Hydroxypropyl-β-Cyclodextrin Enhanced Determination for the Vitamin B<Subscript>12</Subscript> by Fluorescence Quenching Method

A novel fluorescence quenching method for the determination of Vitamin B₁₂(VB₁₂) had been developed. It was based on that the fluorescence intensity of erythrosine sodium(ES) could be enhanced by Hydroxypropyl-β-cyclodextrin(HP-β-CD) due to the formation of inclusion complex (HP-β-CD-ES), while the fluorescence intensity of HP-β-CD-ES was diminished after adding VB₁₂ into the system, and there was a linear relationship between the fluorescence quenching value of the system (ΔF) and the concentration of VB₁₂(c). The mechanism of the determination of VB₁₂was discussed. The results showed that under the optimal conditions, the linear range of calibration curve for the determination of VB₁₂ was 0.0∼2.1 × 10⁻⁵ mol/L, and the detection limit was 1.8×10⁻⁷ mol/ L. It could be satisfactorily applied to the determination of VB₁₂ in injections.     

Fluorescence switch of dye-infiltrated SiO<Subscript>2</Subscript> inverse opal based on acid-base vapors or light

The acid-base vapors/light double responsive dye-infiltrated SiO₂ inverse opal photonic crystals (PCs) were fabricated by sacrificial template method and a subsequent infiltration of spiropyran derivative dye molecules. The fluorescence of ring-open dye molecules infiltrated in PCs can be switched on/off based on different fluorescence properties of spiropyran dye under stimuli of acid-base vapors or light, when PCs with suitable stopband were selected. The fluorescence switch behavior based on PCs has potential applications in data storage, color displays, chemical and biological sensors.     

Fluorescence Spectrum Characteristics of Gold Nanorods

Aqueous solutions containing a high yield of suspended gold nanorods with mean aspect ratio 2.5 have been synthesized via an electrochemical method. The fluorescence emission peaks fixed at 37Onm and 670nm are due to the local field enhancement via coupling to the transverse and longitudinal surface plasmon resonance.The quasi-static calculation results indicate that with the increasing aspect ratio of the nanorods, the longer wavelength emission peak decreases and red shifts, whereas the shorter wavelength emission peak blue shifts slightly.     

An Efficient Fluorescence “Turn-On” Chemosensor Comprising of Coumarin and Rhodamine Moieties for Al<Superscript>3+</Superscript> and Hg<Superscript>2+</Superscript>

A potent fluorescence ‘turn-on’ receptor (HL) based on rhodamine and coumarin moieties for the detection of Hg²⁺ and Al³⁺ is synthesized by condensation of rhodamine 6G hydrazide and 4-hydroxy-3-acetylcoumarin. In presence of Al³⁺ and/or Hg²⁺ the receptor (HL) exhibits deep pink colouration and a sharp band at 528 nm is appeared in UV–vis titration. Upon gradual addition of Al³⁺ and/or Hg²⁺ to the solution of HL significant enhancement of fluorescence intensity is observed at 564 nm in MeCN:H₂O (1:5, v/v) medium. The receptor is strongly bound to Al³⁺ and/or Hg²⁺ and the association constants (K_a) are found to be 1.74?×?10⁴ and 1.04?×?10⁴ M^??1 for Al³⁺ and Hg²⁺ respectively.

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Graphical Abstract A potent fluorescence ‘turn-on’ receptor (HL) based on rhodamine and coumarin moieties for the detection of Hg²⁺ and Al³⁺ is synthesized and characterized. In presence of Al³⁺ and/or Hg²⁺ the receptor (HL) exhibits deep pink colouration and significant enhancement of fluorescence intensity is observed at 564 nm in MeCN:H₂O (1:5, v/v) medium. The receptor is strongly bound to Al³⁺ and/or Hg²⁺ and the association constants (K_a) are found to be 1.74?×?10⁴ and 1.04?×?10⁴ M^??1 for Al³⁺ and Hg²⁺ respectively.

