scholarly journals Subphthalocyanine–tetracyanobuta-1,3-diene–aniline conjugates: stereoisomerism and photophysical properties

2019 ◽  
Vol 10 (48) ◽  
pp. 10997-11005 ◽  
Author(s):  
Kim A. Winterfeld ◽  
Giulia Lavarda ◽  
Julia Guilleme ◽  
Dirk M. Guldi ◽  
Tomás Torres ◽  
...  

We report the stereoisomerism and physicochemical properties of two novel electron donor–acceptor conjugates based on subphthalocyanines decorated at their peripheral, or peripheral/axial positions with multiple tetracyanobutadiene–aniline moieties.

2014 ◽  
Vol 21 (2) ◽  
pp. 746-752 ◽  
Author(s):  
Bin Liu ◽  
Hongyun Fang ◽  
Xiaofang Li ◽  
Wenting Cai ◽  
Lipiao Bao ◽  
...  

2015 ◽  
Vol 127 (23) ◽  
pp. 6879-6883 ◽  
Author(s):  
Francesca M. Toma ◽  
Fausto Puntoriero ◽  
Toan V. Pho ◽  
Marcello La Rosa ◽  
Young-Si Jun ◽  
...  

2015 ◽  
Vol 54 (23) ◽  
pp. 6775-6779 ◽  
Author(s):  
Francesca M. Toma ◽  
Fausto Puntoriero ◽  
Toan V. Pho ◽  
Marcello La Rosa ◽  
Young-Si Jun ◽  
...  

Nanoscale ◽  
2015 ◽  
Vol 7 (3) ◽  
pp. 1145-1160 ◽  
Author(s):  
Sabrina V. Kirner ◽  
Dirk M. Guldi ◽  
Jackson D. Megiatto, Jr. ◽  
David I. Schuster

Nanoscale electron donor–acceptor systems with [2]catenane architectures, with magnesium porphyrin (MgP) or free base porphyrin (H2P) as electron donor and C60as electron acceptor, have been investigated.


2017 ◽  
Vol 5 (36) ◽  
pp. 9345-9358 ◽  
Author(s):  
Abhay Kumar Yadav ◽  
Balaram Pradhan ◽  
Hidayath Ulla ◽  
Subrata Nath ◽  
Joydip De ◽  
...  

Delicate interplay of donor–acceptor interactions in directing the self-assembly and its application.


2020 ◽  
Author(s):  
José Tiago Menezes Correia ◽  
Gustavo Piva da Silva ◽  
Camila Menezes Kisukuri ◽  
Elias André ◽  
Bruno Pires ◽  
...  

A metal- and catalyst-free photoinduced radical cascade hydroalkylation of 1,7-enynes has been disclosed. The process is triggered by a SET event involving a photoexcited electron-donor-aceptor complex between NHPI ester and Hantzsch ester, which decomposes to afford a tertiary radical that is readily trapped by the enyne. <a>The method provides an operationally simple, robust and step-economical approach to the construction of diversely functionalized dihydroquinolinones bearing quaternary-centers. A sequential one-pot hydroalkylation-isomerization approach is also allowed giving access to a family of quinolinones. A wide substrate scope and high functional group tolerance was observed in both approaches</a>.


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