Matrix isolation studies of nucleic acid constituents. 1. Infrared spectra of uracil monomers

M. Szczesniak; M. J. Nowak; H. Rostkowska; K. Szczepaniak; W. B. Person; D. Shugar

doi:10.1021/ja00357a002

Matrix isolation studies of nucleic acid constituents. 1. Infrared spectra of uracil monomers

Journal of the American Chemical Society ◽

10.1021/ja00357a002 ◽

1983 ◽

Vol 105 (19) ◽

pp. 5969-5976 ◽

Cited By ~ 149

Author(s):

M. Szczesniak ◽

M. J. Nowak ◽

H. Rostkowska ◽

K. Szczepaniak ◽

W. B. Person ◽

...

Keyword(s):

Nucleic Acid ◽

Infrared Spectra ◽

Matrix Isolation

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Matrix isolation infrared studies of nucleic acid constituents. 5. Experimental matrix-isolation and theoretical ab initio SCF molecular orbital studies of the infrared spectra of cytosine monomers

Journal of the American Chemical Society ◽

10.1021/ja00233a006 ◽

1988 ◽

Vol 110 (25) ◽

pp. 8319-8330 ◽

Cited By ~ 180

Author(s):

M. Szczesniak ◽

K. Szczepaniak ◽

J. S. Kwiatkowski ◽

K. KuBulat ◽

W. B. Person

Keyword(s):

Nucleic Acid ◽

Ab Initio ◽

Molecular Orbital ◽

Infrared Spectra ◽

Matrix Isolation ◽

Infrared Studies

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ChemInform Abstract: MATRIX ISOLATION STUDIES OF NUCLEIC ACID CONSTITUENTS. 1. INFRARED SPECTRA OF F URACIL MONOMERS

Chemischer Informationsdienst ◽

10.1002/chin.198351039 ◽

1983 ◽

Vol 14 (51) ◽

Author(s):

M. SZCZESNIAK ◽

M. J. NOWAK ◽

H. ROSTKOWSKA ◽

K. SZCZEPANIAK ◽

W. B. PERSON ◽

...

Keyword(s):

Nucleic Acid ◽

Infrared Spectra ◽

Matrix Isolation

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Reevaluation of matrix-isolation infrared spectra of the isotopologues of trans-diazene and attempts to prepare cis-diazene by photoisomerization

Journal of Molecular Spectroscopy ◽

10.1016/j.jms.2014.12.009 ◽

2015 ◽

Vol 310 ◽

pp. 3-7 ◽

Cited By ~ 3

Author(s):

Norman C. Craig ◽

Kwabena J. Appiah ◽

Charles E. Miller ◽

Michael V. Seiden ◽

Joseph E. Varley

Keyword(s):

Infrared Spectra ◽

Matrix Isolation

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Matrix isolation infrared spectra of carbonyl complexes of iron(II) tetraphenylporphyrin

The Journal of Physical Chemistry ◽

10.1021/j100265a032 ◽

1985 ◽

Vol 89 (19) ◽

pp. 4087-4090 ◽

Cited By ~ 3

Author(s):

T. Kuroi ◽

H. Oshio ◽

K. Nakamoto

Keyword(s):

Infrared Spectra ◽

Matrix Isolation ◽

Carbonyl Complexes

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Infrared spectra of syn and anti isomers of benzaldoxime and pyridine-4-aldoxime: an experimental matrix isolation and theoretical density functional theory study

Vibrational Spectroscopy ◽

10.1016/s0924-2031(01)00101-1 ◽

2001 ◽

Vol 26 (1) ◽

pp. 65-82 ◽

Cited By ~ 27

Author(s):

Tetyana Stepanenko ◽

Leszek Lapinski ◽

Maciej J Nowak ◽

Ludwik Adamowicz

Keyword(s):

Density Functional Theory ◽

Infrared Spectra ◽

Density Functional ◽

Matrix Isolation ◽

Theoretical Density ◽

Density Functional Theory Study ◽

Functional Theory

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Infrared spectra of the CF3I dimer: A concurrent application of matrix-isolation spectroscopy and cavity ring-down spectroscopy

The Journal of Chemical Physics ◽

10.1063/1.2206784 ◽

2006 ◽

Vol 124 (23) ◽

pp. 234509 ◽

Cited By ~ 9

Author(s):

Fumiyuki Ito ◽

Shinichi Hirabayashi

Keyword(s):

Infrared Spectra ◽

Matrix Isolation ◽

Cavity Ring Down Spectroscopy ◽

Matrix Isolation Spectroscopy ◽

Cavity Ring Down

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Gas Chromatographic/Matrix Isolation/Fourier Transform Infrared Spectra of the Laterally Chlorinated Dibenzo-p-Dioxins and Dibenzofurans

Applied Spectroscopy ◽

10.1366/0003702894204263 ◽

1989 ◽

Vol 43 (8) ◽

pp. 1317-1324 ◽

Cited By ~ 10

Author(s):

Charles J. Wurrey ◽

Billy J. Fairless ◽

Harry E. Kimball

Keyword(s):

Fourier Transform ◽

Infrared Spectra ◽

Matrix Isolation ◽

Fourier Transform Infrared ◽

Fourier Transform Infrared Spectra ◽

Reference Quality ◽

Ft Ir ◽

Chlorinated Dioxins ◽

Chromatographic Matrix ◽

Ft Ir Spectroscopy

Reference-quality gas chromatographic/matrix isolation/Fourier transform infrared spectra have been recorded for the following fifteen compounds, which collectively are referred to as the “laterally” chlorinated dibenzo- p-dioxins and dibenzofurans: 2,3,7,8-tetrachlorodibenzo- p-dioxin (2,3,7,8-TCDD); 1,2,3,7,8-pentachlorodibenzo- p-dioxin (1,2,3,7,8-PeCDD);l,2,3,4,7,8-hexachlorodibenzo- p-dioxin(1,2,3,4,7,8-HxCDD)>; 1,2,3,6,7,8,-hexachlorodibenzo- p-dioxin(1,2,3,6,7,8-HxCDD); 1,2,3,7,8,9-hexachlorodibenzo- p-dioxin (1,2,3,7,8,9-HxCDD); 1,2,3,4,6,7,8-heptachlorodibenzo- p-dioxin (1,2,3,4,6,7,8-HpCDD); 2,3,7,8-tetrachlorodibenzofuran (2,3,7,8-TCDF); 1,2,3,7,8-pentachlorodibenzofuran (1,2,3,7,8-PeCDF); 2,3,4,7,8-pentachlorodibenzofuran (2,3,4,7,8-PeCDF); 1,2,3,4,7,8-hexachlorodibenzofuran(1,2,3,4,7,8-HxCDF); 1,2,3,6,7,8-hexachlorodibenzofuran (1,2,3,6,7,8-HxCDF); 1,2,3,7,8,9-hexachlorodibenzofuran (1,2,3,7,8,9-HxCDF); 2,3,4,6,7,8-hexachlorodibenzofuran (2,3,4,6,7,8-HxCDF); 1,2,3,4,6,7,8-heptachlorodibenzofnran (1,2,3,4,6,7,8-HpCDF); and 1,2,3,4,7,8,9-heptachlorodibenzofuran (1,2,3,4,7,8,9-HpCDF). These spectra are discussed qualitatively and, for the laterally chlorinated dioxins, are compared to previously recorded gas-phase GC/FT-IR spectra. Estimates of the instrumental detection limits for these compounds, using matrix isolation GC/FT-IR spectroscopy, were found to fall in the mid-to-high picogram and low nanogram ranges.

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