Morpholinyl dendrimer phthalocyanine: synthesis, photophysical properties and photoinduced intramolecular electron transfer

2018 ◽  
Vol 47 (37) ◽  
pp. 13164-13170 ◽  
Author(s):  
Qiumei Guo ◽  
Limin Chen ◽  
Sujuan Pan ◽  
Dongdong Ma ◽  
Xiwen Liu ◽  
...  

The photophysical properties of a novel series of morpholinyl dendrimer phthalocyanines exhibited dependence on the number of morpholinyl groups and the central ion. The photoinduced electron transfer from the morpholinyl units to phthalocyanine ring was evidenced.

2015 ◽  
Vol 6 (4) ◽  
pp. 2419-2426 ◽  
Author(s):  
Karolina A. Korzycka ◽  
Philip M. Bennett ◽  
Eduardo Jose Cueto-Diaz ◽  
Geoffrey Wicks ◽  
Mikhail Drobizhev ◽  
...  

We present a modular approach to photo-labile protecting groups based on photoinduced electron transfer, providing high sensitivity to two-photon excitation.


2019 ◽  
Vol 6 (11) ◽  
pp. 1885-1890 ◽  
Author(s):  
Shengsheng Cui ◽  
Guilin Zhuang ◽  
Jinyi Wang ◽  
Qiang Huang ◽  
Shengda Wang ◽  
...  

A novel multifunctionalized carbon nanoring was facilely synthesized, which demonstrates an unusual hypsochromic shift in the emission spectrum with interesting photophysical properties.


2019 ◽  
Vol 55 (36) ◽  
pp. 5251-5254 ◽  
Author(s):  
Yusen Luo ◽  
Maria Wächtler ◽  
Kevin Barthelmes ◽  
Andreas Winter ◽  
Ulrich S. Schubert ◽  
...  

Photoinduced electron transfer via hopping is generally considered to have a stronger temperature dependence than electron transfer via superexchange.


2014 ◽  
Vol 136 (32) ◽  
pp. 11428-11435 ◽  
Author(s):  
Samantha E. Brown-Xu ◽  
Malcolm H. Chisholm ◽  
Christopher B. Durr ◽  
Terry L. Gustafson ◽  
Thomas F. Spilker

2010 ◽  
Vol 82 (3) ◽  
pp. 613-624 ◽  
Author(s):  
Tien-Yau Luh

A summary of recent advances in the chemistry and photophysics of alternating dialkylsilylene-divinylarene copolymers is presented. The silicon moieties are considered to be insulating tetrahedral spacers in these copolymers. The substituents on silicon can readily be tuned, and the steric environment of these substituents around the silicon may dictate the conformation (or helicity) of the copolymers (the Thorpe–Ingold effect) and hence their photophysical properties. Because different chromophores can be regioregularly introduced into the polymeric chain, these copolymers have been used as models to study energy transfer and photoinduced electron transfer (PET), as well as chiroptical transfer.


2003 ◽  
Vol 07 (06) ◽  
pp. 405-414 ◽  
Author(s):  
Mitsunari Itou ◽  
Mamoru Fujitsuka ◽  
Yasuyuki Araki ◽  
Osamu Ito ◽  
Hiroaki Kido

Photochemical and photophysical properties of self-assembling 5-(4-pyridyl)-10,15,20-triphenylporphinatozinc ( Znpyp 3) have been studied by steady-state and time-resolved absorption in addition to time-resolved fluorescence spectroscopy. Self-assembling oligomers ( Znpyp 3)n( n = 3 at 0.1 mM) were synthetically generated and assigned to a zigzag chain oligomeric structure, where n is dependant on the concentration and temperature. The lifetimes of the singlet and triplet excited states of ( Znpyp 3)n depend on n and the axial ligation. The rate-constant of ( Znpyp 3)n for the intermolecular T-T annihilation process was smaller than that of monomeric porphyrins. In the photoinduced electron-transfer to fullerenes ( C 60 and C 70), it was revealed that the rate-constants and efficiencies for ( Znpyp 3)n were essentially the same as those of the monomer. In the back electron transfer, the rate-constants of oligomers were smaller than that of the monomeric porphyrin, which suggests hole-delocalization along the porphyrin chain.


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