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Journal articles on the topic 'Double resonance ir uv'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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1

Callahan, Michael P., Bridgit Crews, Ali Abo-Riziq, Louis Grace, Mattanjah S. de Vries, Zsolt Gengeliczki, Tiffani M. Holmes, and Glake A. Hill. "IR-UV double resonance spectroscopy of xanthine." Physical Chemistry Chemical Physics 9, no. 32 (2007): 4587. http://dx.doi.org/10.1039/b705042a.

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2

Longarte, Asier, Carolina Redondo, José A. Fernández, and Fernando Castaño. "IR/UV and UV/UV double-resonance study of guaiacol and eugenol dimers." Journal of Chemical Physics 122, no. 16 (April 22, 2005): 164304. http://dx.doi.org/10.1063/1.1881232.

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3

Crews, Bridgit, Ali Abo-Riziq, Louis Grace, Michael Callahan, Martin Kabeláč, Pavel Hobza, and Mattanjah S. de Vries. "IR-UV double resonance spectroscopy of guanine–H2O clusters." Physical Chemistry Chemical Physics 7, no. 16 (2005): 3015. http://dx.doi.org/10.1039/b506107e.

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4

Plützer, Chr, E. Nir, M. S. de Vries, and K. Kleinermanns. "IR–UV double-resonance spectroscopy of the nucleobase adenine." Physical Chemistry Chemical Physics 3, no. 24 (December 5, 2001): 5466–69. http://dx.doi.org/10.1039/b107997b.

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5

Inokuchi, Yoshiya, Yusuke Kobayashi, Takafumi Ito, and Takayuki Ebata. "Conformation ofl-Tyrosine Studied by Fluorescence-Detected UV−UV and IR−UV Double-Resonance Spectroscopy." Journal of Physical Chemistry A 111, no. 17 (May 2007): 3209–15. http://dx.doi.org/10.1021/jp070163a.

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6

Wang, X. M., G. Y. Wu, P. X. Ding, J. D. Chen, W. B. Gao, H. T. Ji, and S. H. Liu. "Vibrational energy transfer study of C6H6 by IR-UV double resonance." Chemical Physics Letters 125, no. 5-6 (April 1986): 537–42. http://dx.doi.org/10.1016/0009-2614(86)87094-4.

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7

Abo-Riziq, Ali G., Bridgit Crews, John E. Bushnell, Michael P. Callahan, and Mattanjah S. De Vries *. "Conformational analysis of cyclo(Phe-Ser) by UV–UV and IR–UV double resonance spectroscopy andab initiocalculations." Molecular Physics 103, no. 11-12 (June 10, 2005): 1491–95. http://dx.doi.org/10.1080/00268970500095923.

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8

Fischer, Kathrin H., Jörg Herterich, Ingo Fischer, Sander Jaeqx, and Anouk M. Rijs. "Phenylpropargyl Radicals and Their Dimerization Products: An IR/UV Double Resonance Study." Journal of Physical Chemistry A 116, no. 33 (August 10, 2012): 8515–22. http://dx.doi.org/10.1021/jp306075a.

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9

Bouchet, Aude, Johanna Klyne, Shun-ichi Ishiuchi, Otto Dopfer, Masaaki Fujii, and Anne Zehnacker. "Stereochemistry-dependent structure of hydrogen-bonded protonated dimers: the case of 1-amino-2-indanol." Physical Chemistry Chemical Physics 20, no. 18 (2018): 12430–43. http://dx.doi.org/10.1039/c8cp00787j.

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Stereochemistry effects on the structure of molecular aggregates are studied in the prototypical 1-amino-2-indanol. Conformer-selective IR-UV double resonance spectroscopy reveals how stereochemistry shapes its dimers.

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10

Fujii, Masaaki, Shigeki Tanabe, Yasuo Okuzawa, and Mitsuo Ito. "IR-UV Double Resonance Spectrum of Acetylene Below and Above the Predissociation Threshold." Laser Chemistry 14, no. 1-3 (January 1, 1994): 161–82. http://dx.doi.org/10.1155/1994/76165.

