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This effect could be due to the more likely occurrence of oxidation under light for the n-type, and/or to its high doping level employed here
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It should be recalled here that monoprotonated 2,2′-bipyridine exists as both syn and anti rotamers, and quantum chemical calculations on the two sets indicate a charge difference of ∼0.6 a.u. between the N atoms of the first set (structures 4-5 in Table 3, but only 0.3-0.4 a.u. for the second set (structures 6-7, This latter result could suggest that a chemical shift of 1 eV is representative of the presence of monoprotonated N atoms selectively in the anti rotamer structures. However, the latter structures are less stable than the syn forms by ∼7 kcal mor-1, and their occurrence on the Si(100) surface should be discarded for thermodynamic reasons
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-1, and their occurrence on the Si(100) surface should be discarded for thermodynamic reasons.
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