scholarly journals Intriguing Heteroleptic ZnII bis(dipyrrinato) Emitters in the Far-Red Region With Large Pseudo-Stokes Shift for Bioimaging

2021 ◽  
Vol 9 ◽  
Author(s):  
Roberta Tabone ◽  
Dominik Feser ◽  
Enrico D. Lemma ◽  
Ute Schepers ◽  
Claudia Bizzarri

Novel heteroleptic ZnII bis(dipyrrinato) complexes were prepared as intriguing emitters. With our tailor-made design, we achieved far-red emissive complexes with a photoluminescence quantum yield up to 45% in dimethylsulfoxide and 70% in toluene. This means that heteroleptic ZnII bis(dipyrrinato) complexes retain very intense emission also in polar solvents, in contrast to their homoleptic counterparts, which we prepared for comparing the photophysical properties. It is evident from the absorption and excitation spectra that heteroleptic complexes present the characteristic features of both ligands: the plain dipyrrin (Lp) and the π-extended dipyrrin (Lπ). On the contrary, the emission comes exclusively from the π-extended dipyrrin Lπ, suggesting an interligand nonradiative transition that causes a large pseudo-Stokes shift (up to 4,600 cm−1). The large pseudo-Stokes shifts and the emissive spectral region of these novel heteroleptic ZnII bis(dipyrrinato) complexes are of great interest for bioimaging applications. Thus, their high biocompatibiliy with four different cell lines make them appealing as new fluorophores for cell imaging.

Chemosensors ◽  
2022 ◽  
Vol 10 (1) ◽  
pp. 19
Author(s):  
Abigail E. Reese ◽  
Charles Lochenie ◽  
Ailsa Geddis ◽  
Luana A. Machado ◽  
Marcos C. de Souza ◽  
...  

Five new disubstituted 2,6-thioaryl-BODIPY dyes were synthesized via selective aromatic electrophilic substitution from commercially available thiophenols. The analysis of the photophysical properties via absorption and emission spectroscopy showed unusually large Stokes shifts for BODIPY fluorophores (70–100 nm), which makes them suitable probes for bioimaging. Selected compounds were evaluated for labelling primary immune cells as well as different cancer cell lines using confocal fluorescence microscopy.


Molecules ◽  
2018 ◽  
Vol 23 (12) ◽  
pp. 3051 ◽  
Author(s):  
Jacqueline Gayton ◽  
Shane Autry ◽  
Ryan Fortenberry ◽  
Nathan Hammer ◽  
Jared Delcamp

Near-infrared emissive materials with tunable Stokes shifts and solid-state emissions are needed for several active research areas and applications. To aid in addressing this need, a series of indolizine-cyanine compounds varying only the anions based on size, dipole, and hydrophilicity were prepared. The effect of the non-covalently bound anions on the absorption and emission properties of identical π-system indolizine-cyanine compounds were measured in solution and as thin films. Interestingly, the anion choice has a significant influence on the Stokes shift and molar absorptivities of the dyes in solution. In the solid-state, the anion choice was found to have an effect on the formation of aggregate states with higher energy absorptions than the parent monomer compound. The dyes were found to be emissive in the NIR region, with emissions peaking at near 900 nm for specific solvent and anion selections.


2016 ◽  
Vol 20 (01n04) ◽  
pp. 475-489 ◽  
Author(s):  
Changjiang Yu ◽  
Qinghua Wu ◽  
Zhonghua Tian ◽  
Tingting Li ◽  
Erhong Hao ◽  
...  

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.


RSC Advances ◽  
2015 ◽  
Vol 5 (87) ◽  
pp. 70958-70967 ◽  
Author(s):  
Ajay Kanungo ◽  
Dipendu Patra ◽  
Sanghamitra Mukherjee ◽  
Tridib Mahata ◽  
Prakas R. Maulik ◽  
...  

Synthesis and live cell imaging of a novel fluorescent scaffold which is emissive in the visible range with large stokes shifts.


2015 ◽  
Vol 56 (21) ◽  
pp. 2749-2753 ◽  
Author(s):  
Yanjun Qiao ◽  
Jingtian Chen ◽  
Xuegang Yi ◽  
Wenfeng Duan ◽  
Baoxiang Gao ◽  
...  

1990 ◽  
Vol 10 (5-6) ◽  
pp. 277-296 ◽  
Author(s):  
Jean-Claude Mialocq ◽  
Martine Meyer

The two styryl dyes, 4-dicyanomethylene-2-methyl-6-P-dimethylaminostyryl-4H-pyran (DCM) and 7- dimethylamino-3-(p-formylstyryl)-l, 4-benzoxazin-2-one (DFSBO) exhibit similar solvent-induced shifts of their absorption and emission spectra related to a large intramolecular charge transfer (ICT) in the first singlet excited state. From the Stokes shift values (vA−vF) and a vectorial analysis of their ground state dipole moment (μg= 6.1 D for DCM and 5.8 D for DFSBO), and using the Lippert-Mataga theory, we have estimated the dipole moments of their fluorescent excited states S1 (μe = 26.3 D for DCM and 27.6 D for DFSBO). Intersystem crossing to the triplet state is totally inefficient in DCM but significant in DFSBO. Moreover the absorption of the DFSBO triplet is quite large in the emission band (600–650 nm), which makes of DFSBO a poor laser dye. Although DCM trans-cis photoisomerization can be quite efficient in non polar solvents (chloroform, tetrahydrofuran), DFSBO does not photoisomerize probably due to steric hindrance and to the S1 character which should be more "benzoxazinone" than ethylenic. DFSBO is also shown to exhibit rotamerism.


2021 ◽  
Vol 18 ◽  
Author(s):  
Amira K. Hajri ◽  
Marzough A. Albalawi ◽  
Souad A. Moussa ◽  
Faouzi Aloui

Background: Three polycyclic aromatic hydrocarbons derived from benzo[c]phenanthrene have been synthesized through a one-step procedure involving palladium Suzuki coupling and are characterized by 1 H and 13C NMR, MS and HRMS spectroscopies. Methods: UV-vis absorption and fluorescence properties of these π-conjugated compounds have been evaluated in solutions and strong emission in the blue region of the visible spectrum was noted. Results: The optical spectra of these small polycyclic aromatic compounds are unusual because absorption is entirely in the UV region (λmax = 281-285 nm), yet fluorescence occurs at 410-422 nm. Conclusion: This equates to a Stokes shift of 1.32-1.39 eV (10756-11256 cm−1 ) and is among the large Stokes shifts that have been reported for small molecules, making them promising candidates for optoelectronic applications.


2014 ◽  
Vol 50 (3) ◽  
pp. 320-322 ◽  
Author(s):  
Peng Hou ◽  
Song Chen ◽  
Hongbo Wang ◽  
Jianxiu Wang ◽  
Kislon Voitchovsky ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document