Fluoreszenz von Distyrylbenzolen und Distyrylstilbenen / Fluorescence of Distyrylbenzenes and Distyrylstilbenes

1982 ◽  
Vol 37 (11) ◽  
pp. 1472-1480 ◽  
Author(s):  
R. Erckel ◽  
H. Frühbeis
Keyword(s):  
Quantum Chemical Calculations ◽  
Quantum Chemical ◽  
Emission Spectra ◽  
Quantum Yields ◽  
Fluorescence Quantum Yields ◽  
Stokes Shifts

Absorption, corrected emission spectra, fluorescence quantum yields, and preparation are reported for distyrylbenzene, distyrylstilbene and substituted derivatives. The Stokes shifts are measured in three solvents and correlated with quantum chemical calculations.

Chlorination vs. fluorination: a study of halogenated benzo[c][1,2,5]thiadiazole-based organic semiconducting dots for near-infrared cellular imaging

2020 ◽  
Vol 44 (19) ◽  
pp. 7740-7748
Author(s):  
Daize Mo ◽  
Li Lin ◽  
Pengjie Chao ◽  
Hanjian Lai ◽  
Qingwen Zhang ◽  
...  
Keyword(s):  
Near Infrared ◽  
Cellular Imaging ◽  
Quantum Yields ◽  
Fluorescence Quantum Yields ◽  
Stokes Shifts

The chlorinated dots based on chlorinated benzo[c][1,2,5]thiadiazole unit possess higher fluorescence quantum yields, larger Stokes shifts, and better photostability than the fluorinated dots.

Synthesis and Photophysical Properties of 3-(Trifluoromethyl)-2H-imidazo[5,1-a]isoquinolinium Chloride Derivatives

Synlett ◽  
2017 ◽  
Vol 29 (03) ◽  
pp. 296-300 ◽  
Author(s):  
Ali Darehkordi ◽  
Fariba Rahmani ◽  
Mahin Ramezani ◽  
Alireza Bazmandegan-Shamili
Keyword(s):  
Blue Light ◽  
Uv Radiation ◽  
Photophysical Properties ◽  
Molecular Probes ◽  
Quantum Yields ◽  
Light Emitting ◽  
Fluorescence Studies ◽  
Fluorescence Quantum Yields ◽  
Fluorescent Molecular Probes ◽  
Stokes Shifts

A series of novel blue-light-emitting 2H-imidazo[5,1-a]isoquinolinium chloride derivatives were synthesized by the reaction of isoquinoline with trifluoroacetimidoyl chlorides and isocyanides in dry CH2Cl2 in excellent yields. Fluorescence studies showed that the compounds absorb UV radiation and then emit blue light at about 481 nm with moderate to good fluorescence quantum yields. These compounds also showed high Stokes shifts, and can be used to develop ­ultrasensitive fluorescent molecular probes to study a variety of biological events and processes.

scholarly journals Thiophene-forming one-pot synthesis of three thienyl-bridged oligophenothiazines and their electronic properties

2016 ◽  
Vol 12 ◽  
pp. 2055-2064 ◽  
Author(s):  
Dominik Urselmann ◽  
Konstantin Deilhof ◽  
Bernhard Mayer ◽  
Thomas J J Müller
Keyword(s):  
Cyclic Voltammetry ◽  
Helical Structure ◽  
Quantum Yields ◽  
Absorption Bands ◽  
One Pot ◽  
Fluorescence Quantum Yields ◽  
Oxidation Potentials ◽  
Td Dft ◽  
Lower Oxidation ◽  
Stokes Shifts

The pseudo five-component Sonogashira–Glaser cyclization synthesis of symmetrically 2,5-diaryl-substituted thiophenes is excellently suited to access thienyl-bridged oligophenothiazines in a one-pot fashion. Three thienyl-bridged systems were intensively studied by UV–vis and fluorescence spectroscopy as well as by cyclic voltammetry. The oxidation proceeds with lower oxidation potentials and consistently reversible oxidations can be identified. The Stokes shifts are large and substantial fluorescence quantum yields can be measured. Computational chemistry indicates lowest energy conformers with sigmoidal and helical structure, similar to oligophenothiazines. TD-DFT and even semiempirical ZINDO calculations reproduce the trends of longest wavelengths absorption bands and allow the assignment of these transitions to possess largely charge-transfer character from the adjacent phenothiazinyl moieties to the central thienyl unit.

