scholarly journals Regulation of bi-color fluorescence changes of AIE supramolecular self-assembly gels by the interaction with Al3+ and energy transfer

2021 ◽  
Author(s):  
Xinxian Ma ◽  
Jinlong Yue ◽  
Bo Qiao ◽  
LIli Zhou ◽  
Yang Gao ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Self Assembly ◽  
Fluorescence Emission ◽  
Fluorescent Materials

Supramolecular fluorescent materials have attracted considerable attention in recent years since they endow specific and unique properties to materials. Nevertheless, the utilization of photo-responsive characteristics to modulate their fluorescence emission...

Tweaking a BODIPY Spherical Self‐Assembly to 2D Supramolecular Polymers Facilitates Excited State Cascade Energy Transfer

2021 ◽  
Author(s):  
Gourab Das ◽  
Sandeep Cherumukkil ◽  
Akhil Padmakumar ◽  
Vijay B. Banakar ◽  
Vakayil K. Praveen ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Excited State ◽  
Self Assembly ◽  
Supramolecular Polymers ◽  
Cascade Energy

Suppressed energy transfer between different rare earth ions to obtain enhanced and tuned fluorescence by using Janus nanofibers

2021 ◽  
Author(s):  
Ping Wu ◽  
Qianli Ma ◽  
Wensheng Yu ◽  
Jinxian Wang ◽  
Gui-Xia Liu ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Rare Earth ◽  
Rare Earth Ions ◽  
Native Fluorescence ◽  
Fluorescent Materials ◽  
Negative Effect

Here, we put forward a viewpoint that the energy transfer between different rare earth (RE) ions plays negative effect in RE ions doped white fluorescent materials if the native fluorescence...

Tweaking a BODIPY Spherical Self‐Assembly to 2D Supramolecular Polymers Facilitates Excited State Cascade Energy Transfer

2021 ◽  
Author(s):  
Gourab Das ◽  
Sandeep Cherumukkil ◽  
Akhil Padmakumar ◽  
Vijay B. Banakar ◽  
Vakayil K. Praveen ◽  
...  
Keyword(s):  
Energy Transfer ◽  
Excited State ◽  
Self Assembly ◽  
Supramolecular Polymers ◽  
Cascade Energy

A New Approach to Fluorescent Chemosensor of Cu2+ Ion

2014 ◽  
Vol 513-517 ◽  
pp. 65-69
Author(s):  
Xiao Jun Hu ◽  
Xin Yan Hu ◽  
Zhi Zhang
Keyword(s):  
Aqueous Solution ◽  
Electron Transfer ◽  
Self Assembly ◽  
Ph Value ◽  
Sodium Dodecyl ◽  
Fluorescence Emission ◽  
Fluorescent Chemosensor ◽  
Dynamic Quenching ◽  
Transfer Effects ◽  
New Approach

According to the principle of dynamic quenching a new ON-OFF fluorescent chemosensor for Cu2+ions was designed, this chemosensor was composed of p-tert-butylthiacalix [arene (TCA),sodium dodecyl sulfate (SDS) and perylene through the form of self-assembly in aqueous solution. Addition of Cu2+ions could result in a quenching of the fluorescence emission of perylene inside micelles, which due to intramicellar complex-fluorophore electron-transfer or energy-transfer effects induced by the complexation of TCA with the Cu2+ions.The experimental results indicated that: Under the condition of TCA/perylene was 800/1, SDS concentration was 150mmol/L and pH value above 9, according to the fluorescence quenching ,within a certain range of the concentration of Cu2+ion can be linearly determined.

