Photophysical properties of meso-substituted octaethylporphines and their zinc complexes

1991 ◽  
Vol 87 (18) ◽  
pp. 2933 ◽  
Author(s):  
Guo-Zhang Wu ◽  
Wei-Xing Gan ◽  
Hiu-Kwong Leung
2015 ◽  
Vol 44 (26) ◽  
pp. 11984-11996 ◽  
Author(s):  
Daniel A. Evans ◽  
Lucia Myongwon Lee ◽  
Ignacio Vargas-Baca ◽  
Alan H. Cowley

Bis(imino)acenaphthene (BIAN) zinc complexes with para-substituted aryl groups have been synthesized and investigated from the standpoint of their photophysical properties.


2012 ◽  
Vol 392 ◽  
pp. 292-299 ◽  
Author(s):  
Zihong Zhou ◽  
Wen Li ◽  
Xiaohua Hou ◽  
Langqiu Chen ◽  
Xiang Hao ◽  
...  

2015 ◽  
Vol 44 (46) ◽  
pp. 20032-20044 ◽  
Author(s):  
Prateeti Chakraborty ◽  
Jaydeep Adhikary ◽  
Sugata Samanta ◽  
Ishani Majumder ◽  
Chiara Massera ◽  
...  

The role of para substituents of three dinuclear zinc(ii) complexes on the structure, photophysical properties and their different weak interactions is investigated.


2007 ◽  
Vol 11 (02) ◽  
pp. 130-138 ◽  
Author(s):  
Eva H. Mørkved ◽  
Nils Kr. Afseth ◽  
Petr Zimcik

Magnesium and zinc complexes of azaphthalocyanines (AzaPc) with eight peripheral aromatic (phenyl) or heteroaromatic (pyridyl, thienyl, furyl) substituents are studied from the point of view of their singlet oxygen (ΦΔ) and fluorescence (Φ F ) quantum yields, and UV-vis absorption spectra. Zn complexes have higher ΦΔ than Mg complexes by a factor of two, whereas the Mg complexes have higher Φ F than Zn complexes, also by a factor of two. Thienyl AzaPc have the highest ΦΔ among all studied substances (0.635 for Zn complex) followed by phenyl and pyridyl derivatives. The order of Φ F values is then reversed - the highest values were reached for pyridyl and phenyl derivatives followed by thienyl AzaPc. Both furyl AzaPc were unstable towards light and decomposed giving very low ΦΔ and Φ F . The Q-bands of the furyl and thienyl AzaPc were red-shifted for approx. 20 nm compared to phenyl and pyridyl derivatives indicating lower sterical hindrance between five-membered rings and thus allowing better conjugation of π-systems. Pyridyl-, thienyl- and furyl-substituted pyrazino[2,3-b]pyrazine-2,3-dicarbonitriles were also prepared but decomposed during attempted cyclotetramerizations.


2016 ◽  
Vol 45 (30) ◽  
pp. 12053-12068 ◽  
Author(s):  
Nidhi Dwivedi ◽  
Sumit Kumar Panja ◽  
Monika Monika ◽  
Satyen Saha ◽  
Sailaja S. Sunkari

In this paper, we report the synthesis, and structure of four new complexes of conformationally flexible 6-chloro-4-phenyl-2-(pyridin-2-yl)quinazoline ligand (L) with Zn(ii). Significance of ring twisting on supramolecular assembly and photophysical properties have also been highlighted.


2021 ◽  
Vol 1229 ◽  
pp. 129793
Author(s):  
Xu-Min Cai ◽  
Tianqi Mu ◽  
Yuting Lin ◽  
Xuedan Zhang ◽  
Zhenguo Tang ◽  
...  

2011 ◽  
Vol 15 (09n10) ◽  
pp. 930-942 ◽  
Author(s):  
Daiki Kuzuhara ◽  
Hiroko Yamada ◽  
Shigeki Mori ◽  
Tetsuo Okujima ◽  
Hidemitsu Uno

A series of benzoporphycenes and naphthoporphycenes and their zinc complexes were prepared from bicyclo[2.2.2]octadiene fused porphycenes by a retro-Diels-Alder reaction and their photophysical properties were studied. Free-base tetranaphthoporphycene was not soluble in common organic solvents, but zinc tetranaphthoporphycene was slightly soluble in pyridine and showed B- and Q-bands at 507 and 690 nm, respectively. Dinaphthoporphycene showed broad B- and Q-bands due to its lower symmetry. Tetrabenzo-, dibenzo-, and dinaphthoporphycenes showed fluorescence at 673, 654, and 670 nm with quantum yields of 0.32, 0.42, and 0.31, respectively, although their precursors were non-fluorescent. Zinc complexes of tetrabenzo-, dibenzo-, tetranaphtho-, dinaphthoporphycenes and their bicyclo[2.2.2]octadiene-fused precursors revealed moderate fluorescence with quantum yields of 0.15–0.37. The crystal structures of tetrabenzo- and dibenzoporphycenes showed herringbone structures, while the zinc tetrabenzoporphycene showed a hexagonal box-structure with six pyridine ligands inside.


2015 ◽  
Vol 121 ◽  
pp. 372-378 ◽  
Author(s):  
Saori Takeda ◽  
Hiroka Yamada ◽  
Toshiki Mutai ◽  
Isao Yoshikawa ◽  
Hirohiko Houjou

Sign in / Sign up

Export Citation Format

Share Document