Tunable Emissive Lanthanidomesogen Derived from a Room-Temperature Liquid-Crystalline Schiff-Base Ligand

2013 ◽  
Vol 19 (39) ◽  
pp. 13151-13159 ◽  
Author(s):  
Harun A. R. Pramanik ◽  
Gobinda Das ◽  
Chira R. Bhattacharjee ◽  
Pradip C. Paul ◽  
Paritosh Mondal ◽  
...  
2012 ◽  
Vol 39 (7) ◽  
pp. 795-801 ◽  
Author(s):  
Lei Wang ◽  
Soo-Yeon Park ◽  
Seong-Min Kim ◽  
Sora Yoon ◽  
Soo-Hyoung Lee ◽  
...  

2017 ◽  
Vol 30 (3) ◽  
pp. 114
Author(s):  
Hasan A. Hasan

 The precursor [W] [2-(2-(naphthalen-5-yl) diazenyl)-4-amino-3-hydroxynaphthalene-1sulfonic acid] was synthesized from reaction of diazonium salt with 1-amino-2-naphtol-4sulfonic acid. Then the tridentate Schiff base ligand type ONO was synthesized from the reaction of the precursor with salicyaldehyde in 1:1 mole ratio to produce the ligand H2L [2-(2-(naphthalen5-yl) diazenyl)-4-(2-hydroxynaphthalen-3-yl)methyleneamino)-3-hydroxy salicyalene-1-sulfonic acid],the reaction achieved in methanol as a solvent under reflux. Spectroscopic methods IR, U.V, 1H,13C-NMR was used to characterize the ligand. Complexes of [CrIII, CoII, NiII and CdII] ions were also prepared through reaction of ligand with metal salts in 2:1 mole ratio at reflux, using KOH as a base, ethanol as a solvent. Chloride content, molar conductivity and melting point measurements along with I.R and U.V-Vis, atomic absorption (A.A) spectroscopy were used to characterize the complexes.1H-NMR spectroscopy was used to characterize Cd complex. Thermal analysis was used to insure the presence of crystallized H2O molecule in the complexes structure. The following formula was proposed for Cr complex: K[Cr(L)2]. H2O, while CoII, NiII and CdII complexes have the K2[M(L)2].H2O formula. The biological activity of the prepared compounds was studied. Fluorescence properties of the prepared compounds were studied (at room temperature) which indicate that the ligand may behave as strong fluorescent emitter. The complexes also showed fluorescence characteristic with the ligand. The ligand revealed high relative intensity and its fluorescence peak were also shifted to the lower or higher wavelength when compared with the complexes.


2010 ◽  
Vol 20 (39) ◽  
pp. 8646 ◽  
Author(s):  
André Wicklein ◽  
Mathis-Andreas Muth ◽  
Mukundan Thelakkat

ChemPlusChem ◽  
2016 ◽  
Vol 82 (3) ◽  
pp. 342-346 ◽  
Author(s):  
Marília Gabriela Belarmino Cabral ◽  
Deise Maria Pereira de Oliveira Santos ◽  
Rodrigo Cristiano ◽  
Hugo Gallardo ◽  
Ahmed Bentaleb ◽  
...  

2014 ◽  
Vol 67 (11) ◽  
pp. 1574 ◽  
Author(s):  
Darunee Sertphon ◽  
David J. Harding ◽  
Phimphaka Harding ◽  
Keith S. Murray ◽  
Boujemaa Moubaraki ◽  
...  

A new sterically bulky Schiff base ligand, N-(8-quinolyl)-5-tert-butylsalicylaldimine (Hqsal-5-tBu) has been prepared and a series of FeIII complexes, [Fe(qsal-5-tBu)2]Y (Y = Cl 1, ClO4 2, NO3 3, BF4 4) utilising this ligand are reported and fully characterised. UV-vis spectroscopic and electrochemical studies indicate that 1–4 are high spin (HS) in solution at room temperature and further suggest that the tBu group only slightly alters the electronic properties of 1–4 compared with related [Fe(qsal-5-X)2]+ systems. The structures of [Fe(qsal-5-tBu)2]Cl·4MeOH·H2O 1, [Fe(qsal-5-tBu)2]ClO4·MeOH 2, and [Fe(qsal-5-tBu)2]NO3 3 determined at 100 K reveal HS FeIII centres in all cases. Four-fold parallel aryl embraces and π–π interactions serve to link the cations forming 2D sheets mirroring the motifs found in other [Fe(qsal-5-X)2]+ complexes. Despite this the tBu group causes strong distortions at the Fe centre which as magnetic studies reveal prevent spin crossover trapping 1–4 in the HS state.


2007 ◽  
Vol 119 (21) ◽  
pp. 3970-3973 ◽  
Author(s):  
Yijin Xu ◽  
Siwei Leng ◽  
Chenming Xue ◽  
Runkun Sun ◽  
Jie Pan ◽  
...  

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