Hydrophobicity and Guest Permeability in Polydimethylsiloxane-Coated MIL-53 as Studied by Solid-State Nuclear Magnetic Resonance Spectroscopy.

Experimental characterization of the hydrophobic porous materials at the atomic and molecular levels is of great significance, but exploring their hydrophobicity characteristics and interactions with guest molecules with distinct polarity is still challenging. In this work, solid-state NMR is employed to characterize the surface hydrophobicity and explore the guest solvent permeability in polydimethylsiloxane (PDMS)-coated MIL-53. It was found that the PDMS-coated MIL-53 was hydrophobic to water and infiltrated to methanol, acetone, benzene, toluene, and ethylbenzene solvents.

Self-Consistent Implementation of a Solvation Free Energy Framework to Predict the Salt Solubilities of Six Alkali Halides.

To assess the salt solubilities of six alkali halides in aqueous systems, we proposed a thermodynamic cycle and an efficient molecular modeling methodology. The Gibbs free energy changes for vaporization, dissociation, and dissolution were calculated using the experimental data of ionic thermodynamic properties obtained from the NBS tables. Additionally, the Marcus' and Tissandier's solvation free energy data for Li, Na, K, Cl, and Br ions were compared with the conventional solvation free energies by substituting into our self-consistent thermodynamic cycle.

Reticulated Polyamide Thin-Film Nanocomposite Membranes Incorporated with 2D Boron Nitride Nanosheets for High-Performance Nanofiltration.

Nanofiltration (NF) technology has been widely used in saline wastewater treatment due to its unique separation mechanism. However, the NF membrane, as the core of the nanofiltration technology, is restricted by the trade-off between permeability and selectivity, which greatly restricts the development of NF membranes. The interlamellar arrangement of 2D boron nitride nanosheets (BNNSs) can provide additional transport channels and selectivity, as well as strong adsorption capacity due to its high specific surface area, exhibiting significant potential for advanced membranes.

Pseudo-resonance structures in chiral alcohols and amines and their possible aggregation states.

We now report that some chiral compounds, like alcohols, which are not sterically hindered atropisomers nor epimer mixtures, exhibit two sets of simultaneous NMR spectra in CDCl. Some other chiral alcohols also simultaneously exhibit two different NMR spectra in the solid state because two different conformers, and had different sizes because their corresponding bond lengths and angles are different. These structures were confirmed in the same solid state by X-ray.

Unravelling the Reactivity of Framework Lewis Acid Sites towards Methanol Activation on H-ZSM-5 Zeolite with Solid-State NMR Spectroscopy.

Understanding the acid sites on zeolites is vital for the establishment of catalyst structure-activity relationship and exploration of their potential applications in heterogeneous catalysis. Here, we report the identification of active framework Lewis acid sites on ZSM-5 zeolites. The structures of framework-associated tri-coordinated Al that is bonding with hydroxyl groups are determined by using one- dimensional (1D) P and two-dimensional (2D) P-{ Al} NMR spectroscopy of trimethylphosphine oxide probe molecule.

Influence of zeolite confinement effects on cation-π interactions in methanol-to-hydrocarbon conversion.

By using 2D C-C correlation MAS NMR spectroscopy and DFT calculations, the nature of cation-π interactions between cyclopentenyl cations and benzene was clarified over H-ZSM-5, H-β and H-SSZ-13 zeolites. The cation-π interactions are favored over H-β and H-SSZ-13 with large channels or cages. The zeolite structure is identified to affect the arrangements of cyclopentenyl cations and benzene in the confined environment, leading to different extents of overlapping of positive-negative charge centers and cation-π interaction strength.

Molecular simulations of the effects of substitutions on the dissolution properties of amorphous cellulose acetate.

The dissolution behavior of cellulose acetate (CA) is an extremely important property in its extensive applications and preparation of derivatives. In this paper, we proposed a molecular model building strategy to construct amorphous CA with various substituent distributions (different degrees of substitution and substitution positions). A protocol combing molecular dynamics simulation and density functional theory (DFT) was applied to systematically investigate the dissolution behavior of CAs, and the structural properties of CAs.

Preferential adsorption sites for propane/propylene separation on ZIF-8 as revealed by solid-state NMR spectroscopy.

Solid-state NMR spectroscopy in conjunction with theoretical calculation was employed to investigate the adsorbent-adsorbate host-guest interactions during propane/propylene separation on ZIF-8. H NMR chemical shifts of free gaseous and adsorbed propane/propylene are unambiguously assigned with the assistance of two-dimensional (2D) H-H correlation spectroscopy (COSY) MAS NMR spectra. Meanwhile, the adsorption selectivity for propane/propylene mixtures on ZIF-8 at a pressure in range of 1.

Application of solid-state NMR techniques for structural characterization of metal-organic frameworks.

Solid-state NMR can afford the structural information about the chemical composition, local environment, and spatial coordination at the atomic level, which has been extensively applied to characterize the detailed structure and host-guest interactions in metal-organic frameworks (MOFs). In this review, recent advances for the structural characterizations of MOFs using versatile solid-state NMR techniques were briefly introduced. High-field sensitivity-enhanced solid-state NMR method enabled the direct observation of metal centers in MOFs containing low-γ nuclei.

Insight into Carbocation-Induced Noncovalent Interactions in the Methanol-to-Olefins Reaction over ZSM-5 Zeolite by Solid-State NMR Spectroscopy.

Carbocations such as cyclic carbenium ions are important intermediates in the zeolite-catalyzed methanol-to-olefins (MTO) reaction. The MTO reaction propagates through a complex hydrocarbon pool process. Understanding the carbocation-involved hydrocarbon pool reaction on a molecular level still remains challenging.