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The Ã1Au ← X˜1∑g+ electronic transition of the vibrationally excited acetylene molecule was studied by IR–UV double resonance spectroscopy in gas and in a supersonic jet. The C–H antisymmetric stretching vibration νCHant in the Ã state was clearly observed when the molecule was excited to the νCHsym + νCHant combination vibration in the X˜ state by the IR laser. When the νCHant fundamental vibration was excited, the C–H in-plane cis-bending vibration νcis(in) in the Ã state was observed strongly, while νCHant almost disappeared. The difference was interpreted in terms of Fermi resonance of the νCHant fundamental vibration in X˜. The predissociation threshold was newly determined to be 46,439˼46,673 cm-1 (133.11 ± 0.33 kcal/mol). In the region above the predissociation threshold, strong vibrational mixing was found. The higher members of the progression of the trans-bending vibration starting from νCHant were assigned. It was suggested that the nonradiative relaxation accelerated in the region above 51,744 cm-1.

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11

Hong, Zhao, Li Li, and Chen Xirong. "IR-UV DOUBLE RESONANCE STUDIES OF THE SINGLE VIBRATIONAL LEVEL RELAXATION OF BENZENE." Acta Physico-Chimica Sinica 4, no. 04 (1988): 406–10. http://dx.doi.org/10.3866/pku.whxb19880416.

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12

Watanabe, Takeshi, Takayuki Ebata, Shigeki Tanabe, and Naohiko Mikami. "Size‐selected vibrational spectra of phenol‐(H2O)n (n=1–4) clusters observed by IR–UV double resonance and stimulated Raman‐UV double resonance spectroscopies." Journal of Chemical Physics 105, no. 2 (July 8, 1996): 408–19. http://dx.doi.org/10.1063/1.471917.

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13

Mahé, Jérôme, Sander Jaeqx, Anouk M. Rijs, and Marie-Pierre Gaigeot. "Can far-IR action spectroscopy combined with BOMD simulations be conformation selective?" Physical Chemistry Chemical Physics 17, no. 39 (2015): 25905–14. http://dx.doi.org/10.1039/c5cp01518a.

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The combination of conformation selective far-IR/UV double resonance spectroscopy with Born–Oppenheimer molecular dynamics (BOMD) simulations is presented here for the structural characterization of the Ac-Phe-Pro-NH₂ peptide in the far-infrared spectral domain, i.e. for radiation below 800 cm⁻¹.

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14

Lettenberger, M., F. Emmerling, N. H. Gottfried, and A. Laubereau. "Orientational motion of anthracene in liquid solution studied by IR/UV double-resonance spectroscopy." Chemical Physics Letters 240, no. 4 (June 1995): 324–29. http://dx.doi.org/10.1016/0009-2614(95)00528-c.

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15

Asami, Hiroya, Shu-hei Urashima, and Hiroyuki Saigusa. "Structural identification of uric acid and its monohydrates by IR-UV double resonance spectroscopy." Physical Chemistry Chemical Physics 13, no. 45 (2011): 20476. http://dx.doi.org/10.1039/c1cp22540e.

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16

Witte, Thomas, Christine Bucher, Françoise Remacle, Detlev Proch, Karl L. Kompa, and R. D. Levine. "IR-UV Double-Resonance Photodissociation of Nitric Acid (HONO2) Viewed as Molecular Information Processing." Angewandte Chemie International Edition 40, no. 13 (July 2, 2001): 2512–14. http://dx.doi.org/10.1002/1521-3773(20010702)40:13<2512::aid-anie2512>3.0.co;2-i.

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17

Abo-Riziq, Ali G., John E. Bushnell, Bridgit Crews, Michael P. Callahan, Louis Grace, and Mattanjah S. De Vries. "Discrimination between diastereoisomeric dipeptides by IR-UV double resonance spectroscopy and ab initio calculations." International Journal of Quantum Chemistry 105, no. 4 (2005): 437–45. http://dx.doi.org/10.1002/qua.20719.

