Browse
Submit Data
Databases
API
Help

Dataset Information

21 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

A Halomanganates(II) with P,P'-Diprotonated Bis(2-Diphenylphosphinophenyl)ether: Wavelength-Excitation Dependence of the Quantum Yield and Role of the Non-Covalent Interactions.

ABSTRACT: A [H₂DPEphos][MnX₄] [X = Br, Cl] tetrahalomanganates(II) with P,P'-diprotonated bis[2-(diphenylphosphino)phenyl]ether cation has been designed and investigated in photophysics and EPR terms. The complexes exhibit a green luminescence resulted from the Mn(II) d-d transitions (⁴T₁→⁶A₁) with the wavelength-excitation dependence of the quantum yield. The solid [H₂DPEphos][MnBr₄] complex exhibits a bright green phosphorescence (λ_max = 515 nm) with the high luminescence quantum yield depending on the excitation energy whereas the solid [H₂DPEphos][MnCl₄] complex exhibits a very weak phosphorescence (λ_max = 523 nm). The unexpected shorter luminescence lifetime for the [H₂DPEphos][MnCl₄] than for the [H₂DPEphos][MnBr₄] at 300 K can be a result of the higher non-radiative relaxation contribution. On the one hand, the non-covalent PH…X(Mn) interactions quench the manganese(II) luminescence. On the other hand, the PH…X(Mn) interactions are a pathway of the excitation transfer from [H₂DPEphos]²⁺ to [MnX₄]^2-.

SUBMITTER: Berezin AS

PROVIDER: S-EPMC8268785 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Camouflaged Nanosilver with Excitation Wavelength Dependent High Quantum Yield for Targeted Theranostic.

Project description:The present study shows the thorough investigations on optical properties and hydrodynamic diameters of glutathione (GSH) stabilized nanosilver clusters (AgNC) at different stages of synthesis and engineering for the optimized absolute quantum yield to generate fluorescent images of Dalton Lymphoma Ascites (DLA) tumour bearing mice. The initial increment of quantum yield was wavelength dependent and finally it became 0.509 which was due to the camouflaging or entrapment of AgNC in macrophages membranes. The potentiality of macrophages membrane camouflaged silver nanoclusters (AgM) was reflected in the cell viability assay and confocal based live dead cell assay where the AgM has better cell killing effect compared to AgNC with reduced dosage and in vivo mice imaging generated the clear visualization at the tumour sites. Therefore, from the present study, it can be considered that the camouflaged nanosilver can be used for targeted theranostic applications.

| S-EPMC6220276 | biostudies-literature

Excitation Wavelength-Dependent Photoluminescence Decay of Hybrid Gold/Quantum Dot Nanostructures.

Project description:Hybrid nanostructures comprised of metal nanoparticles (MNPs) and quantum dots (QDs) have been found to exhibit unique, new optical properties due to the interaction that occurs between the MNPs and QDs. The aim of this work is to understand how the exciton-plasmon interaction in these systems is dependent on the excitation wavelength. The nanoassemblies consisted of gold (Au) NPs coated in a silica (SiO2) shell of a controlled thickness and core/shell CdSe/CdS QDs adsorbed onto the SiO2 shells. Our findings show that the photoluminescence lifetimes of the hybrid constructs are dependent on the excitation wavelength relative to the localized surface plasmon resonance (LSPR) of the Au NPs. When the excitation wavelength is closer to the LSPR, the photoluminescence decay of the hybrid structures is faster. We demonstrate that by tuning the excitation wavelength close to the resonance, there is an enhancement in the exciton-plasmon coupling between the Au NPs and QDs resulting in a shortening in the QD photoluminescence lifetime. We then propose a possible mechanism to explain this excitation wavelength-dependent phenomenon.

| S-EPMC6644928 | biostudies-literature

Effect of Excitation Wavelength on Optical Performances of Quantum-Dot-Converted Light-Emitting Diode.

