Designed non-symmetrical 4,7-pi-extended-2,1,3-benzothiadiazole derivatives: Synthesis guided by DFT predictions-Reference-Cited by-同舟云学术

Designed non-symmetrical 4,7-pi-extended-2,1,3-benzothiadiazole derivatives: Synthesis guided by DFT predictions

Published:2013-10-09 Issue:4 Volume:27 Page:303-309
ISSN:0894-3230
Container-title:Journal of Physical Organic Chemistry
language:en
Short-container-title:J. Phys. Org. Chem.

Author:

Lopes Thiago O.¹,da Silva Filho Demétrio A.²,Lapis Alexandre A. M.³,de Oliveira Heibbe C. B.¹,Neto Brenno A. D.¹

Affiliation:

1. Laboratory of Medicinal and Technological Chemistry and Laboratory of Complex Systems, Chemistry Institute; University of Brasilia (IQ-UnB); Brasilia Federal District Brazil

2. Institute of Physics; University of Brasília; C.P. 04455, DF, CEP 70919-970 Brazil

3. Department of Chemistry; Federal University of Fronteira do Sul, UFFS; 89813-140 Chapecó Santa Catarina Brazil

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/poc.3234/fullpdf

Reference41 articles.

1. 2,1,3-Benzothiadiazole and Derivatives: Synthesis, Properties, Reactions, and Applications in Light Technology of Small Molecules

2. Benzothiadiazoles as DNA intercalators: Docking and simulation

3. The singlet–triplet energy gap in organic and Pt-containing phenylene ethynylene polymers and monomers

4. Synthetic Principles Directing Charge Transport in Low-Band-Gap Dithienosilole–Benzothiadiazole Copolymers

5. Solution-Processed Organic Solar Cells with Power Conversion Efficiencies of 2.5% using Benzothiadiazole/Imide-Based Acceptors

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