THE HYDROSILATION REACTION OF LADDERLIKE POLYALLYLSILSESQUIOXANE(ALLYL-T)AND POLYHYDROSILSESQUIOXANE(H-T)*

Your Location：

Home >

Browse articles >

THE HYDROSILATION REACTION OF LADDERLIKE POLYALLYLSILSESQUIOXANE(ALLYL-T)AND POLYHYDROSILSESQUIOXANE(H-T)*

Papers | Updated：2021-06-21

- THE HYDROSILATION REACTION OF LADDERLIKE POLYALLYLSILSESQUIOXANE(ALLYL-T)AND POLYHYDROSILSESQUIOXANE(H-T)*
- Vol. 20, Issue 1, Pages: 31-38(2002)
- Affiliations：
- Author bio：
- Funds：
- DOI：
  CLC：
- Published：20 February 2002
- Accepted：
Scan QR Code
THE HYDROSILATION REACTION OF LADDERLIKE POLYALLYLSILSESQUIOXANE(ALLYL-T)AND POLYHYDROSILSESQUIOXANE(H-T)*[J]. 2002, 20(1): 31-38.
DOI：

THE HYDROSILATION REACTION OF LADDERLIKE POLYALLYLSILSESQUIOXANE(ALLYL-T)AND POLYHYDROSILSESQUIOXANE(H-T)*[J]. 2002, 20(1): 31-38. DOI：

摘要

The one plus one (1 + 1) mode of hydrosilation reaction of ladderlike cis-isotatic polyallylsilsesquioxane (Allyl-T)and polyhydrosilsesquioxane (H-T) using dicyclopentadienylplatinumdichloride (Cp2PtCl2) as the catalyst leads to theformation of a new polyorganosiloxane (POS). The presence of nanoscale tubular structure in the product POS waspreliminarily proved by IR

1H-NMR

differential scanning calorimetry (DSC)

X-ray diffraction (XRD)

gel permeation chromatography (GPC)

atomic force microscopy(AFM)and molecular simulation.

Abstract

1H-NMR

differential scanning calorimetry (DSC)

X-ray diffraction (XRD)

gel permeation chromatography (GPC)

atomic force microscopy(AFM)and molecular simulation.

关键词

Keywords

references

Views

Downloads

CSCD

Alert me when the article has been cited

Submit

Tools

Publicity Resources

Molecularly Engineered Polyimide Films with Switchable Cavitation for Bidirectional Passive Thermal Regulation

End-group and Side-chain Dual-engineering of Selenium-fused Acceptors for 20.08% Efficiency Polymer Solar Cells with Low Energy Loss

Sequence-encoded Conformation Pathways in Viscoelastic Microphase Separation of Multiblock Copolymers

Special Topic: Chirality in Polymers

Highly Regio- and trans-Selective Ring-opening Metathesis Polymerization of Chiral Aza-norbornene with a Simple Phenylimido-Tungsten Catalyst

Related Author

No data

Related Institution

No data

⁰