     

Enhancement of the Fluorescence Quenching Efficiency of DPPH<Superscript>•</Superscript> on Colloidal Nanocrystalline Quantum Dots in Aqueous Micelles

Luminescent CdS quantum dots capped with thioglycolic acid (CdS-TGA QDs) were demonstrated to serve as a fluorescence probe for a model organic radical, 2,2-diphenyl-1-picrylhydrazyl radical (DPPH^•), employing the quenching of the CdS-TGA QDs emission signal by the radical. Under the optimum conditions, the quenching efficiency of DPPH^• on CdS-TGA QDs was proportional to the concentration of DPPH^•, following Stern-Volmer relationship. Different types of surfactants (cationic, anionic and neutral surfactants) were introduced to CdS-TGA QDs in order to increase the detection sensitivity. The fluorescence intensity of CdS-TGA QDs was greatly enhanced by cationic and neutral surfactants. Moreover, the quenching efficiency of DPPH^• on the QDs in the presence of micelles was remarkably ca. 13 times higher than that in the system without micelles. Effects of pH and concentration of surfactants on the fluorescence quenching of CdS-TGA QDs were investigated. Electron spin resonance (ESR) spectroscopy was also used to monitor the DPPH radical species in CdS-TGA QDs mixtures with and without micelles. Fluorescence quenching mechanisms of CdS-TGA QDs by DPPH^• in the presence and in the absence of CTAB were proposed.     

On the RbBr:Cu☎ Fluorescence

The fluorescence of Cu^? in RbBr was investigated in the temperature range 20–300 K, by recording both emission and excitation spectra and by performing accurate lifetime and quantum yield measurements. The de-excitation mechanism has been interpreted in terms of the traditional Pedrini model. Nevertheless, a change of the compression conditions for Cu^? at low temperature was observed, which implies two temperature regions (above and below 40 K) for the decay parameters. This occurrence is related not only to off-centre configuration but also to a very low value for the Cu^? radius when compared to the Rb^? one in RbBr.     

Study on the New Fluorescence Enhancement System of Tb –N-(2 - Pyridinyl) Ketoacetamide-Et<Subscript>3</Subscript>N-Zn and its Application

A sensitive fluorescence enhancement system was developed for the determination of zinc (II). The fluorescence intensity of the Tb- N- (2 - Pyridinyl) ketoacetamide (PKA) system was greatly enhanced by the addition of triethylamine (Et₃N) and zinc nitrate in the methanol solution. The excitation and emission wavelengths were 329 nm and 546 nm, respectively. Under optimal conditions, the fluorescence intensities varied linearly with the concentration of Zn²⁺ in the range of 8.0×10⁻⁷−5.0×10⁻⁶ M with a detection limit of 9.9×10⁻⁸ M. The interferences of some substances were described. This method was applied to the determination of amounts of Zn²⁺ in soybean, rice, and wheat, respectively. The results showed that the proposed procedure is a high selective, simple, and rapid method to the determination of Zn²⁺ ion. The mechanism of fluorescence enhancement was also studied.     

Fluorescence Microscopy of Nanoscale Silver Oxide Thin Films

The experimental conditions for photoactivated intermittent fluorescence from nanoscale silver oxide were studied with fluorescence microscopy.Strong fluorescence was observed from the Ag2O particles with size of 10-20nm excited with both blue and green light .We observed the saturation of Photoexcitation with blue light and explained the experimental results using the model of agglomeration of silver atoms to form small clusters and the fluorescence of Ag2 and Ag3 clusters.     

Strong Correlation of Fluorescence Photons without Quantum Interference

It has been predicted that a driven three-level V atom can emit strongly correlated fluorescence photons in the presence of quantum interference. Here we examine the effects of quantum interference on the intensity correlation of fluorescence photons emitted from a driven three-level A atom. Unexpectedly, strong correlation occurs without quantum interference. The quantum interference tends to reduce the correlation function to a normal level. The essential difference between these two cases is traced to the different effects of quantum interference on coherent population trapping （OPT）. For the V atom, quantum interference and coherent excitation combine to lead to OPT. For the A atom, however, the quantum interference tends to spoil OPT while the coherent excitation induces the effect.     

