[Spectroscopic investigation of 3-hydroxyflavone in different polarity and pH values solutions].

Guang Pu Xue Yu Guang Pu Fen Xi

Institute of Modern Optics, Nankai University, Key Laboratory of Optoelectronics Information Science and Technology, Ministry of Education, Tianjin 300071, China.

Published: April 2009

The absorption and fluorescence spectra of 3-hydroxyflavone (3-HF) in different polar solvents were observed with UV-Vis spectrometer and fluorescence spectrometer, respectively. There are three absorption bands in the absorption spectra, wherein two absorption bands with absorption peak at 300 and 345 nm, respectively, are strong, and the other one with absorption peak at 415 nm is weak When the samples in different polar solvents were excited by 345 nm light, there appeared two new fluorescence bands peaked at 400 and 526 nm, respectively. The fluorescence band at 400 nm is attributable to the emission from enol structure and its intensity increases with increasing the polarity of protic solvents; that at 526 nm is attributable to the emission from the isomer structure and its intensity decreases with increasing the polarity of protic solvents. The results show that the increase in the polarity of protic solvents prevents the formation of isomer. When the samples in different polar solvents were excited by 415 nm light, three new fluorescence bands peaked at 440, 471 and 515 nm have not been reported so far. In order to identify the three new fluorescence bands, we prepared the samples with pH value of 5.0, 4.0 and 3.0 through incorporating the different amounts of acetic acid into 3-HF solution. The fluorescence spectra in different pH value solution were observed under excitation of 415 nm light, and it was found that the intensity of two fluorescence bands in the region of shorter wavelength changes with pH values changing. For identifying the fluorescence band of 515 nm peak wavelength, we put sodium hydroxide into 3-HF in ethanol solution and prepared 3-HF samples with pH values of 8.0, 8.5, 9.0, and 10.0. When the samples were excited by the 415 nm light, it was found that two fluorescence bands in the region of shorter wavelength disappeared and the intensity of the fluorescence band of 515 nm was enhanced. Since in sodium hydroxide solution 3-HF forms anion easily, we ascribed the fluorescence band with 515 nm peak wavelength to the emission from the 3-HF anion.

Download full-text PDF

Source

Publication Analysis

Top Keywords

fluorescence bands
20
fluorescence band
16
fluorescence
12
polar solvents
12
polarity protic
12
protic solvents
12
415 light
12
band 515
12
fluorescence spectra
8
absorption bands
8

Similar Publications

Nonplanar (butterfly-shaped) phenothiazine () and its derivative's () photophysical and spectral properties have been tuned by varying the solvents and their polarity and investigated employing spectroscopic techniques such as UV-Vis, steady-state and time-resolved fluorescence, and TDDFT calculations. The UV-Vis absorption studies and TDDFT calculations reveal two distinct bands for both compounds: a strong π-π* transition at shorter wavelengths and a weaker -π* transition, which displays a little bathochromic shift in polar solvents. The detailed emission studies reveal that such dual emission is a result of the photoinduced excited-state conjugation enhancement (ESCE) process.

View Article and Find Full Text PDF

To promote the conservation and utilization of the germplasm resources and provide a basis for the breeding of new varieties of Murraya paniculata, this study analyzed the genetic diversity of the germplasm resources and developed the molecular identity(ID) card of M. paniculata. Multiple fluorescence PCR-capillary electrophoresis was performed for 65 germplasm accessions of M.

View Article and Find Full Text PDF

Confined cell migration along extracellular matrix space in vivo.

Proc Natl Acad Sci U S A

January 2025

Center for Complexity and Biosystems, Department of Environmental Science and Policy, University of Milan, 20133 Milan, Italy.

Collective migration of cancer cells is often interpreted using concepts derived from the physics of active matter, but the experimental evidence is mostly restricted to observations made in vitro. Here, we study collective invasion of metastatic cancer cells injected into the mouse deep dermis using intravital multiphoton microscopy combined with a skin window technique and three-dimensional quantitative image analysis. We observe a multicellular but low-cohesive migration mode characterized by rotational patterns which self-organize into antiparallel persistent tracks with orientational nematic order.

View Article and Find Full Text PDF

Herein, a water-soluble, ultrabright, near-infrared (NIR) fluorescent, mechanically interlocked molecules (MIMs)-peptide bioconjugate is designed with dual targeting capabilities. Cancer cell surface overexpressed αβ integrin targeting two RGDS tetrapeptide residues is tethered at the macrocycle of MIMs-peptide bioconjugate via Cu(I)-catalyzed click chemistry on the Wang resin, and mitochondria targeting lipophilic cationic TPP functionality is conjugated at the axle dye. Living carcinoma cell selective active targeting, subsequently cell penetration, mitochondrial imaging, including the ultrastructure of cristae, and real-time tracking of malignant mitochondria by MIMs-peptide bioconjugate (RGDS)-Mito-MIMs-TPP are established by stimulated emission depletion (STED) super-resolved fluorescence microscopy.

View Article and Find Full Text PDF

Electronic spectra for OThF have been recorded using fluorescence excitation and two-photon resonantly enhanced ionization techniques. Multiple vibronic bands were observed in the 340-460 nm range. Dispersed fluorescence spectra provided ground state vibrational constants and evidence of extensive vibronic state mixing at higher excitation energies.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!