화학공학소재연구정보센터
Journal of Chemical Physics, Vol.117, No.19, 8800-8804, 2002
Zero-electron-kinetic-energy photoelectron spectroscopy of transition-metal-ether complexes: Y-O(CH3)(2), Y-O(CD3)(2), Y-[O(CH3)(2)](2), and Y-[O(CD3)(2)](2)
The yttrium complexes with one and two dimethyl ethers and their deuterated derivatives are prepared with laser vaporization molecular beam techniques, identified with photoionization time-of-flight mass spectrometry, and investigated with pulsed-field-ionization zero-electronkinetic-energy (ZEKE) photoelectron spectroscopy and ab initio calculations. Adiabatic ionization potentials and yttrium-oxygen stretch and ether-based vibrations are measured for the 1:1 and 1:2 complexes. Fermi interactions are observed from the ZEKE spectra of the 1:1 species. The ground electronic states of the monoligand complexes are determined to be (2)A(2) for the neutral and (1)A(1) for the singly charged positive ion, both in C-2v symmetry, with yttrium binding to oxygen. The coordination of a second ether forms a diligand complex with a linear oxygen-yttrium-oxygen configuration. This is the first electronic-vibrational spectroscopic study of yttrium-polyatomic molecule complexes and weakly bound metal complexes with two or more polyatomic molecules.