70086-67-8Relevant articles and documents
Non-covalent bridging of bithiophenes through chalcogen bonding grips
Babudri, Francesco,Biot, Nicolas,Bonifazi, Davide,Romito, Deborah
supporting information, p. 6732 - 6738 (2020/05/16)
In this work, chalcogen functionalized dithiophenes, equipped on both extremities with chalcogen-bonding recognition heterocycles, have been prepared following two synthetic pathways. The insertion of the chalcogenazolo[5,4-β]pyridine allows the control of the organization at the solid state. X-Ray diffraction analysis of the single crystals, showed that the Te-doped derivatives give the most persistant assemblies, with the molecules arranging at solid-state in wire-like polymeric structures through Te?N interactions. As expected, the introduction of the Se and Te atoms, dramatically decreases the emission properties, with the Te-bearing congeners being virtually non emissive.
Walking Down the Chalcogenic Group of the Periodic Table: From Singlet to Triplet Organic Emitters
Kremer, Adrian,Aurisicchio, Claudia,Deleo, Federica,Ventura, Barbara,Wouters, Johan,Armaroli, Nicola,Barbieri, Andrea,Bonifazi, Davide
supporting information, p. 15377 - 15387 (2015/11/02)
The synthesis, X-ray crystal structures, ground- and excited-state UV/Vis absorption spectra, and luminescence properties of chalcogen-doped organic emitters equipped on both extremities with benzoxa-, benzothia-, benzoselena- and benzotellurazole (1
Tandem free-radical addition/substitution chemistry and its application to the preparation of novel AT1 receptor antagonists
Staples, Maree K.,Grange, Rebecca L.,Angus, James A.,Ziogas, James,Tan, Nichole P. H.,Taylor, Michelle K.,Schiesser, Carl H.
scheme or table, p. 473 - 479 (2011/03/17)
Benzothiophene and benzoselenophene analogues of the thiophene-containing antihypertensives milfasartan and eprosartan were prepared and tested for AT1 receptor antagonist properties. While the sulfur-containing systems were prepared following
