N-(Anthracen-9-ylmeth-yl)adamantan-1-amine.

In the crystal stucture of the of the title compound, C(25)H(27)N, stong π-π inter-actions are found between adjacent anthracene fragments, with a shortest centroid-centroid distance of 3.5750 (9) Å.

Fabrication and characterization of magnetic mesoporous silica nanospheres covalently bonded with europium complex.

A novel multifunctional nanocomposite has been developed by combining the magnetic (Fe3O4) cores encapsulated in the mesoporous silica nanospheres and the luminescent Eu(TTA)3phen complex covalently bonded to the framework of mesoporous silica through a chelate ligand 5-[N,N-bis-3-(triethoxysilyl)propyl]ureyl-1,10-phenanthroline (phen-Si). The obtained nanocomposite is denoted as Eu(TTA)3phen-MMS. It has been well characterized by field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), N2 adsorption/desorption, Quantum Design SQUID magnetometer and photoluminescence spectroscopy, respectively. The results demonstrated that Eu(TTA)3phen-MMS nanocomposite possess superparamagnetic behavior, intense red emission and mesostructures simultaneously.

Novel multifunctional nanocomposites: magnetic mesoporous silica nanospheres covalently bonded with near-infrared luminescent lanthanide complexes.

In this paper, we report the fabrication and characterization of magnetic mesoporous silica nanospheres covalently bonded with near-infrared (NIR) luminescent lanthanide complexes [denoted as Ln(DBM)(3)phen-MMS (Ln = Nd, Yb)]. Ln(DBM)(3)phen-MMS (Ln = Nd, Yb) nanospheres with an average size of 80-130 nm were synthesized via incorporation of the chelate ligand 5-[N,N-bis-3-(triethoxysilyl)propyl]ureyl-1,10-phenanthroline (phen-Si) into the framework of magnetic mesoporous silica (denoted as phen-MMS), followed by introduction of the Ln(DBM)(3)(H(2)O)(2) (Ln = Nd, Yb) complexes into the nanocomposites via a ligand exchange reaction. The morphological, structural, textural, magnetic, and NIR luminescent properties were well-characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), N(2) adsorption-desorption, a superconducting quantum interference device (SQUID), and photoluminescence spectra. These nanocomposites, which possess high surface area, high pore volume, and well-defined pore size, exhibit two-dimensional hexagonal (P6mm) mesostructures. After ligand-mediated excitation, Ln(DBM)(3)phen-MMS (Ln = Nd, Yb) nanocomposites exhibit the characteristic NIR emission of Nd(3+) and Yb(3+), respectively. Magnetic measurements reveal that these mulfunctional nanocomposites possess superparamagnetic properties at 300 K. The high magnetization values make the nanocomposites respond to the external magnetic field quickly. Additionally, the results indicate that Nd(DBM)(3)phen-MMS nanocomposites may have potential applications for laser systems or the optical amplifiers operating at 1.3 microm and Yb(DBM)(3)phen-MMS nanocomposites have several advantages for potential applications in drug delivery or optical imaging.

Synthesis and optical properties of europium-complex-doped inorganic/organic hybrid materials built from oxo-hydroxo organotin nano building blocks.

Hybrid materials doped with novel europium complexes were synthesized using PMMA-co-Sn(12)Clusters (copolymers from oxohydroxo-organotin dimethacrylate and methylmethacrylate) as the matrix material. Two types of hybrid materials were obtained: the physically doped product, PMMA-co-Sn(12)Cluster/Eu(TTA)(3)phen, and the grafted product, PMMA-co-Sn(12)Cluster-co-[EuAA(TTA)(2)phen] (TTA = 2-thenoyltrifluoroacetone, phen = phenanthroline and AA = acrylic acid). The hybrid materials exhibited characteristic luminescence of the Eu(3+) ions, and also showed relative especial optical properties compared with samples just using PMMA as the matrix material. The PMMA-co-Sn(12)Cluster matrix exhibited a high physical doping quantity of [Eu(TTA)(3)phen], which can be attributed to the special structure of this kind of hybrid material. GPC (gel-permeation chromatography), TGA (thermogravimetric analysis), SEM, (1)H NMR, ICP (inductively coupled plasma), (119)Sn NMR, FTIR, and diffuse reflectance techniques were employed to characterize the structures and properties of these hybrid materials.

A study on the near-infrared luminescent properties of xerogel materials doped with dysprosium complexes.

A series of dysprosium complex doped xerogels with the same first ligand (acac = acetylacetone) and different neutral ligands were synthesized in situ via a sol-gel process. The Fourier transform infrared (FTIR) spectra, diffuse reflectance (DR) spectra, and near-infrared (NIR) luminescent properties of dysprosium complexes and dysprosium complex doped xerogels are described in detail. The results reveal that the dysprosium complex is successfully synthesized in situ in the corresponding xerogel. Excitation at the maximum absorption wavelength of the ligands resulted in the characteristic NIR luminescence of the Dy3+ ion, which contributes to the energy transfer from the ligands to the central Dy3+ ion in both the dysprosium complexes and xerogels via an antenna effect. The NIR luminescent properties of the dysprosium complexes and xerogels were compared, respectively. The evidence showed that the neutral ligand triphenyl phosphine oxide (TPPO) could increase the emission intensity of the dysprosium complex while 1,10-phenanthroline (phen) gave the negative effect. In addition, the coordinated water molecules affect the emission intensity of the dysprosium complex doped xerogel without the neutral ligand.

Near-infrared luminescent xerogel materials covalently bonded with ternary lanthanide [Er(III), Nd(III), Yb(III), Sm(III)] complexes.

A beta-diketone ligand 4,4,5,5,5-pentafluoro-1-(2-naphthyl)-1,3-butanedione (Hpfnp), which contains a pentafluoroalkyl chain, was synthesized as the main sensitizer for synthesizing new near-infrared (NIR) luminescent Ln(pfnp)(3)phen (phen = 1,10-phenanthroline) (Ln = Er, Nd, Yb, Sm) complexes. At the same time, a series of lanthanide complexes covalently bonded to xerogels by the ligand 5-(N,N-bis-3-(triethoxysilyl)propyl)ureyl-1,10-phenanthroline (phen-Si) were synthesized in situvia a sol-gel process. [The obtained materials are denoted as xerogel-bonded Ln complexes (Ln = Er, Nd, Yb, Sm).] The single crystal structures of the Ln(pfnp)(3)phen complexes were determined. The properties of these complexes and the corresponding xerogel materials were investigated by Fourier-transform infrared (FTIR), diffuse reflectance (DR), and field-emission scanning electron microscopy (FE-SEM). After ligand-mediated excitation of these complexes and the corresponding xerogel materials they all show the characteristic NIR luminescence of the corresponding Ln(3+) ion. This is attributed to efficient energy transfer from the ligands to the Ln(3+) ion (the so-called "antenna effect").