Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Donna M. Cyr"'
Publikováno v:
Langmuir. 14:1465-1471
Recent studies have demonstrated that functionalized portions of long-chain hydrocarbons (CH3(CH2)nX, where X = SH, S, SS, NH2, Br, I) physisorbed on graphite at the liquid−solid interface exhibit enhanced contrast (increased tunneling current) whe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73d623d05d66a64dd802dac406badc32
https://doi.org/10.1021/la9707181
https://doi.org/10.1021/la9707181
Publikováno v:
Chemistry of Materials. 8:1600-1615
Investigations of long-chain hydrocarbon and substituted hydrocarbon materials physisorbed at the liquid−solid interface have provided a particularly fruitful area of investigation for the scanning tunneling microscope (STM). Studies of this kind p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4da220c5f915f916d4189fca071e3968
https://doi.org/10.1021/cm960113a
https://doi.org/10.1021/cm960113a
Publikováno v:
The Journal of Physical Chemistry. 100:13747-13759
Monolayer films of several primary substituted hydrocarbons CH3(CH2)nCH2X (X = CH3, OH, NH2, SH, Cl, Br, I; n = 16−30) have been imaged on graphite at the solution−substrate interface using a scanning tunneling microscope (STM). The straight chai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e3c03a35e150c03cab4159c835eac18
https://doi.org/10.1021/jp9606467
https://doi.org/10.1021/jp9606467
Publikováno v:
The Journal of Physical Chemistry. 99:1633-1636
The negative ion zero electron kinetic energy (ZEKE) spectrum of I[sup [minus]]-CH[sub 3]I is presented and discussed. In addition to the high-frequency vibrational structure previously seen in the photoelectron spectrum (PES) of I[sup [minus]]CH[sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b107d9e7746508f740fb4b3c37190638
https://doi.org/10.1021/j100006a002
https://doi.org/10.1021/j100006a002
Autor:
Kenneth B. Wiberg, Donna M. Cyr, Mark A. Johnson, Shinji Nonose, Hideki Tanaka, M. Georgina Scarton, Jun Hirokawa, Tamotsu Kondow, Robert A. Morris
Publikováno v:
Journal of the American Chemical Society. 117:1828-1832
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1148e8cd21cff7a0c7c5c03ef4d4c1f6
https://doi.org/10.1021/ja00111a023
https://doi.org/10.1021/ja00111a023
Publikováno v:
The Journal of Chemical Physics. 101:10507-10520
We describe the reaction dynamics which occur upon excitation of the I−⋅CH3I ion–molecule complex to the first optically allowed excited electronic state. Photoelectron spectroscopy of I−⋅CH3I confirms the identification of the species as e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::631707251aa12d5f6776c7c643236ff2
https://doi.org/10.1063/1.467868
https://doi.org/10.1063/1.467868
Publikováno v:
The Journal of Chemical Physics. 99:4869-4872
The I−⋅CH3I and I−⋅CD3I intermediates in the gas‐phase SN2 identity reaction, I−+CH3I→CH3I+I−, are isolated, cooled in a free jet, and characterized using negative ion photoelectron spectroscopy. The spectra appear similar to bare I
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5ac5b0f3d47580b57f6f22dc91bd6b7
https://doi.org/10.1063/1.466036
https://doi.org/10.1063/1.466036
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ec268441414680c663be8dec366067b
https://doi.org/10.1002/chin.199213051
https://doi.org/10.1002/chin.199213051
Publikováno v:
The Journal of Chemical Physics. 97:5911-5914
Photoelectron spectra of the I−⋅CH3I, I−⋅CH3Br, and I−⋅CH2Br2 complexes each display a relatively sharp main feature shifted from that of I− by the expected binding energies of the ion–dipole bound negative ions. We observe narrow pho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2dc84fb9ffdce49410b22afbba0e0570
https://doi.org/10.1063/1.463752
https://doi.org/10.1063/1.463752
Publikováno v:
Chemical Physics Letters. 181:206-212
We report a rapid increase in the propensity of D 2 O molecules to incorporate into (H 2 O) − n clusters upon collisions between D 2 O and a distribution of (H 2 O − n , 6 n n 2 O) − n distribution are discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bc5968d7ed4ba640d3049234f24eee4
https://doi.org/10.1016/0009-2614(91)90356-e
https://doi.org/10.1016/0009-2614(91)90356-e