Results 41 to 50 of about 3,082 (195)

Chiral perylene materials by ionic self-assembly [PDF]

open access: yes, 2016
Two chiral complexes (1-SDS and 1-SDBS) were prepared via the ionic self-assembly of a chiral perylene diimide tecton with oppositely charged surfactants.
Charl F. J. Faul   +4 more
core   +5 more sources

Ab-Initio Calculation of Molecular Aggregation Effects: a Coumarin-343 Case Study [PDF]

open access: yes, 2013
We present time-dependent density functional theory (TDDFT) calculations for single and dimerized Coumarin-343 molecules in order to investigate the quantum mechanical effects of chromophore aggregation in extended systems designed to function as a new ...
Agranovich V.   +71 more
core   +2 more sources

1,6- and 1,7-Regioisomers of Asymmetric and Symmetric Perylene Bisimides: Synthesis, Characterization and Optical Properties

open access: yesMolecules, 2013
The 1,6- and 1,7-regioisomers of dinitro- (1,6-A and 1,7-A) and diamino-substituted perylene bisimides (1,6-B and 1,7-B), and 1-amino-6-nitro- and 1-amino-7-nitroperylene bisimides (1,6-C and 1,7-C) were synthesized. The 1,6-A and 1,7-A regioisomers were
Hsing-Yang Tsai   +2 more
doaj   +1 more source

Perylene Diimide Aggregates on Sb-Doped SnO2: Charge Transfer Dynamics Relevant to Solar Fuel Generation [PDF]

open access: yes, 2017
open14siThe project leading to this application has received funding from the European Union’s Horizon 2020 Research and Innovation Programme under the Marie Sklodowska-Curie grant agreement no. 705723.The deposition of perylene diimide-based aggregates (

core   +1 more source

A Low Reabsorbing Luminescent Solar Concentrator Employing π-Conjugated Polymers [PDF]

open access: yes, 2015
A highly efficient thin-film luminescent solar concentrator (LSC) utilizing two π-conjugated polymers as antennae for small amounts of the valued perylene bisimide Lumogen F Red 305 is presented. The LSC exhibits high photoluminescence quantum yield, low
Bawendi, Moungi G.   +3 more
core   +1 more source

Switching or blinking? – The switching behaviour of single photochromic triads

open access: yesEPJ Web of Conferences, 2018
Photochromic molecules can be interconverted between two bistable conformations by light [1–3]. Irie and coworkers described a strategy to achieve superior fluorescence characteristics and outstanding switching characteristics of a photochromic unit by ...
Maier Johannes   +4 more
doaj   +1 more source

Understanding and optimising the packing density of perylene bisimide layers on CVD-grown graphene

open access: yes, 2015
The non-covalent functionalisation of graphene is an attractive strategy to alter the surface chemistry of graphene without damaging its superior electrical and mechanical properties.
Backes, Claudia   +9 more
core   +1 more source

Size-dependent exciton dynamics in one-dimensional perylene bisimide aggregates

open access: yesNew Journal of Physics, 2012
The size-dependent exciton dynamics of one-dimensional aggregates of substituted perylene bisimides are studied by ultrafast transient absorption spectroscopy and kinetic Monte-Carlo simulations as a function of the excitation density and the temperature
Steffen Wolter   +6 more
doaj   +1 more source

Kinetically controlled coassembly of multichromophoric peptide hydrogelators and the impacts on energy transport [PDF]

open access: yes, 2017
We report a peptide-based multichromophoric hydrogelator system, wherein π-electron units with different inherent spectral energies are spatially controlled within peptidic 1-D nanostructures to create localized energy gradients in aqueous environments ...
Adams, Dave J   +6 more
core   +2 more sources

Photocatalytic nucleophilic addition of alcohols to styrenes in Markovnikov and anti-Markovnikov orientation

open access: yesBeilstein Journal of Organic Chemistry, 2015
The nucleophilic addition of methanol and other alcohols to 1,1-diphenylethylene (1) and styrene (6) into the Markovnikov- and anti-Markovnikov-type products was selectively achieved with 1-(N,N-dimethylamino)pyrene (Py) and 1,7-dicyanoperylene-3,4:9,10 ...
Martin Weiser   +3 more
doaj   +1 more source

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