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18

Witte, Thomas, Christine Bucher, Françoise Remacle, Detlev Proch, Karl L. Kompa, and R. D. Levine. "IR-UV Double-Resonance Photodissociation of Nitric Acid (HONO2) Viewed as Molecular Information Processing." Angewandte Chemie 113, no. 13 (July 2, 2001): 2580–82. http://dx.doi.org/10.1002/1521-3757(20010702)113:13<2580::aid-ange2580>3.0.co;2-o.

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19

Bhattacherjee, Aditi, and Sanjay Wategaonkar. "Conformational preferences of monohydrated clusters of imidazole derivatives revisited." Physical Chemistry Chemical Physics 17, no. 31 (2015): 20080–92. http://dx.doi.org/10.1039/c5cp02422f.

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IR-UV double resonance spectroscopy was used to identify the conformers of monohydrated benzimidazole andN-methylbenzimidazole in a supersonic jet. A new OH–N bound conformer relevant to histidine containing proteins was discovered. The long standing differences in the literature about the relative energies and abundance of the monohydrated imidazole derivatives have also been resolved.

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20

Chadwick, B. L., A. P. Milce, and B. J. Orr. "Fluorescence-detected infrared– and Raman–ultraviolet double resonance in acetylene gas: studies of spectroscopy and rotational energy transfer." Canadian Journal of Physics 72, no. 11-12 (November 1, 1994): 939–53. http://dx.doi.org/10.1139/p94-124.

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Fluorescence-detected Raman–ultraviolet and infrared–ultraviolet double resonance (DR) spectroscopy enables state-selective studies of rotational and vibrational energy transfer in gas-phase acetylene (C2H2) and its deuterated isotopomers (C2HD, C2D2). The Raman–UV DR approach entails pulsed coherent Raman excitation in the ν2 rovibrational band of C2H2(g), followed by fluorescence-detected rovibronic probing of the resulting rovibrational population distributions. Corresponding IR–UV DR experiments employ a line-tunable, pulsed CO2 laser to excite rovibrational transitions in the 2ν4 band of C2HD(g) and in the (ν4 + ν5) band of C2D2(g), with similar fluorescence-detected rovibronic probing. These time-resolved DR spectroscopic techniques provide rotationally specific information on collision-induced molecular energy transfer in acetylene. This paper extends previous Raman–UV DR spectroscopic studies of C2H2 and presents fresh IR–UV DR spectra of gas-phase C2HD and C2D2, including evidence of a novel two-step excitation sequence in which a single CO2-laser pulse promotes C2D2 by successive transitions in the (ν4 + v5) and (2ν4 + 2ν5−ν4−v5) absorption bands. Kinetic measurements and mechanistic observations are also reported for collision-induced rotational energy transfer in acetylene gas, complementing other investigations of rotationally resolved vibrational energy transfer.

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21

Walther, Th, H. Bitto, T. K. Minton, and J. Robert Huber. "UV-IR double-resonance spectroscopy of jet-cooled propynal detected by the fluorescence dip method." Chemical Physics Letters 231, no. 1 (December 1994): 64–69. http://dx.doi.org/10.1016/0009-2614(94)01224-5.

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22

Fehrensen, Benjamin, Michael Hippler, and Martin Quack. "Isotopomer-selective overtone spectroscopy by ionization detected IR+UV double resonance of jet-cooled aniline." Chemical Physics Letters 298, no. 4-6 (December 1998): 320–28. http://dx.doi.org/10.1016/s0009-2614(98)01216-0.

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23

Rothman, Nancy C., David F. Dever, Dana Garcia, and Ernest Grunwald. "An IR-UV double resonance study of dibromodifluoromethane. Evidence for V-V' vibrational steady states." Journal of Physical Chemistry 90, no. 24 (November 1986): 6464–70. http://dx.doi.org/10.1021/j100282a012.