Sensitizing effect of Yb3+ on near-infrared fluorescence emission of Cr4+-doped calcium aluminate glasses

2000 ◽  
Vol 15 (2) ◽  
pp. 278-281 ◽  
Author(s):  
Yong Gyu Choi ◽  
Kyong Hon Kim ◽  
Yong Seop Han ◽  
Jong Heo
Keyword(s):  
Energy Transfer ◽  
Calcium Aluminate ◽  
Near Infrared ◽  
Fluorescence Emission ◽  
Dipole Interaction ◽  
Energy Transfer Mechanism ◽  
Efficient Energy Transfer ◽  
Efficient Energy ◽  
Sensitizing Effect ◽  
Decay Behavior

We have demonstrated that an efficient energy transfer takes place from Yb3+ to Cr4+ in calcium aluminate glasses. Yb3+ improves excitation efficiency at around 980 nm, enhancing emission intensity of Cr4+ fluorescence at 1.2–1.6 μm. Nonradiative energy transfer via electric dipole–dipole interaction between ytterbium and chromium ions was found to be dominant over radiative Yb3+ → Cr4+ energy transfer. A diffusionlimited energy transfer mechanism well explains the decay behavior of Yb3+/Cr4+- codoped glasses. This codoping scheme may be applicable to other Cr4+-containing crystals and glasses.

A new twofold interpenetrated two-dimensional cadmium(II) coordination polymer constructed from 2,2′-(benzene-1,4-dicarboxamido)dipropionate

2018 ◽  
Vol 74 (11) ◽  
pp. 1434-1439
Author(s):  
Hong-Tao Zhang ◽  
Xiao-Long Wang
Keyword(s):  
Coordination Polymer ◽  
Coordination Polymers ◽  
Self Assembly ◽  
Fluorescence Emission ◽  
Functional Materials ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carboxylate Groups ◽  
Potential Applications

In recent years, much initial interest and enthusiasm has focused on the self-assembly of coordination polymers due to the aesthetics of their crystalline architectures and their potential applications as new functional materials. As part of an exploration of chiral coordination polymers, a new twofold interpenetrated two-dimensional (2D) coordination polymer, namely, poly[[tetraaquabis[μ3-(2R,2′R)-2,2′-(benzene-1,4-dicarboxamido)dipropionato-κ5 O,O′:O′′,O′′′:O′′]dicadmium(II)] trihydrate], {[Cd2(C14H14N2O6)2(H2O)4]·3H2O} n , has been synthesized by the reaction of Cd(CH3COO)2·2H2O with the designed ligand (2R,2′R)-2,2′-(benzene-1,4-dicarboxamido)dipropionic acid (H2 L). The compound has been structurally characterized by elemental analysis, IR spectroscopy, powder X-ray diffraction and single-crystal X-ray diffraction analysis. In the crystal structure, each CdII cation binds to three carboxylate groups from two crystallographically independent L 2− dianions. Four carboxylate groups link two crystallographically independent cadmium cations into a 4,4-connected secondary building unit (SBU). The resulting SBUs are extended into a two-dimensional folding sheet via the terephthalamide moiety of the ligand as a spacer, which can be simplified as a (4,4)-connected 4,4L15 net with the point symbol (3.53.62)(32.52.62). In the lattice, two independent folding sheets interpenetrate each other to yield a double-sheet layer. The resulting 2D layers pack in parallel arrays through intermolecular hydrogen bonds and interlayer π–π interactions. The thermal stability and photoluminescence properties of the title compound have been investigated and it exhibits an enhanced fluorescence emission and a longer lifetime compared with free H2 L.

scholarly journals Impact of nanosizing a host matrix based on a metal–organic framework on solid-state fluorescence emission and energy transfer

2022 ◽  
Author(s):  
Hikaru Sakamoto ◽  
Akitaka Ito ◽  
Masataka Ohtani
Keyword(s):  
Energy Transfer ◽  
Solid State ◽  
Metal Organic Framework ◽  
Fluorescence Emission ◽  
Dye Molecules ◽  
Host Matrix ◽  
Metal Organic ◽  
Solid State Fluorescence ◽  
Organic Framework

We demonstrate that the nanosize effect appears to affect the properties of dye molecules encapsulated in the pores of a metal–organic framework (dye@MOF). The emissive properties of the nanosized dye@MOF...

scholarly journals Stability of Chlorophyll a Monomer Incorporated into Cremophor EL Nano-Micelles under Dark and Moderate Light Conditions

