Cooperative Ligand Engineering Enabling Stepwise Optimization of Metal-Organic Frameworks for Improved CH Separation from CO and CH.

ACS Appl Mater Interfaces

Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, College of Chemistry and Materials Sciences, Zhejiang Normal University, Jinhua 321004, P. R. China.

Published: July 2025


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Acetylene (CH), a critical chemical feedstock, is indispensable in numerous industrial processes. To satisfy the stringent demands for high-purity acetylene, adsorption-based separation techniques have become highly efficient strategies for purifying acetylene from mixtures containing methane and carbon dioxide. In this study, we introduce a novel cooperative ligand engineering strategy that integrates low-symmetry functionalized auxiliary ligands. This innovative approach enables the stepwise synthesis of three zinc-based metal-organic frameworks (MOFs), specifically , , and , which exhibit distinct structural characteristics transitioning from 2D to 3D frameworks. The incorporation of functional groups and framework transformation optimizes the pore environments, thereby creating specific adsorption sites for target gases. Notably, demonstrates superior separation performance, with a CH adsorption capacity of 44.8 cm g at 298 K, and selectivities of 4.28 for CH/CO and 18.6 for CH/CH at 298 K and 1.0 bar. Postsynthetic modification with copper ions further enhances its CH selectivity, achieving values of 6.8 for CH/CO and 20.7 for CH/CH. These results outperform those of many previously reported MOF adsorbents, highlighting the substantial potential of these materials for industrial CH purification.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acsami.5c09790DOI Listing

Publication Analysis

Top Keywords

cooperative ligand
8
ligand engineering
8
metal-organic frameworks
8
engineering enabling
4
enabling stepwise
4
stepwise optimization
4
optimization metal-organic
4
frameworks improved
4
improved separation
4
separation acetylene
4

Similar Publications

We report the synthesis and characterization of a new Schiff base ligand (HL), derived from 2-picolylamine and 2-hydroxy-3-methoxy-5-methylbenzaldehyde. Its reaction with Ni(NO)·6HO and Ln(NO)·HO (Ln = Gd, Tb, Dy) in the presence of triethylamine affords a carbonato-bridged family of heterobimetallic NiLn complexes: [NiLn(L)(L')(μ-CO)(NO)]·MeOH·HO (). During the complexation reaction, ligand HL undergoes an oxidation, followed by C-C coupling to generate a secondary ligand (HL').

View Article and Find Full Text PDF

Multivalent binding and the resulting dynamical clustering of receptors and ligands are known to be key features in biological interactions. For optimizing biomaterials capable of similar dynamical features, it is essential to understand the first step of these interactions, namely the multivalent molecular recognition between ligands and cell receptors. Here, we present the reciprocal cooperation between dynamic ligands in supramolecular polymers and dynamic receptors in model cell membranes, determining molecular recognition and multivalent binding via receptor clustering.

View Article and Find Full Text PDF

Polytantalotungstates Stabilized Iron Catalysts for Carbonylation of Benzylic C-H Bonds.

Inorg Chem

September 2025

Henan Key Laboratory of Polyoxometalate Chemistry, College of Chemistry and Molecular Sciences, Henan University, Kaifeng, Henan 475004, China.

Selective oxidation of benzylic C(sp)-H bonds to ketones is critical to the production of fine chemicals but typically requires toxic/precious metal catalysts under harsh conditions. While iron-based complexes have recently served as catalysts for photocatalytic C-H bond activation, most systems operate via homogeneous catalysis. Developing a light-driven strategy under visible light with O as an oxidant is of major importance.

View Article and Find Full Text PDF

Regio- and chemoselective catalytic partial transfer hydrogenation of quinolines by dinuclear aluminum species.

Nat Commun

September 2025

Department of Chemistry, Institute of Silicon Chemistry and Catalysis Research Center, TUM School of Natural Sciences, Technische Universität München, Garching bei München, Germany.

Catalytic reduction of quinolines has gained continuous interest in both academia and industry, providing direct and efficient access to tetrahydroquinolines or 1,2-dihydroquinolines. The catalytic preparation of tetrahydroquinolines has been extensively studied by transition metal complexes. By contrast, the related catalytic synthesis of 1,2-dihydroquinolines remains underdeveloped due to the difficulties in achieving precise control over both chemo- and regioselectivity.

View Article and Find Full Text PDF

NOTCH signaling orchestrates the inflammatory-fibrotic continuum of macrophages in renal allograft rejection.

Exp Cell Res

September 2025

Organ Transplant Center, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong 510080, China; Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology, Guangzhou, Guangdong 510080, China. Electronic address:

Background: Chronic rejection is a major cause of long-term kidney allograft failure, characterized by persistent inflammation and progressive fibrosis. Macrophages are central mediators of this process, but their phenotypic heterogeneity and regulatory mechanisms in chronic rejection remain incompletely understood.

Methods: We performed single-cell transcriptomic analysis on renal allograft biopsies from patients with different types of rejection and on a time-course rat model of chronic rejection.

View Article and Find Full Text PDF