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24

Palmer, Phillip M., Yu Chen, and Michael R. Topp. "Simple water clusters of Coumarins 151 and 152A studied by IR–UV double resonance spectroscopy." Chemical Physics Letters 318, no. 4-5 (February 2000): 440–47. http://dx.doi.org/10.1016/s0009-2614(00)00036-1.

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25

Bewick, C. P., J. G. Haub, R. G. Hynes, J. F. Martins, and B. J. Orr. "Rotational energy transfer in D2CO (v4=1): IR–UV double resonance studies ofJ‐changing collisions." Journal of Chemical Physics 88, no. 10 (May 15, 1988): 6350–71. http://dx.doi.org/10.1063/1.454473.

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26

Asami, Hiroya, Shu-hei Urashima, and Hiroyuki Saigusa. "Hydration structures of 2′-deoxyguanosine studied by IR-UV double resonance spectroscopy: comparison with guanosine." Physical Chemistry Chemical Physics 11, no. 44 (2009): 10466. http://dx.doi.org/10.1039/b912684h.

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27

Singh, Prashant Chandra, and G. Naresh Patwari. "IR−UV Double Resonance Spectroscopic Investigation of Phenylacetylene−Alcohol Complexes. Alkyl Group Induced Hydrogen Bond Switching." Journal of Physical Chemistry A 112, no. 23 (June 2008): 5121–25. http://dx.doi.org/10.1021/jp800968g.

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28

Plützer, Chr, I. Hünig, and K. Kleinermanns. "Pairing of the nucleobase adenine studied by IR-UV double-resonance spectroscopy and ab initio calculations." Physical Chemistry Chemical Physics 5, no. 6 (February 3, 2003): 1158–63. http://dx.doi.org/10.1039/b212338j.

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29

Nir, Eyal, Christoph Janzen, Petra Imhof, Karl Kleinermanns, and Mattanjah S. de Vries. "Pairing of the nucleobase guanine studied by IR–UV double-resonance spectroscopy and ab initio calculations." Physical Chemistry Chemical Physics 4, no. 5 (January 29, 2002): 740–50. http://dx.doi.org/10.1039/b110360c.

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30

Nagornova, Natalia S., Thomas R. Rizzo, and Oleg V. Boyarkin. "Exploring the Mechanism of IR-UV Double-Resonance for Quantitative Spectroscopy of Protonated Polypeptides and Proteins." Angewandte Chemie International Edition 52, no. 23 (April 25, 2013): 6002–5. http://dx.doi.org/10.1002/anie.201301656.

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31

Nagornova, Natalia S., Thomas R. Rizzo, and Oleg V. Boyarkin. "Exploring the Mechanism of IR-UV Double-Resonance for Quantitative Spectroscopy of Protonated Polypeptides and Proteins." Angewandte Chemie 125, no. 23 (April 25, 2013): 6118–21. http://dx.doi.org/10.1002/ange.201301656.

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32

Broquier, M., F. Lahmani, A. Zehnacker-Rentien, V. Brenner, Ph Millié, and A. Peremans. "Hydrogen-Bonded Bridges in Complexes ofo-Cyanophenol: Laser-Induced Fluorescence and IR/UV Double-Resonance Studies." Journal of Physical Chemistry A 105, no. 28 (July 2001): 6841–50. http://dx.doi.org/10.1021/jp010218n.

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33

Bykov, Sergei, Igor Lednev, Anatoli Ianoul, Aleksandr Mikhonin, Calum Munro, and Sanford A. Asher. "Steady-State and Transient Ultraviolet Resonance Raman Spectrometer for the 193–270 nm Spectral Region." Applied Spectroscopy 59, no. 12 (December 2005): 1541–52. http://dx.doi.org/10.1366/000370205775142511.

