scholarly journals Thorpe−Ingold Effect on Photoinduced Electron Transfer of Dialkylsilylene-Spaced Divinylarene Copolymers Having Alternating Donor and Acceptor Chromophores

2007 ◽  
Vol 40 (26) ◽  
pp. 9238-9243 ◽  
Author(s):  
Mei-Yu Yeh ◽  
Hsin-Chieh Lin ◽  
Tsong-Shin Lim ◽  
Shern-Long Lee ◽  
Chun-hsien Chen ◽  
...  
Molecules ◽  
2019 ◽  
Vol 24 (24) ◽  
pp. 4453
Author(s):  
Mugen Yamawaki ◽  
Akiko Asano ◽  
Toshiki Furutani ◽  
Yuki Izumi ◽  
Yosuke Tanaka ◽  
...  

Directly linked donor and acceptor arenes, such as phenanthrene/naphthalene/biphenyl and 1,3-dicyanobenzene were found to work as photoredox catalysts in the photoreactions of indene, 2,3-dimethyl-2-butene, and 4-methoxyphenylacetic acid. The new stable organic photocatalyst forms an intramolecular exciplex (excited complex) when irradiated in a polar solvent and shows redox catalyst activity, even at low concentrations. To the best of our knowledge, this is the first example of an intramolecular exciplex working as a redox catalyst.


2009 ◽  
Vol 13 (10) ◽  
pp. 1090-1097 ◽  
Author(s):  
Helge Lemmetyinen ◽  
Nikolai Tkachenko ◽  
Alexander Efimov ◽  
Marja Niemi

This paper combines the most important results on studies performed by the authors during the last decade on photoinduced electron transfer reactions of pheophytin-, phthalocyanine-, and porphyrin-fullerene dyads, in which donor and acceptor moieties are covalently linked to each other. Practically all studied molecules form an intramolecular exciplex as a transient state before the formation of the charge separation state or tight ion pair. When the center-to-center distance of the donor and acceptor pair is short (7–10 Å) both the exciplex formation and primary electron transfer are extremely fast with rate constants of 7–23 × 1012 s -1 and 40–1400 × 109 s -1, respectively. Rates become slower when the distance and orientational fluctuation increases. No systematic correlation between free energies and the rates of the formation and recombination of the exciplex and the charge separation state, respectively, were observed. The mechanism is discussed in frames of the Marcus electron transfer and the radiationless quantum transition theories.


CrystEngComm ◽  
2018 ◽  
Vol 20 (38) ◽  
pp. 5663-5666 ◽  
Author(s):  
Jia Huang ◽  
Jie Zhang ◽  
Runhua He ◽  
Zhiyong Fu

A novel Cd(ii)-MOF with tunable photophysical behavior has been developed. The control of color, fluorescence emission and conductivity is achieved in a single crystalline conductance switch by incorporating donor and acceptor building blocks into a molecular wire.


2020 ◽  
Author(s):  
Rishikesh Kulkarni ◽  
Anneliese Gest ◽  
Chun Kei Lam ◽  
Benjamin Raliski ◽  
Feroz James ◽  
...  

<p>High signal-to-noise optical voltage indicators will enable simultaneous interrogation of membrane potential in large ensembles of neurons. However, design principles for voltage sensors with high sensitivity and brightness remain elusive, limiting the applicability of voltage imaging. In this paper, we use molecular dynamics (MD) simulations and density functional theory (DFT) calculations to guide the design of a bright and sensitive green-fluorescent voltage-sensitive fluorophore, or VoltageFluor (VF dye), that uses photoinduced electron transfer (PeT) as a voltage-sensing mechanism. MD simulations predict an 11% increase in sensitivity due to membrane orientation, while DFT calculations predict an increase in fluorescence quantum yield, but a decrease in sensitivity due to a decrease in rate of PeT. We confirm these predictions by synthesizing a new VF dye and demonstrating that it displays the expected improvements by doubling the brightness and retaining similar sensitivity to prior VF dyes. Combining theoretical predictions and experimental validation has resulted in the synthesis of the highest signal-to-noise green VF dye to date. We use this new voltage indicator to monitor the electrophysiological maturation of human embryonic stem cell-derived medium spiny neurons. </p>


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