2020
DOI: 10.1016/j.molstruc.2019.127466
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Crystal structure, thermal behavior and luminescence of a new Manganese(Ⅱ) coordination polymer constructed with 1, 10-phenanthroline-5, 6-dione and 2, 5-dihydroxyl-1, 4-terephthalic acid

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Cited by 11 publications
(3 citation statements)
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“…Because of the potential applications of coordination polymers with transition metal centers in many fields such as chemical sensors, electroluminescence and display photochemistry, they have attracted the interest of a wide range of researchers [36][37][38][39]; thus the luminescence of the complex was detected in a solid state at 25 °C (Figure 4), and the luminescence spectra of free 2,5-dihydroxy-1,4-terephthalic acid ligand (DHTA-1) and free 2,2′-bipyridine ligand (Bpy-1) were also obtained under the same condition. As we know, the emission peak for DHTA-1 is located at 476 nm (λex = 366 nm) [40]. The Bpy-1 that is excited near 398 nm exhibits an obvious emission peak (λex = 366 nm).…”
Section: Luminescent Property Of the Complexmentioning
confidence: 89%
“…Because of the potential applications of coordination polymers with transition metal centers in many fields such as chemical sensors, electroluminescence and display photochemistry, they have attracted the interest of a wide range of researchers [36][37][38][39]; thus the luminescence of the complex was detected in a solid state at 25 °C (Figure 4), and the luminescence spectra of free 2,5-dihydroxy-1,4-terephthalic acid ligand (DHTA-1) and free 2,2′-bipyridine ligand (Bpy-1) were also obtained under the same condition. As we know, the emission peak for DHTA-1 is located at 476 nm (λex = 366 nm) [40]. The Bpy-1 that is excited near 398 nm exhibits an obvious emission peak (λex = 366 nm).…”
Section: Luminescent Property Of the Complexmentioning
confidence: 89%
“…Phendione 867 is probably one of the most versatile building blocks ever used to functionalize phen. A plethora of articles describes the synthesis of 867 . ,,, The common point to all the reported procedures is the strongly acidic (ensuring phen is protonated and increasing the solubility) and oxidizing conditions. Phendione can be further transformed into precious synthons for numerous applications.…”
Section: Divergent Synthesis Pathwaysmentioning
confidence: 99%
“…From these pioneering works, some minor variations in this synthesis of 867 have been described. Some authors first dissolve phen in sulfuric acid then add sodium bromide and then nitric acid (refs , , , , , , ), others first mixed phen with potassium or sodium bromide and cool down the mixture before adding sulfuric acid and nitric acid at −78 (refs , , , , ) or 0 °C (refs , , , , , ,, , , , ,,, , , , , , , , ), and others cool the sulfuric acid solution at 0 or −78 °C and add a mixture of phen and KBr or NaBr then add nitric acid (refs , , , , , , , , ). Other reports advise to cool the sulfuric acid and nitric acid at 0 °C before phen and NaBr are added to the mixture and heated, , or some directly prepare the phen and KBr solid mixture and add the latter to the acidic mixture before heating. , Finally, some authors first dissolved phen in sulfuric acid then add potassium bromide; in this case, no nitric acid was used before heating the reaction. , …”
Section: Divergent Synthesis Pathwaysmentioning
confidence: 99%