2013
Metallosilicates prepared by non-hydrolytic condensation reactions
ŠKODA, David; Aleš STÝSKALÍK; Zdeněk MORAVEC; Jiří PINKAS; Craig BARNES et al.Základní údaje
Originální název
Metallosilicates prepared by non-hydrolytic condensation reactions
Autoři
Vydání
The 246th ACS National Meeting, Indianapolis, Indiana, USA, 2013
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
10402 Inorganic and nuclear chemistry
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14740/13:00069406
Organizační jednotka
Středoevropský technologický institut
UT WoS
Klíčová slova anglicky
non-hydrolytic; inorganic-organic; metallosilicates
Změněno: 11. 10. 2013 16:53, prof. RNDr. Jiří Pinkas, Ph.D.
Anotace
V originále
Non-hydrolytic sol-gel reactions are efficient alternatives to classical aqueous techniques for synthesis of multimetallic oxides and inorganic-organic hybrid materials. We developed non-hydrolytic sol-gel routes to several groups of metallosilicate hybrid inorganic-organic materials based on polycondensation reactions. Titanosilicate xerogels were prepared by reactions between Ti(NEt2)4 or Ti(OR)4, R = OiPr, OtBu and Si(OAc)4. These non-hydrolytic polycondensation reactions led to the formation of Si-O-Ti bonds and to release of acetic acid ester and diethylacetamide as byproducts, respectively. Then the catalytic activity of xerogels in epoxidation of cyclohexene was studied. Alumosilicates were prepared by reactions between Al(NMe2)3 or Al(OiPr)3 and acetoxysilanes R4-nSi(OAc)n, n = 1-4 and R = Me, Ph, H, OtBu. In this case these non-hydrolytic condensation reactions proceeded with the formation of Si-O-Al networks and dimethylacetamide or acetic acid ester and as byproducts as well. As a further step, bridged bis(triacetoxysilyl)alkanes (AcO)3Si(CH2)xSi(OAc)3 , x = 1, 2, 3, 6 were used for the synthesis. Using alkylacetoxysilanes as silicon precursors we can modify some physico-chemical properties (hydrophobicity, porosity) of the resulting xerogels. We have examined also the surface modification of xerogels at the residual organic groups and established their acidic properties. The resulting xerogels and volatile byproducts were characterized by liquid and solid-state NMR, IR, GC-MS, surface area analysis, TGA, and XRD.
Návaznosti
| ED1.1.00/02.0068, projekt VaV |
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| LH11028, projekt VaV |
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