Ligand-Coated Vanadium Oxide Clusters: Capturing Gas-Phase Magic Numbers in Solution

被引:21
作者
Ard, S. [1 ]
Dibble, C. J. [1 ]
Akin, S. T. [1 ]
Duncan, M. A. [1 ]
机构
[1] Univ Georgia, Dept Chem, Athens, GA 30602 USA
关键词
ANION PHOTOELECTRON-SPECTROSCOPY; LASER VAPORIZATION CONDENSATION; DENSITY-FUNCTIONAL THEORY; ELECTRONIC-STRUCTURE; VIBRATIONAL SPECTROSCOPY; LUMINESCENT PROPERTIES; INFRARED-SPECTROSCOPY; METAL; NANOPARTICLES; PHOTODISSOCIATION;
D O I
10.1021/jp200691k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Subnanometer vanadium oxide clusters in the 10-30 atom size range are produced in the gas phase with laser vaporization, coated with gas-phase ligands, and then captured in solution using a laser vaporization flaw reactor. Acetonitrile (MeCN) and tetrahydrofuran (THF) ligands form complexes efficiently with the oxide clusters, rendering them soluble in solutions of these same ligands and other solvents. The structures and compositions of clusters captured in solution are investigated with laser desorption time-of-flight (LD-TOF) mass spectrometry, UV-visible and IR spectroscopy, and density functional theory computations. MeCN forms oxide clusters having the exact stoichiometries found previously to be stable in the gas phase (V3O6, V4O9, and V5O12), in a simple ligand-addition process. THF produces similar oxide cores, but with terminal oxygens displaced. Infrared spectra are consistent with the presence of terminal oxygens for the MeCN complexes and their absence for the THF species. In either case, DFT computations show that the vanadium oxide cores are minimally perturbed by ligand addition. Solutions of both samples exhibit visible photoluminescence with only minor dependence on the ligand, indicating that the core oxide is the source of the emission.
引用
收藏
页码:6438 / 6447
页数:10
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