1998
DOI: 10.1016/s1010-6030(98)00307-4
|View full text |Cite
|
Sign up to set email alerts
|

Intramolecular energy transfer mechanism between ligands in ternary rare earth complexes with aromatic carboxylic acids and 1,10-phenanthroline

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
18
0

Year Published

2007
2007
2015
2015

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 141 publications
(18 citation statements)
references
References 18 publications
0
18
0
Order By: Relevance
“…The energies of the singlet and triplet states of dpp, phen and DDXPO are significantly higher than those for the HPhN ligand (e.g. E S1 = 27,930 cm −1 , E T1 = 21,830 cm −1 for phen; [72] E S1 = 31,850 cm −1 , E T1 = 23,470 cm −1 for DDXPO, Fig. 3).…”
Section: Absorption Spectramentioning
confidence: 92%
“…The energies of the singlet and triplet states of dpp, phen and DDXPO are significantly higher than those for the HPhN ligand (e.g. E S1 = 27,930 cm −1 , E T1 = 21,830 cm −1 for phen; [72] E S1 = 31,850 cm −1 , E T1 = 23,470 cm −1 for DDXPO, Fig. 3).…”
Section: Absorption Spectramentioning
confidence: 92%
“…We can observe that (B) and (C) are rather similar in terms of the same organic ligand 2, 2¢-bipyridyl responsible for the emissions. The peak at 421 nm of (A) shows that the triplet state energy level of STA-APMMES is approximately 23753 cm )1 , which is higher than that of bipy (437 nm, 22880 cm )1 ), therefore, we suppose that energy transfer process will occur from STA-APMMES to 2,2¢-bipyridyl, substantiating that the heterocyclic ligand will become the main energy donor and have the possibility of sensitizing Ln 3+ ions (39,40). Figures 6 and 7 show the excitation and emission spectra of quaternary terbium molecular hybrids with OLA(STA)-AEAPMMS (APMES)-Si and 2, 2¢-bipyridyl.…”
Section: Assembly Of Luminescent Quaternary Molecular Hybridsmentioning
confidence: 77%
“…According to the energy transfer and intramolecular energy mechanism , the energy difference (Δ E ) between the triplet state energy level of the ligand and the lowest excited state energy level of the lanthanide ion is one of the most important factors influencing the luminescence properties of lanthanide complexes. If the energy difference is too large, the energy‐transfer rate constant will decrease due to diminution of the overlap between the energy donor (ligands) and acceptor (lanthanide ions).…”
Section: Resultsmentioning
confidence: 99%