The efficient synthesis of novel unsymmetrical dithienosiloles, 7,7-dimethyl-4,6-di(trimethylsilyl)-dithieno[2,3-b:4',3'-d]silole (1) and 7,7-dimethyl-2,4,6-tri(trimethylsilyl)-dithieno[2,3-b:4',3'-d]silole (2) has been developed by intramolecular silole formation with 4,4'-dibromo-2,2',5,5'-tetrakis(trimethylsilyl)-[3,3']bithienyl (3) as the starting material in the presence of t-BuLi. Upon treatment with N-bromosuccinimide (NBS) under controlled conditions, dithieno[2,3-b:4',3'-d]silole was selectively brominated to produce mono-, di-, and tribrominated dithieno[2,3-b:4',3'-d]siloles in good yields. The crystal structures of the title compounds are described.
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http://dx.doi.org/10.1021/jo202111z | DOI Listing |
RSC Adv
January 2018
Key Laboratory of Jiangxi Province for Persistent Pollutants Control and Resources Recycle, Nanchang Hangkong University Nanchang 330063 PR China
We report here the synthesis and characterizations of a novel series of acceptor copolymers with a broad absorption band. The acceptor polymers were synthesized as a copolymer of perylenediimide (PDI) and naphthalene imide (NDI) along with dithieno[3,2-:2',3'-]silole (DTS) and -alkyl dithieno[3,2-:2',3-]pyrroles (DTP). When the dipole moment and polarizability of the acceptor polymer are compared, it is observed that when the dipole moment decreases, the polarizability becomes larger.
View Article and Find Full Text PDFNanoscale
September 2013
Department of Electrical and Computer Engineering, Ajou University, Woncheon-dong, Yeongtong-gu, Suwon 443-749, Republic of Korea.
We present hybrid solar cells with high efficiency utilizing a novel donor-acceptor combination of poly[2,6-(4,4'-bis-(2-ethylhexyl)dithieno[3,2-b:2',3'-d]silole)-alt-4,7(2,1,3-benzothiadiazole)] (PSBTBT) and a PbSxSe1-x inorganic semiconductor. Several nanocomposite parameters are evaluated in order to improve the hybrid device efficiency, including donor-acceptor materials, surface modification of the inorganic semiconductor, and mixture of quantum dots (QDs) and nanorods (NRs) in the polymer matrix. A high power conversion efficiency (PCE) of ~3.
View Article and Find Full Text PDFMacromol Rapid Commun
September 2012
National Center for Nanoscience and Technology, Beijing, China.
A novel electron-accepting unit cyclopenta[2,1-b:3,4-c']dithiophene-4-one (CPDTO-c'), which is an isomer of CPDTO-b' was developed. CPDTO-c' can be incorporated into the D-A backbone through 5, 7 positions. The 2 position of CPDTO-c' can be easily functionalized with an electron-withdrawing chain.
View Article and Find Full Text PDFJ Org Chem
March 2012
Key Lab for Special Functional Materials of Ministry of Education, Henan University, Kaifeng, 475004, China.
The efficient synthesis of novel unsymmetrical dithienosiloles, 7,7-dimethyl-4,6-di(trimethylsilyl)-dithieno[2,3-b:4',3'-d]silole (1) and 7,7-dimethyl-2,4,6-tri(trimethylsilyl)-dithieno[2,3-b:4',3'-d]silole (2) has been developed by intramolecular silole formation with 4,4'-dibromo-2,2',5,5'-tetrakis(trimethylsilyl)-[3,3']bithienyl (3) as the starting material in the presence of t-BuLi. Upon treatment with N-bromosuccinimide (NBS) under controlled conditions, dithieno[2,3-b:4',3'-d]silole was selectively brominated to produce mono-, di-, and tribrominated dithieno[2,3-b:4',3'-d]siloles in good yields. The crystal structures of the title compounds are described.
View Article and Find Full Text PDFJ Nanosci Nanotechnol
May 2011
Advanced Materials Division, Korea Research Institute of Chemical Technology, Sinseongno 19, Yuseong, Daejeon 305-600, Korea.
A series of dithienosilole-based copolymers, poly [(4,4'-bis(2-hexyl)dithieno[3,2-b:2',3'-d]silole)-2,6-diyl-alt-(2,1,3-benzothiadiazole)-5,5'-diyl] (P1), poly[(4,4'-bis(2-hexyl)dithieno[3,2-b:2',3'-d]silole)-2,6-diyl-alt-(2,2'-bithiazole)-5,5'-diyl] (P2), poly[(4,4'-bis(2-hexyl)dithieno[3,2-b:2',3'-d]silole)-2, 6-diyl-alt-(10 -methyl-phenothiazine)-3,7-diyl](P3), poly[(4,4'-bis(2-hexyl)dithieno[3,2-b:2',3'-d]silole)-2,6-diyl-alt-(4,7-bis(2-thienyl)-9,10-anthracene)-5,5'-diyl] (P4) were synthesized by the Pd-catalyzed Stille polymerization method. Electron-deficient benzothiadiazole and bithiazole units and electron-rich phenothiazine and anthracene moieties were incorporated into the polymer backbone to obtain the broad absorption spectrum and to improve the hole-transporting characteristics, respectively. The polymer solar cell (PSC) was fabricated with a layered structure of ITO/PEDOT:PSS/polymer:C71-PCBM (1:3)/LiF/Al.
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