Synthesis, Electronic Structure, and Electron Transfer Dynamics of (Aryl)ethynyl-Bridged Donor−Acceptor Systems

2003 ◽  
Vol 125 (29) ◽  
pp. 8769-8778 ◽  
Author(s):  
Naomi P. Redmore ◽  
Igor V. Rubtsov ◽  
Michael J. Therien
2014 ◽  
Vol 18 (10n11) ◽  
pp. 982-990 ◽  
Author(s):  
Kei Ohkubo ◽  
Yuki Kawashima ◽  
Kentaro Mase ◽  
Hayato Sakai ◽  
Taku Hasobe ◽  
...  

An electron donor–acceptor supramolecular complex was formed between an anionic zinc chlorin carboxylate ( ZnCh -) and lithium-ion-encapsulated [60]fullerene ( Li +@ C 60) by an electrostatic interaction in benzonitrile ( PhCN ). Photoinduced electron transfer in the supramolecular complex of ZnCh -/ Li +@ C 60 resulted in the formation of the charge-separated state via electron transfer from the triplet excited state of ZnCh - to Li +@ C 60. We report herein photovoltaic cells using ZnCh -/ Li +@ C 60 nanoclusters, which are assembled on the optically transparent electrode (OTE) of nanostructured SnO 2 (OTE/ SnO 2). The photoelectrochemical behavior of the nanostructured SnO 2 film of supramolecular nanoclusters of ZnCh - and Li +@ C 60 denoted as OTE/ SnO 2/( ZnCh -/ Li +@ C 60)n is significantly higher than the single component films of ZnCh - or Li +@ C 60 clusters, denoted as OTE/ SnO 2/( ZnCh -)n or OTE/ SnO 2/( Li +@ C 60)n.


1989 ◽  
Vol 164 (2-3) ◽  
pp. 120-125 ◽  
Author(s):  
James M. Lawson ◽  
Donald C. Craig ◽  
Michael N. Paddon-Row ◽  
Jan Kroon ◽  
Jan W. Verhoeven

2013 ◽  
Vol 117 (48) ◽  
pp. 25259-25268 ◽  
Author(s):  
Robin R. Knauf ◽  
M. Kyle Brennaman ◽  
Leila Alibabaei ◽  
Michael R. Norris ◽  
Jillian L. Dempsey

1981 ◽  
Vol 103 (20) ◽  
pp. 6142-6147 ◽  
Author(s):  
Robert Weiss ◽  
Hilmar Wolf ◽  
Ulrich Schubert ◽  
Timothy Clark

2005 ◽  
Vol 33 (1) ◽  
pp. 20-21 ◽  
Author(s):  
M. Sundararajan ◽  
J.P. McNamara ◽  
M. Mohr ◽  
I.H. Hillier ◽  
H. Wang

We describe the use of the semi-empirical molecular orbital method PM3 (parametric method 3) to study the electronic structure of iron–sulphur proteins. We first develop appropriate parameters to describe models of the redox site of rubredoxins, followed by some preliminary calculations of multinuclear iron systems of relevance to hydrogenases.


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