1621184-24-4

Usage

Type of compound

Silicone-based

Contains groups

Chloroisobutyl and ethoxy groups

Common uses

Surface modifier, adhesion promoter, crosslinking agent

Applications

Adhesives, sealants, coatings, silicone rubbers, and resins

Properties

Increased durability, flexibility, resistance to environmental factors

Siloxane backbone

Provides thermal stability

Suitability

High-temperature applications

Upstream product

• 1627573-20-9 1,1,1,3,3,6-hexachloro-5-methyl-1,3-disilahexane 
• 78-39-7 Triethyl orthoacetate 
• 122-51-0 orthoformic acid triethyl ester 

Relevant academic research and scientific papers

Enhanced hydrolytic stability of siliceous surfaces modified with pendant dipodal silanes

Dipodal silanes possess two silicon atoms that can covalently bond to a surface. They offer a distinct advantage over conventional silanes commonly used for surface modification in terms of maintaining the integrity of surface coatings, adhesive primers, and composites in aqueous environments. New nonfunctional and functional dipodal silanes with structures containing pendant rather than bridged organofunctionality are introduced. The stability of surfaces in aqueous environments prepared from dipodal silanes with hydrophobic alkyl functionality is compared to the stability of similar surfaces prepared from the conventional silanes. In strongly acidic and brine environments, surfaces modified with dipodal silanes demonstrate markedly improved resistance to hydrolysis compared to surfaces prepared from conventional silanes. Pendant dipodal silanes exhibit greater stability than bridged dipodal silanes. The apparent equilibrium constant for the formation of silanol species by the hydrolysis of a disiloxane bond was determined as Kc=[SiOH]2/[Si-O-Si][H2O]= 6±1×10-5 and is helpful in understanding the enhanced hydrolytic stability of surfaces modified with dipodal silanes. Two feet are better than one! Nonfunctional and functional dipodal silanes with structures containing pendant rather than bridged organofunctionality were synthesized. Surfaces modified with pendant dipodal silanes were found to be more resistant to hydrolysis than the bridged structure with single-carbon separated (disilapropyl)silanes, demonstrating the greatest resistance to hydrolysis and best stability (see figure).

PENDANT DIPODAL SILANES HAVING A DISILAPROPYL TERMINUS

Pendant dipodal silanes having formula (I) and methods for their synthesis are provided. In formula (I), R is an organic radical other than methyl and X may be a halogen, an alkoxy group, an acetoxy group, or a dialkylamino group. Films, adhesives, and composites formed from the inventive dipodal silanes generally demonstrate significantly greater hydrolytic resistance and film-forming ability than conventional silanes. [in-line-formulae]RSiX2CH2SiX3??(I)[/in-line-formulae]