Platinum Complexes for Dark-Stable Hydrosilylation

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Solution Overview

Problem

Existing silicone compositions crosslinkable via visible and/or UV radiation lack adequate dark stability, which is crucial for industrial applications, especially in production processes where storage and handling require stability beyond light exposure.

Innovation Solution

Development of platinum complexes with specific cyclopentadienyl radicals, such as trimethyl[(allyldimethylsilyl)cyclopentadienyl]platinum(IV), that are air-stable, moisture-stable, and labile to irradiation, allowing for photochemical activation and catalysis of hydrosilylation reactions, while being easily preparable and having improved solubility in silicone matrices.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Power

If platinum complexes with aromatic substituents are used to increase quantum yield and shift light wavelength, then photochemical activation efficiency is improved, but solubility in silicone matrix deteriorates

Engineering Contradiction:
Improvequantum yieldVSAvoidsolubility in silicone matrix
Core Design Contradiction:
PowerVSStability of the object's composition

Solution Approach 1:

The patent applies local quality by introducing specific silyl-substituted cyclopentadienyl groups at particular positions on the platinum complex structure. The silyl groups are strategically placed to enhance solubility in the silicone matrix without compromising the overall quantum yield, thus creating local structural modifications that address the solubility issue while maintaining the photochemical activation efficiency.

Inventive Principle:
Principle #3Local quality

Solution Approach 2:

The patent employs parameter changes by modifying the substituent groups on the cyclopentadienyl ring from aromatic to silyl-containing aliphatic groups. This chemical parameter change fundamentally alters the solubility characteristics of the platinum complex, making it compatible with silicone matrices while preserving the essential photochemical properties needed for hydrosilylation catalysis.

Inventive Principle:
Principle #35Parameter changes

2Reliability

If thermal means are used for catalyst activation, then crosslinking operation can be performed, but energy consumption and process costs increase

Engineering Contradiction:
Improvecrosslinking operationVSAvoidenergy consumption
Core Design Contradiction:
ReliabilityVSUse of energy by moving object

Solution Approach 1:

The patent replaces the thermal activation mechanism with a photochemical activation mechanism. Instead of using heat (thermal energy) to activate the platinum catalyst, the invention uses light irradiation (electromagnetic radiation) to initiate the hydrosilylation reaction. This substitution of activation method dramatically reduces energy consumption and eliminates the need for costly heating equipment while maintaining reliable crosslinking operation.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

Solution Approach 2:

The patent utilizes the phase transition aspect of energy input by switching from thermal energy (heat) to radiant energy (light) for catalyst activation. This energy phase substitution allows the crosslinking reaction to proceed at ambient or lower temperatures, reducing energy consumption and avoiding thermal warpage of components while ensuring complete crosslinking through the photoinitiated dark reaction.

Inventive Principle:
Principle #36Phase transitions

3Reliability

If high-temperature manufacturing step is used for crosslinking, then crosslinking operation is effective, but thermal warpage of components occurs

Engineering Contradiction:
Improvecrosslinking operationVSAvoidcomponent shape stability
Core Design Contradiction:
ReliabilityVSShape

Solution Approach 1:

The patent replaces thermal activation with photochemical activation, substituting heat-based crosslinking with light-based crosslinking. This eliminates the high-temperature manufacturing step that causes thermal warpage, while the subsequent dark reaction ensures complete and effective crosslinking at lower temperatures, thereby maintaining component shape stability.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

Solution Approach 2:

The patent applies preliminary action by using light irradiation to initiate the crosslinking process before thermal effects can cause warpage. The photoinitiated reaction starts the crosslinking at ambient or low temperatures, and the continuing dark reaction completes the crosslinking without requiring high-temperature exposure, thus preventing thermal deformation of the component shape.

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

The platinum complexes provide enhanced dark stability, allowing for long storage and handling without light-induced degradation, and efficient photochemical activation, leading to improved productivity and reduced energy costs in crosslinking processes.

Implementation Method 1

platinum catalysts activatable by ultraviolet and/or visible radiation

Methodology Applied
Scientific EffectPhotochemical activation: Photoionisation

Implementation Method 2

the crosslinking operation is effected via a hydrosilylation reaction in which the catalyst used is typically platinum or another metal from the platinum group. In the reaction that proceeds catalytically, aliphatically unsaturated groups are reacted with Si-bonded hydrogen

Methodology Applied
Scientific EffectHydrosilylation reaction: Chemical Bonding

Data Source

PatentUS10392479B2Platinum complexes and their use in compounds that can be cross-linked by a hydrosilylation reaction
Publication Date: 2019.08.27 WACKER CHEMIE AG
  • US10392479B2 patent drawing

AI summary

Cyclopentadienyl platinum complexes bearing ethylenic unsaturation are efficient photocatalysts for hydrosilylation of compounds containing aliphatic carbon-carbon multiple bonds, while exhibiting extended dark time, and are particularly useful in addition-curable organopolysiloxane compositions.