Fluorescence Quenching Studies of 1,3‐Diphenyl Benzene

Fluorescence quenching of 1,3‐diphenyl benzene (m‐terphenyl) by carbon tetrachloride (CCl₄) at steady state in different solvents, namely n‐hexane, n‐heptane, cyclohexane, toluene, benzene acetonitrile, 1,4‐dioxane, and with a transient method in benzene has been done at room temperature to understand the role of quenching mechanisms. The Stern–Volmer plot was found to be linear for all the solvents studied. The probability of quenching per encounter p was determined in all the solvents and was found to be less than unity. Further, from the studies of rate parameters and lifetime measurements in benzene at different temperatures (30–60°C), it was shown that the phenomenon of quenching is generally governed by the well‐known Stern–Volmer (S‐V) plot. The activation energy E _a (E′_a) of quenching was determined using literature values of activation energy of diffusion E _d, and it was found to be greater than E _d, which confirms the fact that the quenching mechanism is not solely due to material diffusion but there is also contribution from activation energy.     

Two-photon Induced UV Fluorescence in Photo-active Spiropyran Molecules

Ｔｗｏ－ｐｈｏｔｏｎＩｎｄｕｃｅｄＵＶＦｌｕｏｒｅｓｃｅｎｃｅｉｎＰｈｏｔｏ－ａｃｔｉｖｅＳｐｉｒｏｐｙｒａｎＭｏｌｅｃｕｌｅｓ￥ＣＨＩＬｕｎｇｕａｎｇ；ＷＡＮＧＺｕｇｅｎｇ（ＤｅｐａｒｔｍｅｎｔｏｆＰｈｙｓｉｃｓ，ＥａｓｔＣｈｉｎａＮｏｒｍａｌＵｎ...     

A New Thiosemicarbazone-Based Fluorescence “Turn-on” Sensor for Zn<Superscript>2+</Superscript> Recognition with a Large Stokes Shift and its Application in Live Cell Imaging

Selective fluorescence turn on Zn²⁺ sensor with long-wavelength emission and a large Stokes shift is highly desirable in Zn²⁺ sensing area. We reported herein the synthesis and Zn²⁺ recognition properties of a new thiosemicarbazone-based fluorescent sensor L. L displays high selectivity and sensitivity toward Zn²⁺ over other metal ions in DMSO-H₂O (1:1, v/v, HEPES 10 mM, pH = 7.4) solution with a long-wavelength emission at 572 nm and a large Stokes shift of 222 nm. Confocal fluorescence microscopy experiments demonstrate that L is cell-permeable and capable of monitoring intracellular Zn²⁺.

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Graphical Abstract We report a new thiosemicarbazone-based fluorescent sensor (L) for selective recognition of Zn²⁺ with a long wavelength emission and a large Stokes shift.

     

Time Resolved Fluorescence and Energy Transfer Analysis of Nd<Superscript>3+</Superscript>–Yb<Superscript>3+</Superscript>–Er<Superscript>3+</Superscript> Triply-Doped Ba–Al-Metaphosphate Glasses for an Eye Safe Emission (1.54 μm)

This paper reports on the preparation and systematic analysis of energy transfer mechanisms in Nd³⁺–Yb³⁺–Er³⁺ co-doped new series of barium-alumino-metaphosphate glasses. The time resolved fluorescence of Nd³⁺ in triply doped Ba–Al-metaphosphate glasses have revealed that, Yb³⁺ ions could function as quite efficient bridge for an energy transfer between Nd³⁺ and Er³⁺ ions. As a result, a fourfold emission enhancement at 1.54 μm of Er³⁺ ions has been achieved through an excitation of ⁴F_5/2 level of Nd³⁺ at 806 nm for the glass having 3 mol% Yb³⁺ with an energy transfer efficiency reaching up to 94%. Decay of donor (Nd³⁺) ion fluorescence has been analyzed based on theoretical models such as direct energy transfer model (Inokuti–Hirayama) and migration assisted energy transfer models (Burshtein’s hopping and Yokota–Tanimoto’s diffusion). The corresponding energy transfer parameters have been evaluated and discussed. Primarily, electrostatic dipole–dipole (s ~ 6) interactions are found to be responsible for the occurrence of energy transfer process in theses glasses.     

