TY - JOUR
T1 - Structures and its dipole moments of half-sandwich type metal-benzene (1:1) complexes determined by 2-m long electrostatic hexapole
AU - Imura, Kohei
AU - Ohoyama, Hiroshi
AU - Kasai, Toshio
N1 - Funding Information:
This work was performed as a project research “research and development of system technologies for resource recycling and minimum energy requirement” financially supported by CREST of JST, and was partially supported by a Grant-in-Aid from the Ministry of Education, Culture, Sports, Science and Technology.
PY - 2004/6/21
Y1 - 2004/6/21
N2 - The transition metal-benzene (1:1) complexes are synthesized by laser evaporation method followed by the size and structure selection with 2-m long electrostatic hexapole field. Electric dipole moments of half-sandwich type binary complexes for a series of the transition metals, i.e. Ti, V, Co, and Ni, with benzene molecule were determined by measuring the focusing curves, namely the dependence of the focused beam intensity upon the hexapole field strength. It is found that the dipole moments of Ti-C6H6 and V-C6H6 are larger than the ones of Co-C6H 6 and Ni-C6H6. Such large dipole moments of Ti-C6H6 and V-C6H6 can be ascribed to the strong orbital interaction due to charge transfer between the metal atom and benzene molecule.
AB - The transition metal-benzene (1:1) complexes are synthesized by laser evaporation method followed by the size and structure selection with 2-m long electrostatic hexapole field. Electric dipole moments of half-sandwich type binary complexes for a series of the transition metals, i.e. Ti, V, Co, and Ni, with benzene molecule were determined by measuring the focusing curves, namely the dependence of the focused beam intensity upon the hexapole field strength. It is found that the dipole moments of Ti-C6H6 and V-C6H6 are larger than the ones of Co-C6H 6 and Ni-C6H6. Such large dipole moments of Ti-C6H6 and V-C6H6 can be ascribed to the strong orbital interaction due to charge transfer between the metal atom and benzene molecule.
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U2 - 10.1016/j.chemphys.2004.02.016
DO - 10.1016/j.chemphys.2004.02.016
M3 - Article
AN - SCOPUS:2542426475
SN - 0301-0104
VL - 301
SP - 183
EP - 187
JO - Chemical Physics
JF - Chemical Physics
IS - 2-3
ER -