Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Forrest S. Etheridge"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 1925-1938 (2016)
Homoleptic zinc(II) complexes of di(phenylacetylene)azadipyrromethene (e.g., Zn(WS3)2) are potential non-fullerene electron acceptors for organic photovoltaics. To tune their properties, fluorination of Zn(WS3)2 at various positions was investigated.
Externí odkaz:
https://doaj.org/article/a19d844102d74732b7a7f982c0e59182
Autor:
Danielle Chamberlin, Nisa Zaheer, Alexis Miranda, Richard Schaller, Forrest S. Etheridge, Dmitri Talapin, Yu Kambe
Publikováno v:
SID Symposium Digest of Technical Papers. 53:405-408
Autor:
Dmitri V. Talapin, Yu Kambe, Forrest S. Etheridge, Danielle R. Chamberlin, Richard D. Schaller
Publikováno v:
SID Symposium Digest of Technical Papers. 52:941-944
Autor:
Kenneth D. Singer, Kyle C. Peters, Sandra Pejić, Donald E. Schuele, Forrest S. Etheridge, Lei Gao, Anuj Saini, Geneviève Sauvé, Stuart D. Hellring
Publikováno v:
Organic Electronics. 53:332-338
An aqueous-based deposition of a semiconducting polymer using an electrolysis-based technique is demonstrated here. Regioregular poly (3-alkylthiophene) with a carboxylic acid group in the side chain was synthesized and dispersed in water with trieth
Autor:
Chunlai Wang, Forrest S. Etheridge, Sandra Pejić, Geneviève Sauvé, Roshan Fernando, Anna M. Thomsen
Publikováno v:
Journal of Materials Chemistry C. 6:3990-3998
Structure–property studies were performed on a series of four fluorinated zinc azadipyrromethene derivatives. This series is based on bis[2,8-diphenylethynyl-1,3,7,9-tetraphenylazadipyrromethene]zinc(II) (Zn(WS3)2), with fluorine atoms at the para-
Publikováno v:
New Journal of Chemistry. 39:2506-2514
The effect of styryl imide substitution on optical and electrochemical properties of core-substituted naphthalenediimides was examined by synthesizing a series of naphthalenediimide molecules. 2-Ethylhexylamino and 5-(2-ethylhexyl)thiophene groups we
Publikováno v:
RSC Advances. 5:46534-46539
Selective sulfur substitution of the distal carbonyls of a core-substituted naphthalene diimide was obtained when a combination of core and imide substituents were used. The substituents appear to inhibit thionation of the proximal carbonyl by steric