2013
Metallosilicate and Phosphosilicate Hybrid Materials Prepared by Non-Hydrolytic Sol-Gel Reactions
PINKAS, Jiří, Aleš STÝSKALÍK, David ŠKODA, Zdeněk MORAVEC, Craig BARNES et. al.Základní údaje
Originální název
Metallosilicate and Phosphosilicate Hybrid Materials Prepared by Non-Hydrolytic Sol-Gel Reactions
Autoři
PINKAS, Jiří (203 Česká republika, garant, domácí), Aleš STÝSKALÍK (203 Česká republika, domácí), David ŠKODA (203 Česká republika, domácí), Zdeněk MORAVEC (203 Česká republika, domácí) a Craig BARNES (840 Spojené státy)
Vydání
3rd International Conference on Multifunctional, Hybrid and Nanomaterials, Sorrento, Italy, 2013
Další údaje
Jazyk
angličtina
Typ výsledku
Konferenční abstrakt
Obor
10402 Inorganic and nuclear chemistry
Stát vydavatele
Itálie
Utajení
není předmětem státního či obchodního tajemství
Kód RIV
RIV/00216224:14740/13:00069400
Organizační jednotka
Středoevropský technologický institut
Klíčová slova anglicky
Metallosilicate; Phosphosilicate; Hybrid Materials; Non-Hydrolytic; Sol-Gel
Příznaky
Mezinárodní význam
Změněno: 11. 10. 2013 17:02, prof. RNDr. Jiří Pinkas, Ph.D.
Anotace
V originále
We developed non-hydrolytic sol-gel routes to several families of metallosilicate and phosphosilicate hybrid inorganic-organic materials based on polycondensation reactions between acetoxysilanes 1RxSi(OC(O)CH3)4-x (1R = Me, Ph; n = 0-2), phosphoric and phosphonic acid trimethylsilylesters 2RP(O)(OSiMe3)2 (2R = OSiMe3, c-Hex, Ph), metal amides M(N3R2)n (M = Al, Ti; 3R = Me, Et; n = 3, 4) and metal alkoxides M(O4R)n (M = Al, Ti; 4R = i-Pr, t-Bu, SiMe3; n = 3, 4) in aprotic dry solvents. Alumosilicate xerogels were prepared by polycondensation reactions between Al(NMe2)3 or Al(Oi-Pr)3 and acetoxysilanes. These elimination reactions led to the formation of Si-O-Al networks and released dimethylacetamide or acetic acid ester and as byproducts, respectively. Titanosilicate xerogels were prepared by non-hydrolytic polycondensation reactions between Ti amides Ti(NR2)4 (R = Me, Et) or Ti alkoxides Ti(OR)4 (R = i-Pr, t-Bu, SiMe3) and acetoxysilanes. The acetamide and ester elimination reactions led to Si-O-Ti networks. Phosphosilicates were prepared by the elimination of acetic acid ester from acetoxysilanes and trimethylsilyl phosphates and phosphonates. Two-step sequential polycondensation procedure was used to prepare metallosilicophosphates. The inorganic-organic hybrid xerogels contained residual surface organic groups that were employed for the chemical modification reactions on the surface by a variety of reagents, such as alcohols, chlorosilanes, metal alkyls and chlorides. Our aim was to study the versatility of these reactions, attain stoichiometry control, and tune the properties of resulting xerogels, such as surface area and Bronsted/Lewis acidity. The prepared xerogels were characterized by solid-state 13C, 27Al, 29Si, 31P NMR, IR, surface area analysis, TGA, XANES/EXAFS, and XRD.
Návaznosti
ED1.1.00/02.0068, projekt VaV |
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LH11028, projekt VaV |
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