scholarly journals Effect of Rate and Quantum Yield of 1-alkyl-2-(arylazo) Imidazoles on the Surface of Silver Nps

2021 ◽  
Vol 37 (5) ◽  
pp. 1229-1234
Author(s):  
Pallab Gayen

1-Alkyl-2-(arylazo)imidazole(RaaiR/) exists in trans-structure about –N=N- bond at ambient condition. Upon optical excitation in UV region the trans-RaaiR/ isomerises to cis-RaaiR/. The photochromism is very susceptible to internal substituents and external environment like solvent polarity, viscosity and presence of innocent foreign molecule. The changes from cis-to-trans occurs slowly in visible light excitation it has significantly faster rate at higher temperature. In this work we have studied the effect of silver nanoparticle on the photochromic activity of RaaiR/. The quantum yield of the photoisomerisation is dropped by 9-27% in inclusion phase AgNPs@RaaiR/ than free state and the order of rate is: free state > silver nano particle. The activation energy (Ea) of cis to trans isomerisation is also diminished compared to free state of photochrome.

1987 ◽  
Vol 109 ◽  
Author(s):  
D. Moses ◽  
S. Phillips ◽  
M. Sinclair ◽  
A. J. Heeger

ABSTRACTConducting polymers have been found to be rather good photoconductors in the sub-nansecond time regime. The TP measurement is an effective probe for determining carrier photogeneration quantum yield as well as for investigating transport mechanisms. Here, we present a short survey of our results for a few interesting polymeric systems. We start with the trans-(CH)x grown by the Shirakawa method. We then compared the TP results to those obtained from PDA-TS which currently is the only conjugated polymer in single crystal form. From this comparison, we are able to gauge the improvements in the material quality as was demonstrated by recent TP in trans-(CH)x grown by the Naarmann method


Theranostics ◽  
2013 ◽  
Vol 3 (5) ◽  
pp. 306-316 ◽  
Author(s):  
Qiuqiang Zhan ◽  
Sailing He ◽  
Jun Qian ◽  
Hao Cheng ◽  
Fuhong Cai

2017 ◽  
Vol 56 (14) ◽  
pp. 3842-3846 ◽  
Author(s):  
Alessio Valentini ◽  
Daniel Rivero ◽  
Felipe Zapata ◽  
Cristina García-Iriepa ◽  
Marco Marazzi ◽  
...  

1985 ◽  
Vol 40 (8) ◽  
pp. 859-863
Author(s):  
G. Olbrich ◽  
P. Nikolov ◽  
F. Fratev ◽  
O. E. Polansky

For a series of carbonyl-containing compounds with a stilbene subchromophore the lowest ten singlet and triplet states have been calculated with the aid of the CNDO/S-CI method. The results were used to rationalize the relative ordering of the lowest-lying S(ππ*), S(ππ*), T(ππ*), and T(ππ*) electronic states. Using the calculated energy separation between the singlet ππ*and nπ* states and between the singlet ππ* and triplet nπ* states the fluorescence ability of the compounds studied is interpreted. The connection between the structure of the compounds and their fluorescence is discussed. It is shown that an increase of the solvent polarity in some cases may lead to an inversion of the singlet nπ* and ππ* levels and to an enhancement of the fluorescence quantum yield.


2019 ◽  
Author(s):  
Norah Z. Alqahtani ◽  
Toni G. Blevins ◽  
Catherine McCusker

Photocatalysis is a promising method to harness solar energy and use it to form fuels and other high value chemicals, but most sensitizers used in photocatalytic reactions are complexes of rare and expensive metals such as ruthenium and iridium. Zinc dipyrromethene complexes have potential to be a more earth-abundant alternative, but their photophysical properties are largely unexplored. In this study, triplet state formation was quantified in two zinc dipyrromethene complexes, with a and without heavy atoms, by transient absorption spectroscopy. Without heavy atoms the triplet quantum yield was 16% in toluene and 27% in THF. With the addition of heavy I atoms the triplet quantum yield is increased to 62-63% and is insensitive to solvent polarity. These triplet yields meet or exceed those of successful organic photosensitizers, illustrating the potential for zinc dipyrromethene complexes as photosensitizers