Properties of singlet- and triplet-excited states of hemicyanine dyes

2014 ◽  
Vol 68 (8) ◽  
Author(s):  
Daniel Mártire ◽  
Walter Massad ◽  
Hernán Montejano ◽  
Mónica Gonzalez ◽  
Paula Caregnato ◽  
...  
Keyword(s):  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Fluorescence Emission ◽  
Emission Spectra ◽  
Laser Flash ◽  
Quantum Yields ◽  
Triplet States ◽  
Fluorescence Emission Spectra ◽  
Fluorescence Quantum Yields ◽  
Hemicyanine Dyes

AbstractThe fluorescence emission spectra and fluorescence quantum yields of hemicyanine dyes LDS 698, LDS 722, and LDS 730 were measured in different media. No transient species was detected in the laser flash-photolysis experiments performed with Ar-saturated solutions of the dyes in methanol. However, in the presence of 0.08 M potassium iodide, the absorption of the triplet states was clearly observed. Oxygen consumption measurements in the absence and presence of a chemical trap (furfuryl alcohol) in MeOH: H2O (φ r = 1: 1) solutions of the dyes containing KI confirmed the generation of singlet molecular oxygen.

Synthesis and photophysical properties of meso-aryloxy linked BODIPY monomers, dimers, and trimer

2016 ◽  
Vol 20 (01n04) ◽  
pp. 475-489 ◽  
Author(s):  
Changjiang Yu ◽  
Qinghua Wu ◽  
Zhonghua Tian ◽  
Tingting Li ◽  
Erhong Hao ◽  
...  
Keyword(s):  
Photophysical Properties ◽  
Spatial Arrangement ◽  
Nucleophilic Aromatic Substitution ◽  
Quantum Yields ◽  
Aromatic Substitution ◽  
Polar Solvents ◽  
Fluorescence Quantum Yields ◽  
Species Formation ◽  
The Relationship ◽  
Stokes Shifts

A series of meso-aryloxy linked BODIPY monomers, dimers and trimer were synthesized by nucleophilic aromatic substitution (SNAr) reaction from phenols with meso-chloro BODIPY and their photophysical properties were systematically studied by UV-vis and fluorescence spectroscopy. The relationship between their photophysical properties and the spatial arrangement of meso-aryloxy linked BODIPYs has been discussed. The monomers exhibited different extent solvent-dependent fluorescence, and fluorescence quenching in polar solvents were found relative to the HOMO energies of the donor (meso-phenols), indicating possible PET effect from meso-phenols to the BODIPY fluorophore. Ortho-dimer showed unusual broad red-shifted emission bands centered at 550 nm with a larger Stokes shifts at the range of 2900–3400 cm[Formula: see text], and low fluorescence quantum yields, which was in sharp contrast to those of other dimers and trimer, indicating of possible excimeric species formation due to slipped cofacial arrangement ofortho-dimer.

Aza boron-pyridyl-isoindoline isomers: synthesis and photophysical properties

2014 ◽  
Vol 18 (08n09) ◽  
pp. 679-685 ◽  
Author(s):  
Hui Liu ◽  
Yanping Wu ◽  
Zhifang Li ◽  
Hua Lu
Keyword(s):  
Photophysical Properties ◽  
Emission Spectra ◽  
Quantum Yields ◽  
Structure Property ◽  
X Ray ◽  
X Ray Crystallography ◽  
Fluorescence Quantum Yields ◽  
Structure Property Relationships ◽  
New Type ◽  
Vibrational Bands

By changing benzo-fused position on pyridyl unit, three aza boron-pyridyl-isoindoline isomers, a new type of BODIPY analog, are synthesized through a facile two step reaction. These isomers show broad envelopes of intense vibrational bands in the absorption and emission spectra with moderate fluorescence quantum yields. In comparison to those of classical BODIPYs, significant fluorescence intensity are observed for these isomers in film and powder. An analysis of the structure-property relationships has been carried out based on X-ray crystallography, optical spectroscopy, and theoretical calculation.

scholarly journals A Convenient Synthesis of Diketopyrrolopyrrole Dyes

Molecules ◽  
2021 ◽  
Vol 26 (16) ◽  
pp. 4758
Author(s):  
Vitor A. S. Almodôvar ◽  
Augusto C. Tomé
Keyword(s):  
High Performance ◽  
Coupling Reaction ◽  
Quantum Yields ◽  
Reaction Conditions ◽  
Fluorescence Quantum Yields ◽  
Cross Coupling Reaction ◽  
Convenient Synthesis ◽  
Organic Optoelectronic ◽  
High Fluorescence ◽  
Stokes Shifts

Diketopyrrolo[3,4-c]pyrroles (DPP) are high-performance organic optoelectronic materials. They have applications in solar cells, fluorescent probes, bioimaging, photodynamic/photothermal therapy, and in many other areas. This article reports a convenient two-step synthesis of various DPP dyes from Pigment Red 254, an inexpensive commercial pigment. The synthesis includes a Suzuki–Miyaura cross-coupling reaction of a bis(4-chlorophenyl)DPP derivative with aryl and hetaryl boronic acids under mild reaction conditions. The new dyes show large Stokes shifts and high fluorescence quantum yields, important features for their potential use in technical and biological applications.

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