Synthesis and Fluorescence Properties of Donor-Acceptor-Substituted Novel Dipyrazolo[3,4-<Emphasis Type="Italic">b</Emphasis>:3′,4′-<Emphasis Type="Italic">d</Emphasis>]Pyridines (DPP)

A rapid and efficient method for the synthesis of novel dipyrazolo[3,4-b:3′,4′-d]pyridines (DPP) from pyrazolo[3,4-b]pyridine was successfully developed. The DPP derivative was further N-alkylated (6, 8) as well as N-linked with amino acids (13) and their photophysical properties were studied along with N-aryl DPP 4 and observed that the chromophores at C₄ position in the aryl ring changed the absorption and emission λ_max.     

Investigation of a Tabletop Confocal Micro X-Ray Fluorescence Setup

A new tabletop confocal micro x-ray fluorescence setup with an MCBM 50-0.6B x-ray tube is assembled. The confocal micro x-ray fluorescence setup includes two lenses, a polycapillary full lens in the excitation channel and a polycapillary half lens in the detection channel. A Ni-Cr wire in diameter 25μm is used to investigate the FWHM of three-dimensional confocal volume. A basso-relievo capital letter of a 1-jiao RMB coin of 2005 version is studied with this confocal micro x-ray fluorescence setup.     

The Calibration Kit Spectral Fluorescence Standards—A Simple and Certified Tool for the Standardization of the Spectral Characteristics of Fluorescence Instruments

With the Calibration Kit Spectral Fluorescence Standards BAM-F001-BAM-F005, we developed a simple tool for the characterization of the relative spectral responsivity and the long-term stability of the emission channel of fluorescence instruments under routine measurement conditions thereby providing the basis for an improved comparability of fluorescence measurements and eventually standardization. This first set of traceable fluorescence standards, which links fluorescence measurements to the spectral radiance scale in the spectral range of 300-770 nm and has been optimized for spectrofluorometers, can be employed for different measurement geometries and can be adapted to different fluorescence techniques with proper consideration of the underlying measurement principles.     

Optimal Feedback Control of Two-Photon Fluorescence Based on Genetic Algorithm

An optimal feedback control of two-photon fluorescence in the ethanol solution of 4-dicyanomethylene-2-methyl- 6-p-dimethyl-aminostryryl-4H-pyran （DCM） using pulse-shaping technique based on genetic algorithm is demon- strated experimentally. The two-photon fluorescence of the DCM ethanol solution is enhanced in intensity of about 23%. The second harmonic generation frequency-resolved optical gating （SHG-FROG） trace indicates that the effective population transfer arises from the positively chirped pulse. The experimental results appear the potential applications of coherent control to the complicated molecular system.     

Multi—photon Absorption Induced Fluorescence of a Novel Compound

The linear and nonlinear fluorescence spectra of 5-(9-anthryl)-3-(4-nitrophenyl)-1-phenyl-2-pyrazoline (ANPP) have been studied in different polarity solvents.The linear fluorescence spectrum of ANPP has two emission bands originating from the anthryl and pyrazoline moieties of ANPP on excitation at 355nm.The nonlinear two-photon and three-photon fluorescence from these two moieties are observed simultaneously when ANPP is excited at 1064 nm due to the proximity of the absorption bands of these two moieties to λ/3 and λ/2 of the exciting wavelength.The similar spectrum structure indicates that the nonlinear and linear fluorescence originates from the same relaxation process.