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We describe a state-of-the-art tunable ultraviolet (UV) Raman spectrometer for the 193–270 nm spectral region. This instrument allows for steady-state and transient UV Raman measurements. We utilize a 5 kHz Ti-sapphire continuously tunable laser (∼20 ns pulse width) between 193 nm and 240 nm for steady-state measurements. For transient Raman measurements we utilize one Coherent Infinity YAG laser to generate nanosecond infrared (IR) pump laser pulses to generate a temperature jump (T-jump) and a second Coherent Infinity YAG laser that is frequency tripled and Raman shifted into the deep UV (204 nm) for transient UV Raman excitation. Numerous other UV excitation frequencies can be utilized for selective excitation of chromophoric groups for transient Raman measurements. We constructed a subtractive dispersion double monochromator to minimize stray light. We utilize a new charge-coupled device (CCD) camera that responds efficiently to UV light, as opposed to the previous CCD and photodiode detectors, which required intensifiers for detecting UV light. For the T-jump measurements we use a second camera to simultaneously acquire the Raman spectra of the water stretching bands (2500–4000 cm−1) whose band-shape and frequency report the sample temperature.

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34

Kim, Minho, Sang-Su Kim, Hyuk Kang, and Young Dong Park. "REMPI and IR-UV double resonance spectroscopy of 3-aminophenol·(NH3)1 cluster in the gas phase." Journal of Molecular Spectroscopy 263, no. 1 (September 2010): 51–55. http://dx.doi.org/10.1016/j.jms.2010.06.011.

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35

Matsuda, Yoshiyuki, Takayuki Ebata, and Naohiko Mikami. "IR−UV Double-Resonance Spectroscopic Study of 2-Hydroxypyridine and Its Hydrogen-Bonded Clusters in Supersonic Jets." Journal of Physical Chemistry A 105, no. 14 (April 2001): 3475–80. http://dx.doi.org/10.1021/jp003272x.

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36

Zhang, Weiqing, Hiroshi Kawamata, Anthony J. Merer, and Kopin Liu. "IR−UV Double-Resonance of Methyl Radicals and a Determination of the Detection Sensitivity of REMPI Bands†." Journal of Physical Chemistry A 113, no. 47 (November 26, 2009): 13133–38. http://dx.doi.org/10.1021/jp902969v.

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37

Ishikawa, Haruki, Chioko Nagao, and Naohiko Mikami. "Observation of the νCHExcited Vibrational Levels in theÃ1A″State of HCP by IR–UV Double Resonance Spectroscopy." Journal of Molecular Spectroscopy 194, no. 1 (March 1999): 52–60. http://dx.doi.org/10.1006/jmsp.1998.7757.

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38

Busker, Matthias, Yuriy N. Svartsov, Thomas Häber, and Karl Kleinermanns. "IR–UV double resonance spectra of pyrazine dimers: Competition between CH⋯π, π⋯π and CH⋯N interactions." Chemical Physics Letters 467, no. 4-6 (January 2009): 255–59. http://dx.doi.org/10.1016/j.cplett.2008.10.091.

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39

Mizoguchi, Miwako, Nami Yamakita, Soji Tsuchiya, Atsushi Iwasaki, Kennosuke Hoshina, and Kaoru Yamanouchi. "IR−UV Double Resonance Spectroscopy of Acetylene in the Ã1Aunν3‘+ν4‘ andnν3‘+ν6‘ (n= 2, 3)UngeradeVibrational States†." Journal of Physical Chemistry A 104, no. 45 (November 2000): 10212–19. http://dx.doi.org/10.1021/jp001215y.

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40

Blodgett, Karl N., Joshua L. Fischer, Timothy S. Zwier, and Edwin L. Sibert. "The missing NH stretch fundamental in S1 methyl anthranilate: IR-UV double resonance experiments and local mode theory." Physical Chemistry Chemical Physics 22, no. 25 (2020): 14077–87. http://dx.doi.org/10.1039/d0cp01916j.