Molecules ◽  
2020 ◽  
Vol 25 (21) ◽  
pp. 5059
Author(s):  
Ewa Janik-Zabrotowicz ◽  
Marta Arczewska ◽  
Patrycja Prochniewicz ◽  
Izabela Świetlicka ◽  
Konrad Terpiłowski
Keyword(s):  
Chlorophyll A ◽  
Self Assembly ◽  
Molecular Spectroscopy ◽  
Fluorescence Emission ◽  
Molecular Organization ◽  
Cremophor El ◽  
Light Conditions ◽  
Fluorescence Emission Spectra ◽  
Pigment Stability ◽  
The Stability

In this paper, stability of chlorophyll a monomers encapsulated into the Cremophor EL nano-micelles was studied under dark and moderate light conditions, typical of a room with natural or artificial lighting, in the presence of oxygen. The pigment stability against visible light was determined using the dynamic light scattering and molecular spectroscopy (UV-Vis absorption and stationary fluorescence) methods. Chlorophyll a, at the molar concentration of 10−5 M, was dissolved in the 5 wt% Cremophor emulsion for comparison in the ethanolic solution. The stability of such a self-assembly pigment–detergent nano-system is important in the light of its application on the commercial-scale. The presented results indicate the high stability of the pigment monomeric molecular organization in the nano-emulsion. During the storage in the dark, the half-lifetime was calculated as about 7 months. Additionally, based on the shape of absorption and fluorescence emission spectra, chlorophyll aggregation in the Cremophor EL aqueous solution along with the time was excluded. Moreover, the average size of detergent micelles as chlorophyll carriers was not affected after 70 days of the nano-system storage. Pigment stability against the moderate white light (0.1 mW) did not differ significantly from storage conditions in the dark. The photooxidation products, detected by occurrence of new absorption and fluorescence emission bands, was estimated on the negligible level. The stability of such a self-assembly pigment–detergent nano-system would potentially broaden the field of chlorophyll a (chl a) application in the food industry, medicine or artificial photosynthesis models.

FRET Study Between Carbon Quantum Dots and Malachite Green by Steady-State and Time-Resolved Fluorescence Spectroscopy

2020 ◽  
Vol 10 (3) ◽  
pp. 178-188
Author(s):  
Bipin Rooj ◽  
Ankita Dutta ◽  
Debojyoti Mukherjee ◽  
Sahidul Islam ◽  
Ujjwal Mandal
Keyword(s):  
Quantum Dots ◽  
Energy Transfer ◽  
Fluorescence Spectroscopy ◽  
Malachite Green ◽  
Dye Degradation ◽  
Fluorescence Emission ◽  
Carbon Quantum Dots ◽  
Time Resolved Fluorescence ◽  
Physical Processes ◽  
Time Resolved

Background: Understanding the interaction between different organic dyes and carbon quantum dots helps us to understand several photo physical processes like electron transfer, energy transfer, molecular sensing, drug delivery and dye degradation processes etc. Objective: The primary objective of this study is to whether the carbon quantum dots can act as an electron donor and can participate in the different photo physical processes. Methods: In this work, Carbon Quantum Dots (CQDLs) are synthesized in most economical and simple carbonization method where petals of Nelumbo nucifera L. are used as a carbon precursor. The synthesized CQDLs were characterized by using experimental techniques like UV−Vis absorption, FT-IR, Transmission Electron Microscopy (TEM), steadystate and time-resolved fluorescence spectroscopy. Results: The spectral analysis shows that the so synthesized CQDLs are spherical in shape and its diameter is around 4.2 nm. It shows the fluorescence emission maximum at 495 nm with a quantum yield of 4%. In this work the interaction between Carbon Quantum Dots (CQDLs) and an organic dye Malachite Green (MG) is studied using fluorescence spectroscopic technique under ambient pH condition (At pH 7). The quenching mechanism of CQDLs with MG was investigated using Stern-Volmer equation and time-resolved fluorescence lifetime studies. The results show that the dominant process of fluorescence quenching is attributed to Forster Resonance Energy Transfer (FRET) having a donor acceptor distance of 53 Å where CQDLs act as a donor and MG acts as an acceptor. Conclusion: This work has a consequence that CQDLs can be used as a donor species for different photo physical processes such as photovoltaic cell, dye sensitized solar cell, and also for antioxidant activity study.

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