Lithiated Cyclodextrin MOF Co-Crystallization for Porous Frameworks

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Solution Overview

Problem

The challenge lies in preparing crystalline, highly porous cyclodextrin metal organic frameworks (CD-MOFs) with alkali metal cations other than K+, Rb+, and Cs+, as attempts to incorporate other cations result in non-porous structures due to the inability to obtain stable crystalline frameworks.

Innovation Solution

A co-crystalization methodology using a combination of different cations, specifically Li+ and K+, is employed to create a metal organic framework with a coordinated network of γ-cyclodextrin and metal salt components, allowing for the formation of porous architectures with high surface areas and adsorption capacities.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If alkali metal cations other than K+, Rb+, and Cs+ are used to prepare CD-MOFs, then the diversity of metal cations is improved, but the structural integrity and porosity deteriorate resulting in non-porous structures

Engineering Contradiction:
Improvediversity of metal cationsVSAvoidstructural integrity and porosity
Core Design Contradiction:
Adaptability or versatilityVSStability of the object's composition

Solution Approach 1:

The patent employs mixed-metal cation systems combining Li+ with other alkali metal cations (K+, Rb+, Cs+) to create composite CD-MOF structures. This composite approach allows Li+ to occupy specific coordination sites while other cations maintain the overall framework stability, achieving both cation diversity and structural integrity simultaneously. The mixed-metal strategy enables access to novel porous architectures that cannot be formed with single cation types.

Inventive Principle:
Principle #40Composite materials

2Quantity of substance

If co-crystalization methodology with multiple cations is used, then the adsorption capacity is improved, but the device complexity increases

Engineering Contradiction:
Improveadsorption capacityVSAvoidcrystalization process complexity
Core Design Contradiction:
Quantity of substanceVSDevice complexity

Solution Approach 1:

The patent employs preliminary co-crystalization of multiple metal cations with cyclodextrin before framework formation. By pre-assembling the mixed-metal cation system with the organic linker in a controlled co-crystalization process, the method simplifies the overall synthesis while achieving high adsorption capacity. This preliminary organization of components facilitates subsequent framework assembly and enhances gas adsorption performance.

Inventive Principle:
Principle #10Preliminary action

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

This approach enables the production of CD-MOFs with enhanced CO2 and H2 adsorption capacities, surpassing previous sorption capacities, and maintains structural integrity and porosity, overcoming the limitations of using only K+, Rb+, and Cs+ ions.

Implementation Method 1

a coordinated network of repeating units extending in three dimensions, wherein the repeating unit comprises a cyclodextrin and a metal salt component

Methodology Applied
Scientific EffectCoordination: Chemical Bonding

Implementation Method 2

enhanced CO2 and H2 adsorption capacities, surpassing previous sorption capacities

Methodology Applied
Scientific EffectAdsorption: Adsorption

Data Source

PatentUS11890591B2Lithiated cyclodextrin metal organic frameworks and methods of making and using the same
Publication Date: 2024.02.06 NORTHWESTERN UNIV
  • US11890591B2 patent drawing
  • US11890591B2 patent drawing
  • US11890591B2 patent drawing

AI summary

Disclosed herein are lithiated cyclodextrin metal organic frameworks and method of making and using the same. A metal organic framework comprising a coordinated network of repeating units extending in three dimensions, wherein the repeating unit comprises a cyclodextrin, a first coordinating metal cation, and a second coordinating metal cation.