Zobrazeno 1 - 10
of 51
pro vyhledávání: '"S, Thimon"'
Autor:
Jan Freudenberg, Andrea C. Uptmoor, Frank Rominger, Uwe H. F. Bunz, S. Thimon Schwäbel, Fabian Paulus, Felix Hinkel
Publikováno v:
Angewandte Chemie. 127:14885-14888
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f32fbad97822eca468be217f42b2d6d5
https://doi.org/10.1002/ange.201506905
https://doi.org/10.1002/ange.201506905
Publikováno v:
The Journal of Organic Chemistry. 80:9126-9131
We have prepared a thermally activated delayed fluorescence (TADF) capable molecular system carrying halogen substituents at the carbazole units. The attachment of the halogen atoms considerably decreases the half-life of the delayed fluorescence. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1dcf9c4e0f755053797d79317d0e4324
https://doi.org/10.1021/acs.joc.5b01496
https://doi.org/10.1021/acs.joc.5b01496
Autor:
Uwe H. F. Bunz, Manuel Hamburger, Martin Petzoldt, Uli Lemmer, Kerstin Broedner, Carsten Eschenbaum, S. Thimon Schwaebel
Publikováno v:
Chemistry - A European Journal. 21:14297-14300
Combining the molecular wire effect with a biphasic sensing approach (analyte in water, sensor-dye in 2-methyltetrahydrofuran) and a microfluidic flow setup leads to the construction of a mercury-sensitive module. We so instantaneously detect Hg(2+)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82ca6a5b05dfef6b868cd401406b5db7
https://doi.org/10.1002/chem.201502736
https://doi.org/10.1002/chem.201502736
Publikováno v:
The Journal of Organic Chemistry. 80:5159-5166
Eight acceptor-substituted distyrylbenzene (DSB) derivatives were obtained by postfunctionalization of dialdehyde precursor 1 using Knoevenagel condensation. Solubility in a water/THF 9:1 mixture was achieved through the addition of branched oligoeth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8c5d6bf0db20a7a6635e05a218f5e61
https://doi.org/10.1021/acs.joc.5b00577
https://doi.org/10.1021/acs.joc.5b00577
Publikováno v:
Macromolecules. 47:7014-7020
We have prepared a series of water-soluble, pyridine-containing poly(aryleneethynylene)s (PAEs), consisting of alternating units of substituted ethynylpyridines and ethynylbenzenes. Water solubility is achieved by branched oligoethylene glycol (swall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0f77ca1c542c9a68ae58b75a2530362
https://doi.org/10.1021/ma5018296
https://doi.org/10.1021/ma5018296
Publikováno v:
Macromolecules. 47:2569-2573
We herein describe synthesis and property evaluation of two aldehyde-appended nonconjugated distyrylbenzene polymers as amine sensing platforms and compare their performance to that of their monomers. The monomers and polymers were dissolved in organ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16322cb19e4bc1b6877dd1c8f72450f2
https://doi.org/10.1021/ma500486u
https://doi.org/10.1021/ma500486u
Publikováno v:
Médecine et Santé Tropicales. 24:323-325
Les phaeohyphomycoses sont des mycoses profondes dues a des champignons pigmentes du groupe des dematies. Ces infections apparaissent particulierement en milieu tropical et souvent dans un contexte d’immunodepression. Nous rapportons la premiere ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebc3c64d030235b28914fc9a48a116cf
https://doi.org/10.1684/mst.2014.0342
https://doi.org/10.1684/mst.2014.0342
Autor:
Frank Rominger, S. Thimon Schwäbel, Felix Hinkel, Jan Freudenberg, Andrea C. Uptmoor, Uwe H. F. Bunz, Fabian Paulus
Publikováno v:
Angewandte Chemie (International ed. in English). 54(49)
Two different conjugated microporous polymers (CMPs) based on tetrakis(4-ethynylphenyl)stannane as the repeating unit were synthesized and their BET surfaces and thermal properties were investigated. The first direct method to elucidate the molecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66b680e533dc2e8d2cf572b5486d16ad
https://pubmed.ncbi.nlm.nih.gov/26474306
https://pubmed.ncbi.nlm.nih.gov/26474306
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
La Revue de medecine interne. 30(11)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2727b02ce5c00d5c12e2353dcbdcf823
https://pubmed.ncbi.nlm.nih.gov/19095332
https://pubmed.ncbi.nlm.nih.gov/19095332