scholarly journals Cover Feature: Competitive Energy and Electron Transfer in β-Functionalized Free-Base Porphyrin-Zinc Porphyrin Dimer Axially Coordinated to C60 : Synthesis, Supramolecular Formation and Excited-State Processes (Chem. Eur. J. 52/2017)

2017 ◽  
Vol 23 (52) ◽  
pp. 12679-12679
Author(s):  
Yi Hu ◽  
Michael B. Thomas ◽  
R. G. Waruna Jinadasa ◽  
Hong Wang ◽  
Francis D'Souza
Keyword(s):  
Electron Transfer ◽  
Excited State ◽  
Free Base ◽  
Zinc Porphyrin ◽  
Energy And Electron Transfer ◽  
Porphyrin Dimer

Unusual Photoinduced Electron Transfer from a Zinc Porphyrin to a Tetrapyridyl Free-Base Porphyrin in a Noncovalent Multiporphyrin Array

2010 ◽  
Vol 16 (29) ◽  
pp. 8748-8756 ◽  
Author(s):  
Barbara Ventura ◽  
Lucia Flamigni ◽  
Maryline Beyler ◽  
Valérie Heitz ◽  
Jean-Pierre Sauvage
Keyword(s):  
Electron Transfer ◽  
Photoinduced Electron Transfer ◽  
Free Base ◽  
Zinc Porphyrin

Photoinduced Electron Transfer from a Higher Excited State of a Porphyrin in a Zinc Porphyrin−Ruthenium(II)tris-Bipyridine Dyad

1999 ◽  
Vol 103 (5) ◽  
pp. 557-559 ◽  
Author(s):  
Denis LeGourriérec ◽  
Mikael Andersson ◽  
Jan Davidsson ◽  
Emad Mukhtar ◽  
Licheng Sun ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Excited State ◽  
Photoinduced Electron Transfer ◽  
Zinc Porphyrin

scholarly journals Comparative analysis of lanthanide excited state quenching by electronic energy and electron transfer processes

2021 ◽  
Author(s):  
David Parker ◽  
Jack Fradgley ◽  
Jurriaan M Zwier ◽  
James William Walton ◽  
Martina Delbianco ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Excited State ◽  
Comparative Analysis ◽  
Relative Sensitivity ◽  
Electronic Energy ◽  
Transfer Processes ◽  
Energy And Electron Transfer ◽  
Electron Transfer Processes ◽  
Excited State Quenching ◽  
The Eu

The relative sensitivity of structurally related Eu(III) complexes to quenching by electron and energy transfer processes has been compared. In two sets of 9-coordinate complexes based on 1,4,7-triazacyclonane, the Eu...

scholarly journals Multistep energy and electron transfer processes in novel rotaxane donor–acceptor hybrids generating microsecond-lived charge separated states

2015 ◽  
Vol 6 (12) ◽  
pp. 7293-7304 ◽  
Author(s):  
Sabrina V. Kirner ◽  
Christian Henkel ◽  
Dirk M. Guldi ◽  
Jackson D. Megiatto Jr ◽  
David I. Schuster
Keyword(s):  
Electron Transfer ◽  
Electron Acceptor ◽  
Zinc Phthalocyanine ◽  
Zinc Porphyrin ◽  
Transfer Processes ◽  
Energy And Electron Transfer ◽  
Donor Acceptor ◽  
Electron Transfer Processes

A new set of [Cu(phen)2]+ based rotaxanes, featuring [60]-fullerene as an electron acceptor and a variety of electron donating moieties, namely zinc porphyrin (ZnP), zinc phthalocyanine (ZnPc) and ferrocene (Fc), has been synthesized and fully characterized.

Electron and energy transfer in a porphyrin–oxoporphyrinogen–fullerene triad, ZnP–OxP–C60

2020 ◽  
Vol 22 (25) ◽  
pp. 14356-14363 ◽  
Author(s):  
Mandeep K. Chahal ◽  
Habtom B. Gobeze ◽  
Whitney A. Webre ◽  
Paul A. Karr ◽  
Daniel T. Payne ◽  
...  
Keyword(s):  
Electron Transfer ◽  
Energy Transfer ◽  
Pump Probe ◽  
Zinc Porphyrin ◽  
Energy And Electron Transfer ◽  
Probe Spectroscopy

Competitive energy and electron transfer in a newly synthesized supramolecular triad composed of zinc porphyrin, oxoporphyrinogen and C60 has been demonstrated using ultrafast pump–probe spectroscopy.

Synthesis and the electron transfer reaction of (metallo)-porphyrin linked with a fullerene through an (L)-lysine spacer

2010 ◽  
Vol 14 (12) ◽  
pp. 1019-1026
Author(s):  
Toru Arai ◽  
Yoshikazu Shimote ◽  
Norikazu Nishino ◽  
Akihiko Tsuge
Keyword(s):  
Electron Transfer ◽  
Excited State ◽  
Emission Spectra ◽  
Electron Transfer Reaction ◽  
Free Base ◽  
Intermolecular Electron Transfer ◽  
Amide Bonds ◽  
H Nmr ◽  
Flexible Spacer ◽  
Covalently Linked

A novel visible-light induced electron transfer system composed of the free-base or Zn porphyrin, C60 molecule, and an (L)-lysine was synthesized and characterized. The porphyrin and C60 were covalently linked by the amide bonds through a relatively long and flexible spacer, (L)-lysine. The 1H NMR spectrum of the Zn porphyrin/(L)-lysine/ C60 conjugate (3Zn) suggested that C60 caused the slow molecular motion of this molecule. The steady-state absorption and the emission spectra of 3Zn revealed the intramolecular excited-state electron transfer from the Zn porphyrin moiety to the C60 moiety. The fluorescent lifetime measurement of the excited-state Zn porphyrin in 3Zn indicated the quenching by C60 . The intermolecular electron transfer from the excited-state zinc porphyrin to the viologen derivative in the solution was examined. The Zn porphyrin/(L)-lysine/ C60 conjugate and the free-base porphyrin/(L)-lysine/ C60 conjugate were more effective catalysts than the tetraphenylporphyrin Zn complex, suggesting the intermediacy of the charge separation state, ZnP·+-C60·- .

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