Functionalization of Metal-Organic Frameworks To Achieve Controllable Wettability.

Inorg Chem

Department of Chemistry, ‡School of Biomedical Engineering, and §Department of Chemical & Biological Engineering, Colorado State University, Fort Collins, Colorado 80523, United States.

Published: May 2017

The overall versatility of a material can be immensely expanded by the ability to controllably tune its hydrophobicity. Herein we took advantage of steric bias to demonstrate that tricarboxylate metal-organic frameworks (MOFs) can undergo covalent postsynthetic modification to confer various degrees of hydrophobicity. MOF copper 2-aminobenzene-1,3,5-tricarboxylate was modified with varying-length aliphatic carbon chains. Unmodified Cu(NHBTC) degrades in minutes upon contact with water, whereas modification as low as 14% results in powders that show significantly enhanced hydrophobic character with contact angles up to 147°. The modified material is capable of withstanding direct contact with water for 30 min with no visual evidence of altered surface characteristics. A linear relationship was observed between the length of the tethered chain and the water contact angle. These results reveal a predictable method for achieving a range of desirable sorption rates and highly controllable hydrophobic character. This work thereby expands the possibilities of rationally modifying MOFs for a plethora of target-specific applications.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.inorgchem.7b00373DOI Listing

Publication Analysis

Top Keywords

metal-organic frameworks
8
contact water
8
hydrophobic character
8
functionalization metal-organic
4
frameworks achieve
4
achieve controllable
4
controllable wettability
4
wettability versatility
4
versatility material
4
material immensely
4

Similar Publications

Hierarchical Selenium-Doped Nickel-Cobalt Hybrids on Carbon Paper for the Overall Water-Splitting Electrocatalytic System.

ACS Appl Mater Interfaces

January 2025

Department of Battery and Chemical Engineering, Hanyang University, Ansan, Gyeonggi-do 15588, Republic of Korea.

Designing and constructing hierarchically structured materials with heterogeneous compositions is the key to developing an effective catalyst for overall water-splitting applications. Herein, we report the fabrication of hollow-structured selenium-doped nickel-cobalt hybrids on carbon paper as a self-supported electrode (denoted as Se-Ni|Co/CP, where Ni|Co hybrids consist of nickel-cobalt alloy-incorporated nickel-cobalt oxide). The procedure involves direct growth of zeolitic imidazolate framework-67 (ZIF-67) on bimetal-based nickel-cobalt hydroxide (NiCoOH) electrodeposited on CP, followed by selenous etching and pyrolysis to obtain the final Se-Ni|Co/CP electrocatalytic system.

View Article and Find Full Text PDF

Metal-Organic Frameworks (MOFs) gaining increasing interest in heterogeneous catalysis owing to their advantageous properties such as superior porosity, high surface area, ample catalytic sites. Their properties can be tailored by varying the metal ions or metal clusters (nodes) and organic linkers. Magnetically active nano core-shell MOF composites are also discovered for easy separation and reuse of catalyst.

View Article and Find Full Text PDF

Pressure treatment enables white-light emission in Zn-IPA MOF via asymmetrical metal-ligand chelate coordination.

Nat Commun

January 2025

State Key Laboratory of Superhard Materials, Synergetic Extreme Condition High-Pressure Science Center, College of Physics, Jilin University, Changchun, China.

Metal-organic frameworks that feature hybrid fluorescence and phosphorescence offer unique advantages in white-emitting communities based on their multiple emission centers and high exciton utilization. However, it poses a substantial challenge to realize superior white-light emission in single-component metal-organic frameworks without encapsulating varying chromophores or integrating multiple phosphor subunits. Here, we achieve a high-performance white-light emission with photoluminescence quantum yield of 81.

View Article and Find Full Text PDF

As the global quest for sustainable energy keeps rising, exploring novel efficient and practical photocatalysts remains a research and industrial urge. Particularly, metal organic frameworks were proven to contribute to various stages of the carbon cycle, from CO capture to its conversion. Herein, we report the photo-methanation activity of three isostructural, nickel-based metal organic frameworks incorporating additional niobium, iron, and aluminum sites, having demonstrated exceptional CO capture abilities from thin air in previous reports.

View Article and Find Full Text PDF

Nanocellulose composites based on embedded europium-containing coordination polymers for the detection of antibiotics.

Int J Biol Macromol

January 2025

State Key Laboratory of Biobased Fiber Manufacturing Technology, Tianjin University of Science and Technology, Tianjin 300457, PR China; Tianjin Key Laboratory of Pulp and Paper, Tianjin University of Science and Technology, Tianjin 300457, PR China; China Light Industry Key Laboratory of Papermaking and Biorefinery, Tianjin University of Science and Technology, Tianjin 300457, PR China. Electronic address:

Developing sensitive and reliable methods for detecting antibiotics in water solutions is essential for protecting public health and the environment. Here, we report a novel fluorescent film with superior mechanical properties and detection response to ciprofloxacin (CIP), achieved through the in-situ growth of europium-based metal-organic frameworks on TEMPO-oxidized cellulose nanofibrils (TOCNF). Firstly, Eu(III) and 2,6-pyridinedicarboxylic acid (DPA) served as precursors, and a simple self-assembly strategy was employed to grow the composite film material (Eu-DPA@TOCNF) in situ on TOCNF, which exhibited characteristic emission peaks.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!