Project description:Light-emitting diode (LED) combined with quantum dots (QDs) is an important candidate for next-generation high-quality semiconductor devices. However, the effect of the excitation wavelength on their optical performance has not been fully explored. In this study, green and red QDs are applied to LEDs of different excitation wavelengths from 365 to 455 nm. The blue light is recommended for exciting QDs from the perspective of energy utilization. However, QD LEDs excited at 365 nm have unique advantages in eliminating the original peaks from the LED chip. Moreover, the green or red light excited by ultraviolet light has an advantage in colorimetry. Even for the 455 nm LED with the highest QD concentration at 7.0 wt%, the color quality could not compete with the 365 nm LED with the lowest QD concentration at 0.2 wt%. A 117.5% (NTSC1953) color gamut could be obtained by the 365 nm-excited RGB system, which is 32.6% higher than by the 455 nm-excited solution, and this can help expand the color gamut of LED devices. Consequently, this study provides an understanding of the properties of QD-converted LEDs under different wavelength excitations, and offers a general guide to selecting a pumping source for QDs.

| S-EPMC6723292 | biostudies-literature

Quantum yield and excitation rate of single molecules close to metallic nanostructures.

Project description:The interaction of dyes and metallic nanostructures strongly affects the fluorescence and can lead to significant fluorescence enhancement at plasmonic hot spots, but also to quenching. Here we present a method to distinguish the individual contributions to the changes of the excitation, radiative and non-radiative rate and use this information to determine the quantum yields for single molecules. The method is validated by precisely placing single fluorescent dyes with respect to gold nanoparticles as well as with respect to the excitation polarization using DNA origami nanostructures. Following validation, measurements in zeromode waveguides reveal that suppression of the radiative rate and enhancement of the non-radiative rate lead to a reduced quantum yield. Because the method exploits the intrinsic blinking of dyes, it can generally be applied to fluorescence measurements in arbitrary nanophotonic environments.

| S-EPMC4717520 | biostudies-literature

Excitation wavelength dependence of water-window line emissions from boron-nitride laser-produced plasmas.

Project description:We investigated the effects of laser excitation wavelength on water-window emission lines of laser-produced boron-nitride plasmas. Plasmas are produced by focusing 1064 nm and harmonically generated 532 and 266 nm radiation from a Nd:YAG laser on BN target in vacuum. Soft x-ray emission lines in the water-window region are recorded using a grazing-incidence spectrograph. Filtered photodiodes are used to obtain complementary data for water-window emission intensity and angular dependence. Spectral emission intensity changes in nitrogen Ly-α and He-α are used to show how laser wavelength affects emission. Our results show that the relative intensity of spectral lines is laser wavelength dependent, with the ratio of Ly-α to He-α emission intensity decreasing as laser wavelength is shortened. Filtered photodiode measurements of angular dependence showed that 266 and 532 nm laser wavelengths produce uniform emission.

| S-EPMC3293343 | biostudies-other

Intense, stable and excitation wavelength-independent photoluminescence emission in the blue-violet region from phosphorene quantum dots.

Project description:Nanoscale phosphorene quantum dots (PQDs) with few-layer structures were fabricated by pulsed laser ablation of a bulk black phosphorus target in diethyl ether. An intense and stable photoluminescence (PL) emission of the PQDs in the blue-violet wavelength region is clearly observed for the first time, which is attributed to electronic transitions from the lowest unoccupied molecular orbital (LUMO) to the highest occupied molecular orbital (HOMO) and occupied molecular orbitals below the HOMO (H-1, H-2), respectively. Surprisingly, the PL emission peak positions of the PQDs are not red-shifted with progressively longer excitation wavelengths, which is in contrast to the cases of graphene and molybdenum disulphide quantum dots. This excitation wavelength-independence is derived from the saturated passivation on the periphery and surfaces of the PQDs by large numbers of electron-donating functional groups which cause the electron density on the PQDs to be dramatically increased and the band gap to be insensitive to the quantum size effect in the PQDs. This work suggests that PQDs with intense, stable and excitation wavelength-independent PL emission in the blue-violet region have a potential application as semiconductor-based blue-violet light irradiation sources.

| S-EPMC4893668 | biostudies-literature

Chlorine Modulation Fluorescent Performance of Seaweed-Derived Graphene Quantum Dots for Long-Wavelength Excitation Cell-Imaging Application.

