Sol-Gel Polymerization of Tetraalkoxygermanium and Organotrialkoxygermanium Monomers

1996 ◽  
Vol 431 ◽  
Author(s):  
Brigitta M. Baugher ◽  
Douglas A. Loy

AbstractWhile the sol-gel polymerizations of tetraalkoxy- and organotrialkoxysilanes have been extensively studied, there have been few reports of similar investigations with the analogous tetraalkoxygermanium and organotrialkoxygermanium compounds. Germanium alkoxides have received less attention due, in part to their higher cost, but also their greater reactivity towards hydrolysis and condensation reactions. Germanium oxide materials are potentially interesting because the Ge-O-Ge linkage is labile (compared with the siloxane bond in silica gels and polysilsesquioxanes) opening up the possibility of further chemical modification of the polymeric architecture. This may permit hydrolytic reorganization of germanium oxide networks under relatively mild conditions. In this paper, we will present the results of our investigations of the solgel polymerizations of tetraethoxygermanium 1, tetraisopropoxygermanium 2, and methyltriethoxy-germanium 3 to afford network materials as both xerogels and aerogels.

2018 ◽  
Vol 47 (9) ◽  
pp. 2925-2932 ◽  
Author(s):  
J. Brendlé

The sol–gel process involving hydrolysis and condensation reactions is an attractive way to form siloxane based hybrid materials since it is a one-step method performed under mild conditions.


1994 ◽  
Vol 346 ◽  
Author(s):  
S. Prabakar ◽  
R.A. Assink ◽  
A.D. Irwin

ABSTRACTThe exchange and spinnability of several systems with the general form Si(OR)4 (where R = CH3, C2H5) in ethanol, propanol and butanol were investigated. We have followed the alkoxy group exchange, the hydrolysis and condensation reactions and the Q distributions of these systems using 29Si and 17O NMR. The observed differences in spinnability of the various sol-gel systems are attributed to the effect of the bulkiness of the alkoxy group on its reactivity.


2011 ◽  
Vol 289 (17-18) ◽  
pp. 1875-1883 ◽  
Author(s):  
Amir A. El hadad ◽  
Diogenes Carbonell ◽  
Violeta Barranco ◽  
Antonia Jiménez-Morales ◽  
Blanca Casal ◽  
...  

1999 ◽  
Vol 576 ◽  
Author(s):  
Nicola Hüsing ◽  
Ulrich Schubert

ABSTRACTMonolithic silica aerogels modified by functional organic groups were prepared by basecatalyzed sol-gel processing of Si(OR)4 / R'Si(OMe)3 mixtures (R' = organofunctional group), followed by drying of the wet gels with supercritical CO2. When the functional organic group has only weakly or no basic properties, the microstructure of the obtained aerogels is similar to that of an unmodified silica aerogel prepared under the same conditions and quite independent of the kind of functional group. The experimental findings are explained by a two-stage process in which the R'Si≡ units condense to a pre-formed gel network obtained by hydrolysis and condensation of Si(OR)4. An increasing portion of R'Si(OMe)3 has the same effects on the hydrolysis and condensation reactions as decreasing the bulk density of an unmodified silica aerogel and the same structural consequences as increasing the water / silane ratio and the catalyst concentration acting on Si(OR)4. This leads to larger primary particles and, associated with that, smaller specific surface areas. The two-stage process is not observed when R' contains a strongly basic substituent such as NH2 or NHCH2CH2NH2. The structural parameters indicate that in these cases both R'Si(OMe)3 and Si(OR)4 are involved in the built-up of the gel network. This can be explained by extensive hydrogen bonding between the amino groups and silanol groups.


2000 ◽  
Vol 628 ◽  
Author(s):  
Mark A. Clarner ◽  
Michael J. Lochhead

ABSTRACTOrganically modified silica gels and dye-doped silica gels have been patterned into micrometer-scale structures on a substrate using micro molding in capillaries (MIMIC). This approach is from a class of elastomeric stamping and molding techniques collectively known as soft lithography. Soft lithography and sol-gel processing share attractive features in that they are relatively benign processes performed at ambient conditions, which makes both techniques compatible with a wide variety of organic molecules, molecular assemblies, and biomolecules. The combination of sol-gel and soft lithography, therefore, holds enormous promise as a tool for microfabrication of materials with optical, chemical, or biological functionality that are not readily patterned with conventional methods. This paper describes our investigation of micro-patterned organic-inorganic hybrid materials containing indicator dyes for microfluidic sensor applications. Reversible colorimetric pH sensing via entrapped reagents is demonstrated in a prototype microfluidic sensor element. Patterned structures range from one to tens of micrometers in cross-section and are up to centimeters in length. Fundamental chemical processing issues associated with mold filling, cracking and sensor stability are discussed.


Author(s):  
Agustin Forchetti Casarino ◽  
Santiago Andrés Bortolato ◽  
Diana Alejandra Estenoz ◽  
Marisa Elisabet Spontón
Keyword(s):  
Sol Gel ◽  

Author(s):  
Ewelina Weidner ◽  
Adam Piasecki ◽  
Katarzyna Siwińska-Ciesielczyk ◽  
Teofil Jesionowski ◽  
Filip Ciesielczyk

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