Intramolecular Electron-Transfer Assistance in the Redox Reaction of (μ-Cyano)pentaammineruthenium(III) Pentacyanoferrate(II). Role of the Electronic Isomer and of the Specific Donor−Acceptor Interactions

1997 ◽  
Vol 36 (24) ◽  
pp. 5642-5644 ◽  
Author(s):  
Paula Forlano ◽  
Alejandro R. Parise ◽  
Mariela Videla ◽  
José A. Olabe
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

2018 ◽  
Vol 42 (11) ◽  
pp. 9281-9290 ◽  
Author(s):  
N. Manfredi ◽  
V. Trifiletti ◽  
F. Melchiorre ◽  
G. Giannotta ◽  
P. Biagini ◽  
...  

Suppression of back reaction and enhanced photoinduced intramolecular electron transfer through peripheral functionalization of triphenylamino based dibranched donor–acceptor dyes.


2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Jinseok Kim ◽  
Juwon Oh ◽  
Seongchul Park ◽  
Jose L. Zafra ◽  
Justin R. DeFrancisco ◽  
...  

Abstract The scientific significance of excited-state aromaticity concerns with the elucidation of processes and properties in the excited states. Here, we focus on TMTQ, an oligomer composed of a central 1,6-methano[10]annulene and 5-dicyanomethyl-thiophene peripheries (acceptor-donor-acceptor system), and investigate a two-electron transfer process dominantly stabilized by an aromatization in the low-energy lying excited state. Our spectroscopic measurements quantitatively observe the shift of two π-electrons between donor and acceptors. It is revealed that this two-electron transfer process accompanies the excited-state aromatization, producing a Baird aromatic 8π core annulene in TMTQ. Biradical character on each terminal dicyanomethylene group of TMTQ allows a pseudo triplet-like configuration on the 8π core annulene with multiexcitonic nature, which stabilizes the energetically unfavorable two-charge separated state by the formation of Baird aromatic core annulene. This finding provides a comprehensive understanding of the role of excited-state aromaticity and insight to designing functional photoactive materials.


2019 ◽  
Vol 7 (20) ◽  
pp. 12532-12537 ◽  
Author(s):  
Yuan Guo ◽  
Guangchao Han ◽  
Zeyi Tu ◽  
Yuanping Yi

For the π-bridged multi-PDI derivatives, intramolecular electron transfer is dictated by the super-exchange mechanism and can be greatly tuned by the π-bridge modes.


Biochemistry ◽  
1994 ◽  
Vol 33 (29) ◽  
pp. 8678-8685 ◽  
Author(s):  
Rui-Qin Liu ◽  
Mark A. Miller ◽  
Gye Won Han ◽  
Seung Hahm ◽  
Lois Geren ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document