Unraveling Hydrocarbon Pool Boosted Propane Aromatization on Gallium/ZSM-5 Zeolite by Solid-State Nuclear Magnetic Resonance Spectroscopy.

Propane aromatization on metal-modified zeolites provides a promising route to produce valuable chemicals such as benzene, toluene and xylene via non-petroleum feedstocks. The mechanistic understanding of propane conversion to aromatics is still challenging due to the complexity of the aromatization process. Herein, by using solid-state NMR spectroscopy and GC-MS, it is shown that cyclopentenyl cations are formed as active intermediates during propane aromatization on Ga/ZSM-5 zeolite.

Breathing Effect via Solvent Inclusions on the Linker Rotational Dynamics of Functionalized MIL-53.

The breathing effects of functionalized MIL-53-X (X=H, CH , NH , OH, and NO ) induced by the inclusions of water, methanol, acetone, and N,N-dimethylformamide solvents were comprehensively investigated by solid-state NMR spectroscopy. 2D homo-nuclear correlation NMR provided direct experimental evidence for the host-guest interaction between the guest solvents and the MOF frameworks. The variations of the H and C NMR chemical shifts in functionalized MIL-53 from the narrow pore phase transitions to large pore forms due to solvent inclusions were clearly identified.

Host-Guest Interaction in Ethylene and Ethane Separation on Zeolitic Imidazolate Frameworks as Revealed by Solid-State NMR Spectroscopy.

The separation of ethane/ethylene mixture by using metal-organic frameworks (MOFs) as adsorbents is strongly associated with the pore size-sieving effect and the adsorbent-adsorbate interaction. Herein, solid-state NMR spectroscopy is utilized to explore the host-guest interaction and ethane/ethylene separation mechanism on zeolitic imidazolate frameworks (ZIFs). Preferential access to the ZIF-8 and ZIF-8-90 frameworks by ethane compared to ethylene is directly visualized from two-dimensional H- H spin diffusion MAS NMR spectroscopy and further verified by computational density distributions.

Dual Active Sites on Molybdenum/ZSM-5 Catalyst for Methane Dehydroaromatization: Insights from Solid-State NMR Spectroscopy.

Methane dehydroaromatization (MDA) on Mo/ZSM-5 zeolite catalyst is promising for direct transformation of natural gas. Understanding the nature of active sites on Mo/ZSM-5 is a challenge for applications. Herein, using H{ Mo} double-resonance solid-state NMR spectroscopy, we identify proximate dual active sites on Mo/ZSM-5 catalyst by direct observation of internuclear spatial interaction between Brønsted acid site and Mo species in zeolite channels.

Recent Advances of Solid-State NMR Spectroscopy for Microporous Materials.

Microporous materials have attracted a rapid growth of research interest in materials science and the multidisciplinary area because of their wide applications in catalysis, separation, ion exchange, gas storage, drug release, and sensing. A fundamental understanding of their diverse structures and properties is crucial for rational design of high-performance materials and technological applications in industry. Solid-state NMR (SSNMR), capable of providing atomic-level information on both structure and dynamics, is a powerful tool in the scientific exploration of solid materials.

Probing the active sites for methane activation on Ga/ZSM-5 zeolites with solid-state NMR spectroscopy.

Ga-modified zeolites represent the most effective catalyst for catalytic transformation of light alkanes to aromatics. GaO ions and GaO clusters on Ga/ZSM-5 zeolites are probed by solid-state NMR. These two types of Ga species show strong Lewis acidity and are quantitatively correlated with the catalytic activity of Ga/ZSM-5 for methane C-H bond activation.

Molecular Vises for Precisely Positioning Ligands near Catalytic Metal Centers in Metal-Organic Frameworks.

We report the construction of a molecular vise by pairing a tritopic phenylphosphorus(III) linker and a monotopic linker in opposite positions within a metal-organic framework. The angle between these linkers at metal sites is fixed upon changing the functionality in the monotopic linker, while the distance between them is precisely tuned. This distance within the molecular vise is accurately measured by H-P solid-state nuclear magnetic resonance spectroscopy.

π-Interactions between Cyclic Carbocations and Aromatics Cause Zeolite Deactivation in Methanol-to-Hydrocarbon Conversion.

The understanding of catalyst deactivation represents one of the major challenges for the methanol-to-hydrocarbon (MTH) reaction over acidic zeolites. Here we report the critical role of intermolecular π-interactions in catalyst deactivation in the MTH reaction on zeolites H-SSZ-13 and H-ZSM-5. π-interaction-induced spatial proximities between cyclopentenyl cations and aromatics in the confined channels and/or cages of zeolites are revealed by two-dimensional solid-state NMR spectroscopy.

Solid-state NMR studies of the acidity of functionalized metal-organic framework UiO-66 materials.

The acid strength of metal-organic frameworks plays a key role in their catalytic performance such as activity and selectivity during catalytic reactions. Solid-state nuclear magnetic resonance in combination with probe molecules including 2- C-acetone and pyridine-d was employed to characterize the acid strength of UiO-66-X (X = -H, -2COOH, -SO H). It was found that after introduction of the functional groups, the acid strength of UiO-66-2COOH and UiO-66-SO H is considerably enhanced compared with that of parent UiO-66, with that of the former being similar to that of zeolite H-ZSM-5, and with that of the latter being slightly stronger than that of the former.

Isolated π-Interaction Sites in Mesoporous MOF Backbone for Repetitive and Reversible Dynamics in Water.

We report the introduction of π-interaction sites into a series of chemically robust metal-organic frameworks (MOFs), MOF-526, -527, and -528, with progressively increased pore size, 1.9-3.7 nm, and the inclusion and release of large organic molecules in water.