Photophysical Properties and Electropolymerization of Gold Complexes of 3,3′′-Diethynyl-2,2′:5′,2′′-terthiophene

2010 ◽  
Vol 49 (19) ◽  
pp. 8802-8812 ◽  
Author(s):  
Angela M. Kuchison ◽  
Michael O. Wolf ◽  
Brian O. Patrick
Keyword(s):  
Photophysical Properties ◽  
Gold Complexes

Synthesis, luminescence and electrochemical properties of luminescent dinuclear mixed-valence gold complexes with alkynyl bridges

2015 ◽  
Vol 2 (5) ◽  
pp. 453-466 ◽  
Author(s):  
Ling-Ling Hung ◽  
Wai Han Lam ◽  
Keith Man-Chung Wong ◽  
Eddie Chung-Chin Cheng ◽  
Nianyong Zhu ◽  
...  
Keyword(s):  
Electrochemical Properties ◽  
Photophysical Properties ◽  
Mixed Valence ◽  
Computational Studies ◽  
Gold Complexes

A series of luminescent dinuclear mixed-valence gold alkynyl complexes was synthesized. Their photophysical properties can be tuned by varying the nature of the alkynyl bridges, as supported by computational studies.

scholarly journals Stimuli-Sensitive Aggregation-Induced Emission of Organogelators Containing Mesogenic Au(I) Complexes

Crystals ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 388
Author(s):  
Supattra Panthai ◽  
Ryota Fukuhara ◽  
Kyohei Hisano ◽  
Osamu Tsutsumi
Keyword(s):  
Luminescence Intensity ◽  
Photophysical Properties ◽  
Sol Gel ◽  
Quantum Yields ◽  
Stimuli Responsive ◽  
Gold Complexes ◽  
Aggregation Induced Emission ◽  
Strong Luminescence ◽  
Constrained Environments ◽  
Stimuli Sensitive

As the luminescence from conventional organic luminophores is typically quenched in constrained environments, the aggregation-induced emission (AIE) phenomenon is of interest for the development of materials that exhibit strong luminescence in condensed phases. Herein, new bismesogenic Au complexes were developed as organogelators and their photophysical properties, including their AIE characteristics, were investigated in organogels and crystals. The crystals of the gold complexes exhibited room-temperature phosphorescence with relatively high quantum yields. Moreover, the gold complexes also showed photoluminescence in the organogels and we demonstrated that the reversible switching of the luminescence intensity was induced by the sol-gel phase transition. The intense photoluminescence in the crystal and gel was induced by the restricted internal motion of the luminophore in the molecular aggregates. However, in the sol, the network structure of the organogel was destroyed and the nonradiative deactivation of the excited states was enhanced. As a result, we can conclude that the switching of the luminescence intensity was induced by changes in the aggregated structures of the molecules. The developed Au-complex-based gelators are excellent candidates for the realization of stimuli-responsive soft and smart luminescent materials.

scholarly journals Gold Nanoclusters: Bridging Gold Complexes and Plasmonic Nanoparticles in Photophysical Properties

Nanomaterials ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 933 ◽  
Author(s):  
Meng Zhou ◽  
Chenjie Zeng ◽  
Qi Li ◽  
Tatsuya Higaki ◽  
Rongchao Jin
Keyword(s):  
Excited State ◽  
Photophysical Properties ◽  
Gold Nanoclusters ◽  
Detailed Comparison ◽  
Organometallic Complexes ◽  
Plasmonic Nanoparticles ◽  
Metal Nanoclusters ◽  
Metal Core ◽  
Gold Complexes ◽  
Metal Metal

Recent advances in the determination of crystal structures and studies of optical properties of gold nanoclusters in the size range from tens to hundreds of gold atoms have started to reveal the grand evolution from gold complexes to nanoclusters and further to plasmonic nanoparticles. However, a detailed comparison of their photophysical properties is still lacking. Here, we compared the excited state behaviors of gold complexes, nanolcusters, and plasmonic nanoparticles, as well as small organic molecules by choosing four typical examples including the Au10 complex, Au25 nanocluster (1 nm metal core), 13 diameter Au nanoparticles, and Rhodamine B. To compare their photophysical behaviors, we performed steady-state absorption, photoluminescence, and femtosecond transient absorption spectroscopic measurements. It was found that gold nanoclusters behave somewhat like small molecules, showing both rapid internal conversion (<1 ps) and long-lived excited state lifetime (about 100 ns). Unlike the nanocluster form in which metal–metal transitions dominate, gold complexes showed significant charge transfer between metal atoms and surface ligands. Plasmonic gold nanoparticles, on the other hand, had electrons being heated and cooled (~100 ps time scale) after photo-excitation, and the relaxation was dominated by electron–electron scattering, electron–phonon coupling, and energy dissipation. In both nanoclusters and plasmonic nanoparticles, one can observe coherent oscillations of the metal core, but with different fundamental origins. Overall, this work provides some benchmarking features for organic dye molecules, organometallic complexes, metal nanoclusters, and plasmonic nanoparticles.

