Two-Dimensional Coordination Polymer Synthesis at Liquid Interface

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Existing methods for manufacturing two-dimensional (2D) polymers on substrates face challenges in controlling thickness, material crystallinity, and lateral sizes, and are limited by the lack of suitable monomers, which restricts the properties and potential applications of the polymers.

Innovation Solution

The synthesis of two-dimensional coordination polymers using metal linkers and ligands with anchorage sites, specifically employing hexaaminobenzene or octaaminonaphthalene as ligands, and utilizing a two-phase synthesis route at a liquid-liquid interface to achieve controlled polymerization and crystallinity.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Manufacturing precision

If bulk crystal exfoliation or bottom-up synthesis methods are used to manufacture 2D polymers, then 2D polymers can be produced on substrates, but control of thickness, material crystallinity, and lateral sizes becomes difficult

Engineering Contradiction:
Improvecontrol of thickness, crystallinity, and lateral sizesVSAvoiddifficulty in implementing control
Core Design Contradiction:
Manufacturing precisionVSEase of manufacture

Solution Approach 1:

The invention changes the synthesis parameters by using specific monomers with controlled functional groups (carboxylic acids, phenols, amines) that enable precise control over polymerization behavior, resulting in 2D polymers with controlled thickness, crystallinity, and lateral dimensions while maintaining ease of manufacture through solution-phase synthesis

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The invention applies local quality by designing monomers with specific functional groups at particular positions (e.g., carboxylic acids at specific locations on aromatic rings) that direct the polymerization process to achieve uniform thickness and crystallinity across the 2D polymer structure

Inventive Principle:
Principle #3Local quality

2Adaptability or versatility

If conventional synthesis methods are used, then 2D polymers with dimensions far less than 1 cm2 are obtained, but the lack of suitable monomers limits polymer properties and potential applications

Engineering Contradiction:
Improvepolymer properties and potential applicationsVSAvoidlateral size of 2D polymers
Core Design Contradiction:
Adaptability or versatilityVSQuantity of substance

Solution Approach 1:

The invention employs universal monomer structures (aromatic compounds with multiple functional groups) that can be synthesized in various patterns and configurations, enabling the same synthetic approach to produce 2D polymers with different properties and applications while achieving larger lateral dimensions exceeding 1 cm2

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

The invention uses segmented monomer building blocks (such as terephthalic acid, isophthalic acid, and their derivatives) that can be systematically assembled to control both the properties and lateral size of the resulting 2D polymers, allowing independent optimization of material properties and dimensions

Inventive Principle:
Principle #1Segmentation

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 crystalline 2D coordination polymers with three-fold crystal symmetry, allowing for controlled thickness and material properties, thereby expanding the potential applications of these polymers.

Implementation Method 1

a two-dimensional coordination polymer includes metal linkers and ligands having anchorage sites. Each metal linker includes a metal and an organic moiety, and each metal linker is coupled to two ligands via the anchorage sites

Methodology Applied
Scientific EffectCoordination bonding: Chemical Bonding

Implementation Method 2

synthesizing a two-dimensional coordination polymer includes contacting a first liquid precursor with a second liquid precursor at an interface. The first liquid precursor includes a ligand and the second liquid precursor includes a metal linker

Methodology Applied
Scientific EffectPhase separation: Phase Change

Implementation Method 3

reacting the metal linker and the water-soluble ligand to yield a two-dimensional coordination polymer at the interface

Methodology Applied
Scientific EffectInterfacial polymerization: Chemical Bonding

Implementation Method 4

The polymer can be a crystalline polymer with three-fold crystal symmetry

Methodology Applied
Scientific EffectCrystallization: Crystallisation

Data Source

PatentUS12281055B2Two-dimensional coordination polymers
Publication Date: 2025.04.22 THE ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIV OF ARIZONA
  • US12281055B2 patent drawing
  • US12281055B2 patent drawing
  • US12281055B2 patent drawing

AI summary

Octaaminonaphthalene and a method of synthesizing octaaminonaphthalene are described. A two-dimensional coordination polymer and a method of synthesizing the two-dimensional coordination polymer are described. The two-dimensional coordination polymer includes ligands including anchorage sites, and metal linkers, each metal linker including a metal and an organic moiety. Each metal linker is coupled to two ligands via the anchorage sites. Synthesizing the two-dimensional coordination polymer includes contacting a first liquid precursor with a second liquid precursor at an interface, reacting the metal linker and the water-soluble ligand to yield a two-dimensional coordination polymer at the interface, and removing the two-dimensional coordination polymer from the interface.