ABSTRACT
The layered rare earth hydroxides have attracted increasing interests due to their diverse chemical composition and tunable spectroscopic properties. In this paper, a novel Tb3+ activated layered lutetium hydroxide (LLuH:Tb) was fabricated, in which the inorganic NO3- ions were ion-exchanged with organic (ibuprofen or dodecylsulfonate) anions. After the ion-exchange reaction, the organic anions intercalated LLuH:Tb showed the distinct lamellar structure with the interlayer distance of about 2.56 nm, confirming the formation of inorganic/organic hybrid assembly. The dye ibuprofen-intercalated hybrid effectively promoted the characteristic 5D4 â 7F5 green emission of Tb3+ in the host but failed to be exfoliated into nanosheet colloid. On the contrary, the dodecylsulfonate-intercalated hybrid was readily to be exfoliated into nanosheet colloid by dissolving in formamide solvent, but the green emission of Tb3+ was too weak to be observed. To take advantage of their respective merits and explore the practical uses, certain amounts of dye ibuprofen were directly added to the dodecylsulfonate-intercalated hybrid colloid. Excited with the ultraviolet light, the characteristic green fluorescence of Tb3+ was dramatically enhanced, indicating that the dye was a superior light-harvesting antenna to sensitize the activator Tb3+. The dye sensitized hybrid colloid was very stable at ambient temperature and exhibited excellent fluorescent recognition for Cu2+ ions over other metal ions in aqueous solution due to the large fluorescence quenching. The detection limit for Cu2+ ion reaches 7.63 × 10-7 mol/L, which is far lower than the limitation of Cu2+ in drinking water recommended by the World Health Organization (1.57 × 10-5 mol/L). The fluorescence enhanced/quenched sensor with excellent stability exhibits a high potential for the detection of Cu2+ in routine environmental water.
Subject(s)
Lutetium , Terbium , Fluorescent Dyes/chemistry , Hydroxides/chemistry , Ibuprofen , Spectrometry, Fluorescence , Terbium/chemistryABSTRACT
Amino acids play a very important role in the fields of pharmacy and biochemistry, and the identification of amino acid enantiomers has become a research hotspot. In this study, chiral nanomaterials ZnFe2O4-L-Cys (Cys = cysteine) were prepared by the mechanical stirring method and characterizad by different kinds of techniques. The effect of pH and Cu2+ on the recognition of tryptophan by chiral nanomaterials ZnFe2O4-L-Cys was further explored by ultraviolet-visible spectroscopy. The experimental results show that when the pH of the recognition environment is neutral, ZnFe2O4-L-Cys can be used as chiral selectors for tryptophan enantiomers in the presence of Cu2+ and the absorbance of L-Trp is always stronger than D-Trp within a certain concentration range, which provides a novel and convenient way for the chiral recognition of tryptophan enantiomers.
Subject(s)
Nanoparticles , Tryptophan , Cysteine , Spectrophotometry , StereoisomerismABSTRACT
A new fluorescence coordination polymer [Zn(Py2TTz)(5-OH-IPA)]n (1) (Py2TTz = 2,5-bis(4-pyridyl)thiazolo[5,4-d]thiazole, 5-OH-IPA = 5-hydroxyisophthalic acid dianion) was synthesized, which exhibited the characteristics of fluorescence quenching and bathochromic shift toward Hg(II) in aqueous solution at pH 7.00. Mechanism study showed that the interactions between Hg(II) ions and Py2TTz ligands in 1 were responsible for the fluorescence emission change. Thanks to the specific interactions between 1 and Hg(II), excellent selectivity was achieved both in aqueous solution and in solid test paper. The detection limit of 1 for Hg(II) sensing was 125.76 nmol L-1 and a linear rang was 1.00-10.00 µmol L-1. More importantly, satisfactory recovery and accuracy of 1 for Hg(II) sensing were also obtained in buffer-free real water samples.
Subject(s)
Mercury , Polymers , Spectrometry, Fluorescence , Thiazoles , WaterABSTRACT
In the present paper two series of mixed rare earth complexes Tb(1-x)LnxBTC x nH2O (Ln = Y, Gd, x = 0, 0.1, 0.3, 0.5, 0.7, 0.9) were synthesized by hydrothermal method. The contents of rare earth were measured by using EDTA titration method; the element analyses of C and H were performed by using Vario EL III elemental analyzer, and the IR spectra were recorded by FTIR-8900 infrared spectroscopy with KBr pellet. Then the molecular formula of the complexes were determined to be Tb(1-x)LnxBTC x 0.5H2O (Ln = Y, Gd). The fluorescence spectrum of all the complexes were recorded by using a Hitachi F-4500 fluorescence spectrophotometer at room temperature. The results indicated that all the complexes emitted characteristic fluorescence of Tb3+, and the fluorescence intensities of the complexes were obviously enhanced with doping rare earth ion of Y3+ or Gd3+. It was showed that Tb3+ was sensitized by doping rare earth ions. This may be because there was intra molecular energy transfer in the complexes. Being doped with the rare earth ion the emission peak positions did not change. Among the four emission peaks, 5D4 --> 7F5 (544 nm) was the strongest one, and it was found when the proportion is Y3+ : Tb3+ = 0.5 : 0.5 or Gd3+ : Tb3+ = 0.3 : 0.7, the fluorescence intensity of Tb(1-x)YxBTC x 0.5H2O or Tb(1-x)GdxBTC x 0.5H2O was the greatest, meanwhile the sensitization degree was bigger with doping Gd3+ than doping Y3+ at 544 nm.
ABSTRACT
Three new copper(II) diphosphonates, (NH(4))(2)Cu(3)(hedp)(2)(H(2)O)(4) (1), [NH(3)(CH(2))(4)NH(3)]Cu(3)(hedp)(2).2H(2)O (2), and [NH(2)(C(2)H(4))(2)NH(2)]Cu(3)(hedp)(2) (3), where hedp = 1-hydroxyethylidenediphosphonate, have been synthesized and characterized by single-crystal structural analysis. Crystal data: 1, monoclinic, P2(1)/n, a = 6.2137(13) Å, b = 14.747(2) Å, c = 11.1802(12) Å, beta = 105.83(2) degrees, Z = 2; 2, triclinic, P&onemacr;, a = 7.4840(12) Å, b = 8.032(3) Å, c = 10.007(2) Å, alpha = 111.68(2) degrees, beta = 96.188(14) degrees, gamma = 96.97(2) degrees, Z = 1; 3, triclinic, P&onemacr;, a = 7.0155(6) Å, b = 8.0904(9) Å, c = 9.2644(11) Å, alpha = 112.611(13) degrees, beta = 90.819(8) degrees, gamma = 92.824(7) degrees, Z = 1. The compound 1 is composed of infinite chains with a ladder-type motif. The compounds 2 and 3 adopt a two-dimensional layer structure which contains four- and eight-membered rings assembled from vertex-sharing {CuO(4)} units and {CPO(3)} tetrahedra. The magnetic properties of 3 have been investigated.
