Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Jessica L. Menke"'
Autor:
Jessica L. Menke, Robert J. McMahon
Publikováno v:
Canadian Journal of Chemistry. 89:186-194
Matrix-isolation photochemistry (λ > 299 nm; Ar, 10 K) of 5-cyano-2H-pyran-2-one (5, δ-cyano-α-pyrone) shows complete conversion to a mixture of several ring-opened ketene isomers (6) and a ring-closed Dewar lactone (7), as detected by infrared sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4813afbf5f511f30498771f27fa40b99
https://doi.org/10.1139/v10-094
https://doi.org/10.1139/v10-094
Autor:
Jessica L. Menke
Publikováno v:
Journal of Chemical Education. 91:414-416
Online poster sessions provide the benefits of typical face-to-face poster sessions while eliminating some of the obstacles such a nontraditional assessment presents. It allows students to do in-depth research on a specific topic and then present the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfb0c35373ea3307f28a5afe7c706b31
https://doi.org/10.1021/ed400665n
https://doi.org/10.1021/ed400665n
Publikováno v:
The Journal of Physical Chemistry A. 114:6431-6437
The effects of cyano substitution on cyclobutadiene are explored using density functional, coupled-cluster, CASSCF, and CASPT2 calculations. An isodesmic reaction is employed to gauge the relative stabilization (DeltaH(rxn) degrees) of cyclobutadiene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::773e57466dc5388b234de372216cf0d0
https://doi.org/10.1021/jp101963p
https://doi.org/10.1021/jp101963p
Autor:
Eric V. Patterson, Jessica L. Menke
Publikováno v:
Journal of Molecular Structure: THEOCHEM. 811:281-291
Density functional and correlated ab initio molecular orbital calculations have been carried out in an effort to understand the reaction of ethoxide with O , S -dimethyl methylphosphonothiolate, a model compound for the potent chemical warfare agent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09f72f9b940ac39b940b707a44ced24c
https://doi.org/10.1016/j.theochem.2006.11.033
https://doi.org/10.1016/j.theochem.2006.11.033
Autor:
Jessica L. Menke, Kristin Mutolo, Eric V. Patterson, Anne Saunders, Scott P. Sibley, Pamela L. Crum
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 163:463-471
The absorbance and fluorescence of 2-(1-pyrrolyl)-pyridine and three methylated derivatives have been studied in a variety of solvents. Absorbance spectra of the molecules were found to exhibit minor solvent dependence. The fluorescence spectra for a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37fc29c66f2def5a08c500215eb2bc83
https://doi.org/10.1016/j.jphotochem.2004.01.019
https://doi.org/10.1016/j.jphotochem.2004.01.019
Autor:
Alberto Lesarri, Cornelia Mlynek, Jessica L. Menke, Robert J. McMahon, Henning Hopf, Jens-Uwe Grabow, Michael Rosemeyer
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 16(47)
In support of a deeper understanding of the chemistry of cyanoacetylene--a known constituent of planetary atmospheres and interstellar space--theoretical and experimental studies address the chemical mechanism of dimerization and trimerization, and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d12a6ba67aede89b0f7499d6255f337
https://pubmed.ncbi.nlm.nih.gov/20967903
https://pubmed.ncbi.nlm.nih.gov/20967903
Publikováno v:
Journal of the American Chemical Society. 129(8)
Photolysis (lambda>571 nm) of 1,3-diphenyldiazopropyne (9) affords triplet 1,3-diphenylpropynylidene (3), as characterized by IR, UV/vis, and EPR spectroscopy in low-temperature matrices. Two conformational isomers of triplet 3 are spectroscopically
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f91306561a01b801fa009317e36dd34
https://pubmed.ncbi.nlm.nih.gov/17279747
https://pubmed.ncbi.nlm.nih.gov/17279747
Publikováno v:
The Journal of organic chemistry. 70(22)
[reaction: see text] Potential energy surfaces for the alkaline hydrolysis of sarin and O,S-dimethyl methylphosphonothiolate, a VX model compound, and the perhydrolysis of the latter have been computed at the MP2/6-31+G(d)//mPW1K/MIDI! level of theor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d53b0030429e798ec0611cbd24b5d867
https://pubmed.ncbi.nlm.nih.gov/16238293
https://pubmed.ncbi.nlm.nih.gov/16238293