2011
DOI: 10.1016/j.poly.2011.01.024
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Synthesis and structural studies of some fluorescent group XII metal complexes with a terpyridine based ligand

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Cited by 21 publications
(2 citation statements)
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“…The ligands, 4′-(4chlorophenyl)-2,2′:6′,2″-terpyridine (L 1 ), 4′-(4-bromophenyl)-2,2′:6′,2″-terpyridine (L 2 ), and 4′-(benzothiophen-2-yl)-2,2′:6′,2″terpyridine (L 3 ), were synthesized according to procedures described previously in the literature. [15][16][17] Infrared spectra were recorded on a Nicolet iS5 FT-IR spectrophotometer in the range 4000-400 cm −1 using KBr pellets. Electronic absorption spectra were measured on a Nicolet iS50 UV-VIS-NIR spectrophotometer in the range of 900-180 nm in acetonitrile solution.…”
Section: Methodsmentioning
confidence: 99%
“…The ligands, 4′-(4chlorophenyl)-2,2′:6′,2″-terpyridine (L 1 ), 4′-(4-bromophenyl)-2,2′:6′,2″-terpyridine (L 2 ), and 4′-(benzothiophen-2-yl)-2,2′:6′,2″terpyridine (L 3 ), were synthesized according to procedures described previously in the literature. [15][16][17] Infrared spectra were recorded on a Nicolet iS5 FT-IR spectrophotometer in the range 4000-400 cm −1 using KBr pellets. Electronic absorption spectra were measured on a Nicolet iS50 UV-VIS-NIR spectrophotometer in the range of 900-180 nm in acetonitrile solution.…”
Section: Methodsmentioning
confidence: 99%
“…These bonds are longer as compared to the ve-coordinated mercury thiocyanate complexes with N-donor Schiff base ligands (2.289(3) Å in C 24 H 26 Hg 2 N 10 S 4 and 2.367(5) in C 20 H 23 HgN 5 S 2 ) 52,54. The Hg-S1 and Hg-S2 bond distances are 2.630(5) and 2.480(5) Å, respectively, and comparable to similar structures 55,56. The bond angles of S-donor thiocyanates[S1-C1S-N1S ¼ 174.4(19) and S2-C2S-N2S ¼ 179(2) ] indicates that two thiocyanate groups are quasi-linear and coordinated to the metal center in a bending way [Hg1-S1-C1S ¼ 99.4(7) and Hg1-S2-C2S ¼ 94.7(7)].…”
mentioning
confidence: 50%