Iodine-Containing Polymerization with RTCP for Molecular Weight Control

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Solution Overview

Problem

Conventional methods struggle to achieve controlled molecular weight distribution when using halogen-containing organic iodine compounds, particularly those with fluorine or chlorine atoms, due to difficulties in abstracting iodine from the C—I bond effectively.

Innovation Solution

A method involving reversible chain transfer catalyzed living radical polymerization (RTCP) using specific compounds represented by Formulas (21) and (22) as catalysts to facilitate iodine abstraction from halogen-containing organic iodine compounds, allowing for the production of iodine-containing compounds with controlled molecular weight distribution.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of manufacture

If conventional radical polymerization methods are used, then the polymerization process is simple and easy to carry out, but the molecular weight distribution becomes wide and control over molecular weight is limited

Engineering Contradiction:
Improveease of carrying out polymerizationVSAvoidmolecular weight distribution control
Core Design Contradiction:
Ease of manufactureVSManufacturing precision

Solution Approach 1:

The patent introduces an organic iodine compound as a chain transfer agent that mediates the polymerization process. This intermediary enables reversible chain transfer reactions, allowing the system to maintain ease of operation while achieving precise molecular weight control through the equilibrium between active and dormant species

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The patent changes the chemical parameters by using specific organic iodine compounds with controlled reactivity. By selecting iodine compounds with appropriate bond strengths and reactivity ratios, the system achieves narrow molecular weight distribution while maintaining simple polymerization conditions

Inventive Principle:
Principle #35Parameter changes

2Manufacturing precision

If living radical polymerization methods are used, then molecular weight and molecular weight distribution are controlled, but the process complexity increases due to reversible protection mechanisms

Engineering Contradiction:
Improvemolecular weight distribution controlVSAvoidpolymerization control mechanism complexity
Core Design Contradiction:
Manufacturing precisionVSDevice complexity

Solution Approach 1:

The organic iodine compound serves as a simple intermediary that enables living radical polymerization characteristics without requiring complex protective group mechanisms. The iodine-mediated chain transfer provides molecular weight control through a straightforward reversible reaction mechanism

Inventive Principle:
Principle #24Intermediary (Mediator)

Solution Approach 2:

The system achieves self-regulation of molecular weight through the inherent equilibrium of the iodine-mediated chain transfer reaction. The organic iodine compound automatically adjusts the active/dormant species balance, providing molecular weight control without external intervention or complex control systems

Inventive Principle:
Principle #25Self-service

3Productivity

If halogen-containing organic iodine compounds are used as chain transfer agents, then the polymerization can proceed, but iodine abstraction from the C—I bond becomes difficult and controllability is insufficient

Engineering Contradiction:
Improvepolymerization rateVSAvoidextended product controllability
Core Design Contradiction:
ProductivityVSManufacturing precision

Solution Approach 1:

The patent optimizes the chemical parameters by selecting organic iodine compounds with specific structures and reactivity characteristics. By adjusting the reactivity ratio and bond strength parameters of the iodine compound, the system achieves both adequate polymerization rate and improved controllability of extended products

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The organic iodine compound acts as a mediator that facilitates controlled iodine abstraction. Through the reversible chain transfer mechanism, the iodine compound enables progressive extension while maintaining controllability, resolving the contradiction between productivity and precision

Inventive Principle:
Principle #24Intermediary (Mediator)

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 iodine-containing compounds with controlled molecular weight distribution, including fluorine- or chlorine-containing polymers, and can be applied to the production of cross-linked rubbers.

Implementation Method 1

The RAFT method enables control of the molecular weight distribution by allowing the polymerization to take place through a reversible chain transfer reaction in the presence of a specific chain transfer agent called a RAFT agent

Methodology Applied
Scientific EffectReversible addition fragmentation chain transfer (RAFT):

Implementation Method 2

The ITP method is a polymerization method that uses an organic iodine compound as a chain transfer agent

Methodology Applied
Scientific EffectIodine transfer polymerization (ITP):

Implementation Method 3

A method involving reversible chain transfer catalyzed living radical polymerization (RTCP) using specific compounds represented by Formulas (21) and (22) as catalysts to facilitate iodine abstraction from halogen-containing organic iodine compounds

Methodology Applied
Scientific EffectReversible chain transfer catalyzed living radical polymerization (RTCP):

Data Source

PatentUS12486343B2Method for producing iodine-containing compound, and iodine-containing compound
Publication Date: 2025.12.02 AGC INC
  • US12486343B2 patent drawing
  • US12486343B2 patent drawing
  • US12486343B2 patent drawing

AI summary

A method for producing an iodine-containing compound includes reacting a halogen-containing organic iodine compound and a compound containing a reactive carbon-carbon double bond in the presence of a compound of Formula (21) or Formula (22). Each of R21, R23 and R24 represents a hydrogen atom, an iodine atom, or an organic group having from 1 to 20 carbon atoms; R22 represents a hydrogen atom, an iodine atom, an organic group having from 1 to 20 carbon atoms, or a boron-containing group; R25 represents a hydrogen atom, an iodine atom, an organic group having from 1 to 20 carbon atoms, or a silicon-containing group; and each of A1 and A2 represents a hydrogen atom, a chlorine atom, a bromine atom, or an iodine atom.