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Mono(di)nuclear Europium(III) Complexes of Macrobi(tri)cyclic Cryptands Derived from Diazatetralactams as Luminophores in Aqueous Solution
Author(s) -
Galaup Chantal,
Picard Claude,
Cathala Bernard,
Cazaux Louis,
Tisnès Pierre,
Autiero Hervé,
Aspe Daniel
Publication year - 1999
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/(sici)1522-2675(19990407)82:4<543::aid-hlca543>3.0.co;2-u
Subject(s) - cryptand , chemistry , moiety , luminescence , europium , lanthanide , chromophore , bipyridine , photochemistry , aqueous solution , ion , crystallography , stereochemistry , organic chemistry , crystal structure , physics , optoelectronics
To increase the excellent light‐emitting properties of the Eu 3+ ion, macrobicyclic and macrotricyclic ligands 7 – 10 , incorporating a 18‐membered tetralactam ring (acting as a lanthanide binding site) and a sensitizer group (2,2′‐bipyridine or 2,2′‐bipyridine 1,1′‐dioxide moiety), were synthesized. The mononuclear and dinuclear europium cryptates derived from these ligands were isolated and characterized. Their luminescent properties and those of the corresponding cryptates containing a phenanthroline group (see 11 and 12 ) were examined in H 2 O and D 2 O solutions at 77 and 300 K. It results that the tetralactam moiety plays a major role in the efficient shielding of the complexed Eu 3+ ion from the water environment. The cryptands incorporating the bipyridine unit are the most promising labels according to their photophysical properties (excitation maxima, emission decay lifetime, relative luminescent yield). In contrast with literature data, introduction of N ‐oxide groups in the bipyridine chromophore weakens the luminescence properties of the cryptate.