Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Adhesion promoter for gold substrates in microelectronic applications.1 Forms stable bonds to silica and basic alumina suitable for catalyst immobilization.2 Forms luminescent gels on hydrolysis with (EtO)4Si and Eu(NO3)3.3 Used to immobilize an iridium catalyst for the enantioselective hydrogenation of aryl ketones.4 Used in the preparation of solid-phase Pd catalyst for Suzuki-Miyaura cross-coupling.5 Reference 1. Helbert, J. U.S. Patent 4,497,890, 1985. 2. Merchle, C. H. et al. Chem. Mater. 2001, 13, 3617. 3. Corriu, R. et al. J. Chem. Soc., Chem. Commun. 2001, 1116. 4. Liu, G. et al. Adv. Synth. Catal. 2008, 350, 1464. 5. Zhang, X. et al. Synthesis, 2011, 2975. Safety
Packaging Under Nitrogen 2-(Diphenylphosphino
)ethyltriethoxysilan
e; 2-(triethoxysilyethy
l)diphenylphosphine
Phosphine functional trialkoxy silane
Immobilizing ligand for precious metals
Adhesion promoter for gold substrates in microelectronic applications
Forms stable bonds to silica and basic alumina suitable for catalyst immobilization
Forms luminescent gels on hydrolysis with (EtO)4Si and Eu(NO3)3
Used to immobilize an iridium catalyst for the enantioselective hydrogenation of aryl ketones
Used in the preparation of solid-phase Pd catalyst for Suzuki-Miyaura cross-coupling reaction between organic boron compounds and organic halides
Gelest, Inc.
Done
Datasheet
Description
Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Adhesion promoter for gold substrates in microelectronic applications.1 Forms stable bonds to silica and basic alumina suitable for catalyst immobilization.2 Forms luminescent gels on hydrolysis with (EtO)4Si and Eu(NO3)3.3 Used to immobilize an iridium catalyst for the enantioselective hydrogenation of aryl ketones.4 Used in the preparation of solid-phase Pd catalyst for Suzuki-Miyaura cross-coupling.5 Reference 1. Helbert, J. U.S. Patent 4,497,890, 1985. 2. Merchle, C. H. et al. Chem. Mater. 2001, 13, 3617. 3. Corriu, R. et al. J. Chem. Soc., Chem. Commun. 2001, 1116. 4. Liu, G. et al. Adv. Synth. Catal. 2008, 350, 1464. 5. Zhang, X. et al. Synthesis, 2011, 2975. Safety
Packaging Under Nitrogen 2-(Diphenylphosphino
)ethyltriethoxysilan
e; 2-(triethoxysilyethy
l)diphenylphosphine
Phosphine functional trialkoxy silane
Immobilizing ligand for precious metals
Adhesion promoter for gold substrates in microelectronic applications
Forms stable bonds to silica and basic alumina suitable for catalyst immobilization
Forms luminescent gels on hydrolysis with (EtO)4Si and Eu(NO3)3
Used to immobilize an iridium catalyst for the enantioselective hydrogenation of aryl ketones
Used in the preparation of solid-phase Pd catalyst for Suzuki-Miyaura cross-coupling reaction between organic boron compounds and organic halides
Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water Application Adhesion promoter for gold substrates in microelectronic applications.1 Forms stable bonds to silica and basic alumina suitable for catalyst immobilization.2 Forms luminescent gels on hydrolysis with (EtO)4Si and Eu(NO3)3.3 Used to immobilize an iridium catalyst for the enantioselective hydrogenation of aryl ketones.4 Used in the preparation of solid-phase Pd catalyst for Suzuki-Miyaura cross-coupling.5 Reference 1. Helbert, J. U.S. Patent 4,497,890, 1985. 2. Merchle, C. H. et al. Chem. Mater. 2001, 13, 3617. 3. Corriu, R. et al. J. Chem. Soc., Chem. Commun. 2001, 1116. 4. Liu, G. et al. Adv. Synth. Catal. 2008, 350, 1464. 5. Zhang, X. et al. Synthesis, 2011, 2975. Safety
Packaging Under Nitrogen 2-(Diphenylphosphino
)ethyltriethoxysilan
e; 2-(triethoxysilyethy
l)diphenylphosphine
Phosphine functional trialkoxy silane
Immobilizing ligand for precious metals
Adhesion promoter for gold substrates in microelectronic applications
Forms stable bonds to silica and basic alumina suitable for catalyst immobilization
Forms luminescent gels on hydrolysis with (EtO)4Si and Eu(NO3)3
Used to immobilize an iridium catalyst for the enantioselective hydrogenation of aryl ketones
Used in the preparation of solid-phase Pd catalyst for Suzuki-Miyaura cross-coupling reaction between organic boron compounds and organic halides
Additional Properties
Hydrolytic Sensitivity 7: reacts slowly with moisture/water
Application
Adhesion promoter for gold substrates in microelectronic applications.1 Forms stable bonds to silica and basic alumina suitable for catalyst immobilization.2 Forms luminescent gels on hydrolysis with (EtO)4Si and Eu(NO3)3.3 Used to immobilize an iridium catalyst for the enantioselective hydrogenation of aryl ketones.4 Used in the preparation of solid-phase Pd catalyst for Suzuki-Miyaura cross-coupling.5
Reference
1. Helbert, J. U.S. Patent 4,497,890, 1985. 2. Merchle, C. H. et al. Chem. Mater. 2001, 13, 3617. 3. Corriu, R. et al. J. Chem. Soc., Chem. Commun. 2001, 1116. 4. Liu, G. et al. Adv. Synth. Catal. 2008, 350, 1464. 5. Zhang, X. et al. Synthesis, 2011, 2975.
Safety
Packaging Under Nitrogen
2-(Diphenylphosphino)ethyltriethoxysilane; 2-(triethoxysilyethyl)diphenylphosphine
Phosphine functional trialkoxy silane
Immobilizing ligand for precious metals
Adhesion promoter for gold substrates in microelectronic applications
Forms stable bonds to silica and basic alumina suitable for catalyst immobilization
Forms luminescent gels on hydrolysis with (EtO)4Si and Eu(NO3)3
Used to immobilize an iridium catalyst for the enantioselective hydrogenation of aryl ketones
Used in the preparation of solid-phase Pd catalyst for Suzuki-Miyaura cross-coupling reaction between organic boron compounds and organic halides
