PINKAS, Jiří, Martin KEJÍK, Zdeněk MORAVEC and Craig E. BARNES. Porous aromatic organosilicates by non-hydrolytic sol-gel routes. In 248th American Chemical Society National Meeting & Exposition, San Francisco, California, USA. 2014. ISSN 0009-2347.
Other formats:   BibTeX LaTeX RIS
Basic information
Original name Porous aromatic organosilicates by non-hydrolytic sol-gel routes
Authors PINKAS, Jiří (203 Czech Republic, guarantor, belonging to the institution), Martin KEJÍK (203 Czech Republic, belonging to the institution), Zdeněk MORAVEC (203 Czech Republic, belonging to the institution) and Craig E. BARNES (840 United States of America).
Edition 248th American Chemical Society National Meeting & Exposition, San Francisco, California, USA, 2014.
Other information
Original language English
Type of outcome Conference abstract
Field of Study 10402 Inorganic and nuclear chemistry
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 0.269
RIV identification code RIV/00216224:14740/14:00077574
Organization unit Central European Institute of Technology
ISSN 0009-2347
Keywords in English organosilicates; sol-gel; nonhydrolytic
Tags International impact, Reviewed
Changed by Changed by: Mgr. Zdeněk Moravec, Ph.D., učo 42228. Changed: 20/5/2015 20:26.
Abstract
A series of porous hybrid organosilicate materials was prepared by non-hydrolytic sol-gel reactions of silicon(IV) acetate with rigid aromatic building blocks bearing phenolic hydroxyl functional groups with focus on readily available compounds that were previously utilized for synthesis of materials such as the porous aromatic frameworks (PAFs) and covalent organic frameworks (COFs). Upon elimination of acetic acid as a byproduct, an organosilicate gel is formed in polar ether solvents. Drying in vacuo offers powdered xerogels. The synthesis procedure was optimized in order to reach the maximum degree of condensation as monitored by gravimetry. All of the prepared materials were found to be amorphous, they do however possess large specific surface areas exceeding 800 m2 g-1 and generally exhibit high thermal stability (up to 400 °C under inert gas). The relationship between the size and symmetry of employed organic linker and the surface properties as well as the degree of condensation and thermal behavior were studied. Additionally the chemical properties and stability of these materials were studied in reactions with a variety of organic, inorganic and organometallic reagents (water, alcohols, phenol, chlorosilanes, AlR3, AlCl3, n-BuLi, ...). A method for post-synthetic replacement of the highly coordinating residual acetate functional groups was also found. Products were characterized by elemental analyses, solid-state 13C, 27Al, and 29Si NMR, IR spectroscopy, surface area analysis, thermal analysis TG/DSC, and XRD measurements.
Links
ED1.1.00/02.0068, research and development projectName: CEITEC - central european institute of technology
EE2.3.30.0037, research and development projectName: Zaměstnáním nejlepších mladých vědců k rozvoji mezinárodní spolupráce
LH11028, research and development projectName: Nehydrolytické sol-gelové reakce pro přípravu křemičitanů a fosforečnanů s řízenou porozitou a funkčními skupinami na povrchu (Acronym: NHSGKNOX)
Investor: Ministry of Education, Youth and Sports of the CR
PrintDisplayed: 17/5/2024 03:00