Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Adrian H. Murray"'
Autor:
Martin Drøhse Kilde, Adrian H. Murray, Cecilie Lindholm Andersen, Freja Eilsø Storm, Katrin Schmidt, Anders Kadziola, Kurt V. Mikkelsen, Frank Hampel, Ole Hammerich, Rik R. Tykwinski, Mogens Brøndsted Nielsen
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
6,6,12-graphyne is an intriguing synthetic allotrope of carbon that is predicted to have unique electronic properties but has not been successfully synthesized. Here, the authors prepare a series of radiaannulene oligomers that can be regarded as lar
Externí odkaz:
https://doaj.org/article/692d0972c3a646db833e134adb200408
Autor:
Adrian H. Murray, Robert McDonald, Rik R. Tykwinski, Matthias Adam, Dan Lehnherr, Frank Hampel
Publikováno v:
Canadian Journal of Chemistry. 95:303-314
Pentacenes bearing electron-donating and (or) -withdrawing groups, namely methoxy-, dialkylamino-, and nitroaryl moieties, are synthesized to afford polarized pentacenes. The optical, electrochemical, and chemical properties of these derivatives are
Autor:
Frank Hampel, Martin Drøhse Kilde, Rik R. Tykwinski, Freja Eilsø Storm, Adrian H. Murray, Katrin Schmidt, Cecilie Lindholm Andersen, Kurt V. Mikkelsen, Anders Kadziola, Mogens Brøndsted Nielsen, Ole Hammerich
Publikováno v:
Kilde, M D, Murray, A H, Andersen, C L, Storm, F E, Schmidt, K, Kadziola, A, Mikkelsen, K V, Hampel, F, Hammerich, O, Tykwinski, R R & Nielsen, M B 2019, ' Synthesis of radiaannulene oligomers to model the elusive carbon allotrope 6,6,12-graphyne ', Nature Communications, vol. 10, 3714 . https://doi.org/10.1038/s41467-019-11700-0
Nature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
Nature Communications
Nature Communications, Vol 10, Iss 1, Pp 1-9 (2019)
Nature Communications
Graphyne allotropes of carbon are fascinating materials, and their electronic properties are predicted to rival those of the “wonder material” graphene. One allotrope of graphyne, having rectangular symmetry rather than hexagonal, stands out as p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d8a42d338748d3ad92a60720a04f75f
https://curis.ku.dk/ws/files/231974717/s41467_019_11700_0.pdf
https://curis.ku.dk/ws/files/231974717/s41467_019_11700_0.pdf
Autor:
Lidia De Luca, Rik R. Tykwinski, Adrian H. Murray, Frank Hampel, Dominik Prenzel, Anna Chiara Sale
Publikováno v:
European Journal of Organic Chemistry. 2016:2274-2283
Diels–Alder cycloaddition reactions of 1,3,5-hexatriynes with tetraphenylcyclopentadienone have been performed, and mainly gave 1,2-diethynyl-3,4,5,6-tetraphenylbenzene derivatives as products. The Diels–Alder reactions were optimized under conve
Autor:
Manuel A. S. Aquino, Adrian H. Murray, Luc J. Boudreau, Katherine N. Robertson, T. Stanley Cameron, Terri L. Clarke
Publikováno v:
Inorganica Chimica Acta. 394:152-158
A novel synthetic methodology that involves the “disassembly” of diruthenium(II,III) tetracarboxylates using the modestly π-acidic bidentate 2,2′-bipyridine and 1,10-phenanthroline ligands and their substituted derivatives as disassembling age
ChemInform Abstract: Diels-Alder Cycloaddition of Tetraphenylcyclopentadienone and 1,3,5-Hexatriynes
Autor:
Adrian H. Murray, Rik R. Tykwinski, Dominik Prenzel, Frank Hampel, Anna Chiara Sale, Lidia De Luca
Publikováno v:
ChemInform. 47
Diels–Alder cycloaddition reactions of 1,3,5-hexatriynes with tetraphenylcyclopentadienone have been performed, and mainly gave 1,2-diethynyl-3,4,5,6-tetraphenylbenzene derivatives as products. The Diels–Alder reactions were optimized under conve
Publikováno v:
Angewandte Chemie. 122:6326-6330
Publikováno v:
Chemistry - A European Journal. 15:12580-12584
Autor:
Brian J. MacLean, Zhang Yue, T. Stanley Cameron, Adrian H. Murray, Andrew I. Wallbank, Manuel A. S. Aquino, Ramesh Vadavi
Publikováno v:
Polyhedron. 27:1270-1279
Three 3-thiophenecarboxylate-containing and one 2,2′-bithiophene-5-carboxylate-containing diruthenium complexes, [Ru2(μ-O2CR)4(MeOH)2]PF6 (R = –C4H3S 1, –CH2C4H3S 2, –CH CHC4H3S 3 and –C8H5S2 4), were prepared using a facile carboxylate ex
Autor:
Frank Hampel, Rik R. Tykwinski, Sila Karaca, Robert McDonald, Nuran Elmaci, Hans Peter Lüthi, Adrian H. Murray, Mojtaba Gholami, Sharwatie Ramsaywack
The synthesis of donor- (D) and/or acceptor (A)-expanded [4]radialenes has been developed on the basis of readily available dibromoolefin (7), tetraethynylethene (10 and 20), and vinyl triflate (12) building blocks. The successful formation of D/A ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a20084af3df455bb30cbfb9081310540
http://hdl.handle.net/11147/5393
http://hdl.handle.net/11147/5393