2011
DOI: 10.1016/j.saa.2011.05.030
|View full text |Cite
|
Sign up to set email alerts
|

Homo dinuclear lanthanide(III) complexes of a mesogenic Schiff-base, N,N′-di-(4-decyloxysalicylidene)-1′,6′-diaminohexane: Synthesis and characterization

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
8
0

Year Published

2014
2014
2020
2020

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 18 publications
(8 citation statements)
references
References 32 publications
0
8
0
Order By: Relevance
“…The broad singlets at 5.0 ppm for O 2 H and at 2.0 ppm for O 10 H are due to the aromatic hydroxyl and allylic hydroxyl groups, respectively . The strong singlet at 8.13 ppm for H‐C 7 is assigned to the azomethine proton . The signal for H‐C 11 appears at 1.3 ppm as doublet ( J =9 Hz) assigned to the methyl group.…”
Section: Resultsmentioning
confidence: 88%
“…The broad singlets at 5.0 ppm for O 2 H and at 2.0 ppm for O 10 H are due to the aromatic hydroxyl and allylic hydroxyl groups, respectively . The strong singlet at 8.13 ppm for H‐C 7 is assigned to the azomethine proton . The signal for H‐C 11 appears at 1.3 ppm as doublet ( J =9 Hz) assigned to the methyl group.…”
Section: Resultsmentioning
confidence: 88%
“…According to the antioxidant experiments, the IC 50 of the ligand, Eu III and Ce III complexes are 8.60 × 10 –5 , 6.82 × 10 –6 , and 8.7 × 10 –6 m (Figure a–c). The result suggests that the complexes exhibit better scavenging activity than the ligand, as well as mannitol and vitamin C. Due to the observed IC 50 values, the complexes can be considered as potential drugs to eliminate the hydroxyl radical , …”
Section: Resultsmentioning
confidence: 93%
“…Synthesis, characterization and photoluminescenceproperties 13 following signals б(ppm):3.6(2H,CH 2 g r oup), 7.5(1H,CH group), 6.10(H, -CH= in C3 of coumarin moiety) ,7.8(1H,NH group), 3.4 (1H, Ar-OH), 3.51(1H,OH-coumarin moiety) and 6.2-7.5 ppm are assigned to the proton of both phenolic and coumarin moiety [35,36].…”
Section: H Nmr Studiesmentioning
confidence: 99%