13083-94-8

Usage

Uses

Used in Organic Electronics Industry:
1,6-BIS(TRICHLOROSILYL)HEXANE is used as a cross-linking agent for the synthesis of polymeric blended films. These films serve as dielectrics in organic electronic-based devices, such as organic field-effect transistors (OFETs) and organic thin-film transistors (OTFTs). The cross-linking ability of 1,6-BIS(TRICHLOROSILYL)HEXANE improves the dielectric properties of the films, leading to enhanced performance and stability in these electronic devices.

InChI:InChI=1/C6H12Cl6Si2/c7-13(8,9)5-3-1-2-4-6-14(10,11)12/h1-6H2

Upstream product

• 592-42-7 1,5-Hexadien 
• 13095-00-6 E-1-trichlorosilylhex-1-ene 
• 2163-00-0 1,6-dichlorohexane 
• 10025-78-2 trichlorosilane 
• 693-02-7 hex-1-yne 

Relevant academic research and scientific papers

Process for Preparing Polysilylalkane

Polysilylalkane according to the present invention is represented by following formula. The present invention has an advantage that bis(silyl)alkanes or tri(silyl)alkanes can be manufactured in a high yield by dehydrochlorination with a small amount of catalyst by using a silane compound having a dichloro organic matter or a dichloromethyl group.COPYRIGHT KIPO 2020

Process for Preparing Polysilylalkane

According to the present invention, polysilylalkane is represented by chemical formula 3. In chemical formula 3, m is equal to n, and n is equal to zero; and R^3 is a chloromethyl group. In the case of R^4 is H, -SiMe_2Cl, -SiMe_3, -SiMeCl_2, and -SiCl_3, R^3 is equal to -SiCl_3. In the case of R^4 is H, and R^5 is equal to R^6 and R^6 is equal to Me, or R^5 is equal to Me and R^6 is equal to Et, R^3 is -SiCl_3. In the case of R^4 is H, R^5 is equal to -CH_2SiCl_3, and R^6 is Me, R^3 is equal to -SiCl_3. In the case of R^4 is H, R^5 is equal to R^6 and R^6 is equal to -CH_2SiCl_3, R^3 is equal to Et, SiMe_2Cl, -SiMeCl_2, and -SiCl_3, and m is an integer of zero to nine. The manufacturing method is capable of manufacturing bis(silyl)alkane or tri(silyl)alkane in a high yield with a small amount of a catalyst.COPYRIGHT KIPO 2016

Process for Preparing Polysilylalkane

A polysilyalkane according to the present invention is presented by a formula. Here, m=n=0, R^3 is chloro, and methyl group; when R^4 is H, -SiMe_2Cl, -SiMe_3,-SiMeCl_2, -SiCl_3, R^3=-SiCl_3; R^4 is H, R^5=R^6=Me or R^5=Me, when R6=Et, R^3-SiCl_3; R^4 is H, R^5= -CH_2SiCl_3, when R^6 is Me, R^3=-SiCl_3; R^4 is H, when R5=R6=-CH_2SiCl_3, R^3=Et, SiMe_2Cl, -SiMeCl_2, -SiCl_3, and m is integer number of 0-9.COPYRIGHT KIPO 2015

Effect of ether on regioselectivity in hydrosilylation of 1,5-hexadiene with chlorohydrosilanes catalyzed by homogeneous platinum catalysts

Hydrosilylation of 1,5-hexadiene with chlorohydrosilanes catalyzed by homogeneous platinum catalyst to produce 5-hexenylchlorosilanes was studied. The presence of ether additives was highly effective in improving the regioselectivity and the yield. The formation of a double-bond rearrangement isomer, cis-, or trans-4-hexenylchlorosilanes, during the hydrosilylation was reduced drastically, as well. Copyright Taylor & Francis Group, LLC.

PREPARATION OF A HALOSILYLATED CHAIN HYDROCARBON

A method for the preparation of a chain hydrocarbon halosilylated at its terminal carbon atom or terminal carbon atoms by subjecting a diene-type compound and a hydrogenhalosilane to a hydrosilylation reaction in the presence of a hydrosilylation catalyst and an ether compound having no aliphatic triple bond.A method of conducting a hydrosilylation reaction between a diene-type compound that has vinyl groups on both terminals and a hydrogenhalosilane in the presence of a hydrosilylation catalyst and an ether compound having no aliphatic triple bond.