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41

Urashima, Shu-hei, Mitsuhiko Miyazaki, Masaaki Fujii, and Hiroyuki Saigusa. "IR–UV Double Resonance Spectroscopy as Implemented by Polarized Laser Schemes: Probing Orientations of Vibrational Transition Dipole Moments." Chemistry Letters 42, no. 9 (September 5, 2013): 1070–72. http://dx.doi.org/10.1246/cl.130425.

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42

Okuzawa, Yasuo, Masaaki Fujii, and Mitsuo Ito. "Direct observation of second excited 1,3 (n,π*) states of pyrazine by UV—IR double resonance dip spectroscopy." Chemical Physics Letters 171, no. 4 (August 1990): 341–46. http://dx.doi.org/10.1016/0009-2614(90)85374-l.

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43

Tanabe, Shigeki, Takayuki Ebata, Masaaki Fujii, and Naohiko Mikami. "OH stretching vibrations of phenol—(H2O)n (n=1–3) complexes observed by IR-UV double-resonance spectroscopy." Chemical Physics Letters 215, no. 4 (December 1993): 347–52. http://dx.doi.org/10.1016/0009-2614(93)85726-5.

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44

Payne, Mark A., Angela P. Milce, Michael J. Frost, and Brian J. Orr. "Rovibrational Energy Transfer in the 4νCHManifold of Acetylene, Viewed by IR−UV Double Resonance Spectroscopy. 5. Detailed Kinetic Model†." Journal of Physical Chemistry A 111, no. 49 (December 2007): 12839–53. http://dx.doi.org/10.1021/jp0767617.

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45

Fricke, Holger, Andreas Funk, Thomas Schrader, and Markus Gerhards. "Investigation of Secondary Structure Elements by IR/UV Double Resonance Spectroscopy: Analysis of an Isolated β-Sheet Model System." Journal of the American Chemical Society 130, no. 14 (April 2008): 4692–98. http://dx.doi.org/10.1021/ja076031c.

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46

Matsumoto, Yoshiteru, Takayuki Ebata, and Naohiko Mikami. "OH stretching vibrations and hydrogen-bonded structures of 7-hydroxyquinoline-(H2O)1–3 investigated by IR–UV double-resonance spectroscopy." Chemical Physics Letters 338, no. 1 (April 2001): 52–60. http://dx.doi.org/10.1016/s0009-2614(01)00226-3.

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47

Matsumoto, Y., T. Ebata, and N. Mikami. "Structures and vibrations of 2-naphthol–(NH3) (n=1–3) hydrogen-bonded clusters investigated by IR–UV double-resonance spectroscopy." Journal of Molecular Structure 552, no. 1-3 (September 2000): 257–71. http://dx.doi.org/10.1016/s0022-2860(00)00490-7.

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48

Payne, Mark A., Angela P. Milce, Michael J. Frost, and Brian J. Orr. "Rovibrational Energy Transfer in the 4νCHManifold of Acetylene, Viewed by IR−UV Double Resonance Spectroscopy. 1. Foundation Studies at LowJ†." Journal of Physical Chemistry A 107, no. 49 (December 2003): 10759–70. http://dx.doi.org/10.1021/jp035224t.

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49

Guchhait, Nikhil. "Benzyl alcohol-ammonia (1:1) cluster structure investigated by combined IR-UV double resonance spectroscopy in jet andab initio calculation." Journal of Chemical Sciences 113, no. 3 (June 2001): 235–44. http://dx.doi.org/10.1007/bf02704073.

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50

Wako, Hiromichi, Shun-ichi Ishiuchi, Daichi Kato, Géraldine Féraud, Claude Dedonder-Lardeux, Christophe Jouvet, and Masaaki Fujii. "A conformational study of protonated noradrenaline by UV–UV and IR dip double resonance laser spectroscopy combined with an electrospray and a cold ion trap method." Physical Chemistry Chemical Physics 19, no. 17 (2017): 10777–85. http://dx.doi.org/10.1039/c6cp08426e.

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