研究目的
Reinvestigation of the excited state protonation of 7,8-benzoquinoline through steady state and time-resolved fluorescence study in various solvents and pH conditions.
研究成果
The study provides new insights into the role of hydrogen bonding in excited state proton transfer (ESPT) reactions of 7,8-BQ. It was found that ESPT occurs in both water and TFE, with the process being faster in TFE due to stronger hydrogen bonding. The study also estimated more accurate ESPT rates than previously reported.
研究不足
Sample solubility is low in nonpolar solvents and neutral and basic pH which might reflect in slight uncertainty in the measurement of quantum yield. Low intensity at pH 7 of protonated species may also lead to some uncertainty in lifetime values.
1:Experimental Design and Method Selection:
The study involved steady state and time-resolved fluorescence measurements of 7,8-BQ in a series of organic solvents with varying proticity, polarity, and pH. The effect of hydrogen bonding on protonation was explored in water and trifluoroethanol (TFE).
2:Sample Selection and Data Sources:
7,8-Benzoquinoline (7,8-BQ) was obtained from Sigma Aldrich, USA. Solvents used were of spectroscopic grade. Different pH solutions were prepared using buffer capsules, H2SO4, and NaOH.
3:List of Experimental Equipment and Materials:
Absorption spectra were recorded with Lambda-750, Perkin-Elmer UV/VIS/NIR spectrophotometer and UV–Visible Double beam Systronics Model No: 2203 spectrophotometer. Photoluminescence (PL) spectra were collected by Horiba Jobin Yvon Fluorolog-3. Fluorescence decay times were recorded with Edinburgh-199 time domain spectrometer and Delta Flex TCSPC spectrometer of Horiba Jobin Yvon IBH Ltd.
4:Fluorescence decay times were recorded with Edinburgh-199 time domain spectrometer and Delta Flex TCSPC spectrometer of Horiba Jobin Yvon IBH Ltd. Experimental Procedures and Operational Workflow:
4. Experimental Procedures and Operational Workflow: The concentration of the solutions used was 10-4 M. Steady state and time-resolved measurements were conducted at various pH levels and in different solvents. Decay curves were analyzed using FAST software and Horiba Delta Flex instrument software.
5:Data Analysis Methods:
Time-resolved fluorescence decay curves were analyzed by deconvoluting the observed decay with the instrument response function (IRF) to obtain the intensity decay function represented as a sum of discrete exponentials. Quantum yield was calculated using a reference method.
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Lambda-750
750
Perkin-Elmer
UV/VIS/NIR spectrophotometer for recording absorption spectra
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Edinburgh-199
199
Edinburgh
Time domain spectrometer for recording fluorescence decay times
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UV–Visible Double beam Systronics
2203
Systronics
Spectrophotometer for recording absorption spectra
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Horiba Jobin Yvon Fluorolog-3
Fluorolog-3
Horiba Jobin Yvon
Equipped with double-grating at excitation as well as at emission monochromators and Hamamatsu R928P photomultiplier tube (PMT) for collecting photoluminescence (PL) spectra
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Delta Flex TCSPC spectrometer
Delta Flex
Horiba Jobin Yvon IBH Ltd
Time correlated single photon counting (TCSPC) technique for collecting decay curves
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