Characterization of an organometallic xenon complex using NMR and IR spectroscopy

被引:33
作者
Ball, GE
Darwish, TA
Geftakis, S
George, MW
Lawes, DJ
Portius, P
Rourke, JP
机构
[1] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
[2] Univ New S Wales, NMR Facil, Sydney, NSW 2052, Australia
[3] Univ New S Wales, Sch Chem, Sydney, NSW 2052, Australia
[4] Univ Nottingham, Sch Chem, Nottingham NG7 2RD, England
[5] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
关键词
photolysis; time-resolved IR; multinuclear NMR; xenon chemical shifts;
D O I
10.1073/pnas.0406527102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Photolysis of Re((PrCP)-Pr-i)(CO)(2)(PF3) in liquid or supercritical Xe yields two new compounds [Re((PrCp)-Pr-i)(CO)(2)Xe and Re((PrCp)-Pr-i)(CO)(PF3)Xe]. Re((PrCp)-Pr-i)(CO)(PF3)Xe has been characterized by NMR and IR spectroscopies. The compound is an organometallic Xe complex that has been characterized by using NMR spectroscopy and is shown to be longer-lived than other organometallic Xe complexes by IR spectroscopy. F-19, P-31, and Xe-129 chemical shifts have been determined. The Xe-129 chemical shift of Re((PrCp)-Pr-i)(CO)(PF3)Xe, delta -6,179, is a Xe shift that is significantly shielded, on the order of 1,000 ppm, with respect to free Xe. The coupling constants between coordinated Xe-129 and both the F-19 and P-31 nuclei present have been Extracted, confirming the identity of the compound. Observed line widths give a lower limit to the lifetime of the coordinated Xe of 27 ms at 163 K.
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页码:1853 / 1858
页数:6
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