scholarly journals Synthesis and Characterization of Fused-Ring Iridapyrroles

2008 ◽  
Vol 27 (22) ◽  
pp. 5744-5747 ◽  
Author(s):  
John R. Bleeke ◽  
Phawit Putprasert ◽  
Todsapon Thananatthanachon ◽  
Nigam P. Rath
2013 ◽  
Vol 43 (18) ◽  
pp. 2441-2451 ◽  
Author(s):  
Jason O. E. Young ◽  
Chad A. Snyder ◽  
Nathan C. Tice ◽  
Seth L. Sloan ◽  
Adam C. Smith ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (95) ◽  
pp. 78253-78258 ◽  
Author(s):  
Poulomi Majumdar ◽  
John Mack ◽  
Tebello Nyokong

The synthesis and characterization of an NIR absorbing acenaphthalene fused-ring-expanded aza-BODIPY dye.


2014 ◽  
Vol 25 (6) ◽  
pp. 612-618 ◽  
Author(s):  
Baolin Li ◽  
Shota Tsujimoto ◽  
Yongming Li ◽  
Hayato Tsuji ◽  
Kohei Tamao ◽  
...  

Inorganics ◽  
2018 ◽  
Vol 6 (1) ◽  
pp. 30 ◽  
Author(s):  
Naoki Hayakawa ◽  
Kazuya Sadamori ◽  
Shinsuke Mizutani ◽  
Tomohiro Agou ◽  
Tomohiro Sugahara ◽  
...  

Molecules ◽  
2018 ◽  
Vol 23 (9) ◽  
pp. 2279 ◽  
Author(s):  
Rylan Wolfe ◽  
Evan Culver ◽  
Seth Rasmussen

The synthesis of four N-functionalized bis[1]benzothieno[3,2-b:2′,3′-d]pyrroles (BBTPs) is reported in order to provide a more detailed characterization of these fused-ring units, as well as increase the scope of known BBTP units available for application to conjugated materials. The optical, electronic, and structural properties of the resulting BBTP units have been compared to the parent N-alkyl- and N-aryl-dithieno[3,2-b:2′,3′-d]pyrroles (DTPs), as well as their corresponding 2,6-diphenyl derivatives, in order to fully quantify the relative electronic effects resulting from benzannulation of the parent DTP building block. Such comparative analysis reveals that benzannulation results in a red-shifted absorbance, but to a lesser extent than simple phenyl-capping of the DTP. More surprising is that benzannulation results in stabilization of the BBTP HOMO, compared to the destabilization normally observed with extending the conjugation length of the backbone.


2008 ◽  
Vol 59 (9) ◽  
Author(s):  
Stefania-Felicia Barbuceanu ◽  
Ioana Saramet ◽  
Gabriela Laura Almajan ◽  
Constantin Draghici ◽  
Isabela Tarcomnicu ◽  
...  

In this study, the synthesis and characterization of new thiazolo[3,2-b][1,2,4]triazol-6(5H)-ones 3-5 are described starting from 5-[4-(4-X-phenylsulfonyl)phenyl]-4H-1,2,4-triazole-3-thioles 2. The treatment of 1,2,4-triazole-3-thioles 2 with chloroacetic acid and substituted or non-substituted benzaldehydes in the presence of sodium acetate, acetic acid and acetic anhydride gave fused ring compounds 3-5. The structures of thiazolo-triazolones 3-5 have been elucidate by elemental analysis and IR, UV, 1H-NMR, 13C-NMR, MS spectra. Some of the newly synthesized products were tested for their antimicrobial effects.


1996 ◽  
Vol 61 (10) ◽  
pp. 3572-3572
Author(s):  
Lawrence T. Scott ◽  
Atena Necula

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