Issue 4, 2001

Introduction of per(fluoroorganosilyl) peripheries into carbosilane dendrimers and related core-functionalized monodendrons gives rise to anomalous hydrodynamic and viscosimetric behavior

Abstract

Platinum-catalyzed hydrosilylation of allyl-terminated carbosilane monodendrons using the silanes SiHMe2[(CH2)nRf] (1a, n = 2, Rf = n-C6F13; 1b, n = 3, Rf = −C6F5) yields fluorous, liquid analogues to [G-3], BrC6H4(CH2)3SiMe[(CH2 )3SiMe[(CH2)3SiMe[(CH2) 3SiMe2(CH2)nRf] 2]2]2 (7a, n = 2, Rf = n-C6F13- ; 7b, n = 3, Rf = −C6F5), intrinsic viscosities [η] for which are unusually low, resulting in calculated hydrodynamic radii/Å (ca. 6.3, [G-1]; 8.3, [G-2]; 11.5, [G-3]) that imply unusually compact structures.

Article information

Article type
Communication
Submitted
03 Nov 2000
Accepted
03 Jan 2001
First published
30 Jan 2001

Chem. Commun., 2001, 313-314

Introduction of per(fluoroorganosilyl) peripheries into carbosilane dendrimers and related core-functionalized monodendrons gives rise to anomalous hydrodynamic and viscosimetric behavior

M. A. Casado, J. Roovers and S. R. Stobart, Chem. Commun., 2001, 313 DOI: 10.1039/B008992N

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