On the determination of the number of water molecules, q, coordinated to europium(III) ions in solution from luminescence decay lifetimes

被引:597
作者
Supkowski, RM
Horrocks, WD
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[2] WR Grace & Co Conn, Columbia, MD 21044 USA
基金
美国国家科学基金会;
关键词
luminescence; europium complexes; water ligand complexes;
D O I
10.1016/S0020-1693(02)01022-8
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A refined equation (in its simplest form: q = 1.11[tau(H2O)(-1)-tau(D2O)(-1)-0.31]) which allows the prediction of the number of water molecules in the first coordination sphere of a europium(III) (Eu3+) complex, q, in aqueous solution is presented. It is recognized that in the long history of the determination of the q-values of Eu3+ complexes from luminescent data of the excited metal ions in H2O and D2O solutions, certain inconsistencies are present. In some cases the q-values determined have either been non-integral when they should be integral, or have been in conflict with q-values predicted by other means. The original q-value equation put forth by this laboratory correlated the luminescence lifetime data of crystalline Eu3+ complexes to the known q-values based on XRD data from single crystals. In the current report, the difference in the decay rate of the Eu3+ luminescence of metal complexes in H2O and DO solution is linearly correlated to q-values predicted using the original equation as a guide. Our current interpretation of the luminescence data of 25 Eu3+ complexes taken from the literature, along with the extensive research of many labs involving the effect of oscillators other than water molecules in the first coordination sphere of the Eu3+ ion, has yielded the following equation: q = 1.11[tau(H2O)(-1)-tau(D2O)(-1)-0.31+0.45n(OH)+0.99n(NH)+0.075n(O=CNH)] where n(OH) is the number of alcoholic O-H oscillators in the first coordination sphere of Eu3+, and n(O=CNH) is the number of amide N-H oscillators in the first coordination sphere of Eu3+ n(NH) is the number of amine oscillators in which the amide carboxylic oxygen is in the first coordination sphere of Eu3+. The coefficient of determination parameter of the linear least-squares fit to the data is 0.998 and the standard error of the tit is +/-0.1 in q. The equation is used to account for the effect of water molecules in the second coordination sphere of the Eu3+ ion as well as to cast light on aqueous Eu3+ complexes that have known labile coordination spheres. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:44 / 48
页数:5
相关论文
共 33 条
[21]  
KOSTROMINA NA, 1971, RUSS J INORG CHEM, V16, P1256
[22]   ENHANCEMENT OF FLUORESCENCE YIELD OF RARE-EARTH IONS BY HEAVY WATER [J].
KROP, JL ;
WINDSOR, MW .
JOURNAL OF CHEMICAL PHYSICS, 1963, 39 (10) :2769-&
[23]   LUMINESCENCE AND ENERGY TRANSFER IN SOLUTIONS OF RARE-EARTH COMPLEXES .I. ENHANCEMENT OF FLUORESCENCE BY DEUTERIUM SUBSTITUTION [J].
KROPP, JL ;
WINDSOR, MW .
JOURNAL OF CHEMICAL PHYSICS, 1965, 42 (05) :1599-&
[24]   COMMENT ON FLUORESCENCE OF TRIVALENT EUROPIUM IN D2O-H2O MIXTURES [J].
KROPP, JL ;
WINDSOR, MW .
JOURNAL OF CHEMICAL PHYSICS, 1966, 45 (02) :761-&
[26]   Evaluation of solution structures of highly luminescent europium(III) chelates by using laser induced excitation of the F-7(0)->D-5(0) transition [J].
Latva, M ;
Takalo, H ;
Mukkala, VM ;
Kankare, J .
INORGANICA CHIMICA ACTA, 1998, 267 (01) :63-72
[27]   Solution structures of europium(III) complexes of ethylenediaminetetraacetic acid [J].
Latva, M ;
Kankare, J ;
Haapakka, K .
JOURNAL OF COORDINATION CHEMISTRY, 1996, 38 (1-2) :85-99
[28]  
Rizkalla EN., 1994, HANDB PHYSI, V18, P529
[29]  
Rizkalla EN., 1991, Handb Phys Chem Rare Earths, V15, P393, DOI [10.1016/S0168-1273(05)80009-1, DOI 10.1016/S0168-1273(05)80009-1]
[30]   ENERGY-GAP LAW IN SOLVENT ISOTOPE-EFFECT ON RADIATIONLESS TRANSITIONS OF RARE-EARTH IONS [J].
STEIN, G ;
WURZBERG, E .
JOURNAL OF CHEMICAL PHYSICS, 1975, 62 (01) :208-213