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Saturation typically occurred near an (uncalibrated) exposure of ∼6 L. We believe the RAIRS-based measures are not accurate to more than ±10%.
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11744290429
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note
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We also considered the possibility that the splitting arise from cyclopentene adsorbates bound at chemically different or defect sites on the (111) surface. We discount this possibility for two reasons; first, the splitting seen is indepindent of coverage, and, second, the bands are too intense to arise from molecules bound at sites of low number density.
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11744316890
-
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note
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Some literature reports refer to these groups as exo and endo C - H bonds. In our nomenclature, exo and endo ondicate distal and proximal, respectively.
-
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57
-
-
11744276039
-
-
note
-
5-cycloheptadienyl fragments on Pt(111).
-
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-
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60
-
-
11744262880
-
-
note
-
The intensities seen rule out the possibility that one of these bands arises from the C - H oscillators on the rehybridized olefinic carbons.
-
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62
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11744308164
-
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note
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5-cycloheptadienyl fragments on Pt(111).
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0001029331
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The higher-frequency C - H bend seen in Figure 7 is weaker at lower coverges; this may explain why (other than because of the larger noise levels) this feature is not observable for the benzene generated from 1,4-cyclohexadiene, because the spectrum was obtained by dosing at low temperatures and then warming to 350 K. For 1,3-cylobexadiene, the spectrum shown had a higher benzene coverage because the surface was dosed at 350 K until a saturated overlayer was generated.
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2 group that interacts with the surface (See Hostetler, M. J.; Nuzzo, R. G.; Girolami, G. S. J. Am. Chem. Soc. 1995, 117, 1814-1827). With the data now available, we know that this uncharacteristically high-frequwncy band is more properly assigned to the distal C-H strethes of the surface-contacting methylene units. An identical band is seen for cyclohexene.
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