135746-72-4

Upstream product

• 617-86-7 triethylsilane 
• 1942-46-7 5-decyne 

Downstream Products

• 820-29-1 decan-5-one 

Relevant academic research and scientific papers

Recoverable platinum bis(fluoro-ponytailed) bipyridine complex as catalyst for hydrosilylation of alkynes under thermomorphic condition

The fluorous PtCl2[5,5′-bis-(n-C11F23CH2OCH2)-2,2′-bpy] complex (2) was prepared and employed as recoverable catalyst for the hydrosilylation of alkynes. Pt-catalyst 2 with F-content 0.53 was recovered under the thermomorphic method by design and the catalyst was demonstrated capable of re-usage for 8 times without loss of activity. The leaching of Pt in product mixture was monitored, with ICP-MS, to be at as low as 10?6level per cycle in the 5-decyne reactions and at 10?3level per cycle in the (HO)CMe2C[tbnd]CH reaction. The reaction-catalyst fulfills the principle of green chemistry, and with its addition nature the hydrosilylation delivers 100% atom economy. The easily prepared polyfluorinated (2,2′-bpy)Pt complex 2 is the robust and thermally stable catalyst, which doesn't require specific handling for utilization and storage in laboratory.

Regio- and stereoselective hydrosilylation of alkynes catalyzed by SiO2 supported Pd-Cu bimetallic nanoparticles

An efficient, recyclable Pd-Cu bimetallic nanoparticle catalyst has been prepared, which exhibits superior activity and selectivity toward the hydrosilylation of internal and terminal alkynes under mild reaction conditions with a low catalyst loading. Distinct enhancement in catalytic performance is observed when compared with traditional monometallic catalysts, and the composition of BMNPs is found to be crucial in both selectivity and yield. This kind of elevation in catalytic performance can be ascribed to the enrichment of active sites (Pd) on the catalyst surface and a phenomenon collectively referred to as "synergistic effects". The successful application of BMNPs as catalysts in the alkyne hydrosilylation opens up new possibilities for the excavation of the value of bimetallic nanoparticles in catalysts' development for sustainable chemistry.

Supported Palladium-Gold Alloy Catalysts for Efficient and Selective Hydrosilylation under Mild Conditions with Isolated Single Palladium Atoms in Alloy Nanoparticles as the Main Active Site

Supported Pd-Au alloy catalysts were developed for the highly efficient and selective hydrosilylation of α,β-unsaturated ketones and alkynes. The Pd/Au atomic ratio of the Pd-Au alloy and the supporting material affected the catalytic activity, and supported Pd-Au alloy nanoparticles with a low Pd/Au atomic ratio functioned as highly active heterogeneous catalysts under mild reaction conditions. Structural characterization of supported Pd-Au alloy catalysts by X-ray diffraction, X-ray absorption spectroscopy (XAS), and transmission electron microscopy revealed the formation of random Pd-Au alloy nanoparticles with a uniform size of around 3 nm on the support. Furthermore, XAS and X-ray photoelectron spectroscopy elucidated the charge transfer from Pd to Au and the formation of isolated single Pd atoms in random Pd-Au alloys with a low Pd/Au ratio, which enabled efficient hydrosilylation of a variety of substrates under mild reaction conditions.

Rhodium nanoflowers stabilized by a nitrogen-rich PEG-tagged substrate as recyclable catalyst for the stereoselective hydrosilylation of internal alkynes

Morphology and size controllable rhodium nanoparticles stabilized by a nitrogen-rich polyoxyethylenated derivative have been prepared by reduction of RhCl 3 with NaBH4 in water at room temperature and fully characterized. The flower-like Rh NPs are effective and recyclable catalysts for the stereoselective hydrosilylation of challenging internal alkynes and diynes, affording the (E)-vinylsilanes in quantitative yields for a wide range of substrates. The insolubility of the nanocatalyst in diethyl ether allows its easy separation and recycling.

Hydrosilylation of internal alkynes catalyzed by tris- Imidazolium salt-Stabilized palladium nanoparticles

Palladium nanoparticles stabilized with tris-imidazolium tetrafluoroborates catalyze the stereoselective hydrosilylation of internal alkynes in a dry inert atmosphere to give (E)-vinylsilanes in excellent yields. In the presence of controlled amounts of water a transfer hydrogenation reaction takes place with the formation of (Z)-alkenes or the corresponding alkanes.

Platinum-catalyzed hydrosilylations of internal alkynes: Harnessing substituent effects to achieve high regioselectivity

Rule of thumb: The high yielding title reaction is described with a focus on understanding the factors that govern the regioselectivity of the process (see scheme). Electronic, steric, and functional group properties all influence the selectivity, an understanding of which allows the selective formation of trisubstituted vinylsilanes, which are synthetically useful compounds for accessing stereodefined alkenes. Copyright

Hydrosilylation of alkynes catalysed by platinum on titania

The heterogeneous hydrosilylation of alkynes catalysed by platinum on titania is reported. A variety of hydrosilanes react with both terminal and internal alkynes to furnish the corresponding vinyl silanes in high yields and short reaction times as well as in a regio- and stereoselective manner. The catalyst can be easily recovered and reused in several consecutive cycles.