Co-assembled structures possessing tunable light emission from 510-690 nm have been prepared using various compositions of two different 4,7-substituted benzothiadiazole molecules, 1 and 2. The preferential incorporation and co-localization of 1 and 2 to produce co-assemblies are possible because of structural similarities and allow for tuning of morphology and light emission.

Coordination-driven gelation of a benzothiadiazole-fused tetrathiafulvalene (TTF) is demonstrated. This is the first work reporting highly stable metallogels based on a donor-acceptor conjugate with such a simple structure for the construction of new low-bandgap materials with various functional properties and novel nanostructures.

Novel A-D-A type oligothiophenes incorporating benzothiadiazole (BTDA) and thiadiazolopyridine (TDAPy) as terminal acceptor groups have been developed for small molecule organic solar cells (SMSC). In vacuum-processed planar heterojunction solar cells the TDAPy-based oligomer showed a power conversion efficiency of 3.15% and a high fill factor of 0.67.

Bis(fluorenyl)benzothiadiazole-cored carbazole dendrimers show high thermal and electrochemical stability, and great potential as solution processed hole-transporting non-doped green emitters for OLEDs. A pure green device with CIE coordinates of (0.27, 0.62) and high luminance efficiencies (up to 10.01 cd A(-1)) is achieved, respectively.

A new NbO-type metal-organic framework ZJNU-40 incorporating highly polarized benzothiadiazole moieties exhibits a high CO2 uptake of 108 cm(3) g(-1) at 296 K and 1 atm, as well as good adsorption selectivities of CO2 over CH4 and N2 at room temperature, which is superior to that of the analogous MOF NOTT-101.

We report on two pairs of platinum acetylide based polymers and model oligomers utilizing a 2,1,3-benzothiadiazole (BTD) acceptor moiety flanked on either side by either 2,5-thienyl donor units (Pt2BTD-Th and p-PtBTD-Th) or (3,4-ethylenedioxy)-2,5-thienyl donors (Pt2BTD-EDOT and p-PtBTD-EDOT). Both oligomer/polymer pairs absorb strongly throughout the visible region; however, because the (ethyl...

Two field experiments were carried out in order to investigate the effect of chemicalinducers [benzothiadiazole 0.9 mM l-1, oxalic acid 1.0 mM l-1, salicylic acid 0.2 mM l-1] onphysiological and technological traits as well as on yields and antioxidant enzyme activities ofbarley grown under abiotic stress (i.e. water surplus and deficit conditions). Results showed thatrelative water content, le...

A new photoactive polymer comprising benzo[1,2-b:3,4-b':5,6-d']trithiophene and 2,1,3-benzothiadiazole-5,6-dicarboxylic imide is reported. The synthetic design allows for alkyl chains to be introduced on both electron-rich and electron-deficient components, which in turn allows for rapid optimization of the alkyl chain substitution pattern. Consequently, the optimized polymer shows a maximum ef...

A method to fabricate conjugated polymer waveguides with well defined edge facets is demonstrated. The utility of the approach is explored for application as end-fired ultrafast optical amplifiers based on poly(9,9'-dioctylfluorene-co-benzothiadiazole). An internal gain of 19 dB was achieved on a 760 microm long waveguide at 565 nm wavelength. This fabrication procedure may be applied to a wide...

Novel D–A-?-A organic sensitizers for DSSCs based on benzothiadiazole internal acceptor (A) and N -substituted indolines fused with cyclopentane or cyclohexane as donor (D) the best PCE of 5.8% were reported.