Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Anna Chiara Sale"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 1692-1705 (2014)
A series of 11 new pentacene derivatives has been synthesized, with unsymmetrical substitution based on a trialkylsilylethynyl group at the 6-position and various aryl groups appended to the 13-position. The electronic and physical properties of the
Externí odkaz:
https://doaj.org/article/cc0b2aecbc764e0e94d7f13504ba1932
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
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 1692-1705 (2014)
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry
A series of 11 new pentacene derivatives has been synthesized, with unsymmetrical substitution based on a trialkylsilylethynyl group at the 6-position and various aryl groups appended to the 13-position. The electronic and physical properties of the
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
Autor:
Frank Hampel, Milan Kivala, Ute Meinhardt, Andreas Kunzmann, Tobias A. Schaub, Dirk M. Guldi, Rubén D. Costa, Anna Chiara Sale, Pavlo O. Dral, Fabian Lodermeyer
Publikováno v:
ResearcherID
A series of dimethylmethylene-bridged N-heterotriangulenes decorated with one, two, and three electron-withdrawing 4-pyridyls were synthesized. Their photophysical and electrochemical characteristics were examined and their successful application in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61cda2b23b88e3426fd7fa408f5320d6
https://opus4.kobv.de/opus4-fau/files/9176/Meinhardt_N-heterotriangulene.pdf
https://opus4.kobv.de/opus4-fau/files/9176/Meinhardt_N-heterotriangulene.pdf
Autor:
Tayebeh Ameri, Matthias Adam, Hong Zhang, Jie Min, Yi Hou, Erdmann Spiecker, Anna Chiara Sale, J. Darío Perea, Stefanie Fladischer, Christoph J. Brabec, Nicola Gasparini, Wei Chen, Rik R. Tykwinski, Lili Ke
Publikováno v:
Advanced Energy Materials. 6:1502355
An attractive method to broaden the absorption bandwidth of polymer/fullerene-based bulk heterojunction (BHJ) solar cells is to blend near infrared (near-IR) sensitizers into the host system. Axial substitution of silicon phthalocyanines (Pcs) opens