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Spectroscopy With Polarized Light: Polarized Matrix Infrared Spectra of Cyclopentadieneone THOMAS K. ORMOND, ADAM M. SCHEER, G. BARNEY ELLISON, Department of Chemistry and Biochemistry, University of Colorado, Boulder; MARK R. NIMLOS, Center for Renewable Chemical, Technologies & Materials, NREL, Golden, CO; JOHN W. DAILY, Department of Mechanical Engineering, University of Colorado, Boulder; and JOHN F. STANTON, Institute for Theoretical Chemistry, Department of Chemistry, University of Texas, Austin OSU MOLECULAR SPECTROSCOPY SYMPOSIUM JUNE, 2012 Thomas K. Ormond G. Barney Ellison Group Department of Chemistry and Biochemistry University of Colorado, Boulder
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Intermediate in thermal decomposition pathways of lignin model monomers leading to formation of acetylenes and substituted acetylenes – known precursors to PAHs and soot Partial anti aromatic character and rapid dimerization - cannot be isolated Cyclopentadieneone (C 5 H 4 =O) Depuy & Lyons, J. Am. Chem. Soc. 1960, 82, 631-633.
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Scheer, Mukarakate, Robichaud, Nimlos, & Ellison, Thermal Decomposition Mechanisms of the Methoxyphenols, J. Phys. Chem. A 2011, 115, 13381-13389.
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Cyclopentadieneone (C 5 H 4 =O) Need a clean source of C 5 H 4 =O and deuterated species: C 5 D 4 =O and C 5 H 2 D 2 =O - Synthesis of o-phenylene sulfite DeJongh, D.C.; Van Fossen, R.Y.; Bourgeois, C.F. Tetrahedron Lett., 1967, 271.
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1 mm SiC tube @ 300–1700 K (tubular reactor) 50 µsec Supersonic Jet of Radicals/He into 10 -8 Torr IE( C 5 H 4 =O ) 9.49 eV 118.2 nm VUV Laser (10.487 eV) VUV + C 54 =O C 5 H 4 =O + + e – phenylene sulfite entrained in He/Ar carrier gas. pulsed valve 1 msec open @ 10 Hz Molecular diagnostics: C 5 H 4 =O + VUV-TOF-PIMS detection and matrix isolation FTIR 64 cm Wiley-McLaren TOF spectrometer m/ m 2100 Temperature monitor Optical Pyrometer Supersonic Jet of Radicals/Ar into 10 -6 Torr onto CsI window @ 10 K C 5 H 4 =O molecular beam diagnostics
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C 5 H 4 =O molecular beam diagnostics: 118.2 nm (10.487 eV) photoionization mass spectrometry
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C 5 D 4 =O molecular beam diagnostics: 118.2 nm (10.487 eV) photoionization mass spectrometry – fully deuterated isotopomer
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C 5 H 4 =O and C 5 D 4 =O matrix infrared absorption spectroscopy
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C 5 H 4 =O molecular beam diagnostics: matrix infrared absorption spectroscopy
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C 5 H 4 =O molecular beam diagnostics: matrix infrared absorption spectroscopy
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z x y z x y y-polarized UV radiation photo orients sample via electronic transition y-polarized IR radiation excites b 2 vibrational transitions [Abs(Y)], z- polarized IR excites a 1 vibrations [Abs(Z)] Linear dichroism IR spectroscopy: Carbonyl dissociative transition – formaldehyde test case In this way, we can selectively excite vibrations of a particular symmetry
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Linear dichroism IR spectroscopy: Carbonyl dissociative transition – formaldehyde test case
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Linear dichroism IR spectroscopy: Cyclopentadieneone
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Linear dichroism IR spectroscopy: d4-Cyclopentadieneone
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Linear dichroism IR spectroscopy: d4-Cyclopentadieneone
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This work is funded by the NSF and DOE Ellison (CU Boulder) and Nimlos (NREL) group members Don David and Ken Smith (CIRES machine shop) Chuck Depuy (CU Boulder) Hans-Heinrich Carstensen (Colorado School of Mines) Thanks to:
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