Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jonas Friebel"'
Autor:
Jonas Friebel, Christopher P. Ender, Manfred Wagner, Jiaxu Liang, Tanja Weil, Anna Ermakova, Todd Zapata
Publikováno v:
Diamond and Related Materials
We report mechanistic insights of the bottom-up synthesis of nanodiamonds (NDs) from adamantane derivatives as molecular precursors. Thermal cracking of tetracosane below the decomposition temperature of adamantane, 1-adamantylamine or 2-azaadamantan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53f1bd45320d95a165b5b8795b639a39
https://doi.org/10.5281/zenodo.5827574
https://doi.org/10.5281/zenodo.5827574
Autor:
Markus Mezger, Christopher P. Ender, Tanja Weil, Jonas Friebel, Jasper J. Michels, Kenneth B. Wagener, Manfred Wagner
Publikováno v:
Macromolecules
[Image: see text] Fully saturated, aliphatic polymers containing adamantane moieties evenly distributed along the polymer backbone are of great interest due to their exceptional thermal stability, yet more synthetic strategies toward these polymers w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e40e108ad10fefe01bf1bb181c5a4753
https://doi.org/10.1021/acs.macromol.9b00294
https://doi.org/10.1021/acs.macromol.9b00294
Publikováno v:
European Journal of Organic Chemistry. 2017:2312-2316
The preparation of a chiral derivative of [B(C6F5)4]– in which the fluorine atom in the para position of each of the C6F5 groups is replaced by a 1,1′-binaphthalen-2-yl group is described. The new counteranion was isolated as its lithium, sodium,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33cf7ee619d02bf4268c00228975d4c7
https://doi.org/10.1002/ejoc.201700239
https://doi.org/10.1002/ejoc.201700239
Publikováno v:
European Journal of Organic Chemistry. 2014:2077-2083
An unprecedented transfer silylation of alcohols catalyzed by the strong Lewis acid B(C6F5)3 is described. Gaseous Me3SiH is released in situ by B(C6F5)3-catalyzed decomposition of 3-trimethylsilylcyclohexa-1,4-diene and subsequently reacts with an a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dd1b02b56c0fc7f081814f2f7b8460b
https://doi.org/10.1002/ejoc.201301840
https://doi.org/10.1002/ejoc.201301840
Publikováno v:
ChemInform. 46
Yields of these reactions are determined by NMR-analysis using mesitylene as internal standard.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f320769fa1be27091cc3b96a7954733
https://doi.org/10.1002/chin.201505064
https://doi.org/10.1002/chin.201505064