2012 ◽  
Vol 184-185 ◽  
pp. 868-871
Author(s):  
Jing Liu

Series of the triazene-cinnamic acid polymeric fluorescent brighteners were synthesized through three-step condensation reactions and polymerization reaction with styrene under replacing one of amino compounds of traditional fluorescent brighteners by cinnamic acid. The optical properties in aqueous solutions and N,N’- dimethyl formamide as well as paper coating application test were evaluated. The results showed that the light stability and fluorescence quantum yield of polymeric fluorescent brighteners was improved obviously and photoinduced isomerization was lower. Meanwhile the optical properties of polymeric fluorescent brightener were affected by concentration and solvent polarity, fluorescence quantum yield increasing and hypochromatic shift of fluorescence emmission wavelength with the decrease of solvent polarity. When the concentration was over 1 10-4 g/mL, the fluorescence was quenched.


2021 ◽  
Author(s):  
Shivaprasadagouda Patil ◽  
Mahanthesh M. Basanagouda ◽  
Sudhir M. Hiremath ◽  
Aishwarya Nadgir ◽  
Malatesh S Pujar ◽  
...  

Abstract The electronic absorption and fluorescence emission spectra of N-(2,5-dimethyl-pyrrol-1-yl)-2-(5-methoxybenzofuran-3-yl)acetamide (DPMA) molecule were recorded in various solvents at room temperature with the aim of estimation of ground state (\({\mu }_{g}\)) and excited states (\({\mu }_{e}\)) dipole moments using Lippert’s, Bakshiev’s and Kawski-Chamma-Viallete’s equations. The results were signified that, the excited state dipole moment is greater than the ground state dipole moment, which indicates the excited state dipole moment is more polar than the ground state dipole moment. Ecofriendly green synthesis of silver nanoparticles (Ag NPs) were synthesized using catharanthus roseus (C.R) leaf extract was done. These synthesized Ag NPs were used as fluorescence quenchers. Fluorescence lifetime measurement is carried out using time correlated single photon counting technique of DPMA molecule with various concentrations of Ag NPs. A linear Stern-Volmer (S-V) plot was obtained in steady state and transient state method. Furthermore we have estimated computational calculations such as ground state optimized geometry, molecular electrostatic potential (MEP), highest occupied molecular orbital (HOMO), lowest unoccupied molecular orbital (LUMO), experimental and theoretical energy band gap, solvent polarity and normalized solvent polarity values. Morphology and sizes of green synthesized silver NPs were characterized by transmission electron microscopy (TEM) with energy dispersive X-ray spectroscopy (EDX) and also characterized by UV-Visible absorption.


1987 ◽  
Vol 65 (7) ◽  
pp. 1631-1638 ◽  
Author(s):  
Hélène Deslauriers ◽  
Wlodzimiercz Makulski ◽  
Guy J. Collin

A complete study of the 184.9 nm photolysis of cis- and trans-2-butene has been done in the gas phase. The main primary processes (>90%) are the α(C—C) and β(C—H) bond ruptures. Both processes have similar quantum yield values in cis-2-butene: [Formula: see text]. Conversely, the α(C—C) bond rupture is more important in trans-2-butene: [Formula: see text]. These values are compared with those measured in propene (0.57) and isobutene (0.95). No simple molecular property seems sufficient to explain such an effect.


2019 ◽  
Author(s):  
Norah Z. Alqahtani ◽  
Toni G. Blevins ◽  
Catherine McCusker

Photocatalysis is a promising method to harness solar energy and use it to form fuels and other high value chemicals, but most sensitizers used in photocatalytic reactions are complexes of rare and expensive metals such as ruthenium and iridium. Zinc dipyrromethene complexes have potential to be a more earth-abundant alternative, but their photophysical properties are largely unexplored. In this study, triplet state formation was quantified in two zinc dipyrromethene complexes, with a and without heavy atoms, by transient absorption spectroscopy. Without heavy atoms the triplet quantum yield was 16% in toluene and 27% in THF. With the addition of heavy I atoms the triplet quantum yield is increased to 62-63% and is insensitive to solvent polarity. These triplet yields meet or exceed those of successful organic photosensitizers, illustrating the potential for zinc dipyrromethene complexes as photosensitizers


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