TY - JOUR
T1 - Zero-electron-kinetic-energy photoelectron spectroscopy of transition-metal-ether complexes
T2 - Y-O(CH3)2, Y-O(CD3)2, Y-[O(CH3)2]2, and Y-[O(CD3)2]2
AU - Rothschopf, Gretchen K.
AU - Li, Shenggang
AU - Yang, Dong Sheng
PY - 2002/11/15
Y1 - 2002/11/15
N2 - Adiabatic ionization energies and vibrational frequencies were measured for the yttrium complexes with one and two dimethyl ether ligands. Compared to the metal atom, the ionization energies of the 1:1/1:2 complexes shift to red by 12 147/20 212 cm-1 with O(CH3)2 and 12 172/20 269 cm-1 with O(CD3)2. The energy shifts indicate a large charge effect on the metal-ligand binding and a differential binding for the first and second ligand coordinations. The measurements of the Y+-O, C-O, and C-O-C vibrations show that the complexes are formed through the yttrium binding to the oxygen and that the ether remains unbroken upon coordination.
AB - Adiabatic ionization energies and vibrational frequencies were measured for the yttrium complexes with one and two dimethyl ether ligands. Compared to the metal atom, the ionization energies of the 1:1/1:2 complexes shift to red by 12 147/20 212 cm-1 with O(CH3)2 and 12 172/20 269 cm-1 with O(CD3)2. The energy shifts indicate a large charge effect on the metal-ligand binding and a differential binding for the first and second ligand coordinations. The measurements of the Y+-O, C-O, and C-O-C vibrations show that the complexes are formed through the yttrium binding to the oxygen and that the ether remains unbroken upon coordination.
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U2 - 10.1063/1.1504704
DO - 10.1063/1.1504704
M3 - Article
AN - SCOPUS:0037113229
SN - 0021-9606
VL - 117
SP - 8800
EP - 8804
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 19
ER -