TY - JOUR
T1 - Direct information on structure and energetic features of Cu+-Xe species formed in MFI-Type zeolite at room temperature
AU - Torigoe, Hiroe
AU - Mori, Toshinori
AU - Fujie, Kazuhiko
AU - Ohkubo, Takahiro
AU - Itadani, Atsushi
AU - Gotoh, Kazuma
AU - Ishida, Hiroyuki
AU - Yamashita, Hiroki
AU - Yumura, Takashi
AU - Kobayashi, Hisayoshi
AU - Kuroda, Yasushige
PY - 2010/9/16
Y1 - 2010/9/16
N2 - The interacted species of Xe with metal ions that are stable at room temperature are not known and are a subject of interest for fundamental chemistry. We have experimentally found a new and stable Xe species, XeCu +, which was formed at room temperature in a copper ion-exchanged MFI-type zeolite. The presence of a prominent interaction between Cu+ in MFI and Xe, which has a covalent nature, was for the first time evidenced from experimental in situ synchrotron X-ray absorption fine structure and heat of adsorption measurements: the Cu+-Xe bond length of 2.45 - and the bonding energy of ca. 60 kJ mol-1. The bonding nature between Xe and Cu+ in the MFI zeolite was discussed utilizing density functional theory; the observed significant stabilization comes from the d(Cu+ in MFI)-p(Xe) orbital interaction. These new findings may pave a new way to developing fundamental chemistry of Xe compounds.
AB - The interacted species of Xe with metal ions that are stable at room temperature are not known and are a subject of interest for fundamental chemistry. We have experimentally found a new and stable Xe species, XeCu +, which was formed at room temperature in a copper ion-exchanged MFI-type zeolite. The presence of a prominent interaction between Cu+ in MFI and Xe, which has a covalent nature, was for the first time evidenced from experimental in situ synchrotron X-ray absorption fine structure and heat of adsorption measurements: the Cu+-Xe bond length of 2.45 - and the bonding energy of ca. 60 kJ mol-1. The bonding nature between Xe and Cu+ in the MFI zeolite was discussed utilizing density functional theory; the observed significant stabilization comes from the d(Cu+ in MFI)-p(Xe) orbital interaction. These new findings may pave a new way to developing fundamental chemistry of Xe compounds.
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U2 - 10.1021/jz100838c
DO - 10.1021/jz100838c
M3 - Article
AN - SCOPUS:77956848648
SN - 1948-7185
VL - 1
SP - 2642
EP - 2650
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
IS - 18
ER -