Electronmicroscopic localization of ribonucleic acids in ciliate Bursaria truncatella during cell division

1990 ◽  
Vol 48 (3) ◽  
pp. 132-133
Author(s):  
Vladimir Popenko ◽  
Natalya Cherny ◽  
Maria Yakovleva
Keyword(s):  
Cell Division ◽  
High Specificity ◽  
Longitudinal Axis ◽  
Gold Complexes ◽  
Somatic Nucleus ◽  
Ribonucleic Acids ◽  
Biological Meaning ◽  
Bivalent Cations ◽  
Lowicryl K4m ◽  
Short Time

Highly polyploid somatic nucleus (macronucleus) of ciliate Bursaria truncatella under goes severe changes in morphology during cell division. At first, macronucleus (Ma) condences, diminishes in size and turns perpendicular to longitudinal axis of the cell. After short time, Ma turns again, elongates and only afterwards the process of division itself occurs. The biological meaning of these phenomena is not clear.Localization of RNA in the cells was performed on sections of ciliates B. truncatella, embedded in “Lowicryl K4M” at various stages: (1) before cell division (Figs. 2,3); (11) at the stage of macronucleus condensation; (111) during elongation of Ma (Fig.4); (1111) in young cells (0-5min. after division). For cytochemical labelling we used RNaseAcolloidal gold complexes (RNase-Au), which are known to bind to RNA containing cell ularstructures with high specificity. The influence of different parameters on the reliability and reproducibility of labelling was studied. In addition to the factors, discussed elsewhere, we found that the balance of mono- and bivalent cations is of great significance.

Solvent Dependence of Structural Dynamics and Spin-flip Processes in 3,4,5-tri(9H-carbazole-9-yl)benzonitrile (ortho-3CzBN)

2020 ◽  
Author(s):  
Masaki Saigo ◽  
Kiyoshi Miyata ◽  
Hajime Nakanotani ◽  
Chihaya Adachi ◽  
Ken Onda
Keyword(s):  
Dft Calculations ◽  
Excited States ◽  
Structural Changes ◽  
Photophysical Properties ◽  
Delayed Fluorescence ◽  
Time Resolved ◽  
Thermally Activated Delayed Fluorescence ◽  
Thermally Activated ◽  
Solvent Dependence ◽  
Acetonitrile Solutions

We have investigated the solvent-dependence of structural changes along with intersystem crossing of a thermally activated delayed fluorescence (TADF) molecule, 3,4,5-tri(9H-carbazole-9-yl)benzonitrile (o-3CzBN), in toluene, tetrahydrofuran, and acetonitrile solutions using time-resolved infrared (TR-IR) spectroscopy and DFT calculations. We found that the geometries of the S1 and T1 states are very similar in all solvents though the photophysical properties mostly depend on the solvent. In addition, the time-dependent DFT calculations based on these geometries suggested that the thermally activated delayed fluorescence process of o-3CzBN is governed more by the higher-lying excited states than by the structural changes in the excited states.<br>

Theoretical Framework of 1,3-Thiazolium-5-Thiolates Mesoionic Compounds: Exploring the Nature of Photophysical Properties and Molecular Nonlinearity

2020 ◽  
Author(s):  
Zeyu Liu ◽  
Shugui Hua ◽  
Tian Lu ◽  
Ziqi Tian
Keyword(s):  
Optical Properties ◽  
Rational Design ◽  
Rayleigh Scattering ◽  
Function Analysis ◽  
Theoretical Calculations ◽  
Photophysical Properties ◽  
Optical Nonlinearity ◽  
Nonlinear Properties ◽  
Photoelectric Performance ◽  
Wave Function Analysis

Inspired by a previous experimental study on the first-order hyperpolarizabilities of 1,3-thiazolium-5-thiolates mesoionic compounds using Hyper-Rayleigh scattering technique, we theoretically investigated the UV-Vis absorption spectra and every order polarizabilities of these mesoionic molecules. Based on the fact that the photophysical and nonlinear properties observed in the experiment can be perfectly replicated, our theoretical calculations explored the essential characteristics of the optical properties of the mesoionic compounds with different electron-donating groups at the level of electronic structures through various wave function analysis methods. The influence of the electron-donating ability of the donor on the optical properties of the molecules and the contribution of the mesoionic ring moiety to their optical nonlinearity are clarified, which have not been reported by any research so far. This work will help people understand the nature of optical properties of mesoionic-based molecules and provide guidance for the rational design of molecules with excellent photoelectric performance in the future.

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