Spectral study of interaction between allyl ethers and hydrosiloxanes
摘要:
Interaction of allyl ethers with hydrosiloxanes in the presence of metal complexes has been investigated by spectral methods (H-1 NMR, IR, and GC-MS) as well as by gas-liquid chromatography. It has been shown that the anti-Markovnikov addition predominantly occurs in the studied cases; disproportionation of siloxanes and migration of double bond in the ethers have been identified as side reactions. The tendency to enter the side reactions has decreased in the following series: (HMeSiO)(4) > HMe2Si(OSiMe2)(2)H a parts per thousand HMe2SiOSiMe3 > (HMe2Si)(2)O > (Me3SiOSiMeH)(2)O. The general scheme of disproportionation of siloxanes HMe2Si(OSiMe2) (n) H (n a parts per thousand yen 1) has been proposed. According to mass spectrometry data, the silicon-containing fragment majorly contributes to the fragmentation of hydrosilylation products. Fragmentation of the gamma,gamma-adducts is similar to that of gamma-adducts. The predominant direction of fragmentation in the products of beta,gamma-addition of HMe2Si(OSiMe2)nH (n = 1-3) to allyl ethers is determined by fragmentation of the gamma-component of the molecule. The scheme of fragmentation of the hydrosilylation products ions has been proposed.
A cosmetic containing (A) an organo(poly)siloxane shown by the following general formula (1). A cosmetic with a refreshing feeling, smooth spreadability as well as high stability and favorable cosmetic sustainability is provided.
[where, in the formula, R
1
represents a group except shown by the formula (2), selected from a C1-C20 alkyl group and a C6-C20 aryl group; n represents an integer of 0 to 3; R
2
and R
3
represent R
1
or the formula (2); and either or both of R
2
and R
3
represent formula (2),
(where, in the formula, X represents a C2-C20 alkylene group; and Y represents any one of a hydrogen atom, a C1-C20 alkyl group, a C6-C20 aryl group, a C7-C40 aralkyl group, a C1-C20 alkyloxy group, a C6-C20 aryloxy group, a C7-C40 arylalkyloxy group, and a halogen atom.)]
NOVEL LIQUID TETRACARBOXYLIC DIANHYDRIDES AND PROCESS FOR THE PREPARATION THEREOF
申请人:Kikuchi Tooru
公开号:US20110301362A1
公开(公告)日:2011-12-08
The invention relates to a tetracarboxylic dianhydride represented by the following formula (1).
[In formula (1) R
1
, R
2
, R
3
and R
4
each independently represent an alkyl group having from 1 to 5 carbon atoms, m represents a number from 1 to 30, all of the silicon atoms bonding to the norbornane rings are in an exo-configuration with respect to the norbornane rings, and all of the dicarboxylic anhydride groups bonding to the norbornane rings are in an exo-configuration with respect to the norbornane rings.]
Synthesis and properties of new dibenzoylmethanatoboron difluoride dyads connected by flexible siloxane linkers
作者:Yuriy N. Kononevich、Anastasia S. Belova、Viacheslav A. Sazhnikov、Andrey A. Safonov、Dmitry S. Ionov、Alexander D. Volodin、Alexander A. Korlyukov、Aziz M. Muzafarov
DOI:10.1016/j.tetlet.2020.152176
日期:2020.7
excimer formation) emissions are observed for the dyads in dilute dichloromethane solutions at room temperature. The excimers contribution into the total fluorescence spectrum decreases with increasing siloxane linker length. The parallel-sandwich conformation of intramolecular pre-excimers formed by two terminal DBMBF2 moieties is confirmed by DFT-based calculations.
The invention relates to a method for producing hydridosilanes, in which siloxanes containing Si—H groups are reacted in the presence of a cationic Si(II) compound as a catalyst.
Effect of catalyst structure on the reaction of α-methylstyrene with 1,1,3,3-tetramethyldisiloxane
作者:D. A. de Vekki、N. K. Skvortsov
DOI:10.1134/s107036320904015x
日期:2009.4
Reaction of α-methylstyrene with 1,1,3,3-tetramethyldisiloxane in the presence of the complexes of platinum(II), palladium(II) and rhodium(I) is explored. It is established that in the presence of platinum catalyst predominantly occurs hydrosilylation of α-methylstyrene leading to formation of β-adduct, on palladium catalysts proceeds reduction of α-methylstyrene, on rhodium catalysts both the processes