Project description:Biological imaging is an essential means of disease diagnosis. However, semiconductor quantum dots that are used in bioimaging applications comprise toxic metal elements that are nonbiodegradable, causing serious environmental problems. Herein, we developed a novel ecofriendly solvothermal method that uses ethanol as a solvent and doping with chlorine atoms to prepare highly fluorescent graphene quantum dots (GQDs) from seaweed. The GQDs doped with chlorine atoms exhibit high-intensity white fluorescence. Thus, their preliminary application in bioimaging has been confirmed. In addition, clear cell imaging could be performed at an excitation wavelength of 633 nm.

| S-EPMC8400823 | biostudies-literature

Excitation wavelength dependence of the fluorescence kinetics in Photosystem I particles from Synechocystis PCC 6803 and Synechococcus elongatus.

Project description:The excitation-wavelength dependence of the excited-state dynamics of monomeric and trimeric Photosystem I (PSI) particles from Synechocystis PCC 6803 as well as trimeric PSI particles from Synechococcus elongatus has been studied at room temperature using time-resolved fluorescence spectroscopy. For aselective (400 nm), carotenoid (505 nm), and bulk chlorophyll (approximately 650 nm) excitation in all species, a downhill energy-transfer component is observed, corresponding to a lifetime of 3.4-5.5 ps. For selective red excitation (702-719 nm) in all species, a significantly faster, an approximately 1-ps, uphill transfer component was recorded. In Synechococcus PSI, an additional approximately 10-ps downhill energy-transfer component is found for all wavelengths of excitation, except 719 nm. Each of the species exhibits its own characteristic trap spectrum, the shape of which is independent of the wavelength of excitation. This trap spectrum decays in approximately 23 ps in both monomeric and trimeric Synechocystis PSI and in approximately 35 ps in trimeric Synechococcus PSI. The data were simulated based on the 2.5 A structural model of PSI of Synechococcus elongatus using the Förster equation for energy transfer, and using the 0.6-1-ps charge-separation time and the value of 1.2-1.3 for the index of refraction that were obtained from the dynamics of a hypothetical PSI particle without red chls. The experimentally obtained lifetimes and spectra were reproduced well by assigning three of the chlorophyll-a (chla) dimers observed in the structure to the C708/C702RT pool of red chls present in PSI from both species. Essential for the simulation of the dynamics of Synechococcus PSI is the assignment of the single chla trimer in the structure to the C719/C708RT pool present in this species.

| S-EPMC1303690 | biostudies-literature

Visible to near-IR fluorescence from single-digit detonation nanodiamonds: excitation wavelength and pH dependence.

Project description:Detonation nanodiamonds are of vital significance to many areas of science and technology. However, their fluorescence properties have rarely been explored for applications and remain poorly understood. We demonstrate significant fluorescence from the visible to near-infrared spectral regions from deaggregated, single-digit detonation nanodiamonds dispersed in water produced via post-synthesis oxidation. The excitation wavelength dependence of this fluorescence is analyzed in the spectral region from 400?nm to 700?nm as well as the particles' absorption characteristics. We report a strong pH dependence of the fluorescence and compare our results to the pH dependent fluorescence of aromatic hydrocarbons. Our results significantly contribute to the current understanding of the fluorescence of carbon-based nanomaterials in general and detonation nanodiamonds in particular.

| S-EPMC5802785 | biostudies-other

Dynamical strengthening of covalent and non-covalent molecular interactions by nuclear quantum effects at finite temperature.

Project description:Nuclear quantum effects (NQE) tend to generate delocalized molecular dynamics due to the inclusion of the zero point energy and its coupling with the anharmonicities in interatomic interactions. Here, we present evidence that NQE often enhance electronic interactions and, in turn, can result in dynamical molecular stabilization at finite temperature. The underlying physical mechanism promoted by NQE depends on the particular interaction under consideration. First, the effective reduction of interatomic distances between functional groups within a molecule can enhance the n → π* interaction by increasing the overlap between molecular orbitals or by strengthening electrostatic interactions between neighboring charge densities. Second, NQE can localize methyl rotors by temporarily changing molecular bond orders and leading to the emergence of localized transient rotor states. Third, for noncovalent van der Waals interactions the strengthening comes from the increase of the polarizability given the expanded average interatomic distances induced by NQE. The implications of these boosted interactions include counterintuitive hydroxyl-hydroxyl bonding, hindered methyl rotor dynamics, and molecular stiffening which generates smoother free-energy surfaces. Our findings yield new insights into the versatile role of nuclear quantum fluctuations in molecules and materials.

| S-EPMC7815839 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data